GW501516 25μM R06 exp285

PPARδ receptor agonist, increases metabolism, banned performance enhancer

  • Class / Subclass 1: Gene Regulation / Nuclear Receptor Ligand
  • Class / Subclass 2: Metabolism / Hormone Agonist

Compound References

  • PubChem Name: Endurobol
  • Synonyms: GW 1516; GSK-516
  • CAS #: 317318-70-0
  • PubChem CID: 9803963
  • IUPAC: 2-[2-methyl-4-[[4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]acetic acid
  • INCHI Name: InChI=1S/C21H18F3NO3S2/c1-12-9-16(7-8-17(12)28-10-19(26)27)29-11-18-13(2)25-20(30-18)14-3-5-15(6-4-14)21(22,23)24/h3-9H,10-11H2,1-2H3,(H,26,27)
  • INCHI Key: YDBLKRPLXZNVNB-UHFFFAOYSA-N
  • Molecular Weight: 453.5
  • Canonical SMILES: CC1=C(C=CC(=C1)SCC2=C(N=C(S2)C3=CC=C(C=C3)C(F)(F)F)C)OCC(=O)O
  • Isomeric SMILES: N/A
  • Molecular Formula: C21H18F3NO3S2

Compound Supplier

  • Supplier Name: Sigma-Aldrich
  • Catalog #: SML1491
  • Lot #: 1798

Compound Characterization

  • HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C21H18F3NO3S2 454.0753; found 454.0758

Dose Response Curve

  • Platform ID: GW501516
  • Min: -11.0338; Max: 33.5004





IC Concentration (µM)
IC10 N/A
IC20 N/A
IC30 N/A
IC40 N/A
IC50 N/A
IC60 N/A
IC70 N/A
IC80 N/A
IC90 N/A


  • Round: 06
  • Dose: 25µM
  • Days of incubation: 8
  • Doublings: 7.0
  • Numbers of reads: 8109612
Sensitive/Resistant hits (FDR<0.05)CRANKSScore PlotTop 30 GenesScreen SimilarityTop 30 Sensitive GO termsTop 30 Resistant GO terms
1/0ScoresViewViewViewViewView

  • Last modified: 2026/01/15 21:36
  • by 127.0.0.1