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Table 3 The main flavonoids in HX_1 and ZZ_1

From: Transcriptome and metabolome analysis reveals anthocyanin biosynthesis pathway associated with ramie (Boehmeria nivea (L.) Gaud.) leaf color formation

m/z Metabolites Compound ID Sub Class HX_1 ZZ_1 FC
373.1 3′,4′-Methylenedioxy-2,4,6, beta-tetramethoxychalcone LMPK12020254 Flavonoids 630.56 182.18 3.46
389.1 3-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxy-8 methyl-3,4-dihydro-2H-1-benzopyran-4-one HMDB0129573 O-methylated isoflavonoids 1064.87 330.41 3.22
341.1 Brosimacutin D LMPK12140055 Flavonoids 332.41 41.46 8.02
665.2 Nirurin LMPK12140614 Flavonoids 2797.60 213.74 13.09
523.2 Dichotosinin LMPK12020273 Flavonoids 9362.60 4261.89 2.20
663.2 Flavaprenin 7,4′-diglucoside LMPK12140228 Flavonoids 2945.23 203.81 14.45
538.2 (7′S,8′S)-4,7′-Epoxy-3,8′-bilign-7-ene-3′,5 dimethoxy-4′,9,9′-triol 4′-glucoside HMDB0040636 2-arylbenzofuran flavonoids 610.02 121.62 5.02
583.2 8-trans-[2-(6-Benzoyloxy-4-hydroxy-2-methoxy-3-methylphenyl) ethenyl]-5-methoxyflavan-7-ol LMPK12020254 Flavonoids 993.88 278.95 3.56
903.3 Chamuvaritin LMPK12120473 Flavonoids 4859.48 2062.92 2.36
811.3 3-(3-hydroxyphenyl)-2-phenyl-4-[(E)-2-phenylethenyl] 2,3-dihydro-1-benzofuran-6-ol HMDB0129161 2-arylbenzofuran flavonoids 188.22 11.14 16.90
551.2 4,6,2′,4′-Tetramethoxychalcone 2′-beta-glucoside LMPK12120280 Flavonoids 582.56 161.13 3.62
451.1 Afzelechin 7-apioside HMDB0030824 Flavans 258.82 100.19 2.58
449.1 Koaburanin LMPK12020253 Flavonoids 540.35 119.89 4.51
739.4 Unanisoflavan LMPK12080009 Flavonoids 462.82 123.97 3.73