Anserin
| Nazivi | |
|---|---|
| IUPAC naziv
(2S)-2-[(3-Amino-1-oksopropil)amino]-3-(3-metil-4-imidazolil)propanoinska kiselina
| |
| Drugi nazivi
beta-Alanil-N(pi)-metil-L-histidin
| |
| Identifikacija | |
3D model (Jmol)
|
|
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.008.679 |
| KEGG[1] | |
| |
| Svojstva | |
| C10H16N4O3 | |
| Molarna masa | 240,25904 |
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa). | |
| Reference infokutije | |
Anserin (beta-alanil-N-metilhistidin) je dipeptid prisutan u skeletalnim mišićima i mozgu sisara[4] and birds.
On je antioksidans (oko 5 puta jači od karnozina). pKa vrednost imidazolnog prstena histidina u anserinu je 7,04. Iz tog razloga je arserin efektivan bufer na fiziolopkom pH.[5]
Reference
- ^ 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.
- ^ 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.
- ^ Quantitative studies of carnosine and anserine in mammalian muscle. 1938 (pdf)
- ^ Biochemistry, Garrett & Grisham
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