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| 1 | INN | Class | Route (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 complex | Targets from DrugCentral | Links | |||
| TICLOPIDINE (has an active metabolite)
| TICLOPIDINE | BLOOD | ORAL | Tmax 2 HOUR F 80 PERCENT PPB 98 PERCENT HT 108 HOUR SOLUBILITY FREELY SOLUBLE IN WATER | P2Y PURINOCEPTOR 12 | PURINERGIC RECEPTOR P2Y12 ANTAGONIST CHEMBL2001 PURINERGIC RECEPTOR P2Y12 Q9H244 P2Y PURINOCEPTOR 12 HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 SMALLMOL NUCLEOTIDE-LIKE RECEPTOR PURINE RECEPTOR | ANSM (in French) | |||
