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Details

Stereochemistry RACEMIC
Molecular Formula C24H24ClNO3
Molecular Weight 409.905
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ENICLOBRATE

SMILES

CCC(C)(OC1=CC=C(CC2=CC=C(Cl)C=C2)C=C1)C(=O)OCC3=CC=CN=C3

InChI

InChIKey=VKNSAVOURPMBRN-UHFFFAOYSA-N
InChI=1S/C24H24ClNO3/c1-3-24(2,23(27)28-17-20-5-4-14-26-16-20)29-22-12-8-19(9-13-22)15-18-6-10-21(25)11-7-18/h4-14,16H,3,15,17H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C24H24ClNO3
Molecular Weight 409.905
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Eniclobrate (Sgd 33374), a diphenylmethane derivative, is a lipid-lowering compound. In rodents, eniclobrate lower serum and liver cholesterol levels and reduced the percentage of esterified cholesterol present in the serum but raised liver triglyceride levels. In a clinical trial for the treatment of hyperlipidemia type IIa and type IIb eniclobrate effectively reduced LDL-cholesterol in type IIa, however, there was a remarkable increase in HDL-cholesterol in both types of hyperlipidemia.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Beclobrate and eniclobrate hydrochloride, new diphenylmethane derivatives as agents for lowering cholesterol and triglyceride levels. Part I: Synthesis and consideration of structure-activity relationships (author's transl)].
1979
Lipid-lowering effect of the new drugs eniclobrate and beclobrate in patients with hyperlipidemia type II a and type II b.
1981
Influence of beclobrate and eniclobrate on cholesterol metabolism in rats.
1983
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:30:20 GMT 2023
Edited
by admin
on Fri Dec 15 16:30:20 GMT 2023
Record UNII
M469UFX48N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ENICLOBRATE
INN  
INN  
Official Name English
3-PYRIDYLMETHYL (±)-2-((.ALPHA.-(P-CHLOROPHENYL)-P-TOLYL)OXY)-2-METHYLBUTYRATE
Common Name English
eniclobrate [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29703
Created by admin on Fri Dec 15 16:30:20 GMT 2023 , Edited by admin on Fri Dec 15 16:30:20 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C72992
Created by admin on Fri Dec 15 16:30:20 GMT 2023 , Edited by admin on Fri Dec 15 16:30:20 GMT 2023
PRIMARY
CAS
81126-88-7
Created by admin on Fri Dec 15 16:30:20 GMT 2023 , Edited by admin on Fri Dec 15 16:30:20 GMT 2023
PRIMARY
PUBCHEM
43387
Created by admin on Fri Dec 15 16:30:20 GMT 2023 , Edited by admin on Fri Dec 15 16:30:20 GMT 2023
PRIMARY
INN
4250
Created by admin on Fri Dec 15 16:30:20 GMT 2023 , Edited by admin on Fri Dec 15 16:30:20 GMT 2023
PRIMARY
MESH
C021021
Created by admin on Fri Dec 15 16:30:20 GMT 2023 , Edited by admin on Fri Dec 15 16:30:20 GMT 2023
PRIMARY
SMS_ID
100000080230
Created by admin on Fri Dec 15 16:30:20 GMT 2023 , Edited by admin on Fri Dec 15 16:30:20 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106104
Created by admin on Fri Dec 15 16:30:20 GMT 2023 , Edited by admin on Fri Dec 15 16:30:20 GMT 2023
PRIMARY
EVMPD
SUB06532MIG
Created by admin on Fri Dec 15 16:30:20 GMT 2023 , Edited by admin on Fri Dec 15 16:30:20 GMT 2023
PRIMARY
FDA UNII
M469UFX48N
Created by admin on Fri Dec 15 16:30:20 GMT 2023 , Edited by admin on Fri Dec 15 16:30:20 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY