4μ8C chemical structure
Chemical structureResearch use only
CAT. NO. DC10037Featured

4μ8C

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Product overview

Description & Application

4μ8C (IRE1 Inhibitor III) is a small-molecule inhibitor of IRE1α.

ParameterValue
Chemical Name7-Hydroxy-4-methyl-2-oxo-2H-chromene-8-carbaldehyde
CAS No.14003-96-4
Synonyms7-Hydroxy-4-methyl-2-oxo-2H-chromene-8-carbaldehyde;4Μ8C;7-hydroxy-4-methyl-2-oxochromene-8-carbaldehyde;8-Formyl-4-methylumbelliferone;IRE1 Inhibitor III;4μ7-Hydroxy-4-methyl-2-oxo-2H-1-benzopyran-8-carboxaldehyde;4-Methyl-7-hydroxy-8-formylcoumarin;7-Hydroxy-8-formyl-4-methylcoumarin;8-Formyl-7-hydroxy-4-methyl-2H-1-benzopyran-2-one;4M8C;4u8C;4μIRE1 Inhibitor III, 4μ8C;8-Formyl-7-hydroxy-4-methylcoumarin;4;I8C;4mu8C;2H-1-Benzopyran-8-carboxaldehyde, 7-hydroxy-4-methyl-2-oxo-;4micro8C;HMS3743K09;HMS3653K06;BCP21011;STK504078;s7272;4150AD;BDBM5001379
FormulaC11H8O4
M.Wt204.1788
SMILESO1C(C([H])=C(C([H])([H])[H])C2C([H])=C([H])C(=C(C([H])=O)C1=2)O[H])=O
Purity>98%
Storage2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Biological Activity

4μ8C (IRE1 Inhibitor III) is a small-molecule inhibitor of IRE1α.

In Vitro

When applies to the media of ER stressed cultured cells, 4μ8C inhibits Xbp1 splicing in a concentration-dependent manner. 4μ8C dissociates slowly from IRE1, but ishout of inhibitor leads to rapid recovery of Xbp1 splicing in cells[1].The IRE1 endoribonuclease inhibitor 4μ8c prevents the splicing of the XBP1 mRNA in response to ER stress caused by mutant proinsulin production[2]. The inositol-requiring enzyme 1α (IRE1α) is a serine-threonine kinase that plays crucial roles in activating the unfolded protein response. 4μ8C treatment dramatically inhibits IL-4 production by CD4+ T cells under Th0 conditions because both the IL-4 levels in the culture supernatant and the percentage of IL-4 positive cells are reduced by 4μ8C treatment. In addition, both IL-5 and IL-13 production are significantly reduced upon treatment with 4μ8C[3].

In Vivo

4μ8C reverses the ER stress-dependent loss of several known RIDD targets, with an EC50 of approximately 4 μM, approximating that of inhibition of XBP1 target gene activation[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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