Austrocortirubin

Austrocortirubin
Names
	IUPAC name (5S,7S)-5,7,9,10-Tetrahydroxy-2-methoxy-7-methyl-6,8-dihydro-5H-anthracene-1,4-dione
Identifiers
3D model (JSmol)	Interactive image;
ChemSpider	9384461;
PubChem CID	11209399;
	InChI InChI=1S/C16H16O7/c1-16(22)4-6-10(8(18)5-16)15(21)11-7(17)3-9(23-2)14(20)12(11)13(6)19/h3,8,18-19,21-22H,4-5H2,1-2H3/t8-,16-/m0/s1 Key: WWTHHBSODPGTAK-PWJLMRLQSA-N; InChI=1/C16H16O7/c1-16(22)4-6-10(8(18)5-16)15(21)11-7(17)3-9(23-2)14(20)12(11)13(6)19/h3,8,18-19,21-22H,4-5H2,1-2H3/t8-,16-/m0/s1 Key: WWTHHBSODPGTAK-PWJLMRLQBI;
	SMILES C[C@]1(C[C@@H](C2=C(C3=C(C(=C2C1)O)C(=O)C(=CC3=O)OC)O)O)O;
Properties
Chemical formula	C16H16O7
Molar mass	320.297 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Austrocortirubin is an antibacterial metabolite found in the Dermocybe splendida mushroom.[1][2]

Notes

Beattie KD, Rouf R, Gander L, May TW, Ratkowsky D, Donner CD, et al. (2010). "Antibacterial metabolites from Australian macrofungi from the genus Cortinarius". Phytochemistry. 71 (8–9): 948–55. doi:10.1016/j.phytochem.2010.03.016. PMID 20392467.
Elsworth C, Gill M, Saubern S (2000). "Biosynthesis of tetrahydroanthraquinones in fungi". Phytochemistry. 55 (1): 23–7. doi:10.1016/s0031-9422(00)00181-3. PMID 11021640.

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