Home   >  
PI3K/Akt/mTOR
  >  
mTOR

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

mTOR

Chemical Structure Cat. No. Product Name CAS No.
NV-5138 Chemical Structure
 BCP39080 NV-5138 2095886-80-7
NV-5138, a leucine analog, is the first selective and orally active brain mTORC1 activator, binding to Sestrin2.
MT 63-78 Chemical Structure
 BCP38015 MT 63-78 1179347-65-9
MT 63-78 is a direct activator of AMPK, and an inhibitor of prostate cancer growth by blocking lipogenesis.
MTI-31 Chemical Structure
 BCP36715 MTI-31 1567915-38-1
MTI-31 is a novel potent, selective mTORC1/mTORC2 inhibitor with Kd of 0.2 nM (mTOR), displays >5,000-fold selectivity over PIK3CA, PIK3CB and PIK3G.
PI-103 Hydrochloride Chemical Structure
 BCP36117 PI-103 Hydrochloride 371935-79-4
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.
Rapalink-1 Chemical Structure
 BCP33282 Rapalink-1 Rapalink-1
RapaLink-1, the third-generation bivalent mTOR inhibitor, combines Rapamycin with MLN0128 (a second-generation mTOR kinase inhibitor) by an inert chemical linker.
AZD8055 Fumaric acid Chemical Structure
 BCP25958 AZD8055 Fumaric acid 1201799-05-4
AZD-8055 is a novel ATP-competitive inhibitor of mTOR kinase with an IC50 of 0.8 nM. AZD-8055 inhibits both mTORC1 and mTORC2.
AZD8055 D(-)-Tartaric Acid Chemical Structure
 BCP25959 AZD8055 D(-)-Tartaric Acid 1201799-04-3
AZD-8055 is a novel ATP-competitive inhibitor of mTOR kinase with an IC50 of 0.8 nM. AZD-8055 inhibits both mTORC1 and mTORC2.
mTOR inhibitor-1 Chemical Structure
 BCP32690 mTOR inhibitor-1 468747-17-3
mTOR inhibitor-1 is a novel mTOR pathway inhibitor which can suppress cells proliferation and inducing autophagy.
XL-765 Chemical Structure
 BCP32612 XL-765 1123889-87-1
XL765 is a PI3K/mTOR dual kinase inhibitor and it is more potent compared to an agent that inhibits either PI3K kinase or mTOR kinase alone.
BGT226 Chemical Structure
 BCP26216 BGT226 915020-55-2
BGT226 is a PI3K (with IC50s of 4 nM, 63 nM and 38 nM for PI3Kα, PI3Kβ and PI3Kγ)/mTOR dual inhibitor which displays potent growth-inhibitory activity against human head and neck cancer cells.
123下一页末页共 66 条记录 1 / 7 页 
0086-15971444841