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Carisoprodol

产品号 DB00395 公司名称 DrugBank
CAS号 78-44-4 公司网站 http://www.ualberta.ca/
分子式 C12H24N2O4 电 话 (780) 492-3111
分子量 260.32996 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 278

产品价格信息

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产品别名

标题
Carisoprodol
IUPAC标准名
2-methyl-2-({[(propan-2-yl)carbamoyl]oxy}methyl)pentyl carbamate
IUPAC传统名
2-{[(isopropylcarbamoyl)oxy]methyl}-2-methylpentyl carbamate
商标名
Caridolin
Flexal
Carisoma
Flexidon
Flexagilt
Neotica
Mioartrina
Mioratrina
Atonalyt
Relasom
Somanil
Apesan
Sanoma
Artifar
Chinchen
Fibrosona
Flexagit
Listaflex
Meprodat
Muslax
Scutamil-C
Skutamil
Soma
Miolisodal
Flexartal
Nospasm
Arusal
Mioril
别名
Isoprothane
Carisoprodate
Isoprotane
Isomeprobamate
Carisoprodatum

产品登记号

CAS号 78-44-4
PubChem CID 2576
PubChem SID 46506377

产品性质

疏水性(logP) 2.1
溶解度 0.3 mg/ml

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved
Description A centrally acting skeletal muscle relaxant whose mechanism of action is not completely understood but may be related to its sedative actions. It is used as an adjunct in the symptomatic treatment of musculoskeletal conditions associated with painful muscle spasm. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1202)
Indication For the relief of discomfort associated with acute, painful, musculoskeletal conditions.
Pharmacology Carisoprodol is used as a skeletal muscle relaxant. One of its metabolites, meprobamate, is available as an anxiolytic agent.
Toxicity Symptoms of overdose include drowsiness, giddiness, nausea, indigestion, or rash. Other adverse effects attributed to therapeutic use of carisoprodol include dizziness, irritability, insomnia, diplopia, temporary loss of vision, ataxia, weakness, headache, and dysarthria. Non-CNS adverse effects include gastrointestinal complaints, tachycardia, and postural hypotension. Patients sensitive to sulfites or tartrazine may experience wheezing, allergic rashes including erythema multiforme, or anaphylaxis after using some preparations of carisoprodol which contain such additives
Affected Organisms
Humans and other mammals
Biotransformation Hepatic. Metabolized in the liver via the cytochrome P450 oxidase isozyme CYP2C19.
Half Life 8 hours
Protein Binding 60%
Elimination Carisoprodol is eliminated by both renal and non-renal routes.
Clearance * oral cl=0.772 L/hour/kg [Women]
* oral cl=0.38 L/hour/kg [Men]
References
Toth PP, Urtis J: Commonly used muscle relaxant therapies for acute low back pain: a review of carisoprodol, cyclobenzaprine hydrochloride, and metaxalone. Clin Ther. 2004 Sep;26(9):1355-67. [Pubmed]
Chou R, Peterson K, Helfand M: Comparative efficacy and safety of skeletal muscle relaxants for spasticity and musculoskeletal conditions: a systematic review. J Pain Symptom Manage. 2004 Aug;28(2):140-75. [Pubmed]
Littrell RA, Hayes LR, Stillner V: Carisoprodol (Soma): a new and cautious perspective on an old agent. South Med J. 1993 Jul;86(7):753-6. [Pubmed]
External Links
Wikipedia
RxList
Drugs.com

参考文献

  • Toth PP, Urtis J: Commonly used muscle relaxant therapies for acute low back pain: a review of carisoprodol, cyclobenzaprine hydrochloride, and metaxalone. Clin Ther. 2004 Sep;26(9):1355-67. Pubmed
  • Littrell RA, Hayes LR, Stillner V: Carisoprodol (Soma): a new and cautious perspective on an old agent. South Med J. 1993 Jul;86(7):753-6. Pubmed
  • Chou R, Peterson K, Helfand M: Comparative efficacy and safety of skeletal muscle relaxants for spasticity and musculoskeletal conditions: a systematic review. J Pain Symptom Manage. 2004 Aug;28(2):140-75. Pubmed