变构调节
化学
神经活性类固醇
变构调节剂
孕酮
受体
γ-氨基丁酸受体
药理学
γ-氨基丁酸受体
结构-活动关系
立体化学
生物化学
体外
医学
作者
Gabriel Martinez Botella,Francesco G. Salituro,Boyd L. Harrison,Richard T. Beresis,Zhu Bai,Kaisheng Shen,Gabriel M. Belfort,Carlos M. Loya,Michael A. Ackley,Scott Grossman,Ethan Hoffmann,Shiling Jia,Jiamiao Wang,James Doherty,Albert J. Robichaud
标识
DOI:10.1021/acs.jmedchem.5b00032
摘要
Neuroactive steroids (NASs) have been shown to impact central nervous system (CNS) function through positive allosteric modulation of the GABA(A) receptor (GABA(A)-R). Herein we report the effects on the activity and pharmacokinetic properties of a series of nor-19 pregnanolone analogues bearing a heterocyclic substituent at C-21. These efforts resulted in the identification of SGE-516, a balanced synaptic/extrasynaptic GABA(A) receptor modulator, and SGE-872, a selective extrasynaptic GABA(A) receptor modulator. Both molecules possess excellent druglike properties, making them advanced leads for oral delivery of GABA(A) receptor modulators.
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