BDBM50074289 (4-Methyl-6-phenyl-pyridazin-3-yl)-(2-morpholin-4-yl-ethyl)-amine; hydrochloride::CHEMBL278819::CHEMBL536932::Minaprine hydrochloride
SMILES Cc1cc(nnc1NCCN1CCOCC1)-c1ccccc1
InChI Key InChIKey=LDMWSLGGVTVJPG-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 8 hits for monomerid = 50074289
Affinity DataKi: 1.70E+4nMAssay Description:Binding affinity towards muscarinic M1 receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 1.70E+4nMAssay Description:Displacement of [3H]-pirenzepine from cerebral Muscarinic acetylcholine receptor M1More data for this Ligand-Target Pair
Affinity DataIC50: 8.50E+4nMAssay Description:Inhibition of AChEMore data for this Ligand-Target Pair
TargetCalcium/calmodulin-dependent protein kinase type II subunit gamma(Human)
Northwestern University
Curated by ChEMBL
Northwestern University
Curated by ChEMBL
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of Calcium/calmodulin-dependent protein kinase type IIMore data for this Ligand-Target Pair
TargetO94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139(Human)
Northwestern University
Curated by ChEMBL
Northwestern University
Curated by ChEMBL
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of Protein kinase CMore data for this Ligand-Target Pair
TargetcAMP-dependent protein kinase catalytic subunit gamma(Human)
Northwestern University
Curated by ChEMBL
Northwestern University
Curated by ChEMBL
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of Protein kinase AMore data for this Ligand-Target Pair
Affinity DataIC50: 6.00E+5nMAssay Description:Invitro evaluation against RXR-alpha in CV-1 cells by cotransfection assay was determinedMore data for this Ligand-Target Pair
Affinity DataIC50: 8.50E+4nMAssay Description:In vitro inhibition of acetylcholinesterase in homogenized rat striatum.More data for this Ligand-Target Pair