您当前所在的位置:首页 > 产品中心 > 产品信息
Xli 093 hydrate_分子结构_CAS_646066-59-3(anhydrous))
点击图片或这里关闭

Xli 093 hydrate

产品号 X4628 公司名称 Sigma Aldrich
CAS号 646066-59-3(anhydrous) 公司网站 http://www.sigmaaldrich.com
分子式 C33H28N6O7 电 话 1-800-521-8956
分子量 620.61142 传 真
纯 度 ≥98% (HPLC) 电子邮件
保 存 Chembase数据库ID: 153946

产品价格信息

请登录

产品别名

标题
Xli 093 hydrate
IUPAC标准名
3-{12-ethynyl-8-methyl-9-oxo-2,4,8-triazatricyclo[8.4.0.02,6]tetradeca-1(14),3,5,10,12-pentaene-5-carbonyloxy}propyl 12-ethynyl-8-methyl-9-oxo-2,4,8-triazatricyclo[8.4.0.02,6]tetradeca-1(14),3,5,10,12-pentaene-5-carboxylate hydrate
IUPAC传统名
3-{12-ethynyl-8-methyl-9-oxo-2,4,8-triazatricyclo[8.4.0.02,6]tetradeca-1(14),3,5,10,12-pentaene-5-carbonyloxy}propyl 12-ethynyl-8-methyl-9-oxo-2,4,8-triazatricyclo[8.4.0.02,6]tetradeca-1(14),3,5,10,12-pentaene-5-carboxylate hydrate
别名
Bis[8-ethynyl-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid] 1,3-propanediyl ester hydrate

产品登记号

CAS号 646066-59-3(anhydrous)
PubChem SID 24724668
MDL号 MFCD08705422

产品性质

Empirical Formula (Hill Notation) C33H26N6O6 · xH2O
纯度 ≥98% (HPLC)
外观 off-white powder
溶解度 DMSO: ~16 mg/mL
溶解度 H2O: insoluble
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
Xli 093 is α5 subtype selective benzodiazepine/GABAA receptor antagonist. Xli 093 shows Ki = 5 nM at the α5 receptor in Ltk- cell membranes expressing human α5β3γ2 receptors; little or no affinity at other BDZ/ GABAA subtypes; does not trigger chloride currents in any subtype of tested subtypes, up to 1 μM in concentration; dose-dependently and completely inhibits diazepam stimulated currents in α5β3γ2 receptors.
详细说明 (简体中文)
Biochem/physiol Actions
Xli 093 is α5 subtype selective benzodiazepine/GABAA receptor antagonist. Xli 093 shows Ki = 5 nM at the α5 receptor in Ltk- cell membranes expressing human α5β3γ2 receptors; little or no affinity at other BDZ/ GABAA subtypes; does not trigger chloride currents in any subtype of tested subtypes, up to 1 μM in concentration; dose-dependently and completely inhibits diazepam stimulated currents in α5β3γ2 receptors.

参考文献