CHEBI:2512 - agathisflavone

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ChEBI Name agathisflavone
ChEBI ID CHEBI:2512
Definition A biflavonoid that is obtained by oxidative coupling of two molecules of apigenin resulting in a bond between positions C-6 and C-8 of the two chromene rings.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C30H18O10
Net Charge 0
Average Mass 538.45792
Monoisotopic Mass 538.09000
InChI InChI=1S/C30H18O10/c31-15-5-1-13(2-6-15)22-11-20(36)26-24(39-22)12-21(37)27(29(26)38)28-18(34)9-17(33)25-19(35)10-23(40-30(25)28)14-3-7-16(32)8-4-14/h1-12,31-34,37-38H
InChIKey BACLASYRJRZXMY-UHFFFAOYSA-N
SMILES Oc1ccc(cc1)-c1cc(=O)c2c(O)c(c(O)cc2o1)-c1c(O)cc(O)c2c1oc(cc2=O)-c1ccc(O)cc1
Roles Classification
Biological Role(s): antiviral agent
A substance that destroys or inhibits replication of viruses.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
hepatoprotective agent
Any compound that is able to prevent damage to the liver.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing agathisflavone (CHEBI:2512) has role antineoplastic agent (CHEBI:35610)
agathisflavone (CHEBI:2512) has role antiviral agent (CHEBI:22587)
agathisflavone (CHEBI:2512) has role hepatoprotective agent (CHEBI:62868)
agathisflavone (CHEBI:2512) has role metabolite (CHEBI:25212)
agathisflavone (CHEBI:2512) is a biaryl (CHEBI:64459)
agathisflavone (CHEBI:2512) is a biflavonoid (CHEBI:50128)
agathisflavone (CHEBI:2512) is a hydroxyflavone (CHEBI:24698)
IUPAC Name
5,5',7,7'-tetrahydroxy-2,2'-bis(4-hydroxyphenyl)-6,8'-bichromene-4,4'-dione
Synonyms Sources
5,5',7,7'-tetrahydroxy-2,2'-bis(4-hydroxyphenyl)-(6,8'-bi-4H-1-benzopyran)-4,4'-dione ChemIDplus
6,8''-Biapigenin KEGG COMPOUND
Agathisflavone KEGG COMPOUND
Manual Xrefs Databases
C00001014 KNApSAcK
C10017 KEGG COMPOUND
US2002068757 Patent
WO9700679 Patent
View more database links
Registry Numbers Types Sources
1415839 Beilstein Registry Number Beilstein
1415839 Reaxys Registry Number Reaxys
28441-98-7 CAS Registry Number KEGG COMPOUND
28441-98-7 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
1484886 PubMed citation Europe PMC
21106357 PubMed citation Europe PMC
21281018 PubMed citation Europe PMC
21594945 PubMed citation Europe PMC
Last Modified
28 July 2014