SML0263

PF-04217903

≥98% (HPLC)

• Synonym(e): 4-[1-(6-Quinolinylmethyl)-1H-1,2,3-triazolo[4,5-b]pyrazin-6-yl]-1H-pyrazole-1-ethanol methanesulfonate (1:1)
• Empirische Formel (Hill-System): C₁₉H₁₆N₈O·CH₃SO₃H
• CAS-Nummer: 956906-93-7
• Molekulargewicht: 468.49
• MDL-Nummer: MFCD17392584
• UNSPSC-Code: 12352200
• PubChem Substanz-ID: 329825271
• NACRES: NA.77

Eigenschaften

• Qualitätsniveau: 100
• Assay: ≥98% (HPLC)
• Form: powder
• Farbe: white to beige
• Löslichkeit: DMSO: ≥5 mg/mL (warmed)
• Lagertemp.: 2-8°C
• SMILES String: CS(O)(=O)=O.OCCn1cc(cn1)-c2cnc3nnn(Cc4ccc5ncccc5c4)c3n2
• InChI: 1S/C19H16N8O.CH4O3S/c28-7-6-26-12-15(9-22-26)17-10-21-18-19(23-17)27(25-24-18)11-13-3-4-16-14(8-13)2-1-5-20-16;1-5(2,3)4/h1-5,8-10,12,28H,6-7,11H2;1H3,(H,2,3,4)
• InChIKey: HBEMHKVWZJTVOC-UHFFFAOYSA-N
• Angaben zum Gen: human ... MET(4233)

Beschreibung

Anwendung

PF-04217903 has been used as tyrosine-protein kinase Met (C-Met) selective inhibitor in Madin-Darby Canine kidney (MDCK) cells and NT2D1 non-seminoma cells.

Biochem./physiol. Wirkung

PF-04217903 is a highly selective, potent inhibitor of the hepatocyte growth factor receptor c-Met. PF-04217903 inhibits endogenous, wild type c-Met in A549 human lung carcinoma cells with an IC₅₀ of 4.8 nM. The compund displays 1000-fold selectivity against a panel of 208 other kinases.

PF-04217903 is an ATP-competitive inhibitor. It elicits antiangiogenic functionality. PF-04217903 inhibits c-Met phosphorylation in xenograft models leading to partial tumor growth suppression.

Leistungsmerkmale und Vorteile

This compound is featured on the Met page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable