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Details

Stereochemistry RACEMIC
Molecular Formula C28H35ClN4O.2ClH
Molecular Weight 551.979
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MOSAPRAMINE DIHYDROCHLORIDE

SMILES

Cl.Cl.ClC1=CC2=C(CCC3=CC=CC=C3N2CCCN4CCC5(CC4)N6CCCCC6NC5=O)C=C1

InChI

InChIKey=CVCDAZZJQWLXHM-UHFFFAOYSA-N
InChI=1S/C28H35ClN4O.2ClH/c29-23-12-11-22-10-9-21-6-1-2-7-24(21)32(25(22)20-23)16-5-15-31-18-13-28(14-19-31)27(34)30-26-8-3-4-17-33(26)28;;/h1-2,6-7,11-12,20,26H,3-5,8-10,13-19H2,(H,30,34);2*1H

HIDE SMILES / InChI

Molecular Formula C28H35ClN4O
Molecular Weight 479.057
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/8690306

Mosapramine (Cremin) is used to treat chronic schizophrenia in Japan. It is a potent dopamine antagonist with high affinity to the dopamine receptor subtypes 2, 3 and 4, and with moderate affinity for the 5-HT2 receptors

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: CHEMBL217
Sources: Mosapramine showed the highest affinities for these receptor subtypes among the antipsychotics tested
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Perospirone.
2001
Atypical properties of several classes of antipsychotic drugs on the basis of differential induction of Fos-like immunoreactivity in the rat brain.
2004 Nov 26
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:17:12 GMT 2023
Edited
by admin
on Sat Dec 16 02:17:12 GMT 2023
Record UNII
6M1W6HZL1X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MOSAPRAMINE DIHYDROCHLORIDE
MI  
Common Name English
Y-516
Code English
MOSAPRAMINE DIHYDROCHLORIDE [MI]
Common Name English
CREMIN
Brand Name English
Mosapramine hydrochloride [WHO-DD]
Common Name English
SPIRO(IMIDAZO(1,2-A)PYRIDINE-3(2H),4'-PIPERIDIN)-2-ONE, 1'-(3-(3-CHLORO-10,11-DIHYDRO-5H-DIBENZ(B,F)AZEPIN-5-YL)PROPYL)HEXAHYDRO-, HYDROCHLORIDE (1:2)
Systematic Name English
MOSAPRAMINE HYDROCHLORIDE
WHO-DD  
Common Name English
Code System Code Type Description
CHEBI
135775
Created by admin on Sat Dec 16 02:17:12 GMT 2023 , Edited by admin on Sat Dec 16 02:17:12 GMT 2023
PRIMARY
EVMPD
SUB03337MIG
Created by admin on Sat Dec 16 02:17:12 GMT 2023 , Edited by admin on Sat Dec 16 02:17:12 GMT 2023
PRIMARY
MESH
C046384
Created by admin on Sat Dec 16 02:17:12 GMT 2023 , Edited by admin on Sat Dec 16 02:17:12 GMT 2023
PRIMARY
CAS
98043-60-8
Created by admin on Sat Dec 16 02:17:12 GMT 2023 , Edited by admin on Sat Dec 16 02:17:12 GMT 2023
PRIMARY
FDA UNII
6M1W6HZL1X
Created by admin on Sat Dec 16 02:17:12 GMT 2023 , Edited by admin on Sat Dec 16 02:17:12 GMT 2023
PRIMARY
EPA CompTox
DTXSID30913492
Created by admin on Sat Dec 16 02:17:12 GMT 2023 , Edited by admin on Sat Dec 16 02:17:12 GMT 2023
PRIMARY
MERCK INDEX
m7633
Created by admin on Sat Dec 16 02:17:12 GMT 2023 , Edited by admin on Sat Dec 16 02:17:12 GMT 2023
PRIMARY Merck Index
PUBCHEM
656595
Created by admin on Sat Dec 16 02:17:12 GMT 2023 , Edited by admin on Sat Dec 16 02:17:12 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106650
Created by admin on Sat Dec 16 02:17:12 GMT 2023 , Edited by admin on Sat Dec 16 02:17:12 GMT 2023
PRIMARY
SMS_ID
100000085703
Created by admin on Sat Dec 16 02:17:12 GMT 2023 , Edited by admin on Sat Dec 16 02:17:12 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY