| Literature DB >> 9873680 |
M S Kuo1, M G Bock, R M Freidinger, M T Guidotti, E V Lis, J M Pawluczyk, D S Perlow, D J Pettibone, A G Quigley, D R Reiss, P D Williams, C J Woyden.
Abstract
Structure-activity studies on the oxytocin antagonist 1 (L-371,257) have identified a new series of high affinity, receptor-selective OT antagonists in which the N-acetyl-4-piperidinyl ether terminus in 1 has been replaced with a 1-(aryl)ethoxy group.Mesh:
Substances:
Year: 1998 PMID: 9873680 DOI: 10.1016/S0960-894X(98)00568-X
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823