Compile Data Set for Download or QSAR

Found 31 hits with Last Name = 'parvez' and Initial = 'm'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
D(2) dopamine receptor (Rattus norvegicus (rat))	BDBM50001955 ((-)6-Methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]qu...) Show SMILES CN1CCc2cccc-3c2[C@H]1Cc1ccc(O)c(O)c-31 |r| Show InChI InChI=1S/C17H17NO2/c1-18-8-7-10-3-2-4-12-15(10)13(18)9-11-5-6-14(19)17(20)16(11)12/h2-6,13,19-20H,7-9H2,1H3/t13-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	24	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Compound was tested in vitro for binding affinity towards Dopamine receptor D2 in rat striatal membrane by using [3H]spiperone as radioligand				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50004000 ((3aS,8aR)-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydro...) Show SMILES CNC(=O)Oc1ccc2N(C)[C@H]3N(C)CC[C@@]3(C)c2c1 |r| Show InChI InChI=1S/C15H21N3O2/c1-15-7-8-17(3)13(15)18(4)12-6-5-10(9-11(12)15)20-14(19)16-2/h5-6,9,13H,7-8H2,1-4H3,(H,16,19)/t13-,15+/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	41	n/a	n/a	n/a	n/a	n/a	n/a
University of Karachi Curated by ChEMBL					Assay Description Inhibition of electric eel AChE by modified Ellman method				J Nat Prod 66: 739-42 (2003) Article DOI: 10.1021/np020446o BindingDB Entry DOI: 10.7270/Q2862G6D
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM50007571 (6-Propyl-4,5,5a,6,7,8-hexahydro-thiazolo[4,5-f]qui...) Show SMILES CCCN1CCC=C2C1CCc1sc(N)nc21 |c:6| Show InChI InChI=1S/C13H19N3S/c1-2-7-16-8-3-4-9-10(16)5-6-11-12(9)15-13(14)17-11/h4,10H,2-3,5-8H2,1H3,(H2,14,15)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	138	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Compound was tested in vitro for binding affinity against dopamine receptor D1 in rat striatal membrane by using DA antagonist [3H]NPA				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM50007571 (6-Propyl-4,5,5a,6,7,8-hexahydro-thiazolo[4,5-f]qui...) Show SMILES CCCN1CCC=C2C1CCc1sc(N)nc21 |c:6| Show InChI InChI=1S/C13H19N3S/c1-2-7-16-8-3-4-9-10(16)5-6-11-12(9)15-13(14)17-11/h4,10H,2-3,5-8H2,1H3,(H2,14,15)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	138	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Compound was tested in vitro for binding affinity against dopamine receptor D1 in rat striatal membrane by using DA antagonist [3H]NPA				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM50007571 (6-Propyl-4,5,5a,6,7,8-hexahydro-thiazolo[4,5-f]qui...) Show SMILES CCCN1CCC=C2C1CCc1sc(N)nc21 |c:6| Show InChI InChI=1S/C13H19N3S/c1-2-7-16-8-3-4-9-10(16)5-6-11-12(9)15-13(14)17-11/h4,10H,2-3,5-8H2,1H3,(H2,14,15)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	203	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Compound was tested in vitro for binding affinity against dopamine receptor D1 in rat striatal membrane by using DA antagonist [3H]NPA				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM50001955 ((-)6-Methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]qu...) Show SMILES CN1CCc2cccc-3c2[C@H]1Cc1ccc(O)c(O)c-31 |r| Show InChI InChI=1S/C17H17NO2/c1-18-8-7-10-3-2-4-12-15(10)13(18)9-11-5-6-14(19)17(20)16(11)12/h2-6,13,19-20H,7-9H2,1H3/t13-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank PC cid PC sid PDB UniChem Patents Similars	PDB PubMed	n/a	n/a	384	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Compound was tested in vitro for binding affinity towards dopamine Dopamine receptor D1 in rat striatal membrane by using [3H]-SCH- 23390 as radiolig...				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair				3D Structure (crystal)
D(2) dopamine receptor (Rattus norvegicus (rat))	BDBM50007573 (4-(1-Propyl-1,2,5,6-tetrahydro-pyridin-3-yl)-thiaz...) Show SMILES CCCN1CCC=C(C1)c1csc(N)n1 |c:6| Show InChI InChI=1S/C11H17N3S/c1-2-5-14-6-3-4-9(7-14)10-8-15-11(12)13-10/h4,8H,2-3,5-7H2,1H3,(H2,12,13)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	574	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Binding affinity towards dopamine receptor D2 in rat striatal membrane using [3H]spiperone				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50004000 ((3aS,8aR)-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydro...) Show SMILES CNC(=O)Oc1ccc2N(C)[C@H]3N(C)CC[C@@]3(C)c2c1 |r| Show InChI InChI=1S/C15H21N3O2/c1-15-7-8-17(3)13(15)18(4)12-6-5-10(9-11(12)15)20-14(19)16-2/h5-6,9,13H,7-8H2,1-4H3,(H,16,19)/t13-,15+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	857	n/a	n/a	n/a	n/a	n/a	n/a
University of Karachi Curated by ChEMBL					Assay Description Inhibition of BChE (unknown origin)				J Nat Prod 66: 739-42 (2003) Article DOI: 10.1021/np020446o BindingDB Entry DOI: 10.7270/Q2862G6D
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Rattus norvegicus (rat))	BDBM50007571 (6-Propyl-4,5,5a,6,7,8-hexahydro-thiazolo[4,5-f]qui...) Show SMILES CCCN1CCC=C2C1CCc1sc(N)nc21 |c:6| Show InChI InChI=1S/C13H19N3S/c1-2-7-16-8-3-4-9-10(16)5-6-11-12(9)15-13(14)17-11/h4,10H,2-3,5-8H2,1H3,(H2,14,15)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	860	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Binding affinity towards dopamine receptor D2 in rat striatal membrane using [3H]spiperone				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Rattus norvegicus (rat))	BDBM50007571 (6-Propyl-4,5,5a,6,7,8-hexahydro-thiazolo[4,5-f]qui...) Show SMILES CCCN1CCC=C2C1CCc1sc(N)nc21 |c:6| Show InChI InChI=1S/C13H19N3S/c1-2-7-16-8-3-4-9-10(16)5-6-11-12(9)15-13(14)17-11/h4,10H,2-3,5-8H2,1H3,(H2,14,15)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	860	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Compound was tested in vitro for binding affinity against dopamine receptor D1 in rat striatal membrane by using DA antagonist [3H]NPA				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Rattus norvegicus (rat))	BDBM50007570 (7-Propyl-4,5,5a,6,7,8-hexahydro-thiazolo[4,5-f]iso...) Show SMILES CCCN1CC=C2C(CCc3sc(N)nc23)C1 |c:5| Show InChI InChI=1S/C13H19N3S/c1-2-6-16-7-5-10-9(8-16)3-4-11-12(10)15-13(14)17-11/h5,9H,2-4,6-8H2,1H3,(H2,14,15)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.13E+3	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Binding affinity towards dopamine receptor D2 in rat striatal membrane using [3H]spiperone				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Rattus norvegicus (rat))	BDBM50007575 (6-Propyl-4,5,5a,6,7,8,9,9a-octahydro-thiazolo[4,5-...) Show SMILES CCCN1CCCC2C1CCc1sc(N)nc21 Show InChI InChI=1S/C13H21N3S/c1-2-7-16-8-3-4-9-10(16)5-6-11-12(9)15-13(14)17-11/h9-10H,2-8H2,1H3,(H2,14,15)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	1.24E+3	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Binding affinity towards dopamine receptor D2 in rat striatal membrane using [3H]spiperone				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Rattus norvegicus (rat))	BDBM50007571 (6-Propyl-4,5,5a,6,7,8-hexahydro-thiazolo[4,5-f]qui...) Show SMILES CCCN1CCC=C2C1CCc1sc(N)nc21 |c:6| Show InChI InChI=1S/C13H19N3S/c1-2-7-16-8-3-4-9-10(16)5-6-11-12(9)15-13(14)17-11/h4,10H,2-3,5-8H2,1H3,(H2,14,15)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	2.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Binding affinity towards dopamine receptor D2 in rat striatal membrane using [3H]spiperone				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Rattus norvegicus (rat))	BDBM81924 ((R)-3-(1-Propyl-piperidin-3-yl)-phenol | 3PPP(+/-)...) Show SMILES CCCN1CCCC(C1)c1cccc(O)c1 Show InChI InChI=1S/C14H21NO/c1-2-8-15-9-4-6-13(11-15)12-5-3-7-14(16)10-12/h3,5,7,10,13,16H,2,4,6,8-9,11H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.28E+3	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Binding affinity towards dopamine receptor D2 in rat striatal membrane using [3H]spiperone				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Rattus norvegicus (rat))	BDBM50007574 (7-Propyl-4,5,6,7,8,9-hexahydro-thiazolo[4,5-f]isoq...) Show SMILES CCCN1CCC2=C(CCc3sc(N)nc23)C1 |t:6| Show InChI InChI=1S/C13H19N3S/c1-2-6-16-7-5-10-9(8-16)3-4-11-12(10)15-13(14)17-11/h2-8H2,1H3,(H2,14,15)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.43E+3	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Binding affinity towards dopamine receptor D2 in rat striatal membrane using [3H]spiperone				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM50007570 (7-Propyl-4,5,5a,6,7,8-hexahydro-thiazolo[4,5-f]iso...) Show SMILES CCCN1CC=C2C(CCc3sc(N)nc23)C1 |c:5| Show InChI InChI=1S/C13H19N3S/c1-2-6-16-7-5-10-9(8-16)3-4-11-12(10)15-13(14)17-11/h5,9H,2-4,6-8H2,1H3,(H2,14,15)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description In vitro binding affinity towards dopamine receptor D1 in rat striatal membrane using [3H]-SCH- 23390				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM50007569 (8-Propyl-4,5,6,7,8,9-hexahydro-thiazolo[5,4-h]isoq...) Show SMILES CCCN1CCC2=C(C1)c1nc(N)sc1CC2 |c:6| Show InChI InChI=1S/C13H19N3S/c1-2-6-16-7-5-9-3-4-11-12(10(9)8-16)15-13(14)17-11/h2-8H2,1H3,(H2,14,15)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description In vitro binding affinity towards dopamine receptor D1 in rat striatal membrane using [3H]-SCH- 23390				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM50007571 (6-Propyl-4,5,5a,6,7,8-hexahydro-thiazolo[4,5-f]qui...) Show SMILES CCCN1CCC=C2C1CCc1sc(N)nc21 |c:6| Show InChI InChI=1S/C13H19N3S/c1-2-7-16-8-3-4-9-10(16)5-6-11-12(9)15-13(14)17-11/h4,10H,2-3,5-8H2,1H3,(H2,14,15)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description In vitro binding affinity towards dopamine receptor D1 in rat striatal membrane using [3H]-SCH- 23390				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM50007571 (6-Propyl-4,5,5a,6,7,8-hexahydro-thiazolo[4,5-f]qui...) Show SMILES CCCN1CCC=C2C1CCc1sc(N)nc21 |c:6| Show InChI InChI=1S/C13H19N3S/c1-2-7-16-8-3-4-9-10(16)5-6-11-12(9)15-13(14)17-11/h4,10H,2-3,5-8H2,1H3,(H2,14,15)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description In vitro binding affinity towards dopamine receptor D1 in rat striatal membrane using [3H]-SCH- 23390				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM50007571 (6-Propyl-4,5,5a,6,7,8-hexahydro-thiazolo[4,5-f]qui...) Show SMILES CCCN1CCC=C2C1CCc1sc(N)nc21 |c:6| Show InChI InChI=1S/C13H19N3S/c1-2-7-16-8-3-4-9-10(16)5-6-11-12(9)15-13(14)17-11/h4,10H,2-3,5-8H2,1H3,(H2,14,15)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Compound was tested in vitro for binding affinity against dopamine receptor D1 in rat striatal membrane by using DA antagonist [3H]NPA				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM50007575 (6-Propyl-4,5,5a,6,7,8,9,9a-octahydro-thiazolo[4,5-...) Show SMILES CCCN1CCCC2C1CCc1sc(N)nc21 Show InChI InChI=1S/C13H21N3S/c1-2-7-16-8-3-4-9-10(16)5-6-11-12(9)15-13(14)17-11/h9-10H,2-8H2,1H3,(H2,14,15)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description In vitro binding affinity towards dopamine receptor D1 in rat striatal membrane using [3H]-SCH- 23390				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM81924 ((R)-3-(1-Propyl-piperidin-3-yl)-phenol | 3PPP(+/-)...) Show SMILES CCCN1CCCC(C1)c1cccc(O)c1 Show InChI InChI=1S/C14H21NO/c1-2-8-15-9-4-6-13(11-15)12-5-3-7-14(16)10-12/h3,5,7,10,13,16H,2,4,6,8-9,11H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description In vitro binding affinity towards dopamine receptor D1 in rat striatal membrane using [3H]-SCH- 23390				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM50007573 (4-(1-Propyl-1,2,5,6-tetrahydro-pyridin-3-yl)-thiaz...) Show SMILES CCCN1CCC=C(C1)c1csc(N)n1 |c:6| Show InChI InChI=1S/C11H17N3S/c1-2-5-14-6-3-4-9(7-14)10-8-15-11(12)13-10/h4,8H,2-3,5-7H2,1H3,(H2,12,13)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description In vitro binding affinity towards dopamine receptor D1 in rat striatal membrane using [3H]-SCH- 23390				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM50007574 (7-Propyl-4,5,6,7,8,9-hexahydro-thiazolo[4,5-f]isoq...) Show SMILES CCCN1CCC2=C(CCc3sc(N)nc23)C1 |t:6| Show InChI InChI=1S/C13H19N3S/c1-2-6-16-7-5-10-9(8-16)3-4-11-12(10)15-13(14)17-11/h2-8H2,1H3,(H2,14,15)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description In vitro binding affinity towards dopamine receptor D1 in rat striatal membrane using [3H]-SCH- 23390				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Rattus norvegicus (rat))	BDBM50007569 (8-Propyl-4,5,6,7,8,9-hexahydro-thiazolo[5,4-h]isoq...) Show SMILES CCCN1CCC2=C(C1)c1nc(N)sc1CC2 |c:6| Show InChI InChI=1S/C13H19N3S/c1-2-6-16-7-5-9-3-4-11-12(10(9)8-16)15-13(14)17-11/h2-8H2,1H3,(H2,14,15)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.56E+4	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Binding affinity towards dopamine receptor D2 in rat striatal membrane using [3H]spiperone				J Med Chem 34: 2736-46 (1991) BindingDB Entry DOI: 10.7270/Q2V125FC
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50250634 (CHEMBL466169 | [(20S)-20-(dimethylamino)-3-beta-(2...) Show SMILES C\C=C(/C)C(=O)N[C@H]1CC[C@]2(O)CC3=CC[C@]4(C)[C@H](CC[C@@]4(C)[C@@H]3CC[C@H]2C1(C)C)[C@H](C)N(C)C |r,t:13| Show InChI InChI=1S/C31H52N2O2/c1-10-20(2)27(34)32-26-15-18-31(35)19-22-13-16-29(6)23(21(3)33(8)9)14-17-30(29,7)24(22)11-12-25(31)28(26,4)5/h10,13,21,23-26,35H,11-12,14-19H2,1-9H3,(H,32,34)/b20-10+/t21-,23+,24+,25-,26-,29+,30-,31-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.12E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Karachi Curated by ChEMBL					Assay Description Inhibition of BChE (unknown origin)				J Nat Prod 66: 739-42 (2003) Article DOI: 10.1021/np020446o BindingDB Entry DOI: 10.7270/Q2862G6D
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50250635 (CHEMBL517605 | [(20S)-20-(dimethylamino)-3-beta-(2...) Show SMILES CC(C)C(=O)N[C@H]1CC[C@]2(O)CC3=CC[C@]4(C)[C@H](CC[C@@]4(C)[C@@H]3CC[C@H]2C1(C)C)[C@H](C)N(C)C |r,t:12| Show InChI InChI=1S/C30H52N2O2/c1-19(2)26(33)31-25-14-17-30(34)18-21-12-15-28(6)22(20(3)32(8)9)13-16-29(28,7)23(21)10-11-24(30)27(25,4)5/h12,19-20,22-25,34H,10-11,13-18H2,1-9H3,(H,31,33)/t20-,22+,23+,24-,25-,28+,29-,30-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.37E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Karachi Curated by ChEMBL					Assay Description Inhibition of BChE (unknown origin)				J Nat Prod 66: 739-42 (2003) Article DOI: 10.1021/np020446o BindingDB Entry DOI: 10.7270/Q2862G6D
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50250633 (CHEMBL469289 | [(20S)-3-beta-benzoylamino-20-dimet...) Show SMILES C[C@@H]([C@H]1CC[C@@]2(C)[C@@H]3CC[C@H]4C(C)(C)[C@H](CC[C@]4(O)CC3=CC[C@]12C)NC(=O)c1ccccc1)N(C)C |r,c:22| Show InChI InChI=1S/C33H50N2O2/c1-22(35(6)7)25-16-19-32(5)26-13-14-27-30(2,3)28(34-29(36)23-11-9-8-10-12-23)17-20-33(27,37)21-24(26)15-18-31(25,32)4/h8-12,15,22,25-28,37H,13-14,16-21H2,1-7H3,(H,34,36)/t22-,25+,26+,27-,28-,31+,32-,33-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.11E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Karachi Curated by ChEMBL					Assay Description Inhibition of BChE (unknown origin)				J Nat Prod 66: 739-42 (2003) Article DOI: 10.1021/np020446o BindingDB Entry DOI: 10.7270/Q2862G6D
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50250634 (CHEMBL466169 | [(20S)-20-(dimethylamino)-3-beta-(2...) Show SMILES C\C=C(/C)C(=O)N[C@H]1CC[C@]2(O)CC3=CC[C@]4(C)[C@H](CC[C@@]4(C)[C@@H]3CC[C@H]2C1(C)C)[C@H](C)N(C)C |r,t:13| Show InChI InChI=1S/C31H52N2O2/c1-10-20(2)27(34)32-26-15-18-31(35)19-22-13-16-29(6)23(21(3)33(8)9)14-17-30(29,7)24(22)11-12-25(31)28(26,4)5/h10,13,21,23-26,35H,11-12,14-19H2,1-9H3,(H,32,34)/b20-10+/t21-,23+,24+,25-,26-,29+,30-,31-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.44E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Karachi Curated by ChEMBL					Assay Description Inhibition of electric eel AChE by modified Ellman method				J Nat Prod 66: 739-42 (2003) Article DOI: 10.1021/np020446o BindingDB Entry DOI: 10.7270/Q2862G6D
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50250633 (CHEMBL469289 | [(20S)-3-beta-benzoylamino-20-dimet...) Show SMILES C[C@@H]([C@H]1CC[C@@]2(C)[C@@H]3CC[C@H]4C(C)(C)[C@H](CC[C@]4(O)CC3=CC[C@]12C)NC(=O)c1ccccc1)N(C)C |r,c:22| Show InChI InChI=1S/C33H50N2O2/c1-22(35(6)7)25-16-19-32(5)26-13-14-27-30(2,3)28(34-29(36)23-11-9-8-10-12-23)17-20-33(27,37)21-24(26)15-18-31(25,32)4/h8-12,15,22,25-28,37H,13-14,16-21H2,1-7H3,(H,34,36)/t22-,25+,26+,27-,28-,31+,32-,33-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Karachi Curated by ChEMBL					Assay Description Inhibition of electric eel AChE by modified Ellman method				J Nat Prod 66: 739-42 (2003) Article DOI: 10.1021/np020446o BindingDB Entry DOI: 10.7270/Q2862G6D
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50250635 (CHEMBL517605 | [(20S)-20-(dimethylamino)-3-beta-(2...) Show SMILES CC(C)C(=O)N[C@H]1CC[C@]2(O)CC3=CC[C@]4(C)[C@H](CC[C@@]4(C)[C@@H]3CC[C@H]2C1(C)C)[C@H](C)N(C)C |r,t:12| Show InChI InChI=1S/C30H52N2O2/c1-19(2)26(33)31-25-14-17-30(34)18-21-12-15-28(6)22(20(3)32(8)9)13-16-29(28,7)23(21)10-11-24(30)27(25,4)5/h12,19-20,22-25,34H,10-11,13-18H2,1-9H3,(H,31,33)/t20-,22+,23+,24-,25-,28+,29-,30-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Karachi Curated by ChEMBL					Assay Description Inhibition of electric eel AChE by modified Ellman method				J Nat Prod 66: 739-42 (2003) Article DOI: 10.1021/np020446o BindingDB Entry DOI: 10.7270/Q2862G6D
					More data for this Ligand-Target Pair