您当前所在的位置:首页 > 产品中心 > 产品信息
BIMU8 hydrate_分子结构_CAS_134296-40-5(anhydrous))
点击图片或这里关闭

BIMU8 hydrate

产品号 B4063 公司名称 Sigma Aldrich
CAS号 134296-40-5(anhydrous) 公司网站 http://www.sigmaaldrich.com
分子式 C19H29ClN4O3 电 话 1-800-521-8956
分子量 396.91156 传 真
纯 度 ≥98% (HPLC) 电子邮件
保 存 desiccated Chembase数据库ID: 154634

产品价格信息

请登录

产品别名

标题
BIMU8 hydrate
IUPAC标准名
N-[(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl]-2-oxo-3-(propan-2-yl)-2,3-dihydro-1H-1,3-benzodiazole-1-carboxamide hydrate hydrochloride
IUPAC传统名
3-isopropyl-N-[(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl]-2-oxo-1,3-benzodiazole-1-carboxamide hydrate hydrochloride
别名
2,3-Dihydro-N-[(3-endo)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl]-3-(1-methylethyl)-2-oxo-1H-benzimidazole-1-carboxamide Hydrochloride (1:1) hydrate

产品登记号

CAS号 134296-40-5(anhydrous)

产品性质

Empirical Formula (Hill Notation) C19H26N4O2·HCl · xH2O
纯度 ≥98% (HPLC)
外观 off-white to light tan
溶解度 H2O: ≥5 mg/mL
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H315-H319-H335
欧盟危险性物质标志 刺激性(Irritant) 刺激性(Irritant) (Xi)
MSDS下载 下载链接
GHS警示性声明 P261-P305 + P351 + P338
危险公开号 36/37/38
安全公开号 26
保存条件 desiccated
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
BIMU8 hydrate is a potent 5-HT4 serotonin receptor agonist. Serotonin (5-HT) is a major neurotransmitter that acts through a family of GPCRs and one ion channel. 5-HT4 receptor is GPCR expressed in many tissues, including brain, and modulates dopamine secretion, learning, and memory. BIMU8 is a full agonist at 5-HT4, but it binds differently than the endogenous ligand, 5-HT, shown through site-directed mutagenesis studies. It depolarizes neurons and was used to localize 5-HT4 to somatic but not dendritic regions of CA1 pyramidal neurons.
详细说明 (简体中文)
Biochem/physiol Actions
BIMU8 hydrate is a potent 5-HT4 serotonin receptor agonist. Serotonin (5-HT) is a major neurotransmitter that acts through a family of GPCRs and one ion channel. 5-HT4 receptor is GPCR expressed in many tissues, including brain, and modulates dopamine secretion, learning, and memory. BIMU8 is a full agonist at 5-HT4, but it binds differently than the endogenous ligand, 5-HT, shown through site-directed mutagenesis studies. It depolarizes neurons and was used to localize 5-HT4 to somatic but not dendritic regions of CA1 pyramidal neurons.

参考文献