Fosfatidiletanolamin

Fosfatidiletanolamin (cefalin, PE) je lipid prisutan u biološkim membranama.[4] On se sintetiše adicijom CDP-etanolamina na diglicerid, pri čemu se otpušta CMP. S-adenozil metionin može naknadno da metiliše amin fosfatidiletanolamina i da proizvede fosfatidilholin.

Fosfatidiletanolamin
Phosphatidyl-Ethanolamine.png
Drugi nazivi Cefalin
Identifikacija
PubChem[1][2] 446872
ChemSpider[3] 394115 YesY
MeSH phosphatidylethanolamines
Jmol-3D slike Slika 1

 YesY (šta je ovo?)   (verifikuj)

Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala

Infobox references

ReferenceUredi

  1. Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. http://www.sciencedirect.com/science/article/pii/S1359644610007737.  edit
  2. Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1. 
  3. Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. http://www.jcheminf.com/content/2/1/3.  edit
  4. Wellner N, Diep TA, Janfelt C, Hansen HS (2012-09-08). „N-acylation of phosphatidylethanolamine and its biological functions in mammals.”. Biochim Biophys Acta. DOI:10.1016/j.bbalip.2012.08.019. http://www.ncbi.nlm.nih.gov/pubmed/23000428. 

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