化学
苯并咪唑
药效团
苯胺
点击化学
体外
三唑
立体化学
质子核磁共振
细胞培养
分子
组合化学
有机化学
生物化学
遗传学
生物
作者
Ishani I. Sahay,Prasanna S. Ghalsasi
标识
DOI:10.1080/00397911.2017.1289412
摘要
One pot click chemistry is used to link triazole and benzimidazole pharmacophore to get N-((1-((1H-benzo[d]imidazol-2-yl)methyl)-1H-1,2,3-triazol-4-yl)methyl)aniline and its derivatives. Flexible linkages in the form of –CH2–R or –O–R/–N–R were designed during synthesis. All the newly synthesized compounds were characterized by FT-IR and NMR spectroscopy as well as high-resolution mass spectrometry. Selected compounds were screened for in vitro anti-proliferative activity using National Cancer Institute (NCI)-60 human tumor cell line screening program. The most potent structure N-((1-((1H-benzo[d]imidazol-2-yl)methyl)-1H-1,2,3-triazol-4-yl)methyl)-4-chloroaniline 7e showed 40% growth inhibition in renal cancer cell line (UO-31) at 10 µM concentration.
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