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Details

Stereochemistry ACHIRAL
Molecular Formula C21H18F3NO3S2
Molecular Weight 453.498
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GW-501516

SMILES

CC1=C(CSC2=CC=C(OCC(O)=O)C(C)=C2)SC(=N1)C3=CC=C(C=C3)C(F)(F)F

InChI

InChIKey=YDBLKRPLXZNVNB-UHFFFAOYSA-N
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)

HIDE SMILES / InChI

Description

GW-501516 is a peroxisome proliferator-activator receptor-delta agonist for the potential treatment of dyslipidemia, hyperlipidemia, metabolic diseases and cardiovascular diseases. GW501516 treatment is associated with significant improvements in multiple lipid profile components (TG, LDL-C, HDL-C, free fatty acids and apoB, apoA-I and apoA-II) and a shift in LDL particle size from small dense to larger, less dense particles. Despite these promising early results, the further investigation and development of GW501516 was discontinued after observations in animal studies of its association with the rapid induction of cancers in several organs (liver, stomach, tongue, skin, bladder, ovaries, womb and testes).

CNS Activity

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency
1.1 nM [Ki]

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown
Primary
Unknown
Primary
Unknown

T1/2

ValueDoseCo-administeredAnalytePopulation
24 h
unknown
GW-501516 plasma
Homo sapiens

Doses

PubMed

Sample Use Guides

In Vivo Use Guide
12 weeks of treatment with 2.5 mg, 5.0 mg or 5,0 mg, 10 mg
Route of Administration: Oral
In Vitro Use Guide
In 1BR3N human skin fibroblasts, the 1 uM of GW501516 produced a 3.4-fold increase in ABCA1 expression and a 2-fold increase in apoA1-specific cholesterol efflux. In FHS74 human intestinal cells, the 1 uM of GW501516 produced a 2.1-fold increase in ABCA1 expression.