InChI=1S/C27H29N3O13S/c1-40-13-6-14-19(22-18(13)9-2-4-12(31)17(9)25(39)42-22)20-21(35)27(43-26(20)41-14)44-8-11(23(36)29-7-16(33)34)30-15(32)5-3-10(28)24(37)38/h6,10-11,20-21,26-27,35H,2-5,7-8,28H2,1H3,(H,29,36)(H,30,32)(H,33,34)(H,37,38)/t10-,11-,20+,21+,26-,27-/m0/s1 |
LYDBAPNRLUDIAS-GPQHGYBDSA-N |
[H][C@]12O[C@@H](SC[C@H](NC(=O)CC[C@H](N)C(O)=O)C(=O)NCC(O)=O)[C@H](O)[C@@]1([H])c1c(O2)cc(OC)c2c3CCC(=O)c3c(=O)oc12 |
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xenobiotic metabolite
Any metabolite produced by metabolism of a xenobiotic compound.
mycotoxin
Poisonous substance produced by fungi.
(via aflatoxin )
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View more via ChEBI Ontology
L-γ-glutamyl-S-{(6aS,8S,9R,9aR)-9-hydroxy-4-methoxy-1,11-dioxo-1,2,3,6a,8,9,9a,11-octahydrocyclopenta[c]furo[3',2':4,5]furo[2,3-h]chromen-8-yl}-L-cysteinylglycine
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8,9-Dihydro-8-(S-glutathionyl)-9-hydroxyaflatoxin B1
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KEGG COMPOUND
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Afb(1)-gsh
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ChemIDplus
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Afb1-gsh conjugate
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ChemIDplus
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aflatoxin B1 exo-8,9-epoxide‒GSH
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ChEBI
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Aflatoxin B1exo-8,9-epoxide-GSH
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KEGG COMPOUND
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68385-50-2
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CAS Registry Number
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KEGG COMPOUND
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68385-50-2
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CAS Registry Number
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ChemIDplus
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3933841
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PubMed citation
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Europe PMC
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6411367
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PubMed citation
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Europe PMC
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