Oudenone

Oudenone
Names
	Preferred IUPAC name 2-[(5S)-5-Propyloxolan-2-ylidene]cyclopentane-1,3-dione
Identifiers
CAS Number	31323-50-9 ;
3D model (JSmol)	Interactive image;
ChemSpider	140806 ;
PubChem CID	160199;
UNII	2X2W3L9A37 ;
CompTox Dashboard (EPA)	DTXSID70185252 ;
	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 Key: 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 Key: AFHDYMGMZUYZQT-QMMMGPOBBE;
	SMILES O=C1C(/C(=O)CC1)=C2/O[C@H](CC2)CCC;
Properties
Chemical formula	C12H16O3
Molar mass	208.25 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Oudenone is a molecule found in fungus metabolism.^[1] It is an inhibitor of the enzyme tyrosine hydroxylase.

References

^ 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.

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Names


Preferred IUPAC name 2-[(5S)-5-Propyloxolan-2-ylidene]cyclopentane-1,3-dione
Identifiers
CAS Number	31323-50-9^Y
3D model (JSmol)	Interactive image
ChemSpider	140806^Y
PubChem CID	160199
UNII	2X2W3L9A37^Y
CompTox Dashboard (EPA)	DTXSID70185252
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^Y Key: AFHDYMGMZUYZQT-QMMMGPOBSA-N^Y 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 Key: AFHDYMGMZUYZQT-QMMMGPOBBE
SMILES O=C1C(/C(=O)CC1)=C2/O[C@H](CC2)CCC
Properties
Chemical formula	C₁₂H₁₆O₃
Molar mass	208.25 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is ^YN ?) Infobox references