Skip to main content

Table 3 SwissADME results of compounds derived from N-acylhydrazones

From: Evaluation of antiplasmodial activity in silico and in vitro of N-acylhydrazone derivatives

Compounds

MW < 500

HA < 10

HD < 5

Log P < 5

TPSA < 140 Å

Caco-2 (cm/s)

LR  < 9

Log S > − 5

AH3

285.25

5

2

1.63

107.51

0.55

5

− 3.61

AH4

256.26

4

3

1.18

81.92

0.55

4

− 2.80

AH5

359.38

4

3

2.5

90.79

0.55

7

− 4.18

Chloroquine

305.85

2

1

3.68

28.16

0.56

8

− 4.21

Artemether

298.37

5

0

3.19

46.15

0.55

1

− 3.85

  1. MW molecular weight, HA hydrogen bond acceptors, HD hydrogen bond donors, log P partition coefficient, TPSA polar topological surface area, Caco-2 Human Colon Carcinoma Cell Line, LR rotating bond, Log S solubility