180 results on '"Bouaziz, Zouhair"'
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2. Uncompetitive nanomolar dimeric indenoindole inhibitors of the human breast cancer resistance pump ABCG2
3. Ninhydrins inhibit carbonic anhydrases directly binding to the metal ion
4. Microwave-accelerated multicomponent synthesis and X-ray characterization of novel benzothiadiazinone dioxide derivatives, analogues of Monastrol
5. Mechanistic basis of breast cancer resistance protein inhibition by new indeno[1,2-b]indoles
6. Indenoindoles and cyclopentacarbazoles as bioactive compounds: Synthesis and biological applications
7. Synthesis and antiproliferative activity of oxazinocarbazole and N, N-bis(carbazolylmethyl)amine derivatives
8. Broad-Spectrum Anticancer Activity and Pharmacokinetic Properties of a Prenyloxy-Substituted Indeno[1,2-b]indole Derivative, Discovered as CK2 Inhibitor
9. Solubility enhancement of mefenamic acid by inclusion complex with β-cyclodextrin: in silico modelling, formulation, characterisation, and in vitro studies
10. Indeno[1,2-b]indole scaffold in drug discovery: An effective template in kinase inhibitor medicinal chemistry
11. Isoform specific inhibition of human protein kinase CK2α and CK2α’ by an indenoindole derivative
12. Diacritic Binding of an Indenoindole Inhibitor by CK2 alpha Paralogs Explored by a Reliable Path to Atomic Resolution CK2 alpha ' Structures
13. QSAR Model of Indeno[1,2-b]indole Derivatives and Identification of N-isopentyl-2-methyl-4,9-dioxo-4,9-Dihydronaphtho[2,3-b]furan-3-carboxamide as a Potent CK2 Inhibitor
14. Design, synthesis, X-ray structure and evaluation of functionalized hexacyclic carbazoles as new inhibitors of ABCG2 transporter
15. Diacritic Binding of an Indenoindole Inhibitor by CK2α Paralogs Explored by a Reliable Path to Atomic Resolution CK2α′ Structures
16. A comparative adsorption study of benzophenone-3 onto synthesized lipophilic organosilicate, Laponite and montmorillonite
17. Carbazole scaffolds in cancer therapy: a review from 2012 to 2018
18. Sequential MCR/Fisher indolization strategy for the construction of polycyclic carbazole derivatives
19. Synthesis, Spectroscopic Characterization, and In Vitro Antibacterial Evaluation of Novel Functionalized Sulfamidocarbonyloxyphosphonates
20. Self-Assembled Supramolecular Nanoparticles Improve the Cytotoxic Efficacy of CK2 Inhibitor THN7
21. Inhibition of Shiga toxin-converting bacteriophage development by novel antioxidant compounds
22. Synthesis, X-ray structure, in silico calculation, and carbonic anhydrase inhibitory properties of benzylimidazole metal complexes
23. Unexpected Binding Mode of a Potent Indeno[1,2-b]indole-Type Inhibitor of Protein Kinase CK2 Revealed by Complex Structures with the Catalytic Subunit CK2 alpha and Its Paralog CK2 alpha '
24. Microwave-assisted oxidation of indan-1-ones into ninhydrins
25. Unexpected Binding Mode of a Potent Indeno[1,2-b]indole-Type Inhibitor of Protein Kinase CK2 Revealed by Complex Structures with the Catalytic Subunit CK2α and Its Paralog CK2α′
26. Development of Pharmacophore Model for Indeno[1,2-b]indoles as Human Protein Kinase CK2 Inhibitors and Database Mining
27. DMAP as a new efficient catalyst for the one-pot synthesis of condensed phthalazines
28. Screening of indeno[1,2-b]indoloquinones by MALDI-MS: a new set of potential CDC25 phosphatase inhibitors brought to light
29. Phenolic indeno[1,2-b]indoles as ABCG2-selective potent and non-toxic inhibitors stimulating basal ATPase activity
30. Methyl 3-(Quinolin-2-yl)indolizine-1-carboxylate
31. Crystal structure of 13-phenyl-2,3,4,13-tetrahydro-1H-indazolo[1,2-b]phthalazine-1,6,11-trione
32. ChemInform Abstract: A One-Pot Three-Component Synthesis of Novel α-Sulfamidophosphonates under Ultrasound Irradiation and Catalyst-Free Conditions.
33. Crystal structure of 13-(2-methoxyphenyl)-3,4-dihydro-2H-indazolo[1,2-b]phthalazine-1,6,11(13H)-trione
34. ChemInform Abstract: Microwave-Assisted Oxidation of Indan-1-ones into Ninhydrins.
35. Phenolic indeno[1,2-b]indoles as ABCG2-selective potent and non-toxic inhibitors stimulating basal ATPase activity
36. Synthesis, Biological Evaluation and Molecular Modeling of Substituted Indeno[1,2-b]indoles as Inhibitors of Human Protein Kinase CK2
37. 81: Targeting casein kinase 2 in drug discovery: identification of new chemical entities
38. A one-pot three-component synthesis of novel α-sulfamidophosphonates under ultrasound irradiation and catalyst-free conditions
39. Development of Pharmacophore Model for Indeno[1,2-b]indoles as Human Protein Kinase CK2 Inhibitors and Database Mining.
40. Converting Potent Indeno[1,2-b]indole Inhibitors of Protein Kinase CK2 into Selective Inhibitors of the Breast Cancer Resistance Protein ABCG2
41. Biologically active carbazole derivatives: focus on oxazinocarbazoles and related compounds
42. ChemInform Abstract: Indenoindoles and Cyclopentacarbazoles as Bioactive Compounds: Synthesis and Biological Applications
43. Screening of indeno[1,2- b ]indoloquinones by MALDI-MS: a new set of potential CDC25 phosphatase inhibitors brought to light.
44. ChemInform Abstract: Synthesis and Antiproliferative Activity of Oxazinocarbazole and N,N-Bis(carbazolylmethyl)amine Derivatives.
45. ChemInform Abstract: Regiospecific Synthesis of Pyrido[3,4-b]- and Pyrido[4,3-b]carbazole-5,11-dione Derivatives. Evaluation of Their in vitro Antifungal or Antiprotozoological Activities.
46. ChemInform Abstract: Carbazole-1,4-diones: Syntheses and Properties
47. Synthesis and antiproliferative activity of oxazinocarbazole and N,N-bis(carbazolylmethyl)amine derivatives
48. ChemInform Abstract: Mannich Reaction of 5‐Hydroxy‐β‐carboline. Application to the Synthesis of Novel Oxazinopyrimidocarboline Derivatives.
49. 81: Targeting casein kinase 2 in drug discovery: identification of new chemical entities
50. Mannich Reaction of 5-Hydroxy-b-carboline. Application to the Synthesis of Novel Oxazinopyrimidocarboline Derivatives
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