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 | ![]() |
![]() |
−H | −OH | |
| Sophoraflavanone G | −H2 | ![]() |
![]() |
−H | −OH | |
| Licoflavonol | ![]() |
−OH | −H | ![]() |
![]() |
−OH |
| Mulberrin | ![]() |
![]() |
![]() |
−H | −OH | |
| Kushenol A | −H2 | ![]() |
![]() |
−H | −OH | |
| Isoxanthohumol | −H2 | ![]() |
![]() |
−H | −OCH3 |













