Compile Data Set for Download or QSAR

Found 19 hits of ic50 for UniProtKB: P17597   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50079602 (2,5-Dichloro-N-(4,6-dimethyl-pyrimidin-2-yl)-benze...) Show SMILES Cc1cc(C)nc(NS(=O)(=O)c2cc(Cl)ccc2Cl)n1 Show InChI InChI=1S/C12H11Cl2N3O2S/c1-7-5-8(2)16-12(15-7)17-20(18,19)11-6-9(13)3-4-10(11)14/h3-6H,1-2H3,(H,15,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50079609 (4-Fluoro-N-(4-methyl-pyrimidin-2-yl)-benzenesulfon...) Show SMILES Cc1ccnc(NS(=O)(=O)c2ccc(F)cc2)n1 Show InChI InChI=1S/C11H10FN3O2S/c1-8-6-7-13-11(14-8)15-18(16,17)10-4-2-9(12)3-5-10/h2-7H,1H3,(H,13,14,15)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	3.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50079603 (4-Bromo-N-(4-methyl-pyrimidin-2-yl)-benzenesulfona...) Show SMILES Cc1ccnc(NS(=O)(=O)c2ccc(Br)cc2)n1 Show InChI InChI=1S/C11H10BrN3O2S/c1-8-6-7-13-11(14-8)15-18(16,17)10-4-2-9(12)3-5-10/h2-7H,1H3,(H,13,14,15)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	5.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50216782 (CHEMBL291948) Show SMILES Cc1cccc(c1)C(=O)OCn1ccc(=O)[nH]c1=O Show InChI InChI=1S/C13H12N2O4/c1-9-3-2-4-10(7-9)12(17)19-8-15-6-5-11(16)14-13(15)18/h2-7H,8H2,1H3,(H,14,16,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	6.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50079607 (2,5-Dichloro-N-thiazol-2-yl-benzenesulfonamide | C...) Show SMILES Clc1ccc(Cl)c(c1)S(=O)(=O)Nc1nccs1 Show InChI InChI=1S/C9H6Cl2N2O2S2/c10-6-1-2-7(11)8(5-6)17(14,15)13-9-12-3-4-16-9/h1-5H,(H,12,13)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	8.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50079606 (2,5-Dichloro-N-(4-methyl-pyrimidin-2-yl)-benzenesu...) Show SMILES Cc1ccnc(NS(=O)(=O)c2cc(Cl)ccc2Cl)n1 Show InChI InChI=1S/C11H9Cl2N3O2S/c1-7-4-5-14-11(15-7)16-19(17,18)10-6-8(12)2-3-9(10)13/h2-6H,1H3,(H,14,15,16)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	9.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50079608 (CHEMBL293152 | N-(4-Chloro-6-methoxy-pyrimidin-2-y...) Show SMILES COc1cc(Cl)nc(NS(=O)(=O)c2ccc(F)cc2)n1 Show InChI InChI=1S/C11H9ClFN3O3S/c1-19-10-6-9(12)14-11(15-10)16-20(17,18)8-4-2-7(13)3-5-8/h2-6H,1H3,(H,14,15,16)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	1.11E+5	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50079605 (4-Fluoro-N-(5-methyl-pyridin-2-yl)-benzenesulfonam...) Show SMILES Cc1ccc(NS(=O)(=O)c2ccc(F)cc2)nc1 Show InChI InChI=1S/C12H11FN2O2S/c1-9-2-7-12(14-8-9)15-18(16,17)11-5-3-10(13)4-6-11/h2-8H,1H3,(H,14,15)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	1.52E+5	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50216775 (CHEMBL57654) Show SMILES Brc1ccc(cc1)C(=O)OCn1ccc(=O)[nH]c1=O Show InChI InChI=1S/C12H9BrN2O4/c13-9-3-1-8(2-4-9)11(17)19-7-15-6-5-10(16)14-12(15)18/h1-6H,7H2,(H,14,16,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.69E+5	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50216778 (CHEMBL57215) Show SMILES Clc1ccc(cc1)C(=O)OCn1ccc(=O)[nH]c1=O Show InChI InChI=1S/C12H9ClN2O4/c13-9-3-1-8(2-4-9)11(17)19-7-15-6-5-10(16)14-12(15)18/h1-6H,7H2,(H,14,16,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	1.82E+5	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50216780 (CHEMBL58352) Show SMILES O=C(OCn1ccc(=O)[nH]c1=O)c1ccccc1 Show InChI InChI=1S/C12H10N2O4/c15-10-6-7-14(12(17)13-10)8-18-11(16)9-4-2-1-3-5-9/h1-7H,8H2,(H,13,15,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	2.08E+5	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50216774 (CHEMBL58964) Show SMILES Fc1ccc(cc1)C(=O)OCn1ccc(=O)[nH]c1=O Show InChI InChI=1S/C12H9FN2O4/c13-9-3-1-8(2-4-9)11(17)19-7-15-6-5-10(16)14-12(15)18/h1-6H,7H2,(H,14,16,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.12E+5	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50216779 (CHEMBL58200) Show SMILES FC(F)(F)c1cc(Cl)c(C(=O)OCn2ccc(=O)[nH]c2=O)c(Cl)c1 Show InChI InChI=1S/C13H7Cl2F3N2O4/c14-7-3-6(13(16,17)18)4-8(15)10(7)11(22)24-5-20-2-1-9(21)19-12(20)23/h1-4H,5H2,(H,19,21,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>2.61E+5	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50216773 (CHEMBL61025) Show SMILES Ic1ccc(cc1)C(=O)OCn1ccc(=O)[nH]c1=O Show InChI InChI=1S/C12H9IN2O4/c13-9-3-1-8(2-4-9)11(17)19-7-15-6-5-10(16)14-12(15)18/h1-6H,7H2,(H,14,16,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>2.69E+5	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50079601 (CHEMBL293269 | N-(4-Methyl-pyrimidin-2-yl)-2-nitro...) Show SMILES Cc1ccnc(NS(=O)(=O)c2ccccc2[N+]([O-])=O)n1 Show InChI InChI=1S/C11H10N4O4S/c1-8-6-7-12-11(13-8)14-20(18,19)10-5-3-2-4-9(10)15(16)17/h2-7H,1H3,(H,12,13,14)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	2.87E+5	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50079604 (2,5-Dichloro-N-(5-methyl-thiazol-2-yl)-benzenesulf...) Show SMILES Cc1cnc(NS(=O)(=O)c2cc(Cl)ccc2Cl)s1 Show InChI InChI=1S/C10H8Cl2N2O2S2/c1-6-5-13-10(17-6)14-18(15,16)9-4-7(11)2-3-8(9)12/h2-5H,1H3,(H,13,14)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>3.09E+5	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50216781 (CHEMBL58918) Show SMILES [O-][N+](=O)c1ccc(cc1)C(=O)OCn1ccc(=O)[nH]c1=O Show InChI InChI=1S/C12H9N3O6/c16-10-5-6-14(12(18)13-10)7-21-11(17)8-1-3-9(4-2-8)15(19)20/h1-6H,7H2,(H,13,16,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>3.44E+5	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50216783 (CHEMBL293995) Show SMILES COc1ccc(cc1)C(=O)OCn1ccc(=O)[nH]c1=O Show InChI InChI=1S/C13H12N2O5/c1-19-10-4-2-9(3-5-10)12(17)20-8-15-7-6-11(16)14-13(15)18/h2-7H,8H2,1H3,(H,14,16,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	>3.62E+5	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair
Acetolactate synthase, chloroplastic (Arabidopsis thaliana)	BDBM50216776 (CHEMBL58689) Show SMILES COc1ccccc1C(=O)OCn1ccc(=O)[nH]c1=O Show InChI InChI=1S/C13H12N2O5/c1-19-10-5-3-2-4-9(10)12(17)20-8-15-7-6-11(16)14-13(15)18/h2-7H,8H2,1H3,(H,14,16,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>3.62E+5	n/a	n/a	n/a	n/a	n/a	n/a
Nankai University Curated by ChEMBL					Assay Description Inhibitory activity against Acetolactate synthase (ALS) enzyme by using the rape-root growth method				Bioorg Med Chem Lett 9: 1927-32 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SQC
					More data for this Ligand-Target Pair