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GW 5074, Tocris Bioscience™
GSA_VA

Catalog No. p-4783502 Shop All R&D Systems Products
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Quantity:
10 mg
50 mg
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This item is not returnable. View return policy

Potent, selective c-Raf1 kinase inhibitor

GW 5074 is a potent, selective and cell-permeable c-Raf1 kinase inhibitor (IC50 = 9 nM). GW 5074 displays ≥ 100-fold selectivity for raf kinase over CDK1, CDK2, c-src, ERK2, MEK, p38, Tie2, VEGFR2 and c-fm. GW 5074 binds mutant huntingtin (mHTT) and decreases levels of mHTT in cultured hippocampal neurons and fibroblasts from patients with Huntington's disease. Brain penetrant.

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Chemical Identifiers

CAS 220904-83-6
Molecular Formula C15H8Br2INO2
Molecular Weight (g/mol) 520.95
MDL Number MFCD09971042
InChI Key LMXYVLFTZRPNRV-UHFFFAOYSA-N
Synonym raf1 kinase inhibitor i, chembl72365, 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, 3z-3-3,5-dibromo-4-hydroxyphenyl methylidene-5-iodo-1h-indol-2-one, z-3-3,5-dibromo-4-hydroxybenzylidene-5-iodoindolin-2-one, gw5074, powder, tocris-1381, biomolki_000056
PubChem CID 5924208
IUPAC Name 3-[(3,5-dibromo-4-hydroxyphenyl)methylidene]-5-iodo-2,3-dihydro-1H-indol-2-one
SMILES OC1=C(Br)C=C(C=C2C(=O)NC3=C2C=C(I)C=C3)C=C1Br

Specifications

Quantity 10 mg
Formula Weight 520.94
Percent Purity >98%
Chemical Name or Material GW 5074
Recommended Storage Desiccate at -20°C
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