2733770-48-2

GW2580-d<sub>6</sub> Chemical Structure
2733770-48-2

Chemical Structure

GW2580-d6

  • CAS No.: 2733770-48-2
  • Formula:C20H16D6N4O3
  • Molecular Weight:372.45

IUPAC Name: 5-(3-(methoxy-d3)-4-((4-(methoxy-d3)benzyl)oxy)benzyl)pyrimidine-2,4-diamine

InChIKey: MYQAUKPBNJWPIE-WFGJKAKNSA-N

SMILES: NC1=NC(N)=C(CC2=CC(OC([2H])([2H])[2H])=C(OCC3=CC=C(OC([2H])([2H])[2H])C=C3)C=C2)C=N1

Biological Activity: GW2580-d6 is the deuterium labeled GW2580. GW2580 is an orally bioavailable and selective inhibitor of c-Fms kinase which completely inhibits human cFMS kinase in vitro at 0.06 μM. GW2580 acts as a competitive inhibitor of ATP binding to the cFMS kinase and inhibits colony-stimulating-factor-1 signaling[1].

Cat. No. Product Name Purity Description Pricing
HY-10917S
GW2580-d6 98.36% GW2580-d6 is the deuterium labeled GW2580. GW2580 is an orally bioavailable and selective inhibitor of c-Fms kinase which completely inhibits human cFMS kinase in vitro at 0.06 μM. GW2580 acts as a competitive inhibitor of ATP binding to the cFMS kinase and inhibits colony-stimulating-factor-1 signaling.
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HY-10917R
GW2580 (Standard) ≥98% GW2580 (Standard) is the analytical standard of GW2580. This product is intended for research and analytical applications. GW2580 is an orally bioavailable and selective inhibitor of c-Fms kinase which completely inhibits human cFMS kinase in vitro at 0.06 μM. GW2580 acts as a competitive inhibitor of ATP binding to the cFMS kinase and inhibits colony-stimulating-factor-1 signaling.
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HY-10917
GW2580 99.90% GW2580 is an orally bioavailable and selective inhibitor of c-Fms kinase which completely inhibits human cFMS kinase in vitro at 0.06 μM. GW2580 acts as a competitive inhibitor of ATP binding to the cFMS kinase and inhibits colony-stimulating-factor-1 signaling.
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