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SU3327

Chemical Structure : SU3327

CAS No.: 40045-50-9

SU3327 (Halicin)

Catalog No.: PC-27751Not For Human Use, Lab Use Only.

Halicin (SU3327) is a potent, selective and substrate competitive c-Jun N-terminal kinase (JNK) inhibitor with IC50 of 0.7 uM, inhibits TNF-α stimulated phosphorylation of c-Jun with IC50 of 6.23 uM in HeLa cells.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

Halicin (SU3327) is a potent, selective and substrate competitive c-Jun N-terminal kinase (JNK) inhibitor with IC50 of 0.7 uM, inhibits TNF-α stimulated phosphorylation of c-Jun with IC50 of 6.23 uM in HeLa cells.
Halicin (SU3327) shows an IC50 of 239 nM in displacing pepJIP1, as measured by a DELFIA assay.
Halicin (SU3327) is 142 fold less active against p38α, and completely inactive against Akt kinase, metalloprotease LF (lethal factor) and the proprotein convertase furin.
Halicin (SU3327) improves cardiac function and reduces heart damage during IR.

Physicochemical Properties

M.Wt 261.29
Formula C5H3N5O2S3
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

10 mM in DMSO

Chemical Name/SMILES

5-((5-Nitrothiazol-2-yl)thio)-1,3,4-thiadiazol-2-amine

References

1. De SK, et al. J Med Chem. 2009 Apr 9;52(7):1943-52.

2. Augustine C, et al. Neuroscience. 2014 Aug 22;274:1-10.

3. Jang S, et al. PLoS One. 2014 Nov 25;9(11):e113526.

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