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Synthesis and in vitro antitumor activity of benzimidazole derivatives

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TLDR
In this paper, a series of Schiff bases 1-11, the derivatives of 2-aryl-1H-benzimidazole has been synthesized and evaluated for their cytotoxic activity against the cells of human cancer cell lines, namely K-562 (myelogenous leukemia) and HL-60 (promyelocytic leukemia).
Abstract
One of the most important goals in medicinal chemistry is the development of new heterocyclic compounds with antitumor activity. Thus, a novel series of Schiff bases 1-11, the derivatives of 2-aryl-1H-benzimidazole has been synthesized and evaluated for their cytotoxic activity against the cells of human cancer cell lines, namely K-562 (myelogenous leukemia) and HL-60 (promyelocytic leukemia). Among the compounds tested against K-562 cell line, compounds 1, 7 and 10 showed potent activity and the compound 5 exhibited better activity against HL-60 cell line.

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Journal ArticleDOI

Synthesis and Evaluation of Anticancer Benzoxazoles and Benzimidazoles Related to UK-1

TL;DR: Results support a role of Mg(2+) ion binding in the selective cytotoxicity of UK-1 and provide a minimal pharmacophore for the select cytotoxic activity of the natural product.
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Design, synthesis and biological evaluation of benzimidazole/benzothiazole and benzoxazole derivatives as cyclooxygenase inhibitors.

TL;DR: A series of 2-[[2-alkoxy-6-pentadecylphenyl)methyl]thio]-1H-benzimidazoles/benzothiazoles and benzoxazoles from anacardic acid may serve as excellent candidates for selective COX-2 inhibition.
Book

Pharmacology and Pharmacotherapeutics

TL;DR: It is concluded that chlorpromazine produces a significant immunological inhibition when administered for 7 days prior to TAB vaccine.
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Synthesis and evaluation of some new benzimidazole derivatives as potential antimicrobial agents

TL;DR: The efficient synthesis of novel azetidin-2-ones 6 has been established and structures of the synthesized compounds have been elucidated on the basis of their elemental analyses and spectral data.
Journal ArticleDOI

Synthesis, antibacterial and antifungal activities of electron-rich olefins derived benzimidazole compounds

TL;DR: Nine of the tested compounds showed an antifungal activity with a range of the MICs between 50 and 400 microg/ml, and none of the compounds exhibit antimicrobial activity against Gram-negative bacteria.
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