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120447-62-3

中文名稱 (+/-)-VESAMICOL HYDROCHLORIDE
英文名稱 (+/-)-VESAMICOL HYDROCHLORIDE
CAS 120447-62-3
分子式 C17H26ClNO
分子量 295.85
MOL 文件 120447-62-3.mol
120447-62-3 結(jié)構(gòu)式 120447-62-3 結(jié)構(gòu)式

基本信息

中文別名
鹽酸扎氟普汀
化合物 T22486
英文別名
AH-5183
(+/-)-VESAMICOL HCL
AH-5183 HYDROCHLORIDE
(±)-VesamicolHCl (AH-5183)
rel-Vesamicol Hydrochloride
(+/-)-VESAMICOL HYDROCHLORIDE
(+/-)-VesamicolmiddotHCl(AH-5183)
(+/-)-VESAMICOL HYDROCHLORIDE (AH-5183) >98%
Ah-5183((+/-)-2-(4-phenylpiperidino) cyclohexanol
(+/-)-2-(4-PHENYLPIPERIDINO)CYCLOHEXANOL HYDROCHLORIDE

物理化學(xué)性質(zhì)

儲存條件Store at RT
溶解度aqueous buffers below pH 8: 1 mM
形態(tài)solid
顏色white

安全數(shù)據(jù)

WGK Germany3

常見問題列表

生物活性
(±)-Vesamicol hydrochloride ((±)-AH5183 hydrochloride) 是一種有效的囊泡乙酰膽堿轉(zhuǎn)運 (vesicular acetylcholine transport) 抑制劑,Ki 為 2 nM。(±)-Vesamicol hydrochloride 也對 σ1 和 σ2 受體具有高親和力,Ki 值分別為 26 nM 和 34 nM。
靶點

Ki: 2 nM (Vesicular acetylcholine transport), 26 nM (σ1 receptors) and 34 nM (σ2 receptors)

體外研究

The pharmacological actions of (±)-Vesamicol have been attributed to inhibition of acetylcholine transport into synaptic vesicles and the subsequent quantal release of acetylcholine.

體內(nèi)研究

(±)-Vesamicol (3 mg/kg; intraperitoneal injection; once; male Wistar rats) treatment increases the levels of cytosolic acetylcholine (ACh) in all regions of the brain, while those of vesicular ACh decreased in all regions except for the striatum.

Animal Model: Male Wistar rats (120-300 g)
Dosage: 3 mg/kg
Administration: Intraperitoneal injection; once
Result: The levels of cytosolic acetylcholine (ACh) increased in all regions of the brain, while those of vesicular ACh decreased in all regions except for the striatum.
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