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Details

Stereochemistry ACHIRAL
Molecular Formula C16H22ClNO4
Molecular Weight 327.803
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLOFIBRIDE

SMILES

CN(C)C(=O)CCCOC(=O)C(C)(C)OC1=CC=C(Cl)C=C1

InChI

InChIKey=CXQGFLBVUNUQIA-UHFFFAOYSA-N
InChI=1S/C16H22ClNO4/c1-16(2,22-13-9-7-12(17)8-10-13)15(20)21-11-5-6-14(19)18(3)4/h7-10H,5-6,11H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C16H22ClNO4
Molecular Weight 327.803
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Clofibride is a hypolipaemic drug of p-chlorophenoxyisobutyric type. Clofibride hypolipaemic effects could be due, partially, to a reduction of hormono-dependent lipolysis. Clofibride decreased blood cholesterol and total lipids, increased liver weight and liver catalase content, and decreased biliary excretion of cholesterol in normolipidemic rats after a 7 day treatment.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Medium and long term study of clofibride in the treatment of atherogenic hyperlipidemia. Statistical approach to the results].
1976 Nov
Patents

Sample Use Guides

In Vivo Use Guide
Healthy volunteers received therapeutic doses of clofibrate as 2x500 mg capsules, clofibride as 2x450 mg capsules, twice daily for ten days.
Route of Administration: Oral
In Vitro Use Guide
One dose of clofibride (Cf) is administered, after sacrifice of normal fasting rat, in vitro: 2 mg/100 mg adipocytes in 2 ml medium.
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:21:17 GMT 2023
Edited
by admin
on Sat Dec 16 16:21:17 GMT 2023
Record UNII
0S9SLS3L93
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLOFIBRIDE
INN   MART.   WHO-DD  
INN  
Official Name English
CLOFIBRIDE [MART.]
Common Name English
2-(P-CHLOROPHENOXY)-2-METHYLPROPIONIC ACID, ESTER WITH 4-HYDROXY-N,N-DIMETHYLBUTYRAMIDE
Common Name English
clofibride [INN]
Common Name English
Clofibride [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-ATC C10AB10
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
NCI_THESAURUS C98150
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
WHO-VATC QC10AB10
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
Code System Code Type Description
FDA UNII
0S9SLS3L93
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
PRIMARY
EPA CompTox
DTXSID1022841
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
PRIMARY
MESH
C007089
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
PRIMARY
SMS_ID
100000084335
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
PRIMARY
NCI_THESAURUS
C78055
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
PRIMARY
DRUG BANK
DB13849
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
PRIMARY
ChEMBL
CHEMBL1697831
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
PRIMARY
INN
3245
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
PRIMARY
PUBCHEM
160134
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
PRIMARY
DRUG CENTRAL
696
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
PRIMARY
WIKIPEDIA
CLOFIBRIDE
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
PRIMARY
EVMPD
SUB06708MIG
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
PRIMARY
ECHA (EC/EINECS)
247-912-7
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
PRIMARY
CAS
26717-47-5
Created by admin on Sat Dec 16 16:21:17 GMT 2023 , Edited by admin on Sat Dec 16 16:21:17 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY