BDBM39341 11-[(4-methylpiperazin-1-yl)acetyl]-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one::11-[2-(4-methyl-1-piperazinyl)-1-oxoethyl]-5H-pyrido[2,3-b][1,4]benzodiazepin-6-one;hydrochloride::11-[2-(4-methylpiperazin-1-yl)acetyl]-5H-pyrido[2,3-b][1,4]benzodiazepin-6-one;hydrochloride::11-[2-(4-methylpiperazin-1-yl)ethanoyl]-5H-pyrido[2,3-b][1,4]benzodiazepin-6-one;hydrochloride::11-[2-(4-methylpiperazino)acetyl]-5H-pyrido[2,3-b][1,4]benzodiazepin-6-one;hydrochloride::CHEMBL9967::MLS000069702::PIRENZEPINE::PIRENZEPINE DIHYDROCHLORIDE::SMR000058502::cid_185248
SMILES CN1CCN(CC(=O)N2c3ccccc3C(=O)Nc3cccnc23)CC1
InChI Key InChIKey=RMHMFHUVIITRHF-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 209 hits for monomerid = 39341
Affinity DataIC50: 1.10nMAssay Description:Antagonist activity at human M4 receptor expressed in HEK293T cells assessed as inhibition of carbachol-induced response by beta-arrestin engagement ...More data for this Ligand-Target Pair
Affinity DataIC50: 1.5nMAssay Description:Antagonist activity at human M1 receptor expressed in HEK293T cells assessed as inhibition of carbachol-induced response by BRET based beta-arrestin ...More data for this Ligand-Target Pair
Affinity DataKi: 2.82nMAssay Description:Displacement of [3H]N-methylscopolamine chloride from human cloned muscarinic M1 receptor expressed in CHOK1 cellsMore data for this Ligand-Target Pair
Affinity DataKi: 3.60nMAssay Description:Binding affinity against Muscarinic acetylcholine receptor M1 by displacement of [3H]pirenzepine in bovine striatumMore data for this Ligand-Target Pair
TargetMuscarinic acetylcholine receptor M1(Rat)
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Affinity DataIC50: 3.80nMAssay Description:Displacement of [3H]pirenzepine binding to muscarinic M1 receptor in brain cortex of rat.More data for this Ligand-Target Pair
Affinity DataKi: 4.60nMAssay Description:Compound was evaluated for displacement of [3H]QNB from human Muscarinic m1 receptor in CHO cells.More data for this Ligand-Target Pair
TargetMuscarinic acetylcholine receptor M1(Rat)
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Affinity DataKi: 5.20nMAssay Description:Displacement of [3H]pirenzepine from muscarinic M1 receptor of rat cortex homogenates.More data for this Ligand-Target Pair
TargetMuscarinic acetylcholine receptor M1(Rat)
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Affinity DataKi: 5.20nMAssay Description:Displacement of [3H]pirenzepine from muscarinic acetylcholine receptor M1 in rat cortex homogenatesMore data for this Ligand-Target Pair
TargetMuscarinic acetylcholine receptor M1(Rat)
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Affinity DataKi: 5.20nMAssay Description:Ability to displace [3H]pirenzepine (PZ) from M1 receptor in rat cortex homogenateMore data for this Ligand-Target Pair
TargetMuscarinic acetylcholine receptor M1(Rat)
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
TargetMuscarinic acetylcholine receptor M1(Rat)
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Affinity DataKi: 6.5nMAssay Description:Compound was tested for inhibiting [3H]pirenzepine Binding to Muscarinic receptor (M1) receptor in Rat Cortex HomogenatesMore data for this Ligand-Target Pair
TargetMuscarinic acetylcholine receptor M1(Rat)
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Affinity DataKi: 6.5nMAssay Description:Inhibition of binding of [3H]pirenzepine to muscarinic receptor (M1) in rat cortex homogenatesMore data for this Ligand-Target Pair
TargetMuscarinic acetylcholine receptor M1(Rat)
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
TargetMuscarinic acetylcholine receptor M1(Rat)
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Affinity DataKi: 7.94nMAssay Description:Binding affinity to Muscarinic acetylcholine receptor M1 by measuring its ability to displace [3H]pirenzepine from rat cerebral cortexMore data for this Ligand-Target Pair
TargetMuscarinic acetylcholine receptor M1(Rat)
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Affinity DataKi: 9.10nMAssay Description:Binding affinity to human M1 muscarinic receptorMore data for this Ligand-Target Pair
TargetMuscarinic acetylcholine receptor M1(Rat)
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
TargetMuscarinic acetylcholine receptor M1(Rat)
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Affinity DataKi: 13.8nMAssay Description:Displacement of [3H]N-methylscopolamine chloride from human cloned muscarinic M4 receptor expressed in CHOK1 cellsMore data for this Ligand-Target Pair
Affinity DataKi: 14nMAssay Description:Binding affinity for muscarinic acetylcholine receptor M1 by measuring displacement of [3H]QNB from guinea pig cerebral cortexMore data for this Ligand-Target Pair
Affinity DataKi: 15nMAssay Description:Displacement of [3H]pirenzepine from human recombinant M1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataKi: 15nMAssay Description:Inhibition of muscarinic M1 receptor (unknown origin) assessed as reduction in control ligand bindingMore data for this Ligand-Target Pair
TargetMuscarinic acetylcholine receptor M1(Rat)
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Affinity DataKi: 16nMAssay Description:Displacement of [3H]pirenzepine from human muscarinic M1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 19nMAssay Description:Inhibition of human muscarinic M1 receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 20nMAssay Description:Antagonist activity at human M1 receptor expressed in HEK293T cells assessed as inhibition of carbachol-induced response by BRET based Gq protein act...More data for this Ligand-Target Pair
Affinity DataKi: 20nMAssay Description:Displacement of [3H]-pyrilamine from human recombinant M1 receptor expressed in CHO cells after 60 mins by scintillation countingMore data for this Ligand-Target Pair
Affinity DataKd: 20nMAssay Description:Apparent dissociation constant for human muscarinic receptor M1 from FRET based binding assayMore data for this Ligand-Target Pair
Affinity DataIC50: 21nMAssay Description:Displacement of [3H]pirenzepine from human recombinant M1 receptor expressed in CHO cells measured after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
Affinity DataIC50: 21nMAssay Description:Displacement of [3H]pirenzepine from human recombinant muscarinic M1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataKi: 21.4nMAssay Description:Displacement of [3H]QNB from human muscarinic M1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
TargetMuscarinic acetylcholine receptor M1(Rat)
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Affinity DataIC50: 22nMAssay Description:Inhibitory concentration against human Adenosine A3 receptor expressed in HEK293 cells using 0.1 nM [3H]AB-MECAMore data for this Ligand-Target Pair
TargetMuscarinic acetylcholine receptor M1(Rat)
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Dipartimento Di Scienze Farmaceutiche - Università
Curated by ChEMBL
Affinity DataKi: 23.5nMAssay Description:Displacement of [3H]QNB from EGFP(delta-17)human M1 receptor expressed in HEK cellsMore data for this Ligand-Target Pair
Affinity DataKi: 24nMAssay Description:Displacement of [3H]pirenzepine from human recombinant Muscarinic acetylcholine receptor M1 expressed in CHO cells after 60 mins by scintillation cou...More data for this Ligand-Target Pair
Affinity DataKi: 24nMAssay Description:Inhibition of [3H]QNB binding to human muscarinic receptor M1More data for this Ligand-Target Pair
Affinity DataIC50: 27nMAssay Description:Displacement of [3H]pirenzepine from human recombinant Muscarinic acetylcholine receptor M1 expressed in CHO cells after 60 mins by scintillation cou...More data for this Ligand-Target Pair
Affinity DataKi: 28nMAssay Description:Ability to displace [3H]N-methylscopolamine (NMS) from M3 receptor in rat submaxillary gland homogenateMore data for this Ligand-Target Pair
Affinity DataIC50: 28nMAssay Description:Displacement of [3H]NMS binding to human Muscarinic acetylcholine receptor M1 using membranes from transfected CHO cellsMore data for this Ligand-Target Pair
