3273-78-7Relevant articles and documents
Design of novel bis-benzimidazole derivatives as DNA minor groove binding agents
Wang, Xiu-Jun,Yang, Ming-Li,Zhang, Lan-Ping,Yao, Tong,Chen, Cheng,Mao, Lian-Gang,Wang, Yin,Wu, Jie
, p. 589 - 592 (2014/05/06)
A new series of bis-benzimidazole derivatives were designed and synthesized. In vitro cytotoxicity evaluation showed that these compounds exhibited high activity against the selected tumor cells. Among them, compound 9 owned the best potential, its IC50 values being 5.95 μmol/L (mononuclear tumor cell line (U937)) and 5.58 μmol/L (cervical cancer cell (HeLa)). Fluorescence and UV-vis studies showed that compound 9 could bind into the minor groove of DNA.
Oppi briefs practical and efficient synthesis of 4,4'-dihydroxy-3,3'- dinitrodiphenyl ether and 1,3-bis(4-hydroxy-3-nitrophenoxy)benzene in aqueous alkaline medium
Imoto, Mitsutaka,Takeda, Motonori,Tamaki, Akihiro,Taniguchi, Hisaji,Mizuno, Kazuhiko
scheme or table, p. 161 - 167 (2010/09/05)
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Synthesis and structure of Di[methoxy(ethoxy)carbonylamino-1H-benzimidazol- 5-yl] ethers
Pilyugin,Sapozhnikov,Kiseleva,Sapozhnikova,Vorob'eva,Klimakova
, p. 1509 - 1513 (2007/10/03)
A procedure was developed for preparing di[methoxy(ethoxy)carbonylamino-1H- benzimidazol-5-yl] ethers by the reaction of methyl or ethyl chloroformate with sodium cyanamide, followed by the reaction of the resulting methyl or ethyl cyanocarbamate with 4-(3,4-diaminophenoxy)-1,2-phenylenediamine in acidic solution. 2005 Pleiades Publishing, Inc.