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

Details

Stereochemistry RACEMIC
Molecular Formula C12H19NO2.ClH
Molecular Weight 245.746
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FEPRADINOL HYDROCHLORIDE

SMILES

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

InChI

InChIKey=VJOOWJGUDMCBMI-UHFFFAOYSA-N
InChI=1S/C12H19NO2.ClH/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;1H

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 ( + / - )

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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
Effect of fepradinol on rat hind paw oedema induced by several inflammatory agents.
1993 Nov
Mechanism of anti-inflammatory action of fepradinol.
1994 Jan
Sympathomimetic drug allergy: cross-reactivity study by patch test.
2004
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:06:24 UTC 2023
Edited
by admin
on Sat Dec 16 10:06:24 UTC 2023
Record UNII
47X845AK0J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEPRADINOL HYDROCHLORIDE
WHO-DD  
Common Name English
BENZENEMETHANOL, .ALPHA.-(((2-HYDROXY-1,1-DIMETHYLETHYL)AMINO)METHYL)-, HYDROCHLORIDE
Systematic Name English
BENZENEMETHANOL, .ALPHA.-(((2-HYDROXY-1,1-DIMETHYLETHYL)AMINO)METHYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
Fepradinol hydrochloride [WHO-DD]
Common Name English
Code System Code Type Description
FDA UNII
47X845AK0J
Created by admin on Sat Dec 16 10:06:24 UTC 2023 , Edited by admin on Sat Dec 16 10:06:24 UTC 2023
PRIMARY
EVMPD
SUB35870
Created by admin on Sat Dec 16 10:06:24 UTC 2023 , Edited by admin on Sat Dec 16 10:06:24 UTC 2023
PRIMARY
PUBCHEM
3051696
Created by admin on Sat Dec 16 10:06:24 UTC 2023 , Edited by admin on Sat Dec 16 10:06:24 UTC 2023
PRIMARY
SMS_ID
100000128606
Created by admin on Sat Dec 16 10:06:24 UTC 2023 , Edited by admin on Sat Dec 16 10:06:24 UTC 2023
PRIMARY
CAS
67704-50-1
Created by admin on Sat Dec 16 10:06:24 UTC 2023 , Edited by admin on Sat Dec 16 10:06:24 UTC 2023
PRIMARY
EPA CompTox
DTXSID10987050
Created by admin on Sat Dec 16 10:06:24 UTC 2023 , Edited by admin on Sat Dec 16 10:06:24 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY