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AZ876

Chemical Structure : AZ876

CAS No.: 898800-26-5

AZ876 (AZ-876, AZ 876)

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

AZ876 (AZ 876) 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

AZ876 (AZ 876) is a potent, highly selective LXR agonist with Ki/EC50 of 7/6 nM and 11/73 nM for hLXRα and hLXRβ respectively.
AZ876 is a more potent binder and activator of LXRα and LXRβ than GW3965.
AZ876 is highly selective against FXR, RXR, TRα, TRβ etc.
AZ876 reduces lesion area, and strongly decreases lesion area, lesion number and severity in vivo.
AZ876 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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