4,5-Dihidroorotična kiselina

Izvor: Wikipedia
4,5-Dihidroorotična kiselina
4,5-Dihydroorotic acid.svg
IUPAC ime
Identifikacija
CAS registarski broj 155-54-4
PubChem[1][2] 648
ChemSpider[3] 628 YesY
MeSH 4,5-dihydroorotic+acid
ChEBI 30865
ChEMBL[4] CHEMBL75782 YesY
Jmol-3D slike Slika 1
Svojstva
Molekulska formula C5H6N2O4
Molarna masa 158,112 g/mol

 YesY (šta je ovo?)   (verifikuj)

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

Infobox references

4,5-Dihidroorotična kiselina je derivat orotične kiseline koji služi kao intermedijer u biosintezi pirimidina.[5]

Reference[uredi - уреди]

  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. 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
  5. Francois Lacroute (March 1968). "Regulation of Pyrimidine Biosynthesis in Saccharomyces cerevisiae1". J. Bacteriol. 95: 824–832.