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GW405833 盐酸盐_分子结构_CAS_180002-83-9)
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GW405833 盐酸盐

产品号 G1421 公司名称 Sigma Aldrich
CAS号 180002-83-9 公司网站 http://www.sigmaaldrich.com
分子式 C23H25Cl3N2O3 电 话 1-800-521-8956
分子量 483.8152 传 真
纯 度 ≥98% (HPLC) 电子邮件
保 存 Chembase数据库ID: 155550

产品价格信息

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产品别名

标题
GW405833 hydrochloride
IUPAC标准名
1-(2,3-dichlorobenzoyl)-5-methoxy-2-methyl-3-[2-(morpholin-4-yl)ethyl]-1H-indole hydrochloride
IUPAC传统名
1-(2,3-dichlorobenzoyl)-5-methoxy-2-methyl-3-[2-(morpholin-4-yl)ethyl]indole hydrochloride
别名
1-(2,3-Dichlorobenzoyl)-5-methoxy-2-methyl-(3-(morpholin-4-yl)ethyl)-1H-indole hydrochloride
1-(2,3-Dichlorobenzoyl)-5-methoxy-2-methyl-(3-(morpholin-4-yl)ethyl)-1H-indole 盐酸盐

产品登记号

MDL号 MFCD09832650
CAS号 180002-83-9

产品性质

Empirical Formula (Hill Notation) C23H24Cl2N2O3 · HCl
纯度 ≥98% (HPLC)
外观 tan solid
溶解度 DMSO: soluble >10 mg/mL
溶解度 H2O: insoluble <2 mg/mL
毒品管制信息 regulated under CDSA - not available from Sigma-Aldrich Canada
GHS危险品标识 GHS06
GHS警示词 Danger
GHS危险声明 H301-H413
欧盟危险性物质标志 有毒(Toxic) 有毒(Toxic) (T)
MSDS下载 下载链接
个人保护装置 Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
GHS警示性声明 P301 + P310
RID/ADR UN 2811 6.1/PG 3
危险公开号 25
安全公开号 45
保存温度 2-8°C
联合国危险货物等级 6.1
联合国危险货物编号 2811
联合国危险货物包装类别(PG) 3
德国WGK号 3

产品详细信息

详细说明 (English)
Biochem/physiol Actions
GW405833 is a selective cannabanoid CB2 receptor agonist; analgesic. GW405833 binds with high affinity at both human and rat CB2 receptors (Ki′s 3.9 and 3.6 nM); acts as a partial agonist (50% inhibition of forskolin-stimulated cAMP formation compared to full agonist CP55,940). GW405833 has potent analgesic activity in rat models of inflammatory, neuropathic and incisional pain; devoid of CNS effects common with CB1 agonists.
详细说明 (简体中文)
Biochem/physiol Actions
GW405833 is a selective cannabanoid CB2 receptor agonist; analgesic. GW405833 binds with high affinity at both human and rat CB2 receptors (Ki′s 3.9 and 3.6 nM); acts as a partial agonist (50% inhibition of forskolin-stimulated cAMP formation compared to full agonist CP55,940). GW405833 has potent analgesic activity in rat models of inflammatory, neuropathic and incisional pain; devoid of CNS effects common with CB1 agonists.

参考文献