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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
CIMETIDINE

CIMETIDINE


ATC A02BA01
ATC A02BA51

METABOLISM
HISTAMINE H2 RECEPTOR BLOCKER
ANTIHISTAMINE
INHIBIT GASTRIC ACID SECRETION

ORAL INJECTION

Tmax 1.1 HOUR

VD 78 LITER (65 KILOGRAM)

PPB 22 PERCENT

Cl 31.6 LITER / HOUR (65 KILOGRAM)

HT 2 HOUR

SOLUBILITY SLIGHTLY SOLUBLE IN WATER

HISTAMINE H2 RECEPTOR

HISTAMINE H2 RECEPTOR ANTAGONIST CHEMBL1941 HISTAMINE H2 RECEPTOR P25021 HISTAMINE H2 RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 SMALLMOL MONOAMINE RECEPTOR HISTAMINE RECEPTORANSM (in French)

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