Substance

ID:944

Names and Identifiers
Brand Name
AprobitDipherganDimappFarganFenazilFenerganPipolphenPrometasinPromethainePrometheganProtazineRemsedDormeDuplaminFenetazinaIsophenerganLergiganPhensedylRomerganAllerganDiprazinePhenergan FortisPrometh FortisProrexProviganPyrethiaPyrethiazineAvomineDiprozinFellozineGenphenPharganPhenerganSynalgosThierganVallergineIergiganPhenarganPhencenProcitHibernaTanidilHistarganValergineZipan-25LerciganMymethazine FortisPilpophenPrometazinPrometh PlainPromethacon
IUPAC name
dimethyl[1-(10H-phenothiazin-10-yl)propan-2-yl]amine
Synonyms
Lilly 1516ProazamineProthazinPrometazineProazaiminePromethazinPromezathinePromazinamidePromethazine HclPromethiazineProthazinePromethazineIsopromethazine
IUPAC Traditional name
promethazine
Registration numbers
PubChem SID
CAS Number
PubChem CID
Properties
Physical Property
Hydrophobicity(logP)
4.4
Solubility
Freely soluble
Molecule Details
Drug Groups
approved
Description
A phenothiazine derivative with histamine H1-blocking, antimuscarinic, and sedative properties. It is used as an antiallergic, in pruritus, for motion sickness and sedation, and also in animals. [PubChem]
Indication
For the treatment of allergic disorders, and nausea/vomiting.
Pharmacology
Promethazine, a phenothiazine, is an H1-antagonist with anticholinergic, sedative, and antiemetic effects and some local anesthetic properties. Promethazine is used as an antiemetic or to prevent motion sickness.
Toxicity
Symptoms of overdose include mild depression of the central nervous system and cardiovascular system to profound hypotension, respiratory depression, unconsciousness, and sudden death. Other reported reactions include hyperreflexia, hypertonia, ataxia, athetosis, and extensor-plantar reflexes (Babinski reflex). LD50=55mg/kg (I.V. in mice)
Affected Organisms
Humans and other mammals
Biotransformation
Hepatic
Absorption
On average, 88% of a promethazine dose is absorbed after oral administration; however, the absolute bioavailability is only 25% because of first-pass clearance.
Half Life
16-19 hours
Protein Binding
93%
Elimination
Promethazine hydrochloride is metabolized in the liver, with the sulfoxides of promethazine and N-desmethylpromethazine being the predominant metabolites appearing in the urine.
References
• Peters RJ Jr, Kelder SH, Markham CM, Yacoubian GS Jr, Peters LA, Ellis A: Beliefs and social norms about codeine and promethazine hydrochloride cough syrup (CPHCS) onset and perceived addiction among urban Houstonian adolescents: an addiction trend in the city of lean. J Drug Educ. 2003;33(4):415-25. [Pubmed]
External Links
Molecular Spectra
No Data Available
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References
• Peters RJ Jr, Kelder SH, Markham CM, Yacoubian GS Jr, Peters LA, Ellis A: Beliefs and social norms about codeine and promethazine hydrochloride cough syrup (CPHCS) onset and perceived addiction among urban Houstonian adolescents: an addiction trend in the city of lean. J Drug Educ. 2003;33(4):415-25. Pubmed