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Details

Stereochemistry ACHIRAL
Molecular Formula C22H26FNO2.ClH
Molecular Weight 391.907
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MOPERONE HYDROCHLORIDE

SMILES

Cl.CC1=CC=C(C=C1)C2(O)CCN(CCCC(=O)C3=CC=C(F)C=C3)CC2

InChI

InChIKey=RJTOSFZZYBCYTM-UHFFFAOYSA-N
InChI=1S/C22H26FNO2.ClH/c1-17-4-8-19(9-5-17)22(26)12-15-24(16-13-22)14-2-3-21(25)18-6-10-20(23)11-7-18;/h4-11,26H,2-3,12-16H2,1H3;1H

HIDE SMILES / InChI

Description

Moperone is a first-generation (typical) antipsychotic drug that belongs to the butyrophenone type approved in Japan for the treatment of schizophrenia. It has higher antagonist affinity for D2- than 5-HT2A-receptors. It also has high binding affinity for sigma receptors. It was indicated for schizophrenia, paranoid state, psychoses, epilepsy,alcohol withdrawal syndrome. It can induce extrapyramidal motor side effects, insomnia, and thirst, but it displays generally low toxicity.

CNS Activity

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency
87.0 nM [EC50]
1.5 nM [Ki]
6.1 null [pIC50]

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Luvatrene
Primary
Luvatrene

PubMed

Patents

Sample Use Guides

In Vivo Use Guide
Starting dose is 0.2-0.3 mg/kg/day; then slowly increase to 0.04-0.06 mg/kg/day
Route of Administration: Unknown
In Vitro Use Guide
Moperone was tested at a 3 uM concentration