Determine the necessary mass, volume, or concentration for preparing a solution.
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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G129612-5mg | 5mg | In stock | $71.90 | |
G129612-25mg | 25mg | In stock | $165.90 | |
G129612-100mg | 100mg | In stock | $258.90 |
Potent, selective and cell-permeable c-Raf1 kinase inhibitor
Synonyms | Q27077947 | (3Z)-3-[(3,5-dibromo-4-hydroxy-phenyl)methylene]-5-iodo-indolin-2-one | CS-0092 | GW 5074 | Lopac0_000510 | 5-iodo-3-((3,5-dibromo-4-hydroxyphenyl)methylene)-2-indolinone | EC-000.2403 | NCGC00015478-01 | NCGC00015478-03 | 3-(3,5-Dibromo-4-hyd |
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Specifications & Purity | Moligand™, ≥97% |
Biochemical and Physiological Mechanisms | 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 pot |
Legal Information | Sold for only research purposes |
Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Inhibitor of Raf-1 proto-oncogene; serine/threonine kinase |
Note | Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
Product Description | 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 |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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IUPAC Name | (3Z)-3-[(3,5-dibromo-4-hydroxyphenyl)methylidene]-5-iodo-1H-indol-2-one |
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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)/b10-3- |
InChi Key | LMXYVLFTZRPNRV-KMKOMSMNSA-N |
Canonical SMILES | C1=CC2=C(C=C1I)C(=CC3=CC(=C(C(=C3)Br)O)Br)C(=O)N2 |
Isomeric SMILES | C1=CC2=C(C=C1I)/C(=C/C3=CC(=C(C(=C3)Br)O)Br)/C(=O)N2 |
PubChem CID | 5924208 |
Molecular Weight | 520.94 |
PubChem CID | 5924208 |
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CAS Registry No. | 220904-83-6 |
ChEMBL Ligand | CHEMBL72365 |
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Solubility | DMSO 104 mg/mL Water <1 mg/mL Ethanol <1 mg/mL |
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Sensitivity | Light sensitive |
1. Jiao Ma, Zhechun Hu, Huimin Yue, Yujian Luo, Chao Wang, Xuan Wu, Yan Gu, Lang Wang. (2023) GRM2 Regulates Functional Integration of Adult-Born DGCs by Paradoxically Modulating MEK/ERK1/2 Pathway. JOURNAL OF NEUROSCIENCE, 43 (16): (2822-2836). [PMID:36878727] [10.1523/JNEUROSCI.1886-22.2023] |
1. Chin PC, Liu L, Morrison BE, Siddiq A, Ratan RR, Bottiglieri T, D'Mello SR. (2004) The c-Raf inhibitor GW5074 provides neuroprotection in vitro and in an animal model of neurodegeneration through a MEK-ERK and Akt-independent mechanism.. J Neurochem, 90 (3): (595-608). [PMID:15255937] [10.1021/op500134e] |
2. Jiao Ma, Zhechun Hu, Huimin Yue, Yujian Luo, Chao Wang, Xuan Wu, Yan Gu, Lang Wang. (2023) GRM2 Regulates Functional Integration of Adult-Born DGCs by Paradoxically Modulating MEK/ERK1/2 Pathway. JOURNAL OF NEUROSCIENCE, 43 (16): (2822-2836). [PMID:36878727] [10.1523/JNEUROSCI.1886-22.2023] |