Skip to main content

Table 1 Isoforms tested, marker reactions, incubation conditions, and Km used in the inhibition study

From: Human liver microsomes study on the inhibitory effect of plantainoside D on the activity of cytochrome P450 activity

CYPs

Marker reactions

Substrate concentration (μM)

Protein concentration (mg/mL)

Incubation time (min)

Estimated Km (μM)

Inhibitor concentration (μM)

Inhibitors

Reference

1A2

phenacetin O-deethylation

40

0.2

30

48

10

furafylline

[16, 17]

2A6

coumarin 7-hydroxylation

1.0

0.1

10

1.5

10

tranylcypromine

[16, 17]

2B6

Bupropion to hydroxybuptopion

40

0.25

30

50

50

monoterpenoid

[18, 19]

2C8

paclitaxel 6α-hydroxylation

10

0.5

30

16

5

montelukast

[16, 17]

2C9

diclofenac 4’-hydroxylation

10

0.3

10

13

10

sulphaphenazole

[16, 17]

2C19

S-Mephenytoin 4-hydroxylation

100

0.2

40

105

50

tranylcypromine

[16, 17]

2D6

dextromethorphan O-demethylation

25

0.25

20

4.8

10

quinidine

[20]

2E1

chlorzoxazone 6-hydroxylation

120

0.4

30

126

50

clomethiazole

[16, 17]

3A4

testosterone 6β-hydroxylation

50

0.5

10

53

1

ketoconazole

[16, 17]