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1 INNClassRoute (list)PK parameters= Cmax; Tmax; F: bioavailability; t1/2: half-life; VD: volume of distribution; Cl: clearance; PPB: plasma protein binding;(EQN means that value was calculated using VD=(Cl*t1/2)/0.693)Primary Target and PDB code of Protein-Drug complexTargets from DrugCentral Links
OMEPRAZOLE

OMEPRAZOLE
ESOMEPRAZOLE


ATC A02BC01
ATC A02BD05
ATC A02BD01
ATC A02BD16
ATC A02BC51

METABOLISM
ANTISECRETORY (GASTRIC ACID)
PROTON-PUMP INHIBITORS
ANTI-ULCER AGENTS

ORAL INTRAVENOUS

Cmax 4.09 MICROMOLAR

Tmax 2 HOUR

F 35 PERCENT

VD 16 LITER

PPB 95 PERCENT

Cl 33 LITER / HOUR

HT 0.75 HOUR

SOLUBILITY VERY SLIGHTLY SOLUBLE IN WATER

H+/K+ ATPASE

Potassium-transporting ATPase UNIPROT P20648 ATP4A

more at DrugCentral

EMA

ANSM (in French)

Inxight Drugs
Dailymed
Drugs.com

SIDER side effects

Chemical Probes Portal

ChEMBL
BindingDB
DrugBank



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