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AZ-876

Chemical Structure : AZ-876

CAS No.: 898800-26-5

AZ-876 (AZ876;AZ 876)

Catalog No.: PC-45444Not For Human Use, Lab Use Only.

AZ-876 (AZ876) is a potent, highly selective LXR agonist with Ki/EC50 of 7/6 nM and 11/73 nM for hLXRα and hLXRβ respectively.

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

Biological Activity

AZ-876 (AZ876) is a potent, highly selective LXR agonist with Ki/EC50 of 7/6 nM and 11/73 nM for hLXRα and hLXRβ respectively.
AZ-876 is a more potent binder and activator of LXRα and LXRβ than GW3965.
AZ-876 is highly selective against FXR, RXR, TRα, TRβ etc.
AZ-876 reduces lesion area, and strongly decreases lesion area, lesion number and severity in vivo.
AZ-876 protects against pathological cardiac hypertrophy and fibrosis without lipogenic side effects in mice.

Physicochemical Properties

M.Wt 439.5704
Formula C24H29N3O3S
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: ≥ 2.6 mg/mL

Chemical Name/SMILES

3(2H)-Isothiazolone, 2-(1,1-dimethylethyl)-5-phenyl-4-[[4-(1-piperidinyl)phenyl]amino]-, 1,1-dioxide

References

1. van der Hoorn J, et al. Br J Pharmacol. 2011 Apr;162(7):1553-63.

2. Cannon MV, et al. Eur J Heart Fail. 2015 Mar;17(3):273-82.

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