“…Identification of individual compounds in C. nitidissima Chi leaf extraction was performed by UHPLC–MS/MS, the chromatogram obtained in the UHPLC was shown in Figure 2. Eight compounds were identified in the C. nitidissima Chi leaf extraction which could be seen in Table 1, using UHPLC–MS/MS based on their molecular masses, fragmentation patterns, and literature references (Duc et al, 1993; Karthivashan et al., 2013; Li et al., 2016; Makita et al., 2016; March et al., 2006; Qiu et al., 2015; Taskin et al., 2020; Wang et al., 2016; Zhang, Feng, et al, 2020; Zhang, Wu, et al., 2020). Among these individuals, multiflorin B(5,7‐dihydroxy‐2‐(4‐hydroxyphenyl)‐4‐oxo‐4H‐1‐benzopyran‐3‐yl 6‐deoxy‐4‐O‐β‐D‐glucopyranosyl‐α‐L‐mannopyranoside), kaempferol‐3‐O‐rutinoside, vicenin‐2(5,7‐dihydroxy‐2‐(4‐hydroxyphenyl)‐6,8‐bis[(2S,3R,4R,5S,6R)‐3,4,5‐trihydroxy‐6‐(hydroxymethyl) oxan‐2‐yl] chromen‐4‐one), apigenin‐6‐C‐pentosyl‐8‐C‐hexosyl, vitexin(5,7‐dihydroxy‐2‐(4‐hydroxyphenyl)‐8‐[(2S,3R,4R,5S,6R)‐3,4,5‐trihydroxy‐6‐(hydroxymethyl) oxan‐2‐yl] chromen‐4‐one), kaempferol, vinaginsenoside R9(2‐[4,5‐dihydroxy‐2‐[[12‐hydroxy‐17‐[5‐hydroxy‐6‐methyl‐2‐[3,4,5‐trihydroxy‐6‐(hydroxymethyl)oxan‐2‐yl]oxyhept‐6‐en‐2‐yl]‐4,4,8,10,14‐pentamethyl‐2,3,5,6,7,9,11,12,13,15,16,17‐dodecahydro‐1H‐cyclopenta[a]phenanthren‐3‐yl]oxy]‐6‐(hydroxymethyl)oxan‐3‐yl]oxy‐6‐(hydroxymethyl)oxane‐3,4,5‐triol), and 20‐glc‐ginsenoside Rf((2S,3R,4S,5S,6R)‐2‐[(2R,3R,4S,5S,6R)‐2‐[[(6R,10R,12S,14R,17S)‐3,12‐dihydroxy‐4,4,10,14,15‐pentamethyl‐17‐[(2S)‐6‐methyl‐2‐[(2S,3R,4S,5S,6R)‐3,4,5‐trihydroxy‐6‐(hydroxymethyl)oxan‐2‐yl]oxyhept‐5‐en‐2‐yl]‐1,2,3,5,6,7,8,9,11,12,13,15,16,17‐tetradecahydrocyclopenta[a]phenanthren‐6‐yl]oxy]‐4,5‐dihydroxy‐6‐(hydroxymethyl)oxan‐3‐yl]oxy‐6‐(hydroxymethyl)oxane‐3,4,5‐triol) or its isomer appeared to be the main components in C. nitidissima Chi leaf extracts.…”