Promazine drug data and news

Promazine drug data, resources, and news articles (when available). Onconews.org provides news on cancer research. This section, which includes profiles on medicines that may or not be cancer-related is in beta form. If things run smoothly we will be releasing a new format late in the summer of 2006.

Generic name Promazine
Brand Names/Synonyms 2601A; 3276 R. P.; 4560 R.P.; A 145; AB; Aminazin; Aminazine; Ampazine; Ampliactil; Amplictil; BC 135; Berophen; CPZ; Chlor-Promanyl; Chlordelazin; Chlorderazin; Chlorpromados; Chlorpromazine Hcl; Chlorpromazine Hcl Intensol; Chlropromados; Contomin; Elmarin; Esmind; Esparin; Fenactil; Fenaktyl; Fraction; HL 5746; HSDB 3033; Largactil; Largactilothiazine; Largactyl; Liranol; Megaphen; Neo-Hibernex; Novomazina; Phenactyl; Phenothiazine; Prazin; Prazine; Proma; Promactil; Promapar; Promazil; Promazin; Promazina; Promazine; Promazine Hcl; Promwill; Propaphenin; Protactyl; Prozil; Psychozine; RP 3276; RP 4560; Romtiazin; SKF 2601A; Sanopron; Sinophenin; Sonazine; Sparine; Thorazine; Tomil; Torazina; Verophen; Vesprin; Wintermin; Wy 1094; Wy-1094
Indication Adjunct for short term treatment of moderate and severe psychomotor agitation; agitation or restlessnes in the elderly.
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Description Not Available
Pharmacology Promazine, an atypical antipsychotic agent, is used to treat both negative and positive symptoms of schizophrenia, acute mania with bipolar disorder, agitation, and psychotic symptoms in dementia. Future uses may include the treatment of obsessive-compulsive disorder and severe behavioral disorders in autism. Structurally and pharmacologically similar to clozapine, Promazine binds to alpha(1), dopamine, histamine H1, muscarinic, and serotonin type 2 (5-HT2) receptors.
Mechanism Of Action Promazine is an antagonist at types 1, 2, and 4 dopamine receptors, 5-HT receptor types 2A and 2C, muscarinic receptors 1 through 5, alpha(1)-receptors, and histamine H1-receptors. Promazine's antipsychotic effect is due to antagonism at dopamine and serotonin type 2 receptors, with greater activity at serotonin 5-HT2 receptors than at dopamine type-2 receptors. This may explain the lack of extrapyramidal effects. Promazine does not appear to block dopamine within the tubero-infundibular tract, explaining the lower incidence of hyperprolactinemia than with typical antipsychotic agents or risperidone. Antagonism at muscarinic receptors, H1-receptors, and alpha(1)-receptors also occurs with Promazine.
Promazine News
(When available)

Katsidis suspension reduced  May 2, 2006
Stewards have opened an inquiry into Walk On Crystal testing positive for promazine and hydro-promazine after winning at Ipswich on March 8. ... - FOX SPORTS,

Dosage Forms LIQUID
Drug_Category Antipsychotics; Antiemetics; Phenothiazines; ATC:N05AA01; ATC:N05AA02; ATC:N05AA03; ATC:N05AA04; ATC:N05AA05
Absorption Not Available
Interactions Not Available
Toxicity Not Available
Organisms Affected Humans and other mammals
Chemical IUPAC Name N,N-dimethyl-3-(10H-phenothiazin-10-yl)propan-1-amine
Chemical Formula C17H20N2S
Molecular Weight 284.42 g/mol
Smiles String CN(C)CCCN1C2=CC=CC=C2SC3=CC=CC=C31
Melting Point < 25 °C
Water Solubility 14.2 mg/L
State Liquid
LogP/Hphobicity 4.893
Isoelectric Point 9.36
Biotransformation Not Available
Half Life Not Available
Protein Binding [%] 94%
RxList Link Not Available>RXlist
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Drug Reference http://www.drugs.com/cons/Promazine.html
Drug Type Approved Drug
Accession No APRD00358
CAS Registry Number 58-40-2
KEGG Compound ID C07379
PubChem ID SID:271515
PharmGKB ID PA451126
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] 497509

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