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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
TOFACITINIB

TOFACITINIB


ATC L04AA29

IMMUNOMODULATING
INHIBITOR OF JANUS KINASES (JAKS)
TREATMENT OF RHEUMATOID ARTHRITIS

ORAL

F 74 PERCENT

VD 87 LITER

PPB 40 PERCENT

Cl 20 LITER / HOUR (EQN)

HT 3 HOUR

SOLUBILITY FREELY SOLUBLE IN WATER

JANUS KINASES (JAK)

PDB 3LXK (STRUCTURAL AND THERMODYNAMIC CHARACTERIZATION OF THE TYK2 AND JAK3 KINASE DOMAINS IN COMPLEX WITH CP-690550 AND CMP-6)

LIGAND CODE = MI1 (link to the list of PDB complexes)

Download experimental 3D coordinates of MI1 with added hydrogens

JANUS KINASE (JAK) INHIBITOR CHEMBL2363062 JANUS KINASE (JAK) O60674 TYROSINE-PROTEIN KINASE JAK2 HOMO SAPIENS ENZYME KINASE PROTEIN KINASE TK JAKAEMA

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