76384-45-7Relevant articles and documents
Pyridinium and indole orientation determines the mitochondrial uncoupling and anti-cancer efficiency of F16
Xu, Juan,He, Huan,Zhou, Lian-Jiao,Liu, Yu-Zhu,Li, Dong-Wei,Jiang, Feng-Lei,Liu, Yi
, p. 305 - 313 (2018/05/30)
F16 is a mitochondria-targeted, broad-spectrum anticancer agent in the pre-clinic cancer therapy. Here we developed two fluorescent isomers of F16 (o-F16 and m-F16) with entirely different photophysical properties, uncoupling activity, and cytotoxicity by
Substituted 2-and 4-[2-(3-indolyl)ethenyl]pyridinium salts as MAO-B inhibitors: Quantitative modeling of the structure-activity relationship
Bachurin,Fetisov,Afanas'ev,Afanas'eva,Dubova,Yankovskaya,Mukhina
, p. 41 - 44 (2007/10/03)
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