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Homocistein

Izvor: Wikipedija
Homocistein
Skeletal formula
Ball-and-stick model
IUPAC ime
Identifikacija
CAS registarski broj 454-29-5 DaY, 6027-13-0 (L-isomer) DaY
PubChem[1][2] 778
ChemSpider[3] 757 DaY
UNII 0LVT1QZ0BA DaY
EC-broj 207-222-9
KEGG[4] C05330
ChEBI 17230
ChEMBL[5] CHEMBL310604 DaY
Jmol-3D slike Slika 1
Svojstva
Molekulska formula C4H9NO2S
Molarna masa 135,18 g/mol

 DaY (šta je ovo?)   (verifikuj)

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

Infobox references

Homocistein je neproteinska aminokiselina. On je homolog aminokiseline cisteina, od koje se razlikuje po dodatnoj metilenskoj (-CH2-) grupi. On se biosintetiše iz metionina uklanjanjem terminalne Cε metil grupe. Homocistein se može reciklisati u metionin ili konvertovati u cistein uz pomoć B-vitamina.

Detekcija visokih nivoa homocisteina je povezana sa kardiovaskularnim bolesima, mada snižavanje nivoa homocisteina ne poboljšava ishod oboljenja.[6] Povišeni novoi homocisteina su vezani za više stanja bolesti. Korisnost pokušaja snižavanja nivoa homocisteina je bilo nepotvršena ili neubedljiva.[7][8][9][10]

Reference

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  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.  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.  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. DOI:10.1093/nar/gkr777. PMID 21948594.  edit
  6. Martí-Carvajal AJ, Solà I, Lathyris D, Salanti G (2009). Martí-Carvajal, Arturo J. ur. „Homocysteine lowering interventions for preventing cardiovascular events”. Cochrane Database Syst Rev (4): CD006612. DOI:10.1002/14651858.CD006612.pub2. PMID 19821378. 
  7. Martí-Carvajal, AJ; Solà, I; Lathyris, D; Salanti, G. (2009-10-07). „Homocysteine lowering interventions for preventing cardiovascular events.”. Cochrane database of systematic reviews (Online) (4): CD006612. DOI:10.1002/14651858.CD006612.pub2. PMID 19821378. 
  8. Jardine, MJ; Kang, A; Zoungas, S; Navaneethan, SD; Ninomiya, T; Nigwekar, SU; Gallagher, MP; Cass, A; Strippoli, G; Perkovic, V. (2012-06-13). „The effect of folic acid based homocysteine lowering on cardiovascular events in people with kidney disease: systematic review and meta-analysis.”. BMJ (Clinical research ed.) 344: e3533. PMC 3374481. PMID 22695899. 
  9. Vizzardi, E; Bonadei, I; Zanini, G; Frattini, S; Fiorina, C; Raddino, R; Dei Cas, L. (January 2009). „Homocysteine and heart failure: an overview.”. Recent patents on cardiovascular drug discovery 4 (1): 15–21. PMID 19149701. 
  10. Ahmadieh, H; Arabi, A. (October 2011). „Vitamins and bone health: beyond calcium and vitamin D.”. Nutrition Reviews 69 (10): 584–98. DOI:10.1111/j.1753-4887.2011.00372.x. PMID 21967159. 

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