Compile Data Set for Download or QSAR

Found 24 hits with Last Name = 'hoshino' and Initial = 'm'   

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
C-X-C chemokine receptor type 4 (Homo sapiens (Human))	BDBM50363984 (CHEMBL1949730) Show SMILES [#6]-[#7]-1-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-c2ccc3ccccc3c2)-[#6](=O)-[#7]-[#6]-[#6](=O)-[#7]-[#6@H](-[#6]-c2ccc(-[#8])cc2)-[#6]-1=O |r| Show InChI InChI=1S/C37H49N11O6/c1-48-30(9-5-17-43-37(40)41)34(53)46-27(8-4-16-42-36(38)39)33(52)47-28(20-23-10-13-24-6-2-3-7-25(24)18-23)32(51)44-21-31(50)45-29(35(48)54)19-22-11-14-26(49)15-12-22/h2-3,6-7,10-15,18,27-30,49H,4-5,8-9,16-17,19-21H2,1H3,(H,44,51)(H,45,50)(H,46,53)(H,47,52)(H4,38,39,42)(H4,40,41,43)/t27-,28-,29+,30+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	63	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto University Curated by ChEMBL					Assay Description Displacement of [125I]SDF-1alpha from CXCR4 expressed in HEK293 cell membrane after 1 hr				J Med Chem 55: 2746-57 (2012) Article DOI: 10.1021/jm2016914 BindingDB Entry DOI: 10.7270/Q2FJ2HTW
					More data for this Ligand-Target Pair
C-X-C chemokine receptor type 4 (Homo sapiens (Human))	BDBM50166106 (CHEMBL436283 | N-{3-[(2S,5S,8S,14R)-5-(3-Guanidino...) Show SMILES [#7]\[#6](-[#7])=[#7]\[#6]-[#6]-[#6]-[#6@@H]-1-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#7]-[#6](=O)-[#6@@H](-[#6]-c2ccc(-[#8])cc2)-[#7]-[#6](=O)-[#6]-[#7]-[#6](=O)-[#6@H](-[#6]-c2ccc3ccccc3c2)-[#7]-[#6]-1=O |r| Show InChI InChI=1S/C36H47N11O6/c37-35(38)41-15-3-7-26-32(51)45-27(8-4-16-42-36(39)40)33(52)47-28(19-22-9-12-23-5-1-2-6-24(23)17-22)31(50)43-20-30(49)44-29(34(53)46-26)18-21-10-13-25(48)14-11-21/h1-2,5-6,9-14,17,26-29,48H,3-4,7-8,15-16,18-20H2,(H,43,50)(H,44,49)(H,45,51)(H,46,53)(H,47,52)(H4,37,38,41)(H4,39,40,42)/t26-,27-,28-,29+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	84	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto University Curated by ChEMBL					Assay Description Displacement of [125I]SDF-1alpha from CXCR4 expressed in HEK293 cell membrane after 1 hr				J Med Chem 55: 2746-57 (2012) Article DOI: 10.1021/jm2016914 BindingDB Entry DOI: 10.7270/Q2FJ2HTW
					More data for this Ligand-Target Pair
C-X-C chemokine receptor type 4 (Homo sapiens (Human))	BDBM50383301 (CHEMBL2029611) Show SMILES [#6]\[#6]-1=[#6](-[#6])/[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-c2ccc3ccccc3c2)-[#6](=O)-[#7]-[#6]-[#6](=O)-[#7]-[#6@@H]1-[#6]-c1ccc(-[#8])cc1 |r,t:1| Show InChI InChI=1S/C39H52N10O5/c1-23-24(2)32(20-25-12-15-29(50)16-13-25)47-34(51)22-46-36(53)33(21-26-11-14-27-7-3-4-8-28(27)19-26)49-37(54)31(10-6-18-45-39(42)43)48-35(52)30(23)9-5-17-44-38(40)41/h3-4,7-8,11-16,19,30-33,50H,5-6,9-10,17-18,20-22H2,1-2H3,(H,46,53)(H,47,51)(H,48,52)(H,49,54)(H4,40,41,44)(H4,42,43,45)/b24-23+/t30-,31+,32-,33+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	100	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto University Curated by ChEMBL					Assay Description Displacement of [125I]SDF-1alpha from CXCR4 expressed in HEK293 cell membrane after 1 hr				J Med Chem 55: 2746-57 (2012) Article DOI: 10.1021/jm2016914 BindingDB Entry DOI: 10.7270/Q2FJ2HTW
					More data for this Ligand-Target Pair
C-X-C chemokine receptor type 4 (Homo sapiens (Human))	BDBM50383303 (CHEMBL2029613) Show SMILES [#6]-[#7]-1-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-c2ccc3ccccc3c2)-[#6](=O)-[#7]-[#6]-[#6](=O)-[#7]-[#6@H](-[#6]-c2ccc(-[#8])cc2)-[#6]-1=O |r| Show InChI InChI=1S/C37H49N11O6/c1-48-30(9-5-17-43-37(40)41)34(53)46-27(8-4-16-42-36(38)39)33(52)47-28(20-23-10-13-24-6-2-3-7-25(24)18-23)32(51)44-21-31(50)45-29(35(48)54)19-22-11-14-26(49)15-12-22/h2-3,6-7,10-15,18,27-30,49H,4-5,8-9,16-17,19-21H2,1H3,(H,44,51)(H,45,50)(H,46,53)(H,47,52)(H4,38,39,42)(H4,40,41,43)/t27-,28-,29+,30-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	290	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto University Curated by ChEMBL					Assay Description Displacement of [125I]SDF-1alpha from CXCR4 expressed in HEK293 cell membrane after 1 hr				J Med Chem 55: 2746-57 (2012) Article DOI: 10.1021/jm2016914 BindingDB Entry DOI: 10.7270/Q2FJ2HTW
					More data for this Ligand-Target Pair
C-X-C chemokine receptor type 4 (Homo sapiens (Human))	BDBM50383298 (CHEMBL2029608) Show SMILES [#7]\[#6](-[#7])=[#7]\[#6]-[#6]-[#6]-[#6@@H]-1-[#7]-[#6](=O)-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])\[#6]=[#6]\[#6@@H](-[#6]-c2ccc(-[#8])cc2)-[#7]-[#6](=O)-[#6]-[#7]-[#6](=O)-[#6@H](-[#6]-c2ccc3ccccc3c2)-[#7]-[#6]-1=O |r,t:19| Show InChI InChI=1S/C37H48N10O5/c38-36(39)42-17-3-7-26-13-14-28(20-23-10-15-29(48)16-11-23)45-32(49)22-44-34(51)31(21-24-9-12-25-5-1-2-6-27(25)19-24)47-35(52)30(46-33(26)50)8-4-18-43-37(40)41/h1-2,5-6,9-16,19,26,28,30-31,48H,3-4,7-8,17-18,20-22H2,(H,44,51)(H,45,49)(H,46,50)(H,47,52)(H4,38,39,42)(H4,40,41,43)/b14-13+/t26-,28-,30-,31-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	330	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto University Curated by ChEMBL					Assay Description Displacement of [125I]SDF-1alpha from CXCR4 expressed in HEK293 cell membrane after 1 hr				J Med Chem 55: 2746-57 (2012) Article DOI: 10.1021/jm2016914 BindingDB Entry DOI: 10.7270/Q2FJ2HTW
					More data for this Ligand-Target Pair
C-X-C chemokine receptor type 4 (Homo sapiens (Human))	BDBM50383299 (CHEMBL2029609) Show SMILES [#6]\[#6]-1=[#6]/[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-c2ccc3ccccc3c2)-[#6](=O)-[#7]-[#6]-[#6](=O)-[#7]-[#6@@H]1-[#6]-c1ccc(-[#8])cc1 |r,c:1| Show InChI InChI=1S/C38H50N10O5/c1-23-18-28(8-4-16-43-37(39)40)34(51)47-30(9-5-17-44-38(41)42)36(53)48-32(21-25-10-13-26-6-2-3-7-27(26)19-25)35(52)45-22-33(50)46-31(23)20-24-11-14-29(49)15-12-24/h2-3,6-7,10-15,18-19,28,30-32,49H,4-5,8-9,16-17,20-22H2,1H3,(H,45,52)(H,46,50)(H,47,51)(H,48,53)(H4,39,40,43)(H4,41,42,44)/b23-18+/t28-,30-,31+,32-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto University Curated by ChEMBL					Assay Description Displacement of [125I]SDF-1alpha from CXCR4 expressed in HEK293 cell membrane after 1 hr				J Med Chem 55: 2746-57 (2012) Article DOI: 10.1021/jm2016914 BindingDB Entry DOI: 10.7270/Q2FJ2HTW
					More data for this Ligand-Target Pair
C-X-C chemokine receptor type 4 (Homo sapiens (Human))	BDBM50383300 (CHEMBL2029610) Show SMILES [#6]\[#6]-1=[#6](-[#6])/[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-c2ccc3ccccc3c2)-[#6](=O)-[#7]-[#6]-[#6](=O)-[#7]-[#6@@H]1-[#6]-c1ccc(-[#8])cc1 |r,t:1| Show InChI InChI=1S/C39H52N10O5/c1-23-24(2)32(20-25-12-15-29(50)16-13-25)47-34(51)22-46-36(53)33(21-26-11-14-27-7-3-4-8-28(27)19-26)49-37(54)31(10-6-18-45-39(42)43)48-35(52)30(23)9-5-17-44-38(40)41/h3-4,7-8,11-16,19,30-33,50H,5-6,9-10,17-18,20-22H2,1-2H3,(H,46,53)(H,47,51)(H,48,52)(H,49,54)(H4,40,41,44)(H4,42,43,45)/b24-23+/t30-,31-,32+,33-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL 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
Kyoto University Curated by ChEMBL					Assay Description Displacement of [125I]SDF-1alpha from CXCR4 expressed in HEK293 cell membrane after 1 hr				J Med Chem 55: 2746-57 (2012) Article DOI: 10.1021/jm2016914 BindingDB Entry DOI: 10.7270/Q2FJ2HTW
					More data for this Ligand-Target Pair
C-X-C chemokine receptor type 4 (Homo sapiens (Human))	BDBM50383302 (CHEMBL2029612) Show SMILES [#7]\[#6](-[#7])=[#7]/[#6]-[#6]-[#6]-[#6@H]-1-[#6]-[#6]-[#6@H](-[#6]-c2ccc(-[#8])cc2)-[#7]-[#6](=O)-[#6]-[#7]-[#6](=O)-[#6@H](-[#6]-c2ccc3ccccc3c2)-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#7]-[#6]-1=O |r| Show InChI InChI=1S/C37H50N10O5/c38-36(39)42-17-3-7-26-13-14-28(20-23-10-15-29(48)16-11-23)45-32(49)22-44-34(51)31(21-24-9-12-25-5-1-2-6-27(25)19-24)47-35(52)30(46-33(26)50)8-4-18-43-37(40)41/h1-2,5-6,9-12,15-16,19,26,28,30-31,48H,3-4,7-8,13-14,17-18,20-22H2,(H,44,51)(H,45,49)(H,46,50)(H,47,52)(H4,38,39,42)(H4,40,41,43)/t26-,28+,30-,31-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL 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
Kyoto University Curated by ChEMBL					Assay Description Displacement of [125I]SDF-1alpha from CXCR4 expressed in HEK293 cell membrane after 1 hr				J Med Chem 55: 2746-57 (2012) Article DOI: 10.1021/jm2016914 BindingDB Entry DOI: 10.7270/Q2FJ2HTW
					More data for this Ligand-Target Pair
Beta-galactosidase (Bos taurus (Bovine))	BDBM50204206 (CHEMBL3896958) Show SMILES [H][C@@]12CS\C(=N\CCCCCCCCCCCC)N1[C@@H](CO)[C@H](O)[C@H]2O |r| Show InChI InChI=1S/C19H36N2O3S/c1-2-3-4-5-6-7-8-9-10-11-12-20-19-21-15(13-22)17(23)18(24)16(21)14-25-19/h15-18,22-24H,2-14H2,1H3/b20-19+/t15-,16-,17-,18-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Toyama Curated by ChEMBL					Assay Description Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric method				Bioorg Med Chem 25: 107-115 (2017) Article DOI: 10.1016/j.bmc.2016.10.015 BindingDB Entry DOI: 10.7270/Q26H4KC4
					More data for this Ligand-Target Pair
Beta-galactosidase (Bos taurus (Bovine))	BDBM50204109 (CHEMBL3935498) Show SMILES CCCCCCCCCCCCNC(=S)N1[C@H](CO)[C@@H](O)[C@H](O)[C@H]1CO |r| Show InChI InChI=1S/C19H38N2O4S/c1-2-3-4-5-6-7-8-9-10-11-12-20-19(26)21-15(13-22)17(24)18(25)16(21)14-23/h15-18,22-25H,2-14H2,1H3,(H,20,26)/t15-,16-,17-,18-/m1/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Toyama Curated by ChEMBL					Assay Description Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric method				Bioorg Med Chem 25: 107-115 (2017) Article DOI: 10.1016/j.bmc.2016.10.015 BindingDB Entry DOI: 10.7270/Q26H4KC4
					More data for this Ligand-Target Pair
Beta-galactosidase (Bos taurus (Bovine))	BDBM50204204 (CHEMBL3891002) Show SMILES CCCCCCCCCCCCNC(=S)N1[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]1CO |r| Show InChI InChI=1S/C19H38N2O4S/c1-2-3-4-5-6-7-8-9-10-11-12-20-19(26)21-15(13-22)17(24)18(25)16(21)14-23/h15-18,22-25H,2-14H2,1H3,(H,20,26)/t15-,16-,17-,18-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Toyama Curated by ChEMBL					Assay Description Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric method				Bioorg Med Chem 25: 107-115 (2017) Article DOI: 10.1016/j.bmc.2016.10.015 BindingDB Entry DOI: 10.7270/Q26H4KC4
					More data for this Ligand-Target Pair
Beta-galactosidase (Bos taurus (Bovine))	BDBM50204212 (CHEMBL3901083) Show SMILES [H][C@]12CS\C(=N\CCCCCCCCCCCC)N1[C@H](CO)[C@@H](O)[C@@H]2O |r| Show InChI InChI=1S/C19H36N2O3S/c1-2-3-4-5-6-7-8-9-10-11-12-20-19-21-15(13-22)17(23)18(24)16(21)14-25-19/h15-18,22-24H,2-14H2,1H3/b20-19+/t15-,16-,17-,18-/m1/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Toyama Curated by ChEMBL					Assay Description Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric method				Bioorg Med Chem 25: 107-115 (2017) Article DOI: 10.1016/j.bmc.2016.10.015 BindingDB Entry DOI: 10.7270/Q26H4KC4
					More data for this Ligand-Target Pair
Beta-galactosidase (Bos taurus (Bovine))	BDBM50204205 (CHEMBL3909011) Show SMILES [H][C@@]12CS\C(=N\CCCCCCCCCC)N1[C@@H](CO)[C@H](O)[C@H]2O |r| Show InChI InChI=1S/C17H32N2O3S/c1-2-3-4-5-6-7-8-9-10-18-17-19-13(11-20)15(21)16(22)14(19)12-23-17/h13-16,20-22H,2-12H2,1H3/b18-17+/t13-,14-,15-,16-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Toyama Curated by ChEMBL					Assay Description Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric method				Bioorg Med Chem 25: 107-115 (2017) Article DOI: 10.1016/j.bmc.2016.10.015 BindingDB Entry DOI: 10.7270/Q26H4KC4
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50508732 (CHEMBL4453990) Show SMILES [H][C@]12[C@@H](O)[C@@H](O)[C@@H](C)N1[C@H](CO)[C@@H](O)[C@H]2O |r| Show InChI InChI=1S/C9H17NO5/c1-3-6(12)8(14)5-9(15)7(13)4(2-11)10(3)5/h3-9,11-15H,2H2,1H3/t3-,4-,5-,6+,7-,8-,9+/m1/s1	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Wollongong Curated by ChEMBL					Assay Description Inhibition of human lysosomal alpha-glucosidase				J Nat Prod 82: 358-367 (2019) Article DOI: 10.1021/acs.jnatprod.8b00879 BindingDB Entry DOI: 10.7270/Q2J67M7W
					More data for this Ligand-Target Pair
Beta-galactosidase (Bos taurus (Bovine))	BDBM50204210 (CHEMBL3970812) Show SMILES CCCCCCCCCCNC(=S)N1[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]1CO |r| Show InChI InChI=1S/C17H34N2O4S/c1-2-3-4-5-6-7-8-9-10-18-17(24)19-13(11-20)15(22)16(23)14(19)12-21/h13-16,20-23H,2-12H2,1H3,(H,18,24)/t13-,14-,15-,16-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Toyama Curated by ChEMBL					Assay Description Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric method				Bioorg Med Chem 25: 107-115 (2017) Article DOI: 10.1016/j.bmc.2016.10.015 BindingDB Entry DOI: 10.7270/Q26H4KC4
					More data for this Ligand-Target Pair
Beta-galactosidase (Bos taurus (Bovine))	BDBM50204113 (CHEMBL3897971) Show SMILES [H][C@]12CS\C(=N\CCCCCCCCCC)N1[C@H](CO)[C@@H](O)[C@@H]2O |r| Show InChI InChI=1S/C17H32N2O3S/c1-2-3-4-5-6-7-8-9-10-18-17-19-13(11-20)15(21)16(22)14(19)12-23-17/h13-16,20-22H,2-12H2,1H3/b18-17+/t13-,14-,15-,16-/m1/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Toyama Curated by ChEMBL					Assay Description Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric method				Bioorg Med Chem 25: 107-115 (2017) Article DOI: 10.1016/j.bmc.2016.10.015 BindingDB Entry DOI: 10.7270/Q26H4KC4
					More data for this Ligand-Target Pair
Beta-galactosidase (Bos taurus (Bovine))	BDBM50204209 (CHEMBL3907555) Show SMILES CCCCCCCCCCNC(=S)N1[C@H](CO)[C@@H](O)[C@H](O)[C@H]1CO |r| Show InChI InChI=1S/C17H34N2O4S/c1-2-3-4-5-6-7-8-9-10-18-17(24)19-13(11-20)15(22)16(23)14(19)12-21/h13-16,20-23H,2-12H2,1H3,(H,18,24)/t13-,14-,15-,16-/m1/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Toyama Curated by ChEMBL					Assay Description Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric method				Bioorg Med Chem 25: 107-115 (2017) Article DOI: 10.1016/j.bmc.2016.10.015 BindingDB Entry DOI: 10.7270/Q26H4KC4
					More data for this Ligand-Target Pair
Beta-galactosidase (Bos taurus (Bovine))	BDBM50204111 (CHEMBL3961105) Show SMILES CCCCCCCCNC(=S)N1[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]1CO |r| Show InChI InChI=1S/C15H30N2O4S/c1-2-3-4-5-6-7-8-16-15(22)17-11(9-18)13(20)14(21)12(17)10-19/h11-14,18-21H,2-10H2,1H3,(H,16,22)/t11-,12-,13-,14-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.66E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Toyama Curated by ChEMBL					Assay Description Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric method				Bioorg Med Chem 25: 107-115 (2017) Article DOI: 10.1016/j.bmc.2016.10.015 BindingDB Entry DOI: 10.7270/Q26H4KC4
					More data for this Ligand-Target Pair
Beta-galactosidase (Bos taurus (Bovine))	BDBM50204211 (CHEMBL3944457) Show SMILES CCCCCCCCNC(=S)N1[C@H](CO)[C@@H](O)[C@H](O)[C@H]1CO |r| Show InChI InChI=1S/C15H30N2O4S/c1-2-3-4-5-6-7-8-16-15(22)17-11(9-18)13(20)14(21)12(17)10-19/h11-14,18-21H,2-10H2,1H3,(H,16,22)/t11-,12-,13-,14-/m1/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.14E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Toyama Curated by ChEMBL					Assay Description Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric method				Bioorg Med Chem 25: 107-115 (2017) Article DOI: 10.1016/j.bmc.2016.10.015 BindingDB Entry DOI: 10.7270/Q26H4KC4
					More data for this Ligand-Target Pair
Beta-galactosidase (Bos taurus (Bovine))	BDBM50204114 (CHEMBL3972215) Show SMILES CCCCNC(=S)N1[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]1CO |r| Show InChI InChI=1S/C11H22N2O4S/c1-2-3-4-12-11(18)13-7(5-14)9(16)10(17)8(13)6-15/h7-10,14-17H,2-6H2,1H3,(H,12,18)/t7-,8-,9-,10-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.73E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Toyama Curated by ChEMBL					Assay Description Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric method				Bioorg Med Chem 25: 107-115 (2017) Article DOI: 10.1016/j.bmc.2016.10.015 BindingDB Entry DOI: 10.7270/Q26H4KC4
					More data for this Ligand-Target Pair
Beta-galactosidase (Bos taurus (Bovine))	BDBM50204110 (CHEMBL3905255) Show SMILES CCCCCCNC(=S)N1[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]1CO |r| Show InChI InChI=1S/C13H26N2O4S/c1-2-3-4-5-6-14-13(20)15-9(7-16)11(18)12(19)10(15)8-17/h9-12,16-19H,2-8H2,1H3,(H,14,20)/t9-,10-,11-,12-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.72E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Toyama Curated by ChEMBL					Assay Description Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric method				Bioorg Med Chem 25: 107-115 (2017) Article DOI: 10.1016/j.bmc.2016.10.015 BindingDB Entry DOI: 10.7270/Q26H4KC4
					More data for this Ligand-Target Pair
Beta-galactosidase (Bos taurus (Bovine))	BDBM50204207 (CHEMBL3980259) Show SMILES [H][C@@]12CS\C(=N\CCCCCC)N1[C@@H](CO)[C@H](O)[C@H]2O |r| Show InChI InChI=1S/C13H24N2O3S/c1-2-3-4-5-6-14-13-15-9(7-16)11(17)12(18)10(15)8-19-13/h9-12,16-18H,2-8H2,1H3/b14-13+/t9-,10-,11-,12-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.99E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Toyama Curated by ChEMBL					Assay Description Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric method				Bioorg Med Chem 25: 107-115 (2017) Article DOI: 10.1016/j.bmc.2016.10.015 BindingDB Entry DOI: 10.7270/Q26H4KC4
					More data for this Ligand-Target Pair
Beta-galactosidase (Bos taurus (Bovine))	BDBM50204208 (CHEMBL3910143) Show SMILES [H][C@@]12CS\C(=N\CCCC)N1[C@@H](CO)[C@H](O)[C@H]2O |r| Show InChI InChI=1S/C11H20N2O3S/c1-2-3-4-12-11-13-7(5-14)9(15)10(16)8(13)6-17-11/h7-10,14-16H,2-6H2,1H3/b12-11+/t7-,8-,9-,10-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.19E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Toyama Curated by ChEMBL					Assay Description Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric method				Bioorg Med Chem 25: 107-115 (2017) Article DOI: 10.1016/j.bmc.2016.10.015 BindingDB Entry DOI: 10.7270/Q26H4KC4
					More data for this Ligand-Target Pair
Beta-galactosidase (Bos taurus (Bovine))	BDBM50204112 (CHEMBL3916518) Show SMILES CCCCCCNC(=S)N1[C@H](CO)[C@@H](O)[C@H](O)[C@H]1CO |r| Show InChI InChI=1S/C13H26N2O4S/c1-2-3-4-5-6-14-13(20)15-9(7-16)11(18)12(19)10(15)8-17/h9-12,16-19H,2-8H2,1H3,(H,14,20)/t9-,10-,11-,12-/m1/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Toyama Curated by ChEMBL					Assay Description Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric method				Bioorg Med Chem 25: 107-115 (2017) Article DOI: 10.1016/j.bmc.2016.10.015 BindingDB Entry DOI: 10.7270/Q26H4KC4
					More data for this Ligand-Target Pair