Chemical Name: 5-[(5-Nitro-2-thiazolyl)thio]-1,3,4thiadiazol-2-amine
Purity: ≥99% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Selective inhibitor of c-Jun N-terminal kinase (JNK) (IC50 = 0.7 μM). Inhibits the protein-protein interaction between JNK and JIP (IC50 = 239 nM). Displays selectivity over p38 MAPK and Akt. Restores insulin sensitivity in a mouse model of type-2 diabetes.
Compound Libraries
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Technical Data
M. Wt
261.3
Formula
C5H3N5O2S3
Storage
Store at RT
Purity
≥99% (HPLC)
CAS Number
40045-50-9
PubChem ID
11837140
InChI Key
NQQBNZBOOHHVQP-UHFFFAOYSA-N
Smiles
NC2=NN=C(S2)SC1=NC=C([N+]([O-])=O)S1
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent
Max Conc. mg/mL
Max Conc. mM
Solubility
DMSO
26.13
100
ethanol
2.61
10
Preparing Stock Solutions
The following data is based on the product molecular weight 261.3. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
3.83 mL
19.14 mL
38.27 mL
5 mM
0.77 mL
3.83 mL
7.65 mL
10 mM
0.38 mL
1.91 mL
3.83 mL
50 mM
0.08 mL
0.38 mL
0.77 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products' biological activity.
Deet al (2009) Design, synthesis and structure-activity relationship of substrate competitive, selective, and in vivo active triazole and thiadiazole inhibitors of the c-jun N-terminal kinase. J.Med.Chem. 52 1943 PMID: 19271755