| Literature DB >> 27956751 |
Bereket Mochona1, Timothy Jackson1, DeCoria McCauley1, Elizabeth Mazzio2, Kinfe K Redda2.
Abstract
Azomethine linked pyrrole bishetarylazoles containing benzimidazole/pyrazolone/1,3,4-oxadiazole were synthesized in satisfactory yields. Their structures were confirmed by IR, 1H-NMR, 13C-NMR and elemental analysis. Evaluation for the cytotoxic activities In vitro against a panel of breast cancer cell lines (MDA-AB-231, BT-474 and Ishikawa cells) revealed that the pyrrole-benzimidazole hybrids are more potent than the pyrazolone and 1,3,4-oxadiazole hybrids in all cell lines. Compound (9) displayed promising cytotoxicity against BT-474 cell line with IC50 values, 7.7 µM.Entities:
Year: 2015 PMID: 27956751 PMCID: PMC5147751 DOI: 10.1002/jhet.2501
Source DB: PubMed Journal: J Heterocycl Chem ISSN: 0022-152X Impact factor: 2.193