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

Details

Stereochemistry ACHIRAL
Molecular Formula C20H24ClN3O2
Molecular Weight 373.876
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLEBOPRIDE

SMILES

COC1=C(C=C(Cl)C(N)=C1)C(=O)NC2CCN(CC3=CC=CC=C3)CC2

InChI

InChIKey=BVPWJMCABCPUQY-UHFFFAOYSA-N
InChI=1S/C20H24ClN3O2/c1-26-19-12-18(22)17(21)11-16(19)20(25)23-15-7-9-24(10-8-15)13-14-5-3-2-4-6-14/h2-6,11-12,15H,7-10,13,22H2,1H3,(H,23,25)

HIDE SMILES / InChI

Molecular Formula C20H24ClN3O2
Molecular Weight 373.876
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:04:06 UTC 2023
Edited
by admin
on Fri Dec 15 16:04:06 UTC 2023
Record UNII
I0A84520Y9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLEBOPRIDE
INN   MART.   MI   USAN   WHO-DD  
USAN   INN  
Official Name English
BENZAMIDE, 4-AMINO-5-CHLORO-2-METHOXY-N-(1-(PHENYLMETHYL)-4-PIPERIDINYL)-
Systematic Name English
4-AMINO-5-CHLORO-2-METHOXY-N-(1-(PHENYLMETHYL)-4-PIPERIDINYL)BENZAMIDE
Systematic Name English
Clebopride [WHO-DD]
Common Name English
CLEBOPRIDE [USAN]
Common Name English
CLEBOPRIDE [MART.]
Common Name English
LAS-9273
Code English
CLEBOPRIDE [MI]
Common Name English
LAS 9273
Code English
clebopride [INN]
Common Name English
4-Amino-N-(1-benzyl-4-piperidyl)-5-chloro-O-anisamide
Common Name English
N-(1'-BENZYL-4'-PIPERIDYL)-2-METHOXY-4-AMINO-5-CHLOROBENZAMIDE
Common Name English
Classification Tree Code System Code
WHO-VATC QA03FA06
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
WHO-ATC A03FA06
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
NCI_THESAURUS C66883
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
Code System Code Type Description
ECHA (EC/EINECS)
259-885-9
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY
EPA CompTox
DTXSID7022831
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY
FDA UNII
I0A84520Y9
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY
USAN
Y-100
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY
DRUG CENTRAL
670
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY
CAS
55905-53-8
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY
ChEMBL
CHEMBL325109
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY
RXCUI
21224
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY RxNorm
WIKIPEDIA
CLEBOPRIDE
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY
NCI_THESAURUS
C83627
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY
INN
3699
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY
EVMPD
SUB06646MIG
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY
MERCK INDEX
m3612
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY Merck Index
DRUG BANK
DB13511
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY
SMS_ID
100000092794
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY
PUBCHEM
2780
Created by admin on Fri Dec 15 16:04:07 UTC 2023 , Edited by admin on Fri Dec 15 16:04:07 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY