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539644 UCN-01

A cell-permeable Staurosporine derived anticancer agent that reversibly and ATP-competitively inhibits several protein kinases.

UCN-01: Ficha de datos de seguridad (MSDS o SDS), certificado de análisis y de calidad (CoA y CoQ), expedientes, folletos y otros documentos disponibles.

Sinónimos: 7-Hydroxystaurosporine, Staurosporine, 7β-Hydroxy, Streptomyces sp., Chk1 Inhibitor VI, Chk2 Inhibitor V

Primary Target: PKCα, PKCβ, PKCγ, PKCδ PKCε, Chk1, Cdc25C-associated protein kinase 1, Cdk1, PAK4, Cdk5/p25 and Chk2, PDK1, lck, MAPKAP kinase-2, Akt, GSK-3β and PKA
539644
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Descripción

Replacement Information

Tabla espec. clave

CAS #Empirical Formula
112953-11-4C₂₈H₂₆N₄O₄

Products

Número de referenciaEmbalaje Cant./Env.
539644-500UG Ampolla de plást. 500 μg
Description
OverviewA cell-permeable Staurosporine (Cat. No. 569397) derived anticancer agent that reversibly and ATP-competitively inhibits several protein kinases (IC50 = 29 nM, 34 nM, 30 nM, 590 nM and 530 nM for PKCα, PKCβ, PKCγ, PKCδ and PKCε; IC50 = 7 nM, 27 nM, 50 nM, 50 nM, 150 nM and 1.04 µM for Chk1, Cdc25C-associated protein kinase 1, Cdk1, PAK4, Cdk5/p25 and Chk2; IC50 = 33 nM, 50 nM, 95 nM, 500 nM, 500 nM and 1.0 µM for PDK1, lck, MAPKAP kinase-2, Akt, GSK-3β and PKA, respectively). At higher concentrations (> 15 µM), affects the activities of Src, PIM-1, CKII, DNA-PK, ErK1, ILK-1 and MAPKK1). Reported to suppress thymidylate synthase expression, induce apoptosis with caspase activation, and sensitize tumor cells to a range of DNA-damaging agents.
Catalogue Number539644
Brand Family Calbiochem®
Synonyms7-Hydroxystaurosporine, Staurosporine, 7β-Hydroxy, Streptomyces sp., Chk1 Inhibitor VI, Chk2 Inhibitor V
References
ReferencesReinhardt, H.C., et al. 2007. Cancer Cell 11, 175.
Jiang, X., et al. 2004. Mol. Cancer Ther. 3, 1221.
Sato, S., et al. 2002. Oncogene 21, 1727.
Patel, V., et al. 2002. Clin. Cancer Res. 8, 3549.
Leclerc, S., et al. 2001. J. Biol. Chem. 276, 251.
Busby, E.C., et al. 2000. Cancer Res. 60, 2108.
Hsueh, C.T., et al. 1998. Clin. Cancer Res. 4, 2201.
Akiyama, T., et al. 1997. Cancer Res. 57, 1495.
Seynaeve, C.M., et al. 1994. Mol. Pharmacol. 45, 1207.
Takahashi, I., et al. 1987, J. Antibiot. 40, 1782.
Product Information
CAS number112953-11-4
ATP CompetitiveY
FormWhite to beige solid
Hill FormulaC₂₈H₂₆N₄O₄
Chemical formulaC₂₈H₂₆N₄O₄
ReversibleY
Structure formula ImageStructure formula Image
Quality LevelMQ100
Applications
Biological Information
Primary TargetPKCα, PKCβ, PKCγ, PKCδ PKCε, Chk1, Cdc25C-associated protein kinase 1, Cdk1, PAK4, Cdk5/p25 and Chk2, PDK1, lck, MAPKAP kinase-2, Akt, GSK-3β and PKA
Primary Target IC<sub>50</sub>IC50 = 29 nM, 34 nM, 30 nM, 590 nM, 530 nM, 7 nM, 27 nM, 50 nM, 50 nM, 150 nM, 1.04 µM, 33 nM, 50 nM, 95 nM, 500 nM, 500 nM and 1.0 µM, respectively for primary targets in the order listed
Purity≥95% by HPLC
Physicochemical Information
Cell permeableY
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code Ambient Temperature Only
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 6 months at -20°C.
Packaging Information
Packaged under inert gas Packaged under inert gas
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Número de referencia GTIN
539644-500UG 04055977194821

Documentation

UCN-01 Ficha datos de seguridad (MSDS)

Título

Ficha técnica de seguridad del material (MSDS) 

UCN-01 Certificados de análisis

CargoNúmero de lote
539644

Referencias bibliográficas

Visión general referencias
Reinhardt, H.C., et al. 2007. Cancer Cell 11, 175.
Jiang, X., et al. 2004. Mol. Cancer Ther. 3, 1221.
Sato, S., et al. 2002. Oncogene 21, 1727.
Patel, V., et al. 2002. Clin. Cancer Res. 8, 3549.
Leclerc, S., et al. 2001. J. Biol. Chem. 276, 251.
Busby, E.C., et al. 2000. Cancer Res. 60, 2108.
Hsueh, C.T., et al. 1998. Clin. Cancer Res. 4, 2201.
Akiyama, T., et al. 1997. Cancer Res. 57, 1495.
Seynaeve, C.M., et al. 1994. Mol. Pharmacol. 45, 1207.
Takahashi, I., et al. 1987, J. Antibiot. 40, 1782.
Ficha técnica

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.

Revision22-June-2009 RFH
Synonyms7-Hydroxystaurosporine, Staurosporine, 7β-Hydroxy, Streptomyces sp., Chk1 Inhibitor VI, Chk2 Inhibitor V
DescriptionA cell-permeable Staurosporine (Cat. No. 569397) derived anticancer agent that reversibly and ATP-competitively inhibits several protein kinases (IC50 = 29 nM, 34 nM, 30 nM, 590 nM and 530 nM for PKCα, PKCβ, PKCγ, PKCδ and PKCε; IC50 = 7 nM, 27 nM, 50 nM, 50 nM, 150 nM and 1.04 µM for Chk1, Cdc25C-associated protein kinase 1, Cdk1, PAK4, Cdk5/p25 and Chk2; IC50 = 33 nM, 50 nM, 95 nM, 500 nM, 500 nM and 1.0 µM for PDK1, lck, MAPKAP kinase-2, Akt, GSK-3β and PKA, respectively). At higher concentrations (> 15 µM), affects the activities of Src, PIM-1, CKII, DNA-PK, ErK1, ILK-1 and MAPKK1). Reported to suppress thymidylate synthase expression, induce apoptosis with caspase activation, and sensitize tumor cells to a range of DNA-damaging agents.
FormWhite to beige solid
Intert gas (Yes/No) Packaged under inert gas
CAS number112953-11-4
Chemical formulaC₂₈H₂₆N₄O₄
Structure formulaStructure formula
Purity≥95% by HPLC
SolubilityDMSO (5 mg/ml) or Ethanol (1 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 6 months at -20°C.
Toxicity Standard Handling
ReferencesReinhardt, H.C., et al. 2007. Cancer Cell 11, 175.
Jiang, X., et al. 2004. Mol. Cancer Ther. 3, 1221.
Sato, S., et al. 2002. Oncogene 21, 1727.
Patel, V., et al. 2002. Clin. Cancer Res. 8, 3549.
Leclerc, S., et al. 2001. J. Biol. Chem. 276, 251.
Busby, E.C., et al. 2000. Cancer Res. 60, 2108.
Hsueh, C.T., et al. 1998. Clin. Cancer Res. 4, 2201.
Akiyama, T., et al. 1997. Cancer Res. 57, 1495.
Seynaeve, C.M., et al. 1994. Mol. Pharmacol. 45, 1207.
Takahashi, I., et al. 1987, J. Antibiot. 40, 1782.

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Categorías

Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Protein Phosphorylation / Dephosphorylation > Protein Kinase C (PKC) Inhibitors
Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Protein Phosphorylation / Dephosphorylation > Glycogen Synthase Kinase (GSK) Inhibitors
Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Protein Phosphorylation / Dephosphorylation > Protein Kinase G (PKG; cGMP-Dependent Protein Kinase) Inhibitors
Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Protein Phosphorylation / Dephosphorylation > MAP Kinase Inhibitors
Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Protein Phosphorylation / Dephosphorylation > Protein Tyrosine Kinase (PTK) Inhibitors
Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Cell Cycle/Cell Division > Cyclin-Dependent Kinase (Cdk) Inhibitors