化学
亲脂性
降钙素基因相关肽
偏头痛
药品
铅化合物
药物发现
立体化学
降钙素
敌手
体外
受体
药理学
内科学
生物化学
神经肽
医学
作者
S.J. Bucknell,Mark A. Ator,Alastair Brown,Jason Brown,Andrew D. Cansfield,Julie E. Cansfield,J.A. Christopher,Miles Congreve,G. Cseke,Francesca Deflorian,Christopher R. Jones,Jonathan Mason,Alistair O’Brien,Gregory R. Ott,Mark Pickworth,Stacey M. Southall
标识
DOI:10.1021/acs.jmedchem.0c01003
摘要
Structure-based drug design enabled the discovery of 8, HTL22562, a calcitonin gene-related peptide (CGRP) receptor antagonist. The structure of 8 complexed with the CGRP receptor was determined at a 1.6 Å resolution. Compound 8 is a highly potent, selective, metabolically stable, and soluble compound suitable for a range of administration routes that have the potential to provide rapid systemic exposures with resultant high levels of receptor coverage (e.g., subcutaneous). The low lipophilicity coupled with a low anticipated clinically efficacious plasma exposure for migraine also suggests a reduced potential for hepatotoxicity. These properties have led to 8 being selected as a clinical candidate for acute treatment of migraine.
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