Austrocortirubin
Names
Preferred IUPAC name
(5S,7S)-5,7,9,10-Tetrahydroxy-2-methoxy-7-methyl-5,6,7,8-tetrahydroanthracene-1,4-dione
Identifiers
3D model (JSmol)
ChemSpider
  • 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
  • C[C@]1(C[C@@H](C2=C(C3=C(C(=C2C1)O)C(=O)C(=CC3=O)OC)O)O)O
Properties
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.[2][3]

Notes

  1. ↑ Buckingham, John (2 December 1993). Dictionary of Natural Products. CRC Press. p. 564. ISBN 978-0-412-46620-5.
  2. ↑ 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.
  3. ↑ 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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