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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
RANITIDINE

RANITIDINE


ATC A02BA02
ATC A02BA07

METABOLISM
HISTAMINE H2 RECEPTOR BLOCKER
ANTI-ULCER AGENTS

ORAL INJECTION

Cmax 1.56 MICROMOLAR

Tmax 2.5 HOUR

F 50 PERCENT

VD 91 LITER (65 KILOGRAM)

PPB 15 PERCENT

Cl 45.6 LITER / HOUR

HT 2.75 HOUR

SOLUBILITY 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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