CHEBI:10022 - deoxynivalenol

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ChEBI Name deoxynivalenol ChEBI ID CHEBI:10022 Definition A trichothecene mycotoxin produced by Fusarium to which wheat, barley, maize (corn) and their products are susceptible to contamination. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information ChemicalBook:CB0391546, eMolecules:26757232, eMolecules:474372, ZINC000005457778 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License Read full article at Wikipedia Formula C15H20O6 Net Charge 0 Average Mass 296.319 Monoisotopic Mass 296.12599 InChI InChI=1S/C15H20O6/c1-7-3-9-14(5-16,11(19)10(7)18)13(2)4-8(17)12(21-9)15(13)6-20-15/h3,8-9,11-12,16-17,19H,4-6H2,1-2H3/t8-,9-,11-,12-,13-,14-,15+/m1/s1 InChIKey LINOMUASTDIRTM-QGRHZQQGSA-N SMILES [H][C@@]12O[C@]3([H])C=C(C)C(=O)[C@@H](O)[C@]3(CO)[C@@](C)(C[C@H]1O)[C@]21CO1 Metabolite of Species Details Fusarium (NCBI:txid5506) See: PubMed Roles Classification Biological Role(s): mycotoxin Poisonous substance produced by fungi. (via trichothecene ) View more via ChEBI Ontology ChEBI Ontology Outgoing deoxynivalenol (CHEBI:10022) has role mycotoxin (CHEBI:25442) deoxynivalenol (CHEBI:10022) is a cyclic ketone (CHEBI:3992) deoxynivalenol (CHEBI:10022) is a enone (CHEBI:51689) deoxynivalenol (CHEBI:10022) is a primary alcohol (CHEBI:15734) deoxynivalenol (CHEBI:10022) is a secondary α-hydroxy ketone (CHEBI:2468) deoxynivalenol (CHEBI:10022) is a trichothecene (CHEBI:55517) deoxynivalenol (CHEBI:10022) is a triol (CHEBI:27136) Incoming 15-acetyldeoxynivalenol (CHEBI:146194) has functional parent deoxynivalenol (CHEBI:10022) 3-acetyldeoxynivalenol (CHEBI:146195) has functional parent deoxynivalenol (CHEBI:10022) DON-10-gamma-glutamylcysteine (CHEBI:149450) has functional parent deoxynivalenol (CHEBI:10022) DON-10-glutathione (CHEBI:149452) has functional parent deoxynivalenol (CHEBI:10022) DON-10-isoleucine (CHEBI:149454) has functional parent deoxynivalenol (CHEBI:10022) DON-10-leucine (CHEBI:149456) has functional parent deoxynivalenol (CHEBI:10022) DON-10-phenylalanine (CHEBI:149457) has functional parent deoxynivalenol (CHEBI:10022) DON-10-S-cysteine (CHEBI:149447) has functional parent deoxynivalenol (CHEBI:10022) DON-10-tyrosine (CHEBI:149459) has functional parent deoxynivalenol (CHEBI:10022) DON-13-S-cysteine (CHEBI:149448) has functional parent deoxynivalenol (CHEBI:10022) DON-15-penicillin G (CHEBI:149460) has functional parent deoxynivalenol (CHEBI:10022) DON-15-sulfate (CHEBI:149455) has functional parent deoxynivalenol (CHEBI:10022) DON-3-sulfate (CHEBI:149449) has functional parent deoxynivalenol (CHEBI:10022) DON-sulfonate 1 (CHEBI:149440) has functional parent deoxynivalenol (CHEBI:10022) DON-sulfonate 2 (CHEBI:149442) has functional parent deoxynivalenol (CHEBI:10022) DON-sulfonate 3 (CHEBI:149446) has functional parent deoxynivalenol (CHEBI:10022) IUPAC Name 3α,7α,15-trihydroxy-12,13-epoxytrichothec-9-en-8-one Synonyms Sources 3α,7α,15-trihydroxy-12,13-epoxytrichothec-9-en-8-one ChemIDplus 4-Deoxynivalenol ChemIDplus 4-Desoxynivalenol ChemIDplus Dehydronivalenol ChemIDplus Desoxynivalenol ChemIDplus DON KEGG COMPOUND Vomitoxin KEGG COMPOUND Manual Xrefs Databases 36584 ChemSpider C00003201 KNApSAcK C09747 KEGG COMPOUND LMPR0103180002 LIPID MAPS Vomitoxin Wikipedia View more database links Registry Number Type Source 51481-10-8 CAS Registry Number ChemIDplus Citations Types Sources 28780485 PubMed citation Europe PMC 30284112 PubMed citation Europe PMC 30714884 PubMed citation Europe PMC 30760085 PubMed citation Europe PMC 30802751 PubMed citation Europe PMC 30806951 PubMed citation Europe PMC 30841652 PubMed citation Europe PMC 31394401 PubMed citation Europe PMC 31817218 PubMed citation Europe PMC 31867960 PubMed citation Europe PMC 31960350 PubMed citation Europe PMC 32218143 PubMed citation Europe PMC 32260237 PubMed citation Europe PMC 32560237 PubMed citation Europe PMC 32745571 PubMed citation Europe PMC 32805342 PubMed citation Europe PMC 32851525 PubMed citation Europe PMC 32880717 PubMed citation Europe PMC 32930227 PubMed citation Europe PMC Last Modified 23 November 2020