CYP 450

cyclosporine, macrolides, azoles are all inhibitors
CYP450 Inducers
Inducers
Inhibitors
Substrates
St. John's Wort
Grapefruit Juice
Warfarin
Carbamazepine
Cimetidine
Phenytoin
Phenytoin
Erythromycin
Theophylline
Phenobarbital
Ciprofloxacin
Statin (except pravastatin)
Rifampin
Azoles
Cyclophosphamide
Griseofulvin
Ritonavir
zaleplon
Chronic EtOH
Isoniazid
zolpidem
Modafinil
Bactrim/Metronidazolex
Benzodiazepine
Amiodarone
Simprevir
Diltiazem
Fluoroquinolones


Activated chrome bumper: barbiturates (e.g. phenobarbital) are potent inducers of the cytochrome P450 system

Speeding chrome bumper: rifampin activated cytochrome P450

Greased up chrome bumper: griseofulvin activates cytochrome P-450
CYP450 Inhibitors


Broken chrome bumper: cytochrome P-450 inhibition


Broken chrome bumper: azole antifungals inhibit fungal cytochrome P-450 responsible for the conversion. Also SE because CYP 450

Right on!: ritonovir has greatest cytochrome P-450 inhibitory effect and boosts concentration of other protease inhibitors

Broken chrome bumper: INH inhibits cytochrome P450

Vandalized chrome bumper: inhibition of cytochrome P450

Broken chrome bumper: amiodarone inhibits the cytochrome P450 system

Broken chrome bumper: simeprevir inhibits cytochrome P450
Substrates


chrome tank: all statins except for pravastatin are metabolized by cytochrome p450 (CYP-450) in the liver

Activating chrome bumper: cyclophosphamide is ACTIVATED by hepatic cytochrome P450 enzymes

Liver spot: zaleplon and zolpidem are rapidly metabolized by the liver, P450 system

CYP-450 chrome tank crushing warhead: warfarin is a substrate of cytochrome P-450 (drugs increase CYP activation increase warfarin metabolism)

Chrome bumper hitting energy drinks: methylxanthines (e.g. theophylline) are metabolized by the cytochrome P-450 system
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