Elaidinska kiselina

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Elaidinska kiselina
Elaidic-acid-2D-skeletal-reverse.png
Elaidic-acid-from-xtal-3D-balls.png
Elaidic-acid-from-xtal-3D-vdW.png
IUPAC ime
Identifikacija
CAS registarski broj 112-79-8 YesY
PubChem[1][2] 637517
ChemSpider[3] 553123 YesY
DrugBank DB04224
KEGG[4] C01712
ChEBI 27997
ChEMBL[5] CHEMBL460657 YesY
Jmol-3D slike Slika 1
Svojstva
Molekulska formula C18H34O2
Molarna masa 282,46 g/mol

 YesY (šta je ovo?)   (verifikuj)

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

Infobox references

Elaidinska kiselina je jedna od najzastupljenijih trans-masti prisutnih u hidrogenisanim biljnim uljima. Ona je javlja u manjim količinama u kozjem i goveđem mleku (oko 0,1% masnih kiselina)[6] i u nekim vrstama mesa. Ona je transizomer oleinske kiseline. Naziv reakcija elaidinizacije potiče od elaidinske kiseline.

Elaidinska kiselina povećava aktivnost proteina holesterilesternog transfera activity, koji povišava nivo VLDL i snižava nivo HDL holesterola.[7]

Reference[uredi - уреди | uredi izvor]

  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. PMID 20970519. doi:10.1016/j.drudis.2010.10.003.  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. PMID 20331846. doi:10.1186/1758-2946-2-3.  edit
  4. Joanne Wixon, Douglas Kell (2000). "Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG". Yeast 17 (1): 48–55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H. 
  5. Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). "ChEMBL: a large-scale bioactivity database for drug discovery". Nucleic Acids Res 40 (Database issue): D1100–7. PMID 21948594. doi:10.1093/nar/gkr777.  edit
  6. Alonso L, Fontecha J, Lozada L, Fraga MJ, Juárez M (1999). "Fatty acid composition of caprine milk: major, branched-chain, and trans fatty acids". J. Dairy Sci. 82 (5): 878–84. PMID 10342226. doi:10.3168/jds.S0022-0302(99)75306-3. 
  7. Abbey M, Nestel PJ (1994). "Plasma cholesteryl ester transfer protein activity is increased when trans-elaidic acid is substituted for cis-oleic acid in the diet". Atherosclerosis 106 (1): 99–107. PMID 8018112. doi:10.1016/0021-9150(94)90086-8. 

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