73 results on '"Vitaly I. Kalchenko"'
Search Results
2. Multivalent Calixarene-Based Liposomes as Platforms for Gene and Drug Delivery
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José Antonio Lebrón, Manuel López-López, Clara B. García-Calderón, Ivan V. Rosado, Fernando R. Balestra, Pablo Huertas, Roman V. Rodik, Vitaly I. Kalchenko, Eva Bernal, María Luisa Moyá, Pilar López-Cornejo, and Francisco J. Ostos
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cationic calix[4]arenes ,liposomes ,nucleic acids ,transfection efficiency ,doxorubicin ,encapsulation ,Pharmacy and materia medica ,RS1-441 - Abstract
The formation of calixarene-based liposomes was investigated, and the characterization of these nanostructures was carried out using several techniques. Four amphiphilic calixarenes were used. The length of the hydrophobic chains attached to the lower rim as well as the nature of the polar group present in the upper rim of the calixarenes were varied. The lipid bilayer was formed with one calixarene and with the phospholipid 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine, DOPE. The cytotoxicity of the liposomes for various cell lines was also studied. From the results obtained, the liposomes formed with the least cytotoxic calixarene, (TEAC12)4, were used as nanocarriers of both nucleic acids and the antineoplastic drug doxorubicin, DOX. Results showed that (TEAC12)4/DOPE/p-EGFP-C1 lipoplexes, of a given composition, can transfect the genetic material, although the transfection efficiency substantially increases in the presence of an additional amount of DOPE as coadjuvant. On the other hand, the (TEAC12)4/DOPE liposomes present a high doxorubicin encapsulation efficiency, and a slow controlled release, which could diminish the side effects of the drug.
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- 2021
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- View/download PDF
3. Calix[4]arene-α-hydroxyphosphonic acids. Synthesis, stereochemistry, and inhibition of glutathione S-transferase
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Sergiy O. Cherenok, Olexander A. Yushchenko, Vsevolod Yu. Tanchuk, Iryna M. Mischenko, Nataliya V. Samus, Olexander V. Ruban, Yuriy I. Matvieiev, Julia A. Karpenko, Valery P. Kukhar, Andriy I. Vovk, and Vitaly I. Kalchenko
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Organic chemistry ,QD241-441 - Published
- 2012
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4. Anionic amphiphilic calixarenes for peptide assembly and delivery
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Roman V. Rodik, Sergiy O. Cherenok, Viktoriia Y. Postupalenko, Sule Oncul, Vladyslava Brusianska, Petro Borysko, Vitaly I. Kalchenko, Yves Mely, and Andrey S. Klymchenko
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Anions ,Biomaterials ,Colloid and Surface Chemistry ,Nanoparticles ,Calixarenes ,Peptides ,Micelles ,Surfaces, Coatings and Films ,Electronic, Optical and Magnetic Materials - Abstract
Shape-persistent macrocycles enable superior control on molecular self-assembly, allowing the preparation of well-defined nanostructures with new functions. Here, we report on anionic amphiphilic calixarenes of conic shape and their self-assembly behavior in aqueous media for application in intracellular delivery of peptides. Newly synthesized calixarenes bearing four phosphonate groups and two or four long alkyl chains were found to form micelles of ∼ 10 nm diameter, in contrast to an analogue with short alkyl chains. These amphiphilic calixarenes are able to complex model (oligo-lysine) and biologically relevant (HIV-1 nucleocapsid peptide) cationic peptides into small nanoparticles (20-40 nm). By contrast, a control anionic calixarene with short alkyl chains fails to form small nanoparticles with peptides, highlighting the importance of micellar assembly of amphiphilic calixarenes for peptide complexation. Cellular studies reveal that anionic amphiphilic calixarenes exhibit low cytotoxicity and enable internalization of fluorescently labelled peptides into live cells. These findings suggest anionic amphiphilic macrocycles as promising building blocks for the preparation of peptide delivery vehicles.
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- 2022
5. Тhiacalix[4]arene phosphonate C-800 as a novel fluorescent probe for zinc in living cells
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Bevza Ov, V. I. Yavorovska, Vitaly I. Kalchenko, Labyntseva Rd, S. O. Kosterin Kalchenko, A. B. Drapailo, A. Y. Pugach, and S. O. Cherenok
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mtt assay ,molecular dynamic ,thiacalix[4]arene ,chemistry.chemical_element ,Zinc ,QD415-436 ,Phosphonate ,Combinatorial chemistry ,Fluorescence ,Biochemistry ,chemistry.chemical_compound ,chemistry ,fluorescent probe ,myometrial cells - Abstract
Zn ions are significant for maintaining the proper human organism functioning, thus monitoring the zinc content in living cells and the development of sensitive tracking systems and sensors for Zn is particularly important. The purpose of the work was to study the properties of synthetic thiacalix[4]arene C-800 (5,11,17,23-tetrakis[(hydroxy-ethoxyphosphonyl)methyl])-25,26,27,28-tetrahydroxythiacalix[4]arene) as a fluorescent sensor for zinc ions in living cells. Our studies demonstrated that thiacalix[4]arene C-800 containing four hydroxy-ethoxyphosphonylmethyl groups on the upper rim exhibited fluorescent properties at 340 nm excitation wavelength. Fluorescence intensity of thiacalix[4]arene C-800 was increased significantly in the presence of Zn cations, while cations of other metals, such as Mg2+, Ca2+, Cd2+, and Pb2+ did not affect it. Computer modeling demonstrated that two Zn cations interact with the oxygen atoms of four hydroxy-ethoxyphosphonylmethyl groups. It was shown that thiacalix[4]arene C-800 quickly penetrated rat myometrial cells that led to an increased intracellular fluorescence level. The addition of Zn2+ to cells, stained with thiacalix[4]arene C-800, was followed an even greater increase of intracellular fluorescent signal intensity. No effect of thiacalix[4]arene C-800 on reactive oxygen species production in myometrial cells was detected as well as on cells viability in the range of its 50-250 μM concentrations. Thus, thiacalix[4]arene C-800 can potentially be used as a selective fluorescent probe for the detection of Zn2+ in living cells.
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- 2021
6. Surface Modification of Aminopropylated Silica Gel with Tetraphosphorylated bis-Methoxycarbonylmethoxycalix[4]Arenes for Effective Europium(Iii) Sorption
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Svitlana V. Shishkina, Z. Yu. Bunina, A. A. Golub, R. V. Rodik, Oleksandr A. Yesypenko, Andriy B. Drapailo, L. I. Atamas, K. N. Belikov, A. B. Rozhenko, Vitaly I. Kalchenko, K. Yu. Bryleva, and Yu. S. Boiko
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Phosphine oxide ,Silica gel ,Regioselectivity ,chemistry.chemical_element ,Sorption ,02 engineering and technology ,General Chemistry ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,Phosphonate ,0104 chemical sciences ,chemistry.chemical_compound ,chemistry ,Nitric acid ,Polymer chemistry ,Surface modification ,0210 nano-technology ,Europium - Abstract
bis-Methoxycarbonylmethoxy derivatives capable of reacting with the surface of aminopropylated silica gel with the formation of chemically and thermally stable amide bonds were obtained by regioselective distal dialkylation of hydroxyl groups of phosphorylated tetrahydroxycalix[4]arenes in high yields. It was found that phosphine oxide and phosphonate P=O groups localized on the upper rim cooperatively bind Eu3+ cations and effectively sorb them from nitric acid solutions.
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- 2020
7. Inhibition of Na(+),K(+)-ATPase and activation of myosin ATPase by calix[4]arene C-107 cause stimulation of isolated smooth muscle contractile activity
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Shkrabak Oa, Veklich To, Roman V. Rodik, Kosterin So, Vitaly I. Kalchenko, Labyntseva Rd, and O. V. Tsymbalyuk
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Chemistry ,Myosin ATPase ,myometrium ,myosin atpase ,Stimulation ,plasma membrane ,calix[4]arene ,Biochemistry ,mg(2+)-атраse ,lcsh:Biochemistry ,nа(+)_k(+)-атраse ,Smooth muscle ,Biophysics ,lcsh:QD415-436 ,Na+/K+-ATPase ,smooth muscle cell - Abstract
The discovery of compounds that might modify myometrial contractility is an important area of researches. In our previous experiments, we found that some representatives of macrocyclic compounds family – calix[4]arenes – can modify the enzymatic and transport activity of membrane-bound cation-transport ATP hydrolases. The aim of this work was to study and compare the effect of calix[4]arene C-107 on the enzymatic activities of Mg2+-dependent ATPases of the uterine smooth muscle, namely: ouabain-sensitive Na+,K+-ATPase, plasma membrane Ca2+-independent “basal” Mg2+-ATPase, ATPase of the actomyosin complex and myosin subfragment-1, with effect on the contractile activity of the myometrium. It was shown that calix[4]arene C-107 efficiently inhibited myometrium Na+,K+-ATPase (I50 = 54 ± 6 nM) selectively to other ATP-hydrolases of the plasma membrane and simultaneously activated the enzymatic activity of the myosin ATPase of smooth muscles (A50 = 9.6 ± 0.7 μM). Such reciprocal biochemical effects led to the stimulation of the smooth muscle contractile activity that was demonstrated by the tensometric method using different isolated smooth muscles. Calix[4]arene С-107 was shown to stimulate the increase of the tonic component of myometrium contractions induced by oxytocin, as well as contractions of the caecum muscles induced by high-potassium solution or acetylcholine, and to maintain increased tension for a long time. Thus, calix[4]arene C-107 is a prospective compound for enhancing the smooth muscle basal tone and/or contraction in case of hypotonic dysfunctions.
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- 2020
8. Multivalent Calixarene-Based Liposomes as Platforms for Gene and Drug Delivery
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Manuel López-López, Pablo Huertas, María Luisa Moyá, Eva Bernal, Clara B. García-Calderón, José Antonio Lebrón, Iván V. Rosado, Pilar López-Cornejo, Francisco José Ostos, Fernando R. Balestra, Vitaly I. Kalchenko, Roman V. Rodik, [Lebrón,JA, Bernal,E, Moyá,ML, López-Cornejo,P, Ostos,FJ] Department of Physical Chemistry, Faculty of Chemistry, University of Seville, Seville, Spain. [López-López,M] Department of Chemical Engineering, Physical Chemistry and Materials Science, Faculty of Experimental Sciences, University of Huelva, Huelva, Spain. [García-Calderón,CB, V. Rosado,I] Institute of Biomedicine of Seville (IBiS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain. [Balestra,FR, Huertas,P] Department of Genetics, Faculty of Biology, University of Seville, Seville, Spain. [Balestra,FR, Huertas,P] Andalusian Center of Molecular Biology and Regenerative Medicine (CABIMER), University of Seville-CSIC-University Pablo de Olavide, Seville, Spain. [Rodik,RV, Kalchenko,VI] Institute of Organic Chemistry, National Academy of Science of Ukraine, Kiev, Ukraine., This work was financed by the Consejería de Conocimiento, Innovación y Universidades de la Junta de Andalucía (FQM-206, FQM-274, and PY20-01234), the VI Plan Propio Universidad de Sevilla (PP2019/00000748), RTI2018-100692-B-100, P18-RT-1271, PI18-0005-2018, VI-PP AY.SUPLEM 2019, RYC-2015-18670, The R+D+I grant PID2019-104195G from the Spanish Ministry of Science and Innovation-Agencia Estatal de investigación/10.13039/501100011033 (P.H.) and the European Union (Feder Funds). The authors thank the University of Seville for the grant VPPI-US. J.A.L. also thanks the Fundación ONCE funded by the Fondo Social Europeo., Junta de Andalucía, Universidad de Sevilla, Agencia Estatal de Investigación (España), Ministerio de Ciencia, Innovación y Universidades (España), Ministerio de Economía y Competitividad (España), European Commission, Fundación ONCE, Universidad de Sevilla. Departamento de Química Física, and Universidad de Sevilla. Departamento de Genética
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liposomes ,Chemicals and Drugs::Organic Chemicals::Hydrocarbons::Hydrocarbons, Cyclic::Hydrocarbons, Aromatic::Polycyclic Hydrocarbons, Aromatic::Naphthacenes::Anthracyclines::Daunorubicin::Doxorubicin [Medical Subject Headings] ,Chemicals and Drugs::Pharmaceutical Preparations::Dosage Forms::Delayed-Action Preparations [Medical Subject Headings] ,Doxorrubicina ,Phospholipid ,Pharmaceutical Science ,Technology and Food and Beverages::Technology, Industry, and Agriculture::Manufactured Materials::Nanostructures [Medical Subject Headings] ,doxorubicin ,Chemicals and Drugs::Nucleic Acids, Nucleotides, and Nucleosides::Nucleic Acids [Medical Subject Headings] ,Article ,chemistry.chemical_compound ,Pharmacy and materia medica ,Anatomy::Cells::Cells, Cultured::Cell Line [Medical Subject Headings] ,Amphiphile ,Calixarene ,23 Química ,Lipid bilayer ,transfection efficiency ,cationic calix[4]arenes ,Liposome ,Chemistry ,Chemicals and Drugs::Chemical Actions and Uses::Pharmacologic Actions::Therapeutic Uses::Antineoplastic Agents [Medical Subject Headings] ,technology, industry, and agriculture ,Transfection efficiency ,Combinatorial chemistry ,Controlled release ,Cationic calix[4]arenes ,RS1-441 ,Nucleic acids ,Chemicals and Drugs::Polycyclic Compounds::Macrocyclic Compounds::Calixarenes [Medical Subject Headings] ,nucleic acids ,Liposomas ,Encapsulación celular ,Doxorubicin ,Drug delivery ,Liposomes ,encapsulation ,Ácidos nucleicos ,lipids (amino acids, peptides, and proteins) ,Encapsulation ,Nanocarriers ,Chemicals and Drugs::Biomedical and Dental Materials::Membranes, Artificial::Liposomes [Medical Subject Headings] ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Genetic Techniques::Gene Transfer Techniques::Transfection [Medical Subject Headings] - Abstract
The formation of calixarene-based liposomes was investigated, and the characterization of these nanostructures was carried out using several techniques. Four amphiphilic calixarenes were used. The length of the hydrophobic chains attached to the lower rim as well as the nature of the polar group present in the upper rim of the calixarenes were varied. The lipid bilayer was formed with one calixarene and with the phospholipid 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine, DOPE. The cytotoxicity of the liposomes for various cell lines was also studied. From the results obtained, the liposomes formed with the least cytotoxic calixarene, (TEAC12)4, were used as nanocarriers of both nucleic acids and the antineoplastic drug doxorubicin, DOX. Results showed that (TEAC12)4/DOPE/p-EGFP-C1 lipoplexes, of a given composition, can transfect the genetic material, although the transfection efficiency substantially increases in the presence of an additional amount of DOPE as coadjuvant. On the other hand, the (TEAC12)4/DOPE liposomes present a high doxorubicin encapsulation efficiency, and a slow controlled release, which could diminish the side effects of the drug., This work was financed by the Consejería de Conocimiento, Innovación y Universidades de la Junta de Andalucía (FQM-206, FQM-274, and PY20-01234), the VI Plan Propio Universidad de Sevilla (PP2019/00000748), RTI2018-100692-B-100; P18-RT-1271; PI18-0005-2018; VI-PP AY.SUPLEM- 2019; RYC-2015-18670, The R+D+I grant PID2019-104195G from the Spanish Ministry of Science and Innovation-Agencia Estatal de Investigación/10.13039/501100011033 (P.H.) and the European Union (Feder Funds). The authors thank the University of Seville for the grant VPPI-US. J.A.L. also thanks the Fundación ONCE funded by the Fondo Social Europeo.
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- 2021
9. Recognition and Binding of Aliphatic Dicarboxylic Acids C4 – C10 by Diiminocalix[4]arene
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Vitaly I. Kalchenko, Andrew Solovyov, and O. I. Kalchenko
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Partition coefficient ,Oxygen atom ,chemistry ,Molecular model ,Hydrogen bond ,Calixarene ,Supramolecular chemistry ,chemistry.chemical_element ,Nitrogen ,Medicinal chemistry - Abstract
Host - Guest complexation of 5,17- bis- ( N - tolyliminomethyl )-25,27- dipropoxycalix [4] arene with aliphatic di carboxylic acids C4 – C10 has been studied in water-organic solution by the RP HPLC and molecular modeling methods. T he stability constants (log K A = 2.56 – 3.05) of the supramolecular complexes are depended on structure, pKa and log P values of the acids . The complexation is determined by the hydrogen bonds of the COOH group of the dicarboxylic acids with nitrogen atoms at the upper rim or oxygen atoms at the lower rim of the calixarene.
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- 2019
10. Self-aggregation in aqueous solution of amphiphilic cationic calix[4]arenes. Potential use as vectors and nanocarriers
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Manuel López-López, Vitaly I. Kalchenko, María Luisa Moyá, Iván V. Rosado, Pilar López-Cornejo, Margarita García-Calderón, Clara B. García-Calderón, Francisco José Ostos, José Antonio Lebrón, Roman V. Rodik, Junta de Andalucía, Universidad de Sevilla, Ministerio de Ciencia, Innovación y Universidades (España), Agencia Estatal de Investigación (España), Ministerio de Economía y Competitividad (España), and European Commission
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Compaction ,02 engineering and technology ,010402 general chemistry ,01 natural sciences ,Micelle ,Calixarene ,Amphiphile ,Materials Chemistry ,Vesicles ,Physical and Theoretical Chemistry ,Spectroscopy ,Micelles ,Aqueous solution ,Chemistry ,Vesicle ,Cationic polymerization ,ctDNA ,021001 nanoscience & nanotechnology ,Condensed Matter Physics ,Combinatorial chemistry ,Atomic and Molecular Physics, and Optics ,0104 chemical sciences ,Electronic, Optical and Magnetic Materials ,Polynucleotide ,Doxorubicin ,Nanocarriers ,Calixarenes ,0210 nano-technology - Abstract
The self-aggregation of four amphiphilic cationic calix[4]arenes, CALIX, in aqueous solutions was investigated in this work. The nature of the polar group present at the upper rim as well as the length of the hydrophobic tails attached to the lower rim was varied. All the calixarenes present two critical aggregation concentrations, CAC1 and CAC2. For [CALIX] < CAC1 only micelles are present, within the range CAC1 < [CALIX] < CAC2 micelles as well as vesicles are observed, and for [CALIX] > CAC2 micelles and a wide distribution of vesicles were found. Cell viability experiments show that calixarene micelles and several of the calixarene vesicles investigated could be used as biocompatible nanocarriers. On this basis, the study of the interactions between the cationic calixarene aggregates (micelles and vesicles) and calf thymus DNA, ctDNA, were done and the results indicated that most of them strongly interact with the polynucleotide, inverting its charge. Micelles totally compact the ctDNA, while vesicles only partially cause conformational changes in the nucleic acid. Therefore, the CALIX micelles show potential as vectors in gene therapy. The encapsulation of the antineoplastic drug doxorubicin into the calixarene aggregates was also investigated. A high encapsulation efficiency was found for micelles and, specially, for vesicles. However, DOX-loaded calixarene vesicles present low stability at 37 °C, which is a serious restriction in their use as nanocarriers for this drug. The release of DOX from the calixarene micelles shows that they could lengthen the half-life of free doxorubicin in the body and, as a result, lower amounts of drug could be used in the cancer treatments diminishing the important side effects of DOX., This work was supported by the Consejería de Educación y Ciencia de la Junta de Andalucía (P12-FQM-1105, FQM-206 and FQM-274, and PI-0005-2018), the VI Plan Propio Universidad de Sevilla (PP2018-10338), the Ministerio de Ciencia, Innovación y Universidades (RTI2018-100692-B-I00), the grant Ramon y Cajal RYC2015-1867 and the European Union (Feder Funds). The authors thank the University of Seville for the grant VPPI-US.
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- 2020
11. (Thia)calixarenephosphonic Acids as Potent Inhibitors of the Nucleic Acid Chaperone Activity of the HIV-1 Nucleocapsid Protein with a New Binding Mode and Multitarget Antiviral Activity
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Nicolas Humbert, Maurizio Botta, Federica Poggialini, Eleonore Real, Manuel Pires, Christian Boudier, Vitaly I. Kalchenko, Yves Mély, Alessia Giannini, Maurizio Zazzi, Carole Seguin-Devaux, Sarah Cianférani, S. O. Cherenok, Kamal Kant Sharma, Mattia Mori, Francesco Saladini, Thomas Botzanowski, Lesia Kovalenko, Olga A. Zaporozhets, Laboratoire de Bioimagerie et Pathologies (LBP), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Département Sciences Analytiques et Interactions Ioniques et Biomoléculaires (DSA-IPHC), Institut Pluridisciplinaire Hubert Curien (IPHC), Université de Strasbourg (UNISTRA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), National Taras Shevchenko University of Kiev, Centre de Recherche Public de la Santé, Università degli Studi di Siena = University of Siena (UNISI), Institute of Organic Chemistry of NASU [Kyiv], and National Academy of Sciences of Ukraine (NASU)
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0301 basic medicine ,calixarenes ,Anti-HIV Agents ,030106 microbiology ,Organophosphonates ,Aucun ,Mice, Transgenic ,Molecular Dynamics Simulation ,03 medical and health sciences ,chemistry.chemical_compound ,Inhibitory Concentration 50 ,Mice ,Calixarene ,Animals ,[CHIM]Chemical Sciences ,Zinc finger ,biology ,Chemistry ,Isothermal titration calorimetry ,Nucleocapsid Proteins ,NC inhibitors ,Phosphonate ,Reverse transcriptase ,3. Good health ,030104 developmental biology ,Infectious Diseases ,Biochemistry ,Chaperone (protein) ,biology.protein ,Nucleic acid ,HIV-1 ,fluorescence ,Fluorescence anisotropy ,nucleocapsid protein ,Molecular Chaperones ,Protein Binding - Abstract
International audience; The nucleocapsid protein (NC) is a highly conserved protein that plays key roles in HIV-1 replication through its nucleic acid chaperone properties mediated by its two zinc fingers and basic residues. NC is a promising target for antiviral therapy, particularly to control viral strains resistant to currently available drugs. Since calixarenes with antiviral properties have been described, we explored the ability of calixarene hydroxymethylphosphonic or sulfonic acids to inhibit NC chaperone properties and exhibit antiviral activity. By using fluorescence-based assays, we selected four calixarenes inhibiting NC chaperone activity with submicromolar IC50 values. These compounds were further shown by mass spectrometry, isothermal titration calorimetry, and fluorescence anisotropy to bind NC with no zinc ejection and to compete with nucleic acids for the binding to NC. Molecular dynamic simulations further indicated that these compounds interact via their phosphonate or sulfonate groups with the basic surface of NC but not with the hydrophobic plateau at the top of the folded fingers. Cellular studies showed that the most soluble compound CIP201 inhibited the infectivity of wild-type and drug-resistant HIV-1 strains at low micromolar concentrations, primarily targeting the early steps of HIV-1 replication. Moreover, CIP201 was also found to inhibit the flipping and polymerization activity of reverse transcriptase. Calixarenes thus form a class of noncovalent NC inhibitors, endowed with a new binding mode and multitarget antiviral activity.
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- 2020
12. Calix[4]arene С-956 selectively inhibits plasma membrane Са(2+),Mg(2+)-АТРase in myometrial cells
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Yu. V. Nikonishyna, Kosterin So, O. A. Skrabak, Т. O. Veklich, Roman V. Rodik, and Vitaly I. Kalchenko
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0301 basic medicine ,calix[4]arenes ,M.2 ,Chemistry ,myometrium ,enzymatic hydrolysis of ATP ,Plasma ,plasma membrane ,Biochemistry ,Ca(2+)-Mg(2+)-ATPase ,smooth muscle cells ,lcsh:Biochemistry ,03 medical and health sciences ,030104 developmental biology ,Membrane ,Biophysics ,lcsh:QD415-436 - Abstract
Using enzymatic assays and kinetic analysis, we demonstrated that 100 µM calix[4]arene C-956 (5,11,17,23-tetra(trifluoro)methyl-(phenylsulfonylimino) methylamino-25,27-dioctyloxy-26,28-dipropoxycalix[4]arene) had the most significant inhibitory effect on the plasma membrane Са2+,Mg2+-АТРase activity compared to effects of other calix[4]arenes, and had no effect on specific activities of other membrane ATPases. Using confocal microscopy and fluorescent probe fluo-4, we observed an increase of the intracellular level of Ca2+ after application of calix[4]arene C-956 to immobilized myocytes. Analysis of the effect of calix[4]arene C-956 on the hydrodynamic diameter of myocytes demonstrated that application of calix[4]arene C-956 solution decreased this parameter by 45.5 ± 9.4% compared to control value similarly to the action of uterotonic drug oxytocin.
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- 2018
13. The assessment of sulfonylcalix[4]arene derivatives as inhibitors of protein tyrosine phosphatases
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A. B. Drapailo, Oleksandr L. Kobzar, V. M. Buldenko, Viacheslav V. Trush, Vitaly I. Kalchenko, Andriy I. Vovk, and S. G. Vyshnevsky
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Chemistry ,Stereochemistry ,Protein tyrosine phosphatase - Abstract
Мета роботи. Порівняння похідних сульфонілкалікс[4]арену, які містять здатні та нездатні до іонізації залишки на верхньому вінці макроциклу, як інгібіторів РТР1В та інших протеїнотирозинфосфатаз. Результати та їх обговорення. Властивості сульфонілкалікс[4]арену з чотирма фосфонатними групами, приєднаними до верхнього вінця макроциклу, порівнювалися з властивостями сполук, які містять чотири трет-бутильні або трифторацетамідні замісники. Було встановлено, що сульфонілкалікс[4]арентетракіс-метилфосфонова кислота інгібує PTP1B зі значенням IC50 в низькомікромолярному діапазоні без селективності стосовно інших PTPаз, таких як TC-PTP, MEG1, MEG2, SHP2 та PTPβ. Модифікація сульфонілкалікс[4]арену залишками трифторацетаміду забезпечила інгібування PTP1B зі значенням IC50 1,4 мкМ з 4-28-кратною селективністю відносно інших PTPаз. Для з’ясування інгібувальної здатності похідної сульфонілкалікс[4]арену з трифторацетамідними замісниками відносно PTP1B було застосовано молекулярний докінг та моделювання методом молекулярної динаміки. Обговорюється можливий механізм інгібування. Експериментальна частина. Активність сполук досліджували спектрофотометрично, вимірюючи швидкість ферментативного гідролізу п-нітрофенілфосфату як субстрату протеїнотирозинфосфатаз. Молекулярний докінг було виконано за допомогою AutoDock Vina. Висновки. Це дослідження може бути основою нового підходу до розробки інгібіторів PTPаз шляхом модифікації верхнього вінця сульфонілкалікс[4]аренового каркасу неіоногенними замісниками.
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- 2018
14. Functional Calixarene Nanostructures
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Vitaly I. Kalchenko
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chemistry.chemical_classification ,Fluorescent nanoparticles ,Nanostructure ,010405 organic chemistry ,Chemistry ,Biomolecule ,General Chemistry ,010402 general chemistry ,01 natural sciences ,Combinatorial chemistry ,0104 chemical sciences ,Catalysis ,Organic molecules ,Adsorption ,Organic reaction ,Calixarene - Abstract
The results of the author studies of functional calixarene nanostructures are summarized. Calixarenes modified by various functional groups were created with receptor properties relative to cations, anions, gases, organic molecules and biomolecules. Calixarene nanostructures have been used to develop extraction and adsorption agents for radionuclides, sensitive elements of chemosensors, porous materials for gas adsorption, stereoselective catalysts for organic reactions, biologically-active compounds, inhibitors of therapeutically-important enzymes, vectors for gene transfection, and fluorescent nanoparticles for cell visualization.
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- 2018
15. Phosphorylated thiacalixarenes as molecular receptors for QCM sensors of volatile compounds
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Sergiy G. Kharchenko, Vitaly I. Kalchenko, A.B. Ryabitskii, S.V. Shishkina, Alexander Belyaev, O.V. Shishkin, I.A. Koshets, Z.I. Kazantseva, and A. B. Drapailo
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010405 organic chemistry ,Chemistry ,Biophysics ,Phosphorylation ,General Materials Science ,Characterization and properties ,Quartz crystal microbalance ,010402 general chemistry ,Receptor ,01 natural sciences ,0104 chemical sciences - Abstract
Sorption of volatile organic compounds and ammonia by thin solid films of phosphorylated thiacalixarenes was investigated by the quartz crystal microbalance (QCM), X-ray crystallography and molecular modeling methods The interfacial sorption depends on the number and position (upper or lower rim) of P=O groups on the macrocyclic skeleton, the electronic nature of the substituents at the phosphorus atom. At low concentrations of the analytes their sorption occurs according to the Langmuir isotherm due to specific supramolecular interactions with receptor centers of the thiacalixarenes. The analytes may form either the Host-Guest inclusion complexes stabilized by C-H...π interactions, or extracavity complexes stabilized by hydrogen bonds with oxygen atoms of the peripheral P=O groups. At high concentrations, when the thiacalixarene receptor centers are occupied by the analytes, further sorption occurs nonspecifically according to the linear Henry isotherm due to inclusion of the analytes in voids of the crystal structure of the thiacalixarenes.
- Published
- 2017
16. The inhibitory potential of calixarenes against nucleotide pyrophosphatase/phosphodiesterase 1
- Author
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Lyudmyla A. Kononets, Oleksandr L. Kobzar, Vitaly I. Kalchenko, A. B. Drapailo, S. G. Vyshnevsky, V. M. Buldenko, and Andriy I. Vovk
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chemistry.chemical_classification ,Hydrolysis ,Enzyme ,Chemistry ,Covalent bond ,Stereochemistry ,Calixarene ,Phosphatase ,Phosphodiesterase ,Substrate (chemistry) ,AutoDock - Abstract
It has been previously shown that phosphonic acids covalently attached to the macrocyclic platform of calix[4]arenes are capable of inhibiting alkaline phosphatases. In this paper the effects of the upper-rim functionalized calix[4]arenes on the activity of nucleotide pyrophosphatase/phosphodiesterase 1 (NPP1) have been examined. Aim. To assess the inhibitory potential of calix[4]arene, thiacalix[4]arene and sulfonylcalix[4]arene derivatives against NPP1. Results and discussion. It has been found that calix[4]arene, thiacalix[4]arene, and sulfonylcalix[4]arene tetrakismethylphosphonic acids inhibit NPP1 with the IC50 values in the micromolar range. The derivatives of sulfonylcalix[4]arene demonstrated the selectivity of inhibition of NPP1 over alkaline phosphatases. In addition, sulfonylcalix[4]arene tetrakismethylphosphonic acid was able to inhibit the nucleotide pyrophosphatase/phosphodiesterase activity of the human serum. The possible mechanism of the inhibition has been discussed. Experimental part. The activity of NPP1 was monitored by spectrophotometry measuring the rate of hydrolysis of bis-p-nitrophenyl phosphate. The phosphodiesterase activity of the human serum was assessed in the presence of p-nitrophenyl ester of thymidine-5-monophosphate as a substrate. The homology model of the human NPP1 was generated based on the crystal structure of the murine enzyme. The molecular docking was performed using AutoDock 4.2. Conclusions. The results obtained have shown the ability of sulfonylcalix[4]arene derivatives to inhibit the activity of NPP1 in vitro, including the nucleotide pyrophosphatase/phosphodiesterase activity in the human blood serum.
- Published
- 2017
17. The study of calixarenes complexation with phenols by RP HPLC
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O. I. Kalchenko, S. O. Cherenok, A. V. Solovyov, Vitaly I. Kalchenko, and S. Yu. Suikov
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chemistry.chemical_classification ,Hydrophobic effect ,chemistry.chemical_compound ,chemistry ,Hydrogen bond ,Calixarene ,Supramolecular chemistry ,Organic chemistry ,Molecule ,Phenols ,Resorcinarene ,Aldehyde ,Medicinal chemistry - Abstract
The Host-Guest complexation of octakis(diphenoxyphosphoryloxy)tetramethylcalix[4]resorcinarene, 5,17-bis-(N-tolyliminomethyl)-25,27-dipropoxycalix[4]arene and 5,11,17,23-tetrakis(diisopropoxyphosphonyl)-25,26,27,28-tetrapropoxycalix[4]arene with a series of 11 phenols (phenol, p-fluorophenol, p-chlorophenol, p-bromophenol, pyrogallol, p-cresol, p-aminophenol, p-nitrophenol, salicylic aldehyde, guaiacol and veratrole) has been studied by the high-performance liquid chromatography (RP HPLC) method. Chromatographic characteristics and log P of industrial phenols have been determined. Using the relationship of the phenol retention factor k’ vs the calixarene concentration in the mobile phase the stability constants of the supramolecular complexes K A (29-331 M -1 ) have been determined. The stability constants of the calixarene complexes show that the Host-Guest interaction strongly depends on the nature of the substituents in the Host and Guest molecules. Calixresorcinarene functionalized by diphenoxyphosphoryl groups and calixarene containing tolyliminomethyl groups formed more stable complexes with some phenols compared to calixarene functionalized by diisopropoxyphosphonyl groups. In accordance with the molecular modeling data the complexation does not change the C2v flattened-cone conformation of the calixarene skeleton. The Host-Guest complexes are stabilized by the intermolecular hydrogen bonds of phenolic OH groups with oxygen atoms of P = O groups at the upper rim, and OH groups at the lower rim of the macrocycle. Hydrophobic interactions also participate in the complexation.
- Published
- 2017
18. Sulfonyl-bridged Calix[4]arene as an Inhibitor of Protein Tyrosine Phosphatases
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V. M. Buldenko, Oleksandr L. Kobzar, Viacheslav V. Trush, Andriy I. Vovk, Andriy B. Drapailo, and Vitaly I. Kalchenko
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Sulfonyl ,chemistry.chemical_classification ,biology ,010405 organic chemistry ,Chemistry ,Stereochemistry ,Active site ,Protein tyrosine phosphatase ,010402 general chemistry ,01 natural sciences ,Protein Tyrosine Phosphatase 1B ,0104 chemical sciences ,Phosphonic acid derivatives ,biology.protein ,Lower activity - Abstract
Previously, phosphonic acid derivatives of calix[4]arene and thiacalix[4]arene were found to be potential inhibitors of protein tyrosine phosphatase 1B. In the present paper, the inhibitory activity of unsubstituted sulfonyl-bridget calix[4]arene towards some of the therapeutically important protein tyrosine phosphatases has been established. The obtained results showed that the sulfonylcalix[4]arene is able to inhibit protein tyrosine phosphatase MEG2 with IC50 value in the micromolar range. At the same time, the inhibitor demonstrated lower activity in case of other protein tyrosine phosphatases such as PTP1B, MEG1, TC-PTP, SHP2, and PTPβ. The performed molecular docking indicated that the inhibitor binds to the active site region of MEG2 and PTP1B with WPD-loop in the open conformation.
- Published
- 2017
19. Calixarene Derivatives for (Nano)Biotechnologies
- Author
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Vitaly I. Kalchenko, Roman V. Rodik, and Mykola M. Poberezhnyk
- Subjects
Chemistry ,Organic Chemistry ,Nano ,Calixarene ,Nanotechnology ,Analytical Chemistry - Published
- 2017
20. Study of Calixarene Complexation with Biologically Active
- Author
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Vitaly I. Kalchenko, O. I. Kalchenko, S. O. Cherenok, and Sergiy Suikov
- Subjects
Partition coefficient ,chemistry.chemical_compound ,chemistry ,Hydrogen bond ,Pyridine ,Calixarene ,Supramolecular chemistry ,chemistry.chemical_element ,Molecule ,Resorcinarene ,Oxygen ,Medicinal chemistry - Abstract
Host-Guest complexation of octakis(diphenoxyphosphoryloxy)tetramethylcalix[4]resorcinarene CRA and 5,17-bis-(N-tolyliminomethyl)-25,27-dipropoxycalix[4]arene CA with bio relevant aromatic, pyridine and diterpenoid carboxylic acids in water-organic solution had been studied by the RP HPLC and molecular modelling methods. The stability constants KA (387-1914 М-1) of the supramolecular complexes had been determined. It was shown the Host-Guest interactions are depended on structure of the Host molecules and log P values of the Guests. The complexation is determined by the hydrogen bonds of the COOH group of the carboxylic acids with P=O oxygen atom of diphenoxyphosphoryl group of the calixresorcinarene CRA, and oxygen or nitrogen atoms located on the lower or the upper rim of the calixarene CA.
- Published
- 2017
21. Reaction rates in aqueous solutions of cationic colloidal surfactants and calixarenes: Acceleration and resolution of two steps of fluorescein diesters hydrolysis
- Author
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Nikolay O. Mchedlov-Petrossyan, Vitaly I. Kalchenko, Yulia V. Taranets, Roman V. Rodik, Tatyana A. Cheipesh, Daria V. Kharchenko, and Mykola M. Poberezhnyk
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Aqueous solution ,Cationic polymerization ,02 engineering and technology ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,Micelle ,0104 chemical sciences ,Reaction rate ,chemistry.chemical_compound ,Colloid and Surface Chemistry ,Reaction rate constant ,chemistry ,Bromide ,Micellar solutions ,Calixarene ,Polymer chemistry ,0210 nano-technology - Abstract
The hydrolysis of fluorogenic substrates of fluorescein diester series is a popular and well-documented indicative reaction used in enzyme biochemistry for cholinesterase systems and related fields. The overwhelming majority of studies have been performed using the fluorescence spectroscopy and conventionally considering this two-step reaction as a single-step one. We developed a spectrophotometry-based approach for the separate determination of the rate constants of the first and second hydrolysis steps of fluorescein diesters, such as diacetyl- and dilaurylfluorescein. This approach was applied to micellar solutions of cationic colloidal surfactants and calixarenes in water. Cationic surfactants cetyltrimethylammonium bromide, cetyl-N-pyridinium chloride, cationic Gemini surfactant 16–4–16 bromide, di-n-tetradecyldimethylammonium bromide and a zwitterionic surfactant cetyldimethylammonium propanesulfonate were used. As amphiphilic cationic calixarenes, the wide rim choline or imidazolium derivatives of calix[4,6]arenes decorated at the narrow rim with methyl, propyl, hexyl, octyl, and dodecyl tails in form of tetra- and hexachlorides were used. These systems display marked acceleration of the hydrolysis reaction of diacetylfluorescein in water. The results were compared with the kinetic data in 50 mas. % ethanol. Non-ionic surfactant Triton X-100 displays no influence on kinetics, whereas an anionic surfactant sodium laurylsulfate strongly reduces the reaction rate. In the presence of calixarene aggregates, an expressed catalytic effect was observed for diacetylfluorescein, but not for dilaurylfluorescein. For instance, the rate constants of stepwise hydrolysis of diacetylfluorescein increase by ca. 200–750 times on going from water to aqueous solutions of 5,11,17,23-tetra(N,N-dimethyl-N-hydroxyethylammonium)methylene-25,26,27,28-tetradodecyl-oxycalix[4]arene tetrachloride. At the same time, a distinct macrocyclic effect of calixarene was also observed: the micelles of the “quarter” compound N,N-dimethyl-N-hydroxyethyl-4-dodecyloxybenzylammonium chloride also accelerate the reaction, but in a much less expressed manner.
- Published
- 2020
22. Unprecedented Increase in Affinity for Eu III over Am III through Silica Grafting of a Carbamoylmethylphosphine Oxide‐Calix[4]arene Site
- Author
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Heino Nitsche, Andriy B. Drapailo, Andrew Solovyov, Yury I. Matveev, Alexander Katz, Erin M. May, Yijun Guo, and Vitaly I. Kalchenko
- Subjects
Lanthanide ,Ligand ,Inorganic chemistry ,Supramolecular chemistry ,Oxide ,02 engineering and technology ,010402 general chemistry ,021001 nanoscience & nanotechnology ,Grafting ,01 natural sciences ,0104 chemical sciences ,Inorganic Chemistry ,chemistry.chemical_compound ,chemistry ,Polymer chemistry ,Calixarene ,0210 nano-technology - Abstract
Grafting of a carbamoylmethylphosphine oxide (CMPO) calix[4]arene ligand to the silica surface yields an anchored host site that displays an unusual 22.4-fold higher affinity (kD value) for EuIII relative to AmIII. This selective cation recognition is in stark contrast to a more flexible propoxy-tethered CMPO-calix[4]arene site on silica.
- Published
- 2016
23. Дослідження комплексоутворення калікс[4]aрену та калікс[4]резорцинарену із смоляними кислотами методом ОФ ВЕРХ. Визначення констант зв’язування
- Author
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Vitaly I. Kalchenko, A. V. Solovyov, S. Yu. Suikov, Valery V. Gorbatchuk, O. I. Kalchenko, and S. O. Cherenok
- Subjects
Chemistry ,Hydrogen bond ,Stereochemistry ,УДК 547.03+547.562 ,Supramolecular chemistry ,chemistry.chemical_element ,Resorcinarene ,каликс[4]арены ,смоляные кислоты ,обращенно-фазная высокоэффективная жидкостная хроматография ,комплексы включения ,константы связывания ,молекулярное моделирование ,Nitrogen ,Medicinal chemistry ,Gibbs free energy ,Partition coefficient ,calix[4]arenes ,resin acids ,reversed-phase high performance liquid chromatography ,inclusion complexes ,binding constants ,molecular modelling ,symbols.namesake ,UDC 547.03+547.562 ,Lipophilicity ,symbols ,Solvophobic ,калікс[4]арени ,смоляні кислоти ,обернено-фазна високоефективна рідинна хроматографія ,комплекси включення ,константи зв’язування ,молекулярне моделювання - Abstract
Комплексоутворення типу Гість-Господар oктакіс-(дифеноксифосфорилокси)-тетраметилкалікс[4]резорцинарену (CR) та 5,17-біс-(N-толілімінометил)-25,27-дипропоксикалікс[4]aрену (CA) з 6 дитерпеноїдними (смоляними) кислотами було досліджено методом обернено-фазної високоефективної рідинної хроматографії (ОФ ВЕРХ). Визначені хроматографічні характеристики (час утримання tR тa фактор утримання k’) смоляних кислот. Розраховано значення ліпофільності log P смоляних кислот тa констант зв’язування KA комплексів (395-682 М-1 для CR тa 844-1268 М-1 для CA), а також значення вільних енергій Гіббса ∆G (-14.79 – -16.14 кДж/моль для CR тa -16.70 – -17.67 кДж/моль для CA) із смоляними кислотами. Молекулярне моделювання комплексів CA вказало на присутність водневих зв’язків між карбоксильними групами кислот тa атомами азоту іміно-груп верхнього вінця CA макроцилу або атомами кисню ОН груп його нижнього вінця. Молекулярне моделювання комплексів CR вказало на присутність водневих зв’язків між карбоксильними групами кислот тa атомами кисню дифеноксифосфорилокси-груп верхнього вінця макроциклу CR. Здійснено оцінку впливу log P на константи зв’язування KA комплексів CR/CA. Лінійна залежність КА від log P кислот вказує на роль сольвофобних взаємодій на комплексоутворення. Встановлено взаємозв’язок між супрамолекулярними (KA) тa фізико-хімічними (log P, pKa) характеристиками кислот., The Host-Guest complexation of octakis-(diphenoxyphosphoryloxy)tetramethylcalix[4]resorcinarene (CR) and 5,17-bis-(N-tolyliminomethyl)-25,27-dipropoxycalix[4]arene (CA) with 6 diterpenoid (resin) acids has been studied by the reversed phase high-performance liquid chromatography (RP HPLC). The chromatographic characteristics (retention time tR and retention factor k’) of resin acids have been determined. The lipophilicity values log P of the acids, binding constants KA (395-682 M-1 for CR and 844-1268 M-1 for CA), as well as Gibbs free energies ∆G (-14.79 – -16.14 kJ/mol for CR and -16.70 – -17.67 kJ/mol for CA) of the complexes with resin acids have been calculated. Molecular modelling of CA complexes has revealed the presence of hydrogen bonds between carboxylic groups of acids and nitrogen atoms of imino groups at the upper rim or oxygen atoms of the hydroxyl groups at the lower rim of the CA macrocycle. Molecular modelling of CR complexes has shown the presence of hydrogen bonds between carboxylic groups of acids and oxygen atoms of diphenoxyphosphoryloxy groups at the upper rim of the CR macrocycle. The effect of log P values on KA values of the CR/CA complexes has been assessed. The linear dependence of the binding constants on the acid lipophilicity indicates a significant role of solvophobic interactions on the complexation. The relationship between supramolecular (KA) and physicochemical (log P, pKa) characteristics of acids has been determined., Комплексообразование типа Гость-Хозяин oктакис-(дифеноксифосфорилокси)-тетраэтилкаликс[4]резорцинарена (CR) и 5,17-бис-(N-толилиминометил)-25,27-дипропоксикаликс[4]aрена (CA) с 6 дитерпеноидными ( смоляными) кислотами было исследовано методом обращенно-фазной высокоэффективной жидкостной хроматографии (ОФ ВЭЖХ). Определены хроматографические характеристики (время удерживания tR и фактор удерживания k’) смоляных кислот. Рассчитаны значения липофильности log P смоляных кислот и констант связывания KA их комплексов (395-682 М-1 для CR и 844-1268 М-1 для CA), а также значения свободных энергий Гиббса ∆G (-14.79 – -16.14 кДж/моль для CR и -16.70 – -17.67 кДж/моль для CAL) со смоляными кислотами. Молекулярное моделирование комплексов CA показало наличие водородных связей между карбоксильными группами кислот и атомами азота имино-групп верхнего обода макроцикла CA или атомами кислорода гидроксильных групп его нижнего обода. Молекулярное моделирование комплексов CR показало наличие водородных связей между карбоксильными группами кислот и атомами кислорода дифеноксифосфорилокси-групп верхнего обода макроцикла CR. Оценено влияние log P на константы связывания KA комплексов CR/CA. Линейная зависимость КА от log P кислот свидетельствует о влиянии сольвофобных взаимодействий на процесс комплексообразования.
- Published
- 2016
24. Chiral Phosphinoferrocenyl-Calixarenes
- Author
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Jean-Claude Daran, Rinaldo Poli, V. I. Boiko, Andrii Karpus, Eric Manoury, Zoia Voitenko, Vitaly I. Kalchenko, and Oleksandr A. Yesypenko
- Subjects
010405 organic chemistry ,Organic Chemistry ,Enantioselective synthesis ,Alkylation ,010402 general chemistry ,01 natural sciences ,Medicinal chemistry ,Dimethyl malonate ,Coupling reaction ,0104 chemical sciences ,Catalysis ,chemistry.chemical_compound ,Tsuji–Trost reaction ,chemistry ,Calixarene ,Organic chemistry ,Physical and Theoretical Chemistry ,Phosphine - Abstract
The Mitsunobu alkylation of 4-tert-butylcalix[4]arene with (S)-(2-diphenylthiophosphinoferrocenyl)methanol followed by desulfuration of the thiophosphine unit using tris(dimethylamino)phosphine afforded enantiomerically pure calixarene mono- and di(ferrocenylphosphine) ligands in high yields. The calixarene mono(ferrocenylphosphine) ligands exhibited good catalytic activity but low atropoenantioselectivity when used in the asymmetric Suzuki–Miyaura coupling reaction of 1-naphthaleneboronic acid and 1-bromo-2-methylnaphthalene. However, the di(ferrocenylphosphine) ligand displayed both good catalytic activity and enantioselectivity (ee values up to 86 %) when employed in the asymmetric Tsuji–Trost allylic alkylation of 1,3-diphenylprop-2-enyl acetate with dimethyl malonate.
- Published
- 2016
25. CALIX[4]ARENE C-145 EFFECTS ON СELLULAR HAEMOSTASIS
- Author
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T V Nikolaienko, Pashevin Do, V Е Dosenko, S. O. Cherenok, V. O. Chernyshenko, L V Garmanchuk, E. V. Lugovskoy, D S Korolova, N. N. Khranovska, Vitaly I. Kalchenko, and Serhiy Komisarenko
- Subjects
0106 biological sciences ,0301 basic medicine ,calix[4]arene, haemostasis, antithrombotic drugs, fibrin polymerization ,Chemistry ,lcsh:Biotechnology ,030106 microbiology ,calix[4]arene ,01 natural sciences ,03 medical and health sciences ,fibrin polymerization ,lcsh:TP248.13-248.65 ,010608 biotechnology ,haemostasis ,Polymer chemistry ,Organic chemistry ,antithrombotic drugs - Abstract
The aim of the research was to study a potential antithrombotic sodium salt of calix[4]arene-methylenebis-phosphonic acid (С-145) — on activation and aggregation of platelets in vivo, as well as on proliferation and apoptosis of endothelial cells in the cell culture. Effects of calix[4]arene С-145 estimated in vitro after addition to the platelet rich plasma, and in vivo after intravenous injection into rabbit bloodstream in equivalent amounts (46 μM). Aggregation of platelets was induced by adenosine diphosphate and detected using aggregometer Solar AP2110. Platelet shape and cytoplasmic granularity were monitored on COULTER EPICS XL Flow Cytometer. The level of tissuetype plasminogen activator — tPA — was estimated using enzyme-linked immunosorbent assay ELISA. Effects of calix[4]arene C-145 on culture of endotelial cells cells was studied using 3-(4,5-Dimethylthiazol2-yl)-2,5-Diphenyltetrazolium Bromide — MTT-test. The population of proliferative pool of cells (G2/ M+S) was determined using flow cytometry. Aggregometry and flow cytometry showed that calix[4]arene C-145 did not activate platelets nor affect their aggregation in vitro. However intravenous injection of calix[4]arene C-145 into the bloodstream of healthy rabbits leads to strong inhibition of platelet aggregation and changes of shape and granularity of most of the platelets after 2 hours of administration. Any additional appearance of endothelial cells activation marker tPA in vivo and any inhibition of calix[4]arene C-145 on proliferation of endothelial cells in cell culture did not observe. So calix[4]arene C-145 had strong anti-platelet effect in vivo that was not a result of their direct action on platelets or endothelial cells in vitro. This allowed to assume the possibility of calix[4]arene C-145 use as an effective antithrombotic agent., Целью работы было изучение действия потенциального антитромботического агента — натриевой соли каликс[4]арен-метилен-бисфосфоновой кислоты — каликс[4]арена С-145 на активацию и агрегацию тромбоцитов in vivo, а также на пролиферацию и апоптоз эндотелиоцитов в тканевой культуре. Эффекты каликс[4]арена С-145 оценивали in vitro после добавления в плазму крови, богатую тромбоцитами, а также in vivo после внутривенного введения в кровоток кролика в эквивалентных количествах (46 μМ). Агрегацию тромбоцитов индуцировали ADP и определяли с помощью агрегометра Solar AP2110. Форму и гранулярность цитоплазмы тромбоцитов устанавливали проточным цитометром COULTER EPICS XL. Уровень активатора плазминогена тканевого типа — tPA — измеряли методом иммуноэнзимного анализа ELISA. Эффекты каликс[4] арена C-145 на культуру эндотелиоцитов изучали с помощью 3-(4,5-диметилтиазол-2-ил)-2,5диметилтетразолия бромида — МТТ-теста. Популяцию пролиферативного пула (G2/M+S) клеток эндотелия определяли с применением цито метрии. Методами агрегатометрии и цитометрии установлено, что каликс[4]арен С-145 не активирует тромбоциты и не влияет на их агрегацию in vitro. Однако уже через два часа после введения каликс[4]арена С-145 здоровым лабораторным кролям тромбоциты теряли способность агрегировать, а пул интактных тромбоцитов уменьшался в два раза. В то же время не наблюдали выброса в плазму крови маркера активации эндотелиоцитов tPA in vivo, а также ингибирования пролиферации эндотелиоцитов в культуре клеток. Таким образом, каликс[4]арен С-145 обладает значительным антитромбоцитарным эффектом in vivo, не действуя непосредственно на тромбоциты и эндотелиоциты in vitro. Такие свойства каликсарена позволяют рассматривать возможность его применения в качестве эффективного антитромботического агента.
- Published
- 2016
26. The Upper Rim Functionalized Calixarene Ketocyanines: Synthesis, Structure and Fluorescence Properties
- Author
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Svitlana V. Shishkina, Aleksey B. Ryabitskii, Vitaly I. Kalchenko, Yuriy Matvieiev, Andrii V. Kulinich, Oleg V. Shishkin, and Vasyl G. Pivovarenko
- Subjects
Chemistry ,Organic Chemistry ,Calixarene ,Solvatochromism ,Polymer chemistry ,Organic chemistry ,Knoevenagel condensation ,Fluorescence ,Analytical Chemistry - Published
- 2016
27. Selective inhibition of smooth muscle plasma membrane transport Са2+,Mg2+-АТРase by calixarene C-90 and its activation by IPT-35 compound
- Author
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Anatoly M. Demchenko, Inna V. Gerashchenko, Kosterin So, Vitaly I. Kalchenko, Iuliia I. Mazur, Oleksandr A. Shkrabak, Roman V. Rodik, Tetyana O. Veklich, and Nikolai A. Mohart
- Subjects
030110 physiology ,0301 basic medicine ,Physiology ,Sodium-Potassium-Exchanging ATPase ,Biophysics ,Uterine contraction ,Cell membrane ,03 medical and health sciences ,Uterine Contraction ,parasitic diseases ,Calixarene ,medicine ,Myocyte ,Animals ,Chemistry ,Cell Membrane ,Uterus ,Myometrium ,Muscle, Smooth ,General Medicine ,Membrane transport ,Rats ,Protein Transport ,Membrane ,medicine.anatomical_structure ,Female ,medicine.symptom ,Calixarenes - Abstract
We investigated the influence of calixarene C-90 and IPT-35 on plasma membrane Ca2+- pumping АТРase (PMCA), intracellular calcium homeostasis and myometrium smooth muscle strain contractions. It has been shown that both effectors (100 μM) affect PMCA enzymatic activity: calixarene C-90 inhibits it by 75% and IPT-35 activates it by 40%. These compounds don't affect the Mg2+-АТРase, Mg2+-independent Са2+-АТРase and Na+,K+-АТРase enzymatic activities. C-90 inhibition coefficient I0.5 magnitude was approximately 20 μM and the Hill coefficient nH was 0.55. For IPT-35 activation, constant А0.5 was 6.4 and nH was 0.7. Mathematical modeling demonstrated the implication of calixarene C-90 on unexcited myocytes, which allows for a precise change in cytoplasm Ca2+ concentration and an influence on basal muscle tonus. By the same method, we determined that IPT-35 has a little influence on Ca2+ concentration in unexcited myocytes. It was also shown that calixarene C-90 in vitro can increase velocity of oxytocin-initiated contractions, whereas IPT-35 can suppress this aforementioned parameter. These results are promising for the design of new pharmacological compounds as better regulators of uterine contractions. Calixarene C-90 can be used in obstetric cases for the simultaneous use of oxytocin for enhancing uterine contractions, and IPT-35 for its antispasmodic effect on uterine tone.
- Published
- 2018
28. Synthesis of an enantiomerically pure inherently chiral calix[4]arene phosphonic acid and its evaluation as an organocatalyst
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Eric Manoury, V. I. Boiko, Jean-Claude Daran, Oleksandr A. Yesypenko, Andrii Karpus, Vitaly I. Kalchenko, Zoia Voitenko, Laboratoire de chimie de coordination (LCC), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie de Toulouse (ICT-FR 2599), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), National Taras Shevchenko University of Kiev, Institute of Organic Chemistry, National Academy of Sciences of Ukraine, National Academy of Sciences of Ukraine (NASU), and Institute of Organic Chemistry of NASU [Kyiv]
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Organophosphorus compounds ,Aromatic compounds ,010405 organic chemistry ,Organic Chemistry ,Epoxide ,Reaction products ,Molecules ,010402 general chemistry ,Inherent chirality ,01 natural sciences ,Hydrocarbons ,0104 chemical sciences ,Catalysis ,chemistry.chemical_compound ,chemistry ,Organocatalysis ,Calixarene ,Organic chemistry ,[CHIM.COOR]Chemical Sciences/Coordination chemistry ,Enantiomer ,Brønsted–Lowry acid–base theory ,Benzoic acid - Abstract
International audience; A facile method for the preparation of enantiomerically pure inherently chiral calix[4]arene phosphonic acid (cR,pR)-7 in four steps starting from the readily available and previously synthesized (cS)-enantiomer of calix[4]arene acetic acid 1 or its methyl ester 2 was developed. The first tests of this unique calixarene Brönsted acid with inherent chirality in organocatalysis of the aza-Diels–Alder reaction of imines with Danishefsky’s diene and epoxide ring opening by benzoic acid were performed. The calixarene phosphonic acid (cR,pR)-7 shows good catalytic activities but with low enantioselectivities in these reactions.
- Published
- 2018
29. Thiacalix[4]arenes Remove the Inhibitory Effects of Zn Cations on the Myosin ATPase Activity
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Andriy Drapaylo, Raisa Labyntsevа, Viktoriia Yavorovska, Vitaly I. Kalchenko, Olexander Bevza, and Kosterin So
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0301 basic medicine ,Materials science ,Myosin S1 ,ATPase ,chemistry.chemical_element ,Zinc ,ATPase activity ,03 medical and health sciences ,Hydrolysis ,Smooth muscle ,ATP hydrolysis ,Myosin ,lcsh:TA401-492 ,Zn ,General Materials Science ,Chelation ,biology ,Nano Express ,Uterus ,Myometrium ,Active site ,Condensed Matter Physics ,030104 developmental biology ,chemistry ,Molecular docking ,biology.protein ,Biophysics ,lcsh:Materials of engineering and construction. Mechanics of materials ,Thiacalix[4]arenes - Abstract
Numerous female reproductive abnormalities are caused by uterine smooth muscle (myometrium) disorders. Heavy metals have an adverse effect on the contractility of the uterine smooth muscle. Although zinc is an essential biogenic element for most of the organisms, high doses of this element are toxic. The study of 0.5−5 mM Zn2+ effect on myosin S1 ATPase activity from the uterus found that 5 mM Zn2+ cations have the most pronounced inhibitory effect. The calculation of the kinetic parameters (K m and V max, ATP) revealed that the apparent maximum velocity of the hydrolysis ATP catalyzed by myosin in the presence of 5 mM Zn2+ decreased by 1.6 times. The value of К m for ATP hydrolysis by myosin S1 in the presence of Zn2+ does not change statistically, although it tends to decrease. It was determined that uterine myosin S1 ATPase activity does not depend on the concentration of Mg2+ in the presence of 5 mM Zn2+. Also, it was demonstrated that tetrahydroxythiacalix[4]arene-tetrasulfosphonate (C-798) and tetrahydroxythiacalix[4]arene-tetraphosphonate (C-800) restored myosin S1 ATPase activity to the control level in the presence of 5 mM Zn2+. One of the most probable mechanisms of restoring the action of these thiacalix[4]arenes protective effect is based on its ability to chelate heavy metal cations from the incubation medium. The molecular docking of C-798 and C-800 into the myosin S1 region showed that these thiacalix[4]arenes could interact with Zn cation bond by myosin amino acid residues near the ATPase active site. Therefore, thiacalix[4]arenes may weaken the interaction between this cation and myosin S1. It was speculated that the obtained results could be used for further research with the aim of using this thiacalix[4]arenes as pharmacological compounds in the case of poisoning with high concentrations of zinc.
- Published
- 2017
30. Complexation of Calix[4]arene bis-Hydroxymethylenediphosphonic Acid with Amino acids. Binding Constants Determination by RP HPLC Method
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S. O. Cherenok, O. I. Kalchenko, and Vitaly I. Kalchenko
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Partition coefficient ,chemistry.chemical_classification ,Residue (chemistry) ,Nitrogen atom ,Modelling methods ,Chemistry ,Calixarene ,Organic chemistry ,Electrostatics ,Medicinal chemistry ,Solvophobic ,Amino acid - Abstract
Host-Guest complexation of calixarene-bis-hydroxymethylenediphosphonic acid with 17 amino acids in water solution had been studied by the RP HPLC and molecular modelling methods. It had been shown the binding constants of the complexes are depended on the nature of the amino acid residue, log P and pKa of the acids. The complexation is mainly determined by the electrostatic interactions between the positively charged nitrogen atom of the amino acid and the negatively charged oxygen atom of phosphonic acid residue of the calixarene, the Host-Guest p-p, СН-p and solvophobic interactions.
- Published
- 2015
31. Protective effect of tiacalix[4]arene-tetrasulphonate on heavy metal inhibition of myometrium myosin subfragment-1 ATP-hydrolase activity
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Kharchenko Sh, Vitaly I. Kalchenko, Labyntseva Rd, Kosterin So, Bevza Aa, Bevza Ov, and Liul'ko Ao
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biology ,uterus ,Myosin ATPase ,Chemistry ,thiacalix[4]arene ,Myometrium ,Active site ,Biochemistry ,ATPase activity ,myosin subfragment-1 ,Contractility ,smooth muscle ,lcsh:Biochemistry ,ATP hydrolysis ,Enzymatic hydrolysis ,Myosin ,docking ,biology.protein ,Biophysics ,Chelation ,lcsh:QD415-436 ,heavy metals - Abstract
Heavy metals have a negative effect on the contractility of uterine smooth muscles (myometrium), these effects can lead to various pathologies of a women reproductive system. To overcome these effects the methods for correcting the myometrium contractile activity are to be developed. Catalyzed by myosin ATPase ATP hydrolysis is the most important reaction in the molecular mechanism of myometrium contraction. We have found an inhibitory effect of 0.03-0.3 mM Ni2+, Pb2+ and Cd2+ on enzymatic hydrolysis of ATP by myosin subfragment-1 obtained from swine uterine smooth muscles. We have demonstrated that 100 µM thiacalix[4]arene-tetrasulphonate (C-798) recovered to the control level of ATPase activity of myosin subfragment-1 in the presence of heavy metal cations. One of the most probable mechanisms of C-798 corrective activity is based on its ability to chelate heavy metals, thus cations Pb, Cd and Ni can be removed from the incubation medium. Computer simulation has demonstrated that the protective effect of C-798 may also be the result of weakening the interaction of heavy metal ions with amino acid residues of the myosin molecule near the active site of ATP hydrolase. The obtained results can be used for further research aimed at assessing the prospects of thiacalix[4]arene-tetrasulfonate as pharmacological compounds.
- Published
- 2014
32. Kinetics of inhibitory effect of calix[4]arene С-90 on activity of transporting plasma membrane Cа(2+),Mg(2+)-ATPase of smooth muscle cells
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Roman V. Rodik, Vitaly I. Kalchenko, Kosterin So, Veklich To, Iu Iu Mazur, and Shkrabak Oa
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calix[4]arenes ,chemistry.chemical_classification ,kinetic properties of ATPase ,Magnesium ,Stereochemistry ,myometrium ,Kinetics ,Myometrium ,enzymatic hydrolysis of ATP ,chemistry.chemical_element ,plasma membrane ,Biochemistry ,smooth muscle cells ,Divalent ,lcsh:Biochemistry ,Ca2+ ,chemistry.chemical_compound ,Membrane ,Digitonin ,chemistry ,Mg(2+)-ATPase ,ATP hydrolysis ,lcsh:QD415-436 ,Uncompetitive inhibitor - Abstract
In experiments on the suspension of myometrium cell plasma membrane, processed by 0.1% digitonin, the inhibitory action of calix[4]arene C-90 (5,11,17,23-tetra(threeftor)methyl(phenilsulphonilimino)-methylamino-25,26, 27,28-tetrapropoxy-calix[4]arene) on the activity of Ca2+,Mg2+-ATPase was investigated. The authors also examined the influence of calix[4]arene in different concentration on affinity of enzyme (Ca2+,Mg2+-ATPase) for the ATP and ions of Mg and Ca, and its influence on cooperative effect and maximum velocity of ATP hydrolysis. It is shown that calix[4]arene does not influence the affinity of Ca2+,Mg2+-ATPase for the ATP, which means that these two compounds have different binding centers. Also calix[4]arene has no influence on affinity and cooperative effect of Ca ions, if it is used in concentration lower than 50 µM. Calix[4]arene slightly increases coefficient of Ca2+,Mg2+-ATPase activation by magnesium chloride. In all three cases, where ATP, Mg and Ca ions are used to test the impact of calix[4]arene, maximum velocity of ATP hydrolysis significantly decreases. All these results clarify that calix[4]arene implements its inhibitory action through mechanism of uncompetitive inhibition of Ca2+,Mg2+-ATPase activity.
- Published
- 2014
33. The difference between the aggregates of short-tailed and long-tailed cationic calix[4]arene in water as detected using fluorescein dyes
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Nikolay O. Mchedlov-Petrossyan, Tatyana A. Cheipesh, Vitaly I. Kalchenko, Roman V. Rodik, and E.S. Zagorulko
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Aqueous solution ,Cationic polymerization ,Condensed Matter Physics ,Micelle ,Tautomer ,Atomic and Molecular Physics, and Optics ,Electronic, Optical and Magnetic Materials ,chemistry.chemical_compound ,Colloid ,chemistry ,Calixarene ,Polymer chemistry ,Materials Chemistry ,Alkoxy group ,Organic chemistry ,Physical and Theoretical Chemistry ,Fluorescein ,Spectroscopy - Abstract
Water-soluble cationic calixarenes readily form aggregates in water. The properties of these aggregates, however, markedly vary along with alterations in the molecular structure. In a set of our recent studies, such aggregates were examined by various methods, and first of all using acid–base indicator dyes. The latter acted in fact as monoprotic acids exhibiting one color transition, and their pKa shifts against the values in water were relatively close for different calixarenes. In the present paper, we report the behavior of a much more complicated dye, fluorescein, and two relative compounds, in aqueous solutions of two cationic calix[4]arenes. The last named possess four choline groups on the upper rim and the sole difference is the length of the alkoxy groups at the lower rim: O(CH2)2CH3 and O(CH2)7CH3. In water, both calixarenes form aggregates of similar size and with similar zeta-potential. However, their influence on the acid–base and tautomeric equilibria of fluorescein clearly demonstrate that the aggregates of the long-tailed calixarene resemble the common micelles of colloidal surfactants to a higher degree than those of tetrapropyloxy compound.
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- 2014
34. Calix[4]arene α-hydroxymethylphosphonic acids as potential inhibitors of protein tyrosine phosphatases
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V. Yu. Tanchuk, Andriy I. Vovk, Viacheslav V. Trush, S. O. Cherenok, and Vitaly I. Kalchenko
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chemistry.chemical_classification ,biology ,Stereochemistry ,Active site ,Protein tyrosine phosphatase ,AutoDock ,Phosphonate ,In vitro ,chemistry.chemical_compound ,Enzyme ,chemistry ,Docking (molecular) ,Calixarene ,biology.protein - Abstract
Calix[4]arene are known to be a promising scaffold for designing inhibitors of protein tyrosine phosphatases. In this work calix[4]arene mono- and bis-α-hydroxymethylphosphonic acids have been tested in vitro for the inhibitory activity against some therapeutically important protein tyrosine phosphatases. The results obtained have shown that these macrocyclic compounds can inhibit CD45, PTP1B, and SHP2 with IC50 values in the micromolar range. At the same time the inhibitors have demonstrated lower activity toward other protein tyrosine phosphatases such as TC-PTP and PTPβ. It has been found that mono-substituted calix[4]arene is more potent inhibitor of CD45 than the bis-substituted one and shows about 2-15 fold selectivity over TC-PTP, PTPβ, SHP2 and PTP1B. Model 4-hydroxyphenyl-α-hydroxymethylphosphonate displays at least one order lower activity than the phosphonate derivatives of calix[4]arene. Thus, the combination of a macrocyclic platform and α-hydroxymethylphosphonate group is essential for the inhibition activities of these compounds. Computer-simulated docking studies have been performed using AutoDock 4.2 programme by the example of PTP1B. The data obtained indicate that the inhibitors can bind in the active site of the enzyme. To clarify the inhibition mechanism the possible enzyme-inhibitor complexes have been considered using several crystal structures of PTP1B and all stereoisomeric forms of the inhibitors.
- Published
- 2014
35. Protein-Sized Bright Fluorogenic Nanoparticles Based on Cross- Linked Calixarene Micelles with Cyanine Corona
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Ievgen Shulov, Roman V. Rodik, Youri Arntz, Andreas Reisch, Vitaly I. Kalchenko, and Andrey S. Klymchenko
- Subjects
fluorescence, cyanines, calixarenes, click chemistry, nanoparticles - Abstract
This is the pre-peer reviewed version of the following article: Shulov, I.; Rodik, R. V.; Arntz, Y.; Reisch, A.; Kalchenko, V. I.; Klymchenko, A. S.: Protein-Sized Bright Fluorogenic Nanoparticles Based on Cross-Linked Calixarene Micelles with Cyanine Corona. Angew. Chem.Int. Ed. 2016, 55, 15884-15888, which has been published in final form at http://onlinelibrary.wiley.com/doi/10.1002/ange.201609138/abstract. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
- Published
- 2016
36. Calixarene methylene bisphosphonic acids as promising effectors of biochemical processes
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E. V. Lugovskoy, S. O. Kosterin, Vitaly I. Kalchenko, and Serhiy Komisarenko
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calixarenes ,fibronogen ,Peptide ,ATPase activity ,Biochemistry ,Medicinal chemistry ,Fibrin ,lcsh:Biochemistry ,chemistry.chemical_compound ,fibrin polymerization ,Thrombin ,Calixarene ,Myosin ,medicine ,Organic chemistry ,lcsh:QD415-436 ,fibrin ,Methylene ,chemistry.chemical_classification ,biology ,Chemistry ,Fibrin Monomer ,inhibition ,Polymerization ,docking ,biology.protein ,methylene bisphosphonic acid ,medicine.drug - Abstract
This interdisciplinary study, performed with participation of research workers of Palladin Institute of Biochemistry and Institute of Organic Chemistry of NAS of Ukraine, is devoted to analysis of biochemical effects of some calixarene methylene bisphosphonic acids (cyclic phenol oligomers) on two well-known biological phenomenons – Mg2+-dependent ATP hydrolysis (myosin subfragment-1 of myometrium smooth muscle was used as an example) and fibrin polymerization. Calix[4]arene С-97 (calix[4]arene methylene bisphosphonic acids) is a macrocyclic substance, which contains intramolecular highly ordered lipophilic cavity formed by four aromatic rings, one of which is functionalized at the upper rim with methylene bisphosphonic group. At concentration of 100 µM, this substance was shown to effectively inhibit ATPase activity of pig myometrium myosin subfragment-1 (inhibition coefficient І0.5 = 83 ± 7 µM). At the same time, this calix[4]arene causes significant (vs. control) increase of myosin subfragment-1 hydrodynamic diameter, which may indicate formation of an intermolecular complex between calixarene and myosin head. Computer simulation methods (docking and molecular dynamics with addition of grid technologies) enabled to elucidate the grounds of intermolecular interactions between calix[4]arene С-97 and myometrium myosin subfragment-1, that involve hydrophobic, electrostatic and π-π-stacking interactions, some of which are close to the ATPase active centre. In view of the ability of calixarenes to penetrate into the cell and their low toxicity, the results obtained may be used as a basis for further development of a new generation of supramolecular effectors (starting from the above mentioned substances, in particular calix[4]arene С-97) for regulation of smooth muscle contractile activity at the level of ATP dependent actin-myosin interaction. Calix[4]arenes bearing two or four methylenebisphosphonic acid groups at the macrocyclic upper rim have been studied with respect to their effects on fibrin polymerization. The most potent inhibitor proved to be calix[4]arene tetrakis-methylene-bis-phosphonic acid (C-192), in which case the maximum rate of fibrin polymerization in the fibrinogen + thrombin reaction decreased by 50% at concentrations of 0.52·10-6 M (IC50). At this concentration, the molar ratio of the compound to fibrinogen was 1.7 : 1. For the case of desAB fibrin polymerization, the IC50 was 1.26·10-6 M at a molar ratio of C-192 to fibrin monomer of 4 : 1. Dipropoxycalix[4]-arene bis-methylene-bis-phosphonic acid (C-98) inhibited fibrin desAB polymerization with an IC50 = 1.31·10-4 M. We hypothesized that C-192 blocks fibrin formation by combining with polymerization site ‘A’ (Aa17–19), which ordinarily initiates protofibril formation in a ‘knob-hole’ manner. This suggestion was confirmed by an HPLC assay, which showed a host–guest inclusion complex of C-192 with the synthetic peptide Gly-Pro-Arg-Pro, an analogue of site ‘A’. Further confirmation that the inhibitor was acting at the initial step of the reaction was obtained by electron microscopy, with no evidence of protofibril formation being evident. Calixarene C-192 also doubled both the prothrombin time and the activated partial thromboplastin time in normal human blood plasma at concentrations of 7.13·10-5 and 1.10·10-5 M, respectively. These experiments demonstrate that C-192 is a specific inhibitor of fibrin polymerization and blood coagulation and can be used for the design of a new class of antithrombotic agents.
- Published
- 2013
37. Kinetic regularities of calixarene C-90 action on the myometrial plasma membrane Ca(2+),Mg(2+)-ATPase activity and on the Ca(2+) concentration in unexcited сells of the myometrium
- Author
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Vitaly I. Kalchenko, Mazur IuIu, Boĭko Vi, Kosterin So, Roman V. Rodik, Shkrabak Oa, and Veklich To
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medicine.medical_specialty ,Chemistry ,Kinetics ,Myometrium ,Inhibitory postsynaptic potential ,Biochemistry ,chemistry.chemical_compound ,Digitonin ,Endocrinology ,Membrane ,Muscle tension ,Internal medicine ,Calixarene ,medicine ,Biophysics ,Myocyte - Abstract
Plasma membrane Ca2+,Mg2+-ATPase is an important element of general myometrium tonus control mechanism, which also makes a contribution to muscle tension relaxation after its contraction. Expiriments were done on the myometrial cell plasma membrane suspension, which was treated with 0.1% digitonin solution. The authors have investigated the inhibitory action of calix[4]arene C-90 (5,11,17,23-tetra(trifluor) methyl(phenylsulphonylimino)-methylamino-25,26,27,28-tetra propoxi-calix[4]arene) on the Ca2+,Mg2+-ATPase activity (the magnitude of 10.5 was 20.2 +/- 0.5 mkM). The inhibitory action of calix[4]arene C-90 on the activity of Ca2+, Mg2+-ATPase is explained as cooperative action of four trifluormethyl(phenylsulfonylimino)methylamino groups that are spatially oriented on the calix[4]-arene base rather than with the action of tetra-phenol macrocycle or separate pharmacophore sulphonilamidin groups. Considering established kinetic pattern of calix[4]arene C-90 inhibitory action on the plasma membrane Ca2+,Mg2+-ATPase activity, stationary kinetical model of basal calcium concentration control in unexcited uterus myocytes was developed. It is assumed that obtained results may be promising for creation of new generation ("supramolecular") pharmacological agent - uterus basal tonus stimulator - on the base of calix[4] arene C-90.
- Published
- 2013
38. Effect of the structure of calix[4]arenes, containing phosphine oxide and phosphoryl groups and impregnated on silica gel, on the efficiency of Eu3+ extraction from aqueous solutions
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K. N. Belikov, A. V. Verbytska, K. Y. Bryleva, M. S. Lukashova, and Vitaly I. Kalchenko
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Phosphine oxide ,chemistry.chemical_compound ,Aqueous solution ,Chemistry ,Silica gel ,Extraction (chemistry) ,Inorganic chemistry ,Sorption ,General Chemistry ,Ion - Abstract
We have obtained efficient solid-phase extractants for extraction of Eu3+ ions from aqueous solutions. As the impregnates, we used a series of (thia)calix[4]arenes modified on the upper rim by phosphoryl and phosphine oxide groups. The materials obtained are characterized by sorption capacity 7.5-9.5 mg/g and let us extract up to 99% of the Eu3+ from aqueous solutions of moderate salinity.
- Published
- 2013
39. Enantioselective Recognition of Amino Acids by Enantiomerically Pure Calix[4]arene Carboxylic Acid or Their Diastereomerically Pure N-(1-Phenyl)ethyl Amides
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Elena A. Andreyko, Ivan I. Stoikov, Igor S. Antipin, Andrii O. Karpus, Anton M. Sikorsky, Oleksandr A. Yesypenko, Alexander B. Rozhenko, Vyacheslav I. Boyko, and Vitaly I. Kalchenko
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inorganic chemicals ,chemistry.chemical_classification ,Molecular model ,Chemistry ,Carboxylic acid ,Organic Chemistry ,technology, industry, and agriculture ,Enantioselective synthesis ,Supramolecular chemistry ,Electron spectroscopy ,Analytical Chemistry ,Amino acid ,Calixarene ,Organic chemistry - Abstract
The interaction of inherently chiral calix[4]arene carboxilic acids and their amides with amino acids in the organic phase has been studied using electron spectroscopy. It was found that the chiral calix[4]arenes are able of enantioselective recognition of L- and D-forms of amino acids. Stability constants of the calixarene – amino acid supramolecular complexes were determined and mechanism of the host-guest interaction was examined by molecular modeling method.
- Published
- 2013
40. Dramatic Changes in the Solubilities of Ions Induced by Ligand Addition in Biphasic System D2O/DNO3//[C1C4im][Tf2N]: A Phenomenological Study
- Author
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Laure Cointeaux, Maria Petrova, Dariia Ternova, Ali Ouadi, Vitaly I. Kalchenko, Nicolas Papaiconomou, Isabelle Billard, Valérie Mazan, S. I. Miroshnichenko, Maria Boltoeva, Clotilde Gaillard, Prasanta K. Mohapatra, Département Recherches Subatomiques (DRS-IPHC), Institut Pluridisciplinaire Hubert Curien (IPHC), Université de Strasbourg (UNISTRA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Laboratoire d'Electrochimie et de Physico-chimie des Matériaux et des Interfaces (LEPMI ), Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Université Savoie Mont Blanc (USMB [Université de Savoie] [Université de Chambéry])-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes [2016-2019] (UGA [2016-2019]), Institut de Physique Nucléaire de Lyon (IPNL), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Laboratoire d'Electrochimie et de Physico-chimie des Matériaux et des Interfaces (LEPMI), Université Grenoble Alpes (UGA)-Université Joseph Fourier - Grenoble 1 (UJF)-Institut National Polytechnique de Grenoble (INPG)-Université Savoie Mont Blanc (USMB [Université de Savoie] [Université de Chambéry])-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP)-Centre National de la Recherche Scientifique (CNRS), Institute of Organic Chemistry of NASU [Kyiv], National Academy of Sciences of Ukraine (NASU), Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Institut de Chimie du CNRS (INC)-Université Savoie Mont Blanc (USMB [Université de Savoie] [Université de Chambéry])-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes [2016-2019] (UGA [2016-2019]), Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), Bhabha Atomic Research Centre (BARC), and Government of India, Department of Atomic Energy
- Subjects
Aqueous solution ,Tributylphosphine oxide ,010405 organic chemistry ,Chemistry ,Ligand ,Significant difference ,Inorganic chemistry ,Protonation ,[CHIM.MATE]Chemical Sciences/Material chemistry ,[CHIM.INOR]Chemical Sciences/Inorganic chemistry ,010402 general chemistry ,01 natural sciences ,0104 chemical sciences ,Surfaces, Coatings and Films ,Ion ,chemistry.chemical_compound ,Ionic liquid ,Materials Chemistry ,Physical and Theoretical Chemistry ,ComputingMilieux_MISCELLANEOUS - Abstract
International audience; The solubilities of C 1 C 4 im + and Tf 2 N − in nitric aqueous phases have been measured for several ligand types and concentrations (0.04 M tributylphosphine oxide, 0.05 M N,N′-dimethyl-N,N′-dibutylmalonamide, 0.10 M 1-methyl-3-[4-(dibutylphosphinoyl)butyl]-3H-imidazol-1-ium bis(trifluoromethylsulphonyl)imidate, and 1.1 M N,N-dihexyloctanamide). The data evidence a significant difference between the solubilities of the cations and anions of the ionic liquid as a consequence of several ion-exchange and/or ion-pairing mechanisms involving all ions present in the system as well as the protonation/nitric-extraction ability of the ligand.
- Published
- 2016
41. Calixarenes in Biotechnology and Bio-Medical Research
- Author
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Roman V. Rodik, Vyacheslav I. Boyko, and Vitaly I. Kalchenko
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- 2016
42. Synthesis of thiacalix[4]arene task-specific ionic liquids
- Author
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Alexey B. Ryabitskii, Sergiy G. Kharchenko, Vitaly I. Kalchenko, Z. V. Voitenko, Svetlana V. Shishkinа, and Anna D. Iampolska
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Inorganic Chemistry ,chemistry.chemical_compound ,010405 organic chemistry ,Chemistry ,Computational chemistry ,Organic Chemistry ,Ionic liquid ,010402 general chemistry ,01 natural sciences ,Biochemistry ,0104 chemical sciences ,Task (project management) - Abstract
The preparative methods for the synthesis of imidazolium and pyridinium room temperature task-specific ionic liquids possessing thiacalix[4]arene complexing groups in cationic or anionic fragments of the molecule are described. The cationic imidazolium and pyridinium derivatives of tetrabuthoxythiacalixarene existing in the conformation 1,3-alternate are capable to bind “soft” metal cations due to cooperative cation-π and ion–dipole interactions with spatially contiguous benzene rings and oxygen atoms of the thiacalixarene platform. The cone-shaped imidazolium salts of the tetrahydroxythiacalix[4]arene sulfonic acid can chelate cations of transition metals, lanthanides, and actinides by oxygen and sulfur atoms at the lower rim of macrocycle.
- Published
- 2016
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43. Design, synthesis and structure determination of new inherently chiral para-bromoalkoxycalix[4]arenes
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V. V. Pirozhenko, Svitlana V. Shishkina, Marija A. Klyachina, Vyacheslav I. Boyko, Zoia Voitenko, Vitaly I. Kalchenko, Oleksandr A. Yesypenko, and Maksym V. Dekhtyarenko
- Subjects
Design synthesis ,010405 organic chemistry ,Chemistry ,Computational chemistry ,Stereochemistry ,Absolute configuration ,Regioselectivity ,Propyl bromide ,General Chemistry ,Alkylation ,010402 general chemistry ,01 natural sciences ,0104 chemical sciences - Abstract
The preparative method for the synthesis of inherently chiral para-bromoalkoxycalix[4]arenes based on para-bromination, stepwise regioselective debenzoylation and the following alkylation of the readily available 25-propoxy-26,27-dibenzoyloxycalix[4]arene with propyl bromide or (R)-N-(1-phenylethyl)bromoacetamide has been developed. Three types of the inherently chiral calix[4]arenes in cone or partial cone conformations with asymmetrical (AHHHHBHH, AAHHHBHH, AHBHHCHH) substitution of both upper and lower rims have been obtained in racemic, diastereomerically pure or enantiomerically pure forms. Their structure and the absolute configuration have been determined by NMR and X-ray.
- Published
- 2016
- Full Text
- View/download PDF
44. Calix[4]arene-α-hydroxyphosphonic acids. Synthesis, stereochemistry, and inhibition of glutathione S-transferase
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Olexander A. Yushchenko, S. O. Cherenok, Yuriy Matvieiev, Iryna M. Mischenko, Andriy I. Vovk, Vsevolod Yu. Tanchuk, Vitaly I. Kalchenko, Valery P. Kukhar, Julia A. Karpenko, Nataliya V. Samus, and Olexander V. Ruban
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Ester derivatives ,biology ,Stereochemistry ,Chemistry ,Organic Chemistry ,Glutathione ,Alkylation ,In vitro ,Sodium salt ,lcsh:QD241-441 ,chemistry.chemical_compound ,Glutathione S-transferase ,lcsh:Organic chemistry ,biology.protein ,Proton NMR ,Transferase - Abstract
A series of dipropoxy-, tripropoxy- and tetrapropoxycalix(4)arenes bearing one or two fragments of α-hydroxymethylphosphonic acid at the upper rim of the macrocycle was prepared by the reaction of the corresponding mono- and di-formylcalixarenes with sodium salts of dialkyl phosphites or with trialkyl (tristrimethylsilyl)phosphites followed by dealkylation (desilylation) of the ester derivatives. The conformations of the macrocyclic skeleton and the stereoisomeric forms of the compounds obtained were investigated by 1 H NMR. The resulting α- hydroxymethylphosphonic acids were found to be able to inhibit the activity of glutathione S- transferase in vitro.
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- 2012
45. MPV reduction using AlIII–calix[4]arene Lewis acid catalysts: Molecular-level insight into effect of ketone binding
- Author
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Vitaly I. Kalchenko, Yuriy Matvieiev, Alexander Katz, Kathleen A. Durkin, Vyacheslav I. Boyko, and Partha Nandi
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chemistry.chemical_classification ,Steric effects ,Ketone ,Denticity ,biology ,Molecular model ,Stereochemistry ,Active site ,Medicinal chemistry ,Catalysis ,chemistry.chemical_compound ,chemistry ,Alkoxide ,biology.protein ,Lewis acids and bases ,Physical and Theoretical Chemistry - Abstract
Catalytic Meerwein–Ponndorf–Verley (MPV) reduction using AlIII–calix[4]arene complexes is investigated as a model system that requires the bringing together of two different chemical species, ketone and alkoxide, within a six-membered transition state. Two-point versus one-point ketone binding is demonstrated to be the most salient feature that controls MPV catalysis rate. A 7.7-fold increase in rate is observed when comparing reactants consisting of a bidentate Cl-containing ketone and sterically and electronically similar but looser-binding ketones, which are substituted with H and F. The one-point and two-point nature of ketone binding for the various ketones investigated is independently assessed using a combination of structural data derived from single-crystal X-ray diffraction and DFT-based molecular modeling. Using MPV catalysis with inherently chiral calix[4]arenes, the effect of multiple point reactant binding on enantioselectivity is elucidated. A higher denticity of ketone binding appears to increase the sensitivity of the interplay between chiral active site structure and MPV reduction enantioselectivity.
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- 2011
46. Synthesis and complexation of amphiphilic calix[4]arene phosphonates with organic molecules in solutions and Langmuir-Blodgett films
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S. O. Cherenok, Z.I. Kazantseva, Ivan F. Tsymbal, Vitaly I. Kalchenko, L. I. Atamas, O. I. Kalchenko, I.A. Koshets, and Andrew Solovyov
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chemistry.chemical_classification ,Chemistry ,Butanol ,Infrared spectroscopy ,Aromaticity ,Condensed Matter Physics ,Langmuir–Blodgett film ,Atomic and Molecular Physics, and Optics ,Electronic, Optical and Magnetic Materials ,Organic molecules ,chemistry.chemical_compound ,Amphiphile ,Calixarene ,Polymer chemistry ,Materials Chemistry ,Organic chemistry ,Physical and Theoretical Chemistry ,Spectroscopy ,Alkyl - Abstract
A family of amphiphilic alkoxycalix[4]arenes bearing phosphonyl groups directly attached to para positions of the aromatic rings is synthesized by the Arbuzov reaction of para -bromoalkoxycalix[4]arenes with alkyl esters of phosphorus (III) acid in the presence of NiBr 2 . Amphiphilicity of the calixarene phosphonates is controlled by varying the quantities of the hydrophilic phosphoryl groups at the upper rim and the hydrophobic alkyl groups at the lower rim. Complexation of the calixarenes with benzene derivatives and iso- butanol in solutions is studied by RP HPLC and IR spectroscopy methods. Langmuir-Blodgett films of the calixarene phosphonates are prepared. Physical characteristics and complexation of the films with volatile organic molecules are characterized.
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- 2011
47. Calixarene receptors of environmentally hazardous and biorelevant molecules and ions
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Vitaly I. Kalchenko
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chemistry.chemical_classification ,Chemistry ,General Chemical Engineering ,Biomolecule ,Inorganic chemistry ,Rational design ,Supramolecular chemistry ,General Chemistry ,Combinatorial chemistry ,Organic molecules ,Ion ,Calixarene ,Molecule ,Receptor - Abstract
In the paper, a report on the rational design of the calixarene receptors bearing ligating, H-donor, H-acceptor fragments at the wide and/or narrow rim of the macrocycle is presented. The calixarenes form supramolecular complexes with various cations, anions, organic molecules, and biomolecules in solution, in the crystalline state and even in the gas phase. The calixarenes or their complexes can be used as materials for radionuclide extraction, construction of chemosensors, and drug design.
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- 2008
48. calix[4]arene C-145 Effects on Plasma Haemostasis
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Y M Makogonenko, Chernyshenko Tm, Kravchenko N, Pirogova Lv, Serhiy Komisarenko, D S Korolova, Vitaly I. Kalchenko, V. O. Chernyshenko, Dosenko, Pashevin Do, Lugovska Oe, and E. V. Lugovskoy
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medicine.medical_specialty ,medicine.diagnostic_test ,biology ,medicine.drug_class ,Chemistry ,Anticoagulant ,Thrombin time ,Pharmacology ,Fibrinogen ,Fibrin ,Surgery ,In vivo ,Blood plasma ,medicine ,biology.protein ,Protein C ,medicine.drug ,Partial thromboplastin time - Abstract
Background: Calix[4]arene-methylene-bis-phosphonic acid C-192 and its sodium salt C-145 were shown to be efficient inhibitors of fibrin polymerization in vitro. In presented work we analyze the effects of Nalix[4]arene C-145 on haemostasis in vivo. Methods: Parameters of coagulation system of rabbits intravenously injected with C-145 were monitored. We measured thrombin time (TT), ecamulin time (ET) and activated partial thromboplastin time (APTT), determined the levels of fibrinogen, prothrombin, protein C, PAI-1, monitored overall haemostatic potential before and after the injection. Results: C-145 was administrated intravenously in the dose of 7.5 mg/kg of rabbit weight. 4 hours after the injection the thrombin time and activated partial thromboplastin time of rabbit’s blood plasma were prolonged 2 and 1,5 times respectively. Such prolongation was observed after 24 hours as well. However, the total fibrinogen and prothrombin levels did not change. Parameters of fibrinolytic system (PAI-1, clot lysis half-time) and anticoagulant system (protein C) remained unchanged. Conclusions: Therefore we assumed that calix[4]arene C-145’s effects on haemostasis consisted in selective inhibition of fibrin polymerization and formation of three-dimensional fibrin network.
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- 2015
49. Unusual conformations of 1,3-dialkoxythiacalix[4]arenes in the solid state
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Iris Thondorf, Volker Böhmer, Oleg Kasyan, Michael Bolte, and Vitaly I. Kalchenko
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Molecular Structure ,Sulfur Compounds ,Stereochemistry ,Hydrogen bond ,Molecular Conformation ,Hydrogen Bonding ,Ether ,General Medicine ,Crystal structure ,Crystallography, X-Ray ,Acceptor ,General Biochemistry, Genetics and Molecular Biology ,Solvent ,Crystallography ,chemistry.chemical_compound ,chemistry ,Intramolecular force ,Calixarene ,Molecule ,Calixarenes ,Ethers - Abstract
The structures of three syn-1,3-dialkoxythiacalix[4]arenes with unusual conformations in the solid state are reported. The pinched cone conformation of syn-2 2 ,4 2 -dihydroxy-1 2 ,3 2 -bis-(prop-2-enyloxy)thiacalix[4]arene, C 30 H 24 O 4 S 4 , (3a), is stabilized by two intramolecular hydrogen bonds, remarkably formed from both OH groups to the same ether O atom. In syn-22,42-dihydroxy-1 5 ,2 5 ,3 5 ,4 5 -tetranitro-12,32-bis(prop-2-enyloxy)thiacalix[4]arene acetone disolvate, C 30 H 20 N 4 O 12 S 4 ·-2C 3 H 6 O, (3b1), the molecule is found in the 1,3-alternate conformation. The crystallographic C2 symmetry is due to a twofold rotation axis running through the centre of the calixarene ring. The hydroxy groups cannot form intramolecular hydrogen bonds as in (3a) and both are bonded to an acetone solvent molecule. The molecule of the pseudo-polymorph of (3b1) in which the same compound crystallized without any solvent, viz. (3b2), is located on a crystallographic mirror plane. Only one of the two hydroxy groups forms a hydrogen bond, and this is with a nitro group of a neighbouring molecule as acceptor. Molecular mechanics calculations for syn-1,3-diethers suggest a preference of the 1,3-alternate over the usual cone conformation for thiacalix[4]arene versus calix[4]arene and for para-nitro versus para-H derivatives.
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- 2006
50. Complexation of isoleucine by phosphorylated calix[4]arene in methanol followed by calorimetry, NMR and UV–VIS spectroscopies, and molecular modeling methods
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Sergey Cherenok, A. Marcinowicz, Wojciech Zielenkiewicz, Vitaly I. Kalchenko, and Jarosław Poznański
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Molecular model ,Calorimetry ,Condensed Matter Physics ,Atomic and Molecular Physics, and Optics ,Electronic, Optical and Magnetic Materials ,chemistry.chemical_compound ,Crystallography ,Ultraviolet visible spectroscopy ,chemistry ,Calixarene ,Materials Chemistry ,Molecule ,Organic chemistry ,Titration ,Methanol ,Physical and Theoretical Chemistry ,Isoleucine ,Spectroscopy - Abstract
Complexation of isoleucine with bis (dihydroxyphosphorylhydroxymethyl) dipropoxycalix[4]arene was studied by titration calorimetry, NMR and UV–VIS spectroscopies and in terms of molecular modeling. The experimental data allowed to infer the occurrence of two heterogeneous non-equivalent calixarene moieties complexed by a single isoleucine molecule. The association constants were calculated to be 25,000±3000 and 1700±300 for the (1:1) and (2:1) calixarene–isoleucine complexes, respectively.
- Published
- 2005
Catalog
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