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Chemical Structure| 1222998-36-8 Chemical Structure| 1222998-36-8

Structure of Torin 1
CAS No.: 1222998-36-8

Chemical Structure| 1222998-36-8

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Torin 1 is a potent mTOR inhibitor with an IC50 of 3 nM, inhibiting both mTORC1 and mTORC2 complexes with IC50 values between 2 and 10 nM, and is an effective inducer of autophagy.

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Product Details of Torin 1

CAS No. :1222998-36-8
Formula : C35H28F3N5O2
M.W : 607.62
SMILES Code : O=C1N(C2=CC=C(N3CCN(C(CC)=O)CC3)C(C(F)(F)F)=C2)C4=C(C=NC5=CC=C(C6=CC7=CC=CC=C7N=C6)C=C54)C=C1
MDL No. :MFCD18782653
InChI Key :AKCRNFFTGXBONI-UHFFFAOYSA-N
Pubchem ID :49836027

Safety of Torin 1

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H320-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Related Pathways of Torin 1

PI3K-AKT

Isoform Comparison

Biological Activity

Target
  • mTORC1

    mTORC1, IC50:2 nM

  • mTORC2

    mTORC2, IC50:10 nM

  • mTOR

    mTOR, IC50:4.32 nM

In Vitro:

Cell Line
Concentration Treated Time Description References
HepG2 cells 5 µM 1 h Torin 1 significantly increased rAAV-mediated transgene expression, indicating that induction of autophagy enhances rAAV transduction efficiency. PMC5518300
PHHs (primary human hepatocytes) 10 µM 1 h Torin 1 significantly increased rAAV-mediated transgene expression, indicating that induction of autophagy enhances rAAV transduction efficiency. PMC5518300
IMR90 cells 250 nM 24 h To investigate the effect of Torin 1 on SIRT1 expression under starvation and senescence conditions. Results showed that Torin 1 treatment suppressed the induction of LC3-II levels. PMC7805578
IMR90 cells 250 nM 24 h To investigate the effect of Torin 1 treatment on LC3 nuclear localization. Results showed that Torin 1 treatment increased LC3 localization in the cytoplasm. PMC7805578
Ba/F3-NRAS-G12D cells 300 nM 2 days Screen for compounds that potentiate the efficacy of Torin 1 against NRAS-driven cells PMC4667710
Ba/F3-KRAS-G12D cells 75 nM 2 h Evaluate the effect of MK-1775 combined with mTOR inhibitors on mutant KRAS-expressing cells PMC4667710
LHCN-M2 human skeletal muscle cells 250 nM 2 h Torin 1 completely prevented the reduction in PGC-1α expression caused by tunicamycin, suggesting the involvement of mTOR in the reduction of PGC-1α expression PMC9012021
LHCN-M2 human skeletal muscle cells 250 nM 16 h Torin 1 prevented the reduction in PGC-1α protein levels caused by tunicamycin PMC9012021
Ba/F3-NRAS-G12D cells 20 nM 2 days To identify compounds that synergize with Torin 1 and validate the synergy between MK-1775 and mTOR inhibitors PMC4667710
Ba/F3-KRAS-G12D cells 75 nM 2 h To validate the synergy between MK-1775 and mTOR inhibitors in KRAS mutant cells, observing reduced phosphorylation of 4E-BP1, AKT, and S6K PMC4667710

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
C57BL/6 mice healthy mice intraperitoneal injection 20 mg/kg single dose, lasting 2 hours Torin 1 significantly increased rAAV8-TTR-Epo-mediated hepatic gene expression, indicating that induction of autophagy enhances rAAV transduction efficiency in vivo. PMC5518300
Mice C57BL/6 mice Intraperitoneal injection 5 mg/kg Single injection, sacrificed 24 hours later Torin 1 prevented the reduction in PGC-1α protein levels caused by tunicamycin PMC9012021

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.65mL

0.33mL

0.16mL

8.23mL

1.65mL

0.82mL

16.46mL

3.29mL

1.65mL

References

 

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