U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C21H30N4O4
Molecular Weight 402.4873
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CINITAPRIDE

SMILES

CCOC1=C(C=C(C(N)=C1)[N+]([O-])=O)C(=O)NC2CCN(CC3CCC=CC3)CC2

InChI

InChIKey=ZDLBNXXKDMLZMF-UHFFFAOYSA-N
InChI=1S/C21H30N4O4/c1-2-29-20-13-18(22)19(25(27)28)12-17(20)21(26)23-16-8-10-24(11-9-16)14-15-6-4-3-5-7-15/h3-4,12-13,15-16H,2,5-11,14,22H2,1H3,(H,23,26)

HIDE SMILES / InChI

Molecular Formula C21H30N4O4
Molecular Weight 402.4873
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Cinitapride is an agonist of 5-HT4 and 5-HT1 receptors and antagonist of 5-HT2 receptors. Cinitapride is marketed worldwide for the treatment of gastrointestinal disorders related to motility such as indigestion or functional or non-ulcer dyspepsia, gastroesophageal reflux diseases, delay in gastric emptying and vomiting.

Approval Year

PubMed

PubMed

TitleDatePubMed
Effects of cinitapride on gastric ulceration and secretion in rats.
1998 Mar
The prokinetic cinitapride has no clinically relevant pharmacokinetic interaction and effect on QT during coadministration with ketoconazole.
2007 Jul
Substance Class Chemical
Created
by admin
on Sat Dec 16 18:04:23 UTC 2023
Edited
by admin
on Sat Dec 16 18:04:23 UTC 2023
Record UNII
R8I97I2L24
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CINITAPRIDE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
CINITAPRIDE [MI]
Common Name English
CINITAPRIDE [MART.]
Common Name English
cinitapride [INN]
Common Name English
PAXAPRIDE
Brand Name English
Cinitapride [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-ATC A03FA08
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
NCI_THESAURUS C66885
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
NCI_THESAURUS C47794
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
Code System Code Type Description
CAS
66564-14-5
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
PRIMARY
EVMPD
SUB06298MIG
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
PRIMARY
ChEMBL
CHEMBL2104523
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
PRIMARY
PUBCHEM
68867
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
PRIMARY
SMS_ID
100000081046
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
PRIMARY
DRUG CENTRAL
652
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
PRIMARY
FDA UNII
R8I97I2L24
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
PRIMARY
INN
4555
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
PRIMARY
NCI_THESAURUS
C77257
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
PRIMARY
MERCK INDEX
m3565
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
PRIMARY Merck Index
WIKIPEDIA
CINITAPRIDE
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
PRIMARY
MESH
C045316
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
PRIMARY
RXCUI
21125
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID60867232
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
PRIMARY
DRUG BANK
DB08810
Created by admin on Sat Dec 16 18:04:24 UTC 2023 , Edited by admin on Sat Dec 16 18:04:24 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY