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Continued optimization of the M

Authors :
Kevin M, McGowan
Kellie D, Nance
Hykeyung P, Cho
Thomas M, Bridges
P Jeffrey, Conn
Carrie K, Jones
Craig W, Lindsley
Source :
Bioorganicmedicinal chemistry letters. 27(6)
Publication Year :
2017

Abstract

This letter describes the continued optimization of M5 NAM ML375 (VU0483253). While a valuable in vivo tool compound, ML375 has an excessively long elimination half-life in rat (t1/2 = 80 hours), which can be problematic in certain rodent addiction paradigms (e.g., reinstatement). Thus, we required an M5 NAM of comparable potency to ML375, but with a rat t1/2 of less than 4 hours. Steep SAR plagued this chemotype, and here we detail aniline replacements that offered some improvements over ML375, but failed to advance. Ultimately, incorporation of a single methyl group to the 9b-phenyl ring acted as a metabolic shunt, providing (S)-11 (VU6008667), an equipotent M5 NAM, with high CNS penetration, excellent selectivity versus M1–4 and the desired short half-life (t1/2 = 2.3 hours) in rat.

Details

ISSN :
14643405
Volume :
27
Issue :
6
Database :
OpenAIRE
Journal :
Bioorganicmedicinal chemistry letters
Accession number :
edsair.pmid..........75511e0cc234945cd1241e2c5d65834c