Indole-fused benzooxazepines: a new structural class of anticancer agents
Author(s) -
Ashok Kumar Singh,
Vinit Raj,
Amit Rai,
Amit K. Keshari,
Sudipta Saha
Publication year - 2017
Publication title -
future science oa
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 23
ISSN - 2056-5623
DOI - 10.4155/fsoa-2016-0079
Subject(s) - indole test , docking (animal) , chemistry , stereochemistry , in vitro , hydrogen bond , combinatorial chemistry , cancer cell lines , cancer cell , computational biology , biochemistry , biology , cancer , molecule , medicine , organic chemistry , nursing , genetics
Aim: A new series of compounds ( 1a–16a ) bearing indole-fused benzooxazepine was synthesized, characterized and evaluated for anticancer activity. Materials & methods: In this study, all the synthesized compounds were screened via in vitro anticancer testing on Hep-G2 cancer cell line. A computational study was carried out on cancer-related targets including IL-2, IL-6, COX-2 Caspase-3 and Caspase-8. Results: Some of the synthesized compounds effectively controlled the growth of cancerous cells. Conclusion: The most active compounds – 6a , 10a , 13a , 14a and 15a – exemplify notable anticancer profile with GI 50 <10 μg/ml. Preliminary structure–activity relationship among the tested compounds can produce an assumption that the electronegative groups at phenyl ring attached with indole-fused benzooxazepine are instrumental for the activity. Molecular docking study showed crucial hydrogen bond and π–π stacking interactions, with good ADMET profiling and molecular dynamic simulation.
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