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INT-767

Product Name
INT-767
CAS No.
1000403-03-1
Chemical Name
INT-767
Synonyms
INT-767;INT-767 (INT767);Sodium (R)-3-[(3R,5S,6R,7R,8S,9S,10S,13R,14S,17R)-6-Ethyl-3,7-dihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl]butyl Sulfate
CBNumber
CB33048660
Molecular Formula
C25H45NaO6S
Formula Weight
496.68
MOL File
1000403-03-1.mol
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INT-767 Property

storage temp. 
Store at -20°C
solubility 
DMSO : ≥ 205.5 mg/mL (415.44 mM)
form 
Solid
color 
White to off-white
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

ChemScene
Product number
CS-5007
Product name
INT-767
Purity
>98.0%
Packaging
5mg
Price
$900
Updated
2021/12/16
Biorbyt Ltd
Product number
orb611413
Product name
INT-767
Packaging
5mg
Price
$1089.7
Updated
2021/12/16
ChemScene
Product number
CS-5007
Product name
INT-767
Purity
>98.0%
Packaging
10mg
Price
$1440
Updated
2021/12/16
Biorbyt Ltd
Product number
orb611413
Product name
INT-767
Packaging
10mg
Price
$1771.4
Updated
2021/12/16
Biorbyt Ltd
Product number
orb611413
Product name
INT-767
Packaging
25mg
Price
$3105.9
Updated
2021/12/16
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INT-767 Chemical Properties,Usage,Production

Description

INT-767 is a G-protein coupled/Farnesoid X-activated receptor agonist potentially for the treatment of hepatic fibrosis. INT-767 significantly improved serum liver enzymes, hepatic inflammation, and biliary fibrosis in Mdr2(-/-) mice. INT-767 significantly induced bile flow and biliary HCO?3- output, as well as gene expression of carbonic anhydrase 14, an important enzyme able to enhance HCO?3- transport, in an Fxr-dependent manner. In addition, INT-767 dramatically reduced bile acid synthesis via the induction of ileal Fgf15 and hepatic Shp gene expression, thus resulting in significantly reduced biliary bile acid output in Mdr2(-/-) mice.

Uses

INT-767 is a dual farnesoid X receptor (FXR)/TGR5 agonist with mean EC50s of 30 and 630 nM, respectively[1][2].

in vivo

INT-767 (10-20 mg/kg; i.p.; daily for 2 weeks) decreases plasma total cholesterol and triglyceride levels in db/m and db/db mice [2].

Animal Model:Male 8-week old C57BKS/J db/db mice, control nondiabetic db/m mice[2]
Dosage:10, 20 mg/kg
Administration:Intraperitoneal injection; daily for 2 weeks
Result:Decreased plasma total cholesterol and triglyceride levels.

References

[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. DOI:10.1002/hep.24537
[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. DOI:10.1124/mol.110.064501

INT-767 Preparation Products And Raw materials

Raw materials

Preparation Products

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INT-767 Suppliers

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1000403-03-1, INT-767Related Search:


  • INT-767
  • INT-767 (INT767)
  • Sodium (R)-3-[(3R,5S,6R,7R,8S,9S,10S,13R,14S,17R)-6-Ethyl-3,7-dihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl]butyl Sulfate
  • 1000403-03-1