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94841-17-5

中文名稱 鹽酸螺普利
CAS 94841-17-5
分子式 C22H30N2O5S2.HCl
分子量 503.07
MOL 文件 94841-17-5.mol
更新日期 2023/03/20 15:41:17
94841-17-5 結(jié)構(gòu)式 94841-17-5 結(jié)構(gòu)式

基本信息

中文別名
鹽酸螺普利
英文別名
Renpress
Renormax
Sandopril
TI 211-950
Spirapril HCl
Unii-occ25lm897
Spirapril hydrochloride
(8S)-7-[(2S)-2-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]-1,4-dithia-7-azaspiro[4.4]nonane-8-carboxylic Acid Monohydrochloride
1,4-Dithia-7-azaspiro(4.4)nonane-8-carboxylic acid, 7-(2-((1-(ethoxycarbonyl)-3-phenylpropyl)amino)-1-oxopropyl)-, monohydrochloride, (8S-(7(R*(R*)),8R*))-

物理化學(xué)性質(zhì)

熔點(diǎn)192-1940C (dec.)
比旋光度D26 -11.2° (c = 0.4 in ethanol)
儲(chǔ)存條件-20°C冷凍

常見問題列表

生物活性
Spirapril (SCH 33844) hydrochloride 是一種有效的血管緊張素轉(zhuǎn)換酶 (ACE) 抑制劑,具有降壓作用。Spirapril hydrochloride 競(jìng)爭(zhēng)性地與 ACE 結(jié)合,阻止血管緊張素I向血管緊張素 II 的轉(zhuǎn)化。Spirapril hydrochloride 是螺普利拉的一種口服活性前藥,可用于高血壓、充血性心力衰竭的研究。
靶點(diǎn)

IC50: angiotensin converting enzyme

體內(nèi)研究

Spirapril (feeding needle; 10 mg/kg; 3 weeks) decreases alcohol intake in TGM123 mice and dose not reduce the alcohol consumption in TLM mice. Spirapril shows a 40.2% reduction in ACE activity in brain membrane from treated-mice. It crosses the blood-brain barrier and suppresses the transgene effect in the experiments.

Animal Model: TGM123 mice (expressing a rat angiotensinogen transgene) and TLM ( lacking the angiotensinogen gene) mice
Dosage: 10 mg/kg
Administration: Feeding needle; 10 mg/kg; 3 weeks
Result: Alter voluntary alcohol consumption in animals. Crossed the blood-brain barrier and may influences alcohol consumption mainly by decreasing central angiotensin II (AII) levels.
"94841-17-5" 相關(guān)產(chǎn)品信息
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