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. 2025 Apr 1;46(9):2482–2495. doi: 10.1038/s41401-025-01533-7

Table 4.

Chemical structure analysis of the top four analogs and the last one from Table 3.

R1 R2 R3 R4 R5
Licoflavone C −H graphic file with name 41401_2025_1533_Tabq_HTML.gif graphic file with name 41401_2025_1533_Tabr_HTML.gif −H −OH
Sophoraflavanone G −H2 graphic file with name 41401_2025_1533_Tabs_HTML.gif graphic file with name 41401_2025_1533_Tabt_HTML.gif −H −OH
Licoflavonol graphic file with name 41401_2025_1533_Tabu_HTML.gif −OH −H graphic file with name 41401_2025_1533_Tabv_HTML.gif graphic file with name 41401_2025_1533_Tabw_HTML.gif −OH
Mulberrin graphic file with name 41401_2025_1533_Tabx_HTML.gif graphic file with name 41401_2025_1533_Taby_HTML.gif graphic file with name 41401_2025_1533_Tabz_HTML.gif −H −OH
Kushenol A −H2 graphic file with name 41401_2025_1533_Tabaa_HTML.gif graphic file with name 41401_2025_1533_Tabab_HTML.gif −H −OH
Isoxanthohumol −H2 graphic file with name 41401_2025_1533_Tabac_HTML.gif graphic file with name 41401_2025_1533_Tabad_HTML.gif −H −OCH3