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Torin1

Chemical Structure : Torin1

CAS No.: 1222998-36-8

Torin1 (Torin 1;Torin-1)

Catalog No.: PC-43314Not For Human Use, Lab Use Only.

Torin1 is a highly potent, selective inhibitor of mTORC1 and mTORC2 with IC50 of 2 and 10 nM in cell-free assays, exhibits 1,000-fold selectivity PI3K (EC50=1,800 nM).

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

Torin1 is a highly potent, selective inhibitor of mTORC1 and mTORC2 with IC50 of 2 and 10 nM in cell-free assays, exhibits 1,000-fold selectivity PI3K (EC50=1,800 nM).
Torin1 exhibits 100-fold binding selectivity relative to 450 other protein kinases.
Torin1 causes cell cycle arrest through a rapamycin-resistant mechanism that is also independent of mTORC2, disrupts mTORC1-dependent phenotypes more completely than rapamycin.
Torin1 prevents the anti-inflammatory potency of GC both in human monocytes and myeloid dendritic cells.

Physicochemical Properties

M.Wt 607.6243
Formula C35H28F3N5O2
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

DMSO: 6.6 mg/mL (Need ultrasonic or warming)

Chemical Name/SMILES

Benzo[h]-1,6-naphthyridin-2(1H)-one, 1-[4-[4-(1-oxopropyl)-1-piperazinyl]-3-(trifluoromethyl)phenyl]-9-(3-quinolinyl)-

References

1. Thoreen CC, et al. J Biol Chem. 2009 Mar 20;284(12):8023-32.

2. Liu Q, et al. J Med Chem. 2010 Oct 14;53(19):7146-55.

3. Weichhart T, et al. Blood. 2011 Apr 21;117(16):4273-83.

4. Thoreen CC, et al. Autophagy. 2009 Jul;5(5):725-6.

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