Synthesis and evaluation of some novel precursors of oxazolidinone analogues of chloroquinoline for their antimicrobial and cytotoxic potential

10Citations
Citations of this article
9Readers
Mendeley users who have this article in their library.

Abstract

Some 3-(3-(7-chloroquinolin-4-ylamino)propyl-2-imino-5-(4-chloro/nitro/ methoxy benzylidene) oxazolidin-4-one 4(a-c) and 4-(3-(7-chloroquinolin-4- ylamino) propyl)-2(4-chloro/nitro/methoxy benzylidene)-1,6-diox-4,9 diazaspiro[4,4]nonane-3,8-dione 5(a-c) derivatives were synthesized using appropriate synthetic route. The newly prepared compounds 5a-c demonstrated inhibitory effects on the growth of a MCF7 (hormone-dependant breast carcinoma cell line), HT29 (colon carcinoma cell line on leukemia). The MCF7 cell line was found to be very susceptible towards compound 5a with IC50 values of 16 μg/ml. Similarly, the HT29 cell line was found to be moderately susceptible towards compounds 5a and 5c with IC 50 values of 32 and 49 μg/ml, respectively. [Figure not available: see fulltext.] © 2013 Indian Academy of Sciences.

Cite

CITATION STYLE

APA

Devi, K., Asmat, K., Agrawal, M., Sharma, S., & Dwivedi, J. (2013). Synthesis and evaluation of some novel precursors of oxazolidinone analogues of chloroquinoline for their antimicrobial and cytotoxic potential. Journal of Chemical Sciences, 125(5), 1093–1101. https://doi.org/10.1007/s12039-013-0492-9

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free