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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