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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
CYCLOBENZAPRINE

CYCLOBENZAPRINE


ATC M03BX08

MUSCULO-SKELETAL
MUSCLE RELAXANT (SKELETAL)
RELIEVES SKELETAL MUSCLE SPASM OF LOCAL ORIGIN WITHOUT INTERFERING WITH MUSCLE FUNCTION
5-HT2 RECEPTOR ANTAGONIST (PMID12498911)
STRUCTURAL ANALOG OF TRICYCLIC ANTIDEPRESSANTS

ORAL

Cmax 167 NANOMOLAR

Tmax 7.1 HOUR

F 44 PERCENT

VD 1939 LITER (EQN)

Cl 42 LITER / HOUR

HT 32 HOUR

SOLUBILITY FREELY SOLUBLE IN WATER

5-HYDROXYTRYPTAMINE 2A RECEPTOR

5-hydroxytryptamine receptor 2A UNIPROT P28223 HTR2A

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