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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
FAMCICLOVIR (has an active metabolite)

FAMCICLOVIR


ATC J05AB09
ATC S01AD07

ANTIINFECTIVES
ANTIVIRAL
DNA POLYMERASE INHIBITOR
PRODRUG OF PENCICLOVIR
TREATMENT OF HERPES VIRUS HSV-1 AND HSV-2

ORAL

F 77 PERCENT

SOLUBILITY IS FREELY SOLUBLE (>25 PERCENT) IN WATER INITIALLY BUT RAPIDLY PRECIPITATES AS THE SPARINGLY SOLUBLE (2-3 PERCENT) MONOHYDRATE

HUMAN HERPESVIRUS 1 DNA POLYMERASE INHIBITOR CHEMBL1872 HUMAN HERPESVIRUS 1 DNA POLYMERASE P04293 DNA POLYMERASE CATALYTIC SUBUNIT HERPES SIMPLEX VIRUS (TYPE 1 / STRAIN 17) ENZYME TRANSFERASEEMA

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