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533298 TNIK Inhibitor, KY-05009 - CAS 1228280-29-2 - Calbiochem

TNIK inhibitor, KY-05009, is a cell-permeable, highly potent inhibitor of TNIK (IC₅₀ = 9 nM). Blocks multiple effects of TGF-β1 in tumor cells.

FDS (Fiches de données de sécurité), certificats d’analyse (CoA) et de qualité (CoQ), dossiers, brochures et autres documents disponibles.

Synonymes: Traf2- and Nck-interacting Kinase Inhibitor, KY-05009, KY05009, 5-(4-Methylbenzamido)-2-(phenylamino)thiazole-4-carboxamide

Primary Target: TNIK
533298
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Aperçu

Replacement Information

Tableau de caractéristiques principal

CAS #Empirical Formula
1228280-29-2C₁₈H₁₆N₄O₂S

Products

RéférenceConditionnement Qté
5332980001 Flacon en verre 10 mg
Description
OverviewA cell-permeable, non-toxic, 2-phenylaminothiazole derivative that acts as a highly potent, ATP competitive inhibitor of Traf2- and Nck-interacting kinase (TNIK; Ki = 100 nM, IC50 = 9 nM). Also shown to inhibit the activity of MLK1 (IC50 = 18 nM). Blocks multiple effects of TGF-β1 in A549 human lung adenocarcinoma cells, including nuclear translocation of β-catenin, TNIK binding to TCF4, phosphorylation of TCF4, and phosphorylation and nuclear translocation of Smad2/3. Significantly reduces TGF-β1 induced epithelial-to-mesenchymal transition (EMT). Reduces TGF-β1-induced migration and invasion in A549 cells and inhibits gelatinase activity of MMP2 and 9. Shown to diminish TGF-β1-induced phosphorylation of focal adhesion kinase (at Tyr925), Src (at Tyr416), and paxillin (at Tyr118) and of ERK1/2 (at Thr202/Tyr204), JNK1 (Thr183/Tyr221), and JNK2 (at Thr185/Tyr223).

Please note that the molecular weight for this compound is batch-specific due to variable water content. Please refer to the vial label or the certificate of analysis for the batch-specific molecular weight. The molecular weight provided represents the baseline molecular weight without water.
Catalogue Number533298
Brand Family Calbiochem®
SynonymsTraf2- and Nck-interacting Kinase Inhibitor, KY-05009, KY05009, 5-(4-Methylbenzamido)-2-(phenylamino)thiazole-4-carboxamide
References
ReferencesKim, J., et al. 2014. PLOS One. 9, e110180.
Product Information
CAS number1228280-29-2
FormYellow solid
Hill FormulaC₁₈H₁₆N₄O₂S
Chemical formulaC₁₈H₁₆N₄O₂S
Quality LevelMQ100
Applications
Biological Information
Primary TargetTNIK
Primary Target K<sub>i</sub>100 nM, IC₅₀
Purity≥98% by HPLC
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
Toxicity Standard Handling
Storage +2°C to +8°C
Protect from Light Protect from light
Do not freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Packaging Information
Packaged under inert gas Packaged under inert gas
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Référence GTIN
5332980001 04055977281521

Documentation

TNIK Inhibitor, KY-05009 - CAS 1228280-29-2 - Calbiochem FDS

Titre

Fiche de données de sécurité des matériaux (FDS) 

Références bibliographiques

Aperçu de la référence bibliographique
Kim, J., et al. 2014. PLOS One. 9, e110180.
Fiche technique

Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

Revision20-November-2015 JSW
SynonymsTraf2- and Nck-interacting Kinase Inhibitor, KY-05009, KY05009, 5-(4-Methylbenzamido)-2-(phenylamino)thiazole-4-carboxamide
DescriptionA cell-permeable, non-toxic, 2-phenylaminothiazole derivative that acts as a highly potent, ATP competitive inhibitor of Traf2- and Nck-interacting kinase (TNIK; Ki = 100 nM, IC50 = 9 nM). Also shown to inhibit the activity of MLK1 (IC50 = 18 nM). Blocks multiple effects of TGF-β1 in A549 human lung adenocarcinoma cells, including nuclear translocation of β-catenin, TNIK binding to TCF4, phosphorylation of TCF4, and phosphorylation and nuclear translocation of Smad2/3. Significantly reduces TGF-β1 induced epithelial-to-mesenchymal transition (EMT). Reduces TGF-β1-induced migration and invasion in A549 cells and inhibits gelatinase activity of MMP2 and 9. Shown to diminish TGF-β1-induced phosphorylation of focal adhesion kinase (at Tyr925), Src (at Tyr416), and paxillin (at Tyr118) and of ERK1/2 (at Thr202/Tyr204), JNK1 (Thr183/Tyr221), and JNK2 (at Thr185/Tyr223).
FormYellow solid
Intert gas (Yes/No) Packaged under inert gas
CAS number1228280-29-2
Chemical formulaC₁₈H₁₆N₄O₂S
Purity≥98% by HPLC
SolubilityDMSO (50 mg/ml)
Storage Protect from light
+2°C to +8°C
Do Not Freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Toxicity Standard Handling
ReferencesKim, J., et al. 2014. PLOS One. 9, e110180.