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
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)
| 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
| Title | Date | PubMed |
|---|---|---|
| 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
Edited
Mon Mar 31 22:59:50 GMT 2025
by
admin
on
Mon Mar 31 22:59:50 GMT 2025
|
| Record UNII |
H32ABL87X4
|
| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID10179493
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9870304
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H32ABL87X4
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289722-11-8
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