MK-2206

469 Cited Publications
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Based on 469 publication(s) in Google Scholar

MK-2206 is an orally active pan-AKT inhibitor, with IC50 values of 8 nM, 12 nM and 65 nM against AKT1, AKT2 and AKT3, respectively. MK-2206 inhibits the Akt/mTOR signaling pathway and reduces the levels of downstream GSK3β and Mcl-1 via proteasomal degradation. MK-2206 induces G1-phase cell cycle arrest, apoptosis, epithelial-mesenchymal transition, fibroblast activation and extracellular matrix deposition. MK-2206 causes transient hyperglycemia and hyperinsulinemia in animals. MK-2206 can be used in research related to solid tumors, renal fibrosis and hypercholesterolemia.

For research use only. We do not sell to patients.

  • Purity: 99.72%
  • CAS No.: 1032349-77-1
  • Formula: C25H22ClN5O
  • Molecular Weight:443.93
  • Storage:

    4°C, sealed storage, away from moisture

    * In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

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Publications Citing Use of MedChemExpress (MCE) MK-2206

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All Bcl-2 Family Isoforms

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All Akt Isoforms

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All mTOR Isoforms

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All GSK-3 Isoforms

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