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Synthesis, characterization and evaluation of benzimidazole derivative and its precursors as inhibitors of MDA-MB-231 human breast cancer cell proliferation

A novel series of trisubstituted benzimidazole and its precursors ( 3– 7) were synthesised and characterized by using 1H NMR, LC/MS, FTIR and elemental analysis techniques. The title compounds were evaluated for inhibition against MDA-MB-231 breast cancer cell proliferation. The results revealed tha...

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Published in:Bioorganic & medicinal chemistry 2008, Vol.18 (1), p.432-435
Main Authors: Thimmegowda, N.R., Nanjunda Swamy, S., Ananda Kumar, C.S., Sunil Kumar, Y.C., Chandrappa, S., Yip, George W., Rangappa, K.S.
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cited_by cdi_FETCH-LOGICAL-c415t-fb4dd47cac9cb8d034d2094dfe5d2f09b79d2141f817844c193ba227a5ce9a393
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container_title Bioorganic & medicinal chemistry
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creator Thimmegowda, N.R.
Nanjunda Swamy, S.
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description A novel series of trisubstituted benzimidazole and its precursors ( 3– 7) were synthesised and characterized by using 1H NMR, LC/MS, FTIR and elemental analysis techniques. The title compounds were evaluated for inhibition against MDA-MB-231 breast cancer cell proliferation. The results revealed that the compound N-(4-cyano-3-(trifluoromethyl) phenyl)-4-fluoro-3-nitrobenzamide ( 3) was the potent inhibitor.
doi_str_mv 10.1016/j.bmcl.2007.08.078
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source ScienceDirect Journals
subjects Antineoplastic agents
Antineoplastic Agents - chemical synthesis
Antineoplastic Agents - chemistry
Antineoplastic Agents - pharmacology
Benzimidazoles - chemical synthesis
Benzimidazoles - chemistry
Benzimidazoles - pharmacology
Biological and medical sciences
Breast Neoplasms - drug therapy
Breast Neoplasms - pathology
Cell Growth Processes - drug effects
Cell Line, Tumor
Cell proliferation
General aspects
Humans
MDA-MB-231
Medical sciences
Nuclear Magnetic Resonance, Biomolecular
Pharmacology. Drug treatments
Spectroscopy, Fourier Transform Infrared
Trisubstituted benzimidazole
title Synthesis, characterization and evaluation of benzimidazole derivative and its precursors as inhibitors of MDA-MB-231 human breast cancer cell proliferation
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