Psychology Wiki
Register
Advertisement

Assessment | Biopsychology | Comparative | Cognitive | Developmental | Language | Individual differences | Personality | Philosophy | Social |
Methods | Statistics | Clinical | Educational | Industrial | Professional items | World psychology |

Biological: Behavioural genetics · Evolutionary psychology · Neuroanatomy · Neurochemistry · Neuroendocrinology · Neuroscience · Psychoneuroimmunology · Physiological Psychology · Psychopharmacology (Index, Outline)


Carisoprodol chemical structure
Carisoprodol

[2-methyl-2-(1-methylethylcarbamoyloxymethyl) pentyl]aminomethanoate
IUPAC name
CAS number
78-44-4
ATC code

M03BA02

PubChem
2576
DrugBank
APRD00417
Chemical formula {{{chemical_formula}}}
Molecular weight 260.33 g/mol
Bioavailability
Metabolism Hepatic (CYP2C19-mediated)
Elimination half-life 8 hours
Excretion Renal
Pregnancy category
Legal status Scheduled in some U.S. states
Routes of administration Oral

Carisoprodol is a skeletal muscle relaxant whose active metabolite is meprobamate. Although several case reports have shown that carisoprodol has abuse potential, it continues to be widely prescribed (not so in the United Kingdom where use of benzodiazepines is preferred). Carisoprodol is a colorless, crystalline powder, having a mild, characteristic odor and a bitter taste. It is slightly soluble in water and freely soluble in alcohol, chloroform and acetone. Its solubility is practically independent of pH. It is marketed in the United States under the brand name Soma, and in the United Kingdom and other countries under the brand name Carisoma.

Chemistry[]

It is a carbamic acid ester. Carisoprodol is a racemic mixture of two stereoisomers.

Effects[]

Side effects[]

These are somewhat rare when used at normal doses.

Pharmacokinetics[]

Carisoprodol has a rapid, 30 minute onset of action, with the aforementioned effects lasting for approximately 2–6 hours. It is metabolized in the liver via the cytochrome P450 oxidase isozyme CYP2C19, excreted by the kidneys and has an approximate 8 hour half-life.

References[]

APhA Drug Information Handbook

External links[]


|}

This page uses Creative Commons Licensed content from Wikipedia (view authors).
Advertisement