- GW 5074
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- $36.00 / 2mg
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2025-09-11
- CAS:220904-83-6
- Min. Order:
- Purity: 99.32%
- Supply Ability: 10g
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| Product Name: | GW5074 | | Synonyms: | RAF1 KINASE INHIBITOR I;(3Z)-3-[(3,5-DIBROMO-4-HYDROXYPHENYL)METHYLIDENE]-5-IODO-1H-INDOL-2-ONE;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-HYDROXYBENZYLIDINE)-5-IODO-1,3-DIHYDRO-INDOL-2-ONE;GW5074;2H-Indol-2-one, 3-[(3,5-dibromo-4-hydroxyphenyl)methylene]-1,3-dihydro-5-iodo-;3-(3,5-dibromo-4-hydroxybenzyliden)-5-iodo-1,3-dihydroindol-2-one | | CAS: | 220904-83-6 | | MF: | C15H8Br2INO2 | | MW: | 520.94 | | EINECS: | | | Product Categories: | MAPK;Inhibitors | | Mol File: | 220904-83-6.mol |  |
| | GW5074 Chemical Properties |
| Boiling point | 561.4±50.0 °C(Predicted) | | density | 2.248±0.06 g/cm3(Predicted) | | storage temp. | room temp | | solubility | DMSO: soluble | | form | solid | | pka | 5.86±0.25(Predicted) | | color | yellow to orange-brown | | Stability: | Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 1 month. | | InChI | InChI=1S/C15H8Br2INO2/c16-11-4-7(5-12(17)14(11)20)3-10-9-6-8(18)1-2-13(9)19-15(10)21/h1-6,20H,(H,19,21) | | InChIKey | LMXYVLFTZRPNRV-XCVCLJGOSA-N | | SMILES | N1C2=C(C=C(I)C=C2)C(=CC2=CC(Br)=C(O)C(Br)=C2)C1=O | | CAS DataBase Reference | 220904-83-6 |
| WGK Germany | 3 | | HS Code | 2933790090 |
| | GW5074 Usage And Synthesis |
| Description | GW-5074 (220904-83-6) is a potent inhibitor of cRAF1 kinase (IC50 = 9 nM). Displays 100-fold selectivity for cRAF1 over CDK1, CDK2, c-src, ERK2, MEK, p38, Tie2, VEGFR2 and c-fm. GW-5074 displays neuroprotective effects in vivo via a mechanism that is independent of MEK, ERK, and Akt signaling. Cell permeable. | | Uses | GW5074 has been used as a specific inhibitor of cRaf1 in C2 murine skeletal myoblasts, HT-29 colorectal adenocarcinoma cell line and neutrophils. | | Biological Activity | Potent, selective and cell-permeable c-Raf1 kinase inhibitor (IC 50 = 9 nM). Displays ≥ 100-fold selectivity for raf kinase over CDK1, CDK2, c-src, ERK2, MEK, p38, Tie2, VEGFR2 and c-fm. | | Biochem/physiol Actions | GW5074 is a cRaf1 kinase inhibitor, which is placed immediately downstream of Ras in the Motogen activated protein kinase (MAPK) signaling pathway. It elicits protection in GW5074 prevents degeneration in Huntington′s disease and also have therapeutic potential in treating neurodegenerative disorders. GW5074 in combination with anti-inflammatory drug, dexamethasone, attenuates sidestream smoke-induced airway inflammation. | | storage | Desiccate at -20°C | | References | [1] MING-SHYAN CHANG . Phorbol 12-myristate 13-acetate upregulates cyclooxygenase-2 expression in human pulmonary epithelial cells via Ras, Raf-1, ERK, and NF-κB, but not p38 MAPK, pathways[J]. Cellular signalling, 2005, 17 3: Pages 299-310. DOI:10.1016/j.cellsig.2004.07.008
[2] JIAN HUANG . Fibroblast Growth Factor-2 Suppresses Oridonin-Induced L929 Apoptosis Through Extracellular Signal-Regulated Kinase-Dependent and Phosphatidylinositol 3-Kinase-Independent Pathway[J]. Journal of pharmacological sciences, 2006, 102 3: Pages 305-313. DOI:10.1254/jphs.fpj06004x
[3] KAREN LACKEY. The discovery of potent cRaf1 kinase inhibitors[J]. Bioorganic & Medicinal Chemistry Letters, 2000, 10 3: Pages 223-226. DOI:10.1016/s0960-894x(99)00668-x
[4] BING-CHANG CHEN. Bradykinin B2 receptor mediates NF-kappaB activation and cyclooxygenase-2 expression via the Ras/Raf-1/ERK pathway in human airway epithelial cells.[J]. Journal of immunology, 2004, 173 8: 5219-5228. DOI:10.4049/jimmunol.173.8.5219 |
| | GW5074 Preparation Products And Raw materials |
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