mTOR

mTOR (mechanistic Target Of Rapamycin, mammalian Target Of Rapamycin) plays a key role in coordinating cell signaling pathways. mTOR is a large (>280kD), multidomain protein with a kinase domain and a FKBP12 binding domain.

Products for mTOR

  1. Cat.No. Product Name Information/Activity
  2. BCC7622 Compound 401 Compound 401 is a synthetic inhibitor of DNA-PK (IC50 = 0.28 μM) that also targets mTOR but not PI3K in vitro. Compound 401 chemical structure
  3. BCC2484 KU-0063794 KU-0063794 is a potent and specific mTOR inhibitor, inhibiting both the mTORC1 and mTORC2 complexes with IC50s of 10 nM. KU-0063794 chemical structure
  4. BCC5081 Niclosamide Niclosamide (BAY2353) is an orally bioavailable chlorinated salicylanilide, with anthelmintic and potential antineoplastic activity. Niclosamide (BAY2353) inhibits STAT3 with IC50 of 0.25 μM in HeLa cells and inhibits DNA replication in a cell-free assay. Niclosamide chemical structure
  5. BCC3837 PF-04691502 PF-04691502 is a potent and selective inhibitor of PI3K and mTOR. PF-04691502 binds to human PI3Kα, β, δ, γ and mTOR with Kis of 1.8, 2.1, 1.6, 1.9 and 16 nM, respectively. PF-04691502 chemical structure
  6. BCC4987 PF-05212384 (PKI-587) Gedatolisib (PKI-587) is a highly potent dual inhibitor of PI3Kα, PI3Kγ, and mTOR with IC50s of 0.4 nM, 5.4 nM and 1.6 nM, respectively. PKI-587 is equally effective in both complexes of mTOR, mTORC1 and mTORC2. PF-05212384 (PKI-587) chemical structure
  7. BCC1860 PI-103 Hydrochloride PI-103 Hydrochloride is a dual PI3K and mTOR inhibitor with IC50s of 8 nM, 88 nM, 48 nM, 150 nM, 20 nM, and 83 nM for p110α, p110β, p110δ, p110γ, mTORC1, and mTORC2. PI-103 Hydrochloride also inhibits DNA-PK with an IC50 of 2 nM. PI-103 Hydrochloride induces autophagy. PI-103 Hydrochloride chemical structure
  8. BCC4980 PP121 PP121 is a multi-targeted kinase inhibitor with IC50s of 10, 60, 12, 14, 2 nM for mTOR, DNK-PK, VEGFR2, Src, PDGFR, respectively. PP121 chemical structure
  9. BCC3682 PP242 Torkinib (PP 242) is a selective and ATP-competitive mTOR inhibitor with an IC50 of 8 nM. PP242 inhibits both mTORC1 and mTORC2 with IC50s of 30 nM and 58 nM, respectively. PP242 chemical structure
  10. BCC3592 Rapamycin (Sirolimus) Rapamycin (Sirolimus) is a potent and specific mTOR inhibitor with an IC50 of 0.1 nM in HEK293 cells. Rapamycin binds to FKBP12 and specifically acts as an allosteric inhibitor of mTORC1. Rapamycin is an autophagy activator, an immunosuppressant. Rapamycin (Sirolimus) chemical structure
  11. BCC3678 Temsirolimus Temsirolimus is an inhibitor of mTOR with an IC50 of 1.76 μM. Temsirolimus chemical structure

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