3D model (JSmol)
|Molar mass||364.44 g·mol−1|
|Melting point||250 to 251 °C (482 to 484 °F; 523 to 524 K)|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Phorbol is a natural, plant-derived organic compound. It is a member of the tigliane family of diterpenes. Phorbol was first isolated in 1934 as the hydrolysis product of croton oil, which is derived from the seeds of the purging croton, Croton tiglium. The structure of phorbol was determined in 1967. Various esters of phorbol have important biological properties, the most notable of which is the capacity to act as tumor promoters through activation of protein kinase C. They mimic diacylglycerols, glycerol derivatives in which two hydroxyl groups have reacted with fatty acids to form esters. The most common and potent phorbol ester is 12-O-tetradecanoylphorbol-13-acetate (TPA), also called phorbol-12-myristate-13-acetate (PMA), which is used as a biomedical research tool in models of carcinogenesis.
History and source
Phorbol is a natural product found in many plants, especially those of the Euphorbiaceae and Thymelaeaceae families. Phorbol is identified as the active constituent of the highly toxic New World tropical manchineel or 'beach apple' Hippomane mancinella. It is very soluble in most polar organic solvents, as well as in water. In the manchineel, this leads to an additional exposure risk during rain, where liquid splashing from an undamaged tree may also be injurious. Contact with the tree or consumption of its fruit can lead to symptoms such as severe pain and swelling. Another plant of particular note is Croton tiglium, the source of croton oil from which phorbol was initially isolated. The seeds and oil of C. tiglium have been used for hundreds of years in traditional medicine, generally as a purgative. The seeds have been mentioned in Chinese herbal texts as early as 2000 years ago. The purgative effects of the oil are largely attributed to the high percentage of phorbol esters contained in the oil. Although products derived from the croton plant have been used for thousands of years, phorbol was only isolated from C. Tiglium seeds in 1934. The structure of the compound was determined in 1967, and a total synthesis was described in 2015
Mechanism of action
Phorbol derivatives work primarily by interacting with protein kinase C (PKC), although they can interact with other phospholipid membrane receptors. The esters bind to PKC in a similar way to its natural ligand, diacylglycerol, and activate the kinase. Diacylglycerol is degraded quickly by the body, allowing PKC to be reversibly activated. When phorbol esters bind to the receptor, they are not degraded as efficiently by the body, leading to constitutively active PK. Protein kinase C is involved in a number of important cell signaling pathways. Thus, phorbol ester exposure can show a wide range of results.
The main results of phorbol exposure are tumor promotion and inflammatory response. Although phorbol is not a carcinogen itself, it greatly enhances the action of other substances and promotes tumor proliferation. PKC is a key component in biological pathways controlling cell growth and differentiation. When phorbol esters bind to PKC, cell proliferation pathways are activated. This effect greatly promotes tumors when the cells are exposed to even a sub-carcinogenic amount of a substance. Protein kinase C is also involved in activation of inflammation pathways such as the NF-KB pathway. Thus, exposure to phorbol products can induce an inflammatory response in tissues. Symptoms can include edema and pain, especially to the skin and mucus membranes. While phorbol itself doesn’t have irritant activity, nearly all phorbol esters are highly irritant, with a wide range of ID50s. The LD50 of phorbol esters for male mice was found to be about 27 mg/kg, with the mice showing hemorrhage and congestion of pulmonary blood vessels, as well as lesions throughout the body.
A total synthesis of enantiopure phorbol was developed in 2015. While this synthesis will not replace natural isolation products, it will enable researchers to create phorbol analogues for use in research, especially creating phorbol derivatives that can be used for anti-cancer activity. Previously, the difficulty with synthesizing phorbol had been creating C-C bonds, especially in the 6 membered ring at the top of the molecule. This synthesis starts from (+)-3-carene, and uses a series of 19 steps to eventually create (+) phorbol.
Uses in biomedical research and treatments
Because of their mechanism of action, phorbol esters can be used to study tumor proliferation and pain response. TPA is most commonly used in the laboratory to induce a cellular response. For example, TPA can be used to measure response to pain and test compounds that may mitigate the inflammatory response. TPA and other phorbol esters can also be used to induce tumor formation and elucidate its mechanism. Some phorbol esters have shown anti-cancer activities and can potentially be used as a defense against certain viruses and bacteria. TPA, together with ionomycin, can also be used to stimulate T-cell activation, proliferation, and cytokine production, and is used in protocols for intracellular staining of these cytokines. Phorbol, in the form of croton oil, is also in folk medicine as a purgative, counter irritant, or anthelmintic.
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