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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
TEDIZOLID (is an active metabolite)

TEDIZOLID


ATC J01XX11

ANTIINFECTIVES
ANTIBACTERIAL AGENT OF THE OXAZOLIDINONE
BINDING TO THE 50S SUBUNIT OF THE BACTERIAL RIBOSOME

-

Cmax 8.1 MICROMOLAR

Tmax 1.2 HOUR

F 91 PERCENT

VD 73.5 LITER

PPB 80 PERCENT

Cl 5.9 LITER / HOUR

HT 12 HOUR

RIBOSOME 50S SUBUNIT

PDB 6WRS (STRUCTURE OF THE 50S SUBUNIT OF THE RIBOSOME FROM METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS IN COMPLEX WITH THE ANTIBIOTIC, TEDIZOLID)

LIGAND CODE = U7V (link to the list of PDB complexes)

Download experimental 3D coordinates of U7V with added hydrogens

Unknown

more at DrugCentral

EMA

ANSM (in French)

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SIDER side effects

Chemical Probes Portal

ChEMBL
BindingDB
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