
Journal of Medicinal Chemistry p. 2591 - 2600 (1992)
Update date:2022-08-04
Topics:
Lowe, John A.
Drozda, Suzan E.
Snider, R. Michael
Longo, Kelly P.
Zorn, Stevin H.
et al.
We describe the structure-activity relationship development of a series of quinuclidines which culminated in the first potent, selective, nonpeptide substance P (SP) antagonist, (2S,3S)-cis-2-(diphenylmethyl)-N-<(2-methoxyphenyl)methyl>-1-azabicyclo<2.2.2
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