DC_AC50

DC_AC50

CAT N°: 19283
Price:

From 54.00 45.90

DC_AC50 is an inhibitor of the copper-trafficking proteins Atox1 and CCS.{53558} It binds to purified Atox1 and CCS (Kds = 6.8 and 8.2 ?M, respectively) and inhibits the interaction between Atox1 and domain 4 of the Cu+-ATPase ATP7B in the presence of zinc in a FRET-based assay when used at a concentration of 100 ?M. DC_AC50 increases copper and reactive oxygen species (ROS) levels and decreases COX activity and lipid biosynthesis in H1299 cells when used at a concentration of 10 ?M. It inhibits the proliferation of H1299, K562, MDA-MB-231, and 212LN cancer cells, but not PIG1, HDF, HaCaT, or MCF-10A cells, in a concentration-dependent manner. DC_AC50 (100 mg/kg per day) reduces tumor growth in an H1299 mouse xenograft model.

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • 3-amino-N-(2-bromo-4,6-difluorophenyl)-6,7-dihydro-5H-cyclopenta[b]thieno[3,2-e]pyridine-2-carboxamide
  • Correlated keywords
    • DCAC50 DC-AC-50 DCAC-50 Atox-1 ATP-7B H-1299 K-562 MDAMB-231 MDAMB231 212-LN PIG-1 MCF10A
  • Product Overview:
    DC_AC50 is an inhibitor of the copper-trafficking proteins Atox1 and CCS.{53558} It binds to purified Atox1 and CCS (Kds = 6.8 and 8.2 ?M, respectively) and inhibits the interaction between Atox1 and domain 4 of the Cu+-ATPase ATP7B in the presence of zinc in a FRET-based assay when used at a concentration of 100 ?M. DC_AC50 increases copper and reactive oxygen species (ROS) levels and decreases COX activity and lipid biosynthesis in H1299 cells when used at a concentration of 10 ?M. It inhibits the proliferation of H1299, K562, MDA-MB-231, and 212LN cancer cells, but not PIG1, HDF, HaCaT, or MCF-10A cells, in a concentration-dependent manner. DC_AC50 (100 mg/kg per day) reduces tumor growth in an H1299 mouse xenograft model.

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