Foretinib
CAS No. 849217-64-7
Foretinib( XL880 | GSK1363089 | GSK089 | EXEL-2880 )
Catalog No. M16164 CAS No. 849217-64-7
Foretinib (XL880, GSK1363089, GSK089, EXEL-2880) is a potent, multikinase inhibitor that inhibits c-Met and VEGFR, also KIT, Flt-3, PDGFRβ, and Tie-2.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 68 | In Stock |
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| 2MG | 31 | In Stock |
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| 5MG | 49 | In Stock |
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| 10MG | 68 | In Stock |
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| 25MG | 128 | In Stock |
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| 50MG | 202 | In Stock |
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| 100MG | 347 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | 830 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameForetinib
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NoteResearch use only, not for human use.
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Brief DescriptionForetinib (XL880, GSK1363089, GSK089, EXEL-2880) is a potent, multikinase inhibitor that inhibits c-Met and VEGFR, also KIT, Flt-3, PDGFRβ, and Tie-2.
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DescriptionForetinib (XL880, GSK1363089, GSK089, EXEL-2880) is a potent, multikinase inhibitor that inhibits c-Met and VEGFR, also KIT, Flt-3, PDGFRβ, and Tie-2; inhibits HGFR family tyrosine kinases with IC50 of 0.4 nM for Met and 3 nM for Ron, also inhibits KDR, Flt-1, and Flt-4 with IC50 of 0.9, 6.8, and 2.8 nM, respectively; exhibits modest activity against FGFR1 and EGFR, no activity against 50 serine/threonine kinases, including CDKs and PKC isoforms; inhibits cellular HGF-induced Met phosphorylation and VEGF-induced ERK phosphorylation and prevents both HGF-induced responses of tumor cells and HGF/VEGF-induced responses of endothelial cells; exhibits significant inhibition of tumor burden in animal model of lung metastasis.Lung Cancer Phase 2 Discontinued.
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In Vitro——
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In Vivo——
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SynonymsXL880 | GSK1363089 | GSK089 | EXEL-2880
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PathwayAngiogenesis
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Targetc-Met/HGFR
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RecptorMet|RON|Tie-2|VEGFR2?(KDR)|VEGFR3/FLT4|KDR|Flt-4|Flt-3
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Research AreaCancer
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IndicationLung Cancer
Chemical Information
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CAS Number849217-64-7
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Formula Weight632.6537
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Molecular FormulaC34H34F2N4O6
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Purity>98% (HPLC)
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SolubilityDMSO: ≥ 38 mg/mL
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SMILESO=C(C1(C(NC2=CC=C(F)C=C2)=O)CC1)NC3=CC=C(OC4=CC=NC5=CC(OCCCN6CCOCC6)=C(OC)C=C45)C(F)=C3
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Chemical Name1,1-Cyclopropanedicarboxamide, N-[3-fluoro-4-[[6-methoxy-7-[3-(4-morpholinyl)propoxy]-4-quinolinyl]oxy]phenyl]-N'-(4-fluorophenyl)-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Dihexa
Dihexa is an activator of the hepatocyte growth factor/c-Met (HGF/c-Met) systemit binds to HGF (Kd = 65 pM)and an analog of the peptide angiotensin IV.
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Capmatinib hydrochlo...
Capmatinib hydrochloride is an orally bioavailable inhibitor of the proto-oncogene c-Met (HGFR)with potential antineoplastic activity.Capmatinib was found to be highly selective for MET over other kinases.?It was active against cancer models that are characterized by MET amplification, marked MET overexpression, MET exon 14 skipping mutations, or MET activation via expression of the ligand hepatocyte growth factor (HGF).
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SAR125884 hydrochlor...
SAR125844 is a potent and selective MET kinase inhibitor with a favorable preclinical toxicity profile(IC50=4.2 nM).
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