Oudenon

Oudenon
	(5S)-2-(5-propil-2-tetrahidrofuraniliden)ciklopentan-1,3-dion
Identifikacija
CAS registarski broj	31323-50-9
PubChem	160199
ChemSpider	140806
Jmol-3D slike	Slika 1
SMILES
	O=C1C(/C(=O)CC1)=C2/O[C@H](CC2)CCC
InChI
	InChI=1S/C12H16O3/c1-2-3-8-4-7-11(15-8)12-9(13)5-6-10(12)14/h8H,2-7H2,1H3/t8-/m0/s1 ; Kod: AFHDYMGMZUYZQT-QMMMGPOBSA-N InChI=1/C12H16O3/c1-2-3-8-4-7-11(15-8)12-9(13)5-6-10(12)14/h8H,2-7H2,1H3/t8-/m0/s1; Kod: AFHDYMGMZUYZQT-QMMMGPOBBE
Svojstva
Molekulska formula	C12H16O3
Molarna masa	208,25 g/mol
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Oudenon je molekul koji učestvuje u metabolizmu gljiva.^[4] On je inhibitor enzima tirozinska hidroksilaza.

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
↑ Tsantrizos YS, Yang X, McClory A (September 1999). „Studies on the Biosynthesis of the Fungal Metabolite Oudenone. 2. Synthesis and Enzymatic Cyclization of an alpha-Diketone, Open-Chain Precursor into Oudenone in Cultures of Oudemansiella radicata”. J. Org. Chem. 64 (18): 6609–6614. DOI:10.1021/jo9901135. PMID 11674663.

Portal Hemija