Compile Data Set for Download or QSAR

Found 97 hits with Last Name = 'grabowiecka' and Initial = 'a'   

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
Urease subunit alpha/beta/gamma (Bacillus pasteurii)	BDBM24969 ([(2-{[(benzyloxy)carbonyl]amino}acetamido)methyl](...) Show SMILES CP(O)(=S)CNC(=O)CNC(=O)OCc1ccccc1 Show InChI InChI=1S/C12H17N2O4PS/c1-19(17,20)9-14-11(15)7-13-12(16)18-8-10-5-3-2-4-6-10/h2-6H,7-9H2,1H3,(H,13,16)(H,14,15)(H,17,20)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	170	-39.3	1.80E+3	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534783 (CHEMBL4575318) Show SMILES [#6]-[#8]-[#6](=O)-[#6]-[#6]-[#6]-[#7]-[#6](=O)-c1ccccc1[Se;v2][Se;v2]c1ccccc1-[#6](=O)-[#7]-[#6]-[#6]-[#6]-[#6](=O)-[#8]-[#6] Show InChI InChI=1S/C24H28N2O6Se2/c1-31-21(27)13-7-15-25-23(29)17-9-3-5-11-19(17)33-34-20-12-6-4-10-18(20)24(30)26-16-8-14-22(28)32-2/h3-6,9-12H,7-8,13-16H2,1-2H3,(H,25,29)(H,26,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	184	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant Helicobacter pylori urease expressed in Escherichia coli rosetta DE3 after 120 mins by Berthelot colorimetric analysis				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM34233 (2-Phenyl-benzo[d]isoselenazol-3-one | 2-Phenyl-ben...) Show SMILES O=c1n([se]c2ccccc12)-c1ccccc1 Show InChI InChI=1S/C13H9NOSe/c15-13-11-8-4-5-9-12(11)16-14(13)10-6-2-1-3-7-10/h1-9H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	226	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant Helicobacter pylori urease expressed in Escherichia coli rosetta DE3 after 120 mins by Berthelot colorimetric analysis				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit alpha [F36L]/beta/gamma (Proteus vulgaris)	BDBM24969 ([(2-{[(benzyloxy)carbonyl]amino}acetamido)methyl](...) Show SMILES CP(O)(=S)CNC(=O)CNC(=O)OCc1ccccc1 Show InChI InChI=1S/C12H17N2O4PS/c1-19(17,20)9-14-11(15)7-13-12(16)18-8-10-5-3-2-4-6-10/h2-6H,7-9H2,1H3,(H,13,16)(H,14,15)(H,17,20)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	450	-36.8	3.10E+3	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50197347 (Ebselen Diselenide) Show SMILES O=C(Nc1ccccc1)c1ccccc1[Se][Se]c1ccccc1C(=O)Nc1ccccc1 Show InChI InChI=1S/C26H20N2O2Se2/c29-25(27-19-11-3-1-4-12-19)21-15-7-9-17-23(21)31-32-24-18-10-8-16-22(24)26(30)28-20-13-5-2-6-14-20/h1-18H,(H,27,29)(H,28,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	651	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant Helicobacter pylori urease expressed in Escherichia coli rosetta DE3 after 120 mins by Berthelot colorimetric analysis				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534782 (CHEMBL4471428) Show SMILES [#6]-[#8]-[#6](=O)-[#6]-[#7]-[#6](=O)-c1ccccc1[Se;v2][Se;v2]c1ccccc1-[#6](=O)-[#7]-[#6]-[#6](=O)-[#8]-[#6] Show InChI InChI=1S/C20H20N2O6Se2/c1-27-17(23)11-21-19(25)13-7-3-5-9-15(13)29-30-16-10-6-4-8-14(16)20(26)22-12-18(24)28-2/h3-10H,11-12H2,1-2H3,(H,21,25)(H,22,26)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	915	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant Helicobacter pylori urease expressed in Escherichia coli rosetta DE3 after 120 mins by Berthelot colorimetric analysis				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534776 (CHEMBL4539240) Show SMILES [#6]-[#6]-[#6](-[#6]-[#8])-[#7]-[#6](=O)-c1ccccc1[Se;v2][Se;v2]c1ccccc1-[#6](=O)-[#7]-[#6](-[#6]-[#6])-[#6]-[#8] Show InChI InChI=1S/C22H28N2O4Se2/c1-3-15(13-25)23-21(27)17-9-5-7-11-19(17)29-30-20-12-8-6-10-18(20)22(28)24-16(4-2)14-26/h5-12,15-16,25-26H,3-4,13-14H2,1-2H3,(H,23,27)(H,24,28)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.26E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant Helicobacter pylori urease expressed in Escherichia coli rosetta DE3 after 120 mins by Berthelot colorimetric analysis				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit alpha [F36L]/beta/gamma (Proteus vulgaris)	BDBM24971 (({[(benzyloxy)carbonyl]amino}methyl)(methyl)sulfan...) Show SMILES CP(O)(=S)CNC(=O)OCc1ccccc1 Show InChI InChI=1S/C10H14NO3PS/c1-15(13,16)8-11-10(12)14-7-9-5-3-2-4-6-9/h2-6H,7-8H2,1H3,(H,11,12)(H,13,16)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.40E+4	-28.2	1.58E+5	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha/beta/gamma (Bacillus pasteurii)	BDBM24971 (({[(benzyloxy)carbonyl]amino}methyl)(methyl)sulfan...) Show SMILES CP(O)(=S)CNC(=O)OCc1ccccc1 Show InChI InChI=1S/C10H14NO3PS/c1-15(13,16)8-11-10(12)14-7-9-5-3-2-4-6-9/h2-6H,7-8H2,1H3,(H,11,12)(H,13,16)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.75E+4	-27.6	1.12E+5	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha/beta/gamma (Bacillus pasteurii)	BDBM24967 (methyl[(methylamino)methyl]phosphinic acid | organ...) Show SMILES CN=CP(C)(O)O |w:1.0| Show InChI InChI=1S/C3H10NO2P/c1-4-3-7(2,5)6/h3,5-7H,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.80E+4	-27.5	6.00E+4	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha/beta/gamma (Bacillus pasteurii)	BDBM24962 ([(2-aminoacetamido)methyl](methyl)phosphinic acid ...) Show SMILES CP(O)(=O)CNC(=O)CN Show InChI InChI=1S/C4H11N2O3P/c1-10(8,9)3-6-4(7)2-5/h2-3,5H2,1H3,(H,6,7)(H,8,9)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.10E+4	-27.1	6.00E+4	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha/beta/gamma (Bacillus pasteurii)	BDBM24965 (organophosphorus derivative, 6 | {[(2S)-2-amino-3-...) Show SMILES CP(O)(=O)CNC(=O)[C@@H](N)COCc1ccccc1 |r| Show InChI InChI=1S/C12H19N2O4P/c1-19(16,17)9-14-12(15)11(13)8-18-7-10-5-3-2-4-6-10/h2-6,11H,7-9,13H2,1H3,(H,14,15)(H,16,17)/t11-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.50E+4	-26.7	8.00E+4	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha [F36L]/beta/gamma (Proteus vulgaris)	BDBM24967 (methyl[(methylamino)methyl]phosphinic acid | organ...) Show SMILES CN=CP(C)(O)O |w:1.0| Show InChI InChI=1S/C3H10NO2P/c1-4-3-7(2,5)6/h3,5-7H,1-2H3	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.70E+4	-26.5	1.53E+5	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha [F36L]/beta/gamma (Proteus vulgaris)	BDBM24962 ([(2-aminoacetamido)methyl](methyl)phosphinic acid ...) Show SMILES CP(O)(=O)CNC(=O)CN Show InChI InChI=1S/C4H11N2O3P/c1-10(8,9)3-6-4(7)2-5/h2-3,5H2,1H3,(H,6,7)(H,8,9)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.00E+4	-26.2	8.60E+4	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha [F36L]/beta/gamma (Proteus vulgaris)	BDBM24965 (organophosphorus derivative, 6 | {[(2S)-2-amino-3-...) Show SMILES CP(O)(=O)CNC(=O)[C@@H](N)COCc1ccccc1 |r| Show InChI InChI=1S/C12H19N2O4P/c1-19(16,17)9-14-12(15)11(13)8-18-7-10-5-3-2-4-6-10/h2-6,11H,7-9,13H2,1H3,(H,14,15)(H,16,17)/t11-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.26E+4	-26.0	1.83E+5	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha/beta/gamma (Bacillus pasteurii)	BDBM24966 (organophosphorus derivative, 7 | {[(2S)-2-amino-3-...) Show SMILES CP(O)(=O)CNC(=O)[C@@H](N)CO |r| Show InChI InChI=1S/C5H13N2O4P/c1-12(10,11)3-7-5(9)4(6)2-8/h4,8H,2-3,6H2,1H3,(H,7,9)(H,10,11)/t4-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.70E+4	-25.7	1.50E+5	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha [F36L]/beta/gamma (Proteus vulgaris)	BDBM24966 (organophosphorus derivative, 7 | {[(2S)-2-amino-3-...) Show SMILES CP(O)(=O)CNC(=O)[C@@H](N)CO |r| Show InChI InChI=1S/C5H13N2O4P/c1-12(10,11)3-7-5(9)4(6)2-8/h4,8H,2-3,6H2,1H3,(H,7,9)(H,10,11)/t4-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	4.10E+4	-25.5	3.42E+5	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha/beta/gamma (Bacillus pasteurii)	BDBM24968 (({[(benzyloxy)carbonyl]amino}methyl)(methyl)phosph...) Show SMILES CP(O)(=O)CNC(=O)OCc1ccccc1 Show InChI InChI=1S/C10H14NO4P/c1-16(13,14)8-11-10(12)15-7-9-5-3-2-4-6-9/h2-6H,7-8H2,1H3,(H,11,12)(H,13,14)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	4.30E+4	-25.3	1.23E+5	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha [F36L]/beta/gamma (Proteus vulgaris)	BDBM24968 (({[(benzyloxy)carbonyl]amino}methyl)(methyl)phosph...) Show SMILES CP(O)(=O)CNC(=O)OCc1ccccc1 Show InChI InChI=1S/C10H14NO4P/c1-16(13,14)8-11-10(12)15-7-9-5-3-2-4-6-9/h2-6H,7-8H2,1H3,(H,11,12)(H,13,14)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	6.50E+4	-24.3	3.19E+5	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50099857 (ACETOHYDROXAMIC ACID (AHA) | AHA | Acethydroxamsae...) Show SMILES CC(=O)NO Show InChI InChI=1S/C2H5NO2/c1-2(4)3-5/h5H,1H3,(H,3,4)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents	PDB Article PubMed	9.60E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant Helicobacter pylori urease expressed in Escherichia coli rosetta DE3 after 120 mins by Berthelot colorimetric analysis				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair				3D Structure (crystal)
Urease subunit alpha/beta/gamma (Bacillus pasteurii)	BDBM24963 (organophosphorus derivative, 4 | {[(2S)-2-amino-3-...) Show SMILES CC(C)[C@H](N)C(=O)NCP(C)(O)=O |r| Show InChI InChI=1S/C7H17N2O3P/c1-5(2)6(8)7(10)9-4-13(3,11)12/h5-6H,4,8H2,1-3H3,(H,9,10)(H,11,12)/t6-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.20E+5	-22.8	4.85E+5	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha/beta/gamma (Bacillus pasteurii)	BDBM24970 ([(2-{[(benzyloxy)carbonyl]amino}acetamido)methyl](...) Show SMILES CP(O)(=O)CNC(=O)CNC(=O)OCc1ccccc1 Show InChI InChI=1S/C12H17N2O5P/c1-20(17,18)9-14-11(15)7-13-12(16)19-8-10-5-3-2-4-6-10/h2-6H,7-9H2,1H3,(H,13,16)(H,14,15)(H,17,18)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.35E+5	-22.5	4.50E+5	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha [F36L]/beta/gamma (Proteus vulgaris)	BDBM24964 (organophosphorus derivative, 5 | {[(2S)-2-amino-3-...) Show SMILES CP(O)(=O)CNC(=O)[C@@H](N)Cc1ccccc1 |r| Show InChI InChI=1S/C11H17N2O3P/c1-17(15,16)8-13-11(14)10(12)7-9-5-3-2-4-6-9/h2-6,10H,7-8,12H2,1H3,(H,13,14)(H,15,16)/t10-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.76E+5	-21.8	7.54E+5	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha [F36L]/beta/gamma (Proteus vulgaris)	BDBM24970 ([(2-{[(benzyloxy)carbonyl]amino}acetamido)methyl](...) Show SMILES CP(O)(=O)CNC(=O)CNC(=O)OCc1ccccc1 Show InChI InChI=1S/C12H17N2O5P/c1-20(17,18)9-14-11(15)7-13-12(16)19-8-10-5-3-2-4-6-10/h2-6H,7-9H2,1H3,(H,13,16)(H,14,15)(H,17,18)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.78E+5	-21.8	6.40E+5	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha [F36L]/beta/gamma (Proteus vulgaris)	BDBM24963 (organophosphorus derivative, 4 | {[(2S)-2-amino-3-...) Show SMILES CC(C)[C@H](N)C(=O)NCP(C)(O)=O |r| Show InChI InChI=1S/C7H17N2O3P/c1-5(2)6(8)7(10)9-4-13(3,11)12/h5-6H,4,8H2,1-3H3,(H,9,10)(H,11,12)/t6-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.08E+5	-21.4	6.17E+5	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha/beta/gamma (Bacillus pasteurii)	BDBM24964 (organophosphorus derivative, 5 | {[(2S)-2-amino-3-...) Show SMILES CP(O)(=O)CNC(=O)[C@@H](N)Cc1ccccc1 |r| Show InChI InChI=1S/C11H17N2O3P/c1-17(15,16)8-13-11(14)10(12)7-9-5-3-2-4-6-9/h2-6,10H,7-8,12H2,1H3,(H,13,14)(H,15,16)/t10-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.15E+5	-21.3	6.00E+5	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha/beta/gamma (Bacillus pasteurii)	BDBM24960 ((aminomethyl)(methyl)phosphinic acid | organophosp...) Show SMILES CP(O)(O)C=N Show InChI InChI=1S/C2H8NO2P/c1-6(4,5)2-3/h2-6H,1H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	3.40E+5	-20.1	1.10E+6	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit alpha [F36L]/beta/gamma (Proteus vulgaris)	BDBM24960 ((aminomethyl)(methyl)phosphinic acid | organophosp...) Show SMILES CP(O)(O)C=N Show InChI InChI=1S/C2H8NO2P/c1-6(4,5)2-3/h2-6H,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	4.25E+5	-19.6	2.53E+6	n/a	n/a	n/a	n/a	7.0	30
Wroclaw University of Technology					Assay Description Progress curves were obtained by initiation of urease reaction with addition of purified enzyme into assay mixtures containing increasing concentrati...				J Med Chem 51: 5736-44 (2008) Article DOI: 10.1021/jm800570q BindingDB Entry DOI: 10.7270/Q2PR7T91
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50070209 (Aciphex | CHEBI:8768 | LY-307640 | Rabeprazole) Show SMILES COCCCOc1ccnc(C[S+]([O-])c2nc3ccccc3[nH]2)c1C Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	290	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of Helicobacter pylori ATCC 43504 urease assessed as amount of ammonia after 15 mins by indophenol method				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM106944 (US8592468, EbSe2) Show SMILES O=c1[nH][se]c2ccccc12 Show InChI InChI=1S/C7H5NOSe/c9-7-5-3-1-2-4-6(5)10-8-7/h1-4H,(H,8,9)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.28E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant Helicobacter pylori urease expressed in Escherichia coli rosetta DE3 using urea as substrate assessed as transformed cell u...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534774 (CHEMBL4089739) Show SMILES [#6]-[#8]-[#6](=O)-[#6]-n1[se;v2]c2ccccc2c1=O Show InChI InChI=1S/C10H9NO3Se/c1-14-9(12)6-11-10(13)7-4-2-3-5-8(7)15-11/h2-5H,6H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.12E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of urease in Helicobacter pylori J99 in Brucella broth using urea as substrate preincubated for 2 hrs followed by substrate addition measu...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534779 (CHEMBL4469463) Show SMILES [#6]-[#8]-[#6](=O)-[#6@@H](-[#6]-[#6](-[#6])-[#6])-n1[se;v2]c2ccccc2c1=O |r| Show InChI InChI=1S/C14H17NO3Se/c1-9(2)8-11(14(17)18-3)15-13(16)10-6-4-5-7-12(10)19-15/h4-7,9,11H,8H2,1-3H3/t11-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.14E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of urease in Helicobacter pylori J99 in Brucella broth using urea as substrate preincubated for 2 hrs followed by substrate addition measu...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534787 (CHEMBL4444060) Show SMILES [#6]-[#8]-[#6](=O)-[#6@H](-[#6]-[#6](-[#6])-[#6])-n1[se;v2]c2ccccc2c1=O |r| Show InChI InChI=1S/C14H17NO3Se/c1-9(2)8-11(14(17)18-3)15-13(16)10-6-4-5-7-12(10)19-15/h4-7,9,11H,8H2,1-3H3/t11-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of urease in Helicobacter pylori J99 in Brucella broth using urea as substrate preincubated for 2 hrs followed by substrate addition measu...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534774 (CHEMBL4089739) Show SMILES [#6]-[#8]-[#6](=O)-[#6]-n1[se;v2]c2ccccc2c1=O Show InChI InChI=1S/C10H9NO3Se/c1-14-9(12)6-11-10(13)7-4-2-3-5-8(7)15-11/h2-5H,6H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.47E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of urease in Helicobacter pylori J99 in Brucella broth using urea as substrate after 2 hrs by Berthelot assay				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM34233 (2-Phenyl-benzo[d]isoselenazol-3-one | 2-Phenyl-ben...) Show SMILES O=c1n([se]c2ccccc12)-c1ccccc1 Show InChI InChI=1S/C13H9NOSe/c15-13-11-8-4-5-9-12(11)16-14(13)10-6-2-1-3-7-10/h1-9H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.69E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of urease in Helicobacter pylori J99 in Brucella broth using urea as substrate preincubated for 2 hrs followed by substrate addition measu...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM34233 (2-Phenyl-benzo[d]isoselenazol-3-one | 2-Phenyl-ben...) Show SMILES O=c1n([se]c2ccccc12)-c1ccccc1 Show InChI InChI=1S/C13H9NOSe/c15-13-11-8-4-5-9-12(11)16-14(13)10-6-2-1-3-7-10/h1-9H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant Helicobacter pylori urease expressed in Escherichia coli rosetta DE3 using urea as substrate assessed as transformed cell u...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534778 (CHEMBL4563587) Show SMILES [#6]-[#8]-[#6](=O)-[#6@H](-[#6])-n1[se;v2]c2ccccc2c1=O |r| Show InChI InChI=1S/C11H11NO3Se/c1-7(11(14)15-2)12-10(13)8-5-3-4-6-9(8)16-12/h3-7H,1-2H3/t7-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.91E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of urease in Helicobacter pylori J99 in Brucella broth using urea as substrate preincubated for 2 hrs followed by substrate addition measu...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534772 (CHEMBL4563580) Show SMILES [#6]-[#6]-[#6](-[#6])-[#6@@H](-[#6](=O)-[#8]-[#6])-n1[se;v2]c2ccccc2c1=O |r| Show InChI InChI=1S/C14H17NO3Se/c1-4-9(2)12(14(17)18-3)15-13(16)10-7-5-6-8-11(10)19-15/h5-9,12H,4H2,1-3H3/t9?,12-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.07E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of urease in Helicobacter pylori J99 in Brucella broth using urea as substrate preincubated for 2 hrs followed by substrate addition measu...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534780 (CHEMBL4469439) Show SMILES [#8]-[#6]-[#6@H](-c1ccccc1)-n1[se;v2]c2ccccc2c1=O |r| Show InChI InChI=1S/C15H13NO2Se/c17-10-13(11-6-2-1-3-7-11)16-15(18)12-8-4-5-9-14(12)19-16/h1-9,13,17H,10H2/t13-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.03E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of urease in Helicobacter pylori J99 in Brucella broth using urea as substrate preincubated for 2 hrs followed by substrate addition measu...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534773 (CHEMBL4524305) Show SMILES [#6]-[#6@H](-c1ccccc1)-n1[se;v2]c2ccccc2c1=O |r| Show InChI InChI=1S/C15H13NOSe/c1-11(12-7-3-2-4-8-12)16-15(17)13-9-5-6-10-14(13)18-16/h2-11H,1H3/t11-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.04E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of urease in Helicobacter pylori J99 in Brucella broth using urea as substrate preincubated for 2 hrs followed by substrate addition measu...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50197347 (Ebselen Diselenide) Show SMILES O=C(Nc1ccccc1)c1ccccc1[Se][Se]c1ccccc1C(=O)Nc1ccccc1 Show InChI InChI=1S/C26H20N2O2Se2/c29-25(27-19-11-3-1-4-12-19)21-15-7-9-17-23(21)31-32-24-18-10-8-16-22(24)26(30)28-20-13-5-2-6-14-20/h1-18H,(H,27,29)(H,28,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of urease in Helicobacter pylori J99 in Brucella broth using urea as substrate preincubated for 2 hrs followed by substrate addition measu...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM106944 (US8592468, EbSe2) Show SMILES O=c1[nH][se]c2ccccc12 Show InChI InChI=1S/C7H5NOSe/c9-7-5-3-1-2-4-6(5)10-8-7/h1-4H,(H,8,9)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.92E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of urease in Helicobacter pylori J99 in Brucella broth using urea as substrate preincubated for 2 hrs followed by substrate addition measu...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534774 (CHEMBL4089739) Show SMILES [#6]-[#8]-[#6](=O)-[#6]-n1[se;v2]c2ccccc2c1=O Show InChI InChI=1S/C10H9NO3Se/c1-14-9(12)6-11-10(13)7-4-2-3-5-8(7)15-11/h2-5H,6H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	9.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant Helicobacter pylori urease expressed in Escherichia coli rosetta DE3 using urea as substrate assessed as transformed cell u...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50197347 (Ebselen Diselenide) Show SMILES O=C(Nc1ccccc1)c1ccccc1[Se][Se]c1ccccc1C(=O)Nc1ccccc1 Show InChI InChI=1S/C26H20N2O2Se2/c29-25(27-19-11-3-1-4-12-19)21-15-7-9-17-23(21)31-32-24-18-10-8-16-22(24)26(30)28-20-13-5-2-6-14-20/h1-18H,(H,27,29)(H,28,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.09E+4	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant Helicobacter pylori urease expressed in Escherichia coli rosetta DE3 using urea as substrate assessed as transformed cell u...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534783 (CHEMBL4575318) Show SMILES [#6]-[#8]-[#6](=O)-[#6]-[#6]-[#6]-[#7]-[#6](=O)-c1ccccc1[Se;v2][Se;v2]c1ccccc1-[#6](=O)-[#7]-[#6]-[#6]-[#6]-[#6](=O)-[#8]-[#6] Show InChI InChI=1S/C24H28N2O6Se2/c1-31-21(27)13-7-15-25-23(29)17-9-3-5-11-19(17)33-34-20-12-6-4-10-18(20)24(30)26-16-8-14-22(28)32-2/h3-6,9-12H,7-8,13-16H2,1-2H3,(H,25,29)(H,26,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.18E+4	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of urease in Helicobacter pylori J99 in Brucella broth using urea as substrate preincubated for 2 hrs followed by substrate addition measu...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534778 (CHEMBL4563587) Show SMILES [#6]-[#8]-[#6](=O)-[#6@H](-[#6])-n1[se;v2]c2ccccc2c1=O |r| Show InChI InChI=1S/C11H11NO3Se/c1-7(11(14)15-2)12-10(13)8-5-3-4-6-9(8)16-12/h3-7H,1-2H3/t7-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant Helicobacter pylori urease expressed in Escherichia coli rosetta DE3 using urea as substrate assessed as transformed cell u...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534783 (CHEMBL4575318) Show SMILES [#6]-[#8]-[#6](=O)-[#6]-[#6]-[#6]-[#7]-[#6](=O)-c1ccccc1[Se;v2][Se;v2]c1ccccc1-[#6](=O)-[#7]-[#6]-[#6]-[#6]-[#6](=O)-[#8]-[#6] Show InChI InChI=1S/C24H28N2O6Se2/c1-31-21(27)13-7-15-25-23(29)17-9-3-5-11-19(17)33-34-20-12-6-4-10-18(20)24(30)26-16-8-14-22(28)32-2/h3-6,9-12H,7-8,13-16H2,1-2H3,(H,25,29)(H,26,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.01E+4	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant Helicobacter pylori urease expressed in Escherichia coli rosetta DE3 using urea as substrate assessed as transformed cell u...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534780 (CHEMBL4469439) Show SMILES [#8]-[#6]-[#6@H](-c1ccccc1)-n1[se;v2]c2ccccc2c1=O |r| Show InChI InChI=1S/C15H13NO2Se/c17-10-13(11-6-2-1-3-7-11)16-15(18)12-8-4-5-9-14(12)19-16/h1-9,13,17H,10H2/t13-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.27E+4	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant Helicobacter pylori urease expressed in Escherichia coli rosetta DE3 using urea as substrate assessed as transformed cell u...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534773 (CHEMBL4524305) Show SMILES [#6]-[#6@H](-c1ccccc1)-n1[se;v2]c2ccccc2c1=O |r| Show InChI InChI=1S/C15H13NOSe/c1-11(12-7-3-2-4-8-12)16-15(17)13-9-5-6-10-14(13)18-16/h2-11H,1H3/t11-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.53E+4	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant Helicobacter pylori urease expressed in Escherichia coli rosetta DE3 using urea as substrate assessed as transformed cell u...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair
Urease subunit beta (Helicobacter pylori (strain ATCC 700392 / 26695) (...)	BDBM50534777 (CHEMBL4592440) Show SMILES [#6]-[#6](-[#6])-[#6@@H](-[#6](-[#8])=O)-n1[se;v2]c2ccccc2c1=O |r| Show InChI InChI=1S/C12H13NO3Se/c1-7(2)10(12(15)16)13-11(14)8-5-3-4-6-9(8)17-13/h3-7,10H,1-2H3,(H,15,16)/t10-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.54E+4	n/a	n/a	n/a	n/a	n/a	n/a
Wroc?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of urease in Helicobacter pylori J99 in Brucella broth using urea as substrate preincubated for 2 hrs followed by substrate addition measu...				J Med Chem 59: 8125-33 (2016) Article DOI: 10.1021/acs.jmedchem.6b00986 BindingDB Entry DOI: 10.7270/Q2FR0130
					More data for this Ligand-Target Pair

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