化学
CXCR3型
趋化因子
药理学
受体
敌手
小分子
趋化因子受体
生物
生物化学
作者
Stephen P. Andrews,Rhona J. Cox
标识
DOI:10.1021/acs.jmedchem.5b01337
摘要
Chemokines and their receptors are known to play important roles in disease. More than 40 chemokine ligands and 20 chemokine receptors have been identified, but, to date, only two small molecule chemokine receptor antagonists have been approved by the FDA. The chemokine receptor CXCR3 was identified in 1996, and nearly 20 years later, new areas of CXCR3 disease biology continue to emerge. Several classes of small molecule CXCR3 antagonists have been developed, and two have shown efficacy in preclinical models of inflammatory disease. However, only one CXCR3 antagonist has been evaluated in clinical trials, and there remain many opportunities to further investigate known classes of CXCR3 antagonists and to identify new chemotypes. This Perspective reviews the known CXCR3 antagonists and considers future opportunities for the development of small molecules for clinical evaluation.
科研通智能强力驱动
Strongly Powered by AbleSci AI