Beta-Ureidoizobutirinska kiselina

Beta-Ureidoizobutirinska kiselina
Skeletal formula of beta-ureidoisobutyric acid
Preferentno IUPAC ime

2-Metil-3-ureidopropanoinska kiselina

Naziv po klasifikaciji 3-(Karbamoilamino)-2-metilpropanoinska kiselina[1]
Identifikacija
CAS registarski broj 2905-86-4 DaY
PubChem[2][3] 160663
55289370 R
ChemSpider[4] 141172 DaY
KEGG[5] C05100
MeSH beta-ureidoisobutyric+acid
ChEBI 1670
Bajlštajn 1768736
3DMet B00750
Jmol-3D slike Slika 1
Slika 2
SMILES

CC(C[nH]:c(:[nH2]):[o])c(:[o]):[oH]


CC(CNC(N)=O)C(O)=O

InChI

InChI=1S/C5H10N2O3/c1-3(4(8)9)2-7-5(6)10/h3H,2H2,1H3,(H,8,9)(H3,6,7,10) DaY
Kod: PHENTZNALBMCQD-UHFFFAOYSA-N DaY

Svojstva
Molekulska formula C5H10N2O3
Molarna masa 146.14 g mol−1
Srodna jedinjenja
Srodna alkanoinske kiseline
  • 3-Ureidopropionska kiselina
  • Karbamoil aspartinska kiselina
  • N-Acetilaspartinska kiselina
Srodna jedinjenja
  • Biuret
  • Bromizoval
  • Karbromal

 DaY (šta je ovo?)   (verifikuj)

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

Infobox references

β-Ureidoizobutirinska kiselina je intermedijer u katabolizmu timina.

Reference

  1. „beta-ureidoisobutyric acid - 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. 

Spoljašnje veze

Portal Hemija
  • p
  • r
  • u
Metabolizam purina
R5PIMP: 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)