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Details

Stereochemistry ABSOLUTE
Molecular Formula C27H21F3N2O6S
Molecular Weight 558.526
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CEVOGLITAZAR

SMILES

CC1=C(COC2=CC=C(C=C2)S(=O)(=O)N3[C@H](CC4=C3C=CC=C4)C(O)=O)N=C(O1)C5=CC=C(C=C5)C(F)(F)F

InChI

InChIKey=KVVODNUBDFULSC-XMMPIXPASA-N
InChI=1S/C27H21F3N2O6S/c1-16-22(31-25(38-16)17-6-8-19(9-7-17)27(28,29)30)15-37-20-10-12-21(13-11-20)39(35,36)32-23-5-3-2-4-18(23)14-24(32)26(33)34/h2-13,24H,14-15H2,1H3,(H,33,34)/t24-/m1/s1

HIDE SMILES / InChI

Description

Cevoglitazar is a dual agonist for the peroxisome proliferator-activated receptor (PPAR)-alpha and -gamma subtypes. Cevoglitazar was as effective as pioglitazone at improving glucose tolerance, normalizes intramyocellular lipids and reduces body weight gain and adiposity, independent of food intake. Metabolic profiling showed that in the muscle cevoglitazar improves the lipid profile via both PPARα‐ and PPARγ‐mediated mechanisms. Cevoglitazar only induced small changes to the lipid composition of visceral fat. In subcutaneous fat, however, cevoglitazar induced changes similar to those observed with fenofibrate suggesting export of fatty acids from this depot.

Originator

Approval Year

PubMed

Sample Use Guides

In Vivo Use Guide
rat 5 mg/kg
Route of Administration: Oral