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New Indolyl‐Arylaminopropenone Conjugates: Synthesis, Cytotoxicity and Apoptotic Inducing Studies
Author(s) -
Adil Shareef Mohd,
Ganapathi Thipparapu,
Khan Irfan,
Rani Sunitha,
Rajanna Ajumeera,
Akbar Syed,
Kumar C. Ganesh,
Babu Bathini Nagendra
Publication year - 2020
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201904077
Subject(s) - apoptosis , cytotoxicity , cell culture , cell cycle , annexin , chemistry , stereochemistry , aryl , cell cycle checkpoint , amino acid , conjugate , programmed cell death , docking (animal) , cancer cell , cell growth , biochemistry , biology , in vitro , cancer , medicine , organic chemistry , mathematical analysis , genetics , alkyl , mathematics , nursing
In view of the antiproliferative potential of indoles and aryl amino propenones, a series of indolyl tethered aryl aminopropenones have been synthesized and investigated for their anti‐proliferative activity against selected human cancer cell lines. These compounds exhibited good to moderate activity against the tested cell lines. Among them, (Z)‐1‐(1‐(4‐chlorobenzyl)‐1 H ‐indol‐3‐yl)‐3‐((3,4,5‐trimethoxyphenyl)amino)prop‐2‐en‐1‐one ( 6a ) and (Z)‐1‐(1‐benzyl‐1 H ‐indol‐3‐yl)‐3‐((3,4,5‐trimethoxyphenyl)amino)prop‐2‐en‐1‐one ( 6g ) exhibited promising IC 50 values of 2.3 μM and 1.9 μM, respectively, against MCF‐7 (human breast cancer cell line). The morphological studies indicated that compounds showed a dose dependent decrease of viable cells in MCF‐7 cell line. The flow cytometric analysis of these potential compounds revealed that they caused cell cycle arrest at G0/G1 phase. Furthermore, Annexin‐V FITC study revealed that the potential compounds induced cell death by apoptosis. In addition, molecular docking studies of the most potential compounds provided insights about the binding interactions of the compounds with Bcl‐2 protein.