118578-91-9Relevant articles and documents
Structure-guided design, synthesis, and evaluation of guanine-derived inhibitors of the eIF4E mRNA-cap interaction
Chen, Xiaoqi,Kopecky, David J.,Mihalic, Jeff,Jeffries, Shawn,Min, Xiaoshan,Heath, Julie,Deignan, Jeff,Lai, Sujen,Fu, Zice,Guimaraes, Cristiano,Shen, Shanling,Li, Shyun,Johnstone, Sheree,Thibault, Stephen,Xu, Haoda,Cardozo, Mario,Shen, Wang,Walker, Nigel,Kayser, Frank,Wang, Zhulun
, p. 3837 - 3851 (2012/07/28)
The eukaryotic initiation factor 4E (eIF4E) plays a central role in the initiation of gene translation and subsequent protein synthesis by binding the 5′ terminal mRNA cap structure. We designed and synthesized a series of novel compounds that display pot
Synthesis and biological activity of the metabolites of diethyl 4-[(4- bromo-2-cyanophenyl)carbamoyl]benzylphosphonate (NO-1886)
Goto,Nakamura,Morioka,Kondo,Naito,Tsutsumi
, p. 547 - 551 (2007/10/03)
Five metabolites of diethyl 4-[(4-bromo-2- cyanophenyl)carbamoyl]benzylphosphonate (NO-1886) (1) were synthesized to confirm their proposed structures. The metabolites (2-6) were found to be identical with the synthesized compounds. These metabolites were
Negative inotropic activity of para-substituted diethyl benzylphosphonates related to fostedil
Bellucci, Christina,Gualtieri, Fulvio,Chiarini, Alberto
, p. 473 - 478 (2007/10/02)
Several para-substituted diethyl benzylphosphonates related to the calcium antagonist diethyl 4-(2-benzothiazolyl)benzylphosphonate (fostedil) have been studied.They produce a dose-dependent negative inotropic effect on left atrial muscle isolated from guinea pig heart.Some of the compounds are equipotent or slightly more potent than fostedil and diltiazem taken as reference drugs.Structure-activity relationships are discussed.Keywords: calcium antagonists / p-substituted diethyl benzylphosphonates / cardiodepressant activity