Synthesis, characterization and biological evaluation of bile acid-aromatic/heteroaromatic amides linked via amino acids as anti-cancer agents

被引:33
作者
Agarwal, Devesh S. [1 ]
Anantaraju, Hasitha Shilpa [2 ]
Sriram, Dharmarajan [2 ]
Yogeeswari, Perumal [2 ]
Nanjegowda, Shankara H. [3 ]
Mallu, P. [3 ]
Sakhuja, Rajeev [1 ]
机构
[1] Birla Inst Technol, Dept Chem, Pilani 333031, Rajasthan, India
[2] Birla Inst Technol & Sci Pilani, Dept Pharm, Drug Discovery Res Lab, Hyderabad Campus, Hyderabad 500078, Andhra Pradesh, India
[3] Sri Jayachamarajendra Coll Engn, Dept Chem, Mysore 570006, Karnataka, India
关键词
Cancer; Cholic acid; Coupling; Cytotoxicity; Amino acid; Heteroaryl amines; URSODEOXYCHOLIC ACID; INDUCE APOPTOSIS; CELL-CYCLE; DERIVATIVES; PATHWAY; MODULATION; DESIGN;
D O I
10.1016/j.steroids.2015.12.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of bile acid (Cholic acid and Deoxycholic acid) aryl/heteroaryl amides linked via alpha-amino acid were synthesized and tested against 3 human cancer cell-lines (HT29, MDAMB231, U87MG) and 1 human normal cell line (HEK293T). Some of the conjugates showed promising results to be new anticancer agents with good in vitro results. More specifically, Cholic acid derivatives 6a (1.35 mu M), 6c (1.41 mu M) and 6m (4.52 mu M) possessing phenyl, benzothiazole and 4-methylphenyl groups showed fairly good activity against the breast cancer cell line with respect to Cisplatin (7.21 mu M) and comparable with respect to Doxorubicin (1 mu M), while 6e (2.49 mu M), 6i (2.46 mu M) and 6m (1.62 mu M) showed better activity against glioblastoma cancer cell line with respect to both Cisplatin (2.60 mu M) and Doxorubicin (3.78 mu M) drugs used as standards. Greater than 65% of the compounds were found to be safer on human normal cell line. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:87 / 97
页数:11
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