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HJC0350

Chemical Structure : HJC0350

CAS No.: 885434-70-8

HJC0350 (HJC-0350)

Catalog No.: PC-44643Not For Human Use, Lab Use Only.

HJC0350 is a potent and specific EPAC2 antagonist with IC50 of 0.3 uM for competing with 8-NBD-cAMP in binding EPAC2, about 133-fold more potent than cAMP.

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10 mg $78 In stock
25 mg $128 In stock
50 mg $218 In stock
100 mg $358 In stock
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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

HJC0350 is a potent and specific EPAC2 antagonist with IC50 of 0.3 uM for competing with 8-NBD-cAMP in binding EPAC2, about 133-fold more potent than cAMP.
HJC0350 exhibits no inhibition of EPAC1-mediated Rap1-GDP exchange activity at 25 uM.
HJC0350 selectively blocks cAMP-induced EPAC2 activation but does not inhibit cAMP-mediated PKA activation, fully blocks the 007-AM induced decrease of FRET in HEK293/EPAC2-FL cells at 10 uM.

Physicochemical Properties

M.Wt 277.38
Formula C15H19NO2S
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

DMSO: 10 mM

Chemical Name/SMILES

1H-Pyrrole, 2,4-dimethyl-1-[(2,4,6-trimethylphenyl)sulfonyl]-

References

1. Chen H, et al. J Med Chem. 2013 Feb 14;56(3):952-62.

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