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promazine

Structure via PubChem · Public domain (PubChem)

EntityQ419822· pop 22· linked from 625 articles

Also known as N,N-dimethyl-3-(10H-phenothiazin-10-yl)-propan-1-amine, N-dimethylamino-1-methylethyl thiodiphenylamine, N-(3-dimethylaminopropyl)phenothiazine, 10-[3-(dimethylamino)propyl]phenothiazine

Promazine (brand name Sparine among others), is used as a short-term add-on treatment for psychomotor agitation. Its approved uses in people is limited, but is used as a tranquilizer in veterinary medicine. It has weak antipsychotic effects but is generally not used to treat psychosis.

Chemical data

Formula
C17H20N2S
Molecular weight
284.4 g/mol
IUPAC name
N,N-dimethyl-3-phenothiazin-10-ylpropan-1-amine
SMILES
CN(C)CCCN1C2=CC=CC=C2SC3=CC=CC=C31
InChIKey
ZGUGWUXLJSTTMA-UHFFFAOYSA-N
XLogP
4.5
Polar surface area
31.8 Ų
H-bond donors
0
H-bond acceptors
3
Formal charge
0

via PubChem

Research

1,380 papers

via PubMed

Wikidata facts

Has part
carbon
Mass
284.135
Has use
medication
Show 7 more facts
subject has role
antiemetic
chemical formula
C₁₇H₂₀N₂S
World Health Organisation international non-proprietary name
promazine
medical condition treated
vomiting
canonical SMILES
CN(C)CCCN1C2=CC=CC=C2SC3=CC=CC=C31
physically interacts with
Dopamine receptor D3
Commons category
Promazine
Sources (4)

via Wikidata · CC0

~2 min read

Encyclopedic overview

6 sections
Contents
  • Uses
  • Adverse effects
  • Overdose
  • Other animals
  • Synthesis
  • References

Promazine (brand name Sparine among others), is used as a short-term add-on treatment for psychomotor agitation. Its approved uses in people is limited, but is used as a tranquilizer in veterinary medicine. It has weak antipsychotic effects but is generally not used to treat psychosis.

It acts similar to chlorpromazine and causes sedation. It has predominantly anticholinergic side effects, though extrapyramidal side effects are not uncommon. It belongs to the typical antipsychotic and phenothiazine class of drugs.

Excerpted from Wikipedia’s “promazine” article, available under the CC BY-SA 4.0 licence.

Gallery (2)