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xylindein

Structure via PubChem · Public domain (PubChem)

EntityQ10856929· pop 6· linked from 5 articles

Xylindein is a quinone pigment, a dimeric naphthoquinone derivative. It is produced by fungi in the genus Chlorociboria. This pigment causes green staining of wood infected by the fungi.

Chemical data

Formula
C32H24O10
Molecular weight
568.5 g/mol
IUPAC name
(7S,20S)-11,24-dihydroxy-7,20-dipropyl-8,16,21,30-tetraoxaoctacyclo[15.11.1.14,28.02,15.03,12.05,10.018,23.025,29]triaconta-1,3,5(10),11,14,17(29),18(23),24,27-nonaene-9,13,22,26-tetrone
SMILES
CCC[C@H]1CC2=C(C(=C3C(=O)C=C4C5=C6C(=CC(=O)C7=C(C8=C(C[C@@H](OC8=O)CCC)C(=C67)O4)O)OC2=C53)O)C(=O)O1
InChIKey
BZFKYROURDRMSO-RYUDHWBXSA-N
XLogP
4.9
Polar surface area
146 Ų
H-bond donors
2
H-bond acceptors
10
Formal charge
0

via PubChem

Wikidata facts

Mass
568.136946968
Show 5 more facts
canonical SMILES
CCCC1CC2=C3C4=C(C(=O)C=C5C4=C6C(=CC(=O)C7=C6C(=C8CC(OC(=O)C8=C7O)CCC)O5)O3)C(=C2C(=O)O1)O
isomeric SMILES
CCC[C@H]1CC2=C3C4=C(C(=O)C=C5C4=C6C(=CC(=O)C7=C6C(=C8C[C@@H](OC(=O)C8=C7O)CCC)O5)O3)C(=C2C(=O)O1)O
chemical formula
C₃₂H₂₄O₁₀
Commons category
Xylindein
Sources (2)

via Wikidata · CC0

~1 min read

Encyclopedic overview

3 sections
Contents
  • Etymology
  • References
  • External links

Xylindein is a quinone pigment, a dimeric naphthoquinone derivative. It is produced by fungi in the genus Chlorociboria. This pigment causes green staining of wood infected by the fungi.

==Etymology==

Excerpted from Wikipedia’s “xylindein” article, available under the CC BY-SA 4.0 licence.

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