5-Formamidoimidazol-4-karboksamid ribotid

5-Formamidoimidazol-4-karboksamid ribotid
	[(2R,3S,4R,5R)-5-(4-karbamoil-5-formamidoimidazol-1-il)- 3,4-dihidroksioksolan-2-il]metil dihidrogen fosfat
Drugi nazivi	5-Formamidoimidazol-4-karboksamid ribonukleotid,; FAICAR
Identifikacija
CAS registarski broj	13018-54-7
PubChem	166760
ChemSpider	145893
MeSH	5-formamidoimidazole-4-carboxamide+ribotide
ChEBI	18381
ChEMBL	CHEMBL521310
Jmol-3D slike	Slika 1; Slika 2
SMILES
	C1=NC(=C(N1[C@H]2[C@@H]([C@@H]([C@H] (O2)COP(=O)(O)O)O)O)NC=O)C(=O)N O=P(O)(O)OC[C@H]2O[C@@H](n1cnc(C(=O)N)c1NC=O)[C@H](O)[C@@H]2O
InChI
	InChI=1S/C10H15N4O9P/c11-8(18)5-9(13-3-15)14(2-12-5)10-7(17)6(16)4(23-10)1-22-24(19,20)21/h2-4,6-7,10,16-17H,1H2,(H2,11,18)(H,13,15)(H2,19,20,21)/t4-,6-,7-,10-/m1/s1 ; Kod: ABCOOORLYAOBOZ-KQYNXXCUSA-N InChI=1/C10H15N4O9P/c11-8(18)5-9(13-3-15)14(2-12-5)10-7(17)6(16)4(23-10)1-22-24(19,20)21/h2-4,6-7,10,16-17H,1H2,(H2,11,18)(H,13,15)(H2,19,20,21)/t4-,6-,7-,10-/m1/s1; Kod: ABCOOORLYAOBOZ-KQYNXXCUBS
Svojstva
Molekulska formula	C10H15N4O9P
Molarna masa	366,22 g/mol
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

5-Formamidoimidazol-4-karboksamid ribotid (FAICAR) je intermedijer pri formiranju purina. On se formira posredstvom enzima AICAR transformilaza iz AICAR i 10-formiltetrahidrofolata.

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
↑ 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

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