Literature DB >> 27240276

Synthesis, anti-proliferative and genotoxicity studies of 6-chloro-5-(2-substituted-ethyl)-1,3-dihydro-2H-indol-2-ones and 6-chloro-5-(2-chloroethyl)-3-(alkyl/ary-2-ylidene)indolin-2-ones.

Gangadhar Y Meti1, Atulkumar A Kamble2, Ravindra R Kamble3, Shilpa M Somagond2, H C Devarajegowda4, Sandhya Kumari5, Guruprasad Kalthur5, Satish K Adiga5.   

Abstract

A series of 6-chloro-5-(2-substituted-ethyl)-1,3-dihydro-2H-indol-2-ones (3a-h) and 6-chloro-5-(2-chloroethyl)-3-(alkyl/aryl-2-ylidene)indolin-2-ones (5i-x) were synthesized. Compounds 3a-e, 5i-l and 5q-r were selected by NIH, USA for in vitro anti-proliferative screening. Based on the impressive growth inhibitory (GI %) effect by the compounds 3a-b and 3e which showed growth inhibition in the range 1.22-76.30%, 2.85-76.03% and 10.98-82.05% respectively at 10(-5) concentration, these compounds were further analyzed for anti-proliferative activity at 5 dose concentration and genotoxicity.
Copyright © 2016 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  2H-Indol-2-ones; Anti-proliferative activity; Cell line; Genotoxicity

Mesh:

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Year:  2016        PMID: 27240276     DOI: 10.1016/j.ejmech.2016.05.028

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  1 in total

1.  Discovery and Anticancer Activity of Novel 1,3,4-Thiadiazole- and Aziridine-Based Indolin-2-ones via In Silico Design Followed by Supramolecular Green Synthesis.

Authors:  Prashant J Chaudhari; Sanjaykumar B Bari; Sanjay J Surana; Atul A Shirkhedkar; Chandrakant G Bonde; Saurabh C Khadse; Vinod G Ugale; Akhil A Nagar; Rameshwar S Cheke
Journal:  ACS Omega       Date:  2022-05-12
  1 in total

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