Compile Data Set for Download or QSAR

Found 160 hits of ic50 for UniProtKB: P32929   

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
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM60996 (5-[(3-carboxy-4-hydroxy-phenyl)-(3-carboxy-4-keto-...) Show SMILES [#8]-[#6](=O)-[#6]-1=[#6]\[#6](-[#6]=[#6]-[#6]-1=O)=[#6](\c1ccc(-[#8])c(c1)-[#6](-[#8])=O)-c1ccc(-[#8])c(c1)-[#6](-[#8])=O |c:6,t:3| Show InChI InChI=1S/C22H14O9/c23-16-4-1-10(7-13(16)20(26)27)19(11-2-5-17(24)14(8-11)21(28)29)12-3-6-18(25)15(9-12)22(30)31/h1-9,23-24H,(H,26,27)(H,28,29)(H,30,31)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	600	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human CSE using L-Cys as the substrate by tandem well based HTS assay				Citation and Details Article DOI: 10.1021/acs.jmedchem.8b01720 BindingDB Entry DOI: 10.7270/Q2W380Z9
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50280040 (CHEMBL1619821) Show SMILES NCCO\C=C\[C@H](N)C(O)=O Show InChI InChI=1S/C6H12N2O3/c7-2-4-11-3-1-5(8)6(9)10/h1,3,5H,2,4,7-8H2,(H,9,10)/b3-1+/t5-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin)				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50280013 (CHEMBL4163832) Show SMILES COc1ccc(NC(=O)CSC(=S)N\N=C\c2ncccc2F)cc1 Show InChI InChI=1S/C16H15FN4O2S2/c1-23-12-6-4-11(5-7-12)20-15(22)10-25-16(24)21-19-9-14-13(17)3-2-8-18-14/h2-9H,10H2,1H3,(H,20,22)(H,21,24)/b19-9+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM60996 (5-[(3-carboxy-4-hydroxy-phenyl)-(3-carboxy-4-keto-...) Show SMILES [#8]-[#6](=O)-[#6]-1=[#6]\[#6](-[#6]=[#6]-[#6]-1=O)=[#6](\c1ccc(-[#8])c(c1)-[#6](-[#8])=O)-c1ccc(-[#8])c(c1)-[#6](-[#8])=O |c:6,t:3| Show InChI InChI=1S/C22H14O9/c23-16-4-1-10(7-13(16)20(26)27)19(11-2-5-17(24)14(8-11)21(28)29)12-3-6-18(25)15(9-12)22(30)31/h1-9,23-24H,(H,26,27)(H,28,29)(H,30,31)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	1.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human CSE using H-Cys as the substrate by tandem well based HTS assay				Citation and Details Article DOI: 10.1021/acs.jmedchem.8b01720 BindingDB Entry DOI: 10.7270/Q2W380Z9
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM60996 (5-[(3-carboxy-4-hydroxy-phenyl)-(3-carboxy-4-keto-...) Show SMILES [#8]-[#6](=O)-[#6]-1=[#6]\[#6](-[#6]=[#6]-[#6]-1=O)=[#6](\c1ccc(-[#8])c(c1)-[#6](-[#8])=O)-c1ccc(-[#8])c(c1)-[#6](-[#8])=O |c:6,t:3| Show InChI InChI=1S/C22H14O9/c23-16-4-1-10(7-13(16)20(26)27)19(11-2-5-17(24)14(8-11)21(28)29)12-3-6-18(25)15(9-12)22(30)31/h1-9,23-24H,(H,26,27)(H,28,29)(H,30,31)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human CSE using L-Cys as the substrate in presence of 0.025% Triton X-100 by tandem well based HTS assay				Citation and Details Article DOI: 10.1021/acs.jmedchem.8b01720 BindingDB Entry DOI: 10.7270/Q2W380Z9
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM60996 (5-[(3-carboxy-4-hydroxy-phenyl)-(3-carboxy-4-keto-...) Show SMILES [#8]-[#6](=O)-[#6]-1=[#6]\[#6](-[#6]=[#6]-[#6]-1=O)=[#6](\c1ccc(-[#8])c(c1)-[#6](-[#8])=O)-c1ccc(-[#8])c(c1)-[#6](-[#8])=O |c:6,t:3| Show InChI InChI=1S/C22H14O9/c23-16-4-1-10(7-13(16)20(26)27)19(11-2-5-17(24)14(8-11)21(28)29)12-3-6-18(25)15(9-12)22(30)31/h1-9,23-24H,(H,26,27)(H,28,29)(H,30,31)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human CSE using L-Cys as the substrate in presence of 0.01% Triton X-100 by tandem well based HTS assay				Citation and Details Article DOI: 10.1021/acs.jmedchem.8b01720 BindingDB Entry DOI: 10.7270/Q2W380Z9
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50280015 (CHEMBL4159854) Show SMILES COc1ccc(NC(=O)CSC(=S)N\N=C\c2cccc(C)n2)cc1 Show InChI InChI=1S/C17H18N4O2S2/c1-12-4-3-5-14(19-12)10-18-21-17(24)25-11-16(22)20-13-6-8-15(23-2)9-7-13/h3-10H,11H2,1-2H3,(H,20,22)(H,21,24)/b18-10+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50279931 (CHEMBL4166278) Show SMILES COc1ccc(NC(=O)CSC(=S)N\N=C\c2ccccn2)cc1 Show InChI InChI=1S/C16H16N4O2S2/c1-22-14-7-5-12(6-8-14)19-15(21)11-24-16(23)20-18-10-13-4-2-3-9-17-13/h2-10H,11H2,1H3,(H,19,21)(H,20,23)/b18-10+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50280022 (CHEMBL4171052) Show SMILES CC(C)(C)c1ccc(NC(=O)CSC(=S)N\N=C\c2ncccc2F)cc1 Show InChI InChI=1S/C19H21FN4OS2/c1-19(2,3)13-6-8-14(9-7-13)23-17(25)12-27-18(26)24-22-11-16-15(20)5-4-10-21-16/h4-11H,12H2,1-3H3,(H,23,25)(H,24,26)/b22-11+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50280014 (CHEMBL4160453) Show SMILES Cc1ccc(NC(=O)CSC(=S)N\N=C\c2ncccc2F)cc1 Show InChI InChI=1S/C16H15FN4OS2/c1-11-4-6-12(7-5-11)20-15(22)10-24-16(23)21-19-9-14-13(17)3-2-8-18-14/h2-9H,10H2,1H3,(H,20,22)(H,21,23)/b19-9+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50280026 (CHEMBL4162824) Show SMILES Cc1ccc(NC(=O)CSC(=S)N\N=C\c2ccccn2)cc1 Show InChI InChI=1S/C16H16N4OS2/c1-12-5-7-13(8-6-12)19-15(21)11-23-16(22)20-18-10-14-4-2-3-9-17-14/h2-10H,11H2,1H3,(H,19,21)(H,20,22)/b18-10+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50279935 (CHEMBL4168463) Show SMILES COc1ccc(NC(=O)CSC(=S)N\N=C\c2cscn2)cc1 Show InChI InChI=1S/C14H14N4O2S3/c1-20-12-4-2-10(3-5-12)17-13(19)8-23-14(21)18-16-6-11-7-22-9-15-11/h2-7,9H,8H2,1H3,(H,17,19)(H,18,21)/b16-6+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50280019 (CHEMBL4167775) Show SMILES Cc1ccc(NC(=O)CSC(=S)N\N=C\c2ncccc2C)cc1 Show InChI InChI=1S/C17H18N4OS2/c1-12-5-7-14(8-6-12)20-16(22)11-24-17(23)21-19-10-15-13(2)4-3-9-18-15/h3-10H,11H2,1-2H3,(H,20,22)(H,21,23)/b19-10+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM60996 (5-[(3-carboxy-4-hydroxy-phenyl)-(3-carboxy-4-keto-...) Show SMILES [#8]-[#6](=O)-[#6]-1=[#6]\[#6](-[#6]=[#6]-[#6]-1=O)=[#6](\c1ccc(-[#8])c(c1)-[#6](-[#8])=O)-c1ccc(-[#8])c(c1)-[#6](-[#8])=O |c:6,t:3| Show InChI InChI=1S/C22H14O9/c23-16-4-1-10(7-13(16)20(26)27)19(11-2-5-17(24)14(8-11)21(28)29)12-3-6-18(25)15(9-12)22(30)31/h1-9,23-24H,(H,26,27)(H,28,29)(H,30,31)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	2.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human CSE by methylene blue method				Citation and Details Article DOI: 10.1021/acs.jmedchem.8b01720 BindingDB Entry DOI: 10.7270/Q2W380Z9
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50279998 (CHEMBL4166122) Show SMILES COc1ccc(NC(=O)CSC(=S)N\N=C\c2nn(C)cc2Cl)cc1 Show InChI InChI=1S/C15H16ClN5O2S2/c1-21-8-12(16)13(20-21)7-17-19-15(24)25-9-14(22)18-10-3-5-11(23-2)6-4-10/h3-8H,9H2,1-2H3,(H,18,22)(H,19,24)/b17-7+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50279999 (CHEMBL4169541) Show SMILES Cc1ccc(NC(=O)CSC(=S)N\N=C\c2nn(C)cc2Cl)cc1 Show InChI InChI=1S/C15H16ClN5OS2/c1-10-3-5-11(6-4-10)18-14(22)9-24-15(23)19-17-7-13-12(16)8-21(2)20-13/h3-8H,9H2,1-2H3,(H,18,22)(H,19,23)/b17-7+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50279979 (CHEMBL4176894) Show SMILES CC(C)(C)c1ccc(NC(=O)CSC(=S)N\N=C\c2ccccn2)cc1 Show InChI InChI=1S/C19H22N4OS2/c1-19(2,3)14-7-9-15(10-8-14)22-17(24)13-26-18(25)23-21-12-16-6-4-5-11-20-16/h4-12H,13H2,1-3H3,(H,22,24)(H,23,25)/b21-12+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM60996 (5-[(3-carboxy-4-hydroxy-phenyl)-(3-carboxy-4-keto-...) Show SMILES [#8]-[#6](=O)-[#6]-1=[#6]\[#6](-[#6]=[#6]-[#6]-1=O)=[#6](\c1ccc(-[#8])c(c1)-[#6](-[#8])=O)-c1ccc(-[#8])c(c1)-[#6](-[#8])=O |c:6,t:3| Show InChI InChI=1S/C22H14O9/c23-16-4-1-10(7-13(16)20(26)27)19(11-2-5-17(24)14(8-11)21(28)29)12-3-6-18(25)15(9-12)22(30)31/h1-9,23-24H,(H,26,27)(H,28,29)(H,30,31)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	3.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human CSE using H-Cys as the substrate by LC/MS/MS-based assay				Citation and Details Article DOI: 10.1021/acs.jmedchem.8b01720 BindingDB Entry DOI: 10.7270/Q2W380Z9
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50280025 (CHEMBL4170080) Show SMILES Cc1ccc(NC(=O)CSC(=S)N\N=C\c2cccc(C)n2)cc1 Show InChI InChI=1S/C17H18N4OS2/c1-12-6-8-14(9-7-12)20-16(22)11-24-17(23)21-18-10-15-5-3-4-13(2)19-15/h3-10H,11H2,1-2H3,(H,20,22)(H,21,23)/b18-10+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50280023 (CHEMBL4177072) Show SMILES CSC(=S)N\N=C\c1ncccc1F Show InChI InChI=1S/C8H8FN3S2/c1-14-8(13)12-11-5-7-6(9)3-2-4-10-7/h2-5H,1H3,(H,12,13)/b11-5+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50279975 (CHEMBL4170257) Show SMILES CSC(=S)N\N=C\c1cccc(C)n1 Show InChI InChI=1S/C9H11N3S2/c1-7-4-3-5-8(11-7)6-10-12-9(13)14-2/h3-6H,1-2H3,(H,12,13)/b10-6+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50280027 (CHEMBL4176749) Show SMILES Cn1cc(Cl)c(\C=N\NC(=S)SCC(=O)Nc2ccc(cc2)C(C)(C)C)n1 Show InChI InChI=1S/C18H22ClN5OS2/c1-18(2,3)12-5-7-13(8-6-12)21-16(25)11-27-17(26)22-20-9-15-14(19)10-24(4)23-15/h5-10H,11H2,1-4H3,(H,21,25)(H,22,26)/b20-9+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50280012 (CHEMBL4174491) Show SMILES Fc1cccnc1\C=N\NC(=S)SCC(=O)Nc1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C16H12F4N4OS2/c17-12-2-1-7-21-13(12)8-22-24-15(26)27-9-14(25)23-11-5-3-10(4-6-11)16(18,19)20/h1-8H,9H2,(H,23,25)(H,24,26)/b22-8+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50279978 (CHEMBL4173530) Show SMILES O=C(CSC(=S)N\N=C\c1ccccn1)Nc1ccccc1 Show InChI InChI=1S/C15H14N4OS2/c20-14(18-12-6-2-1-3-7-12)11-22-15(21)19-17-10-13-8-4-5-9-16-13/h1-10H,11H2,(H,18,20)(H,19,21)/b17-10+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50279974 (CHEMBL4159631) Show SMILES CSC(=S)N\N=C\c1nn(C)cc1Cl Show InChI InChI=1S/C7H9ClN4S2/c1-12-4-5(8)6(11-12)3-9-10-7(13)14-2/h3-4H,1-2H3,(H,10,13)/b9-3+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50279943 (CHEMBL4160479) Show SMILES CSC(=S)N\N=C\c1ccccn1 Show InChI InChI=1S/C8H9N3S2/c1-13-8(12)11-10-6-7-4-2-3-5-9-7/h2-6H,1H3,(H,11,12)/b10-6+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50279940 (CHEMBL4159463) Show SMILES Cc1cccc(\C=N\NC(=S)SCC(=O)Nc2ccc(cc2)C(C)(C)C)n1 Show InChI InChI=1S/C20H24N4OS2/c1-14-6-5-7-17(22-14)12-21-24-19(26)27-13-18(25)23-16-10-8-15(9-11-16)20(2,3)4/h5-12H,13H2,1-4H3,(H,23,25)(H,24,26)/b21-12+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50279933 (CHEMBL4169868) Show SMILES CSC(=S)N\N=C\c1ncccc1C Show InChI InChI=1S/C9H11N3S2/c1-7-4-3-5-10-8(7)6-11-12-9(13)14-2/h3-6H,1-2H3,(H,12,13)/b11-6+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50279932 (CHEMBL3318351) Show SMILES CSC1=NNC(S1)c1ccccn1 |t:2| Show InChI InChI=1S/C8H9N3S2/c1-12-8-11-10-7(13-8)6-4-2-3-5-9-6/h2-5,7,10H,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM64987 (5-nitro-8-quinolinol | 5-nitroquinolin-8-ol | 8-HY...) Show SMILES Oc1ccc([N+]([O-])=O)c2cccnc12 Show InChI InChI=1S/C9H6N2O3/c12-8-4-3-7(11(13)14)6-2-1-5-10-9(6)8/h1-5,12H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase DrugBank MCE PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human CSE using H-Cys as the substrate by LC/MS/MS-based assay				Citation and Details Article DOI: 10.1021/acs.jmedchem.8b01720 BindingDB Entry DOI: 10.7270/Q2W380Z9
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50548267 (CHEMBL4761159) Show SMILES COc1cccc2C(=O)C3=C([C@H](C)O[C@@H](CC(O)=O)C3)C(=O)c12 |r,t:9| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human CSE using L-Cys as the substrate by tandem well based HTS assay				Citation and Details Article DOI: 10.1021/acs.jmedchem.8b01720 BindingDB Entry DOI: 10.7270/Q2W380Z9
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50548267 (CHEMBL4761159) Show SMILES COc1cccc2C(=O)C3=C([C@H](C)O[C@@H](CC(O)=O)C3)C(=O)c12 |r,t:9| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Non-covalent reversible inhibition of human CSE				Citation and Details Article DOI: 10.1021/acs.jmedchem.8b01720 BindingDB Entry DOI: 10.7270/Q2W380Z9
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50279937 (CHEMBL1985550) Show SMILES NC1=CC(=N)c2ccc(=O)[nH]c2C1=O |t:1| Show InChI InChI=1S/C9H7N3O2/c10-5-3-6(11)9(14)8-4(5)1-2-7(13)12-8/h1-3,10H,11H2,(H,12,13)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin)				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50280028 (CHEMBL4162997) Show SMILES CSC(=S)N\N=C\c1cscn1 Show InChI InChI=1S/C6H7N3S3/c1-11-6(10)9-8-2-5-3-12-4-7-5/h2-4H,1H3,(H,9,10)/b8-2+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50548267 (CHEMBL4761159) Show SMILES COc1cccc2C(=O)C3=C([C@H](C)O[C@@H](CC(O)=O)C3)C(=O)c12 |r,t:9| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	7.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human CSE using H-Cys as the substrate by tandem well based HTS assay				Citation and Details Article DOI: 10.1021/acs.jmedchem.8b01720 BindingDB Entry DOI: 10.7270/Q2W380Z9
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM64987 (5-nitro-8-quinolinol | 5-nitroquinolin-8-ol | 8-HY...) Show SMILES Oc1ccc([N+]([O-])=O)c2cccnc12 Show InChI InChI=1S/C9H6N2O3/c12-8-4-3-7(11(13)14)6-2-1-5-10-9(6)8/h1-5,12H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase DrugBank MCE PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	8.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human CSE using L-Cys as the substrate by tandem well based HTS assay				Citation and Details Article DOI: 10.1021/acs.jmedchem.8b01720 BindingDB Entry DOI: 10.7270/Q2W380Z9
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM330317 (US9725426, 21) Show SMILES CC(C)=NNc1nnn[nH]1 |(3.85,.15,;2.52,-.62,;2.52,-2.16,;1.18,.15,;-.15,-.62,;-1.48,.15,;-2.95,-.33,;-3.85,.92,;-2.95,2.16,;-1.48,1.69,)| Show InChI InChI=1S/C4H8N6/c1-3(2)5-6-4-7-9-10-8-4/h1-2H3,(H2,6,7,8,9,10)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	US Patent	n/a	n/a	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
SOVA PHARMACEUTICALS, INC. US Patent					Assay Description Test compounds (from DMSO stock solutions) were added to (final concentrations) 20 ug/ml enzyme solution (human, mouse or rat recombinant CSE) plus 5...				US Patent US9725426 (2017) BindingDB Entry DOI: 10.7270/Q2765HG7
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50279938 (CHEMBL4161944) Show SMILES CSC(=S)N\N=C\c1ccc(Br)cn1 Show InChI InChI=1S/C8H8BrN3S2/c1-14-8(13)12-11-5-7-3-2-6(9)4-10-7/h2-5H,1H3,(H,12,13)/b11-5+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of cystathionine gamma-lyase (unknown origin) assessed as reduction in cysteine formation from CPM using L-cystathionine pre-incubated for...				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM50279936 (CHEMBL4167285) Show SMILES Cc1ccc(NC(=O)CSC(=S)N\N=C\c2cccc(Br)n2)cc1 Show InChI InChI=1S/C16H15BrN4OS2/c1-11-5-7-12(8-6-11)20-15(22)10-24-16(23)21-18-9-13-3-2-4-14(17)19-13/h2-9H,10H2,1H3,(H,20,22)(H,21,23)/b18-9+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Chicago Curated by ChEMBL					Assay Description Binding affinity against sigma receptor				ACS Med Chem Lett 8: 1241-1245 (2017) Article DOI: 10.1021/acsmedchemlett.7b00313 BindingDB Entry DOI: 10.7270/Q2N300GT
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM330339 (US9725426, (E)-5-(2-(furan-2-ylmethylene)hydraziny...) Show SMILES N(\N=C\c1ccco1)c1nnn[nH]1 Show InChI InChI=1S/C6H6N6O/c1-2-5(13-3-1)4-7-8-6-9-11-12-10-6/h1-4H,(H2,8,9,10,11,12)/b7-4+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	US Patent	n/a	n/a	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
SOVA PHARMACEUTICALS, INC. US Patent					Assay Description Test compounds (from DMSO stock solutions) were added to (final concentrations) 20 ug/ml enzyme solution (human, mouse or rat recombinant CSE) plus 5...				US Patent US9725426 (2017) BindingDB Entry DOI: 10.7270/Q2765HG7
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM330331 (US9725426, 2-hydrazinylacetic acid) Show SMILES NNCC(O)=O Show InChI InChI=1S/C2H6N2O2/c3-4-1-2(5)6/h4H,1,3H2,(H,5,6)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	US Patent	n/a	n/a	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
SOVA PHARMACEUTICALS, INC. US Patent					Assay Description Test compounds (from DMSO stock solutions) were added to (final concentrations) 20 ug/ml enzyme solution (human, mouse or rat recombinant CSE) plus 5...				US Patent US9725426 (2017) BindingDB Entry DOI: 10.7270/Q2765HG7
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM330299 (US9725426, 3) Show SMILES NN(CC#C)c1nnn[nH]1 Show InChI InChI=1S/C4H6N6/c1-2-3-10(5)4-6-8-9-7-4/h1H,3,5H2,(H,6,7,8,9)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
SOVA PHARMACEUTICALS, INC. US Patent					Assay Description Test compounds (from DMSO stock solutions) were added to (final concentrations) 20 ug/ml enzyme solution (human, mouse or rat recombinant CSE) plus 5...				US Patent US9725426 (2017) BindingDB Entry DOI: 10.7270/Q2765HG7
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM330300 (US9725426, 4) Show SMILES CCN(N)c1nnn[nH]1 Show InChI InChI=1S/C3H8N6/c1-2-9(4)3-5-7-8-6-3/h2,4H2,1H3,(H,5,6,7,8)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
SOVA PHARMACEUTICALS, INC. US Patent					Assay Description Test compounds (from DMSO stock solutions) were added to (final concentrations) 20 ug/ml enzyme solution (human, mouse or rat recombinant CSE) plus 5...				US Patent US9725426 (2017) BindingDB Entry DOI: 10.7270/Q2765HG7
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM330307 (US9725426, 11) Show SMILES CN(N)c1nnn[nH]1 Show InChI InChI=1S/C2H6N6/c1-8(3)2-4-6-7-5-2/h3H2,1H3,(H,4,5,6,7)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
SOVA PHARMACEUTICALS, INC. US Patent					Assay Description Test compounds (from DMSO stock solutions) were added to (final concentrations) 20 ug/ml enzyme solution (human, mouse or rat recombinant CSE) plus 5...				US Patent US9725426 (2017) BindingDB Entry DOI: 10.7270/Q2765HG7
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM330308 (US9725426, 12) Show SMILES NCCCN(N)c1nnn[nH]1 Show InChI InChI=1S/C4H11N7/c5-2-1-3-11(6)4-7-9-10-8-4/h1-3,5-6H2,(H,7,8,9,10)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
SOVA PHARMACEUTICALS, INC. US Patent					Assay Description Test compounds (from DMSO stock solutions) were added to (final concentrations) 20 ug/ml enzyme solution (human, mouse or rat recombinant CSE) plus 5...				US Patent US9725426 (2017) BindingDB Entry DOI: 10.7270/Q2765HG7
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM330309 (US9725426, 13) Show SMILES NCCN(N)c1nnn[nH]1 Show InChI InChI=1S/C3H9N7/c4-1-2-10(5)3-6-8-9-7-3/h1-2,4-5H2,(H,6,7,8,9)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
SOVA PHARMACEUTICALS, INC. US Patent					Assay Description Test compounds (from DMSO stock solutions) were added to (final concentrations) 20 ug/ml enzyme solution (human, mouse or rat recombinant CSE) plus 5...				US Patent US9725426 (2017) BindingDB Entry DOI: 10.7270/Q2765HG7
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM330311 (US9725426, 15) Show SMILES CNCCCN(N)c1nnn[nH]1 Show InChI InChI=1S/C5H13N7/c1-7-3-2-4-12(6)5-8-10-11-9-5/h7H,2-4,6H2,1H3,(H,8,9,10,11)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
SOVA PHARMACEUTICALS, INC. US Patent					Assay Description Test compounds (from DMSO stock solutions) were added to (final concentrations) 20 ug/ml enzyme solution (human, mouse or rat recombinant CSE) plus 5...				US Patent US9725426 (2017) BindingDB Entry DOI: 10.7270/Q2765HG7
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM330316 (US9725426, 20) Show SMILES Clc1ccc(\C=N\Nc2nnn[nH]2)cc1 Show InChI InChI=1S/C8H7ClN6/c9-7-3-1-6(2-4-7)5-10-11-8-12-14-15-13-8/h1-5H,(H2,11,12,13,14,15)/b10-5+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	US Patent	n/a	n/a	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
SOVA PHARMACEUTICALS, INC. US Patent					Assay Description Test compounds (from DMSO stock solutions) were added to (final concentrations) 20 ug/ml enzyme solution (human, mouse or rat recombinant CSE) plus 5...				US Patent US9725426 (2017) BindingDB Entry DOI: 10.7270/Q2765HG7
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM330318 (US9725426, 22) Show SMILES CN(C)c1ccc(cc1)C(\C)=N\Nc1nnn[nH]1 Show InChI InChI=1S/C11H15N7/c1-8(12-13-11-14-16-17-15-11)9-4-6-10(7-5-9)18(2)3/h4-7H,1-3H3,(H2,13,14,15,16,17)/b12-8+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
SOVA PHARMACEUTICALS, INC. US Patent					Assay Description Test compounds (from DMSO stock solutions) were added to (final concentrations) 20 ug/ml enzyme solution (human, mouse or rat recombinant CSE) plus 5...				US Patent US9725426 (2017) BindingDB Entry DOI: 10.7270/Q2765HG7
					More data for this Ligand-Target Pair
Cystathionine gamma-lyase (Homo sapiens (Human))	BDBM330319 (US9725426, 23) Show SMILES C1CCC(CC1)=NNc1nnn[nH]1 |(4.52,-1.78,;3.19,-2.55,;1.85,-1.78,;1.85,-.24,;3.19,.53,;4.52,-.24,;.52,.53,;-.82,-.24,;-2.15,.53,;-3.61,.06,;-4.52,1.3,;-3.61,2.55,;-2.15,2.07,)| Show InChI InChI=1S/C7H12N6/c1-2-4-6(5-3-1)8-9-7-10-12-13-11-7/h1-5H2,(H2,9,10,11,12,13)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	US Patent	n/a	n/a	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
SOVA PHARMACEUTICALS, INC. US Patent					Assay Description Test compounds (from DMSO stock solutions) were added to (final concentrations) 20 ug/ml enzyme solution (human, mouse or rat recombinant CSE) plus 5...				US Patent US9725426 (2017) BindingDB Entry DOI: 10.7270/Q2765HG7
					More data for this Ligand-Target Pair

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