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Details

Stereochemistry RACEMIC
Molecular Formula C21H23NO4S
Molecular Weight 385.477
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RACECADOTRIL

SMILES

CC(=O)SCC(CC1=CC=CC=C1)C(=O)NCC(=O)OCC2=CC=CC=C2

InChI

InChIKey=ODUOJXZPIYUATO-UHFFFAOYSA-N
InChI=1S/C21H23NO4S/c1-16(23)27-15-19(12-17-8-4-2-5-9-17)21(25)22-13-20(24)26-14-18-10-6-3-7-11-18/h2-11,19H,12-15H2,1H3,(H,22,25)

HIDE SMILES / InChI

Molecular Formula C21H23NO4S
Molecular Weight 385.477
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:27:17 UTC 2023
Edited
by admin
on Fri Dec 15 16:27:17 UTC 2023
Record UNII
76K53XP4TO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RACECADOTRIL
EP   INN   MART.   MI   WHO-DD  
INN  
Official Name English
NSC-759828
Code English
RACECADOTRIL [MART.]
Common Name English
TIORFIX
Brand Name English
TIORFAN
Brand Name English
ACETORPHAN
VANDF  
Common Name English
racecadotril [INN]
Common Name English
RACECADOTRIL [MI]
Common Name English
RACECADOTRIL [EP MONOGRAPH]
Common Name English
HIDRASEC
Brand Name English
N-((R,S)-3-ACETYLTHIO-2-BENZYLPROPANOYL)GLYCINE BENZYL ESTER
Common Name English
Racecadotril [WHO-DD]
Common Name English
ACETORPHAN [VANDF]
Common Name English
(±)-N-(.ALPHA.-(MERCAPTOMETHYL)HYDROCINNAMOYL)GLYCINE, BENZYL ESTER, ACETATE (ESTER)
Common Name English
Classification Tree Code System Code
WHO-ATC A07XA04
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
FDA ORPHAN DRUG 732920
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
WHO-VATC QA07XA04
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
Code System Code Type Description
WIKIPEDIA
RACECADOTRIL
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY
EPA CompTox
DTXSID8045513
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY
DRUG CENTRAL
60
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY
FDA UNII
76K53XP4TO
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY
MERCK INDEX
m9477
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY Merck Index
EVMPD
SUB12435MIG
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY
SMS_ID
100000089968
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY
ChEMBL
CHEMBL2103772
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY
INN
7378
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY
CAS
81110-73-8
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY
RXCUI
16738
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY RxNorm
MESH
C049331
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY
PUBCHEM
107751
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY
NCI_THESAURUS
C66503
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY
DRUG BANK
DB11696
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY
NSC
759828
Created by admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
PRIMARY
Related Record Type Details
METABOLITE ACTIVE -> PRODRUG
bulk of its inhibitory actions on enkephalinase.
MAJOR
PLASMA
Related Record Type Details
IMPURITY -> PARENT
REFERENCE SOLUTION USED
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity F = 0.7
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity E = 0.6
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity C = 1.4
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP