Phosphorylethanolamine
Names
Preferred IUPAC name
2-Aminoethyl dihydrogen phosphate
Other names
Phosphoethanolamine; PHOS
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.012.717
MeSH phosphorylethanolamine
UNII
  • InChI=1S/C2H8NO4P/c3-1-2-7-8(4,5)6/h1-3H2,(H2,4,5,6) checkY
    Key: SUHOOTKUPISOBE-UHFFFAOYSA-N checkY
  • C(COP(=O)(O)O)N
Properties
C2H8NO4P
Molar mass 141.063 g·mol−1
Appearance White powder
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Phosphorylethanolamine or phosphoethanolamine is an ethanolamine derivative that is used to construct two different categories of phospholipids. One category termed a glycerophospholipid and the other a sphingomyelin, or more specifically within the sphingomyelin class, a sphingophospholipid. Phosphorylethanolamine is a polyprotic acid with two pKa values at 5.61 and 10.39.[1]

Phosphorylethanolamine has been falsely promoted as a cancer treatment.[2]

Effectiveness

As a potential drug, phosphorylethanolamine has undergone human clinical trials. These were halted when no evidence of benefit was found.[3][2]

Edzard Ernst has called Phosphorylethanolamine "the most peculiar case of Brazilian quackery".[2]

Legality

There has been ongoing controversy and litigation in Brazil with regard to its use as a cancer treatment without approval by the National Health Surveillance Agency. For years, Gilberto Chierice, a Chemistry Professor at the São Carlos campus of the University of São Paulo, used resources from a campus laboratory to unofficially manufacture, distribute, and promote the drug to cancer patients without it having gone through clinical testing. In September 2015, university administrators began preventing the Professor from continuing with this practice. In October 2015, several courts in Brazil ruled in favor of plaintiffs who wanted the right to try the compound. However, a state court overturned the lower courts' decision a month later. Jailson Bittencourt de Andrade, secretary for Brazil's science and technology ministry, said the ministry plans to fund further research on the compound, but that it will be years before a determination can be made about phosphorylethanolamine's safety and efficacy in humans.[4][5]

On April 14, 2016, a law was passed in Brazil allowing the use of synthetic phosphorylethanolamine for cancer treatment,[6] despite opposition from the Brazilian Medical Association, the Brazilian Society of Clinical Oncology, and the regulatory agency Anvisa.[7] However, shortly after, the country's Supreme Court suspended the law.[8]

See also

References

  1. ↑ Myller, AT; et al. (2010). "Preparation of aminofunctionalized TiO2 surfaces by binding of organophosphates". Applied Surface Science. 257 (5): 1616–1622. Bibcode:2010ApSS..257.1616M. doi:10.1016/j.apsusc.2010.08.109.
  2. 1 2 3 Edzard Ernst (28 November 2018). "The amazing story of a Brazilian cancer 'cure'".
  3. ↑ "Fosfoetanolamina: Instituto do Câncer suspende novos testes devido a 'ausência de benefício clínico significativo'" [Phosphorylethanolamine: Cancer Institute suspends new tests due to 'lack of significant clinical benefits'] (in Portuguese). 31 March 2017. Retrieved 10 January 2018.
  4. ↑ Heidi Ledford (24 November 2015). "Brazilian courts tussle over unproven cancer treatment". Nature. 527 (7579): 420–421. Bibcode:2015Natur.527..420L. doi:10.1038/527420a. PMID 26607521. S2CID 3011466.
  5. ↑ Escobar, H. (2016). "Brazil bill would legalize renegade cancer pill". Science. 352 (6281): 18. Bibcode:2016Sci...352...18E. doi:10.1126/science.352.6281.18. PMID 27034350.
  6. ↑ Escobar, Herton (2016). "Brazil president signs law legalizing renegade cancer pill". Science. doi:10.1126/science.aaf9915.
  7. ↑ Noam Pondé; Felipe Ades; Evandro de Azambuja (2016). "Threat posed by unproven drugs in medical oncology". ESMO Open. 1 (3): e000064. doi:10.1136/esmoopen-2016-000064. PMC 5070266. PMID 27843615.
  8. ↑ "Human tests start on controversial Brazil cancer pill". 25 July 2016. Archived from the original on 2016-07-27.

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