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INT-767

Catalog No. T11661   CAS 1000403-03-1

INT-767 is a potent farnesoid X receptor (FXR)/TGR5 dual agonist that prevents NASH and promotes visceral adipose brown lipogenesis and mitochondrial function for the study of non-alcoholic steatohepatitis.

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INT-767 Chemical Structure
INT-767, CAS 1000403-03-1
Pack Size Availability Price/USD Quantity
25 mg 8-10 weeks $ 2,120.00
50 mg 8-10 weeks $ 2,780.00
100 mg 8-10 weeks $ 3,700.00
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Biological Description
Chemical Properties
Storage & Solubility Information
Description INT-767 is a potent farnesoid X receptor (FXR)/TGR5 dual agonist that prevents NASH and promotes visceral adipose brown lipogenesis and mitochondrial function for the study of non-alcoholic steatohepatitis.
In vitro INT-767 does not inhibit hERG, indicating that this compound should not induce cardiac toxicity because of inhibition of the potassium channel[2].
In vivo Mice were treated daily with INT-767 (10 and 20 mg/kg) or vehicle alone (40% 2-hydroxypropyl-β-cyclodextrin) via intraperitoneal injection for 2 weeks. The results showed that INT-767 reduced the levels of plasma total cholesterol, high-density lipoprotein cholesterol, and triglycerides in both db/m and db/db mice [2].
Molecular Weight 494.66
Formula C25H43NaO6S
CAS No. 1000403-03-1

Storage

keep away from moisture

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 80 mg/mL (161.62 mM), Sonification is recommended.

H2O: 80 mg/mL (161.62 mM)

TargetMolReferences and Literature

1. Baghdasaryan A, et al. Dual farnesoid X receptor/TGR5 agonist INT-767 reduces liver injury in the Mdr2-/- (Abcb4-/-) mousecholangiopathy model by promoting biliary HCO3- output. Hepatology. 2011 Oct;54(4):1303-1312. 2. Rizzo G, et al. Functional characterization of the semisynthetic bile acid derivative INT-767, a dual farnesoid X receptor andTGR5 agonist. Mol Pharmacol. 2010 Oct;78(4):617-630.

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Keywords

INT-767 1000403-03-1 GPCR/G Protein Metabolism FXR GPCR19 INT767 INT 767 inhibitor inhibit

 

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