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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
DONEPEZIL

DONEPEZIL


ATC N06DA02
ATC N06DA52
ATC N06DA53

NERVOUS SYSTEM
ACETYLCHOLINESTERASE INHIBITOR (REVERSIBLE)
COGNITIVE ENHANCER
ANTI-ALZHEIMER'S DISEASE
CHOLINESTERASE INHIBITORS
INCREASES CONCENTRATION OF ACETYLCHOLINE

ORAL TRANSDERMAL

Cmax 160 NANOMOLAR (PMID18621671)

Tmax 3 HOUR

VD 910 LITER (65 KILOGRAM)

PPB 96 PERCENT

Cl 8.4 LITER / HOUR (65 KILOGRAM)

HT 70 HOUR

SOLUBILITY SOLUBLE IN WATER

ACETYLCHOLINESTERASE

PDB 4EY7 (CRYSTAL STRUCTURE OF RECOMBINANT HUMAN ACETYLCHOLINESTERASE IN COMPLEX WITH DONEPEZIL)

LIGAND CODE = E20 (link to the list of PDB complexes)

Download experimental 3D coordinates of E20 with added hydrogens

Acetylcholinesterase UNIPROT P22303 ACHE

more at DrugCentral

EMA

ANSM (in French)

Inxight Drugs
Dailymed
Drugs.com

SIDER side effects

Chemical Probes Portal

ChEMBL
BindingDB
DrugBank



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