N-Acetilaspartinska kiselina
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IUPAC ime
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2-Acetamidobutandioinska kiselina[1] |
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Identifikacija
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CAS registarski broj
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2545-40-6 Y, 997-55-7 S Y
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PubChem[2][3]
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97508, 774916 R, 65065 S
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ChemSpider[4]
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88007 Y, 677387 R Y
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EINECS broj
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219-827-5
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KEGG[5]
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C01042
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MeSH
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N-acetylaspartate
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ChEBI
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21547
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ChEMBL[6]
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CHEMBL1162493 Y
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RTECS registarski broj toksičnosti
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CI9098600
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Bajlštajn
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1726198 S
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3DMet
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B00227
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Jmol-3D slike
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Slika 1 Slika 2
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Cc(:[o]):[nH]C(Cc(:[o]):[oH])c(:[o]):[oH]
CC(=O)NC(CC(O)=O)C(O)=O |
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InChI=1S/C6H9NO5/c1-3(8)7-4(6(11)12)2-5(9)10/h4H,2H2,1H3,(H,7,8)(H,9,10)(H,11,12) N Kod: OTCCIMWXFLJLIA-UHFFFAOYSA-N N |
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Svojstva
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Molekulska formula
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C6H9NO5
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Molarna masa
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175.14 g mol−1
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Agregatno stanje
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Bezbojni, transparentni kristali
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Tačka ključanja
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141-144 °C, 414-417 K, 286-291 °F
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log P
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−2.209
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pKa
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3.142
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Baznost (pKb)
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10.855
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Opasnost
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S-oznake
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S22, S24/25
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Srodna jedinjenja
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Srodna alkanoinske kiseline
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Srodna jedinjenja
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Y (šta je ovo?)
(verifikuj)
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
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Infobox references
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N-Acetilaspartic acid (N-acetilaspartat, NAA) je derivat aspartinske kiseline sa formulom C6H9NO5 i molekulskom težinom 175,139.
NAA je drugi po zastupljenosti neurotransmiter u mozgu, posle glutamatne aminokiseline. On je prisutan u mozgu odraslih osoba jedino u neuronima.[7] Sintetiše se u mitochondrijama[8] iz aspartinske kiseline i acetil-koenzimA A.
- ↑ „N-acetylaspartate - Compound Summary”. PubChem Compound. USA: National Center for Biotechnology Information. 26. 3. 2005.. Identification. Pristupljeno 8. 1. 2012.
- ↑ 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
- ↑ 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.
- ↑ 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
- ↑ 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.
- ↑ 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
- ↑ Simmons, Frondoza et al. 1991 PMID 1754068; Moffett, Namboodiri et al. 1991
- ↑ Patel, T. B. and J. B. Clark (1979). "Synthesis of N-acetyl-L-aspartate by rat brain mitochondria and its involvement in mitochondrial/cytosolic carbon transport." Biochem J 184(3): 539-46.
- N-Acetylaspartate: A Unique Neuronal Molecule in the Central Nervous System, eds., J.R.Moffett, S.B.Tieman, D.R.Weinberger, J.T.Coyle, and M.A.Namboodiri, pp. 7–26. New York, NY: Springer Science + Business Media, 2006.
- Biochemical Support for the "Threshold" Theory of Creativity: A Magnetic Resonance Spectroscopy Study, Rex E. Jung et al., April 22, 2009, 29(16):5319-5325; DOI:10.1523/JNEUROSCI.0588-09.2009