985-13-7

985-13-7结构式
985-13-7结构式

化源商城直购

中文名 盐酸依沙维林
英文名 ethaverine hydrochloride
英文别名 Isoquinoline,1-(3,4-diethoxybenzyl)-6,7-diethoxy-,hydrochloride
6,7-Diethoxy-1-(3,4-diethoxybenzyl)isoquinoline hydrochloride
Consenil
Balborin
Isovex
Barbonin hydrochloride
Cebral
Ethaquin
Ethylpapaverin hydrochloride
描述 罂粟碱的衍生物盐酸伊沙韦林抑制心脏L型钙通道。盐酸乙威林是一种外周血管扩张剂和解痉药。盐酸乙威林可用于外周血管疾病的研究[1][2][3]。
相关类别
体外研究 盐酸乙威林(10μM,PC12细胞) 通过阻断 L型电压敏感 钙离子通道来减少儿茶酚胺分泌[2]。 盐酸乙威林(12小时)通过抑制 第12页细胞中的酪氨酸羟化酶 (第)活性来降低多巴胺含量,国际50为 1.4μM[3]盐酸乙威林抑制小鼠脑中的单胺氧化酶 (毛)(分离自小鼠全脑) 活性,国际50为 25.5μM[6]
体内研究 将盐酸乙威林(2-10mg/kg静脉滴注,静脉注射)引起豚鼠耳蜗内电位显着升高[4]。 Ethaverine(1-10mg/kg静脉注射) 抑制麻醉狗的房室传导和心率[5]。 动物模型:狗[5]剂量:1和10 mg/kg给药:静脉注射结果:抑制房室传导和心率。
参考文献

[1]. Wang Y, et al. Ethaverine, a derivative of papaverine, inhibits cardiac L-type calcium channels. Mol Pharmacol. 1991 Nov;40(5):750-5.  

[2]. Suh BC, et al. Inhibition by ethaverine of catecholamine secretion through blocking L-type Ca2+ channels in PC12 cells. Biochem Pharmacol. 1994 Mar 29;47(7):1262-6.  

[3]. Shin JS, et al. Inhibitory effects of ethaverine, a homologue of papaverine, on dopamine content in PC12 cells. Biol Pharm Bull. 2001 Jan;24(1):103-5.  

[4]. Prazma J, et al. Effect of ethaverine hydrochloride on cochlear microcirculation. Arch Otolaryngol. 1981 Apr;107(4):227-9.  

[5]. Lacroix P, et al. [Comparative activity of ethaverine and papaverine on chronotropic and dromotropic cardiac functions in the anesthetized dog]. Arch Int Pharmacodyn Ther. 1976 May;221(1):163-76. French.  

[6]. Lee SS, et al. Inhibitory effects of ethaverine, a homologue of papaverine, on monoamine oxidase activity in mouse brain. Biol Pharm Bull. 2001 Jul;24(7):838-40.  

密度 1.104g/cm3
沸点 527.1ºC at 760 mmHg
熔点 187ºC
分子式 C24H30ClNO4
分子量 431.95200
闪点 185.9ºC
精确质量 431.18600
PSA 49.81000
LogP 6.22240
外观性状 固体
储存条件 -20°C, 密封, 干燥

CHEMICAL IDENTIFICATION

RTECS NUMBER :
NW7524100
CHEMICAL NAME :
Isoquinoline, 1-(3,4-diethoxybenzyl)-6,7-diethoxy-, hydrochloride
CAS REGISTRY NUMBER :
985-13-7
LAST UPDATED :
199701
DATA ITEMS CITED :
4
MOLECULAR FORMULA :
C24-H29-N-O4.Cl-H
MOLECULAR WEIGHT :
432.00
WISWESSER LINE NOTATION :
T66 CNJ B1R CO2 DO2& HO2 FO2 &GH

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
660 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
THERAP Therapie. (Doin, Editeurs, 8, Place de l'Odeon, F-75006 Paris, France) V.1- 1946- Volume(issue)/page/year: 5,69,1950
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
86 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
APFRAD Annales Pharmaceutiques Francaises. (SPPIF, B.P.22, F-41353 Vineuil, France) V.1- 1943- Volume(issue)/page/year: 9,585,1951 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X5434 No. of Facilities: 26 (estimated) No. of Industries: 1 No. of Occupations: 1 No. of Employees: 1324 (estimated) No. of Female Employees: 667 (estimated)

危险品运输编码 UN 3249
包装等级 II
危险类别 6.1(a)
海关编码 2933499090
海关编码 2933499090
中文概述 2933499090. 其他含喹琳或异喹啉环系的化合物〔但未进一步稠合的〕. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%
申报要素 品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期
Summary 2933499090. other compounds containing in the structure a quinoline or isoquinoline ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%