“…Based on the analysis and comparison of NMR data reported in the literature, thirty‐five known compounds were identified, including fraxinuacidoside ( 3 ), [7] 3‐ O ‐methylkaempferol ( 4 ), [8] 8‐methylretusin ( 5 ), [9] 7‐hydroxy‐3′,4′‐methylenedioxyisoflavone ( 6 ), [10] formononetin ( 7 ), [11] calycosin ( 8 ), [12] (2 S )‐pinostrobin ( 9 ), [13] daidzein ( 10 ), [14] 3′,4′,7‐trihydroxyisoflavone ( 11 ), [15] neochamaejasmin A ( 12 ), [16] chamaejasmin D ( 13 ), [17] 3′,4′‐methylenedioxyisoflavone‐7‐ O ‐ β ‐D‐glucopyranoside ( 14 ), [17] ononin ( 15 ), [18] 4′,8‐dimethoxyisoflavone‐7‐ O ‐ β ‐D‐glucopyranoside ( 16 ), [19] sissotorin ( 17 ), [20] genistin ( 18 ), [15] calycosin‐7‐ O ‐ β ‐D‐glucopyranoside ( 19 ), [21] trilobatin ( 20 ), [22] cantoniensin A ( 21 ), [23] hirsutissimiside C ( 22 ), [24] (+)‐pinoresinol ( 23 ), [25] (−)‐syringaresinol ( 24 ), [25] (+)‐medioresinol ( 25 ), [25] (+)‐de‐4′‐ O ‐methylyangabin ( 26 ), [26] (−)‐pinoresinol‐4,4′‐ O ‐ β ‐D‐di‐glucopyranoside ( 27 ), [27] (+)‐medioresinol‐4,4′‐ O ‐ β ‐D‐diglucopyranoside ( 28 ), [28] (−)‐syringaresinol‐4,4′‐ O ‐ β ‐D‐diglucopyranoside ( 29 ), [29] (−)‐isolariciresinol ( 30 ), [30] (−)‐lariciresinol‐4′‐ O ‐ β ‐D‐glucopyranoside ( 31 ), [31] syringin ( 32 ), [32] daphnin ( 33 ), [33] ( S )‐hypaphorine ( 34 ), [34] (3 R )‐1,2,3,4‐tetrahydro‐ β ‐carboline‐3‐carboxylic acid ( 35 ), [35] N ‐ trans‐ caffeoyltyramine ( 36 ), [36] cannabisin B ( 37 ) [37] …”