Compile Data Set for Download or QSAR

Found 325 hits Enz. Inhib. hit(s) with Target = 'Protein-lysine 6-oxidase'   

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
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM50526737 (CHEMBL4528500 | US10807974, Example 82 | US1099508...) Show SMILES Cc1ccc(cc1)-c1cc(ccc1S(C)(=O)=O)S(=O)(=O)c1ccc(CN)s1 Show InChI InChI=1S/C19H19NO4S3/c1-13-3-5-14(6-4-13)17-11-16(8-9-18(17)26(2,21)22)27(23,24)19-10-7-15(12-20)25-19/h3-11H,12,20H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	<180	n/a	n/a	n/a	n/a	n/a	n/a
THE INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL US Patent					Assay Description Cell Culture and TransfectionAll cell lines used in this study was purchased from American Type Culture Collection (ATCC). Mycoplasma contamination w...				US Patent US10995088 (2021) BindingDB Entry DOI: 10.7270/Q2125WSK
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Mus musculus)	BDBM50526737 (CHEMBL4528500 | US10807974, Example 82 | US1099508...) Show SMILES Cc1ccc(cc1)-c1cc(ccc1S(C)(=O)=O)S(=O)(=O)c1ccc(CN)s1 Show InChI InChI=1S/C19H19NO4S3/c1-13-3-5-14(6-4-13)17-11-16(8-9-18(17)26(2,21)22)27(23,24)19-10-7-15(12-20)25-19/h3-11H,12,20H2,1-2H3	KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	<180	n/a	n/a	n/a	n/a	n/a	n/a
The Institute of Cancer Research: Royal Cancer Hospital US Patent					Assay Description To produce MDCK cysts, cells were cultured on Matrigel (Corning) with 2% Matrigel supplemented in DMEM with 10% FBS. Cysts were allowed to form for 1...				US Patent US10807974 (2020) BindingDB Entry DOI: 10.7270/Q2TH8QS8
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM50526721 (CHEMBL4444163 | US10807974, Example 111 | US109950...) Show SMILES CCc1cc(cc(c1)S(=O)(=O)c1cnc(CN)s1)-c1cnn(C)c1 Show InChI InChI=1S/C16H18N4O2S2/c1-3-11-4-12(13-8-19-20(2)10-13)6-14(5-11)24(21,22)16-9-18-15(7-17)23-16/h4-6,8-10H,3,7,17H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	190	n/a	n/a	n/a	n/a	n/a	n/a
THE INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL US Patent					Assay Description Cell Culture and TransfectionAll cell lines used in this study was purchased from American Type Culture Collection (ATCC). Mycoplasma contamination w...				US Patent US10995088 (2021) BindingDB Entry DOI: 10.7270/Q2125WSK
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Mus musculus)	BDBM50526721 (CHEMBL4444163 | US10807974, Example 111 | US109950...) Show SMILES CCc1cc(cc(c1)S(=O)(=O)c1cnc(CN)s1)-c1cnn(C)c1 Show InChI InChI=1S/C16H18N4O2S2/c1-3-11-4-12(13-8-19-20(2)10-13)6-14(5-11)24(21,22)16-9-18-15(7-17)23-16/h4-6,8-10H,3,7,17H2,1-2H3	KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	190	n/a	n/a	n/a	n/a	n/a	n/a
The Institute of Cancer Research: Royal Cancer Hospital US Patent					Assay Description To produce MDCK cysts, cells were cultured on Matrigel (Corning) with 2% Matrigel supplemented in DMEM with 10% FBS. Cysts were allowed to form for 1...				US Patent US10807974 (2020) BindingDB Entry DOI: 10.7270/Q2TH8QS8
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Sus scrofa)	BDBM469007 (US10807974, Example 16 | US10995088, Example 16 | ...) Show SMILES NCc1ccc(s1)S(=O)(=O)c1ccc(cc1)S(=O)(=O)CCO Show InChI InChI=1S/C13H15NO5S3/c14-9-10-1-6-13(20-10)22(18,19)12-4-2-11(3-5-12)21(16,17)8-7-15/h1-6,15H,7-9,14H2	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	300	n/a	n/a	n/a	n/a	n/a	n/a
The Institute of Cancer Research: Royal Cancer Hospital US Patent					Assay Description LOX enzyme was obtained from pig skin by the method of Shackleton et al 1990.				US Patent US10807974 (2020) BindingDB Entry DOI: 10.7270/Q2TH8QS8
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM469007 (US10807974, Example 16 | US10995088, Example 16 | ...) Show SMILES NCc1ccc(s1)S(=O)(=O)c1ccc(cc1)S(=O)(=O)CCO Show InChI InChI=1S/C13H15NO5S3/c14-9-10-1-6-13(20-10)22(18,19)12-4-2-11(3-5-12)21(16,17)8-7-15/h1-6,15H,7-9,14H2	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	300	n/a	n/a	n/a	n/a	n/a	n/a
THE INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL US Patent					Assay Description The following reagents were prepared:Reagents500 mM CHES, pH 9 (with NaOH), filtered (MW=207.29)20.7 g in 200 ml in dH2O10% Pluronic F-127 (store at ...				US Patent US10995088 (2021) BindingDB Entry DOI: 10.7270/Q2125WSK
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633180 (4-((1-((Z)-4-amino-2-fluorobut-2-en-1-yl)-2-methyl...) Show SMILES CN(C)S(=O)(=O)c1ccc(Cc2c(C)n(C\C(F)=C\CN)c3ccc(cc23)C(=O)N2CCN(CC2)C(=O)CCCC[C@@H]2SC[C@@H]3NC(=O)N[C@H]23)cc1 |r| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633181 (1-((Z)-4-amino-2-fluorobut-2-en-1-yl)-3-(3-(N,N-di...) Show SMILES CN(C)S(=O)(=O)c1ccc(Cc2c(C)n(C\C(F)=C\CN)c3ccc(cc23)C(=O)NCCCCCNC(=O)CCCC[C@@H]2SC[C@@H]3NC(=O)N[C@H]23)cc1 |r| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633197 (N,N′-((((((((((5-(1-((Z)-4-amino-2-fluorobut...) Show SMILES CN(C)S(=O)(=O)c1cccc(c1)-c1c(C)n(C\C(F)=C\CN)c2ccc(cc12)C(=O)Nc1ccc2n(Cc3cn(CCOCCOCCOCCNC(=O)CCCC[C@@H]4SC[C@@H]5NC(=O)N[C@H]45)nn3)c(=O)n(Cc3cn(CCOCCOCCOCCNC(=O)CCCC[C@@H]4SC[C@@H]5NC(=O)N[C@H]45)nn3)c2c1 |r| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633202 (N,N′-((((5-(1-((Z)-4-amino-2-fluorobut-2-en-...) Show SMILES CN(C)S(=O)(=O)c1cccc(c1)-c1c(C)n(C\C(F)=C\CN)c2ccc(cc12)C(=O)Nc1ccc2n(CCn3cc(CCNC(=O)CCCC[C@@H]4SC[C@@H]5NC(=O)N[C@H]45)nn3)c(=O)n(CCn3cc(CCNC(=O)CCCC[C@@H]4SC[C@@H]5NC(=O)N[C@H]45)nn3)c2c1 |r| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633203 (5-(1-((Z)-4-amino-2-fluorobut-2-en-1-yl)-3-(3-(N,N...) Show SMILES CN(C)S(=O)(=O)c1cccc(c1)-c1c(C)n(C\C(F)=C\CN)c2ccc(cc12)C(=O)Nc1cc(cc(c1)C(=O)NCCCCCNC(=O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@H]12)C(=O)NCCCCCNC(=O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@H]12 |r| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633204 (5-(4-(1-((Z)-4-amino-2-fluorobut-2-en-1-yl)-3-(3-(...) Show SMILES CN(C)S(=O)(=O)c1cccc(c1)-c1c(C)n(C\C(F)=C\CN)c2ccc(cc12)-c1cn(nn1)-c1cc(cc(c1)C(=O)NCCCCCNC(=O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@H]12)C(=O)NCCCCCNC(=O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@H]12 |r| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633224 (4-(((Z)-4-amino-2-fluorobut-2-en-1-yl)sulfonyl)-N-...) Show SMILES NC\C=C(/F)CS(=O)(=O)c1ccc(cc1)C(=O)NCc1cn(CCOCCOCCOCCNC(=O)CCCC[C@@H]2SC[C@@H]3NC(=O)N[C@H]23)nn1 |r| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633227 (2-(((Z)-4-amino-2-fluorobut-2-en-1-yl)sulfonyl)-N-...) Show SMILES NC\C=C(/F)CS(=O)(=O)c1ccccc1C(=O)NCCCCCNC(=O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@H]12 |r| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633233 (3-(((Z)-4-amino-2-fluorobut-2-en-1-yl)sulfonyl)-N-...) Show SMILES NC\C=C(/F)CS(=O)(=O)c1cccc(c1)C(=O)NCCCCCNC(=O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@H]12 |r| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633244 (3-(((Z)-4-amino-2-fluorobut-2-en-1-yl)sulfonyl)-N-...) Show SMILES NC\C=C(/F)CS(=O)(=O)c1cccc(c1)C(=O)Nc1cc(cc(c1)C(=O)N1CCN(CC1)C(=O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@H]12)C(=O)N1CCN(CC1)C(=O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@H]12 |r| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633245 ((3aS,4S,6aR)-4-(5-(4-(3-(3-(((Z)-4-amino-2-fluorob...) Show SMILES NC\C=C(/F)CS(=O)(=O)c1cccc(OCCCc2cn(CCCCC[C@@H]3SC[C@@H]4NC(=O)N[C@H]34)nn2)c1 |r| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633246 ((3aS,3a'S,4S,4'S,6aR,6a′R)-4,4′-(((((5...) Show SMILES NC\C=C(/F)CS(=O)(=O)c1cccc(Cn2cc(nn2)-c2cc(OCCCc3cn(CCCCC[C@@H]4SC[C@@H]5NC(=O)N[C@H]45)nn3)cc(OCCCc3cn(CCCCC[C@@H]4SC[C@@H]5NC(=O)N[C@H]45)nn3)c2)c1 |r| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633247 ((3aS,3a'S,4S,4'S,6aR,6a′R)-4,4′-(((((3...) Show SMILES NC\C=C(/F)CS(=O)(=O)c1cccc(c1)N(CCCc1cn(CCCCC[C@@H]2SC[C@@H]3NC(=O)N[C@H]23)nn1)CCCc1cn(CCCCC[C@@H]2SC[C@@H]3NC(=O)N[C@H]23)nn1 |r| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633248 ((3aS,4S,6aR)-4-(4-(4-(3-((3-(((Z)-4-amino-2-fluoro...) Show SMILES NC\C=C(/F)CS(=O)(=O)c1cccc(NCCCc2cn(CCCCC[C@@H]3SC[C@@H]4NC(=O)N[C@H]34)nn2)c1 |r| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633249 (N-((1-(4-(((1-((Z)-4-amino-2-fluorobut-2-en-1-yl)-...) Show SMILES CN(C)S(=O)(=O)c1ccc(cc1)C(OCc1ccc(cc1)-n1cc(CNC(=O)CCCC[C@@H]2SC[C@@H]3NC(=O)N[C@H]23)nn1)c1cn(C\C(F)=C\CN)nn1 |r,w:13.13| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	<300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM633250 (N-((1-(4-(((1-((Z)-4-amino-2-fluorobut-2-en-1-yl)-...) Show SMILES CN(C)S(=O)(=O)c1ccc(cc1)C(OCc1ccc(cc1)-n1cc(CNC(=O)CCOCCOCCOCCOCCNC(=O)CCCC[C@@H]2SC[C@@H]3NC(=O)N[C@H]23)nn1)c1cn(C\C(F)=C\CN)nn1 |r,w:13.13| Show InChI	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>300	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM50058655 (1,1',1'',1'''-[disulfanediylbis(carbonothioylnitri...) Show SMILES CCN(CC)C(=S)SSC(=S)N(CC)CC Show InChI InChI=1S/C10H20N2S4/c1-5-11(6-2)9(13)15-16-10(14)12(7-3)8-4/h5-8H2,1-4H3	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	320	n/a	n/a	n/a	n/a	n/a	n/a
Hungarian Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of recombinant human LOX expressed in HEK293 cells using diaminopentane as substrate preincubated for 30 mins followed by substrate additi...				Bioorg Med Chem Lett 28: 3113-3118 (2018) Article DOI: 10.1016/j.bmcl.2018.07.001 BindingDB Entry DOI: 10.7270/Q28P6366
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Sus scrofa)	BDBM469005 (US10807974, Example 9 | US10995088, Example 9 | US...) Show SMILES CS(=O)(=O)c1cccc(c1)S(=O)(=O)c1ccc(CN)s1 Show InChI InChI=1S/C12H13NO4S3/c1-19(14,15)10-3-2-4-11(7-10)20(16,17)12-6-5-9(8-13)18-12/h2-7H,8,13H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	340	n/a	n/a	n/a	n/a	n/a	n/a
The Institute of Cancer Research: Royal Cancer Hospital US Patent					Assay Description LOX enzyme was obtained from pig skin by the method of Shackleton et al 1990.				US Patent US10807974 (2020) BindingDB Entry DOI: 10.7270/Q2TH8QS8
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM469005 (US10807974, Example 9 | US10995088, Example 9 | US...) Show SMILES CS(=O)(=O)c1cccc(c1)S(=O)(=O)c1ccc(CN)s1 Show InChI InChI=1S/C12H13NO4S3/c1-19(14,15)10-3-2-4-11(7-10)20(16,17)12-6-5-9(8-13)18-12/h2-7H,8,13H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	340	n/a	n/a	n/a	n/a	n/a	n/a
THE INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL US Patent					Assay Description The following reagents were prepared:Reagents500 mM CHES, pH 9 (with NaOH), filtered (MW=207.29)20.7 g in 200 ml in dH2O10% Pluronic F-127 (store at ...				US Patent US10995088 (2021) BindingDB Entry DOI: 10.7270/Q2125WSK
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM50505633 (CHEMBL4448713) Show SMILES Cl.CN(C)S(=O)(=O)c1cccc(c1)-c1c(C)n(C\C(F)=C\CN)c2ccc(cc12)S(C)(=O)=O Show InChI InChI=1S/C22H26FN3O4S2/c1-15-22(16-6-5-7-19(12-16)32(29,30)25(2)3)20-13-18(31(4,27)28)8-9-21(20)26(15)14-17(23)10-11-24/h5-10,12-13H,11,14,24H2,1-4H3/b17-10-	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	398	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaxis Ltd Curated by ChEMBL					Assay Description Inhibition of LOX in bovine aorta using putrescine as substrate preincubated with enzyme for 30 mins followed by substrate addition and measured ever...				J Med Chem 62: 9874-9889 (2019) Article DOI: 10.1021/acs.jmedchem.9b01283 BindingDB Entry DOI: 10.7270/Q2VM4GJ2
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM50505649 (CHEMBL4439437) Show SMILES Cl.C[C@H](NS(=O)(=O)c1ccc(OC\C(F)=C\CN)cc1)c1ccccc1 |r| Show InChI InChI=1S/C18H21FN2O3S.ClH/c1-14(15-5-3-2-4-6-15)21-25(22,23)18-9-7-17(8-10-18)24-13-16(19)11-12-20;/h2-11,14,21H,12-13,20H2,1H3;1H/b16-11-;/t14-;/m0./s1	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	398	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaxis Ltd Curated by ChEMBL					Assay Description Inhibition of LOX in bovine aorta using putrescine as substrate preincubated with enzyme for 30 mins followed by substrate addition and measured ever...				J Med Chem 62: 9874-9889 (2019) Article DOI: 10.1021/acs.jmedchem.9b01283 BindingDB Entry DOI: 10.7270/Q2VM4GJ2
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Sus scrofa)	BDBM469011 (US10807974, Example 27 | US10995088, Example 27 | ...) Show SMILES CCNCCS(=O)(=O)c1ccc(cc1)S(=O)(=O)c1ccc(CN)s1 Show InChI InChI=1S/C15H20N2O4S3/c1-2-17-9-10-23(18,19)13-4-6-14(7-5-13)24(20,21)15-8-3-12(11-16)22-15/h3-8,17H,2,9-11,16H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
The Institute of Cancer Research: Royal Cancer Hospital US Patent					Assay Description LOX enzyme was obtained from pig skin by the method of Shackleton et al 1990.				US Patent US10807974 (2020) BindingDB Entry DOI: 10.7270/Q2TH8QS8
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM469011 (US10807974, Example 27 | US10995088, Example 27 | ...) Show SMILES CCNCCS(=O)(=O)c1ccc(cc1)S(=O)(=O)c1ccc(CN)s1 Show InChI InChI=1S/C15H20N2O4S3/c1-2-17-9-10-23(18,19)13-4-6-14(7-5-13)24(20,21)15-8-3-12(11-16)22-15/h3-8,17H,2,9-11,16H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
THE INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL US Patent					Assay Description The following reagents were prepared:Reagents500 mM CHES, pH 9 (with NaOH), filtered (MW=207.29)20.7 g in 200 ml in dH2O10% Pluronic F-127 (store at ...				US Patent US10995088 (2021) BindingDB Entry DOI: 10.7270/Q2125WSK
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Sus scrofa)	BDBM469032 (US10807974, Example 43 | US10995088, Example 43 | ...) Show SMILES NCc1ccc(s1)S(=O)(=O)c1cccc(c1)S(=O)(=O)N1CCC[C@H]1CO |r| Show InChI InChI=1S/C16H20N2O5S3/c17-10-13-6-7-16(24-13)25(20,21)14-4-1-5-15(9-14)26(22,23)18-8-2-3-12(18)11-19/h1,4-7,9,12,19H,2-3,8,10-11,17H2/t12-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	420	n/a	n/a	n/a	n/a	n/a	n/a
The Institute of Cancer Research: Royal Cancer Hospital US Patent					Assay Description LOX enzyme was obtained from pig skin by the method of Shackleton et al 1990.				US Patent US10807974 (2020) BindingDB Entry DOI: 10.7270/Q2TH8QS8
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM469032 (US10807974, Example 43 | US10995088, Example 43 | ...) Show SMILES NCc1ccc(s1)S(=O)(=O)c1cccc(c1)S(=O)(=O)N1CCC[C@H]1CO |r| Show InChI InChI=1S/C16H20N2O5S3/c17-10-13-6-7-16(24-13)25(20,21)14-4-1-5-15(9-14)26(22,23)18-8-2-3-12(18)11-19/h1,4-7,9,12,19H,2-3,8,10-11,17H2/t12-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	420	n/a	n/a	n/a	n/a	n/a	n/a
THE INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL US Patent					Assay Description The following reagents were prepared:Reagents500 mM CHES, pH 9 (with NaOH), filtered (MW=207.29)20.7 g in 200 ml in dH2O10% Pluronic F-127 (store at ...				US Patent US10995088 (2021) BindingDB Entry DOI: 10.7270/Q2125WSK
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM469023 (US10807974, Example 39 | US10995088, Example 39 | ...) Show SMILES NCc1ccc(s1)S(=O)(=O)c1ccc(cc1)S(=O)(=O)CCCO Show InChI InChI=1S/C14H17NO5S3/c15-10-11-2-7-14(21-11)23(19,20)13-5-3-12(4-6-13)22(17,18)9-1-8-16/h2-7,16H,1,8-10,15H2	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	440	n/a	n/a	n/a	n/a	n/a	n/a
THE INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL US Patent					Assay Description The following reagents were prepared:Reagents500 mM CHES, pH 9 (with NaOH), filtered (MW=207.29)20.7 g in 200 ml in dH2O10% Pluronic F-127 (store at ...				US Patent US10995088 (2021) BindingDB Entry DOI: 10.7270/Q2125WSK
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Sus scrofa)	BDBM469023 (US10807974, Example 39 | US10995088, Example 39 | ...) Show SMILES NCc1ccc(s1)S(=O)(=O)c1ccc(cc1)S(=O)(=O)CCCO Show InChI InChI=1S/C14H17NO5S3/c15-10-11-2-7-14(21-11)23(19,20)13-5-3-12(4-6-13)22(17,18)9-1-8-16/h2-7,16H,1,8-10,15H2	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	440	n/a	n/a	n/a	n/a	n/a	n/a
The Institute of Cancer Research: Royal Cancer Hospital US Patent					Assay Description LOX enzyme was obtained from pig skin by the method of Shackleton et al 1990.				US Patent US10807974 (2020) BindingDB Entry DOI: 10.7270/Q2TH8QS8
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Sus scrofa)	BDBM469019 (US10807974, Example 35 | US10995088, Example 35 | ...) Show SMILES NCc1ccc(s1)S(=O)(=O)c1ccc(cc1)S(=O)(=O)CCN1CCCNCC1 Show InChI InChI=1S/C18H25N3O4S3/c19-14-15-2-7-18(26-15)28(24,25)17-5-3-16(4-6-17)27(22,23)13-12-21-10-1-8-20-9-11-21/h2-7,20H,1,8-14,19H2	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	450	n/a	n/a	n/a	n/a	n/a	n/a
The Institute of Cancer Research: Royal Cancer Hospital US Patent					Assay Description LOX enzyme was obtained from pig skin by the method of Shackleton et al 1990.				US Patent US10807974 (2020) BindingDB Entry DOI: 10.7270/Q2TH8QS8
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM469008 (US10807974, Example 17 | US10995088, Example 17 | ...) Show SMILES CN(C)CCS(=O)(=O)c1ccc(cc1)S(=O)(=O)c1ccc(CN)s1 Show InChI InChI=1S/C15H20N2O4S3/c1-17(2)9-10-23(18,19)13-4-6-14(7-5-13)24(20,21)15-8-3-12(11-16)22-15/h3-8H,9-11,16H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	450	n/a	n/a	n/a	n/a	n/a	n/a
THE INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL US Patent					Assay Description The following reagents were prepared:Reagents500 mM CHES, pH 9 (with NaOH), filtered (MW=207.29)20.7 g in 200 ml in dH2O10% Pluronic F-127 (store at ...				US Patent US10995088 (2021) BindingDB Entry DOI: 10.7270/Q2125WSK
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Sus scrofa)	BDBM469008 (US10807974, Example 17 | US10995088, Example 17 | ...) Show SMILES CN(C)CCS(=O)(=O)c1ccc(cc1)S(=O)(=O)c1ccc(CN)s1 Show InChI InChI=1S/C15H20N2O4S3/c1-17(2)9-10-23(18,19)13-4-6-14(7-5-13)24(20,21)15-8-3-12(11-16)22-15/h3-8H,9-11,16H2,1-2H3	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	450	n/a	n/a	n/a	n/a	n/a	n/a
The Institute of Cancer Research: Royal Cancer Hospital US Patent					Assay Description LOX enzyme was obtained from pig skin by the method of Shackleton et al 1990.				US Patent US10807974 (2020) BindingDB Entry DOI: 10.7270/Q2TH8QS8
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM469019 (US10807974, Example 35 | US10995088, Example 35 | ...) Show SMILES NCc1ccc(s1)S(=O)(=O)c1ccc(cc1)S(=O)(=O)CCN1CCCNCC1 Show InChI InChI=1S/C18H25N3O4S3/c19-14-15-2-7-18(26-15)28(24,25)17-5-3-16(4-6-17)27(22,23)13-12-21-10-1-8-20-9-11-21/h2-7,20H,1,8-14,19H2	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	450	n/a	n/a	n/a	n/a	n/a	n/a
THE INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL US Patent					Assay Description The following reagents were prepared:Reagents500 mM CHES, pH 9 (with NaOH), filtered (MW=207.29)20.7 g in 200 ml in dH2O10% Pluronic F-127 (store at ...				US Patent US10995088 (2021) BindingDB Entry DOI: 10.7270/Q2125WSK
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Sus scrofa)	BDBM469024 (US10807974, Example 40 | US10995088, Example 40 | ...) Show SMILES NCc1ccc(s1)S(=O)(=O)c1ccc(cc1)S(=O)(=O)CCCN=[N+]=[N-] Show InChI InChI=1S/C14H16N4O4S3/c15-10-11-2-7-14(23-11)25(21,22)13-5-3-12(4-6-13)24(19,20)9-1-8-17-18-16/h2-7H,1,8-10,15H2	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	470	n/a	n/a	n/a	n/a	n/a	n/a
The Institute of Cancer Research: Royal Cancer Hospital US Patent					Assay Description LOX enzyme was obtained from pig skin by the method of Shackleton et al 1990.				US Patent US10807974 (2020) BindingDB Entry DOI: 10.7270/Q2TH8QS8
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM469024 (US10807974, Example 40 | US10995088, Example 40 | ...) Show SMILES NCc1ccc(s1)S(=O)(=O)c1ccc(cc1)S(=O)(=O)CCCN=[N+]=[N-] Show InChI InChI=1S/C14H16N4O4S3/c15-10-11-2-7-14(23-11)25(21,22)13-5-3-12(4-6-13)24(19,20)9-1-8-17-18-16/h2-7H,1,8-10,15H2	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	470	n/a	n/a	n/a	n/a	n/a	n/a
THE INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL US Patent					Assay Description The following reagents were prepared:Reagents500 mM CHES, pH 9 (with NaOH), filtered (MW=207.29)20.7 g in 200 ml in dH2O10% Pluronic F-127 (store at ...				US Patent US10995088 (2021) BindingDB Entry DOI: 10.7270/Q2125WSK
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Sus scrofa)	BDBM469004 (US10807974, Example 5 | US10995088, Example 5 | US...) Show SMILES CS(=O)(=O)c1ccc(cc1)S(=O)(=O)c1ccc(CN)s1 Show InChI InChI=1S/C12H13NO4S3/c1-19(14,15)10-3-5-11(6-4-10)20(16,17)12-7-2-9(8-13)18-12/h2-7H,8,13H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	480	n/a	n/a	n/a	n/a	n/a	n/a
The Institute of Cancer Research: Royal Cancer Hospital US Patent					Assay Description LOX enzyme was obtained from pig skin by the method of Shackleton et al 1990.				US Patent US10807974 (2020) BindingDB Entry DOI: 10.7270/Q2TH8QS8
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM469004 (US10807974, Example 5 | US10995088, Example 5 | US...) Show SMILES CS(=O)(=O)c1ccc(cc1)S(=O)(=O)c1ccc(CN)s1 Show InChI InChI=1S/C12H13NO4S3/c1-19(14,15)10-3-5-11(6-4-10)20(16,17)12-7-2-9(8-13)18-12/h2-7H,8,13H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	480	n/a	n/a	n/a	n/a	n/a	n/a
THE INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL US Patent					Assay Description The following reagents were prepared:Reagents500 mM CHES, pH 9 (with NaOH), filtered (MW=207.29)20.7 g in 200 ml in dH2O10% Pluronic F-127 (store at ...				US Patent US10995088 (2021) BindingDB Entry DOI: 10.7270/Q2125WSK
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM50505657 (CHEMBL4467234) Show SMILES Cl.CN(C)S(=O)(=O)c1ccc(NCc2cn(C\C(F)=C\CN)nn2)cc1 Show InChI InChI=1S/C15H21FN6O2S/c1-21(2)25(23,24)15-5-3-13(4-6-15)18-9-14-11-22(20-19-14)10-12(16)7-8-17/h3-7,11,18H,8-10,17H2,1-2H3/b12-7-	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	501	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaxis Ltd Curated by ChEMBL					Assay Description Inhibition of LOX in bovine aorta using putrescine as substrate preincubated with enzyme for 30 mins followed by substrate addition and measured ever...				J Med Chem 62: 9874-9889 (2019) Article DOI: 10.1021/acs.jmedchem.9b01283 BindingDB Entry DOI: 10.7270/Q2VM4GJ2
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM50505659 (CHEMBL4459524) Show SMILES Cl.CC(C)(C)c1ccc(OCc2cn(C\C(F)=C\CN)nn2)cc1 Show InChI InChI=1S/C17H23FN4O/c1-17(2,3)13-4-6-16(7-5-13)23-12-15-11-22(21-20-15)10-14(18)8-9-19/h4-8,11H,9-10,12,19H2,1-3H3/b14-8-	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	501	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaxis Ltd Curated by ChEMBL					Assay Description Inhibition of LOX in bovine aorta using putrescine as substrate preincubated with enzyme for 30 mins followed by substrate addition and measured ever...				J Med Chem 62: 9874-9889 (2019) Article DOI: 10.1021/acs.jmedchem.9b01283 BindingDB Entry DOI: 10.7270/Q2VM4GJ2
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Bos taurus)	BDBM50505655 (CHEMBL4441299) Show SMILES Cl.NC\C=C(/F)Cn1cc(COc2ccccc2)nn1 Show InChI InChI=1S/C13H15FN4O/c14-11(6-7-15)8-18-9-12(16-17-18)10-19-13-4-2-1-3-5-13/h1-6,9H,7-8,10,15H2/b11-6-	MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	501	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaxis Ltd Curated by ChEMBL					Assay Description Inhibition of LOX in bovine aorta using putrescine as substrate preincubated with enzyme for 30 mins followed by substrate addition and measured ever...				J Med Chem 62: 9874-9889 (2019) Article DOI: 10.1021/acs.jmedchem.9b01283 BindingDB Entry DOI: 10.7270/Q2VM4GJ2
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Sus scrofa)	BDBM469027 (US10807974, Example 12 | US10995088, Example 12 | ...) Show SMILES CN(C)S(=O)(=O)c1ccc(cc1)S(=O)(=O)c1ccc(CN)s1 Show InChI InChI=1S/C13H16N2O4S3/c1-15(2)22(18,19)12-6-4-11(5-7-12)21(16,17)13-8-3-10(9-14)20-13/h3-8H,9,14H2,1-2H3	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	510	n/a	n/a	n/a	n/a	n/a	n/a
The Institute of Cancer Research: Royal Cancer Hospital US Patent					Assay Description LOX enzyme was obtained from pig skin by the method of Shackleton et al 1990.				US Patent US10807974 (2020) BindingDB Entry DOI: 10.7270/Q2TH8QS8
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM469027 (US10807974, Example 12 | US10995088, Example 12 | ...) Show SMILES CN(C)S(=O)(=O)c1ccc(cc1)S(=O)(=O)c1ccc(CN)s1 Show InChI InChI=1S/C13H16N2O4S3/c1-15(2)22(18,19)12-6-4-11(5-7-12)21(16,17)13-8-3-10(9-14)20-13/h3-8H,9,14H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	510	n/a	n/a	n/a	n/a	n/a	n/a
THE INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL US Patent					Assay Description The following reagents were prepared:Reagents500 mM CHES, pH 9 (with NaOH), filtered (MW=207.29)20.7 g in 200 ml in dH2O10% Pluronic F-127 (store at ...				US Patent US10995088 (2021) BindingDB Entry DOI: 10.7270/Q2125WSK
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Sus scrofa)	BDBM469018 (US10807974, Example 34 | US10995088, Example 34 | ...) Show SMILES CS(=O)(=O)N1CCN(CCS(=O)(=O)c2ccc(cc2)S(=O)(=O)c2ccc(CN)s2)CC1 Show InChI InChI=1S/C18H25N3O6S4/c1-29(22,23)21-10-8-20(9-11-21)12-13-30(24,25)16-3-5-17(6-4-16)31(26,27)18-7-2-15(14-19)28-18/h2-7H,8-14,19H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	530	n/a	n/a	n/a	n/a	n/a	n/a
The Institute of Cancer Research: Royal Cancer Hospital US Patent					Assay Description LOX enzyme was obtained from pig skin by the method of Shackleton et al 1990.				US Patent US10807974 (2020) BindingDB Entry DOI: 10.7270/Q2TH8QS8
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM469018 (US10807974, Example 34 | US10995088, Example 34 | ...) Show SMILES CS(=O)(=O)N1CCN(CCS(=O)(=O)c2ccc(cc2)S(=O)(=O)c2ccc(CN)s2)CC1 Show InChI InChI=1S/C18H25N3O6S4/c1-29(22,23)21-10-8-20(9-11-21)12-13-30(24,25)16-3-5-17(6-4-16)31(26,27)18-7-2-15(14-19)28-18/h2-7H,8-14,19H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	530	n/a	n/a	n/a	n/a	n/a	n/a
THE INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL US Patent					Assay Description The following reagents were prepared:Reagents500 mM CHES, pH 9 (with NaOH), filtered (MW=207.29)20.7 g in 200 ml in dH2O10% Pluronic F-127 (store at ...				US Patent US10995088 (2021) BindingDB Entry DOI: 10.7270/Q2125WSK
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM50232678 (CHEBI:27413 | CHEMBL1618272 | US10717734, Compound...) Show SMILES NCCC#N Show InChI InChI=1S/C3H6N2/c4-2-1-3-5/h1-2,4H2	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	550	n/a	n/a	n/a	n/a	n/a	n/a
PharmAkea Inc. Curated by ChEMBL					Assay Description Inhibition of full length recombinant human LOX expressed in HEK cells assessed as reduction in H2O2 production using DAP as substrate preincubated f...				ACS Med Chem Lett 8: 423-427 (2017) Article DOI: 10.1021/acsmedchemlett.7b00014 BindingDB Entry DOI: 10.7270/Q2542QV6
					More data for this Ligand-Target Pair
Protein-lysine 6-oxidase (Homo sapiens (Human))	BDBM469010 (US10807974, Example 26 | US10995088, Example 26 | ...) Show SMILES NCc1ccc(s1)S(=O)(=O)c1ccc(cc1)S(=O)(=O)CCN1CCCC1 Show InChI InChI=1S/C17H22N2O4S3/c18-13-14-3-8-17(24-14)26(22,23)16-6-4-15(5-7-16)25(20,21)12-11-19-9-1-2-10-19/h3-8H,1-2,9-13,18H2	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	550	n/a	n/a	n/a	n/a	n/a	n/a
THE INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL US Patent					Assay Description The following reagents were prepared:Reagents500 mM CHES, pH 9 (with NaOH), filtered (MW=207.29)20.7 g in 200 ml in dH2O10% Pluronic F-127 (store at ...				US Patent US10995088 (2021) BindingDB Entry DOI: 10.7270/Q2125WSK
					More data for this Ligand-Target Pair

Displayed 1 to 50 (of 325 total )  |  Next  |  Last  >>

Jump to: