Urotensin-II receptor antagonists: Synthesis and SAR of N-cyclic azaalkyl benzamides
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Add time:09/07/2019 Source:sciencedirect.com
SAR exploration of the central diamine, benzyl, and terminal aminoalkoxy regions of the N-cyclic azaalkyl benzamide series led to the identification of very potent human urotensin-II receptor antagonists such as 1a with a Ki of 4 nM. The synthesis and structure–activity relationships (SAR) of N-cyclic azaalkyl benzamides are described.
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