InChI=1S/C29H26O10/c1- 10(30) 5- 12- 18- 19- 13(6- 11(2) 31) 29(37- 4) 27(35) 21- 15(33) 8- 17- 23(25(19) 21) 22- 16(38- 9- 39- 17) 7- 14(32) 20(24(18) 22) 26(34) 28(12) 36- 3/h7- 8,10- 11,30- 33H,5- 6,9H2,1- 4H3/t10- ,11- /m1/s1 |
DGAZLNHJYDOWLG-GHMZBOCLSA-N |
C1=2C3=C4C5=C(C(=O)C(=C4C[C@@H](C)O)OC)C(O)=CC6=C5C1=C(C=C(C2C(=O)C(=C3C[C@@H](C)O)OC)O)OCO6 |
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Pseudocercosporella capsellae
(NCBI:txid1873268)
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See:
PubMed
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Cercospora coffeicola
(NCBI:txid225974)
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See:
DOI
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Cercospora
(NCBI:txid29002)
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See:
DOI
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Cercospora kikuchii
(NCBI:txid84275)
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Isolated from dried mycelia.
See:
DOI
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reactive oxygen species generator
Any entity used to generate reactive oxygen species.
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phytotoxin
Any toxin produced by a plant.
fungal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
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photosensitizing agent
A chemical compound that can be excited by light of a specific wavelength and subsequently transfer energy to a chosen reactant. This is commonly molecular oxygen within a cancer tissue, which is converted to (highly rective) singlet state oxygen. This rapidly reacts with any nearby biomolecules, ultimately killing the cancer cells.
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View more via ChEBI Ontology
5,12- dihydroxy- 8,9- bis[(2R)- 2- hydroxypropyl]- 7,10- dimethoxyperylo[1,12- def][1,3]dioxepine- 6,11- dione
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(+)-cercosporin
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ChEBI
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cercosporin
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KEGG COMPOUND
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35082-49-6
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CAS Registry Number
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ChemIDplus
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