ChemicalBook--->CAS DataBase List--->985-13-7

985-13-7

985-13-7 Structure

985-13-7 Structure
IdentificationBack Directory
[Name]

ethaverine hydrochloride
[CAS]

985-13-7
[Synonyms]

Cebral
Isovex
Consenil
Ethaquin
Balborin
Barbonin hydrochloride
ethaverine hydrochloride
Ethylpapaverin hydrochloride
6,7-Diethoxy-1-(3,4-diethoxybenzyl)isoquinoline hydrochloride
Isoquinoline, 1-(3,4-diethoxybenzyl)-6,7-diethoxy-, hydrochloride
Isoquinoline, 1-[(3,4-diethoxyphenyl)methyl]-6,7-diethoxy-, hydrochloride
[EINECS(EC#)]

213-573-9
[Molecular Formula]

C24H29NO4.ClH
[MOL File]

985-13-7.mol
[Molecular Weight]

431.957
Chemical PropertiesBack Directory
[Melting point ]

186-188° (dec)
[form ]

Solid
[color ]

Light yellow to yellow
[EPA Substance Registry System]

Ethaverine hydrochloride (985-13-7)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[RIDADR ]

3249
[TSCA ]

TSCA listed
[HazardClass ]

6.1(a)
[PackingGroup ]

II
[Toxicity]

LD50 scu-mus: 660 mg/kg THERAP5,69,50
Hazard InformationBack Directory
[Uses]

Ethaverine hydrochloride, a derivative of papaverine, inhibits cardiac L-type calcium channel. Ethaverine hydrochloride is a peripheral vasodilator and antispasmodic agent. Ethaverine hydrochloride can be used for research of peripheral vascular disease[1][2][3].
[Safety Profile]

Poison by intravenous route. Moderately toxic by subcutaneous route. When heated to decomposition it emits toxic vapors of NOx, HCl, and Clí
[in vivo]

Ethaverine hydrochloride (2-10 mg/kg, intravenous infusion, i.v.) causes significant elevation of endocochlear potential in guinea pigs[4].
Ethaverine (1-10 mg/kg, i.v.) inhibits atrioventricular conduction and heart rate in the anaesthetized dog[5].

Animal Model:Dog[5]
Dosage:1 and 10 mg/kg
Administration:i.v.
Result:Inhibited atrioventricular conduction and heart rate.
[References]

[1] Wang Y, et al. Ethaverine, a derivative of papaverine, inhibits cardiac L-type calcium channels. Mol Pharmacol. 1991 Nov;40(5):750-5. PMID:1658607
[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. DOI:10.1016/0006-2952(94)90399-9
[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. DOI:10.1248/bpb.24.103
[4] Prazma J, et al. Effect of ethaverine hydrochloride on cochlear microcirculation. Arch Otolaryngol. 1981 Apr;107(4):227-9. DOI:10.1001/archotol.1981.00790400029006
[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. PMID:962426
[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. DOI:10.1248/bpb.24.838
Spectrum DetailBack Directory
[Spectrum Detail]

ethaverine hydrochloride(985-13-7)1HNMR
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