Compile Data Set for Download or QSAR

Found 63 hits Enz. Inhib. hit(s) with all data for entry = 50034779   

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
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50283602 (6a-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro...) Show SMILES OCC12OC(Nc3ccccc3)=NC1C(O)C(O)C2O |c:12| Show InChI InChI=1S/C13H16N2O5/c16-6-13-10(8(17)9(18)11(13)19)15-12(20-13)14-7-4-2-1-3-5-7/h1-5,8-11,16-19H,6H2,(H,14,15)	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against baker's yeast Alpha-Glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283601 (2-Phenylamino-4,5,6,6a-tetrahydro-3aH-cyclopentaox...) Show SMILES OC1C(O)C2OC(Nc3ccccc3)=NC2C1O |c:14| Show InChI InChI=1S/C12H14N2O4/c15-8-7-11(10(17)9(8)16)18-12(14-7)13-6-4-2-1-3-5-6/h1-5,7-11,15-17H,(H,13,14)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283601 (2-Phenylamino-4,5,6,6a-tetrahydro-3aH-cyclopentaox...) Show SMILES OC1C(O)C2OC(Nc3ccccc3)=NC2C1O |c:14| Show InChI InChI=1S/C12H14N2O4/c15-8-7-11(10(17)9(8)16)18-12(14-7)13-6-4-2-1-3-5-6/h1-5,7-11,15-17H,(H,13,14)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Bos taurus)	BDBM50283601 (2-Phenylamino-4,5,6,6a-tetrahydro-3aH-cyclopentaox...) Show SMILES OC1C(O)C2OC(Nc3ccccc3)=NC2C1O |c:14| Show InChI InChI=1S/C12H14N2O4/c15-8-7-11(10(17)9(8)16)18-12(14-7)13-6-4-2-1-3-5-6/h1-5,7-11,15-17H,(H,13,14)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	240	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50283602 (6a-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro...) Show SMILES OCC12OC(Nc3ccccc3)=NC1C(O)C(O)C2O |c:12| Show InChI InChI=1S/C13H16N2O5/c16-6-13-10(8(17)9(18)11(13)19)15-12(20-13)14-7-4-2-1-3-5-7/h1-5,8-11,16-19H,6H2,(H,14,15)	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>999	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against baker's yeast Alpha-Glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50283602 (6a-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro...) Show SMILES OCC12OC(Nc3ccccc3)=NC1C(O)C(O)C2O |c:12| Show InChI InChI=1S/C13H16N2O5/c16-6-13-10(8(17)9(18)11(13)19)15-12(20-13)14-7-4-2-1-3-5-7/h1-5,8-11,16-19H,6H2,(H,14,15)	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>999	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against baker's yeast Alpha-Glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50283598 (5-Amino-1-hydroxymethyl-cyclopentane-1,2,3,4-tetra...) Show SMILES NC1C(O)C(O)C(O)C1(O)CO Show InChI InChI=1S/C6H13NO5/c7-4-2(9)3(10)5(11)6(4,12)1-8/h2-5,8-12H,1,7H2	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	1.34E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against baker's yeast Alpha-galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Bos taurus)	BDBM50283602 (6a-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro...) Show SMILES OCC12OC(Nc3ccccc3)=NC1C(O)C(O)C2O |c:12| Show InChI InChI=1S/C13H16N2O5/c16-6-13-10(8(17)9(18)11(13)19)15-12(20-13)14-7-4-2-1-3-5-7/h1-5,8-11,16-19H,6H2,(H,14,15)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1.89E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against bovine liver beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283601 (2-Phenylamino-4,5,6,6a-tetrahydro-3aH-cyclopentaox...) Show SMILES OC1C(O)C2OC(Nc3ccccc3)=NC2C1O |c:14| Show InChI InChI=1S/C12H14N2O4/c15-8-7-11(10(17)9(8)16)18-12(14-7)13-6-4-2-1-3-5-6/h1-5,7-11,15-17H,(H,13,14)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	2.16E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against almonds Beta-glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283601 (2-Phenylamino-4,5,6,6a-tetrahydro-3aH-cyclopentaox...) Show SMILES OC1C(O)C2OC(Nc3ccccc3)=NC2C1O |c:14| Show InChI InChI=1S/C12H14N2O4/c15-8-7-11(10(17)9(8)16)18-12(14-7)13-6-4-2-1-3-5-6/h1-5,7-11,15-17H,(H,13,14)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	2.16E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against almonds Beta-glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50283603 (4-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro-...) Show SMILES OCC1C(O)C(O)C2OC(Nc3ccccc3)=NC12 |c:17| Show InChI InChI=1S/C13H16N2O4/c16-6-8-9-12(11(18)10(8)17)19-13(15-9)14-7-4-2-1-3-5-7/h1-5,8-12,16-18H,6H2,(H,14,15)	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	2.32E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against baker's yeast Alpha-Glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50283604 (6-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro-...) Show SMILES OCC1(O)C(O)C(O)C2N=C(Nc3ccccc3)OC12 |t:9| Show InChI InChI=1S/C13H16N2O5/c16-6-13(19)10(18)9(17)8-11(13)20-12(15-8)14-7-4-2-1-3-5-7/h1-5,8-11,16-19H,6H2,(H,14,15)	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	2.93E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against baker's yeast Alpha-Glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Bos taurus)	BDBM50283603 (4-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro-...) Show SMILES OCC1C(O)C(O)C2OC(Nc3ccccc3)=NC12 |c:17| Show InChI InChI=1S/C13H16N2O4/c16-6-8-9-12(11(18)10(8)17)19-13(15-9)14-7-4-2-1-3-5-7/h1-5,8-12,16-18H,6H2,(H,14,15)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against bovine liver beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283602 (6a-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro...) Show SMILES OCC12OC(Nc3ccccc3)=NC1C(O)C(O)C2O |c:12| Show InChI InChI=1S/C13H16N2O5/c16-6-13-10(8(17)9(18)11(13)19)15-12(20-13)14-7-4-2-1-3-5-7/h1-5,8-11,16-19H,6H2,(H,14,15)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	4.89E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli Alpha-galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283601 (2-Phenylamino-4,5,6,6a-tetrahydro-3aH-cyclopentaox...) Show SMILES OC1C(O)C2OC(Nc3ccccc3)=NC2C1O |c:14| Show InChI InChI=1S/C12H14N2O4/c15-8-7-11(10(17)9(8)16)18-12(14-7)13-6-4-2-1-3-5-6/h1-5,7-11,15-17H,(H,13,14)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	6.39E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against almonds Beta-glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283600 (5-Amino-cyclopentane-1,2,3,4-tetraol | CHEMBL87120) Show SMILES NC1C(O)C(O)C(O)C1O Show InChI InChI=1S/C5H11NO4/c6-1-2(7)4(9)5(10)3(1)8/h1-5,7-10H,6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	Article	n/a	n/a	7.78E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283600 (5-Amino-cyclopentane-1,2,3,4-tetraol | CHEMBL87120) Show SMILES NC1C(O)C(O)C(O)C1O Show InChI InChI=1S/C5H11NO4/c6-1-2(7)4(9)5(10)3(1)8/h1-5,7-10H,6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	Article	n/a	n/a	7.78E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Bos taurus)	BDBM50283599 (5,7a-Bis-hydroxymethyl-3-phenylamino-2,4a,5,6,7,7a...) Show SMILES OCC1(O)C(O)C(O)C2(CO)OCC(Nc3ccccc3)=NC12 |c:21| Show InChI InChI=1S/C15H20N2O6/c18-7-14(22)11(20)12(21)15(8-19)13(14)17-10(6-23-15)16-9-4-2-1-3-5-9/h1-5,11-13,18-22H,6-8H2,(H,16,17)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	2.39E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against bovine liver beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283598 (5-Amino-1-hydroxymethyl-cyclopentane-1,2,3,4-tetra...) Show SMILES NC1C(O)C(O)C(O)C1(O)CO Show InChI InChI=1S/C6H13NO5/c7-4-2(9)3(10)5(11)6(4,12)1-8/h2-5,8-12H,1,7H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	2.93E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against almonds beta-glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Bos taurus)	BDBM50283600 (5-Amino-cyclopentane-1,2,3,4-tetraol | CHEMBL87120) Show SMILES NC1C(O)C(O)C(O)C1O Show InChI InChI=1S/C5H11NO4/c6-1-2(7)4(9)5(10)3(1)8/h1-5,7-10H,6H2	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	Article	n/a	n/a	4.69E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against bovine liver beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Bos taurus)	BDBM50283600 (5-Amino-cyclopentane-1,2,3,4-tetraol | CHEMBL87120) Show SMILES NC1C(O)C(O)C(O)C1O Show InChI InChI=1S/C5H11NO4/c6-1-2(7)4(9)5(10)3(1)8/h1-5,7-10H,6H2	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	Article	n/a	n/a	4.69E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against bovine liver beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Bos taurus)	BDBM50283602 (6a-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro...) Show SMILES OCC12OC(Nc3ccccc3)=NC1C(O)C(O)C2O |c:12| Show InChI InChI=1S/C13H16N2O5/c16-6-13-10(8(17)9(18)11(13)19)15-12(20-13)14-7-4-2-1-3-5-7/h1-5,8-11,16-19H,6H2,(H,14,15)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	5.17E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against bovine liver beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Bos taurus)	BDBM50283602 (6a-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro...) Show SMILES OCC12OC(Nc3ccccc3)=NC1C(O)C(O)C2O |c:12| Show InChI InChI=1S/C13H16N2O5/c16-6-13-10(8(17)9(18)11(13)19)15-12(20-13)14-7-4-2-1-3-5-7/h1-5,8-11,16-19H,6H2,(H,14,15)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	5.17E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against bovine liver beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283600 (5-Amino-cyclopentane-1,2,3,4-tetraol | CHEMBL87120) Show SMILES NC1C(O)C(O)C(O)C1O Show InChI InChI=1S/C5H11NO4/c6-1-2(7)4(9)5(10)3(1)8/h1-5,7-10H,6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	Article	n/a	n/a	8.38E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against almonds beta-glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283600 (5-Amino-cyclopentane-1,2,3,4-tetraol | CHEMBL87120) Show SMILES NC1C(O)C(O)C(O)C1O Show InChI InChI=1S/C5H11NO4/c6-1-2(7)4(9)5(10)3(1)8/h1-5,7-10H,6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	Article	n/a	n/a	8.38E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against almonds beta-glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM18351 ((2R,3R,4R,5S)-2-(Hydroxymethyl)piperidine-3,4,5-tr...) Show SMILES OC[C@H]1NC[C@H](O)[C@@H](O)[C@@H]1O Show InChI InChI=1S/C6H13NO4/c8-2-3-5(10)6(11)4(9)1-7-3/h3-11H,1-2H2/t3-,4+,5-,6-/m1/s1	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article	n/a	n/a	9.19E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against baker's yeast Alpha-Glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50283599 (5,7a-Bis-hydroxymethyl-3-phenylamino-2,4a,5,6,7,7a...) Show SMILES OCC1(O)C(O)C(O)C2(CO)OCC(Nc3ccccc3)=NC12 |c:21| Show InChI InChI=1S/C15H20N2O6/c18-7-14(22)11(20)12(21)15(8-19)13(14)17-10(6-23-15)16-9-4-2-1-3-5-9/h1-5,11-13,18-22H,6-8H2,(H,16,17)	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	>1.18E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli Alpha-galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM18351 ((2R,3R,4R,5S)-2-(Hydroxymethyl)piperidine-3,4,5-tr...) Show SMILES OC[C@H]1NC[C@H](O)[C@@H](O)[C@@H]1O Show InChI InChI=1S/C6H13NO4/c8-2-3-5(10)6(11)4(9)1-7-3/h3-11H,1-2H2/t3-,4+,5-,6-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article	n/a	n/a	1.18E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli Alpha-galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Bos taurus)	BDBM50283604 (6-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro-...) Show SMILES OCC1(O)C(O)C(O)C2N=C(Nc3ccccc3)OC12 |t:9| Show InChI InChI=1S/C13H16N2O5/c16-6-13(19)10(18)9(17)8-11(13)20-12(15-8)14-7-4-2-1-3-5-7/h1-5,8-11,16-19H,6H2,(H,14,15)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1.53E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against bovine liver beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50283598 (5-Amino-1-hydroxymethyl-cyclopentane-1,2,3,4-tetra...) Show SMILES NC1C(O)C(O)C(O)C1(O)CO Show InChI InChI=1S/C6H13NO5/c7-4-2(9)3(10)5(11)6(4,12)1-8/h2-5,8-12H,1,7H2	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	1.62E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against baker's yeast Alpha-Glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50283598 (5-Amino-1-hydroxymethyl-cyclopentane-1,2,3,4-tetra...) Show SMILES NC1C(O)C(O)C(O)C1(O)CO Show InChI InChI=1S/C6H13NO5/c7-4-2(9)3(10)5(11)6(4,12)1-8/h2-5,8-12H,1,7H2	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	1.62E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against baker's yeast Alpha-Glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283599 (5,7a-Bis-hydroxymethyl-3-phenylamino-2,4a,5,6,7,7a...) Show SMILES OCC1(O)C(O)C(O)C2(CO)OCC(Nc3ccccc3)=NC12 |c:21| Show InChI InChI=1S/C15H20N2O6/c18-7-14(22)11(20)12(21)15(8-19)13(14)17-10(6-23-15)16-9-4-2-1-3-5-9/h1-5,11-13,18-22H,6-8H2,(H,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	2.11E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against almonds Beta-glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283601 (2-Phenylamino-4,5,6,6a-tetrahydro-3aH-cyclopentaox...) Show SMILES OC1C(O)C2OC(Nc3ccccc3)=NC2C1O |c:14| Show InChI InChI=1S/C12H14N2O4/c15-8-7-11(10(17)9(8)16)18-12(14-7)13-6-4-2-1-3-5-6/h1-5,7-11,15-17H,(H,13,14)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50283603 (4-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro-...) Show SMILES OCC1C(O)C(O)C2OC(Nc3ccccc3)=NC12 |c:17| Show InChI InChI=1S/C13H16N2O4/c16-6-8-9-12(11(18)10(8)17)19-13(15-9)14-7-4-2-1-3-5-7/h1-5,8-12,16-18H,6H2,(H,14,15)	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli Alpha-galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283600 (5-Amino-cyclopentane-1,2,3,4-tetraol | CHEMBL87120) Show SMILES NC1C(O)C(O)C(O)C1O Show InChI InChI=1S/C5H11NO4/c6-1-2(7)4(9)5(10)3(1)8/h1-5,7-10H,6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against almonds beta-glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50283600 (5-Amino-cyclopentane-1,2,3,4-tetraol | CHEMBL87120) Show SMILES NC1C(O)C(O)C(O)C1O Show InChI InChI=1S/C5H11NO4/c6-1-2(7)4(9)5(10)3(1)8/h1-5,7-10H,6H2	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against baker's yeast Alpha-Glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283598 (5-Amino-1-hydroxymethyl-cyclopentane-1,2,3,4-tetra...) Show SMILES NC1C(O)C(O)C(O)C1(O)CO Show InChI InChI=1S/C6H13NO5/c7-4-2(9)3(10)5(11)6(4,12)1-8/h2-5,8-12H,1,7H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50283602 (6a-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro...) Show SMILES OCC12OC(Nc3ccccc3)=NC1C(O)C(O)C2O |c:12| Show InChI InChI=1S/C13H16N2O5/c16-6-13-10(8(17)9(18)11(13)19)15-12(20-13)14-7-4-2-1-3-5-7/h1-5,8-11,16-19H,6H2,(H,14,15)	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli Alpha-galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283598 (5-Amino-1-hydroxymethyl-cyclopentane-1,2,3,4-tetra...) Show SMILES NC1C(O)C(O)C(O)C1(O)CO Show InChI InChI=1S/C6H13NO5/c7-4-2(9)3(10)5(11)6(4,12)1-8/h2-5,8-12H,1,7H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against almonds beta-glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50283600 (5-Amino-cyclopentane-1,2,3,4-tetraol | CHEMBL87120) Show SMILES NC1C(O)C(O)C(O)C1O Show InChI InChI=1S/C5H11NO4/c6-1-2(7)4(9)5(10)3(1)8/h1-5,7-10H,6H2	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli Alpha-galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283600 (5-Amino-cyclopentane-1,2,3,4-tetraol | CHEMBL87120) Show SMILES NC1C(O)C(O)C(O)C1O Show InChI InChI=1S/C5H11NO4/c6-1-2(7)4(9)5(10)3(1)8/h1-5,7-10H,6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against almonds beta-glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Bos taurus)	BDBM50283600 (5-Amino-cyclopentane-1,2,3,4-tetraol | CHEMBL87120) Show SMILES NC1C(O)C(O)C(O)C1O Show InChI InChI=1S/C5H11NO4/c6-1-2(7)4(9)5(10)3(1)8/h1-5,7-10H,6H2	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli Alpha-galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283602 (6a-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro...) Show SMILES OCC12OC(Nc3ccccc3)=NC1C(O)C(O)C2O |c:12| Show InChI InChI=1S/C13H16N2O5/c16-6-13-10(8(17)9(18)11(13)19)15-12(20-13)14-7-4-2-1-3-5-7/h1-5,8-11,16-19H,6H2,(H,14,15)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against almonds Beta-glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50283598 (5-Amino-1-hydroxymethyl-cyclopentane-1,2,3,4-tetra...) Show SMILES NC1C(O)C(O)C(O)C1(O)CO Show InChI InChI=1S/C6H13NO5/c7-4-2(9)3(10)5(11)6(4,12)1-8/h2-5,8-12H,1,7H2	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Bos taurus)	BDBM50283598 (5-Amino-1-hydroxymethyl-cyclopentane-1,2,3,4-tetra...) Show SMILES NC1C(O)C(O)C(O)C1(O)CO Show InChI InChI=1S/C6H13NO5/c7-4-2(9)3(10)5(11)6(4,12)1-8/h2-5,8-12H,1,7H2	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli Alpha-galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283599 (5,7a-Bis-hydroxymethyl-3-phenylamino-2,4a,5,6,7,7a...) Show SMILES OCC1(O)C(O)C(O)C2(CO)OCC(Nc3ccccc3)=NC12 |c:21| Show InChI InChI=1S/C15H20N2O6/c18-7-14(22)11(20)12(21)15(8-19)13(14)17-10(6-23-15)16-9-4-2-1-3-5-9/h1-5,11-13,18-22H,6-8H2,(H,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283604 (6-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro-...) Show SMILES OCC1(O)C(O)C(O)C2N=C(Nc3ccccc3)OC12 |t:9| Show InChI InChI=1S/C13H16N2O5/c16-6-13(19)10(18)9(17)8-11(13)20-12(15-8)14-7-4-2-1-3-5-7/h1-5,8-11,16-19H,6H2,(H,14,15)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against baker's yeast Alpha-Glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Bos taurus)	BDBM50283601 (2-Phenylamino-4,5,6,6a-tetrahydro-3aH-cyclopentaox...) Show SMILES OC1C(O)C2OC(Nc3ccccc3)=NC2C1O |c:14| Show InChI InChI=1S/C12H14N2O4/c15-8-7-11(10(17)9(8)16)18-12(14-7)13-6-4-2-1-3-5-6/h1-5,7-11,15-17H,(H,13,14)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against baker's yeast Alpha-Glucosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50283603 (4-Hydroxymethyl-2-phenylamino-4,5,6,6a-tetrahydro-...) Show SMILES OCC1C(O)C(O)C2OC(Nc3ccccc3)=NC12 |c:17| Show InChI InChI=1S/C13H16N2O4/c16-6-8-9-12(11(18)10(8)17)19-13(15-9)14-7-4-2-1-3-5-7/h1-5,8-12,16-18H,6H2,(H,14,15)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli Alpha-galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50283601 (2-Phenylamino-4,5,6,6a-tetrahydro-3aH-cyclopentaox...) Show SMILES OC1C(O)C2OC(Nc3ccccc3)=NC2C1O |c:14| Show InChI InChI=1S/C12H14N2O4/c15-8-7-11(10(17)9(8)16)18-12(14-7)13-6-4-2-1-3-5-6/h1-5,7-11,15-17H,(H,13,14)	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity was determined against Escherichia coli beta galactosidase				Bioorg Med Chem Lett 4: 2643-2648 (1994) Article DOI: 10.1016/S0960-894X(01)80688-0 BindingDB Entry DOI: 10.7270/Q21V5FFN
					More data for this Ligand-Target Pair

Displayed 1 to 50 (of 63 total )  |  Next  |  Last  >>

Jump to: