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

Details

Stereochemistry EPIMERIC
Molecular Formula C21H30N4O4.C4H6O6
Molecular Weight 552.5741
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CINITAPRIDE TARTRATE

SMILES

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

InChI

InChIKey=HVANMRCHFMTSEG-LREBCSMRSA-N
InChI=1S/C21H30N4O4.C4H6O6/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;5-1(3(7)8)2(6)4(9)10/h3-4,12-13,15-16H,2,5-11,14,22H2,1H3,(H,23,26);1-2,5-6H,(H,7,8)(H,9,10)/t;1-,2-/m.1/s1

HIDE SMILES / InChI

Molecular Formula C4H6O6
Molecular Weight 150.0868
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

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
[Efficacy and tolerance of cinitapride on the disturbances of gastrointestinal transit].
1991 Jul-Sep
[Cinitapride in the treatment of gastroesophageal reflux. Comparative study with metoclopramide and placebo].
1992 Jan-Mar
[Metoclopramide versus cinitapride in the treatment of functional dyspepsia].
1993 Jul
Cinitapride protects against ethanol-induced gastric mucosal injury in rats: role of 5-hydroxytryptamine, prostaglandins and sulfhydryl compounds.
1997 Apr
Effects of cinitapride on gastric ulceration and secretion in rats.
1998 Mar
[Prokinetic agents as a cause of granulomatous interstitial nephritis].
2007 Dec
The prokinetic cinitapride has no clinically relevant pharmacokinetic interaction and effect on QT during coadministration with ketoconazole.
2007 Jul
[Efficacy and tolerability of cinitapride in the treatment of functional dyspepsia and delayed gastric emptying].
2009 Dec
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:46:11 GMT 2023
Edited
by admin
on Sat Dec 16 09:46:11 GMT 2023
Record UNII
2Z90GEN540
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CINITAPRIDE TARTRATE
MI   WHO-DD  
Common Name English
BENZAMIDE, 4-AMINO-N-(1-(3-CYCLOHEXEN-1-YLMETHYL)-4-PIPERIDINYL)-2-ETHOXY-5-NITRO-, (2R,3R)-2,3-DIHYDROXYBUTANEDIOATE (1:1)
Systematic Name English
Cinitapride tartrate [WHO-DD]
Common Name English
CIDINE
Brand Name English
CINITAPRIDE TARTRATE [MI]
Common Name English
LAS-17177
Code English
Code System Code Type Description
SMS_ID
100000090189
Created by admin on Sat Dec 16 09:46:11 GMT 2023 , Edited by admin on Sat Dec 16 09:46:11 GMT 2023
PRIMARY
EVMPD
SUB01312MIG
Created by admin on Sat Dec 16 09:46:11 GMT 2023 , Edited by admin on Sat Dec 16 09:46:11 GMT 2023
PRIMARY
CAS
1207859-16-2
Created by admin on Sat Dec 16 09:46:11 GMT 2023 , Edited by admin on Sat Dec 16 09:46:11 GMT 2023
PRIMARY
FDA UNII
2Z90GEN540
Created by admin on Sat Dec 16 09:46:11 GMT 2023 , Edited by admin on Sat Dec 16 09:46:11 GMT 2023
PRIMARY
MERCK INDEX
m3565
Created by admin on Sat Dec 16 09:46:11 GMT 2023 , Edited by admin on Sat Dec 16 09:46:11 GMT 2023
PRIMARY Merck Index
DRUG BANK
DBSALT002860
Created by admin on Sat Dec 16 09:46:11 GMT 2023 , Edited by admin on Sat Dec 16 09:46:11 GMT 2023
PRIMARY
PUBCHEM
6917844
Created by admin on Sat Dec 16 09:46:11 GMT 2023 , Edited by admin on Sat Dec 16 09:46:11 GMT 2023
PRIMARY
CAS
96623-56-2
Created by admin on Sat Dec 16 09:46:11 GMT 2023 , Edited by admin on Sat Dec 16 09:46:11 GMT 2023
NON-SPECIFIC STOICHIOMETRY