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Details

Stereochemistry ACHIRAL
Molecular Formula C26H34F2N2O3S
Molecular Weight 492.622
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GW-9578

SMILES

CCCCCCCN(CCC1=CC=C(SC(C)(C)C(O)=O)C=C1)C(=O)NC2=CC=C(F)C=C2F

InChI

InChIKey=KYQNYMXQHLMADB-UHFFFAOYSA-N
InChI=1S/C26H34F2N2O3S/c1-4-5-6-7-8-16-30(25(33)29-23-14-11-20(27)18-22(23)28)17-15-19-9-12-21(13-10-19)34-26(2,3)24(31)32/h9-14,18H,4-8,15-17H2,1-3H3,(H,29,33)(H,31,32)

HIDE SMILES / InChI

Molecular Formula C26H34F2N2O3S
Molecular Weight 492.622
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
PPARalpha agonists suppress osteopontin expression in macrophages and decrease plasma levels in patients with type 2 diabetes.
2007-06
Identification of a subtype selective human PPARalpha agonist through parallel-array synthesis.
2001-05-07
A ureido-thioisobutyric acid (GW9578) is a subtype-selective PPARalpha agonist with potent lipid-lowering activity.
1999-09-23
A novel N-aryl tyrosine activator of peroxisome proliferator-activated receptor-gamma reverses the diabetic phenotype of the Zucker diabetic fatty rat.
1999-07
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:59:50 GMT 2025
Edited
by admin
on Mon Mar 31 22:59:50 GMT 2025
Record UNII
H32ABL87X4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GW-9578
Common Name English
PROPANOIC ACID, 2-((4-(2-((((2,4-DIFLUOROPHENYL)AMINO)CARBONYL)HEPTYLAMINO)ETHYL)PHENYL)THIO)-2-METHYL-
Preferred Name English
Code System Code Type Description
CAS
247923-29-1
Created by admin on Mon Mar 31 22:59:50 GMT 2025 , Edited by admin on Mon Mar 31 22:59:50 GMT 2025
PRIMARY
EPA CompTox
DTXSID10179493
Created by admin on Mon Mar 31 22:59:50 GMT 2025 , Edited by admin on Mon Mar 31 22:59:50 GMT 2025
PRIMARY
PUBCHEM
9870304
Created by admin on Mon Mar 31 22:59:50 GMT 2025 , Edited by admin on Mon Mar 31 22:59:50 GMT 2025
PRIMARY
FDA UNII
H32ABL87X4
Created by admin on Mon Mar 31 22:59:50 GMT 2025 , Edited by admin on Mon Mar 31 22:59:50 GMT 2025
PRIMARY
CAS
289722-11-8
Created by admin on Mon Mar 31 22:59:50 GMT 2025 , Edited by admin on Mon Mar 31 22:59:50 GMT 2025
SUPERSEDED
Related Record Type Details
ACTIVE MOIETY