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TMPH hydrochloride_分子结构_CAS_849461-91-2)
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TMPH hydrochloride

产品号 T5576 公司名称 Sigma Aldrich
CAS号 849461-91-2 公司网站 http://www.sigmaaldrich.com
分子式 C16H32ClNO2 电 话 1-800-521-8956
分子量 305.88378 传 真
纯 度 (Product is pure based on CHN, NMR and MS results) 电子邮件
保 存 under inert gas Chembase数据库ID: 153937

产品价格信息

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产品别名

标题
TMPH hydrochloride
IUPAC标准名
2,2,6,6-tetramethylpiperidin-4-yl heptanoate hydrochloride
IUPAC传统名
2,2,6,6-tetramethylpiperidin-4-yl heptanoate hydrochloride
别名
2,2,6,6-Tetramethylpiperidin-4-yl heptanoate hydrochloride

产品登记号

PubChem SID 24724633
CAS号 849461-91-2
MDL号 MFCD08277030

产品性质

Empirical Formula (Hill Notation) C16H32ClNO2
纯度 (Product is pure based on CHN, NMR and MS results)
外观 white solid
溶解度 H2O: soluble22 mg/mL at ~60 °C
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H315-H317-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
个人保护装置 dust mask type N95 (US), Eyeshields, Faceshields, Gloves
GHS警示性声明 P261-P280-P305 + P351 + P338
危险公开号 36/37/38-43
安全公开号 26-36/37
保存条件 under inert gas
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
2,2,6,6-tetramethylpiperidin-4-yl heptanoate (TMPH) is a potent inhibitor of neuronal nicotinic receptors. Evaluation of nicotinic acetylcholine receptor (nAChR) subunits expressed in Xenopus laevis oocytes indicated that TMPH can produce a potent and long-lasting inhibition of neuronal nAChR formed by the pairwise combination of the most abundant neuronal alpha (i.e., alpha3 and alpha4) and beta subunits (beta2 and beta4), with relatively little effect, because of rapid reversibility of inhibition, on muscle-type (alpha1beta1gammadelta) or alpha7 receptors. However, the inhibition of neuronal beta subunit-containing receptors was also decreased if any of the nonessential subunits alpha5, alpha6, or beta3 were coexpressed. This decrease in inhibition is shown to be associated with a single amino acid present in the second transmembrane domain of these subunits. TMPH abilitty to relate the diverse central nervous system effects to specific nAChR subtypes makes it a useful tool for studying the functional roles of nAChR.
详细说明 (简体中文)
Biochem/physiol Actions
2,2,6,6-tetramethylpiperidin-4-yl heptanoate (TMPH) is a potent inhibitor of neuronal nicotinic receptors. Evaluation of nicotinic acetylcholine receptor (nAChR) subunits expressed in Xenopus laevis oocytes indicated that TMPH can produce a potent and long-lasting inhibition of neuronal nAChR formed by the pairwise combination of the most abundant neuronal alpha (i.e., alpha3 and alpha4) and beta subunits (beta2 and beta4), with relatively little effect, because of rapid reversibility of inhibition, on muscle-type (alpha1beta1gammadelta) or alpha7 receptors. However, the inhibition of neuronal beta subunit-containing receptors was also decreased if any of the nonessential subunits alpha5, alpha6, or beta3 were coexpressed. This decrease in inhibition is shown to be associated with a single amino acid present in the second transmembrane domain of these subunits. TMPH abilitty to relate the diverse central nervous system effects to specific nAChR subtypes makes it a useful tool for studying the functional roles of nAChR.

参考文献