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4?-Phorbol 12-myristate 13-acetate

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    4?-Phorbol 12-myristate 13-acetate
  • 4?-Phorbol 12-myristate 13-acetate
Cat No: 16806
Biochemicals - Small Molecule Activators
Cayman

Phorbol 12-myristate 13-acetate (PMA; Item No. 10008014) is a phorbol ester that is commonly used to activate certain types of PKC, including group A (α, βI, βII, γ) and group B (δ, ε, η, θ) isoforms.{17804} 4α-PMA is a structural analog of PMA that do...

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: 1 mg

This product can only be bought through Cayman Chemical. Please contact us.

Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • tetradecanoic acid, (4aS,7bS,8R,9R,9aS)-9a-(acetyloxy)-1aR,1bS,4,4a,5,7aS,7b,8,9,9a-decahydro-4a,7b-dihydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-5-oxo-1H-cyclopropa[3,4]benz[1,2-e]azulen-9-yl ester
Correlated keywords:
  • biochemicals intracellular signaling 12-O-tetradecanoylphorbol 4?-TPA ? 4?Phorbol 12myristate 13acetate 4?phorbol12myristate13acetate negative control PMA structural analog PKC signal
Product Overview:
Phorbol 12-myristate 13-acetate (PMA; Item No. 10008014) is a phorbol ester that is commonly used to activate certain types of PKC, including group A (α, βI, βII, γ) and group B (δ, ε, η, θ) isoforms.{17804} 4α-PMA is a structural analog of PMA that does not activate PKC.{27366,27365} It is used as a negative control for PMA signaling through PKC.{27365}
Size 1 mg
Shipping dry ice
CAS Number 63597-44-4
Molecular Formula C36H56O8
SMILES OCC1=C[C@]2([H])[C@]([C@@](C=C(C)C3=O)([H])[C@@]3(O)C1)(O)[C@H](C)[C@@H](OC(CCCCCCCCCCCCC)=O)[C@]4(OC(C)=O)[C@H]2C4(C)C
Molecular Weight 616,8
Formulation A solid
Purity ≥98%
Custom Code 2915.90
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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