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Details

Stereochemistry RACEMIC
Molecular Formula C11H16O
Molecular Weight 164.2441
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENIPENTOL

SMILES

CCCCC(O)C1=CC=CC=C1

InChI

InChIKey=OVGORFFCBUIFIA-UHFFFAOYSA-N
InChI=1S/C11H16O/c1-2-3-9-11(12)10-7-5-4-6-8-10/h4-8,11-12H,2-3,9H2,1H3

HIDE SMILES / InChI

Description

Fenipentol is a choleretic agent indicated for the treatment of chronic liver disease and bile duct disease. The drug is sold without prescription.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
FEBICHOL

Approved Use

Febichol capsules are to be used by adult patients to treat digestive problems in chronic (long-term) liver disease and bile duct disease (disorders of gall bladder activity, chronic cholecystitis, chronic development of gall bladder stones, chronic liver disease associated with digestive symptoms caused by impairment or disorder of biliary tree) and conditions after surgical removal of gall bladder or after hepatitis.
Primary
FEBICHOL

Approved Use

Febichol capsules are to be used by adult patients to treat digestive problems in chronic (long-term) liver disease and bile duct disease (disorders of gall bladder activity, chronic cholecystitis, chronic development of gall bladder stones, chronic liver disease associated with digestive symptoms caused by impairment or disorder of biliary tree) and conditions after surgical removal of gall bladder or after hepatitis.
PubMed

PubMed

TitleDatePubMed
[Contact sensitization to pharmaceutic aids in dermatologic cosmetic and external use preparations].
2004 May
Synthesis and antioxidant properties of some indole ethylamine derivatives as melatonin analogs.
2005 Sep
Running speed in mammals increases with muscle n-6 polyunsaturated fatty acid content.
2006 Dec 20
Dietary exposure of children and teenagers to benzoates, sulphites, butylhydroxyanisol (BHA) and butylhydroxytoluen (BHT) in Beirut (Lebanon).
2007 Feb
Improved and efficient synthesis of chiral N,P-ligands via cyclic sulfamidates for asymmetric addition of butyllithium to benzaldehyde.
2007 Sep 13
Monocytes of patients with familial hypercholesterolemia show alterations in cholesterol metabolism.
2008 Nov 28
Hypercholesterolemia in rats impairs the cholinergic system and leads to memory deficits.
2010 Dec
Contribution of dietary intakes of antioxidants to homocysteine-induced low density lipoprotein (LDL) oxidation in atherosclerotic patients.
2010 Jul
Patents

Sample Use Guides

In Vivo Use Guide
Standard dosage for adults and youths over 15 years of age is 2 capsules (each capsule of contains 100 mg of active ingredient fenipentol) three times a day (always immediately before meals).
Route of Administration: Oral
In Vitro Use Guide
Unknown
Name Type Language
FENIPENTOL
INN   JAN   MART.   MI   WHO-DD  
INN  
Official Name English
BENZYL ALCOHOL, .ALPHA.-BUTYL-
Systematic Name English
PHENYLBUTYLCARBINOL
Systematic Name English
FENIPENTOL [JAN]
Common Name English
FENIPENTOL [MART.]
Common Name English
FENIPENTOL [MI]
Common Name English
1-PHENYL-1-HYDROXY-N-PENTANE
Common Name English
(±)-.ALPHA.-BUTYLBENZYL ALCOHOL
Systematic Name English
PH-BC
Code English
1-PHENYL-1-HYDROXYPENTANE
Systematic Name English
fenipentol [INN]
Common Name English
(±)-1-PHENYL-1-PENTANOL
Systematic Name English
PC-1
Code English
NSC-8478
Code English
PANCORAL
Brand Name English
1-PENTANOL, 1-PHENYL-
Systematic Name English
Fenipentol [WHO-DD]
Common Name English
.ALPHA.-BUTYLBENZYL ALCOHOL
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C66913
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
Code System Code Type Description
CAS
583-03-9
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
PRIMARY
NSC
8478
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
PRIMARY
ChEMBL
CHEMBL2104321
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
PRIMARY
MESH
C013992
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
PRIMARY
NCI_THESAURUS
C65652
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
PRIMARY
CAS
21632-19-9
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
SUPERSEDED
PUBCHEM
3338
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
PRIMARY
FDA UNII
X3FZE77O60
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
PRIMARY
CAS
136264-41-0
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
SUPERSEDED
EVMPD
SUB07567MIG
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
PRIMARY
INN
3413
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
PRIMARY
DRUG CENTRAL
1151
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
PRIMARY
ECHA (EC/EINECS)
209-493-9
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
PRIMARY
RXCUI
24846
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID4046818
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
PRIMARY
SMS_ID
100000081296
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
PRIMARY
MERCK INDEX
m5276
Created by admin on Fri Dec 15 15:54:50 UTC 2023 , Edited by admin on Fri Dec 15 15:54:50 UTC 2023
PRIMARY Merck Index