加压素
加压素受体
加压素拮抗剂
精氨酸加压素受体2
受体
精氨酸加压素受体1B
药理学
神经科学
医学
生物信息学
生物
内科学
敌手
作者
Ferenc Baska,Éva Bozó,Tamás Patócs
标识
DOI:10.1080/13543776.2023.2218546
摘要
In recent years, vasopressin receptor antagonists have been in the spotlight of drug discovery, especially V1a selective molecules. Publishing balovaptan as a possible treatment for autism spectrum disorder (ASD), greatly increased the interest in CNS-acting vasopressin antagonists. In addition, peripherally active selective V2 and dual-acting V1a/V2 antagonists have also been developed. Although clinical trials were unsuccessful in many cases, there is still potential in the research of vasopressin receptor antagonists as shown by several currently ongoing clinical trials.
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