您当前所在的位置:首页 > 产品中心 > 产品信息
α5IA_分子结构_CAS_215874-86-5)
点击图片或这里关闭

α5IA

产品号 A2734 公司名称 Sigma Aldrich
CAS号 215874-86-5 公司网站 http://www.sigmaaldrich.com
分子式 C17H14N8O2 电 话 1-800-521-8956
分子量 362.34546 传 真
纯 度 ≥98% (HPLC) 电子邮件
保 存 Chembase数据库ID: 130268

产品价格信息

请登录

产品别名

标题
α5IA
IUPAC标准名
1-methyl-4-({[3-(5-methyl-1,2-oxazol-3-yl)-[1,2,4]triazolo[3,4-a]phthalazin-6-yl]oxy}methyl)-1H-1,2,3-triazole
IUPAC传统名
Α5IA
别名
3-(5-Methylisoxazol-3-yl)-6-(1-methyl-1,2,3-triazol-4-yl)methoxy-1,2,4-triazolo[3,4-a]phthalazine
1,2,4-Triazolo[3,4-a]phthalazine, 3-(5-methyl-3-isoxazolyl)-6-[(1-methyl-1H-1,2,3-triazol-4-yl)methoxy]-

产品登记号

MDL号 MFCD09832717
CAS号 215874-86-5

产品性质

Empirical Formula (Hill Notation) C17H14N8O2
纯度 ≥98% (HPLC)
外观 off-white to light yellow powder
溶解度 DMSO: >2 mg/mL
MSDS下载 下载链接
个人保护装置 Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
保存温度 2-8°C
德国WGK号 3

产品详细信息

详细说明 (English)
Biochem/physiol Actions
α5IA is a selective inverse agonist for Α5 subtype of GABAA receptor with a higher intrinsic activity at the A5 subtype than other drugs. α5IA enhances cognition in laboratory animals without being proconvulsant or anxiogenic. α5IA acts as an "alcohol antagonist," markedly reducing the amnesic effect of alcohol and partially attenuating sedation, similar to Ro15-4513, but without the anxiogenic effect. α5IA offers promise as a tool to study cognitive disorders, memory function, and treatment of alcohol-related disorders.
详细说明 (简体中文)
Biochem/physiol Actions
α5IA is a selective inverse agonist for Α5 subtype of GABAA receptor with a higher intrinsic activity at the A5 subtype than other drugs. α5IA enhances cognition in laboratory animals without being proconvulsant or anxiogenic. α5IA acts as an "alcohol antagonist," markedly reducing the amnesic effect of alcohol and partially attenuating sedation, similar to Ro15-4513, but without the anxiogenic effect. α5IA offers promise as a tool to study cognitive disorders, memory function, and treatment of alcohol-related disorders.

参考文献