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

Details

Stereochemistry RACEMIC
Molecular Formula C16H15F3O
Molecular Weight 280.2849
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLUMECINOL

SMILES

CCC(O)(C1=CC=CC=C1)C2=CC(=CC=C2)C(F)(F)F

InChI

InChIKey=DVASNQYQOZHAJN-UHFFFAOYSA-N
InChI=1S/C16H15F3O/c1-2-15(20,12-7-4-3-5-8-12)13-9-6-10-14(11-13)16(17,18)19/h3-11,20H,2H2,1H3

HIDE SMILES / InChI
FLUMECINOL, a benzhydrol derivative, is a hepatic microsomal drug-metabolizing enzyme inducer. It was in clinical development for the treatment of pruritus associated with primary biliary cirrhosis.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Efficiency of enzyme-inducing agents in rats with intrahepatic cholestasis.
2002 Sep
Patents

Patents

Sample Use Guides

600 mg once weekly for 3 weeks.
Route of Administration: Oral
Name Type Language
FLUMECINOL
INN   MART.   MI   WHO-DD  
INN  
Official Name English
1-(3-TRIFLUOROMETHYLPHENYL)-1-PHENYLPROPAN-1-OL
Systematic Name English
flumecinol [INN]
Common Name English
.ALPHA.-ETHYL-3-(TRIFLUOROMETHYL)BENZHYDROL
Systematic Name English
BENZENEMETHANOL, .ALPHA.-ETHYL-.ALPHA.-PHENYL-3-(TRIFLUOROMETHYL)-
Systematic Name English
Flumecinol [WHO-DD]
Common Name English
FLUMECINOL [MART.]
Common Name English
ZYXORIN
Brand Name English
FLUMECINOL [MI]
Common Name English
3-(TRIFLUOROMETHYL)-.ALPHA.-ETHYLBENZHYDROL
Systematic Name English
(±)-FLUMECINOL
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 2984
Created by admin on Fri Dec 15 15:13:45 GMT 2023 , Edited by admin on Fri Dec 15 15:13:45 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID80866560
Created by admin on Fri Dec 15 15:13:45 GMT 2023 , Edited by admin on Fri Dec 15 15:13:45 GMT 2023
PRIMARY
MESH
C016914
Created by admin on Fri Dec 15 15:13:45 GMT 2023 , Edited by admin on Fri Dec 15 15:13:45 GMT 2023
PRIMARY
CAS
56430-99-0
Created by admin on Fri Dec 15 15:13:45 GMT 2023 , Edited by admin on Fri Dec 15 15:13:45 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107440
Created by admin on Fri Dec 15 15:13:45 GMT 2023 , Edited by admin on Fri Dec 15 15:13:45 GMT 2023
PRIMARY
CAS
113755-17-2
Created by admin on Fri Dec 15 15:13:45 GMT 2023 , Edited by admin on Fri Dec 15 15:13:45 GMT 2023
SUPERSEDED
FDA UNII
JB0YA8LDOW
Created by admin on Fri Dec 15 15:13:45 GMT 2023 , Edited by admin on Fri Dec 15 15:13:45 GMT 2023
PRIMARY
EVMPD
SUB07694MIG
Created by admin on Fri Dec 15 15:13:45 GMT 2023 , Edited by admin on Fri Dec 15 15:13:45 GMT 2023
PRIMARY
PUBCHEM
41870
Created by admin on Fri Dec 15 15:13:45 GMT 2023 , Edited by admin on Fri Dec 15 15:13:45 GMT 2023
PRIMARY
SMS_ID
100000080685
Created by admin on Fri Dec 15 15:13:45 GMT 2023 , Edited by admin on Fri Dec 15 15:13:45 GMT 2023
PRIMARY
ECHA (EC/EINECS)
260-176-1
Created by admin on Fri Dec 15 15:13:45 GMT 2023 , Edited by admin on Fri Dec 15 15:13:45 GMT 2023
PRIMARY
INN
4445
Created by admin on Fri Dec 15 15:13:45 GMT 2023 , Edited by admin on Fri Dec 15 15:13:45 GMT 2023
PRIMARY
MERCK INDEX
m5437
Created by admin on Fri Dec 15 15:13:45 GMT 2023 , Edited by admin on Fri Dec 15 15:13:45 GMT 2023
PRIMARY Merck Index
DRUG CENTRAL
1196
Created by admin on Fri Dec 15 15:13:45 GMT 2023 , Edited by admin on Fri Dec 15 15:13:45 GMT 2023
PRIMARY
NCI_THESAURUS
C169987
Created by admin on Fri Dec 15 15:13:45 GMT 2023 , Edited by admin on Fri Dec 15 15:13:45 GMT 2023
PRIMARY