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session 63240 - Total of 3 hits - Display hits per page:

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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
FESOTERODINE (has an active metabolite)	FESOTERODINE	ATC G04BD11 ANTISPASMODICS ANTIMUSCARINIC MUSCARINIC ANTAGONIST OVERACTIVE BLADDER WITH SYMPTOMS OF URGE URINARY INCONTINENCE URINARY ANTISPASMODICS GENITO HYDROLYSIS BY NONSPECIFIC ESTERASES	ORAL	SOLUBILITY FREELY SOLUBLE IN WATER	MUSCARINIC RECEPTOR ANTAGONIST	MUSCARINIC ACETYLCHOLINE RECEPTOR M2 ANTAGONIST CHEMBL211 MUSCARINIC ACETYLCHOLINE RECEPTOR M2 P08172 MUSCARINIC ACETYLCHOLINE RECEPTOR M2 HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 SMALLMOL MONOAMINE RECEPTOR ACETYLCHOLINE RECEPTOR	EMA ANSM (in French) Inxight Drugs Dailymed Drugs.com SIDER side effects Chemical Probes Portal ChEMBL BindingDB DrugBank
2	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
M FESOTERODINE (is an active metabolite)	FESOTERODINE	ATC G04BD11 ANTISPASMODICS ANTIMUSCARINIC MUSCARINIC ANTAGONIST OVERACTIVE BLADDER WITH SYMPTOMS OF URGE URINARY INCONTINENCE URINARY ANTISPASMODICS GENITO HYDROLYSIS BY NONSPECIFIC ESTERASES	-	Cmax 11.6 NANOMOLAR (8 MILLIGRAM) Tmax 1.8 HOUR F 52 PERCENT VD 169 LITER PPB 50 PERCENT Cl 13.6 LITER / HOUR (EQN) HT 8.59 HOUR	MUSCARINIC RECEPTOR	MUSCARINIC ACETYLCHOLINE RECEPTOR M2 ANTAGONIST CHEMBL211 MUSCARINIC ACETYLCHOLINE RECEPTOR M2 P08172 MUSCARINIC ACETYLCHOLINE RECEPTOR M2 HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 SMALLMOL MONOAMINE RECEPTOR ACETYLCHOLINE RECEPTOR	EMA ANSM (in French) Inxight Drugs Dailymed Drugs.com SIDER side effects Chemical Probes Portal ChEMBL BindingDB DrugBank
3	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
TOLTERODINE (has an active metabolite)	TOLTERODINE	ATC G04BD07 GENITO ANTICHOLINERGIC ANTI-INCONTINENCE AGENTS ANTISPASMODICS GENITOURINARY SMOOTH MUSCLE RELAXANTS MUSCARINIC RECEPTOR ANTAGONISTS	ORAL	Cmax 4.92 NANOMOLAR Tmax 1.5 HOUR VD 113 LITER PPB 96.3 PERCENT Cl 534 LITER / HOUR HT 2 HOUR SOLUBILITY IN WATER 12 MILLIGRAM / MILLILITER	MUSCARINIC ACETYLCHOLINE RECEPTOR	MUSCARINIC ACETYLCHOLINE RECEPTOR M2 ANTAGONIST CHEMBL211 MUSCARINIC ACETYLCHOLINE RECEPTOR M2 P08172 MUSCARINIC ACETYLCHOLINE RECEPTOR M2 HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 SMALLMOL MONOAMINE RECEPTOR ACETYLCHOLINE RECEPTOR	EMA ANSM (in French) Inxight Drugs Dailymed Drugs.com SIDER side effects Chemical Probes Portal ChEMBL BindingDB DrugBank