870766-46-4Relevant academic research and scientific papers
Tricyclononene carboxamide derivatives as novel anti-HIV-1 agents
Dong, Ming-Xin,Zhang, Jian,Peng, Xu-Qing,Lu, Hong,Yun, Liu-Hong,Jiang, Shibo,Dai, Qiu-Yun
experimental part, p. 4096 - 4103 (2010/10/02)
By modifying the chemical structure of anti-orthopoxvirus compound ST-246, we designed and synthesized a series of tricyclononene carboxamide derivatives and tested their anti-HIV-1 activity and cytotoxicity. We found that benzoimidazol-containing compound 7g was highly effective in inhibiting HIV-1 R5 infection with an IC50 value of 0.41 μM and a selectivity index of 292, but it exhibited no significant inhibitory activity on HIV-1 reverse transcriptase, integrase and protease. CoMFA was used to analyze structure-activity relationships with good predictive power (r2 = 0.921; q2 = 0.582). Moreover, the CoMFA model showed that the length of the molecule, the amide, and the amine moieties all played crucial roles in anti-HIV activity. These results suggest that 7g may serve as a lead for the development of novel anti-HIV-1 therapies. A series of tricyclononene carboxamide derivatives based on anti-orthopoxvirus compound ST-246 were synthesized and characterized as novel anti-HIV-1 agents.
Synthesis of 4-(1H-Azol-1-ylmethyl)benzohydrazides and their acyclic and heterocyclic derivatives
Osyanin,Purygin,Belousova
, p. 111 - 117 (2007/10/03)
4-(1H-Azol-1-ylmethyl)benzohydrazides were prepared from methyl 4-(bromomethyl)benzoate, azoles, and hydrazine hydrate. Reactions of 4-(1H-imidazol-1-ylmethyl)benzohydrazide with carbonyl compounds gave hydrazones whose tautomerism was studied. From the h
