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Details

Stereochemistry RACEMIC
Molecular Formula C12H19NO2
Molecular Weight 209.2848
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FEPRADINOL

SMILES

CC(C)(CO)NCC(O)C1=CC=CC=C1

InChI

InChIKey=PVOOBRUZWPQOER-UHFFFAOYSA-N
InChI=1S/C12H19NO2/c1-12(2,9-14)13-8-11(15)10-6-4-3-5-7-10/h3-7,11,13-15H,8-9H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C12H19NO2
Molecular Weight 209.2848
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

FEPRADINOL is an analgesic, antipyretic and anti-inflammatory agent. Its anti-inflammatory activity does not seem to be related to an inhibitory effect on prostaglandin biosynthesis.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Sympathomimetic drug allergy: cross-reactivity study by patch test.
2004
Mechanism of anti-inflammatory action of fepradinol.
1994-01
Effect of fepradinol on rat hind paw oedema induced by several inflammatory agents.
1993-11
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:20:18 GMT 2025
Edited
by admin
on Mon Mar 31 18:20:18 GMT 2025
Record UNII
860MHI4WBA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEPRADINOL
INN   MART.   MI   WHO-DD  
INN  
Official Name English
FEPRADINOL [MI]
Preferred Name English
fepradinol [INN]
Common Name English
Fepradinol [WHO-DD]
Common Name English
(±)-.ALPHA.-(((2-HYDROXY-1,1-DIMETHYLETHYL)AMINO)METHYL)BENZYL ALCOHOL USAN SYNONYM
Common Name English
1-PHENYL-4,4-DIMETHYL-3-AZAPENTANE-1,5-DIOL
Systematic Name English
BENZENEMETHANOL, .ALPHA.-(((2-HYDROXY-1,1-DIMETHYLETHYL)AMINO)METHYL)-
Systematic Name English
FEPRADINOL [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C28394
Created by admin on Mon Mar 31 18:20:18 GMT 2025 , Edited by admin on Mon Mar 31 18:20:18 GMT 2025
Code System Code Type Description
ChEMBL
CHEMBL2106269
Created by admin on Mon Mar 31 18:20:18 GMT 2025 , Edited by admin on Mon Mar 31 18:20:18 GMT 2025
PRIMARY
PUBCHEM
68819
Created by admin on Mon Mar 31 18:20:18 GMT 2025 , Edited by admin on Mon Mar 31 18:20:18 GMT 2025
PRIMARY
EVMPD
SUB07606MIG
Created by admin on Mon Mar 31 18:20:18 GMT 2025 , Edited by admin on Mon Mar 31 18:20:18 GMT 2025
PRIMARY
CAS
36981-91-6
Created by admin on Mon Mar 31 18:20:18 GMT 2025 , Edited by admin on Mon Mar 31 18:20:18 GMT 2025
PRIMARY
SMS_ID
100000080958
Created by admin on Mon Mar 31 18:20:18 GMT 2025 , Edited by admin on Mon Mar 31 18:20:18 GMT 2025
PRIMARY
MESH
C078462
Created by admin on Mon Mar 31 18:20:18 GMT 2025 , Edited by admin on Mon Mar 31 18:20:18 GMT 2025
PRIMARY
CAS
63075-47-8
Created by admin on Mon Mar 31 18:20:18 GMT 2025 , Edited by admin on Mon Mar 31 18:20:18 GMT 2025
SUPERSEDED
FDA UNII
860MHI4WBA
Created by admin on Mon Mar 31 18:20:18 GMT 2025 , Edited by admin on Mon Mar 31 18:20:18 GMT 2025
PRIMARY
INN
5456
Created by admin on Mon Mar 31 18:20:18 GMT 2025 , Edited by admin on Mon Mar 31 18:20:18 GMT 2025
PRIMARY
DRUG CENTRAL
1168
Created by admin on Mon Mar 31 18:20:18 GMT 2025 , Edited by admin on Mon Mar 31 18:20:18 GMT 2025
PRIMARY
NCI_THESAURUS
C65674
Created by admin on Mon Mar 31 18:20:18 GMT 2025 , Edited by admin on Mon Mar 31 18:20:18 GMT 2025
PRIMARY
MERCK INDEX
m5308
Created by admin on Mon Mar 31 18:20:18 GMT 2025 , Edited by admin on Mon Mar 31 18:20:18 GMT 2025
PRIMARY Merck Index
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY