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251650
Sigma-AldrichDamnacanthal - CAS 477-84-9 - Calbiochem
A cell-permeable, potent, reversible, and selective inhibitor of p56lck tyrosine kinase.
More>>A cell-permeable, potent, reversible, and selective inhibitor of p56lck tyrosine kinase. Less<<
Damnacanthal - CAS 477-84-9 - Calbiochem MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
A cell-permeable, potent, reversible, and selective inhibitor of p56lck tyrosine kinase. Inhibits p56lck autophosphorylation (IC50 = 17 nM) and phosphorylation of an exogenous peptide by p56lck (IC50 = 620 nM). Exhibits over 100-fold greater selectivity for p56lck over PKA and PKC, 40-fold greater selectivity for p56lck over EGF receptor kinase, c-ErbB2, insulin receptor kinase, and PDGF receptor kinase, and 7 - 20-fold greater selectivity for p56lck over p60src and p59fyn. Inhibition of p56lck is not significantly affected by the presence of sulfhydryl reagents. Also known to have antimalarial properties and to reverse the phenotype of ras-transformed cells.
Catalogue Number
251650
Brand Family
Calbiochem®
Synonyms
3-Hydroxy-1-methoxyanthraquinone-2-aldehyde
References
References
Faltynek, C.R., et al. 1995. Biochemistry34, 12404. Hiramatsu, T., et al. 1993. Cancer Lett.73, 161. Koumaglo, K., et al. 1992. Planta Med.58, 533.
Damnacanthal - CAS 477-84-9 - Calbiochem Certificates of Analysis
Title
Lot Number
251650
References
Reference overview
Faltynek, C.R., et al. 1995. Biochemistry34, 12404. Hiramatsu, T., et al. 1993. Cancer Lett.73, 161. Koumaglo, K., et al. 1992. Planta Med.58, 533.
Data Sheet
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.
Revision
21-April-2011 JSW
Synonyms
3-Hydroxy-1-methoxyanthraquinone-2-aldehyde
Description
A cell-permeable, potent, reversible, and selective inhibitor of p56lck tyrosine kinase activity. Inhibits p56lck autophosphorylation (IC50 = 17 nM) and phosphorylation of an exogenous peptide by p56lck over PKA and PKC and >40 fold selectivity for p56lck over EGF, c-erbB2, insulin, and the PDGF receptor tyrosine kinases. In addition, damnacanthal exhibits 7-20 fold selectivity for p56lck over pp60src and pp59fyn. Inhibition of p56lck by damnacanthal appears to be reversible, not time-dependent and not significantly affected by the presence of sulfhydryl reagents. Also known to have antimalarial properties, and to reverse the phenotype of ras-transformed cells.
Form
Orange-yellow solid
Intert gas (Yes/No)
Packaged under inert gas
CAS number
477-84-9
Chemical formula
C₁₆H₁₀O₅
Structure formula
Purity
≥95% by HPLC
Solubility
DMSO (5 mg/ml)
Storage
Protect from light -20°C
Do Not Freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 1 month at -20°C.
Toxicity
Standard Handling
References
Faltynek, C.R., et al. 1995. Biochemistry34, 12404. Hiramatsu, T., et al. 1993. Cancer Lett.73, 161. Koumaglo, K., et al. 1992. Planta Med.58, 533.