Tetradecanoic acid, (1aR,1bS,4aR,7aS,7bS,8R,9R,9aS)-9a-(acetyloxy)-1a,1b,4,4a,5,7a,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, 95%, 95%

cas: 16561-29-8 — see every product listed under this CAS number, including other names

Tetradecanoic acid, (1aR,1bS,4aR,7aS,7bS,8R,9R,9aS)-9a-(acetyloxy)-1a,1b,4,4a,5,7a,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, 95%, 95% (CAS 16561-29-8) is a chemical reagent available from Chemat. Available pack sizes: 100mg. Offered by: Chemat.

brandChemat
catalog numberCh11AOO5-100mg
cas16561-29-8
size100mg
availability 1g
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Available pack sizes

brand size price
Chemat 100mg 2877.20 Pln

properties

purity95%
delivery time3 weeks

Phorbol 13-acetate 12-myristate is a phorbol ester that is phorbol in which the hydroxy groups at the cyclopropane ring juction (position 13) and the adjacent carbon (position 12) have been converted into the corresponding acetate and myristate esters. It is a major active constituent of the seed oil of Croton tiglium. It has been used as a tumour promoting agent for skin carcinogenesis in rodents and is associated with increased cell proliferation of malignant cells. However its function is controversial since a decrease in cell proliferation has also been observed in several cancer cell types. It has a role as an antineoplastic agent, a carcinogenic agent, a mitogen, a protein kinase C agonist, an apoptosis inducer, a reactive oxygen species generator and a plant metabolite. It is a tertiary alpha-hydroxy ketone, a phorbol ester, an acetate ester, a diester and a tetradecanoate ester.

Source: ChEBI

Identity
Molecular formulaC36H56O8
Molecular weight616.8 g/mol
IUPAC name[(1S,2S,6R,10S,11R,13S,14R,15R)-13-acetyloxy-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] tetradecanoate
InChIKeyPHEDXBVPIONUQT-RGYGYFBISA-N
SMILESCCCCCCCCCCCCCC(=O)O[C@@H]1[C@H]([C@]2([C@@H](C=C(C[C@]3([C@H]2C=C(C3=O)C)O)CO)[C@H]4[C@@]1(C4(C)C)OC(=O)C)O)C

Computed by PubChem (NCBI)

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