Compile Data Set for Download or QSAR

Found 45 hits with Last Name = 'khobragade' and Initial = 'cn'   

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))	BDBM50324036 (2-[5-(2,4-Dimethoxy-phenyl)-1H-pyrazol-3-yl]-6-(2-...) Show SMILES COc1ccc(-c2cc([nH]n2)-c2c(OC)cc(OC)c(C3CCN(C)C3CO)c2O)c(OC)c1 Show InChI InChI=1S/C25H31N3O6/c1-28-9-8-16(19(28)13-29)23-21(33-4)12-22(34-5)24(25(23)30)18-11-17(26-27-18)15-7-6-14(31-2)10-20(15)32-3/h6-7,10-12,16,19,29-30H,8-9,13H2,1-5H3,(H,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	840	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50324036 (2-[5-(2,4-Dimethoxy-phenyl)-1H-pyrazol-3-yl]-6-(2-...) Show SMILES COc1ccc(-c2cc([nH]n2)-c2c(OC)cc(OC)c(C3CCN(C)C3CO)c2O)c(OC)c1 Show InChI InChI=1S/C25H31N3O6/c1-28-9-8-16(19(28)13-29)23-21(33-4)12-22(34-5)24(25(23)30)18-11-17(26-27-18)15-7-6-14(31-2)10-20(15)32-3/h6-7,10-12,16,19,29-30H,8-9,13H2,1-5H3,(H,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	960	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase assessed as oxidation of L-DOPA				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50491384 (CHEMBL2380377) Show SMILES COc1ccc(NC2=NC(=O)\C(S2)=C\c2cn(nc2-c2ccc(Cl)cc2)-c2ccccc2)c(OC)c1 |t:7| Show InChI InChI=1S/C27H21ClN4O3S/c1-34-21-12-13-22(23(15-21)35-2)29-27-30-26(33)24(36-27)14-18-16-32(20-6-4-3-5-7-20)31-25(18)17-8-10-19(28)11-9-17/h3-16H,1-2H3,(H,29,30,33)/b24-14-	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	5.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Competitive inhibition of mushroom tyrosinase diphenolase activity assessed as L-DOPA conversion to dopachrome by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50491381 (CHEMBL2380379) Show SMILES COc1ccc(NC2=NC(=O)\C(S2)=C\c2cn(nc2-c2ccc(F)cc2)-c2ccccc2)c(OC)c1 |t:7| Show InChI InChI=1S/C27H21FN4O3S/c1-34-21-12-13-22(23(15-21)35-2)29-27-30-26(33)24(36-27)14-18-16-32(20-6-4-3-5-7-20)31-25(18)17-8-10-19(28)11-9-17/h3-16H,1-2H3,(H,29,30,33)/b24-14-	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	7.18E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Competitive inhibition of mushroom tyrosinase diphenolase activity assessed as L-DOPA conversion to dopachrome by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50491382 (CHEMBL2380378) Show SMILES COc1ccc(NC2=NC(=O)\C(S2)=C\c2cn(nc2-c2ccc(Br)cc2)-c2ccccc2)c(OC)c1 |t:7| Show InChI InChI=1S/C27H21BrN4O3S/c1-34-21-12-13-22(23(15-21)35-2)29-27-30-26(33)24(36-27)14-18-16-32(20-6-4-3-5-7-20)31-25(18)17-8-10-19(28)11-9-17/h3-16H,1-2H3,(H,29,30,33)/b24-14-	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	9.46E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Competitive inhibition of mushroom tyrosinase diphenolase activity assessed as L-DOPA conversion to dopachrome by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50324035 (2-[5-(2-Chloro-4-nitro-phenyl)-1H-pyrazol-3-yl]-6-...) Show SMILES COc1cc(OC)c(-c2cc(n[nH]2)-c2ccc(cc2Cl)[N+]([O-])=O)c(O)c1C1CCN(C)C1CO Show InChI InChI=1S/C23H25ClN4O6/c1-27-7-6-14(18(27)11-29)21-19(33-2)10-20(34-3)22(23(21)30)17-9-16(25-26-17)13-5-4-12(28(31)32)8-15(13)24/h4-5,8-10,14,18,29-30H,6-7,11H2,1-3H3,(H,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.85E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50324034 (2-[5-(2-Chloro-phenyl)-1H-pyrazol-3-yl]-6-(2-hydro...) Show SMILES COc1cc(OC)c(-c2cc(n[nH]2)-c2ccccc2Cl)c(O)c1C1CCN(C)C1CO Show InChI InChI=1S/C23H26ClN3O4/c1-27-9-8-14(18(27)12-28)21-19(30-2)11-20(31-3)22(23(21)29)17-10-16(25-26-17)13-6-4-5-7-15(13)24/h4-7,10-11,14,18,28-29H,8-9,12H2,1-3H3,(H,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.06E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50324037 (2-[5-(4-Fluoro-phenyl)-1H-pyrazol-3-yl]-6-(2-hydro...) Show SMILES COc1cc(OC)c(-c2cc(n[nH]2)-c2ccc(F)cc2)c(O)c1C1CCN(C)C1CO Show InChI InChI=1S/C23H26FN3O4/c1-27-9-8-15(18(27)12-28)21-19(30-2)11-20(31-3)22(23(21)29)17-10-16(25-26-17)13-4-6-14(24)7-5-13/h4-7,10-11,15,18,28-29H,8-9,12H2,1-3H3,(H,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.12E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50324034 (2-[5-(2-Chloro-phenyl)-1H-pyrazol-3-yl]-6-(2-hydro...) Show SMILES COc1cc(OC)c(-c2cc(n[nH]2)-c2ccccc2Cl)c(O)c1C1CCN(C)C1CO Show InChI InChI=1S/C23H26ClN3O4/c1-27-9-8-14(18(27)12-28)21-19(30-2)11-20(31-3)22(23(21)29)17-10-16(25-26-17)13-6-4-5-7-15(13)24/h4-7,10-11,14,18,28-29H,8-9,12H2,1-3H3,(H,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.18E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase assessed as oxidation of L-DOPA				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50324037 (2-[5-(4-Fluoro-phenyl)-1H-pyrazol-3-yl]-6-(2-hydro...) Show SMILES COc1cc(OC)c(-c2cc(n[nH]2)-c2ccc(F)cc2)c(O)c1C1CCN(C)C1CO Show InChI InChI=1S/C23H26FN3O4/c1-27-9-8-15(18(27)12-28)21-19(30-2)11-20(31-3)22(23(21)29)17-10-16(25-26-17)13-4-6-14(24)7-5-13/h4-7,10-11,15,18,28-29H,8-9,12H2,1-3H3,(H,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.26E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase assessed as oxidation of L-DOPA				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50324035 (2-[5-(2-Chloro-4-nitro-phenyl)-1H-pyrazol-3-yl]-6-...) Show SMILES COc1cc(OC)c(-c2cc(n[nH]2)-c2ccc(cc2Cl)[N+]([O-])=O)c(O)c1C1CCN(C)C1CO Show InChI InChI=1S/C23H25ClN4O6/c1-27-7-6-14(18(27)11-29)21-19(33-2)10-20(34-3)22(23(21)30)17-9-16(25-26-17)13-5-4-12(28(31)32)8-15(13)24/h4-5,8-10,14,18,29-30H,6-7,11H2,1-3H3,(H,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.46E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase assessed as oxidation of L-DOPA				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					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	1.49E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Competitive inhibition of mushroom tyrosinase diphenolase activity assessed as L-DOPA conversion to dopachrome by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50491386 (CHEMBL2380491) Show SMILES COc1ccc(NC2=NC(=O)\C(S2)=C\c2cn(nc2-c2ccc(Cl)cc2Cl)-c2ccccc2)c(OC)c1 |t:7| Show InChI InChI=1S/C27H20Cl2N4O3S/c1-35-19-9-11-22(23(14-19)36-2)30-27-31-26(34)24(37-27)12-16-15-33(18-6-4-3-5-7-18)32-25(16)20-10-8-17(28)13-21(20)29/h3-15H,1-2H3,(H,30,31,34)/b24-12-	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.69E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Competitive inhibition of mushroom tyrosinase diphenolase activity assessed as L-DOPA conversion to dopachrome by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50491380 (CHEMBL2380380) Show SMILES COc1ccc(NC2=NC(=O)\C(S2)=C\c2cn(nc2-c2cccc(Cl)c2)-c2ccccc2)c(OC)c1 |t:7| Show InChI InChI=1S/C27H21ClN4O3S/c1-34-21-11-12-22(23(15-21)35-2)29-27-30-26(33)24(36-27)14-18-16-32(20-9-4-3-5-10-20)31-25(18)17-7-6-8-19(28)13-17/h3-16H,1-2H3,(H,29,30,33)/b24-14-	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.15E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Competitive inhibition of mushroom tyrosinase diphenolase activity assessed as L-DOPA conversion to dopachrome by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50491383 (CHEMBL2380490) Show SMILES COc1ccc(NC2=NC(=O)\C(S2)=C\c2cn(nc2-c2ccccc2Cl)-c2ccccc2)c(OC)c1 |t:7| Show InChI InChI=1S/C27H21ClN4O3S/c1-34-19-12-13-22(23(15-19)35-2)29-27-30-26(33)24(36-27)14-17-16-32(18-8-4-3-5-9-18)31-25(17)20-10-6-7-11-21(20)28/h3-16H,1-2H3,(H,29,30,33)/b24-14-	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.91E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Competitive inhibition of mushroom tyrosinase diphenolase activity assessed as L-DOPA conversion to dopachrome by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50324036 (2-[5-(2,4-Dimethoxy-phenyl)-1H-pyrazol-3-yl]-6-(2-...) Show SMILES COc1ccc(-c2cc([nH]n2)-c2c(OC)cc(OC)c(C3CCN(C)C3CO)c2O)c(OC)c1 Show InChI InChI=1S/C25H31N3O6/c1-28-9-8-16(19(28)13-29)23-21(33-4)12-22(34-5)24(25(23)30)18-11-17(26-27-18)15-7-6-14(31-2)10-20(15)32-3/h6-7,10-12,16,19,29-30H,8-9,13H2,1-5H3,(H,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.75E+3	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50324036 (2-[5-(2,4-Dimethoxy-phenyl)-1H-pyrazol-3-yl]-6-(2-...) Show SMILES COc1ccc(-c2cc([nH]n2)-c2c(OC)cc(OC)c(C3CCN(C)C3CO)c2O)c(OC)c1 Show InChI InChI=1S/C25H31N3O6/c1-28-9-8-16(19(28)13-29)23-21(33-4)12-22(34-5)24(25(23)30)18-11-17(26-27-18)15-7-6-14(31-2)10-20(15)32-3/h6-7,10-12,16,19,29-30H,8-9,13H2,1-5H3,(H,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.84E+3	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase assessed as oxidation of L-DOPA				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Rattus norvegicus)	BDBM35440 (ALLOPURINOL | MLS000069453 | SMR000059083 | cid_20...) Show SMILES O=c1[nH]cnc2n[nH]cc12 Show InChI InChI=1S/C5H4N4O/c10-5-3-1-8-9-4(3)6-2-7-5/h1-2H,(H2,6,7,8,9,10)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase 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
Swami Ramanand Teerth Marathwada University Curated by ChEMBL					Assay Description Inhibition of Wistar albino rat xanthine oxidase isolated from liver using xanthine as substrate incubated for 15 mins prior to substrate addition by...				Bioorg Med Chem 21: 365-72 (2012) Article DOI: 10.1016/j.bmc.2012.09.060 BindingDB Entry DOI: 10.7270/Q2RV0Q0R
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Rattus norvegicus)	BDBM50423923 (CHEMBL2313040) Show SMILES CN(C)c1ccc(cc1)C1CC(=NN1c1nc(cs1)-c1ccc(Cl)cc1)c1cc(Cl)sc1SCc1ccccc1 |c:12| Show InChI InChI=1S/C31H26Cl2N4S3/c1-36(2)24-14-10-22(11-15-24)28-17-26(25-16-29(33)40-30(25)38-18-20-6-4-3-5-7-20)35-37(28)31-34-27(19-39-31)21-8-12-23(32)13-9-21/h3-16,19,28H,17-18H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Swami Ramanand Teerth Marathwada University Curated by ChEMBL					Assay Description Inhibition of Wistar albino rat xanthine oxidase isolated from liver using xanthine as substrate incubated for 15 mins prior to substrate addition by...				Bioorg Med Chem 21: 365-72 (2012) Article DOI: 10.1016/j.bmc.2012.09.060 BindingDB Entry DOI: 10.7270/Q2RV0Q0R
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Rattus norvegicus)	BDBM50423922 (CHEMBL2313041) Show SMILES CN(C)c1ccc(cc1)C1CC(=NN1c1nc(cs1)-c1ccc(Cl)cc1)c1cc(Cl)sc1S(N)(=O)=O |c:12| Show InChI InChI=1S/C24H21Cl2N5O2S3/c1-30(2)17-9-5-15(6-10-17)21-12-19(18-11-22(26)35-23(18)36(27,32)33)29-31(21)24-28-20(13-34-24)14-3-7-16(25)8-4-14/h3-11,13,21H,12H2,1-2H3,(H2,27,32,33)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Swami Ramanand Teerth Marathwada University Curated by ChEMBL					Assay Description Inhibition of Wistar albino rat xanthine oxidase isolated from liver using xanthine as substrate incubated for 15 mins prior to substrate addition by...				Bioorg Med Chem 21: 365-72 (2012) Article DOI: 10.1016/j.bmc.2012.09.060 BindingDB Entry DOI: 10.7270/Q2RV0Q0R
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Rattus norvegicus)	BDBM50423924 (CHEMBL2313039) Show SMILES CN(C)c1ccc(cc1)C1CC(=NN1c1nc(cs1)-c1ccc(Cl)cc1)c1cc(Cl)sc1Cl |c:12| Show InChI InChI=1S/C24H19Cl3N4S2/c1-30(2)17-9-5-15(6-10-17)21-12-19(18-11-22(26)33-23(18)27)29-31(21)24-28-20(13-32-24)14-3-7-16(25)8-4-14/h3-11,13,21H,12H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Swami Ramanand Teerth Marathwada University Curated by ChEMBL					Assay Description Inhibition of Wistar albino rat xanthine oxidase isolated from liver using xanthine as substrate incubated for 15 mins prior to substrate addition by...				Bioorg Med Chem 21: 365-72 (2012) Article DOI: 10.1016/j.bmc.2012.09.060 BindingDB Entry DOI: 10.7270/Q2RV0Q0R
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50324037 (2-[5-(4-Fluoro-phenyl)-1H-pyrazol-3-yl]-6-(2-hydro...) Show SMILES COc1cc(OC)c(-c2cc(n[nH]2)-c2ccc(F)cc2)c(O)c1C1CCN(C)C1CO Show InChI InChI=1S/C23H26FN3O4/c1-27-9-8-15(18(27)12-28)21-19(30-2)11-20(31-3)22(23(21)29)17-10-16(25-26-17)13-4-6-14(24)7-5-13/h4-7,10-11,15,18,28-29H,8-9,12H2,1-3H3,(H,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.55E+4	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50324035 (2-[5-(2-Chloro-4-nitro-phenyl)-1H-pyrazol-3-yl]-6-...) Show SMILES COc1cc(OC)c(-c2cc(n[nH]2)-c2ccc(cc2Cl)[N+]([O-])=O)c(O)c1C1CCN(C)C1CO Show InChI InChI=1S/C23H25ClN4O6/c1-27-7-6-14(18(27)11-29)21-19(33-2)10-20(34-3)22(23(21)30)17-9-16(25-26-17)13-5-4-12(28(31)32)8-15(13)24/h4-5,8-10,14,18,29-30H,6-7,11H2,1-3H3,(H,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.78E+4	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50324037 (2-[5-(4-Fluoro-phenyl)-1H-pyrazol-3-yl]-6-(2-hydro...) Show SMILES COc1cc(OC)c(-c2cc(n[nH]2)-c2ccc(F)cc2)c(O)c1C1CCN(C)C1CO Show InChI InChI=1S/C23H26FN3O4/c1-27-9-8-15(18(27)12-28)21-19(30-2)11-20(31-3)22(23(21)29)17-10-16(25-26-17)13-4-6-14(24)7-5-13/h4-7,10-11,15,18,28-29H,8-9,12H2,1-3H3,(H,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.96E+4	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase assessed as oxidation of L-DOPA				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Rattus norvegicus)	BDBM50423932 (CHEMBL2313031) Show SMILES CCCCc1nc(Cl)c([nH]1)C1CC(=NN1c1nc(cs1)-c1ccc(Cl)cc1)c1cc(Cl)sc1SCc1ccccc1 |c:13| Show InChI InChI=1S/C30H26Cl3N5S3/c1-2-3-9-26-35-27(28(33)36-26)24-15-22(21-14-25(32)41-29(21)39-16-18-7-5-4-6-8-18)37-38(24)30-34-23(17-40-30)19-10-12-20(31)13-11-19/h4-8,10-14,17,24H,2-3,9,15-16H2,1H3,(H,35,36)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Swami Ramanand Teerth Marathwada University Curated by ChEMBL					Assay Description Inhibition of Wistar albino rat xanthine oxidase isolated from liver using xanthine as substrate incubated for 15 mins prior to substrate addition by...				Bioorg Med Chem 21: 365-72 (2012) Article DOI: 10.1016/j.bmc.2012.09.060 BindingDB Entry DOI: 10.7270/Q2RV0Q0R
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50324035 (2-[5-(2-Chloro-4-nitro-phenyl)-1H-pyrazol-3-yl]-6-...) Show SMILES COc1cc(OC)c(-c2cc(n[nH]2)-c2ccc(cc2Cl)[N+]([O-])=O)c(O)c1C1CCN(C)C1CO Show InChI InChI=1S/C23H25ClN4O6/c1-27-7-6-14(18(27)11-29)21-19(33-2)10-20(34-3)22(23(21)30)17-9-16(25-26-17)13-5-4-12(28(31)32)8-15(13)24/h4-5,8-10,14,18,29-30H,6-7,11H2,1-3H3,(H,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.15E+4	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase assessed as oxidation of L-DOPA				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					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	2.25E+4	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate preincubated for 10 mins by spectrophotometric analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50324034 (2-[5-(2-Chloro-phenyl)-1H-pyrazol-3-yl]-6-(2-hydro...) Show SMILES COc1cc(OC)c(-c2cc(n[nH]2)-c2ccccc2Cl)c(O)c1C1CCN(C)C1CO Show InChI InChI=1S/C23H26ClN3O4/c1-27-9-8-14(18(27)12-28)21-19(30-2)11-20(31-3)22(23(21)29)17-10-16(25-26-17)13-6-4-5-7-15(13)24/h4-7,10-11,14,18,28-29H,8-9,12H2,1-3H3,(H,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.28E+4	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Rattus norvegicus)	BDBM50423931 (CHEMBL2313032) Show SMILES CCCCc1nc(Cl)c([nH]1)C1CC(=NN1c1nc(cs1)-c1ccc(Cl)cc1)c1cc(Cl)sc1S(N)(=O)=O |c:13| Show InChI InChI=1S/C23H21Cl3N6O2S3/c1-2-3-4-19-29-20(21(26)30-19)17-10-15(14-9-18(25)36-22(14)37(27,33)34)31-32(17)23-28-16(11-35-23)12-5-7-13(24)8-6-12/h5-9,11,17H,2-4,10H2,1H3,(H,29,30)(H2,27,33,34)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.39E+4	n/a	n/a	n/a	n/a	n/a	n/a
Swami Ramanand Teerth Marathwada University Curated by ChEMBL					Assay Description Inhibition of Wistar albino rat xanthine oxidase isolated from liver using xanthine as substrate incubated for 15 mins prior to substrate addition by...				Bioorg Med Chem 21: 365-72 (2012) Article DOI: 10.1016/j.bmc.2012.09.060 BindingDB Entry DOI: 10.7270/Q2RV0Q0R
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Rattus norvegicus)	BDBM50423933 (CHEMBL2313030) Show SMILES CCCCc1nc(Cl)c([nH]1)C1CC(=NN1c1nc(cs1)-c1ccc(Cl)cc1)c1cc(Cl)sc1Cl |c:13| Show InChI InChI=1S/C23H19Cl4N5S2/c1-2-3-4-19-29-20(21(26)30-19)17-10-15(14-9-18(25)34-22(14)27)31-32(17)23-28-16(11-33-23)12-5-7-13(24)8-6-12/h5-9,11,17H,2-4,10H2,1H3,(H,29,30)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
Swami Ramanand Teerth Marathwada University Curated by ChEMBL					Assay Description Inhibition of Wistar albino rat xanthine oxidase isolated from liver using xanthine as substrate incubated for 15 mins prior to substrate addition by...				Bioorg Med Chem 21: 365-72 (2012) Article DOI: 10.1016/j.bmc.2012.09.060 BindingDB Entry DOI: 10.7270/Q2RV0Q0R
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50324034 (2-[5-(2-Chloro-phenyl)-1H-pyrazol-3-yl]-6-(2-hydro...) Show SMILES COc1cc(OC)c(-c2cc(n[nH]2)-c2ccccc2Cl)c(O)c1C1CCN(C)C1CO Show InChI InChI=1S/C23H26ClN3O4/c1-27-9-8-14(18(27)12-28)21-19(30-2)11-20(31-3)22(23(21)29)17-10-16(25-26-17)13-6-4-5-7-15(13)24/h4-7,10-11,14,18,28-29H,8-9,12H2,1-3H3,(H,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.94E+4	n/a	n/a	n/a	n/a	n/a	n/a
Solapur University Curated by ChEMBL					Assay Description Inhibition of mashroom tyrosinase assessed as oxidation of L-DOPA				Bioorg Med Chem 18: 6149-55 (2010) Article DOI: 10.1016/j.bmc.2010.06.046 BindingDB Entry DOI: 10.7270/Q2GQ6XXR
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Rattus norvegicus)	BDBM50423929 (CHEMBL2313034) Show SMILES Clc1cc(C2=NN(C(C2)c2ccc(Cl)cc2)c2nc(cs2)-c2ccc(Cl)cc2)c(SCc2ccccc2)s1 |t:4| Show InChI InChI=1S/C29H20Cl3N3S3/c30-21-10-6-19(7-11-21)25-17-37-29(33-25)35-26(20-8-12-22(31)13-9-20)15-24(34-35)23-14-27(32)38-28(23)36-16-18-4-2-1-3-5-18/h1-14,17,26H,15-16H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD 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
Swami Ramanand Teerth Marathwada University Curated by ChEMBL					Assay Description Inhibition of Wistar albino rat xanthine oxidase isolated from liver using xanthine as substrate incubated for 15 mins prior to substrate addition by...				Bioorg Med Chem 21: 365-72 (2012) Article DOI: 10.1016/j.bmc.2012.09.060 BindingDB Entry DOI: 10.7270/Q2RV0Q0R
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50491383 (CHEMBL2380490) Show SMILES COc1ccc(NC2=NC(=O)\C(S2)=C\c2cn(nc2-c2ccccc2Cl)-c2ccccc2)c(OC)c1 |t:7| Show InChI InChI=1S/C27H21ClN4O3S/c1-34-19-12-13-22(23(15-19)35-2)29-27-30-26(33)24(36-27)14-17-16-32(18-8-4-3-5-9-18)31-25(17)20-10-6-7-11-21(20)28/h3-16H,1-2H3,(H,29,30,33)/b24-14-	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.41E+4	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate preincubated for 10 mins by spectrophotometric analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Rattus norvegicus)	BDBM50423928 (CHEMBL2313035) Show SMILES NS(=O)(=O)c1sc(Cl)cc1C1=NN(C(C1)c1ccc(Cl)cc1)c1nc(cs1)-c1ccc(Cl)cc1 |t:11| Show InChI InChI=1S/C22H15Cl3N4O2S3/c23-14-5-1-12(2-6-14)18-11-32-22(27-18)29-19(13-3-7-15(24)8-4-13)10-17(28-29)16-9-20(25)33-21(16)34(26,30)31/h1-9,11,19H,10H2,(H2,26,30,31)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.42E+4	n/a	n/a	n/a	n/a	n/a	n/a
Swami Ramanand Teerth Marathwada University Curated by ChEMBL					Assay Description Inhibition of Wistar albino rat xanthine oxidase isolated from liver using xanthine as substrate incubated for 15 mins prior to substrate addition by...				Bioorg Med Chem 21: 365-72 (2012) Article DOI: 10.1016/j.bmc.2012.09.060 BindingDB Entry DOI: 10.7270/Q2RV0Q0R
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Rattus norvegicus)	BDBM50423930 (CHEMBL2313033) Show SMILES Clc1cc(C2=NN(C(C2)c2ccc(Cl)cc2)c2nc(cs2)-c2ccc(Cl)cc2)c(Cl)s1 |t:4| Show InChI InChI=1S/C22H13Cl4N3S2/c23-14-5-1-12(2-6-14)18-11-30-22(27-18)29-19(13-3-7-15(24)8-4-13)10-17(28-29)16-9-20(25)31-21(16)26/h1-9,11,19H,10H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD 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
Swami Ramanand Teerth Marathwada University Curated by ChEMBL					Assay Description Inhibition of Wistar albino rat xanthine oxidase isolated from liver using xanthine as substrate incubated for 15 mins prior to substrate addition by...				Bioorg Med Chem 21: 365-72 (2012) Article DOI: 10.1016/j.bmc.2012.09.060 BindingDB Entry DOI: 10.7270/Q2RV0Q0R
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Rattus norvegicus)	BDBM50423926 (CHEMBL2313037) Show SMILES Fc1ccc(cc1)C1CC(=NN1c1nc(cs1)-c1ccc(Cl)cc1)c1cc(Cl)sc1SCc1ccccc1 |c:10| Show InChI InChI=1S/C29H20Cl2FN3S3/c30-21-10-6-19(7-11-21)25-17-37-29(33-25)35-26(20-8-12-22(32)13-9-20)15-24(34-35)23-14-27(31)38-28(23)36-16-18-4-2-1-3-5-18/h1-14,17,26H,15-16H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.66E+4	n/a	n/a	n/a	n/a	n/a	n/a
Swami Ramanand Teerth Marathwada University Curated by ChEMBL					Assay Description Inhibition of Wistar albino rat xanthine oxidase isolated from liver using xanthine as substrate incubated for 15 mins prior to substrate addition by...				Bioorg Med Chem 21: 365-72 (2012) Article DOI: 10.1016/j.bmc.2012.09.060 BindingDB Entry DOI: 10.7270/Q2RV0Q0R
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Rattus norvegicus)	BDBM50423925 (CHEMBL2313038) Show SMILES NS(=O)(=O)c1sc(Cl)cc1C1=NN(C(C1)c1ccc(F)cc1)c1nc(cs1)-c1ccc(Cl)cc1 |t:11| Show InChI InChI=1S/C22H15Cl2FN4O2S3/c23-14-5-1-12(2-6-14)18-11-32-22(27-18)29-19(13-3-7-15(25)8-4-13)10-17(28-29)16-9-20(24)33-21(16)34(26,30)31/h1-9,11,19H,10H2,(H2,26,30,31)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Swami Ramanand Teerth Marathwada University Curated by ChEMBL					Assay Description Inhibition of Wistar albino rat xanthine oxidase isolated from liver using xanthine as substrate incubated for 15 mins prior to substrate addition by...				Bioorg Med Chem 21: 365-72 (2012) Article DOI: 10.1016/j.bmc.2012.09.060 BindingDB Entry DOI: 10.7270/Q2RV0Q0R
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Rattus norvegicus)	BDBM50423927 (CHEMBL2313036) Show SMILES Fc1ccc(cc1)C1CC(=NN1c1nc(cs1)-c1ccc(Cl)cc1)c1cc(Cl)sc1Cl |c:10| Show InChI InChI=1S/C22H13Cl3FN3S2/c23-14-5-1-12(2-6-14)18-11-30-22(27-18)29-19(13-3-7-15(26)8-4-13)10-17(28-29)16-9-20(24)31-21(16)25/h1-9,11,19H,10H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Swami Ramanand Teerth Marathwada University Curated by ChEMBL					Assay Description Inhibition of Wistar albino rat xanthine oxidase isolated from liver using xanthine as substrate incubated for 15 mins prior to substrate addition by...				Bioorg Med Chem 21: 365-72 (2012) Article DOI: 10.1016/j.bmc.2012.09.060 BindingDB Entry DOI: 10.7270/Q2RV0Q0R
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50491380 (CHEMBL2380380) Show SMILES COc1ccc(NC2=NC(=O)\C(S2)=C\c2cn(nc2-c2cccc(Cl)c2)-c2ccccc2)c(OC)c1 |t:7| Show InChI InChI=1S/C27H21ClN4O3S/c1-34-21-11-12-22(23(15-21)35-2)29-27-30-26(33)24(36-27)14-18-16-32(20-9-4-3-5-10-20)31-25(18)17-7-6-8-19(28)13-17/h3-16H,1-2H3,(H,29,30,33)/b24-14-	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.26E+4	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate preincubated for 10 mins by spectrophotometric analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50491384 (CHEMBL2380377) Show SMILES COc1ccc(NC2=NC(=O)\C(S2)=C\c2cn(nc2-c2ccc(Cl)cc2)-c2ccccc2)c(OC)c1 |t:7| Show InChI InChI=1S/C27H21ClN4O3S/c1-34-21-12-13-22(23(15-21)35-2)29-27-30-26(33)24(36-27)14-18-16-32(20-6-4-3-5-7-20)31-25(18)17-8-10-19(28)11-9-17/h3-16H,1-2H3,(H,29,30,33)/b24-14-	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	7.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate preincubated for 10 mins by spectrophotometric analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50491386 (CHEMBL2380491) Show SMILES COc1ccc(NC2=NC(=O)\C(S2)=C\c2cn(nc2-c2ccc(Cl)cc2Cl)-c2ccccc2)c(OC)c1 |t:7| Show InChI InChI=1S/C27H20Cl2N4O3S/c1-35-19-9-11-22(23(14-19)36-2)30-27-31-26(34)24(37-27)12-16-15-33(18-6-4-3-5-7-18)32-25(16)20-10-8-17(28)13-21(20)29/h3-15H,1-2H3,(H,30,31,34)/b24-12-	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.17E+4	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate preincubated for 10 mins by spectrophotometric analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50491381 (CHEMBL2380379) Show SMILES COc1ccc(NC2=NC(=O)\C(S2)=C\c2cn(nc2-c2ccc(F)cc2)-c2ccccc2)c(OC)c1 |t:7| Show InChI InChI=1S/C27H21FN4O3S/c1-34-21-12-13-22(23(15-21)35-2)29-27-30-26(33)24(36-27)14-18-16-32(20-6-4-3-5-7-20)31-25(18)17-8-10-19(28)11-9-17/h3-16H,1-2H3,(H,29,30,33)/b24-14-	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.04E+5	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate preincubated for 10 mins by spectrophotometric analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50491379 (CHEMBL2380376) Show SMILES COc1ccc(cc1)-c1nn(cc1\C=C1/SC(Nc2ccc(OC)cc2OC)=NC1=O)-c1ccccc1 |c:30| Show InChI InChI=1S/C28H24N4O4S/c1-34-21-11-9-18(10-12-21)26-19(17-32(31-26)20-7-5-4-6-8-20)15-25-27(33)30-28(37-25)29-23-14-13-22(35-2)16-24(23)36-3/h4-17H,1-3H3,(H,29,30,33)/b25-15-	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.14E+5	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate preincubated for 10 mins by spectrophotometric analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50491382 (CHEMBL2380378) Show SMILES COc1ccc(NC2=NC(=O)\C(S2)=C\c2cn(nc2-c2ccc(Br)cc2)-c2ccccc2)c(OC)c1 |t:7| Show InChI InChI=1S/C27H21BrN4O3S/c1-34-21-12-13-22(23(15-21)35-2)29-27-30-26(33)24(36-27)14-18-16-32(20-6-4-3-5-7-20)31-25(18)17-8-10-19(28)11-9-17/h3-16H,1-2H3,(H,29,30,33)/b24-14-	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.31E+5	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate preincubated for 10 mins by spectrophotometric analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50491385 (CHEMBL2380375) Show SMILES COc1ccc(NC2=NC(=O)\C(S2)=C\c2cn(nc2-c2ccc(C)cc2)-c2ccccc2)c(OC)c1 |t:7| Show InChI InChI=1S/C28H24N4O3S/c1-18-9-11-19(12-10-18)26-20(17-32(31-26)21-7-5-4-6-8-21)15-25-27(33)30-28(36-25)29-23-14-13-22(34-2)16-24(23)35-3/h4-17H,1-3H3,(H,29,30,33)/b25-15-	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.94E+5	n/a	n/a	n/a	n/a	n/a	n/a
Bahirji Smarak Mahavidyalaya Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA as substrate preincubated for 10 mins by spectrophotometric analysis				Bioorg Med Chem 21: 2772-7 (2013) Article DOI: 10.1016/j.bmc.2012.12.053 BindingDB Entry DOI: 10.7270/Q2G44T6G
					More data for this Ligand-Target Pair