Karbamoil aspartinska kiselina
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Nazivi | |
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IUPAC naziv 2-(Karbamoilamino)butandioinska kiselina[1] | |
Identifikacija | |
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3D model (Jmol) |
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3DMet | B00115 |
Bajlštajn | 1726861, 1726860 S |
ChEBI |
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ChemSpider |
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DrugBank |
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ECHA InfoCard | 100.011.906 |
EC broj | 213-096-6 |
KEGG[2] |
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MeSH | ureidosuccinic+acid |
PubChem[3][4] C ID |
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SMILES
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Svojstva | |
C5H8N2O5 | |
Molarna masa | 176,13 g·mol−1 |
log P | −0,663 |
Kiselost (pKa) | 3,649 |
Baznost (pKb) | 10,348 |
Srodna jedinjenja | |
Srodne alkanoinske kiesline |
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Srodna jedinjenja |
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Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa). | |
Reference infokutije | |
Karbamoil aspartinska kiselina (ureidosukcinska kiselina) je karbamatni derivat koji služi kao intermedijar u biosintezi pirimidina.
Reference
- ^ „ureidosuccinic acid - Compound Summary”. PubChem Compound. USA: National Center for Biotechnology Information. 26. 3. 2005. Identification. Приступљено 27. 6. 2012.
- ^ 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.
- ^ 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. уреди
- ^ 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.
Spoljašnje veze
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