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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 | |||
| TIMOLOL
| TIMOLOL |
CARDIOVASCULAR | ORAL OPHTHALMIC | Cmax 1.45 NANOMOLAR VD 97.5 LITER (65 KILOGRAM) PPB 10 PERCENT Cl 33.1 LITER / HOUR (65 KILOGRAM) HT 2.2 HOUR SOLUBILITY SOLUBLE IN WATER | BETA-1 ADRENERGIC RECEPTOR BETA-2 ADRENERGIC RECEPTOR PDB 3D4S (CHOLESTEROL BOUND FORM OF HUMAN BETA2 ADRENERGIC RECEPTOR.) LIGAND CODE = TIM (link to the list of PDB complexes) Download experimental 3D coordinates of TIM with added hydrogens | BETA-2 ADRENERGIC RECEPTOR ANTAGONIST CHEMBL210 BETA-2 ADRENERGIC RECEPTOR P07550 BETA-2 ADRENERGIC RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 SMALLMOL MONOAMINE RECEPTOR ADRENERGIC RECEPTOR | EMA | |||
