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Details

Stereochemistry ACHIRAL
Molecular Formula C16H14Cl2O3
Molecular Weight 325.187
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DULOFIBRATE

SMILES

CC(C)(OC1=CC=C(Cl)C=C1)C(=O)OC2=CC=C(Cl)C=C2

InChI

InChIKey=NIVDRJXCJCEFDD-UHFFFAOYSA-N
InChI=1S/C16H14Cl2O3/c1-16(2,21-14-9-5-12(18)6-10-14)15(19)20-13-7-3-11(17)4-8-13/h3-10H,1-2H3

HIDE SMILES / InChI

Molecular Formula C16H14Cl2O3
Molecular Weight 325.187
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Dulofibrate is a fibrate derivative with antilipidemic activity. Unlike clofibrate, dulofibrate is selective for a reduction in triglycerides. Dulofibrate decreased the conjugation of nopol. Dulofibrate exhibited a clofibrate-like effect on the induction of hepatic drug-metabolizing enzymes, characterized by an increase in lauric acid 12-hydroxylation and bilirubin UDP-glucuronosyltransferase activities. Dulofibrate and fenofibrate have been shown to possess an equal potency as peroxisome proliferators.

Approval Year

PubMed

PubMed

TitleDatePubMed
Influence of food on the absorption of the p-chlorophenolic ester of chlorophenoxyisobutyric acid in man.
1984 Mar
Differential induction profile of drug-metabolizing enzymes after treatment with hypolipidaemic agents.
1987 Apr
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Rat data
200 mg/kg per day once a day for five days
Route of Administration: Other
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:38:21 GMT 2023
Edited
by admin
on Fri Dec 15 16:38:21 GMT 2023
Record UNII
5K0215OMQX
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DULOFIBRATE
INN  
INN  
Official Name English
dulofibrate [INN]
Common Name English
P-CHLOROPHENYL 2-(P-CHLOROPHENOXY)-2-METHYLPROPIONATE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C98150
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
Code System Code Type Description
EVMPD
SUB06423MIG
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
INN
4776
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
PUBCHEM
68812
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
EPA CompTox
DTXSID10866891
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
SMS_ID
100000081012
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
CAS
61887-16-9
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106328
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
MESH
C041053
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
FDA UNII
5K0215OMQX
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
NCI_THESAURUS
C65494
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY