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Medchemexpress LLC Cyclo(L-arginylglycyl-L-α-aspartyl-D-phenylalanyl-L-lysyl), 2,2,2-trifluoroacetate (1:1) | 500577-51-5 | 99.6% | 717.69 | 25 MG
SDP

Catalog No. 5000426240
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Cyclo(-RGDfK) TFA is a potent and selective inhibitor of the αvβ3 integrin, with an IC50 of 0.94 nM. This compound targets tumor microvasculature and cancer cells through specific binding to the αvβ3 integrin on the cell surface. It can be prepared with high radiochemical purity and specific activity, showing in vitro stability and moderate protein binding.

  • Potent and selective inhibitor of αvβ3 integrin.
  • IC50 of 0.94 nM for αvβ3 integrin.
  • Targets tumor microvasculature and cancer cells.
  • Exhibits high radiochemical purity (>97%).
  • Shows in vitro stability.
  • Suitable for MicroPET imaging to reflect αvβ3-targeted tracer accumulation.

Catalog No. 50-004-26240 Supplier Medchemexpress LLC Supplier No. 25MGHYP0023A
May include imposed supplier surcharges.
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Cyclo(-RGDfK) TFA is a potent and selective inhibitor of the αvβ3 integrin, with an IC50 of 0.94 nM. This compound targets tumor microvasculature and cancer cells through specific binding to the αvβ3 integrin on the cell surface. It can be prepared with high radiochemical purity and specific activity, showing in vitro stability and moderate protein binding.

  • Potent and selective inhibitor of αvβ3 integrin.
  • IC50 of 0.94 nM for αvβ3 integrin.
  • Targets tumor microvasculature and cancer cells.
  • Exhibits high radiochemical purity (>97%).
  • Shows in vitro stability.
  • Suitable for MicroPET imaging to reflect αvβ3-targeted tracer accumulation.

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