GW-5074 chemical structure
Chemical structureResearch use only
CAT. NO. DC8810Featured

GW-5074

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TotalUS$350
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Product overview

Description & Application

GW 5074 is a potent and selective c-Raf inhibitor with IC50 of 9 nM, and has no effect on the activities of JNK1/2/3, MEK1, MKK6/7, CDK1/2, c-Src, p38 MAP, VEGFR2 or c-Fms.

ParameterValue
Chemical Name5-Iodo-3-[(3,5-dibromo-4-hydroxyphenyl)methylene]-2-indolinone
CAS No.220904-83-6
Synonyms2H-Indol-2-one,3-[(3,5-dibromo-4-hydroxyphenyl)methylene]-1,3-dihydro-5-iodo-;GW5074;(3Z)-3-[(3,5-dibromo-4-hydroxyphenyl)methylidene]-5-iodo-1H-indol-2-one;3-(3,5-Dibromo-4-hydroxybenzylidene)-5-iodo-1,3-dihydroindol-2-one;GW 5074 (GW-5074,GW5074);3-(3,5-Dibromo-4-hydroxybenzyliden)-5-iodo-1,3-dihydroindol-2-one;GW-5074;Raf1 Kinase Inhibitor I;STO521;Tocris-1381;GW 5074;B7W8RS1GG2;InSolution™ Raf1 Kinase Inhibitor I;5-Iodo-3-[(3,5-dibromo-4-hydroxyphenyl)methylene]-2-indolinone;3-(3,5-Dibromo-4-hydroxy-benzylidene)-5-iodo-1,3-dihydro-indol-2-one;3-(3,5-dibromo-4-hydroxybenzylidene)-5-iodoindolin-2-one;(Z)-3-(3,5-Dibromo-4-hydroxybenzylidene)-5-iodoindolin-2-one;3-(3,5-Dibro
FormulaC15H8Br2INO2
M.Wt520.942
SMILESIC1C([H])=C([H])C2=C(C=1[H])/C(=C(\[H])/C1C([H])=C(C(=C(C=1[H])Br)O[H])Br)/C(N2[H])=O
Purity>98%
Storage2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Biological Activity

GW 5074 is a potent and selective c-Raf inhibitor with IC50 of 9 nM, and has no effect on the activities of JNK1/2/3, MEK1, MKK6/7, CDK1/2, c-Src, p38 MAP, VEGFR2 or c-Fms.

In Vitro

GW5074 is a potent and specific inhibitor of c-Raf with IC50 of 9 nM and has no effect of MKK6, MKK7, p38 MAP kinase and cdks in vitro. However, treatment of neuronal cultures with GW5074 permits accumulation of activating modifications on c-Raf and also B-Raf. The inhibition of LK-induced apoptosis by GW5074 in cerebellar granule neurons is not MEK-ERK-dependent. GW5074 delays down-regulation of Akt activity but inhibits apoptosis by an Akt-independent mechanism. GW5074 affects Ras, nuclear factor-kappa B and c-jun. GW5074 inhibits cell death caused by neurotoxins in granule cells and other neuronal types[1].

In Vivo

GW5074 (5 mg/Kg) completely prevents extensive bilateral striatal lesions induced by 3-NP in mice[1]. GW5074 suppresses sidestream smoke-induced airway hyperresponsiveness in mice[2]. GW5074 completely abolishes chronic morphine-mediated AC superactivation I in CHO cells stably expressing the humanμ-opioid receptor[3].

References & source

DC Chemicals original product information

Published experimental findings depend on the model and assay conditions. They do not guarantee equivalent performance in every application. For laboratory research use only.

Product documentation

Refer to the certificate supplied with your lot for batch-specific release results.

Handling guide

2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

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