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 CDK S protein. Lower inhibition constant, relative to one of 4-OH-coumarine, proved stronger and more numerous interactions with CDK S protein. These interactions were carefully examined for both parent molecule and derivative and explained from a structural point of view. © 2019 Dušan S. Dimić et al.

Synthesis and characterization of 3-(1-((3,4-dihydroxyphenethyl)amino)ethylidene)-chroman-2,4-dione as a potential antitumor agent / Dimić, D. S.; Marković, Z. S.; Saso, L.; Avdović, E. H.; Dorović, J. R.; Petrović, I. P.; Stanisavljević, D. D.; Stevanović, M. J.; Potočňák, I.; Samoľová, E.; Trifunović, S. R.; Dimitrić Marković, J. M.. - In: OXIDATIVE MEDICINE AND CELLULAR LONGEVITY. - ISSN 1942-0900. - 2019:(2019). [10.1155/2019/2069250]

Synthesis and characterization of 3-(1-((3,4-dihydroxyphenethyl)amino)ethylidene)-chroman-2,4-dione as a potential antitumor agent

Saso, L.;
2019

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 CDK S protein. Lower inhibition constant, relative to one of 4-OH-coumarine, proved stronger and more numerous interactions with CDK S protein. These interactions were carefully examined for both parent molecule and derivative and explained from a structural point of view. © 2019 Dušan S. Dimić et al.
2019
amines; cell culture; cells; hydrogen bonds; proteins, anti-tumor agents; carcinoma cell lines; coumarin derivatives; hepatocellular carcinoma; Inhibition constants; molecular docking; squamous cell carcinoma; synthesis and characterizations, X ray crystallography, 3 [1 [(3,4 dihydroxyphenethyl)amino]ethylidene]chroman 2,4 dione; antineoplastic agent; unclassified drug; antineoplastic agent; chroman derivative, Article; controlled study; drug synthesis; HaCat cell line; Hep-G2 cell line; human; human cell; in vitro study; molecular docking; SiHa cell line; cell survival; chemistry; drug effect; MCF-7 cell line; synthesis; X ray crystallography, Amines; Cancers; Cells; Control Systems; Crystallography; Hydrogen Bonds; Inhibition; Proteins, Antineoplastic Agents; Cell Survival; Chromans; Crystallography, X-Ray; Humans; MCF-7 Cells; Molecular Docking Simulation
01 Pubblicazione su rivista::01a Articolo in rivista
Synthesis and characterization of 3-(1-((3,4-dihydroxyphenethyl)amino)ethylidene)-chroman-2,4-dione as a potential antitumor agent / Dimić, D. S.; Marković, Z. S.; Saso, L.; Avdović, E. H.; Dorović, J. R.; Petrović, I. P.; Stanisavljević, D. D.; Stevanović, M. J.; Potočňák, I.; Samoľová, E.; Trifunović, S. R.; Dimitrić Marković, J. M.. - In: OXIDATIVE MEDICINE AND CELLULAR LONGEVITY. - ISSN 1942-0900. - 2019:(2019). [10.1155/2019/2069250]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1302403
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