3-Ureidopropionska kiselina

3-Ureidopropionska kiselina
Skeletal formula of 3-ureidopropionic acid
Preferentno IUPAC ime

3-Ureidopropanoinska kiselna

Naziv po klasifikaciji 3-(Karbamoilamino)propanoinska kiselina[1]
Identifikacija
CAS registarski broj 462-88-4 DaY
PubChem[2][3] 111
ChemSpider[4] 109 DaY
KEGG[5] C02642
MeSH N-carbamoyl-beta-alanine
ChEBI 18261
ChEMBL[6] CHEMBL20962 DaY
Bajlštajn 1705263
Gmelin Referenca 675230
3DMet B00472
Jmol-3D slike Slika 1
Slika 2
SMILES

[nH2]:c(:[o]):[nH]CCc(:[o]):[oH]

NC(=O)NCCC(O)=O

InChI

InChI=1S/C4H8N2O3/c5-4(9)6-2-1-3(7)8/h1-2H2,(H,7,8)(H3,5,6,9) DaY
Kod: JSJWCHRYRHKBBW-UHFFFAOYSA-N DaY

Svojstva
Molekulska formula C4H8N2O3
Molarna masa 132.12 g mol−1
Agregatno stanje Beli kristali
log P −1,23
pKa 4,408
Baznost (pKb) 9,589
Opasnost
S-oznake S22, S24/25
Srodna jedinjenja
Srodna alkanoinske kiseline
Srodna jedinjenja

 DaY (šta je ovo?)   (verifikuj)

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

Infobox references

3-Ureidopropionska kiselna je intermedijer u metabolizmu uracila. Ona je derivat ureje i beta-alanina.

Reference

  1. ↑ „N-carbamoyl-beta-alanine - Compound Summary”. PubChem Compound. USA: National Center for Biotechnology Information. 16. 9. 2004.. Identification. Pristupljeno 28. 6. 2012. 
  2. ↑ 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
  3. ↑ 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. 
  4. ↑ 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
  5. ↑ 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. 
  6. ↑ 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
  • p
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Metabolizam purina
R5P→IMP: R5P • PRPP • PRA • GAR • FGAR • FGAM • AIR • CAIR • SAICAR • AICAR • FAICAR

IMP→AMP: Adenilosukcinat

IMP→GMP: Ksantozin monofosfat
Metabolizam pirimidina

M: MET

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)