CAROVERINEHYDROCHLORIDE

CAROVERINEHYDROCHLORIDE Suppliers list
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Products Intro: Product Name:1-[2-(diethylamino)ethyl]-3-[(4-methoxyphenyl)methyl]quinoxalin-2-one,hydrochloride
CAS:55750-05-5
Purity:0.99 Package:5KG;1KG Remarks:C22H28ClN3O2
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Products Intro: Product Name:Caroverine hydrochloride
CAS:55750-05-5
Purity:98.75% Package:5mg;39USD|10mg;64USD|25mg;133USD
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Products Intro: Product Name:Caroverine hydrochloride
CAS:55750-05-5
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Products Intro: Product Name:Caroverine hydrochloride
CAS:55750-05-5
Purity:98% Package:1g,10g,25g,100g,500g,1kg
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Products Intro: Product Name:Caroverine HCL
CAS:55750-05-5
Purity:99% Package:5KG;1KG Remarks:Caroverine HCL

CAROVERINEHYDROCHLORIDE manufacturers

CAROVERINEHYDROCHLORIDE Basic information
Product Name:CAROVERINEHYDROCHLORIDE
Synonyms:CAROVERINEHYDROCHLORIDE;1-(2-diethylaminoethyl)-3-[(4-methoxyphenyl)methyl]quinoxalin-2-one;1-[2-(Diethylamino)ethyl]-3-[(4-methoxyphenyl)methyl]-2(1H)-quinoxalinone monohydrochloride;1-(2-Diethylamino)ethyl-3-((4-methoxyphenyl)methyl)-2(1H)-quinoxalinone hydrochloride;1-Diethylaminoethyl-3-(p-methoxybenzyl)-2-quinoxaone hydrochloride;2(1H)-Quinoxalinone, 1-(2-diethylamino)ethyl-3-(4-methoxybenzyl)-, hydrochloride;p 201-1;1-[2-(diethylamino)ethyl]-3-[(4-methoxyphenyl)methyl]quinoxalin-2-one,hydrochloride
CAS:55750-05-5
MF:C22H27N3O2
MW:0
EINECS:
Product Categories:APIs
Mol File:55750-05-5.mol
CAROVERINEHYDROCHLORIDE Structure
CAROVERINEHYDROCHLORIDE Chemical Properties
storage temp. 2-8°C
solubility DMSO: >10mg/mL
form solid
color White to off-white
Safety Information
Hazard Codes Xn
Risk Statements 22
WGK Germany 3
MSDS Information
CAROVERINEHYDROCHLORIDE Usage And Synthesis
UsesCaroverine hydrochloride is a potent, competitive and reversible antagonist of NMDA and AMPA glutamate receptor. Caroverine hydrochloride is also an antioxidant and calcium-blocking agent that exhibits vasorelaxant action. Caroverine hydrochloride can be used for the research of inner ear tinnitus[1][2][3].
in vivo

Caroverine (1.44 mg/rat; s.c; 1.0 mL/h for 72 h) attenuates impulse noise-induced hearing loss in the rat[4].

Animal Model:Sprague-Dawley rats of either sex (250-300 g) received impulse noise exposure[4]
Dosage:1.44 mg/rat
Administration:20 mg/mL; s.c. 1.0 mL/h for 72 h
Result:Significantly protected the cochlea against impulse noise trauma.
References[1] Chen Z, et, al. Pharmacokinetics of caroverine in the inner ear and its effects on cochlear function after systemic and local administrations in Guinea pigs. Audiol Neurootol. Jan-Feb 2003;8(1):49-56. DOI:10.1159/000067893
[2] Denk DM, et, al. Caroverine in tinnitus treatment. A placebo-controlled blind study. Acta Otolaryngol. 1997 Nov;117(6):825-30. DOI:10.3109/00016489709114208
[3] Ishida Y, et, al. Vasorelaxant action of caroverine fumarate (a quinoxaline derivative), a calcium-blocking agent. Br J Pharmacol. 1980;71(1):343-8. DOI:10.1111/j.1476-5381.1980.tb10945.x
[4] Duan M, et, al. Low-dose, long-term caroverine administration attenuates impulse noise-induced hearing loss in the rat. Acta Otolaryngol. 2006 Dec;126(11):1140-7. DOI:10.1080/00016480500540519
CAROVERINEHYDROCHLORIDE Preparation Products And Raw materials
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