The identification of potent, orally bioavailable tricyclic CGRP receptor antagonists
作者:Ian M. Bell、Rodney A. Bednar、Halea A. Corcoran、John F. Fay、Steven N. Gallicchio、Victor K. Johnston、James C. Hershey、Cynthia M. Miller-Stein、Eric L. Moore、Scott D. Mosser、Shane A. Roller、Christopher A. Salvatore、Cory R. Theberge、Bradley K. Wong、C. Blair Zartman、Stefanie A. Kane、Theresa M. Williams、Samuel L. Graham、Joseph P. Vacca
DOI:10.1016/j.bmcl.2009.06.057
日期:2009.8
A series of tricyclic CGRP receptor antagonists was optimized in order to improve oral bioavailability. Attenuation of polar surface area and incorporation of a weakly basic indoline nitrogen led to compound 5, a potent antagonist with good oral bioavailability in three species. (C) 2009 Elsevier Ltd. All rights reserved.
[EN] TRICYCLIC ANILIDE SPIROLACTAM CGRP RECEPTOR ANTAGONISTS<br/>[FR] ANTAGONISTES DES RECEPTEURS CGRP SOUS FORME DE SPIROLACTAME D'ANILIDE TRICYCLIQUE