Compile Data Set for Download or QSAR

Found 29 hits with Last Name = 'iwadate' and Initial = 't'   

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
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50503718 (CHEMBL4439507) Show SMILES OC[C@H]1O[C@@H](OCCCCCCCCCCCCCCc2ccc(O)cc2O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C26H44O8/c27-18-22-23(30)24(31)25(32)26(34-22)33-16-12-10-8-6-4-2-1-3-5-7-9-11-13-19-14-15-20(28)17-21(19)29/h14-15,17,22-32H,1-13,16,18H2/t22-,23-,24+,25-,26-/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	390	n/a	n/a	n/a	n/a	n/a	n/a
Utsunomiya University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric method				Bioorg Med Chem Lett 29: 313-316 (2019) Article DOI: 10.1016/j.bmcl.2018.11.029 BindingDB Entry DOI: 10.7270/Q22V2KCK
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50503713 (CHEMBL4462064) Show SMILES OC[C@H]1O[C@@H](OCCCCCCCCCCc2ccc(O)cc2O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C22H36O8/c23-14-18-19(26)20(27)21(28)22(30-18)29-12-8-6-4-2-1-3-5-7-9-15-10-11-16(24)13-17(15)25/h10-11,13,18-28H,1-9,12,14H2/t18-,19-,20+,21-,22-/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	410	n/a	n/a	n/a	n/a	n/a	n/a
Utsunomiya University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric method				Bioorg Med Chem Lett 29: 313-316 (2019) Article DOI: 10.1016/j.bmcl.2018.11.029 BindingDB Entry DOI: 10.7270/Q22V2KCK
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50292636 (4-hexyl resorcinol | ACRISORCIN | CHEMBL443605) Show SMILES CCCCCCc1ccc(O)cc1O Show InChI InChI=1S/C12H18O2/c1-2-3-4-5-6-10-7-8-11(13)9-12(10)14/h7-9,13-14H,2-6H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	560	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometry				Bioorg Med Chem Lett 24: 122-5 (2014) Article DOI: 10.1016/j.bmcl.2013.11.063 BindingDB Entry DOI: 10.7270/Q2NZ8BMD
					More data for this Ligand-Target Pair
Tyrosinase (Homo sapiens (Human))	BDBM50292636 (4-hexyl resorcinol | ACRISORCIN | CHEMBL443605) Show SMILES CCCCCCc1ccc(O)cc1O Show InChI InChI=1S/C12H18O2/c1-2-3-4-5-6-10-7-8-11(13)9-12(10)14/h7-9,13-14H,2-6H2,1H3	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	560	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysis				Bioorg Med Chem 23: 6650-8 (2015) Article DOI: 10.1016/j.bmc.2015.09.014 BindingDB Entry DOI: 10.7270/Q2DR2X9W
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50292636 (4-hexyl resorcinol | ACRISORCIN | CHEMBL443605) Show SMILES CCCCCCc1ccc(O)cc1O Show InChI InChI=1S/C12H18O2/c1-2-3-4-5-6-10-7-8-11(13)9-12(10)14/h7-9,13-14H,2-6H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	610	n/a	n/a	n/a	n/a	n/a	n/a
Utsunomiya University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric method				Bioorg Med Chem Lett 29: 313-316 (2019) Article DOI: 10.1016/j.bmcl.2018.11.029 BindingDB Entry DOI: 10.7270/Q22V2KCK
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50503714 (CHEMBL4456030) Show SMILES OC[C@H]1O[C@@H](OCCCCCCc2ccc(O)cc2O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C18H28O8/c19-10-14-15(22)16(23)17(24)18(26-14)25-8-4-2-1-3-5-11-6-7-12(20)9-13(11)21/h6-7,9,14-24H,1-5,8,10H2/t14-,15-,16+,17-,18-/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	630	n/a	n/a	n/a	n/a	n/a	n/a
Utsunomiya University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric method				Bioorg Med Chem Lett 29: 313-316 (2019) Article DOI: 10.1016/j.bmcl.2018.11.029 BindingDB Entry DOI: 10.7270/Q22V2KCK
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50503717 (CHEMBL4465094) Show SMILES OC[C@H]1O[C@@H](OCCCCc2ccc(O)cc2O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C16H24O8/c17-8-12-13(20)14(21)15(22)16(24-12)23-6-2-1-3-9-4-5-10(18)7-11(9)19/h4-5,7,12-22H,1-3,6,8H2/t12-,13-,14+,15-,16-/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.36E+3	n/a	n/a	n/a	n/a	n/a	n/a
Utsunomiya University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric method				Bioorg Med Chem Lett 29: 313-316 (2019) Article DOI: 10.1016/j.bmcl.2018.11.029 BindingDB Entry DOI: 10.7270/Q22V2KCK
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50120802 (CHEMBL3100130) Show SMILES [H][C@@]1(O[C@H](C)CCc2ccc(O)cc2O)O[C@H](CO)[C@@H](O[C@]2([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C22H34O13/c1-9(2-3-10-4-5-11(25)6-12(10)26)32-21-19(31)17(29)20(14(8-24)34-21)35-22-18(30)16(28)15(27)13(7-23)33-22/h4-6,9,13-31H,2-3,7-8H2,1H3/t9-,13-,14-,15-,16+,17-,18-,19-,20-,21-,22+/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.51E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometry				Bioorg Med Chem Lett 24: 122-5 (2014) Article DOI: 10.1016/j.bmcl.2013.11.063 BindingDB Entry DOI: 10.7270/Q2NZ8BMD
					More data for this Ligand-Target Pair
Tyrosinase (Homo sapiens (Human))	BDBM50120802 (CHEMBL3100130) Show SMILES [H][C@@]1(O[C@H](C)CCc2ccc(O)cc2O)O[C@H](CO)[C@@H](O[C@]2([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C22H34O13/c1-9(2-3-10-4-5-11(25)6-12(10)26)32-21-19(31)17(29)20(14(8-24)34-21)35-22-18(30)16(28)15(27)13(7-23)33-22/h4-6,9,13-31H,2-3,7-8H2,1H3/t9-,13-,14-,15-,16+,17-,18-,19-,20-,21-,22+/m1/s1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.51E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysis				Bioorg Med Chem 23: 6650-8 (2015) Article DOI: 10.1016/j.bmc.2015.09.014 BindingDB Entry DOI: 10.7270/Q2DR2X9W
					More data for this Ligand-Target Pair
Tyrosinase (Homo sapiens (Human))	BDBM50120803 (CHEMBL3100134) Show SMILES [H][C@@]1(O[C@H](C)CCc2ccc(O)cc2O)OC[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C15H22O7/c1-8(2-3-9-4-5-10(16)6-11(9)17)22-15-14(20)13(19)12(18)7-21-15/h4-6,8,12-20H,2-3,7H2,1H3/t8-,12-,13+,14-,15+/m1/s1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.72E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysis				Bioorg Med Chem 23: 6650-8 (2015) Article DOI: 10.1016/j.bmc.2015.09.014 BindingDB Entry DOI: 10.7270/Q2DR2X9W
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50120803 (CHEMBL3100134) Show SMILES [H][C@@]1(O[C@H](C)CCc2ccc(O)cc2O)OC[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C15H22O7/c1-8(2-3-9-4-5-10(16)6-11(9)17)22-15-14(20)13(19)12(18)7-21-15/h4-6,8,12-20H,2-3,7H2,1H3/t8-,12-,13+,14-,15+/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.72E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometry				Bioorg Med Chem Lett 24: 122-5 (2014) Article DOI: 10.1016/j.bmcl.2013.11.063 BindingDB Entry DOI: 10.7270/Q2NZ8BMD
					More data for this Ligand-Target Pair
Tyrosinase (Homo sapiens (Human))	BDBM50120804 (CHEMBL3618459) Show SMILES C[C@@H](O)CCc1ccc(O)cc1O |r| Show InChI InChI=1S/C10H14O3/c1-7(11)2-3-8-4-5-9(12)6-10(8)13/h4-7,11-13H,2-3H2,1H3/t7-/m1/s1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.78E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysis				Bioorg Med Chem 23: 6650-8 (2015) Article DOI: 10.1016/j.bmc.2015.09.014 BindingDB Entry DOI: 10.7270/Q2DR2X9W
					More data for this Ligand-Target Pair
Tyrosinase (Homo sapiens (Human))	BDBM50120800 (CHEMBL3618460) Show SMILES [H][C@]1(O[C@@H]2[C@@H](CO)O[C@@H](O[C@H](C)CCc3ccc(O)cc3O)[C@H](O)[C@H]2O)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C22H34O13/c1-9(2-3-10-4-5-11(25)6-12(10)26)32-21-19(31)17(29)20(14(8-24)34-21)35-22-18(30)16(28)15(27)13(7-23)33-22/h4-6,9,13-31H,2-3,7-8H2,1H3/t9-,13-,14-,15-,16+,17-,18-,19-,20-,21-,22-/m1/s1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.98E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysis				Bioorg Med Chem 23: 6650-8 (2015) Article DOI: 10.1016/j.bmc.2015.09.014 BindingDB Entry DOI: 10.7270/Q2DR2X9W
					More data for this Ligand-Target Pair
Tyrosinase (Homo sapiens (Human))	BDBM50120813 (CHEMBL3618457) Show SMILES C[C@H](O)CCc1ccc(O)cc1O |r| Show InChI InChI=1S/C10H14O3/c1-7(11)2-3-8-4-5-9(12)6-10(8)13/h4-7,11-13H,2-3H2,1H3/t7-/m0/s1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.17E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysis				Bioorg Med Chem 23: 6650-8 (2015) Article DOI: 10.1016/j.bmc.2015.09.014 BindingDB Entry DOI: 10.7270/Q2DR2X9W
					More data for this Ligand-Target Pair
Tyrosinase (Homo sapiens (Human))	BDBM50120806 (CHEMBL3100132) Show SMILES [H][C@@]1(O[C@H](C)CCc2ccc(O)cc2O)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C16H24O8/c1-8(2-3-9-4-5-10(18)6-11(9)19)23-16-15(22)14(21)13(20)12(7-17)24-16/h4-6,8,12-22H,2-3,7H2,1H3/t8-,12-,13-,14+,15-,16-/m1/s1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysis				Bioorg Med Chem 23: 6650-8 (2015) Article DOI: 10.1016/j.bmc.2015.09.014 BindingDB Entry DOI: 10.7270/Q2DR2X9W
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50120806 (CHEMBL3100132) Show SMILES [H][C@@]1(O[C@H](C)CCc2ccc(O)cc2O)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C16H24O8/c1-8(2-3-9-4-5-10(18)6-11(9)19)23-16-15(22)14(21)13(20)12(7-17)24-16/h4-6,8,12-22H,2-3,7H2,1H3/t8-,12-,13-,14+,15-,16-/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometry				Bioorg Med Chem Lett 24: 122-5 (2014) Article DOI: 10.1016/j.bmcl.2013.11.063 BindingDB Entry DOI: 10.7270/Q2NZ8BMD
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50503712 (CHEMBL4541503) Show SMILES OC[C@H]1O[C@@H](OCCCc2ccc(O)cc2O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C15H22O8/c16-7-11-12(19)13(20)14(21)15(23-11)22-5-1-2-8-3-4-9(17)6-10(8)18/h3-4,6,11-21H,1-2,5,7H2/t11-,12-,13+,14-,15-/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.62E+3	n/a	n/a	n/a	n/a	n/a	n/a
Utsunomiya University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric method				Bioorg Med Chem Lett 29: 313-316 (2019) Article DOI: 10.1016/j.bmcl.2018.11.029 BindingDB Entry DOI: 10.7270/Q22V2KCK
					More data for this Ligand-Target Pair
Tyrosinase (Homo sapiens (Human))	BDBM50120810 (CHEMBL3100135) Show SMILES [H][C@@]1(O[C@@H](C)CCc2ccc(O)cc2O)O[C@H](CO)[C@@H](O[C@]2([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C22H34O13/c1-9(2-3-10-4-5-11(25)6-12(10)26)32-21-19(31)17(29)20(14(8-24)34-21)35-22-18(30)16(28)15(27)13(7-23)33-22/h4-6,9,13-31H,2-3,7-8H2,1H3/t9-,13+,14+,15+,16-,17+,18+,19+,20+,21+,22-/m0/s1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.83E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysis				Bioorg Med Chem 23: 6650-8 (2015) Article DOI: 10.1016/j.bmc.2015.09.014 BindingDB Entry DOI: 10.7270/Q2DR2X9W
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50120810 (CHEMBL3100135) Show SMILES [H][C@@]1(O[C@@H](C)CCc2ccc(O)cc2O)O[C@H](CO)[C@@H](O[C@]2([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C22H34O13/c1-9(2-3-10-4-5-11(25)6-12(10)26)32-21-19(31)17(29)20(14(8-24)34-21)35-22-18(30)16(28)15(27)13(7-23)33-22/h4-6,9,13-31H,2-3,7-8H2,1H3/t9-,13+,14+,15+,16-,17+,18+,19+,20+,21+,22-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.83E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometry				Bioorg Med Chem Lett 24: 122-5 (2014) Article DOI: 10.1016/j.bmcl.2013.11.063 BindingDB Entry DOI: 10.7270/Q2NZ8BMD
					More data for this Ligand-Target Pair
Tyrosinase (Homo sapiens (Human))	BDBM50120807 (CHEMBL3618458) Show SMILES [H][C@]1(O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H](C)CCc3ccc(O)cc3O)[C@H](O)[C@H]2O)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C22H34O13/c1-9(2-3-10-4-5-11(25)6-12(10)26)32-21-19(31)17(29)20(14(8-24)34-21)35-22-18(30)16(28)15(27)13(7-23)33-22/h4-6,9,13-31H,2-3,7-8H2,1H3/t9-,13+,14+,15+,16-,17+,18+,19+,20+,21+,22+/m0/s1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.13E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysis				Bioorg Med Chem 23: 6650-8 (2015) Article DOI: 10.1016/j.bmc.2015.09.014 BindingDB Entry DOI: 10.7270/Q2DR2X9W
					More data for this Ligand-Target Pair
Tyrosinase (Homo sapiens (Human))	BDBM50120811 (CHEMBL3100133) Show SMILES [H][C@@]1(O[C@@H](C)CCc2ccc(O)cc2O)OC[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C15H22O7/c1-8(2-3-9-4-5-10(16)6-11(9)17)22-15-14(20)13(19)12(18)7-21-15/h4-6,8,12-20H,2-3,7H2,1H3/t8-,12+,13-,14+,15-/m0/s1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.56E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysis				Bioorg Med Chem 23: 6650-8 (2015) Article DOI: 10.1016/j.bmc.2015.09.014 BindingDB Entry DOI: 10.7270/Q2DR2X9W
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50120811 (CHEMBL3100133) Show SMILES [H][C@@]1(O[C@@H](C)CCc2ccc(O)cc2O)OC[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C15H22O7/c1-8(2-3-9-4-5-10(16)6-11(9)17)22-15-14(20)13(19)12(18)7-21-15/h4-6,8,12-20H,2-3,7H2,1H3/t8-,12+,13-,14+,15-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.56E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometry				Bioorg Med Chem Lett 24: 122-5 (2014) Article DOI: 10.1016/j.bmcl.2013.11.063 BindingDB Entry DOI: 10.7270/Q2NZ8BMD
					More data for this Ligand-Target Pair
Tyrosinase (Homo sapiens (Human))	BDBM50120814 (CHEMBL3100131) Show SMILES [H][C@@]1(O[C@@H](C)CCc2ccc(O)cc2O)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C16H24O8/c1-8(2-3-9-4-5-10(18)6-11(9)19)23-16-15(22)14(21)13(20)12(7-17)24-16/h4-6,8,12-22H,2-3,7H2,1H3/t8-,12+,13+,14-,15+,16+/m0/s1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.72E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysis				Bioorg Med Chem 23: 6650-8 (2015) Article DOI: 10.1016/j.bmc.2015.09.014 BindingDB Entry DOI: 10.7270/Q2DR2X9W
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50120814 (CHEMBL3100131) Show SMILES [H][C@@]1(O[C@@H](C)CCc2ccc(O)cc2O)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C16H24O8/c1-8(2-3-9-4-5-10(18)6-11(9)19)23-16-15(22)14(21)13(20)12(7-17)24-16/h4-6,8,12-22H,2-3,7H2,1H3/t8-,12+,13+,14-,15+,16+/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.72E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometry				Bioorg Med Chem Lett 24: 122-5 (2014) Article DOI: 10.1016/j.bmcl.2013.11.063 BindingDB Entry DOI: 10.7270/Q2NZ8BMD
					More data for this Ligand-Target Pair
Tyrosinase (Homo sapiens (Human))	BDBM50031467 (5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE | 5-Hyd...) Show SMILES OCc1cc(=O)c(O)co1 Show InChI InChI=1S/C6H6O4/c7-2-4-1-5(8)6(9)3-10-4/h1,3,7,9H,2H2	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	9.15E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysis				Bioorg Med Chem 23: 6650-8 (2015) Article DOI: 10.1016/j.bmc.2015.09.014 BindingDB Entry DOI: 10.7270/Q2DR2X9W
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50031467 (5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE | 5-Hyd...) Show SMILES OCc1cc(=O)c(O)co1 Show InChI InChI=1S/C6H6O4/c7-2-4-1-5(8)6(9)3-10-4/h1,3,7,9H,2H2	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	9.15E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tokyo University of Agriculture and Technology Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometry				Bioorg Med Chem Lett 24: 122-5 (2014) Article DOI: 10.1016/j.bmcl.2013.11.063 BindingDB Entry DOI: 10.7270/Q2NZ8BMD
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50031467 (5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE | 5-Hyd...) Show SMILES OCc1cc(=O)c(O)co1 Show InChI InChI=1S/C6H6O4/c7-2-4-1-5(8)6(9)3-10-4/h1,3,7,9H,2H2	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.07E+4	n/a	n/a	n/a	n/a	n/a	n/a
Utsunomiya University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric method				Bioorg Med Chem Lett 29: 313-316 (2019) Article DOI: 10.1016/j.bmcl.2018.11.029 BindingDB Entry DOI: 10.7270/Q22V2KCK
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50503716 (CHEMBL4453823) Show SMILES OC[C@H]1O[C@@H](OCCc2ccc(O)cc2O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C14H20O8/c15-6-10-11(18)12(19)13(20)14(22-10)21-4-3-7-1-2-8(16)5-9(7)17/h1-2,5,10-20H,3-4,6H2/t10-,11-,12+,13-,14-/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.59E+4	n/a	n/a	n/a	n/a	n/a	n/a
Utsunomiya University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric method				Bioorg Med Chem Lett 29: 313-316 (2019) Article DOI: 10.1016/j.bmcl.2018.11.029 BindingDB Entry DOI: 10.7270/Q22V2KCK
					More data for this Ligand-Target Pair
Tyrosinase (Homo sapiens (Human))	BDBM50503715 (CHEMBL4586957) Show SMILES OC[C@H]1O[C@@H](Oc2ccc(O)cc2O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C12H16O8/c13-4-8-9(16)10(17)11(18)12(20-8)19-7-2-1-5(14)3-6(7)15/h1-3,8-18H,4H2/t8-,9-,10+,11-,12-/m1/s1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.17E+5	n/a	n/a	n/a	n/a	n/a	n/a
Utsunomiya University Curated by ChEMBL					Assay Description Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate preincubated with substrate for 5 mins followed by enzyme addition and measured i...				Bioorg Med Chem Lett 29: 313-316 (2019) Article DOI: 10.1016/j.bmcl.2018.11.029 BindingDB Entry DOI: 10.7270/Q22V2KCK
					More data for this Ligand-Target Pair