Millipore Sigma Vibrant Logo
Atención: Nos hemos mudado. Los productos Merck Millipore ya no pueden adquirirse en MerckMillipore.comMás información

420320 KT5720 - CAS 108068-98-0 - Calbiochem

420320
Purchase on Sigma-Aldrich

Descripción

Replacement Information

Tabla espec. clave

CAS #Empirical Formula
108068-98-0C₃₂H₃₁N₃O₅

Products

Número de referenciaEmbalaje Cant./Env.
420320-100UG Frasco de vidrio 100 μg
420320-50UG Ampolla de plást. 50 μg
Description
OverviewA potent, specific, cell-permeable, reversible and ATP-competitive inhibitor of protein kinase A (Ki = 56 nM) that is prepared by a chemical modification of K-252a. Does not significantly affect the activities of PKC, PKG, and MLCK. Inhibits axon branching in cultured neurons. A 2 mM (50 µg/47 µl) solution of KT 5720 (Cat. No. 420323) in DMSO is also available.
Catalogue Number420320
Brand Family Calbiochem®
SynonymsPKA Inhibitor VII
References
ReferencesSimpson, C.S., and Morris, B.J. 1995. Neuroscience 68, 97.
Cabell, L., and Audesirk, G. 1993. Int. J. Dev. Neurosci. 11, 357.
Gadbois, D.M., et al. 1992. Proc. Natl. Acad. Sci. USA 89, 8626.
Kase, H., et al. 1987. Biochem. Biophys. Res. Commun. 142, 436.
Product Information
CAS number108068-98-0
ATP CompetitiveY
FormWhite solid
Hill FormulaC₃₂H₃₁N₃O₅
Chemical formulaC₃₂H₃₁N₃O₅
ReversibleY
Structure formula ImageStructure formula Image
Quality LevelMQ100
Applications
ApplicationKT5720, CAS 108068-98-0, is a cell-permeable, potent, specific, reversible, ATP-competitive inhibitor of protein kinase A (Ki = 56 nM). Has no significant effect on PKC, PKG & MLCK.
Biological Information
Primary TargetPKA
Primary Target K<sub>i</sub>56 nM for protein kinase A
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 -20°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
Transport Information
Supplemental Information
Specifications

Documentation

KT5720 - CAS 108068-98-0 - Calbiochem Ficha datos de seguridad (MSDS)

Título

Ficha técnica de seguridad del material (MSDS) 

KT5720 - CAS 108068-98-0 - Calbiochem Certificados de análisis

CargoNúmero de lote
420320

Referencias bibliográficas

Visión general referencias
Simpson, C.S., and Morris, B.J. 1995. Neuroscience 68, 97.
Cabell, L., and Audesirk, G. 1993. Int. J. Dev. Neurosci. 11, 357.
Gadbois, D.M., et al. 1992. Proc. Natl. Acad. Sci. USA 89, 8626.
Kase, H., et al. 1987. Biochem. Biophys. Res. Commun. 142, 436.

Citas

Título
  • Mike T. Lin, et al. (2005) Ca2+-activated K+ channel-associated phosphatase and kinase activities during development. American Journal of Physiology Heart and Circulatory Physiology 289, H414-H425.
  • 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.

    Revision08-January-2010 RFH
    SynonymsPKA Inhibitor VII
    DescriptionPrepared by a chemical modification of K-252a. A potent, specific, cell-permeable, reversible and ATP-competitive inhibitor of protein kinase A (Ki = 56 nM). Does not significantly affect the activity of PKC, PKG, or MLCK. Inhibits axon branching in cultured neurons.
    FormWhite solid
    CAS number108068-98-0
    Chemical formulaC₃₂H₃₁N₃O₅
    Structure formulaStructure formula
    Purity≥95% by HPLC
    SolubilityDMSO (1 mg/ml). Further dilute with aqueous buffers just prior to use.
    Storage Protect from light
    -20°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
    ReferencesSimpson, C.S., and Morris, B.J. 1995. Neuroscience 68, 97.
    Cabell, L., and Audesirk, G. 1993. Int. J. Dev. Neurosci. 11, 357.
    Gadbois, D.M., et al. 1992. Proc. Natl. Acad. Sci. USA 89, 8626.
    Kase, H., et al. 1987. Biochem. Biophys. Res. Commun. 142, 436.
    Citation
  • Mike T. Lin, et al. (2005) Ca2+-activated K+ channel-associated phosphatase and kinase activities during development. American Journal of Physiology Heart and Circulatory Physiology 289, H414-H425.