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. Author manuscript; available in PMC: 2013 Apr 2.
Published in final edited form as: Mol Pharm. 2012 Mar 16;9(4):862–873. doi: 10.1021/mp200400s

Table 1.

Chemical structures of flavonoids used in this study.

Compound Abbreviation Chemical Structure Sub-classes
Naringenin Nar graphic file with name nihms359953t1.jpg flavanone
Phloretin Phlor graphic file with name nihms359953t2.jpg chalcone
Genistein Gen graphic file with name nihms359953t3.jpg isoflavone
Apigenin
5,7,4'-Trihydroxyflavone
Api
5,7,4'-THF
graphic file with name nihms359953t4.jpg flavone
Kaempferol
3,5,7,4’tetrahydroxyflavone
Kamp
3,5,7,4’QHF
graphic file with name nihms359953t5.jpg flavonol
4'-Hydroxyflavone 4HF graphic file with name nihms359953t6.jpg

flavones
5-Hydroxyflavone 5HF graphic file with name nihms359953t7.jpg
7-Hydroxyflavone 7HF graphic file with name nihms359953t8.jpg
5,4'-Dihydroxyflavone 5,4’DHF graphic file with name nihms359953t9.jpg
5,7-Dihydroxyflavone 5,7DHF graphic file with name nihms359953t10.jpg
7,4'-Dihydroxyflavone 7,4’DHF graphic file with name nihms359953t11.jpg
3-Hydroxyflavone 3HF graphic file with name nihms359953t12.jpg flavonols
3,4'-Dihydroxyflavone 3,4’DHF graphic file with name nihms359953t13.jpg
3,7-Dihydroxyflavone 3,7DHF graphic file with name nihms359953t14.jpg
3,5,7-Trihydroxyflavone 3,5,7THF graphic file with name nihms359953t15.jpg
3,7,4'-Trihydroxyflavone 3,7,4’THF graphic file with name nihms359953t16.jpg