[CAS NO. 1032823-75-8]  GSK1292263

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PRODUCTS SPECIFICATIONS [1032823-75-8]

Catalog
SLK-S2149
Brand
Selleck
CAS
1032823-75-8

DESCRIPTION [1032823-75-8]

Overview

MDLMFCD18385004
Molecular Weight456.56
Molecular FormulaC23H28N4O4S
SMILESO=S(C1=CC=C(C2=CC=C(OCC3CCN(C4=NC(C(C)C)=NO4)CC3)C=N2)C=C1)(C)=O

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM2.1903 mL10.9515 mL21.9029 mL
5 mM0.4381 mL2.1903 mL4.3806 mL
10 mM0.2190 mL1.0951 mL2.1903 mL
50 mM0.0438 mL0.2190 mL0.4381 mL

Description

GSK1292263 is a novel agonist, showing potential for the treatment of type 2 diabetes. Phase 2.

Targets

GPR119 [1]

In vitro

GSK-1292263 is selected from 1538 compounds by using Hypo1, the Fit-Value and Estimate of GSK-1292263 that is aligned in Hypo1 are 8.8 and 7.7 (nM), respectively.

In vivo

GSK-1292263 administrated at a single dose of 3-30 mg/kg in the absence of nutrients correlates with increased levels of circulating gastrointestinal peptides, including glucagon-like peptide 1 (GLP-1), gastric inhibitory polypeptide (GIP), peptide YY (PYY) and glucagon in male Sprague-Dawley rats, the increase is enhanced following administration of glucose in the oral glucose tolerance test (OGTT). GSK-129226 significant increases in the peak insulin response and insulin AUC(0-15 min) of 30-60% compared with values in the vehicle control cohort in the intravenous glucose tolerance test in rats, this insulin upregulation correlated with a significant increase in the glucose disposal rate. GSK-1292263 is associated with a statistically significant increase in insulin immunoreactivity in pancreatic sections in a 6-week study performed in Zucker diabetic fatty rats, compared with insulin immunoreactivity in samples obtained from rats receiving vehicle control. GSK-1292263 administrated at dose of 10 or 30 mg/kg or vehicle control at 2 hours prior to insulin infusion in hyperinsulinemic-euglycemic clamps stimulates glucagon secretion without increasing blood glucose levels Sprague-Dawley rats.