Drotaverine hydrochloride
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Drotaverine hydrochloride
structure -
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CAS No:
985-12-6
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Formula:
C24H31NO4.ClH
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Chemical Name:
Drotaverine hydrochloride
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Synonyms:
Isoquinoline,1-[(3,4-diethoxyphenyl)methylene]-6,7-diethoxy-1,2,3,4-tetrahydro-,hydrochloride (1:1);Isoquinoline,1-(3,4-diethoxybenzylidene)-6,7-diethoxy-1,2,3,4-tetrahydro-,hydrochloride;Isoquinoline,1-[(3,4-diethoxyphenyl)methylene]-6,7-diethoxy-1,2,3,4-tetrahydro-,hydrochloride;No-Spa hydrochloride;Drotaverinium chloride;Isodihydroperparine hydrochloride;Tetraspasmin-Lefa;Drotaverin hydrochloride;Drotaverine hydrochloride;No-Spa;NOSH-BRA;Drotin;1-(3,4-Diethoxy-benzylidene)-6,7-diethoxy-1,2,3,4-tetrahydro-isoquinoline hydrochloride;53908-09-1
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CAS No:
Drotaverine hydrochloride Basic Attributes
433.97
433.201996
1308068-626-2
DTXSID40243590
2933990090
Safety Information
|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P301+P312, P330, and P501|Aggregated GHS information provided by 72 companies from 6 notifications to the ECHA C&L Inventory.
Drug Information
Agents that inhibit the actions of the parasympathetic nervous system. The major group of drugs used therapeutically for this purpose is the MUSCARINIC ANTAGONISTS. (See all compounds classified as Parasympatholytics.)|Compounds capable of relieving pain without the loss of CONSCIOUSNESS. (See all compounds classified as Analgesics.)|Drugs used to cause dilation of the blood vessels. (See all compounds classified as Vasodilator Agents.)
dihydroisoperparine
Computed Properties
Molecular Weight:434.0
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:9
Exact Mass:433.2019862
Monoisotopic Mass:433.2019862
Topological Polar Surface Area:49
Heavy Atom Count:30
Complexity:511
Undefined Bond Stereocenter Count:1
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Drotaverine inhibits phosphodiesterase, increases CAMP concentration, activates CAMP-dependent protein kinase, affects the phosphorylation of myosin light chain kinase (MLCK) and its affinity with the calcium ion-calmodulin complex, thereby leading to muscle relaxation; at the same time, it reduces the calcium ion concentration in the cytoplasm through the CAMP pathway, exhibiting a calcium ion antagonist effect.
Registered Holders
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Biobetta Pharmaceuticals (Shanghai) Co., Ltd.
Active
China
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EuroAPI Shanghai Ltd.
Active
China
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Jiangxi Yiyou Pharmaceutical Co., Ltd.
Active
China
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