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Medchemexpress LLC 3-[4-methyl-2-(2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-1H-pyrrol-3-yl]-propionic acid | 215543-92-3 | MFCD08235144 | 99.9% | 296.32 g·mol⁻¹ | C17H16N2O3 | 1 MG
SDP

Catalog No. 5000242521
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SU 5402 is a small-molecule receptor tyrosine kinase inhibitor used in research to probe FGFR, VEGFR2, and PDGFRβ signaling. Supplied as a purified solid for in vitro applications, it exhibits low-nanomolar potency against VEGFR2 and FGFR1 and sub-micromolar activity against PDGFRβ.

  • Inhibits VEGFR2, FGFR1, and PDGFRβ (IC50: 20 nM, 30 nM, 510 nM).
  • Supplied as a high-purity solid suitable for biochemical and cell-based assays.
  • Molecular weight 296.32 g·mol⁻¹; formula C17H16N2O3.
  • Recommended storage: powder frozen (-20°C) and solutions at -80°C for long-term stability.
  • Commonly used to study angiogenesis and receptor tyrosine kinase signaling pathways.

Catalog No. 50-002-42521 Supplier Medchemexpress LLC Supplier No. HY104071MG
May include imposed supplier surcharges.
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SU 5402 is a small-molecule receptor tyrosine kinase inhibitor used in research to probe FGFR, VEGFR2, and PDGFRβ signaling. Supplied as a purified solid for in vitro applications, it exhibits low-nanomolar potency against VEGFR2 and FGFR1 and sub-micromolar activity against PDGFRβ.

  • Inhibits VEGFR2, FGFR1, and PDGFRβ (IC50: 20 nM, 30 nM, 510 nM).
  • Supplied as a high-purity solid suitable for biochemical and cell-based assays.
  • Molecular weight 296.32 g·mol⁻¹; formula C17H16N2O3.
  • Recommended storage: powder frozen (-20°C) and solutions at -80°C for long-term stability.
  • Commonly used to study angiogenesis and receptor tyrosine kinase signaling pathways.

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