University of Belgrade, Faculty of Physical Chemistry, Studentski trg 12-16, 11000 Belgrade, Serbia.
Department of Chemical-Technological Sciences, State University of Novi Pazar, Vuka Karadžića bb, 36300 Novi Pazar, Serbia.
Oxid Med Cell Longev. 2019 Feb 13;2019:2069250. doi: 10.1155/2019/2069250. eCollection 2019.
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 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 protein. Lower inhibition constant, relative to one of 4-OH-coumarine, proved stronger and more numerous interactions with CDK protein. These interactions were carefully examined for both parent molecule and derivative and explained from a structural point of view.
新合成的多巴胺香豆素衍生物,3-(1-((3,4-二羟基苯乙基)氨基)亚乙基)-2,4-二酮,通过 X 射线晶体学得到了完全的结构表征。结果表明存在几种类型的氢键,这进一步稳定了结构。该化合物被测试了对不同细胞系的作用,包括健康人角质形成细胞 HaCaT、宫颈鳞状细胞癌 SiHa、乳腺癌 MCF7 和肝癌 HepG2。与对照相比,新衍生物对健康细胞系和癌细胞系都表现出更强的作用,对乳腺癌 MCF7 细胞系的作用最为显著。对新化合物的十种不同构象进行的分子对接研究表明,它具有抑制 CDK 蛋白的特性。与 4-OH-香豆素相比,更低的抑制常数证明了与 CDK 蛋白更强和更多的相互作用。对母体分子和衍生物都进行了仔细的检查,并从结构的角度进行了解释。