Compile Data Set for Download or QSAR

Found 210 hits with Last Name = 'lewis' and Initial = 'p'   

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
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096606 (CHEMBL3577279) Show SMILES OC(=O)CNC(=O)Cn1c2C[C@@H](CCc2c2cc(Br)ccc12)C(O)=O |r| Show InChI InChI=1S/C17H17BrN2O5/c18-10-2-4-13-12(6-10)11-3-1-9(17(24)25)5-14(11)20(13)8-15(21)19-7-16(22)23/h2,4,6,9H,1,3,5,7-8H2,(H,19,21)(H,22,23)(H,24,25)/t9-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	PDB Article PubMed	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair				3D Structure (crystal)
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096604 (CHEMBL3577290) Show SMILES OC(=O)[C@H](Cc1ccccc1)NC(=O)Cn1c2C[C@@H](CCc2c2cc(Br)ccc12)C(O)=O |r| Show InChI InChI=1S/C24H23BrN2O5/c25-16-7-9-20-18(12-16)17-8-6-15(23(29)30)11-21(17)27(20)13-22(28)26-19(24(31)32)10-14-4-2-1-3-5-14/h1-5,7,9,12,15,19H,6,8,10-11,13H2,(H,26,28)(H,29,30)(H,31,32)/t15-,19+/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	1.50E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair				3D Structure (crystal)
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096605 (CHEMBL3577289) Show SMILES OC(=O)[C@@H](Cc1ccccc1)NC(=O)Cn1c2C[C@@H](CCc2c2cc(Br)ccc12)C(O)=O |r| Show InChI InChI=1S/C24H23BrN2O5/c25-16-7-9-20-18(12-16)17-8-6-15(23(29)30)11-21(17)27(20)13-22(28)26-19(24(31)32)10-14-4-2-1-3-5-14/h1-5,7,9,12,15,19H,6,8,10-11,13H2,(H,26,28)(H,29,30)(H,31,32)/t15-,19-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	1.70E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair				3D Structure (crystal)
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096608 (CHEMBL3577288) Show SMILES CC(C)C[C@H](NC(=O)Cn1c2C[C@@H](CCc2c2cc(Br)ccc12)C(O)=O)C(O)=O |r| Show InChI InChI=1S/C21H25BrN2O5/c1-11(2)7-16(21(28)29)23-19(25)10-24-17-6-4-13(22)9-15(17)14-5-3-12(20(26)27)8-18(14)24/h4,6,9,11-12,16H,3,5,7-8,10H2,1-2H3,(H,23,25)(H,26,27)(H,28,29)/t12-,16+/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.70E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096611 (CHEMBL3577285) Show SMILES NC(=O)c1ccc(CNC(=O)Cn2c3C[C@@H](CCc3c3cc(Br)ccc23)C(O)=O)cc1 |r| Show InChI InChI=1S/C23H22BrN3O4/c24-16-6-8-19-18(10-16)17-7-5-15(23(30)31)9-20(17)27(19)12-21(28)26-11-13-1-3-14(4-2-13)22(25)29/h1-4,6,8,10,15H,5,7,9,11-12H2,(H2,25,29)(H,26,28)(H,30,31)/t15-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.60E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096607 (CHEMBL3577278) Show SMILES OC(=O)CNC(=O)Cn1c2C[C@@H](CCc2c2cc(Cl)ccc12)C(O)=O |r| Show InChI InChI=1S/C17H17ClN2O5/c18-10-2-4-13-12(6-10)11-3-1-9(17(24)25)5-14(11)20(13)8-15(21)19-7-16(22)23/h2,4,6,9H,1,3,5,7-8H2,(H,19,21)(H,22,23)(H,24,25)/t9-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	4.70E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096609 (CHEMBL3577287) Show SMILES CC(C)(C)OC(=O)NCCCC[C@@H](NC(=O)Cn1c2C[C@@H](CCc2c2cc(Br)ccc12)C(O)=O)C(O)=O |r| Show InChI InChI=1S/C26H34BrN3O7/c1-26(2,3)37-25(36)28-11-5-4-6-19(24(34)35)29-22(31)14-30-20-10-8-16(27)13-18(20)17-9-7-15(23(32)33)12-21(17)30/h8,10,13,15,19H,4-7,9,11-12,14H2,1-3H3,(H,28,36)(H,29,31)(H,32,33)(H,34,35)/t15-,19-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.40E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096638 (CHEMBL3577268) Show SMILES OC(=O)[C@@H]1CCc2c(C1)[nH]c1ccc(Cl)cc21 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	7.40E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair				3D Structure (crystal)
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096614 (CHEMBL3577282) Show SMILES CC(C)(C)OC(=O)N1CCC(CNC(=O)Cn2c3C[C@@H](CCc3c3cc(Br)ccc23)C(O)=O)CC1 |r| Show InChI InChI=1S/C26H34BrN3O5/c1-26(2,3)35-25(34)29-10-8-16(9-11-29)14-28-23(31)15-30-21-7-5-18(27)13-20(21)19-6-4-17(24(32)33)12-22(19)30/h5,7,13,16-17H,4,6,8-12,14-15H2,1-3H3,(H,28,31)(H,32,33)/t17-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.30E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096634 (CHEMBL3577272) Show SMILES OC(=O)[C@@H]1CCc2c(C1)[nH]c1ccc(Br)cc21 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.70E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096612 (CHEMBL3577284) Show SMILES NC(=O)CNC(=O)Cn1c2C[C@@H](CCc2c2cc(Br)ccc12)C(O)=O |r| Show InChI InChI=1S/C17H18BrN3O4/c18-10-2-4-13-12(6-10)11-3-1-9(17(24)25)5-14(11)21(13)8-16(23)20-7-15(19)22/h2,4,6,9H,1,3,5,7-8H2,(H2,19,22)(H,20,23)(H,24,25)/t9-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.50E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096635 (CHEMBL3577271) Show SMILES OC(=O)[C@@H]1CCc2c(C1)[nH]c1ccc(I)cc21 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	9.70E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096613 (CHEMBL3577283) Show SMILES OC(=O)[C@@H]1CCc2c(C1)n(CC(=O)NCC1CCNCC1)c1ccc(Br)cc21 |r| Show InChI InChI=1S/C21H26BrN3O3/c22-15-2-4-18-17(10-15)16-3-1-14(21(27)28)9-19(16)25(18)12-20(26)24-11-13-5-7-23-8-6-13/h2,4,10,13-14,23H,1,3,5-9,11-12H2,(H,24,26)(H,27,28)/t14-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.16E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096618 (CHEMBL3577276) Show SMILES NC(=O)Cn1c2C[C@@H](CCc2c2cc(Br)ccc12)C(O)=O |r| Show InChI InChI=1S/C16H10O7/c1-21-13-5-12-7(3-10(13)19)15-14(16(20)23-12)6-2-8(17)9(18)4-11(6)22-15/h2-5,17-19H,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	PDB Article PubMed	1.37E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair				3D Structure (crystal)
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096617 (CHEMBL3577277) Show SMILES NC(=O)Cn1c2C[C@H](CCc2c2cc(Br)ccc12)C(O)=O |r| Show InChI InChI=1S/C15H15BrN2O3/c16-9-2-4-12-11(6-9)10-3-1-8(15(20)21)5-13(10)18(12)7-14(17)19/h2,4,6,8H,1,3,5,7H2,(H2,17,19)(H,20,21)/t8-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.58E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096641 (CHEMBL3277053) Show SMILES OC(=O)C1CCc2c(C1)[nH]c1ccc(Cl)cc21 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	1.66E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair				3D Structure (crystal)
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096610 (CHEMBL3577286) Show SMILES NC(=O)CN1CCC(CC1)NC(=O)Cn1c2C[C@@H](CCc2c2cc(Br)ccc12)C(O)=O |r| Show InChI InChI=1S/C22H27BrN4O4/c23-14-2-4-18-17(10-14)16-3-1-13(22(30)31)9-19(16)27(18)12-21(29)25-15-5-7-26(8-6-15)11-20(24)28/h2,4,10,13,15H,1,3,5-9,11-12H2,(H2,24,28)(H,25,29)(H,30,31)/t13-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.71E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096633 (CHEMBL3577273) Show SMILES OC(=O)[C@H]1CCc2c(C1)[nH]c1ccc(Br)cc21 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.82E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096616 (CHEMBL3577280) Show SMILES CCNC(=O)Cn1c2C[C@@H](CCc2c2cc(Cl)ccc12)C(O)=O |r| Show InChI InChI=1S/C17H19ClN2O3/c1-2-19-16(21)9-20-14-6-4-11(18)8-13(14)12-5-3-10(17(22)23)7-15(12)20/h4,6,8,10H,2-3,5,7,9H2,1H3,(H,19,21)(H,22,23)/t10-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.93E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096615 (CHEMBL3577281) Show SMILES NC(=O)Cc1ccc(NC(=O)Cn2c3C[C@@H](CCc3c3cc(Cl)ccc23)C(O)=O)cc1 |r| Show InChI InChI=1S/C23H22ClN3O4/c24-15-4-8-19-18(11-15)17-7-3-14(23(30)31)10-20(17)27(19)12-22(29)26-16-5-1-13(2-6-16)9-21(25)28/h1-2,4-6,8,11,14H,3,7,9-10,12H2,(H2,25,28)(H,26,29)(H,30,31)/t14-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.01E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096632 (CHEMBL3577274) Show SMILES NC(=O)Cn1c2C[C@@H](CCc2c2cc(Cl)ccc12)C(O)=O |r| Show InChI InChI=1S/C15H15ClN2O3/c16-9-2-4-12-11(6-9)10-3-1-8(15(20)21)5-13(10)18(12)7-14(17)19/h2,4,6,8H,1,3,5,7H2,(H2,17,19)(H,20,21)/t8-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	2.04E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair				3D Structure (crystal)
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096637 (CHEMBL3577269) Show SMILES OC(=O)[C@H]1CCc2c(C1)[nH]c1ccc(Cl)cc21 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.46E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096636 (CHEMBL3577270) Show SMILES OC(=O)[C@@H]1CCc2c(C1)[nH]c1ccc(F)cc21 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.54E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
Beta sliding clamp (Escherichia coli (strain K12))	BDBM50096631 (CHEMBL3577275) Show SMILES NC(=O)Cn1c2C[C@H](CCc2c2cc(Cl)ccc12)C(O)=O |r| Show InChI InChI=1S/C15H15ClN2O3/c16-9-2-4-12-11(6-9)10-3-1-8(15(20)21)5-13(10)18(12)7-14(17)19/h2,4,6,8H,1,3,5,7H2,(H2,17,19)(H,20,21)/t8-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	4.93E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Wollongong and The Illawarra Health and Medical Research Institute Curated by ChEMBL					Assay Description Inhibition of Escherichia coli DNA sliding clamp protein using N-fluorescein (FAM)-QLDLF-OH tracer by fluorescence polarization assay				J Med Chem 58: 4693-702 (2015) Article DOI: 10.1021/acs.jmedchem.5b00232 BindingDB Entry DOI: 10.7270/Q2KK9DJ9
					More data for this Ligand-Target Pair
D(1A)/D(1B)/D(2)/D(3)/D(4) dopamine receptor (Rattus norvegicus (rat)-RAT-Rattus norvegicus (Rat...)	BDBM21398 (4-[4-(4-Chloro-phenyl)-4-hydroxy-piperidin-1-yl]-1...) Show SMILES OC1(CCN(CCCC(=O)c2ccc(F)cc2)CC1)c1ccc(Cl)cc1 Show InChI InChI=1S/C21H23ClFNO2/c22-18-7-5-17(6-8-18)21(26)11-14-24(15-12-21)13-1-2-20(25)16-3-9-19(23)10-4-16/h3-10,26H,1-2,11-15H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	0.280	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Ability to inhibit [3H]haloperidol binding to dopamine receptor in rat striatal homogenate				J Med Chem 28: 1811-7 (1985) BindingDB Entry DOI: 10.7270/Q2KW5J7H
					More data for this Ligand-Target Pair
D(1A)/D(1B)/D(2)/D(3)/D(4) dopamine receptor (Rattus norvegicus (rat)-RAT-Rattus norvegicus (Rat...)	BDBM50334150 (1-(1-(4,4-bis(4-fluorophenyl)butyl)piperidin-4-yl)...) Show SMILES Fc1ccc(cc1)C(CCCN1CCC(CC1)n1c2ccccc2[nH]c1=O)c1ccc(F)cc1 Show InChI InChI=1S/C28H29F2N3O/c29-22-11-7-20(8-12-22)25(21-9-13-23(30)14-10-21)4-3-17-32-18-15-24(16-19-32)33-27-6-2-1-5-26(27)31-28(33)34/h1-2,5-14,24-25H,3-4,15-19H2,(H,31,34)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of [3H]haloperidol binding to dopamine receptors in rat striatal membranes.				J Med Chem 28: 606-12 (1985) BindingDB Entry DOI: 10.7270/Q2TB193Z
					More data for this Ligand-Target Pair
D(1A)/D(1B)/D(2)/D(3)/D(4) dopamine receptor (Rattus norvegicus (rat)-RAT-Rattus norvegicus (Rat...)	BDBM50334150 (1-(1-(4,4-bis(4-fluorophenyl)butyl)piperidin-4-yl)...) Show SMILES Fc1ccc(cc1)C(CCCN1CCC(CC1)n1c2ccccc2[nH]c1=O)c1ccc(F)cc1 Show InChI InChI=1S/C28H29F2N3O/c29-22-11-7-20(8-12-22)25(21-9-13-23(30)14-10-21)4-3-17-32-18-15-24(16-19-32)33-27-6-2-1-5-26(27)31-28(33)34/h1-2,5-14,24-25H,3-4,15-19H2,(H,31,34)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of [3H]haloperidol binding to dopamine receptors in rat striatal membranes.				J Med Chem 28: 606-12 (1985) BindingDB Entry DOI: 10.7270/Q2TB193Z
					More data for this Ligand-Target Pair
D(1A)/D(1B)/D(2)/D(3)/D(4) dopamine receptor (Rattus norvegicus (rat)-RAT-Rattus norvegicus (Rat...)	BDBM50225369 (CHEMBL295712) Show SMILES Fc1ccc(cc1)N(CCCN1CCC2(CC1)N(CNC2=O)c1ccccc1)c1ccc(F)cc1 Show InChI InChI=1S/C28H30F2N4O/c29-22-7-11-24(12-8-22)33(25-13-9-23(30)10-14-25)18-4-17-32-19-15-28(16-20-32)27(35)31-21-34(28)26-5-2-1-3-6-26/h1-3,5-14H,4,15-21H2,(H,31,35)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	0.610	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of [3H]haloperidol binding to dopamine receptors in rat striatal membranes.				J Med Chem 28: 606-12 (1985) BindingDB Entry DOI: 10.7270/Q2TB193Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353767 (CHEMBL1829430) Show SMILES CCC(N(CCCN)C(=O)c1ccc(C)cc1)c1nc2snc(C)c2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C27H31N5O2S/c1-4-22(31(16-8-15-28)26(33)21-13-11-18(2)12-14-21)24-29-25-23(19(3)30-35-25)27(34)32(24)17-20-9-6-5-7-10-20/h5-7,9-14,22H,4,8,15-17,28H2,1-3H3	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	1	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353767 (CHEMBL1829430) Show SMILES CCC(N(CCCN)C(=O)c1ccc(C)cc1)c1nc2snc(C)c2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C27H31N5O2S/c1-4-22(31(16-8-15-28)26(33)21-13-11-18(2)12-14-21)24-29-25-23(19(3)30-35-25)27(34)32(24)17-20-9-6-5-7-10-20/h5-7,9-14,22H,4,8,15-17,28H2,1-3H3	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	1	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353788 (CHEMBL1829433) Show SMILES CC(C)C(N(CCCN)C(=O)c1ccc(C)cc1)c1nc2snc(C)c2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C28H33N5O2S/c1-18(2)24(32(16-8-15-29)27(34)22-13-11-19(3)12-14-22)25-30-26-23(20(4)31-36-26)28(35)33(25)17-21-9-6-5-7-10-21/h5-7,9-14,18,24H,8,15-17,29H2,1-4H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353788 (CHEMBL1829433) Show SMILES CC(C)C(N(CCCN)C(=O)c1ccc(C)cc1)c1nc2snc(C)c2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C28H33N5O2S/c1-18(2)24(32(16-8-15-29)27(34)22-13-11-19(3)12-14-22)25-30-26-23(20(4)31-36-26)28(35)33(25)17-21-9-6-5-7-10-21/h5-7,9-14,18,24H,8,15-17,29H2,1-4H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353767 (CHEMBL1829430) Show SMILES CCC(N(CCCN)C(=O)c1ccc(C)cc1)c1nc2snc(C)c2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C27H31N5O2S/c1-4-22(31(16-8-15-28)26(33)21-13-11-18(2)12-14-21)24-29-25-23(19(3)30-35-25)27(34)32(24)17-20-9-6-5-7-10-20/h5-7,9-14,22H,4,8,15-17,28H2,1-3H3	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	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353799 (CHEMBL1829424) Show SMILES CCC(N(CCCN)C(=O)c1ccc(C)cc1)c1nc2sccc2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C27H30N4O2S/c1-3-23(30(16-7-15-28)26(32)21-12-10-19(2)11-13-21)24-29-25-22(14-17-34-25)27(33)31(24)18-20-8-5-4-6-9-20/h4-6,8-14,17,23H,3,7,15-16,18,28H2,1-2H3	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	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353799 (CHEMBL1829424) Show SMILES CCC(N(CCCN)C(=O)c1ccc(C)cc1)c1nc2sccc2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C27H30N4O2S/c1-3-23(30(16-7-15-28)26(32)21-12-10-19(2)11-13-21)24-29-25-22(14-17-34-25)27(33)31(24)18-20-8-5-4-6-9-20/h4-6,8-14,17,23H,3,7,15-16,18,28H2,1-2H3	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	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353820 (CHEMBL1829432) Show SMILES CCC(N(CCCN)C(=O)c1ccc(C)cc1)c1nc2c(C)nsc2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C27H31N5O2S/c1-4-22(31(16-8-15-28)26(33)21-13-11-18(2)12-14-21)25-29-23-19(3)30-35-24(23)27(34)32(25)17-20-9-6-5-7-10-20/h5-7,9-14,22H,4,8,15-17,28H2,1-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353799 (CHEMBL1829424) Show SMILES CCC(N(CCCN)C(=O)c1ccc(C)cc1)c1nc2sccc2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C27H30N4O2S/c1-3-23(30(16-7-15-28)26(32)21-12-10-19(2)11-13-21)24-29-25-22(14-17-34-25)27(33)31(24)18-20-8-5-4-6-9-20/h4-6,8-14,17,23H,3,7,15-16,18,28H2,1-2H3	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	8	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353821 (CHEMBL1829246) Show SMILES CCC(N(CCCN)C(=O)c1ccc(C)cc1)c1nc2ccsc2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C27H30N4O2S/c1-3-23(30(16-7-15-28)26(32)21-12-10-19(2)11-13-21)25-29-22-14-17-34-24(22)27(33)31(25)18-20-8-5-4-6-9-20/h4-6,8-14,17,23H,3,7,15-16,18,28H2,1-2H3	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	10	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353823 (CHEMBL1829422) Show SMILES CCC(N(CCCN)C(=O)c1ccc(C)cc1)c1nc2ccoc2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C27H30N4O3/c1-3-23(30(16-7-15-28)26(32)21-12-10-19(2)11-13-21)25-29-22-14-17-34-24(22)27(33)31(25)18-20-8-5-4-6-9-20/h4-6,8-14,17,23H,3,7,15-16,18,28H2,1-2H3	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	13	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
D(1A)/D(1B)/D(2)/D(3)/D(4) dopamine receptor (Rattus norvegicus (rat)-RAT-Rattus norvegicus (Rat...)	BDBM50225510 (CHEMBL156395) Show SMILES COc1ccccc1N1CCN(CCCN(c2ccc(F)cc2)c2ccc(F)cc2)CC1 Show InChI InChI=1S/C26H29F2N3O/c1-32-26-6-3-2-5-25(26)30-19-17-29(18-20-30)15-4-16-31(23-11-7-21(27)8-12-23)24-13-9-22(28)10-14-24/h2-3,5-14H,4,15-20H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	13	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of [3H]haloperidol binding to dopamine receptors in rat striatal membranes.				J Med Chem 28: 606-12 (1985) BindingDB Entry DOI: 10.7270/Q2TB193Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353822 (CHEMBL1829431) Show SMILES CCC(N(CCCN)C(=O)c1ccc(C)cc1)c1nc2onc(C)c2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C27H31N5O3/c1-4-22(31(16-8-15-28)26(33)21-13-11-18(2)12-14-21)24-29-25-23(19(3)30-35-25)27(34)32(24)17-20-9-6-5-7-10-20/h5-7,9-14,22H,4,8,15-17,28H2,1-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353761 (CHEMBL1829406) Show SMILES CCC(N(CCCN)C(=O)c1ccc(C)c(F)c1)c1nc2ccsc2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C27H29FN4O2S/c1-3-23(31(14-7-13-29)26(33)20-11-10-18(2)21(28)16-20)25-30-22-12-15-35-24(22)27(34)32(25)17-19-8-5-4-6-9-19/h4-6,8-12,15-16,23H,3,7,13-14,17,29H2,1-2H3	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	20	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Alpha-1A/Alpha-1B/Alpha-1D adrenergic receptor (Rattus norvegicus (rat)-Rattus norvegicus (Rat))	BDBM50001884 (2-[4-(4-Methyl-benzyl)-piperazin-1-yl]-1-(2-methyl...) Show SMILES CN1CCN(CC1)C1=Nc2cc(Cl)ccc2Nc2ccccc12 |t:8| Show InChI InChI=1S/C18H19ClN4/c1-22-8-10-23(11-9-22)18-14-4-2-3-5-15(14)20-16-7-6-13(19)12-17(16)21-18/h2-7,12,20H,8-11H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars	DrugBank PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description The compound was tested for inhibition of [3H]WB-4101 binding to alpha-1 adrenergic receptor of rat frontal cortex				J Med Chem 28: 1811-7 (1985) BindingDB Entry DOI: 10.7270/Q2KW5J7H
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353760 (CHEMBL1829248) Show SMILES CCC(N(CCCN)C(=O)c1ccc(C)cc1)c1nc2ccsc2c(=O)n1Cc1cccc(F)c1 Show InChI InChI=1S/C27H29FN4O2S/c1-3-23(31(14-5-13-29)26(33)20-10-8-18(2)9-11-20)25-30-22-12-15-35-24(22)27(34)32(25)17-19-6-4-7-21(28)16-19/h4,6-12,15-16,23H,3,5,13-14,17,29H2,1-2H3	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	20	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353762 (CHEMBL1829423) Show SMILES CCC(N(CCCN)C(=O)c1ccc(C)cc1)c1nc2ccn(C)c2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C28H33N5O2/c1-4-24(32(17-8-16-29)27(34)22-13-11-20(2)12-14-22)26-30-23-15-18-31(3)25(23)28(35)33(26)19-21-9-6-5-7-10-21/h5-7,9-15,18,24H,4,8,16-17,19,29H2,1-3H3	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	21	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353763 (CHEMBL1829401) Show SMILES CCC(N(CCCN)C(=O)c1ccc(Br)cc1)c1nc2ccsc2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C26H27BrN4O2S/c1-2-22(30(15-6-14-28)25(32)19-9-11-20(27)12-10-19)24-29-21-13-16-34-23(21)26(33)31(24)17-18-7-4-3-5-8-18/h3-5,7-13,16,22H,2,6,14-15,17,28H2,1H3	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	30	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353764 (CHEMBL1829420) Show SMILES CCC(N(CCCN)C(=O)c1ccc2ccccc2c1)c1nc2ccsc2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C30H30N4O2S/c1-2-26(33(17-8-16-31)29(35)24-14-13-22-11-6-7-12-23(22)19-24)28-32-25-15-18-37-27(25)30(36)34(28)20-21-9-4-3-5-10-21/h3-7,9-15,18-19,26H,2,8,16-17,20,31H2,1H3	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	30	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Kinesin-like protein KIF11 (Homo sapiens (Human))	BDBM50353765 (CHEMBL1829418) Show SMILES CCC(N(CCCN)C(=O)c1cc2ccccc2s1)c1nc2ccsc2c(=O)n1Cc1ccccc1 Show InChI InChI=1S/C28H28N4O2S2/c1-2-22(31(15-8-14-29)27(33)24-17-20-11-6-7-12-23(20)36-24)26-30-21-13-16-35-25(21)28(34)32(26)18-19-9-4-3-5-10-19/h3-7,9-13,16-17,22H,2,8,14-15,18,29H2,1H3	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	40	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant C-terminal His6-tagged KSP ATPase activity after 1 hr by malachite green assay				J Med Chem 54: 6734-50 (2011) Article DOI: 10.1021/jm200629m BindingDB Entry DOI: 10.7270/Q2ZC838Z
					More data for this Ligand-Target Pair
Cytochrome P450 2C19 (Homo sapiens (Human))	BDBM50113978 (CHEMBL3605543) Show SMILES CCn1c(nc2ccc(cc12)C(F)(F)F)[C@@H](C)NS(=O)(=O)c1ccncc1 |r| Show InChI InChI=1S/C17H17F3N4O2S/c1-3-24-15-10-12(17(18,19)20)4-5-14(15)22-16(24)11(2)23-27(25,26)13-6-8-21-9-7-13/h4-11,23H,3H2,1-2H3/t11-/m1/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	40	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of CYP2C19 in human liver microsomes incubated for 5 mins in presence of NADPH and specific substrates by LC/MS/MS method				J Med Chem 58: 7057-75 (2015) Article DOI: 10.1021/acs.jmedchem.5b01078 BindingDB Entry DOI: 10.7270/Q2Z89F6J
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M1/M2/M3/M4/M5 (RAT)	BDBM50001884 (2-[4-(4-Methyl-benzyl)-piperazin-1-yl]-1-(2-methyl...) Show SMILES CN1CCN(CC1)C1=Nc2cc(Cl)ccc2Nc2ccccc12 |t:8| Show InChI InChI=1S/C18H19ClN4/c1-22-8-10-23(11-9-22)18-14-4-2-3-5-15(14)20-16-7-6-13(19)12-17(16)21-18/h2-7,12,20H,8-11H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	48	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description The compound was tested for inhibition of [3H]QNB binding to Muscarinic acetylcholine receptor				J Med Chem 28: 1811-7 (1985) BindingDB Entry DOI: 10.7270/Q2KW5J7H
					More data for this Ligand-Target Pair

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