AICA ribonukleotid

AICA ribonukleotid
	[(2R,3S,4R,5R)-5-(4-karbamoil-5-aminoimidazol-1-il)-3,4-dihidroksioksolan-2-il]metil dihidrogen fosfat
Drugi nazivi	AICAR,; Aminoimidazol karboksamid ribonukleotid,; AICA ribonukleotid,; ZMP
Identifikacija
CAS registarski broj	3031-94-5
PubChem	65110
ChemSpider	58620
MeSH	AICA+ribonucleotide
ChEBI	18406
ChEMBL	CHEMBL483849
Jmol-3D slike	Slika 1
SMILES
	O=P(O)(O)OC[C@H]2O[C@@H](n1cnc(C(=O)N)c1N)[C@H](O)[C@@H]2O
InChI
	InChI=1S/C9H15N4O8P/c10-7-4(8(11)16)12-2-13(7)9-6(15)5(14)3(21-9)1-20-22(17,18)19/h2-3,5-6,9,14-15H,1,10H2,(H2,11,16)(H2,17,18,19)/t3-,5-,6-,9-/m1/s1 ; Kod: NOTGFIUVDGNKRI-UUOKFMHZSA-N InChI=1/C9H15N4O8P/c10-7-4(8(11)16)12-2-13(7)9-6(15)5(14)3(21-9)1-20-22(17,18)19/h2-3,5-6,9,14-15H,1,10H2,(H2,11,16)(H2,17,18,19)/t3-,5-,6-,9-/m1/s1; Kod: NOTGFIUVDGNKRI-UUOKFMHZBG
Svojstva
Molekulska formula	C9H15N4O8P
Molarna masa	338,211 g/mol
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

5-Aminoimidazol-4-karboksamid ribonukleotid (5-amino-1-β-D-ribofuranozil-imidazol-4-karboksamid, ZMP) je intermedijer u formiranju inozin monofosfata.

AICA-Ribonukleotid (AICAR)

AICAR je analog AMP molekula. On ima sposobnost stimulisanja aktivnosti AMP-zavisne proteinske kinaze (AMPK). AICAR se klinički koristi za tretiranje i zaštitu od srčanih ishemijskih povreda. U odsustvu tretmana dolazi do srčanog udara. Srčana ishemija je uzrokovana nedovljnim krvnim protokom i dovodom kiseonika do miokarda^[5] Ovaj lek je prvobitno korišten tokom 1980-tih kao metod za očuvanje krvnog protoka do srca tokom operacija.^[6] U današnje vreme se lek koristi i za treatment dijabetesa, jer povećava metaboličku aktivnost tkiva putem promena fizičke kompozicije mišića.^[7]

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
↑ Corton JM, Gillespie JG, Hawley SA, Hardie DG. 5-aminoimidazole-4-carboxamide ribonucleoside. A specific method for activating AMP-activated protein kinase in intact cells? Eur J Biochem 229:558–565(1995)
↑ Galinanes M, Bullough D, Mullane KM, Hearse DJ. Sustained protection by acadesine against ischemia- and reperfusion-induced injury. Studies in the transplanted rat heart.Circulation 86:589–597 (1992)
↑ Zarembo, Alan. "'Exercise pill' could take the work out of workouts." Los Angeles Times [Los Angeles] 01 08 2008, n. pag. Web. 21 Jan. 2012.

Povezano

Inozin monofosfat sintaza

Šablon:Nukleotidni metabolički intermedijari

[1] 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

[2] 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.

[3] 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

[4] 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

[5] Corton JM, Gillespie JG, Hawley SA, Hardie DG. 5-aminoimidazole-4-carboxamide ribonucleoside. A specific method for activating AMP-activated protein kinase in intact cells? Eur J Biochem 229:558–565(1995)

[6] Galinanes M, Bullough D, Mullane KM, Hearse DJ. Sustained protection by acadesine against ischemia- and reperfusion-induced injury. Studies in the transplanted rat heart.Circulation 86:589–597 (1992)

[7] Zarembo, Alan. "'Exercise pill' could take the work out of workouts." Los Angeles Times [Los Angeles] 01 08 2008, n. pag. Web. 21 Jan. 2012.

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