@article{APS7566,
author = {Michael H Chen and Fu-zon Chung and Bruce D Roth and Be-sheng Kuo and James Atherton and Helen T Lee},
title = {Syntheses and biological activities of chiral piperidines-tachykinin NK3 antagonists},
journal = {Acta Pharmacologica Sinica},
volume = {20},
number = {3},
year = {2016},
keywords = {},
abstract = {AIM:
To develop nonpeptide tachykinin NK3 antagonists.
METHODS:
Five tachykinin NK3 antagonists were synthesized. Receptor binding assay and oral absorption study were made.
RESULTS:
The 4,4-disubstituted piperidine compounds (1b, 1c, and 1d) showed stronger activities (IC50 = 5.9, 6.2, and 11 nmol.L-1, respectively) than the monosubstituted ring compound 1e (IC50 = 17 nmol.L-1). 4-Phenyl (1b) and 4-phenylsulfonylmethyl (1c) compounds were more active than the 4-fluorobenzyl compound (1d). All antagonists were found to be orally absorbable, the T1/2 of 1b (6.4 h) was more than three-fold longer than that of 1a (1.9 h).
CONCLUSION:
Compound 1b had the best binding activity (IC50 = 5.9 nmol.L-1) and the best AUC (2081 micrograms.h.L-1).},
issn = {1745-7254}, url = {http://www.chinaphar.com/article/view/7566}
}