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Details

Stereochemistry RACEMIC
Molecular Formula C21H28N2O
Molecular Weight 324.4598
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BIFEPRAMIDE

SMILES

CCN(CC)CCNC(=O)C(C)C1=CC=C(C=C1)C2=CC=CC=C2

InChI

InChIKey=GXLWOFJVIBEMCS-UHFFFAOYSA-N
InChI=1S/C21H28N2O/c1-4-23(5-2)16-15-22-21(24)17(3)18-11-13-20(14-12-18)19-9-7-6-8-10-19/h6-14,17H,4-5,15-16H2,1-3H3,(H,22,24)

HIDE SMILES / InChI

Molecular Formula C21H28N2O
Molecular Weight 324.4598
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Bifepramide, (+)- belong to the class of parasympatholytic agents that reduce the activity of the parasympathetic nervous system.

Approval Year

Patents
Substance Class Chemical
Created
by admin
on Wed Apr 02 09:24:22 GMT 2025
Edited
by admin
on Wed Apr 02 09:24:22 GMT 2025
Record UNII
B1H2FS2WPP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BIFEPRAMIDE
INN  
INN  
Official Name English
bifepramide [INN]
Preferred Name English
(±)-N-(2-(DIETHYLAMINO)ETHYL)-.ALPHA.-METHYL-4-BIPHENYLACETAMIDE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C241
Created by admin on Wed Apr 02 09:24:22 GMT 2025 , Edited by admin on Wed Apr 02 09:24:22 GMT 2025
Code System Code Type Description
SMS_ID
100000085903
Created by admin on Wed Apr 02 09:24:22 GMT 2025 , Edited by admin on Wed Apr 02 09:24:22 GMT 2025
PRIMARY
PUBCHEM
68900
Created by admin on Wed Apr 02 09:24:22 GMT 2025 , Edited by admin on Wed Apr 02 09:24:22 GMT 2025
PRIMARY
ECHA (EC/EINECS)
275-076-3
Created by admin on Wed Apr 02 09:24:22 GMT 2025 , Edited by admin on Wed Apr 02 09:24:22 GMT 2025
PRIMARY
FDA UNII
B1H2FS2WPP
Created by admin on Wed Apr 02 09:24:22 GMT 2025 , Edited by admin on Wed Apr 02 09:24:22 GMT 2025
PRIMARY
CAS
70976-76-0
Created by admin on Wed Apr 02 09:24:22 GMT 2025 , Edited by admin on Wed Apr 02 09:24:22 GMT 2025
PRIMARY
EVMPD
SUB05828MIG
Created by admin on Wed Apr 02 09:24:22 GMT 2025 , Edited by admin on Wed Apr 02 09:24:22 GMT 2025
PRIMARY
ChEMBL
CHEMBL2107594
Created by admin on Wed Apr 02 09:24:22 GMT 2025 , Edited by admin on Wed Apr 02 09:24:22 GMT 2025
PRIMARY
EPA CompTox
DTXSID20867975
Created by admin on Wed Apr 02 09:24:22 GMT 2025 , Edited by admin on Wed Apr 02 09:24:22 GMT 2025
PRIMARY
INN
5204
Created by admin on Wed Apr 02 09:24:22 GMT 2025 , Edited by admin on Wed Apr 02 09:24:22 GMT 2025
PRIMARY
NCI_THESAURUS
C72110
Created by admin on Wed Apr 02 09:24:22 GMT 2025 , Edited by admin on Wed Apr 02 09:24:22 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY