2′ Biaryl amides as novel and subtype selective M1 agonists. Part II: Further optimization and profiling
摘要:
Further optimization of the biaryl amide series via extensively exploring structure-activity relationships resulted in potent and subtype selective M-1 agonists exemplified by compounds 9a and 9j with good rat PK properties including CNS penetration. Synthesis, structure-activity relationships, subtype selectivity for M-1 over M2-5, and DMPK properties of these novel compounds are described. (C) 2010 Elsevier Ltd. All rights reserved.
2′ Biaryl amides as novel and subtype selective M1 agonists. Part II: Further optimization and profiling
摘要:
Further optimization of the biaryl amide series via extensively exploring structure-activity relationships resulted in potent and subtype selective M-1 agonists exemplified by compounds 9a and 9j with good rat PK properties including CNS penetration. Synthesis, structure-activity relationships, subtype selectivity for M-1 over M2-5, and DMPK properties of these novel compounds are described. (C) 2010 Elsevier Ltd. All rights reserved.