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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
ROSUVASTATIN

ROSUVASTATIN


ATC C10AA07
ATC C10BX05
ATC C10BA06
ATC C10BX09
ATC C10BX10
ATC C10BX07
ATC C10BX14
ATC C10BX13
ATC A10BH52
ATC C10BA09
ATC C10BX16
ATC C10BA07
ATC C10BX17

CARDIOVASCULAR
ANTICHOLESTEREMIC AGENTS
HMG-COA REDUCTASE INHIBITORS

ORAL

Tmax 4 HOUR

F 20 PERCENT

VD 134 LITER

PPB 88 PERCENT

Cl 42.9 LITER / HOUR (65 KILOGRAM)

HT 19 HOUR

SOLUBILITY SPARINGLY SOLUBLE IN WATER

3-HYDROXY-3-METHYLGLUTARYL-COENZYME A REDUCTASE

HMG-COA REDUCTASE INHIBITOR CHEMBL402 HMG-COA REDUCTASE P04035 3-HYDROXY-3-METHYLGLUTARYL-COENZYME A REDUCTASE HOMO SAPIENS ENZYME REDUCTASEANSM (in French)

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