Synthesis and Characterization of 3-(1-((3,4-Dihydroxyphenethyl)amino)ethylidene)-chroman-2,4-dione as a Potential Antitumor Agent

Author:

Dimić Dušan S.1ORCID,Marković Zoran S.2ORCID,Saso Luciano3ORCID,Avdović Edina H.4,Đorović Jelena R.5ORCID,Petrović Isidora P.6,Stanisavljević Danijela D.6ORCID,Stevanović Milena J.678ORCID,Potočňák Ivan9,Samoľová Erika9,Trifunović Srećko R.4,Dimitrić Marković Jasmina M.1ORCID

Affiliation:

1. University of Belgrade, Faculty of Physical Chemistry, Studentski trg 12-16, 11000 Belgrade, Serbia

2. Department of Chemical-Technological Sciences, State University of Novi Pazar, Vuka Karadžića bb, 36300 Novi Pazar, Serbia

3. Department of Physiology and Pharmacology “Vittorio Erspamer”, Sapienza University of Rome, Rome, Italy

4. University of Kragujevac, Faculty of Science, Radoja Domanovića 12, 34000 Kragujevac, Serbia

5. BioIRC, Bioengineering R&D Center, Prvoslava Stojanovića 6, 34000 Kragujevac, Serbia

6. University of Belgrade, Institute of Molecular Genetics and Genetic Engineering, Vojvode Stepe 444a, PO Box 23, 11010 Belgrade, Serbia

7. University of Belgrade, Faculty of Biology, Studentski trg 16, 11000 Belgrade, Serbia

8. Serbian Academy of Sciences and Art, Knez Mihajlova 35, 11000 Belgrade, Serbia

9. Institute of Chemistry, P. J. Šafárik University in Košice, Moyzesova 11, 04154 Košice, Slovak Republic, Slovakia

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.

Funder

Ministarstvo Prosvete, Nauke i Tehnološkog Razvoja

Publisher

Hindawi Limited

Subject

Cell Biology,Aging,General Medicine,Biochemistry

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