| Literature DB >> 28753313 |
Gabriel Martinez Botella1, Francesco G Salituro1, Boyd L Harrison1, Richard T Beresis2, Zhu Bai3, Maria-Jesus Blanco1, Gabriel M Belfort1, Jing Dai1, Carlos M Loya1, Michael A Ackley1, Alison L Althaus1, Scott J Grossman1, Ethan Hoffmann1, James J Doherty1, Albert J Robichaud1.
Abstract
Certain classes of neuroactive steroids (NASs) are positive allosteric modulators (PAM) of synaptic and extrasynaptic GABAA receptors. Herein, we report new SAR insights in a series of 5β-nor-19-pregnan-20-one analogues bearing substituted pyrazoles and triazoles at C-21, culminating in the discovery of 3α-hydroxy-3β-methyl-21-(4-cyano-1H-pyrazol-1'-yl)-19-nor-5β-pregnan-20-one (SAGE-217, 3), a potent GABAA receptor modulator at both synaptic and extrasynaptic receptor subtypes, with excellent oral DMPK properties. Compound 3 has completed a phase 1 single ascending dose (SAD) and multiple ascending dose (MAD) clinical trial and is currently being studied in parallel phase 2 clinical trials for the treatment of postpartum depression (PPD), major depressive disorder (MDD), and essential tremor (ET).Entities:
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Year: 2017 PMID: 28753313 DOI: 10.1021/acs.jmedchem.7b00846
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446