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Details

Stereochemistry ACHIRAL
Molecular Formula C28H28N2O2
Molecular Weight 424.5341
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIFENOXIN

SMILES

OC(=O)C1(CCN(CCC(C#N)(C2=CC=CC=C2)C3=CC=CC=C3)CC1)C4=CC=CC=C4

InChI

InChIKey=UFIVBRCCIRTJTN-UHFFFAOYSA-N
InChI=1S/C28H28N2O2/c29-22-28(24-12-6-2-7-13-24,25-14-8-3-9-15-25)18-21-30-19-16-27(17-20-30,26(31)32)23-10-4-1-5-11-23/h1-15H,16-21H2,(H,31,32)

HIDE SMILES / InChI

Molecular Formula C28H28N2O2
Molecular Weight 424.5341
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 15:59:39 UTC 2023
Edited
by admin
on Fri Dec 15 15:59:39 UTC 2023
Record UNII
3ZZ5BJ9F2Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIFENOXIN
INN   MART.   MI   USAN   VANDF   WHO-DD  
USAN   INN  
Official Name English
Difenoxin [WHO-DD]
Common Name English
DIPHENOXYLATE RELATED COMPOUND A [USP-RS]
Common Name English
1-(3-Cyano-3,3-diphenylpropyl)-4-phenylisonipecotic acid
Systematic Name English
R-15403 FREE BASE
Code English
4-PIPERIDINECARBOXYLIC ACID, 1-(3-CYANO-3,3-DIPHENYLPROPYL)-4-PHENYL-
Common Name English
MCN-JR 15403-11
Common Name English
DIFENOXIN [MART.]
Common Name English
DIFENOXIN [USAN]
Common Name English
IDS-ND-007
Code English
DIFENOXINE
Common Name English
ACSCN-9168
Common Name English
LYSPAFEN
Common Name English
DIFENOXIN [MI]
Common Name English
DIFENOXIN [VANDF]
Common Name English
difenoxin [INN]
Common Name English
DIPHENOXYLATE RELATED COMPOUND A CI
USP-RS  
Common Name English
R 15,403 FREE BASE
Code English
MCN-JR-15,403-11
Code English
DIPHENOXYLIC ACID
Common Name English
Classification Tree Code System Code
LIVERTOX 304
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
DEA NO. 9168
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
DEA NO. 9167
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
WHO-ATC A07DA04
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
WHO-VATC QA07DA04
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
NCI_THESAURUS C266
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
NDF-RT N0000178374
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
Code System Code Type Description
DAILYMED
3ZZ5BJ9F2Q
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
EPA CompTox
DTXSID0022931
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
CHEBI
4534
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
IUPHAR
7592
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
DRUG CENTRAL
878
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
RS_ITEM_NUM
1219019
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
SMS_ID
100000083174
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
RXCUI
23024
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY RxNorm
MESH
C100010
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
ChEMBL
CHEMBL1201321
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
EVMPD
SUB07123MIG
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
NCI_THESAURUS
C65381
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
INN
2903
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
DRUG BANK
DB01501
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
PUBCHEM
34328
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
FDA UNII
3ZZ5BJ9F2Q
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
CAS
28782-42-5
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
MERCK INDEX
m4425
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY Merck Index
WIKIPEDIA
DIFENOXIN
Created by admin on Fri Dec 15 15:59:39 UTC 2023 , Edited by admin on Fri Dec 15 15:59:39 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
APPROXIMATE PURE ANHYDROUS DRUG CONTENT (IN PERCENT)
Related Record Type Details
PARENT -> METABOLITE
Metabolite to parent drug ratio in non-uraemic human plasma.
URINE
PARENT -> METABOLITE
Percent of dose excreted in urine as metabolite.
URINE
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Related Record Type Details
ACTIVE MOIETY