cyclazosin hcl

Cyclazosin HCl 是一种具有亚型选择性的 α-肾上腺素能受体拮抗剂，竞争性拮抗去甲肾上腺素诱导的 α（1B）-肾上腺素能受体收缩，可用于研究非动脉前性缺血性视神经病变和其他神经系统疾病。

Cyclazosin Free Base is a monocarboxylic acid amide obtained by formal condensation of the carboxy group of furoic acid with the secondary amino group of 6,7-dimethoxy-2-[(4aR,8aS)-octahydroquinoxalin-1-yl]quinazolin-4-amine. It has a role as an adenosine A2A receptor antagonist. It is a member of quinazolines, a member of furans, an aromatic ether, a quinoxaline derivative, an aromatic amide and a monocarboxylic acid amide.