Phosphorylethanolamine

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Phosphorylethanolamine
Phosphorylethanolamine.svg
Names
IUPAC name
2-Aminoethyl dihydrogen phosphate
Other names
Phosphoethanolamine; PHOS
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
DrugBank
ECHA InfoCard 100.012.717
MeSH phosphorylethanolamine
UNII
Properties
C2H8NO4P
Molar mass 141.06 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).
N verify (what is YesYN ?)
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]

Research[edit]

Research is being conducted with Ehrlich ascites tumor cells in vitro to see if phosphoethanolamine could be used in cancer treatment.[2] In studies in rats, phosphorylethanolamine failed to stop the growth of tumors.[3][4]

There is, however, an experiment with mice that stated synthetic phosphoethanolamine has in vitro and in vivo anti-leukemia effects.[5]

As a potential drug, phosphorylethanolamine has never been evaluated in human clinical trials.[6][7]

The main synthetic form of phosphorylethanolamine is calcium 2-aminoethylphosphate.

Legality[edit]

There has been ongoing controversy and litigation in Brazil with regard to its use as a cancer treatment prior to approval by the National Health Surveillance Agency. In September 2015, administrators at the University of São Paulo attempted to prevent chemists at the São Carlos campus from continuing to unofficially manufacture, distribute, and promote the drug to cancer patients since it had not been tested in humans yet. 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 phosphoethanolamine's safety and efficacy in humans.[8][9]

On April 14, 2016, a law was passed in Brazil allowing the use of synthetic phosphoethanolamine for cancer treatment,[10] despite opposition from the Brazilian Medical Association, the Brazilian Society of Clinical Oncology, and the regulatory agency ANVISA.[11] However, shortly after, the country's Supreme Court suspended the law.[12]

See also[edit]

References[edit]

  1. ^ Myller, AT; et al. (2010). "Preparation of aminofunctionalized TiO2 surfaces by binding of organophosphates". Applied Surface Science. 257 (5): 1616. Bibcode:2010ApSS..257.1616M. doi:10.1016/j.apsusc.2010.08.109. 
  2. ^ Ferreira, Adilson Kleber; Meneguelo, Renato; Pereira, Alexandre; Mendonça Filho, Otaviano R.; Chierice, Gilberto Orivaldo; Maria, Durvanei Augusto (2012-01-01). "Anticancer effects of synthetic phosphoethanolamine on Ehrlich ascites tumor: an experimental study". Anticancer Research. 32 (1): 95–104. ISSN 1791-7530. PMID 22213293. 
  3. ^ "Cancer Pill Fails. Again.". June 2, 2016. 
  4. ^ "Effectiveness of 'Cancer Pill' Disproved in New Test". June 1, 2016. 
  5. ^ Ferreira, A K; Santana-Lemos, B A A; Rego, E M; Filho, O M R; Chierice, G O; Maria, D A (2013). "Synthetic phosphoethanolamine has in vitro and in vivo anti-leukemia effects". British Journal of Cancer. 109: 2819–2828. doi:10.1038/bjc.2013.510. 
  6. ^ "Drugs on demand". Nature. 527 (7579): 410. 2015. Bibcode:2015Natur.527R.410.. doi:10.1038/527410b. 
  7. ^ Pondé, Noam; De Azambuja, Evandro; Ades, Felipe (2016). "Phosphoethanolamine and the danger of unproven drugs". Ecancermedicalscience. 10. doi:10.3332/ecancer.2016.681. 
  8. ^ Heidi Ledford (24 November 2015). "Brazilian courts tussle over unproven cancer treatment". Nature. 527 (7579): 420. Bibcode:2015Natur.527..420L. PMID 26607521. doi:10.1038/527420a. 
  9. ^ Escobar, H. (2016). "Brazil bill would legalize renegade cancer pill". Science. 352 (6281): 18. PMID 27034350. doi:10.1126/science.352.6281.18. 
  10. ^ Herton Escobar (14 April 2016). "Brazil president signs law legalizing renegade cancer pill". Sciencemag.com. doi:10.1126/science.aaf4126. 
  11. ^ Noam Pondé; Felipe Ades; Evandro de Azambuja (2016). "Threat posed by unproven drugs in medical oncology". Cancer Horizons. 1 (3): e000064. doi:10.1136/esmoopen-2016-000064. 
  12. ^ "Human tests start on controversial Brazil cancer pill". 25 July 2016. Archived from the original on 2016-07-27. 

Additional images[edit]