AS1842856 chemical structure
Chemical structureResearch use only
CAT. NO. DC10086Featured

AS1842856

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TotalUS$450
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Product overview

Description & Application

AS1842856 is a potent and cell-permeable Foxo1 inhibitor with an IC50 of 30 nM.

ParameterValue
Chemical Name3-Quinolinecarboxylic acid,5-amino-7-(cyclohexylamino)-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-
CAS No.836620-48-5
Synonyms3-Quinolinecarboxylic acid,5-amino-7-(cyclohexylamino)-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-;AS1842856;AS-1842856
FormulaC18H22FN3O3
M.Wt347.383987903595
SMILESO=C(C1=CN(CC)C2=C(C(N)=C(F)C(NC3CCCCC3)=C2)C1=O)O
Purity>98%
Storage2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Biological Activity

AS1842856 is a potent and cell-permeable Foxo1 inhibitor with an IC50 of 30 nM.

In Vitro

AS1842856 potently inhibits human Foxo1 transactivation and reduces glucose production through the inhibition of glucose-6 phosphatase and phosphoenolpyruvate carboxykinase mRNA levels in a rat hepatic cell line[1].

In Vivo

Oral administration of AS1842856 to diabetic db/db mice leads to a drastic decrease in fasting plasma glucose level via the inhibition of hepatic gluconeogenic genes, whereas administration to normal mice has no effect on the fasting plasma glucose level. Treatment with AS1842856 also suppresses an increase in plasma glucose level caused by pyruvate injection in both normal and db/db mice[1].

References & source

DC Chemicals original product information

Published experimental findings depend on the model and assay conditions. They do not guarantee equivalent performance in every application. For laboratory research use only.

Product documentation

Refer to the certificate supplied with your lot for batch-specific release results.

Handling guide

2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

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