Millipore Sigma Vibrant Logo
Attention: We have moved. Merck Millipore products are no longer available for purchase on MerckMillipore.com.Learn More

524390 Phorbol-12,13-dibutyrate - CAS 37558-16-0 - Calbiochem

Strong irritant for mouse skin, but only moderately active as a tumor promoter.

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

Synonymes: PDBu, PKC Activator II

Primary Target: Na+,K+- ATPase
524390
Purchase on Sigma-Aldrich

Aperçu

Replacement Information

Tableau de caractéristiques principal

CAS #Empirical Formula
37558-16-0C₂₈H₄₀O₈

Products

RéférenceConditionnement Qté
524390-1MG Bidon alu 1 mg
524390-5MG Bidon alu 5 mg
Description
OverviewStrong irritant for mouse skin, but only moderately active as a tumor promoter. Activates protein kinase C. Stimulates the phosphorylation of Na+,K+- ATPase, thereby inhibiting its activity. Promotes the expression of inducible NOS in cultured hepatocytes. Commonly used in binding studies or in applications requiring high concentrations of phorbol compounds.
Catalogue Number524390
Brand Family Calbiochem®
SynonymsPDBu, PKC Activator II
References
ReferencesFisone, G., et al. 1995. J. Biol. Chem. 270, 2427.
Lee, E.J., et al. 1994. Brain Res. 665, 127.
Critz, S.D., et al. 1993. J. Neurochem. 60, 1175.
Iredale, P.A., et al. 1993. Biochem. Pharmacol. 45, 611.
Critz, S.D., and Byrne J.H. 1992. J. Neurophys. 68, 1079.
Hortelano, S., et al. 1992. J. Biol. Chem. 267, 24937.
Ward C.A., and Moffat, M.P. 1992. J. Mol. Cell. Cardiol. 24, 937.
Product Information
CAS number37558-16-0
ATP CompetitiveN
FormClear film or white crystalline solid
Hill FormulaC₂₈H₄₀O₈
Chemical formulaC₂₈H₄₀O₈
ReversibleN
Structure formula ImageStructure formula Image
Quality LevelMQ100
Applications
Biological Information
Primary TargetNa+,K+- ATPase
Purity≥99% by HPLC
Physicochemical Information
Cell permeableN
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
RTECSEK7767000
Safety Information
R PhraseR: 26/27/28-36/37/38-40-41

Very toxic by inhalation, in contact with skin and if swallowed.
Irritating to eyes, respiratory system and skin.
Limited evidence of a carcinogenic effect.
Risk of serious damage to eyes.
S PhraseS: 26-36/37/39-45

In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
Wear suitable protective clothing, gloves and eye/face protection.
In case of accident or if you feel unwell, seek medical advice immediately (show the label where possible).
Product Usage Statements
Storage and Shipping Information
Ship Code Ambient Temperature Only
Toxicity Highly Toxic & Carcinogenic / Teratogenic
Hazardous Materials Attention: Due to the nature of the Hazardous Materials in this shipment, additional shipping charges may be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
Storage -20°C
Do not freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). DMSO stock solutions are stable for up to 6 months at -20°C. With frequent use, the DMSO stock solutions may accumulate water. The presence of water in the stock solution will accelerate the decomposition of the product, resulting in significant loss of activity in 2-3 months.
Packaging Information
Packaged under inert gas Packaged under inert gas
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Référence GTIN
524390-1MG 04055977271546
524390-5MG 04055977271553

Documentation

Phorbol-12,13-dibutyrate - CAS 37558-16-0 - Calbiochem FDS

Titre

Fiche de données de sécurité des matériaux (FDS) 

Phorbol-12,13-dibutyrate - CAS 37558-16-0 - Calbiochem Certificats d'analyse

TitreNuméro de lot
524390

Références bibliographiques

Aperçu de la référence bibliographique
Fisone, G., et al. 1995. J. Biol. Chem. 270, 2427.
Lee, E.J., et al. 1994. Brain Res. 665, 127.
Critz, S.D., et al. 1993. J. Neurochem. 60, 1175.
Iredale, P.A., et al. 1993. Biochem. Pharmacol. 45, 611.
Critz, S.D., and Byrne J.H. 1992. J. Neurophys. 68, 1079.
Hortelano, S., et al. 1992. J. Biol. Chem. 267, 24937.
Ward C.A., and Moffat, M.P. 1992. J. Mol. Cell. Cardiol. 24, 937.

Brochure

Titre
Caspases and other Apoptosis Related Tools Brochure
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.

Revision19-August-2008 RFH
SynonymsPDBu, PKC Activator II
DescriptionStrong irritant for mouse skin, but only moderately active as a tumor promoter. Activates protein kinase C (PKC). Stimulates the phosphorylation of Na+-K+ ATPase, thereby inhibiting its activity. Promotes the expression of iNOS in cultured hepatocytes. PDBu can be diluted to 30 µM in aqueous solutions, so it is commonly used in binding studies or in applications requiring high concentrations. It is easier to remove PDBu than PMA from cells in culture.
FormClear film or white crystalline solid
Intert gas (Yes/No) Packaged under inert gas
CAS number37558-16-0
RTECSEK7767000
Chemical formulaC₂₈H₄₀O₈
Structure formulaStructure formula
Purity≥99% by HPLC
SolubilityDMSO (10 mg/ml). Further dilute with aqueous buffers just prior to use.
Storage -20°C
Do Not Freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). DMSO stock solutions are stable for up to 6 months at -20°C. With frequent use, the DMSO stock solutions may accumulate water. The presence of water in the stock solution will accelerate the decomposition of the product, resulting in significant loss of activity in 2-3 months.
Toxicity Highly Toxic & Carcinogenic / Teratogenic
ReferencesFisone, G., et al. 1995. J. Biol. Chem. 270, 2427.
Lee, E.J., et al. 1994. Brain Res. 665, 127.
Critz, S.D., et al. 1993. J. Neurochem. 60, 1175.
Iredale, P.A., et al. 1993. Biochem. Pharmacol. 45, 611.
Critz, S.D., and Byrne J.H. 1992. J. Neurophys. 68, 1079.
Hortelano, S., et al. 1992. J. Biol. Chem. 267, 24937.
Ward C.A., and Moffat, M.P. 1992. J. Mol. Cell. Cardiol. 24, 937.