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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
MEMANTINE

MEMANTINE


ATC N06DX01
ATC N06DA52
ATC N06DA53

NERVOUS SYSTEM
MUSCLE RELAXANT (SKELETAL)
NMDA RECEPTOR ANTAGONIST (OPEN CHANNEL)
ANTI-ALZHEIMER'S DISEASE

ORAL

Tmax 5 HOUR

VD 650 LITER (65 KILOGRAM)

PPB 45 PERCENT

Cl 6.4 LITER / HOUR (EQN)

HT 70 HOUR

SOLUBILITY SOLUBLE IN WATER

GLUTAMATE [NMDA] RECEPTOR SUBUNIT
5HT3 RECEPTOR
NICOTINIC ACETYLCHOLINE RECEPTOR

PDB 4TWD (X-RAY STRUCTURE OF A PENTAMERIC LIGAND GATED ION CHANNEL FROM ERWINIA CHRYSANTHEMI (ELIC) IN COMPLEX WITH MEMANTINE)

LIGAND CODE = 377 (link to the list of PDB complexes)

Download experimental 3D coordinates of 377 with added hydrogens

GLUTAMATE [NMDA] RECEPTOR NEGATIVE ALLOSTERIC MODULATOR CHEMBL2094124 GLUTAMATE [NMDA] RECEPTOR O15399 GLUTAMATE RECEPTOR IONOTROPIC, NMDA 2D HOMO SAPIENS ION CHANNEL LGIC GLUT NMDAANSM (in French)

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