1. Synthesis and Characterization of 3-(1-((3,4-Dihydroxyphenethyl)amino)ethylidene)-chroman-2,4-dione as a Potential Antitumor Agent
- Author
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Edina H. Avdović, Srećko R. Trifunović, Milena Stevanovic, Luciano Saso, Isidora Petrovic, Ivan Potočňák, Danijela Stanisavljevic, Jelena Đorović, Erika Samoľová, Dušan Dimić, Zoran Marković, and Jasmina M. Dimitrić Marković
- Subjects
squamous cell carcinoma ,Aging ,synthesis ,Control Systems ,MCF-7 cell line ,Crystallography, X-Ray ,01 natural sciences ,Biochemistry ,Inhibition constants ,synthesis and characterizations ,chemistry.chemical_compound ,carcinoma cell lines ,Amines ,antineoplastic agent ,Inhibition ,4 dihydroxyphenethyl)amino]ethylidene]chroman 2 ,Crystallography ,biology ,lcsh:Cytology ,Chemistry ,drug effect ,hepatocellular carcinoma ,General Medicine ,HaCat cell line ,unclassified drug ,3. Good health ,Molecular Docking Simulation ,chroman derivative ,MCF-7 Cells ,Cancers ,Breast carcinoma ,Research Article ,in vitro study ,Article Subject ,Cell Survival ,Stereochemistry ,Cells ,Antineoplastic Agents ,anti-tumor agents ,Hep-G2 cell line ,chemistry ,010402 general chemistry ,3 [1 [(3 ,Article ,4 dione ,Cyclin-dependent kinase ,amines ,cell culture ,cells ,hydrogen bonds ,proteins, anti-tumor agents ,coumarin derivatives ,molecular docking ,synthesis and characterizations, X ray crystallography, 3 [1 [(3,4 dihydroxyphenethyl)amino]ethylidene]chroman 2,4 dione ,chroman derivative, Article ,controlled study ,drug synthesis ,human ,human cell ,SiHa cell line ,cell survival ,X ray crystallography, Amines ,Hydrogen Bonds ,Proteins, Antineoplastic Agents ,Chromans ,Humans ,Molecule ,lcsh:QH573-671 ,010405 organic chemistry ,Proteins ,X ray crystallography ,Cell Biology ,Coumarin ,In vitro ,0104 chemical sciences ,HaCaT ,Cell culture ,X-Ray ,biology.protein ,Derivative (chemistry) - Abstract
The newly synthesized coumarin derivative with dopamine, 3-(1-((3,4-dihydroxyphenethyl)amino)ethylidene)-chroman-2,4-dione, was completely structurally characterized by X-ray crystallography. It was shown that several types of hydrogen bonds are present, which additionally stabilize the structure. The compound was tested in vitro against different cell lines, healthy human keratinocyte HaCaT, cervical squamous cell carcinoma SiHa, breast carcinoma MCF7, and hepatocellular carcinoma HepG2. Compared to control, the new derivate showed a stronger effect on both healthy and carcinoma cell lines, with the most prominent effect on the breast carcinoma MCF7 cell line. The molecular docking study, obtained for ten different conformations of the new compound, showed its inhibitory nature against CDKS protein. Lower inhibition constant, relative to one of 4-OH-coumarine, proved stronger and more numerous interactions with CDKS protein. These interactions were carefully examined for both parent molecule and derivative and explained from a structural point of view.
- Published
- 2019
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