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124009 Akt Inhibitor III - Calbiochem

124009
Purchase on Sigma-Aldrich

Descripción

Replacement Information

Tabla espec. clave

Empirical Formula
C₂₈H₅₇O₉P

Products

Número de referenciaEmbalaje Cant./Env.
124009-1MG Ampolla de plást. 1 mg
Description
OverviewA cell permeable, reversible, and substrate competitive phosphatidylinositol analog that inhibits the activation of Akt and select downstream substrates without decreasing phosphorylation of PDK-1 or other kinases downstream of Ras, such as MAPK. Also acts as a potent inducer of apoptosis and selectively kills a variety of cancer cell lines that contain high levels of active Akt. When used at a concentration of 10 µM, it is reported to activate p38α/SAPK2α MAP kinase. At 10 µM it will also inhibit PKA activity.
Catalogue Number124009
Brand Family Calbiochem®
SynonymsSH-6
References
ReferencesGills, J.J., et al. 2007. J. Biol. Chem. in press.
Kozikowski, A.P., et al. 2003. J. Am. Chem. Soc.125, 1144.
Product Information
ATP CompetitiveN
FormWhite solid
Hill FormulaC₂₈H₅₇O₉P
Chemical formulaC₂₈H₅₇O₉P
ReversibleY
Structure formula ImageStructure formula Image
Applications
Biological Information
Primary TargetAkt
Purity≥98% by NMR
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 -20°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.
Packaging Information
Packaged under inert gas Packaged under inert gas
Transport Information
Supplemental Information
Specifications

Documentation

Akt Inhibitor III - Calbiochem Ficha datos de seguridad (MSDS)

Título

Ficha técnica de seguridad del material (MSDS) 

Akt Inhibitor III - Calbiochem Certificados de análisis

CargoNúmero de lote
124009

Referencias bibliográficas

Visión general referencias
Gills, J.J., et al. 2007. J. Biol. Chem. in press.
Kozikowski, A.P., et al. 2003. J. Am. Chem. Soc.125, 1144.

Folleto

Cargo
Akt
Biologics 31.1
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.

Revision03-October-2007 RFH
SynonymsSH-6
DescriptionA phosphatidylinositol analog that inhibits the activation of Akt and selected downstream substrates without affecting the phosphorylation of PDK-1 and other downstream kinases. Decreases phosphorylation of Akt without affecting the total Akt level. Reported to be a potent inducer of apoptosis and to selectively kill a variety of cancer cell lines expressing high levels of active Akt. When used at a concentration of 10 µM, it is reported to activate p38α/SAPK2α MAP kinase. At 10 µM it will also inhibit PKA activity.
FormWhite solid
Intert gas (Yes/No) Packaged under inert gas
Chemical formulaC₂₈H₅₇O₉P
Structure formulaStructure formula
Purity≥98% by NMR
SolubilityDMSO (10 mg/ml)
Storage -20°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
ReferencesGills, J.J., et al. 2007. J. Biol. Chem. in press.
Kozikowski, A.P., et al. 2003. J. Am. Chem. Soc.125, 1144.