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Medchemexpress LLC IK-930 | 2563892-44-2 | C19H19F3N4O2S | 200 MG
SDP

Catalog No. 5000372743
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IK-930 is a potent and orally active inhibitor of TEAD, exhibiting an EC50 value of less than 0.1 μM. It has been evaluated in vivo, demonstrating favorable pharmacokinetic properties in BALB/c mice with a Cmax of 1088 ng/mL and an AUC 0-last of 4581 ng*h/mL when administered orally at 10 mg/kg. The compound is being investigated in clinical trials for solid tumors, including those with NF2 deficiency and YAP1 or TAZ gene fusions.

  • Potent TEAD inhibitor with an EC50 < 0.1 μM.
  • Orally active.
  • Demonstrates good pharmacokinetic parameters in animal models.
  • Currently in clinical trials for various solid tumors, including those linked to NF2 deficiency and YAP1/TAZ gene fusions.

Catalog No. 50-003-72743 Supplier Medchemexpress LLC Supplier No. HY153585200MG
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IK-930 is a potent and orally active inhibitor of TEAD, exhibiting an EC50 value of less than 0.1 μM. It has been evaluated in vivo, demonstrating favorable pharmacokinetic properties in BALB/c mice with a Cmax of 1088 ng/mL and an AUC 0-last of 4581 ng*h/mL when administered orally at 10 mg/kg. The compound is being investigated in clinical trials for solid tumors, including those with NF2 deficiency and YAP1 or TAZ gene fusions.

  • Potent TEAD inhibitor with an EC50 < 0.1 μM.
  • Orally active.
  • Demonstrates good pharmacokinetic parameters in animal models.
  • Currently in clinical trials for various solid tumors, including those linked to NF2 deficiency and YAP1/TAZ gene fusions.

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