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PI3K/Akt/mTOR Signaling

Research Areas

Products Related to PI3K/Akt/mTOR Signaling(719)

  • GC10463 structure
    GC10463SB 216763
    CAS: 280744-09-4
    Purity: >99.00%

    SB 216763 stands out as a powerful, selective, and ATP-competitive inhibitor of GSK-3, effectively targeting both GSK-3α and GSK-3β with an impressive IC 50 of 34.3 nM [1-3] .

  • GC10518 structure
    GC10518AICAR
    CAS: 2627-69-2
    Purity: >99.00%

    AICAR (also called acadesine) is a purine nucleoside.

  • GC10573 structure
    GC10573L803-mts
    CAS: 1043881-55-5
    Purity: >98%

    Selective peptide inhibitor of glycogen synthase kinase-3 (GSK-3)

  • GC10649 structure
    GC10649TTP 22
    CAS: 329907-28-0
    Purity: >98.00%

    A CK2 inhibitor

  • GC10662 structure
    GC10662WYE-354
    CAS: 1062169-56-5
    Purity: >98.00%

    MTOR inhibitor,potent,ATP-competitive and cell-permeable

  • GC10710 structure
    GC107103-Methyladenine
    CAS: 5142-23-4
    Purity: >98.00%

    3-Methyladenine is a PI3K inhibitor with IC 50 values of 25μM and 60μM for Vps34 and PtdIns3Kγ, respectively.

  • GC10752 structure
    GC10752Bikinin
    CAS: 188011-69-0
    Purity: >99.50%

    Bikinin is a non-steroidal, ATP-competitive inhibitor of plant GSK-3 (glycogen synthase kinase 3)/Shaggy-like kinases.

  • GC10812 structure
    GC10812Compound 401
    CAS: 168425-64-7
    Purity: >99.50%

    DNA-PK and mTOR inhibitor

  • GC10857 structure
    GC10857UCN-01
    CAS: 112953-11-4
    Purity: >98%

    inhibitor of Akt, protein kinase C, PDK1 and cyclin-dependent kinases

  • GC10860 structure
    GC10860Acalisib (GS-9820)
    CAS: 870281-34-8
    Purity: >99.50%

    Acalisib (GS-9820) is a potent and selective PI3Kδ inhibitor with an IC50 of 12.7 nM.

  • GC10900 structure
    GC10900GDC-mTOR inhibitor
    CAS: 1207358-59-5
    Purity: >99.00%
  • GC10918 structure
    GC10918AT7867 dihydrochloride
    CAS: 1431697-86-7
    Purity: >99.00%

    A potent and orally bioavailable pan-Akt inhibitor

  • GC11003 structure
    GC11003PP121
    CAS: 1092788-83-4
    Purity: >99.00%

    Dual inhibitor of tyrosine and phosphoinositide kinases

  • GC11018 structure
    GC11018GSK1059615
    CAS: 958852-01-2
    Purity: >98.00%

    PI3K and mTOR inhibitor,potent and reversible

  • GC11135 structure
    GC11135CAL-130 Hydrochloride
    CAS: 1431697-78-7
    Purity: >99.50%
  • GC11165 structure
    GC11165PI-103
    CAS: 371935-74-9
    Purity: >98.00%

    PI-103 is a potent cell-permeable multi-target inhibitor that primarily acts on the PI3K and mTOR signaling pathways.

  • GC11177 structure
    GC11177GDC-0980 (RG7422)
    CAS: 1032754-93-0
    Purity: >98.00%

    GDC-0980 (RG7422) (GDC-0980; GNE 390; RG 7422) is a selective, potent, orally bioavailable Class I PI3 kinase and mTOR kinase (TORC1/2) inhibitor with IC50s of 5 nM/27 nM/7 nM/14 nM for PI3Kα/PI3Kβ/PI3Kδ/PI3Kγ, and with aKiof 17 nM for mTOR.

  • GC11190 structure
    GC11190AMPK activator
    CAS: 849727-81-7
    Purity: >98%

    AMPK activator is a cell penetrant AMPK activator and partially inhibits the mitochondrial complex I. In multiple myeloma cells, AMPK activator inhibits cell growth.

  • GC11214 structure
    GC11214GDC-0068 (RG7440)
    CAS: 1001264-89-6
    Purity: >98.00%

    GDC-0068 (RG7440) is an orally active, highly selective and ATP-competitive pan-Akt inhibitor with IC 50 values of 5, 18, 8nM for Akt1, Akt2, and Akt3, respectively.

  • GC11234 structure
    GC11234A-769662
    CAS: 844499-71-4
    Purity: >98.50%

    A-769662 is an activator of AMP-activated protein kinase, which has an EC 50 value of 0.8μM.

  • GC11248 structure
    GC11248AZD8835
    CAS: 1620576-64-8
    Purity: >98.50%

    PI3Kα and PI3Kδ inhibitor

  • GC11325 structure
    GC11325CX-4945 sodium salt
    CAS: 1309357-15-0
    Purity: >99.50%

    CX-4945 sodium salt is an orally bioavailable, highly selective and potent CK2 inhibitor, with IC50 values of 1 nM against CK2α and CK2α'.

  • GC11471 structure
    GC11471SAR405
    CAS: 1523406-39-4
    Purity: >98.00%

    SAR405 is a highly selective, ATP-competitive class III phosphoinositide 3-kinase (PIK3C3/Vps34) inhibitor with an IC 50 value of 1.2nM.

  • GC11515 structure
    GC11515TCS 184
    CAS: 1315378-71-2
    Purity: >98%

    Scrambled control peptide for use with TCS 183