Ksantozin monofosfat

Ksantozin monofosfat
	5'-ksantilinska kiselina
Drugi nazivi	ksantinski ribotid,; XMP
Identifikacija
CAS registarski broj	523-98-8
PubChem	122280
ChemSpider	66054
KEGG	C00655
MeSH	Xanthosine+monophosphate
ChEBI	CHEBI:15652
Jmol-3D slike	Slika 1
SMILES
	C1=NC2=C(N1[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O)NC(=O)NC2=O
InChI
	InChI=1S/C10H13N4O9P/c15-5-3(1-22-24(19,20)21)23-9(6(5)16)14-2-11-4-7(14)12-10(18)13-8(4)17/h2-3,5-6,9,15-16H,1H2,(H2,19,20,21)(H2,12,13,17,18)/t3-,5-,6-,9-/m1/s1 ; Kod: DCTLYFZHFGENCW-UUOKFMHZSA-N InChI=1/C10H13N4O9P/c15-5-3(1-22-24(19,20)21)23-9(6(5)16)14-2-11-4-7(14)12-10(18)13-8(4)17/h2-3,5-6,9,15-16H,1H2,(H2,19,20,21)(H2,12,13,17,18)/t3-,5-,6-,9-/m1/s1; Kod: DCTLYFZHFGENCW-UUOKFMHZBH
Svojstva
Molekulska formula	C10H13N4O9P
Molarna masa	364,206 g/mol
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Ksantozin monofosfat (XMP^[5]) je intermedijer u purinskom metabolizmu.^[6] On je ribonukleosidni monofosfat. XMP se formira iz inozin monofosfata posredstvom IMP dehidrogenaze, dok se guanozin monofosfat (GMP) formira posredstvom GMP sintaze.

Reference

↑ 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.
↑ Gogia, S.; Balaram, H.; Puranik, M. (May 2011). „Hypoxanthine guanine phosphoribosyltransferase distorts the purine ring of nucleotide substrates and perturbs the pKa of bound xanthosine monophosphate.”. Biochemistry 50 (19): 4184-93. DOI:10.1021/bi102039b. PMID 21486037.
↑ McMurry 2007: str. 1007

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