【摘 要】
:
A series of novel compounds(8a-21b)were designed and synthesized based on lH-benzo[d]imidazole.Their biological activities were evaluated as potential tubulin polymerization inhibitors and anticancer
【机 构】
:
State Key Laboratory of Pharmaceutical Biotechnology,Nanjing University,Nanjing 210093,People's Rep
【出 处】
:
第八届国际分子模拟与信息技术应用学术会议
论文部分内容阅读
A series of novel compounds(8a-21b)were designed and synthesized based on lH-benzo[d]imidazole.Their biological activities were evaluated as potential tubulin polymerization inhibitors and anticancer agents.Among all the compounds,compound 18b showed the most potent in vitro growth inhibitory activity against A549,MCF-7,K562 cancer cell lines,with IC50 values of 0.12 μM,0.15 μM,0.21 μM,respectively.And,compound 18b also exhibited significant tubulin polymerization inhibitory activity(IC50=2.1 μM),which was comparable with the positive control.Furthermore,docking simulation and 3D-QSAR modeling of inhibitor analogues provide determination of the probable binding model and an important basis that compound 18b with potent inhibitory activity in tumor growth may be a potential anticancer agent.
其他文献
Metronidazole-sulfonamide derivatives 4a-4l,a new class of human carbonic anhydrase inhibitors(hCA),were designed,synthesized,isolated,and evaluated for their ability to inhibit the enzymatic activity
The aim of this study was to investigate the angiogenic effects of curcumin on an ischemia and lung cancer model.To induce ischemia combined with lung cancer models,unilateral femoral arteries of C57B
Background: Quantitative description of dose-response of a drug for complex systems is essential fortreatment of diseases and drug discovery.Given the growth of large-scale biological data obtained by
Cytochrome P450(CYP)17A1 is a dual-function monooxygenase with a critical role in the synthesis or many human steroid hormones The enzyme is an important target for Lrealment of breast and prostate ca
Anticoagulants and anti-platelet agents are simultaneously administrated in clinical practice(i.e.percutaneous coronary intervention),which cause significant risk of systemic bleeding.Targeted deliver
Fatty actci biosynthesis is essential for bacterial survival.FabH,β-ketoacyl-acyl carrier protein(ACP)synthase Ⅲ,is a particularly attractive target,since it is central to the initiation of fatty acid
Series of novel Schiffs base derivatives have been synthesized by combining 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl 4-formylbenzoate 5,6 with aromatic/heterocyclic amine 7a-r,8,9a-r in ethanol.All
A series of aryl-2H-pyrazole derivatives were synthesized and evaluated for inhibitory activity against xanthine oxidase in vitro as potent xanthine oxidase inhibitors.Among them,2 aryl-2H-pyrazole de
A series of 1-methyl-1H-indole-pyrazoline hybrids were designed,synthesized,and biologically evaluated as potential tubulin polymerization inhibitors.Among them,compound e19 [5-(5-bromo-1-methyl-1H-in
A series of novel compounds(6a-6v)containing l-methylindol and 31-(4,5-dihydro-lH-pyraxol-1-yl)ethanone skeleton were designed,synthesized and biologically evaluated as potential tubulin polymerizatio