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T0901317

Chemical Structure : T0901317

CAS No.: 293754-55-9

T0901317 (TO901317;T-0901317)

Catalog No.: PC-42684Not For Human Use, Lab Use Only.

T0901317 (TO901317) is a potent, high affinity LXR agonist (EC50=50 nM, Kd are 7 and 22 nM for LXR-α and LXR-β respectively).

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

Biological Activity

T0901317 (TO901317) is a potent, high affinity LXR agonist (EC50=50 nM, Kd are 7 and 22 nM for LXR-α and LXR-β respectively).
T0901317 (TO901317) upregulates expression of the ABCA1 gene associated with cholesterol efflux regulation and HDL metabolism.
T0901317 (TO901317) decreases amyloid-β production in primary neurons in vitro.
T0901317 (TO901317) displays an EC50 of ~ 5 μM for activation of FXRs.
T0901317 (TO901317) also is an inverse agonist of human constitutive androstane receptor (hCAR), blocks the interaction of hCAR with steroid receptor co-activator 1 (SRC1).
 

Physicochemical Properties

M.Wt 481.3327
Formula C17H12F9NO3S
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: ≥ 27 mg/mL

Chemical Name/SMILES

Benzenesulfonamide, N-(2,2,2-trifluoroethyl)-N-[4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl]-

References

1. Repa JJ, et al. Science. 2000 Sep 1;289(5484):1524-9.

2. Koldamova RP, et al. J Biol Chem. 2005 Feb 11;280(6):4079-88.

3. Kanno Y, et al. J Toxicol Sci. 2013;38(3):309-15.

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