Table 5 Binding energies (Kcalmol−1) from molecular studies for H1H6 and acarbose.

From: Evaluating the antidiabetes and antioxidant activities of halogenated Schiff bases derived from 4-(diethylamino)salicylaldehyde: in vitro antidiabetes, antioxidant and computational investigation

Compounds

H1

H2

H3

H4

H5

H6

acarbose

α-amylase (binding energy)

 − 7.3

 − 7.3

 − 7.4

 − 7.0

 − 6.9

 − 7.6

 − 7.2

α-glucosidase (binding energy)

 − 7.1

 − 7.1

 − 7.1

 − 6.8

 − 6.9

 − 7.5

 − 6.4