has role is conjugate acid of apigenin 2-(p-hydroxyphenyl)-5,7-dihydroxychromone 270.23690 4',5,7-Trihydroxyflavone 5,7,4'-Trihydroxyflavone 5,7-dihydroxy-2-(4-hydroxyphenyl)-4-benzopyrone 5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one 5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one A trihydroxyflavone that is flavone substituted by hydroxy groups at positions 4', 5 and 7. Apigenin Beilstein:262620 C.I. Natural Yellow 1 C15H10O5 CAS:520-36-5 CHEBI:12084 CHEBI:18388 CHEBI:22588 CHEBI:2768 HMDB:HMDB02124 InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)13-7-12(19)15-11(18)5-10(17)6-14(15)20-13/h1-7,16-18H KEGG:C01477 KNApSAcK:C00003817 KZNIFHPLKGYRTM-UHFFFAOYSA-N LINCS:LSM-5206 LIPID_MAPS_instance:LMPK12110005 MetaCyc:CPD-431 Oc1ccc(cc1)-c1cc(=O)c2c(O)cc(O)cc2o1 PDBeChem:AGI PMID:23304222 PMID:23344191 PMID:23354402 PMID:23359392 Reaxys:262620 Wikipedia:Apigenin chamomile chebi_ontology spigenin versulin metabolite trihydroxyflavone antineoplastic agent apigenin-7-olate