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Table 1 Detailed information on active compounds in L. sinense

From: Integrated network pharmacology and cellular assay reveal the biological mechanisms of Limonium sinense (Girard) Kuntze against Breast cancer

Compound Name

Compound Type

Molecular weight

nRB

nHA

nHD

TPSA

LogP

Gallic acid

Phenolic acid

170.12

1

5

4

97.99

-0.16

Ethyl gallate

Phenolic acid

198.17

3

5

3

86.99

0.49

Apigenin

Flavone

270.24

1

5

3

90

0.52

Naringenin

Flavanone

272.25

1

5

3

86.99

0.71

Luteolin

Flavone

286.24

1

6

4

111.13

-0.03

Kaempferol

Flavonol

286.24

1

6

4

111.13

-0.03

Eriodictyol

Flavanone

288.25

1

6

4

107.22

0.16

( +)-Catechin

Flavan-3-ol

290.27

1

6

5

110.38

0.24

N-trans-caffeoyltyramine

Alkaloid

299.32

6

4

4

89.79

1.65

Quercetin

Flavonol

302.24

1

7

5

131.36

-0.56

Morin

Flavonol

302.24

1

7

5

131.36

-0.56

Homoeriodictyol

Flavanone

302.28

2

6

3

96.22

0.41

N-trans-feruloyltyramine

Alkaloid

313.35

7

4

3

78.79

1.89

Isorhamnetin

Flavonol

316.26

2

7

4

120.36

-0.31

Isodihydrosyringetin

Flavanone

348.3

3

8

4

125.68

-0.66

  1. nRB Number of Rotatable bonds, optimal 0–10, nHA Number of Hydrogen bond acceptors, optimal: 0–10; nHD Number of Hydrogen bond donors, optimal: 0–5, TPSA Topological Polar Surface Area, optimal: 0–140, LogP Log of the octanol/water partition coefficient, optimal: ≤ 5