CHEBI:5970 - irilone

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ChEBI Name irilone
ChEBI ID CHEBI:5970
Definition A hydroxyisoflavone that is 6,7-methylenedioxyisoflavone substituted by hydroxy groups at positions 5 and 4'.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C16H10O6
Net Charge 0
Average Mass 298.24700
Monoisotopic Mass 298.048
InChI InChI=1S/C16H10O6/c17-9-3-1-8(2-4-9)10-6-20-11-5-12-16(22-7-21-12)15(19)13(11)14(10)18/h1-6,17,19H,7H2
InChIKey NUGRQNBDTZWXTP-UHFFFAOYSA-N
SMILES Oc1ccc(cc1)-c1coc2cc3OCOc3c(O)c2c1=O
Roles Classification
Biological Role(s): immunomodulator
Biologically active substance whose activity affects or plays a role in the functioning of the immune system.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application(s): immunomodulator
Biologically active substance whose activity affects or plays a role in the functioning of the immune system.
antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing irilone (CHEBI:5970) has role antineoplastic agent (CHEBI:35610)
irilone (CHEBI:5970) has role immunomodulator (CHEBI:50846)
irilone (CHEBI:5970) has role metabolite (CHEBI:25212)
irilone (CHEBI:5970) is a hydroxyisoflavone (CHEBI:38755)
irilone (CHEBI:5970) is a organic heterotricyclic compound (CHEBI:26979)
irilone (CHEBI:5970) is a oxacycle (CHEBI:38104)
Incoming irilone-4'-O-[β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside] (CHEBI:66084) has functional parent irilone (CHEBI:5970)
IUPAC Name
9-hydroxy-7-(4-hydroxyphenyl)-8H-[1,3]dioxolo[4,5-g]chromen-8-one
Synonyms Sources
5,4'-dihydroxy-6,7-methylenedioxyisoflavone ChEBI
9-Hydroxy-7-(4-hydroxyphenyl)-8H-1,3-dioxolo[4,5-g]-1-benzopyran-8-one ChEBI
Irilone KEGG COMPOUND
Irolone HMDB
Manual Xrefs Databases
C00002539 KNApSAcK
C10467 KEGG COMPOUND
HMDB0033820 HMDB
Irilone Wikipedia
LMPK12050383 LIPID MAPS
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Registry Numbers Types Sources
1264266 Reaxys Registry Number Reaxys
41653-81-0 CAS Registry Number KEGG COMPOUND
Citations Waiting for Citations Types Sources
12567273 PubMed citation Europe PMC
19003948 PubMed citation Europe PMC
20349151 PubMed citation Europe PMC
21495101 PubMed citation Europe PMC
22388969 PubMed citation Europe PMC
Last Modified
28 July 2014