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GW0742

GW0742

CAS: 317318-84-6

Molecular Formula: C21H17F4NO3S2

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GW0742 - Names and Identifiers

Name GW0742
Synonyms GW0742
GW0742X
GW610742
GW 0742X
GW 610742
GWdelta0742
GWdelta 0742
2-(4-(((2-(3-Fluoro-4-(trifluoromethyl)phenyl)-4-methylthiazol-5-yl)methyl)thio)-2-methylpheno
2-(4-(((2-(3-Fluoro-4-(trifluoromethyl)phenyl)-4-methylthiazol-5-yl)methyl)thio)-2-methylphenoxy)
4-[2-(3-FLUORO-4-TRIFLUOROMETHYL-PHENYL)-4-METHYL-THIAZOL-5-YLMETHYLSULFANYL]-2-METHYL-PHENOXY-ACETIC ACID
[4-[[[2-[3-FLUORO-4-(TRIFLUOROMETHYL)PHENYL]-4-METHYL-5-THIAZOLYL]METHYL]THIO]-2-METHYLPHENOXY]ACETIC ACID
CAS 317318-84-6
EINECS 1532714-185-1
InChIKey HWVNEWGKWRGSRK-UHFFFAOYSA-N

GW0742 - Physico-chemical Properties

Molecular FormulaC21H17F4NO3S2
Molar Mass471.49
Density1.46±0.1 g/cm3(Predicted)
Melting Point134.5-135.5 °C
Boling Point591.5±60.0 °C(Predicted)
Solubility DMSO: >5mg/mL
Appearancesolid
Colorwhite
pKa3.17±0.10(Predicted)
Storage Condition2-8°C
MDLMFCD07369423
Physical and Chemical PropertiesBioactive GW0742 is a potent, selective PPAR β/δ agonist with an IC50 of 1 nM, which is 1000-fold more selective than hPPAR α and hPPAR γ.
UseUses GW0742 is a small molecule agonist of the human peroxisome proliferator-activated receptor δ(PPAR δ). It shows an EC50 of 1.1 nM for PPAR δ, which is 100-fold more selective than other human subtypes.
In vitro studyIn basic cell transcription experiments, GW0742 effectively acted on hPPAR α,hPPAR γ, and hPPAR δ with EC50 of 1.1 μm, 2 μm, and 1 nM, respectively. GW0742 (0.2 μm and 1 μm) significantly increased PPAR β/δ activity in N/TERT-1 keratinocytes. GW0742 (1 μm) significantly inhibited the average cell number of N/TERT-1 keratinocytes. GW0742 (1 M) increased the number of cells in G1 phase, decreased the number of cells in S phase. GW0742 (1 μm) acts on N/TERT-1 keratinocytes and mouse primary keratinocytes to significantly increase mRNA-encoded ADRP, a PPAR β/δ target gene. GW0742 (1 μm) significantly reduced phosphorylation of retinoblastoma (Rb) and p42/44 ERK levels in N/TERT-1 cells. 100 μm GW0742 significantly reduced low KCl-induced neuronal cell death in cerebellar granule neurons. By measuring LDH release, it was observed that 100 μm GW0742 significantly enhanced cell death. Treatment of cerebellar granule neuron medium with 100 μm GW0742 for 6 hours significantly enhanced c-Jun expression. 100 μm GW0742 acts on MCF-7 cells to increase PPARα-mediated transcription in the presence of 1.5% BSA.
In vivo studyGW0742 (10 mg/kg) treatment of C57BL6/J mice promoted reverse cholesterol transport. GW0742 (10 mg/kg) treatment of C57BL6/J mice promoted fecal excretion of HDL cholesterol, although there was no effect on HDL cholesterol metabolism. GW0742 acts on the small intestine of mice to reduce the expression of NPC1L1 mRNA. GW0742 (30 mg/kg) treatment of Male BALB/c mice significantly reduced leukocyte recruitment into the lung space prior to induction of LPS-mediated lung inflammation. GW0742 (30 mg/kg) treatment of mouse bronchoalveolar lavage fluid significantly reduced the protein and mRNA levels of proinflammatory cytokines IL-6,IL-1β and TNF-α.

GW0742 - Risk and Safety

WGK Germany3

GW0742 - Preparation solution concentration reference

 1mg5mg10mg
1 mM2.121 ml10.605 ml21.209 ml
5 mM0.424 ml2.121 ml4.242 ml
10 mM0.212 ml1.06 ml2.121 ml
5 mM0.042 ml0.212 ml0.424 ml
Last Update:2024-01-02 23:10:35
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Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
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CAS: 317318-84-6
Tel: 18301782025
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View History
GW0742
BOC-VAL-PRO-ARG-MCA
Benzofuran, 7-(chloromethyl)-
155486-33-2
2-Nathphalenyl disulfide
potassium benzenolate
3-(4-Chlorophenyl)-2-[[[phenylamino]thiocarbonylamino]iminomethyl]quinazolin-4(3H)-one
2307-11-1
55608-72-5
2,12-Diaza-3,7,11-triboratridecane, 3,7,11-tris(dimethylamino)-2,12-dimethyl- (7CI,8CI)
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