Unknown

Dataset Information

0

Synthesis and antitumor activity of novel N-substituted carbazole imidazolium salt derivatives.


ABSTRACT: A series of novel N-substituted carbazole imidazolium salt derivatives has been prepared and investigated for their cytotoxic activity against five human tumor cell lines by MTS assay. The results indicated that the existence of 5,6-dimethyl-benzimidazole ring, substitution of the imidazolyl-3-position with a 2-bromobenzyl or naphthylacyl group, as well as alkyl chain length between carbazole and imidazole ring were important for the antitumor activity. Compound 61, bearing a 2-bromobenzyl substituent at position-3 of the 5,6-dimethyl-benzimidazole, showed powerful inhibitory activities and was more selective to HL-60, SMMC-7721, MCF-7 and SW480 cell lines with IC50 values 0.51-2.48??M. Mechanism of action studies revealed that this new compound could remarkably induce cell cycle arrest and apoptosis in SMMC-7721 cells. This work provides alternative novel way for future drug development based on carbazole and imidazolium salt scaffolds.

SUBMITTER: Liu LX 

PROVIDER: S-EPMC4642527 | biostudies-literature | 2015 Aug

REPOSITORIES: biostudies-literature

altmetric image

Publications

Synthesis and antitumor activity of novel N-substituted carbazole imidazolium salt derivatives.

Liu Lan-Xiang LX   Wang Xue-Quan XQ   Zhou Bei B   Yang Li-Juan LJ   Li Yan Y   Zhang Hong-Bin HB   Yang Xiao-Dong XD  

Scientific reports 20150819


A series of novel N-substituted carbazole imidazolium salt derivatives has been prepared and investigated for their cytotoxic activity against five human tumor cell lines by MTS assay. The results indicated that the existence of 5,6-dimethyl-benzimidazole ring, substitution of the imidazolyl-3-position with a 2-bromobenzyl or naphthylacyl group, as well as alkyl chain length between carbazole and imidazole ring were important for the antitumor activity. Compound 61, bearing a 2-bromobenzyl subst  ...[more]

Similar Datasets

| S-EPMC6598646 | biostudies-literature
| S-EPMC8198100 | biostudies-literature
| S-EPMC6151509 | biostudies-literature
| S-EPMC6225359 | biostudies-literature
| S-EPMC5609566 | biostudies-literature
| S-EPMC7865355 | biostudies-literature
| S-EPMC6272846 | biostudies-literature
| S-EPMC4337696 | biostudies-literature
| S-EPMC10889159 | biostudies-literature
| S-EPMC6264406 | biostudies-literature