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Details

Stereochemistry ACHIRAL
Molecular Formula C20H21Cl2NO4
Molecular Weight 410.291
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LIFIBRATE

SMILES

CN1CCC(CC1)OC(=O)C(OC2=CC=C(Cl)C=C2)OC3=CC=C(Cl)C=C3

InChI

InChIKey=QDGIAPPCJRFVEK-UHFFFAOYSA-N
InChI=1S/C20H21Cl2NO4/c1-23-12-10-18(11-13-23)25-19(24)20(26-16-6-2-14(21)3-7-16)27-17-8-4-15(22)5-9-17/h2-9,18,20H,10-13H2,1H3

HIDE SMILES / InChI

Molecular Formula C20H21Cl2NO4
Molecular Weight 410.291
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Lifibrate is the antihyperlipidemic agent. It is a potent hepatic peroxisome proliferator. Administration of lifibrate at a dietary concentration of 0.15% for 3 weeks, increased the activity of catalase in both liver and kidney of male wild type (Cs-a strain) mice. The hypolipidemic activity of lifibrate is eight to nine times greater than that of chlorphenoxy isobutyric acid ethyl ester in the male Wistar rat.

Approval Year

PubMed

PubMed

TitleDatePubMed
Laboratory studies of 1-methyl-4-piperidyl bis(p-chlorophenoxy) acetate (SaH 42-348)--a new hypolipidemic agent.
1969 Aug
Effect of SaH 42-348, an analog of clofibrate, on lipid metabolism in rats.
1973 Jun
1-methyl-4piperidyl-bis (P-chlorophenoxy) acetate: a new hypolipidemic peroxisome proliferator.
1975 Mar
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:11:41 GMT 2023
Edited
by admin
on Fri Dec 15 15:11:41 GMT 2023
Record UNII
Y4X961F8Z1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LIFIBRATE
INN   USAN  
INN   USAN  
Official Name English
42-348
Code English
lifibrate [INN]
Common Name English
LIFIBRATE [USAN]
Common Name English
ACETIC ACID, BIS(4-CHLOROPHENOXY)-, 1-METHYL-4-PIPERIDINYL ESTER
Common Name English
1-METHYL-4-PIPERIDYL GLYOXYLATE 2-(BIS(P-CHLOROPHENYL) ACETAL)
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C98150
Created by admin on Fri Dec 15 15:11:41 GMT 2023 , Edited by admin on Fri Dec 15 15:11:41 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL1883563
Created by admin on Fri Dec 15 15:11:41 GMT 2023 , Edited by admin on Fri Dec 15 15:11:41 GMT 2023
PRIMARY
FDA UNII
Y4X961F8Z1
Created by admin on Fri Dec 15 15:11:41 GMT 2023 , Edited by admin on Fri Dec 15 15:11:41 GMT 2023
PRIMARY
SMS_ID
100000082312
Created by admin on Fri Dec 15 15:11:41 GMT 2023 , Edited by admin on Fri Dec 15 15:11:41 GMT 2023
PRIMARY
ECHA (EC/EINECS)
244-839-2
Created by admin on Fri Dec 15 15:11:41 GMT 2023 , Edited by admin on Fri Dec 15 15:11:41 GMT 2023
PRIMARY
CAS
22204-91-7
Created by admin on Fri Dec 15 15:11:41 GMT 2023 , Edited by admin on Fri Dec 15 15:11:41 GMT 2023
PRIMARY
MESH
C100041
Created by admin on Fri Dec 15 15:11:41 GMT 2023 , Edited by admin on Fri Dec 15 15:11:41 GMT 2023
PRIMARY
NCI_THESAURUS
C82243
Created by admin on Fri Dec 15 15:11:41 GMT 2023 , Edited by admin on Fri Dec 15 15:11:41 GMT 2023
PRIMARY
EVMPD
SUB08511MIG
Created by admin on Fri Dec 15 15:11:41 GMT 2023 , Edited by admin on Fri Dec 15 15:11:41 GMT 2023
PRIMARY
EPA CompTox
DTXSID1046217
Created by admin on Fri Dec 15 15:11:41 GMT 2023 , Edited by admin on Fri Dec 15 15:11:41 GMT 2023
PRIMARY
INN
3473
Created by admin on Fri Dec 15 15:11:41 GMT 2023 , Edited by admin on Fri Dec 15 15:11:41 GMT 2023
PRIMARY
PUBCHEM
31060
Created by admin on Fri Dec 15 15:11:41 GMT 2023 , Edited by admin on Fri Dec 15 15:11:41 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY