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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
SOLIFENACIN

SOLIFENACIN


ATC G04BD08
ATC G04CA53

GENITO
ANTI-INCONTINENCE AGENTS
ANTISPASMODICS
MUSCARINIC ANTAGONISTS

ORAL

Cmax 173.7 NANOMOLAR (10 MILLIGRAM)

F 90 PERCENT

VD 600 LITER

PPB 98 PERCENT

Cl 7.3 LITER / HOUR (EQN)

HT 56.5 HOUR

SOLUBILITY FREELY SOLUBLE IN WATER

MUSCARINIC ACETYLCHOLINE RECEPTOR

Muscarinic acetylcholine receptor M2 UNIPROT P08172 CHRM2 -- Muscarinic acetylcholine receptor M3 UNIPROT P20309 CHRM3

more at DrugCentral

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BindingDB
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