Compile Data Set for Download or QSAR

Found 64 hits with Last Name = 'thanigaimalai' and Initial = 'p'   

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))	BDBM50356166 (CHEMBL1088657) Show SMILES Cc1cccc(NC(N)=S)c1 Show InChI InChI=1S/C8H10N2S/c1-6-3-2-4-7(5-6)10-8(9)11/h2-5H,1H3,(H3,9,10,11)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	600	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase activity using L-tyrosine as substrate by spectrometric analysis				Bioorg Med Chem Lett 21: 6824-8 (2011) Article DOI: 10.1016/j.bmcl.2011.09.024 BindingDB Entry DOI: 10.7270/Q2M9093C
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50356164 (CHEMBL1088361) Show SMILES CCc1ccc(NC(N)=S)cc1 Show InChI InChI=1S/C9H12N2S/c1-2-7-3-5-8(6-4-7)11-9(10)12/h3-6H,2H2,1H3,(H3,10,11,12)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	800	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase activity using L-tyrosine as substrate by spectrometric analysis				Bioorg Med Chem Lett 21: 6824-8 (2011) Article DOI: 10.1016/j.bmcl.2011.09.024 BindingDB Entry DOI: 10.7270/Q2M9093C
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50356167 (CHEMBL1088658) Show SMILES Cc1ccccc1NC(N)=S Show InChI InChI=1S/C8H10N2S/c1-6-4-2-3-5-7(6)10-8(9)11/h2-5H,1H3,(H3,9,10,11)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	840	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase activity using L-tyrosine as substrate by spectrometric analysis				Bioorg Med Chem Lett 21: 6824-8 (2011) Article DOI: 10.1016/j.bmcl.2011.09.024 BindingDB Entry DOI: 10.7270/Q2M9093C
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50242276 (CHEMBL486626 | Sophoricoside) Show SMILES OC[C@H]1O[C@@H](Oc2ccc(cc2)-c2coc3cc(O)cc(O)c3c2=O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C21H20O10/c22-7-15-18(26)19(27)20(28)21(31-15)30-11-3-1-9(2-4-11)12-8-29-14-6-10(23)5-13(24)16(14)17(12)25/h1-6,8,15,18-24,26-28H,7H2/t15-,18-,19+,20-,21-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50242276 (CHEMBL486626 | Sophoricoside) Show SMILES OC[C@H]1O[C@@H](Oc2ccc(cc2)-c2coc3cc(O)cc(O)c3c2=O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C21H20O10/c22-7-15-18(26)19(27)20(28)21(31-15)30-11-3-1-9(2-4-11)12-8-29-14-6-10(23)5-13(24)16(14)17(12)25/h1-6,8,15,18-24,26-28H,7H2/t15-,18-,19+,20-,21-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50356163 (CHEMBL1088360) Show SMILES Cc1ccc(NC(N)=S)cc1 Show InChI InChI=1S/C8H10N2S/c1-6-2-4-7(5-3-6)10-8(9)11/h2-5H,1H3,(H3,9,10,11)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase activity using L-tyrosine as substrate by spectrometric analysis				Bioorg Med Chem Lett 21: 6824-8 (2011) Article DOI: 10.1016/j.bmcl.2011.09.024 BindingDB Entry DOI: 10.7270/Q2M9093C
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50242276 (CHEMBL486626 | Sophoricoside) Show SMILES OC[C@H]1O[C@@H](Oc2ccc(cc2)-c2coc3cc(O)cc(O)c3c2=O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C21H20O10/c22-7-15-18(26)19(27)20(28)21(31-15)30-11-3-1-9(2-4-11)12-8-29-14-6-10(23)5-13(24)16(14)17(12)25/h1-6,8,15,18-24,26-28H,7H2/t15-,18-,19+,20-,21-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50240041 (1-phenyl-2-thiourea | 1-phenylthiourea | CHEMBL263...) Show SMILES NC(=S)Nc1ccccc1 Show InChI InChI=1S/C7H8N2S/c8-7(10)9-6-4-2-1-3-5-6/h1-5H,(H3,8,9,10)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase activity using L-tyrosine as substrate by spectrometric analysis				Bioorg Med Chem Lett 21: 6824-8 (2011) Article DOI: 10.1016/j.bmcl.2011.09.024 BindingDB Entry DOI: 10.7270/Q2M9093C
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50356165 (CHEMBL1088498) Show SMILES CC(C)(C)c1ccc(NC(N)=S)cc1 Show InChI InChI=1S/C11H16N2S/c1-11(2,3)8-4-6-9(7-5-8)13-10(12)14/h4-7H,1-3H3,(H3,12,13,14)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase activity using L-tyrosine as substrate by spectrometric analysis				Bioorg Med Chem Lett 21: 6824-8 (2011) Article DOI: 10.1016/j.bmcl.2011.09.024 BindingDB Entry DOI: 10.7270/Q2M9093C
					More data for this Ligand-Target Pair
Tyrosinase (Homo sapiens (Human))	BDBM50240041 (1-phenyl-2-thiourea | 1-phenylthiourea | CHEMBL263...) Show SMILES NC(=S)Nc1ccccc1 Show InChI InChI=1S/C7H8N2S/c8-7(10)9-6-4-2-1-3-5-6/h1-5H,(H3,8,9,10)	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of tyrosinase				Bioorg Med Chem 18: 1555-62 (2010) Article DOI: 10.1016/j.bmc.2010.01.005 BindingDB Entry DOI: 10.7270/Q23F4PQ7
					More data for this Ligand-Target Pair
Tyrosinase (Mus musculus (Mouse))	BDBM50240041 (1-phenyl-2-thiourea | 1-phenylthiourea | CHEMBL263...) Show SMILES NC(=S)Nc1ccccc1 Show InChI InChI=1S/C7H8N2S/c8-7(10)9-6-4-2-1-3-5-6/h1-5H,(H3,8,9,10)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of tyrosinase in alpha-MSH-induced mouse B16 cells				Bioorg Med Chem Lett 20: 4771-3 (2010) Article DOI: 10.1016/j.bmcl.2010.06.123 BindingDB Entry DOI: 10.7270/Q27M0BR0
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50320916 (5-(cyclohexylmethoxy)-3-(4-hydroxyphenyl)-4H-chrom...) Show SMILES Oc1ccc(cc1)-c1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C22H22O4/c23-17-11-9-16(10-12-17)18-14-26-20-8-4-7-19(21(20)22(18)24)25-13-15-5-2-1-3-6-15/h4,7-12,14-15,23H,1-3,5-6,13H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50320923 (5-(Cyclohexylmethoxy)-3-(3,4,5-trimethoxyphenyl)-4...) Show SMILES COc1ccc(c(OC)c1OC)-c1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C25H28O6/c1-27-21-13-12-17(24(28-2)25(21)29-3)18-15-31-20-11-7-10-19(22(20)23(18)26)30-14-16-8-5-4-6-9-16/h7,10-13,15-16H,4-6,8-9,14H2,1-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321929 (3-((1-Cyclohexyl-3-hydroxypropan-2-ylamino)methyl)...) Show SMILES OCC(CC1CCCCC1)NCc1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C26H37NO4/c28-16-22(14-19-8-3-1-4-9-19)27-15-21-18-31-24-13-7-12-23(25(24)26(21)29)30-17-20-10-5-2-6-11-20/h7,12-13,18-20,22,27-28H,1-6,8-11,14-17H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.73E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50320921 (3-(4-(Benzyloxy)-3-methoxyphenyl)-5-(cyclohexylmet...) Show SMILES COc1cc(ccc1OCc1ccccc1)-c1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C30H30O5/c1-32-28-17-23(15-16-25(28)33-18-21-9-4-2-5-10-21)24-20-35-27-14-8-13-26(29(27)30(24)31)34-19-22-11-6-3-7-12-22/h2,4-5,8-10,13-17,20,22H,3,6-7,11-12,18-19H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.74E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321926 (5-(Cyclohexylmethoxy)-3-((2-hydroxy-1-phenylethyla...) Show SMILES OCC(NCc1coc2cccc(OCC3CCCCC3)c2c1=O)c1ccccc1 Show InChI InChI=1S/C25H29NO4/c27-15-21(19-10-5-2-6-11-19)26-14-20-17-30-23-13-7-12-22(24(23)25(20)28)29-16-18-8-3-1-4-9-18/h2,5-7,10-13,17-18,21,26-27H,1,3-4,8-9,14-16H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.85E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50356170 (CHEMBL1087841) Show SMILES NC(=S)NCc1ccccc1 Show InChI InChI=1S/C8H10N2S/c9-8(11)10-6-7-4-2-1-3-5-7/h1-5H,6H2,(H3,9,10,11)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MMDB PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.54E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase activity using L-tyrosine as substrate by spectrometric analysis				Bioorg Med Chem Lett 21: 6824-8 (2011) Article DOI: 10.1016/j.bmcl.2011.09.024 BindingDB Entry DOI: 10.7270/Q2M9093C
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321928 (5-(Cyclohexylmethoxy)-3-((1-hydroxy-3-phenylpropan...) Show SMILES OCC(Cc1ccccc1)NCc1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C26H31NO4/c28-16-22(14-19-8-3-1-4-9-19)27-15-21-18-31-24-13-7-12-23(25(24)26(21)29)30-17-20-10-5-2-6-11-20/h1,3-4,7-9,12-13,18,20,22,27-28H,2,5-6,10-11,14-17H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.57E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50354850 (BUDESONIDE | US10869929, Compound Budesonide | US1...) Show SMILES CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@@]2(O1)C(=O)CO |r,c:15,t:11| Show InChI InChI=1S/C25H34O6/c1-4-5-21-30-20-11-17-16-7-6-14-10-15(27)8-9-23(14,2)22(16)18(28)12-24(17,3)25(20,31-21)19(29)13-26/h8-10,16-18,20-22,26,28H,4-7,11-13H2,1-3H3/t16-,17-,18-,20+,21?,22+,23-,24-,25+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase DrugBank MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.62E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50354850 (BUDESONIDE | US10869929, Compound Budesonide | US1...) Show SMILES CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@@]2(O1)C(=O)CO |r,c:15,t:11| Show InChI InChI=1S/C25H34O6/c1-4-5-21-30-20-11-17-16-7-6-14-10-15(27)8-9-23(14,2)22(16)18(28)12-24(17,3)25(20,31-21)19(29)13-26/h8-10,16-18,20-22,26,28H,4-7,11-13H2,1-3H3/t16-,17-,18-,20+,21?,22+,23-,24-,25+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase DrugBank MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.62E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321941 (5-(Cyclohexylmethoxy)-3-((1-hydroxy-3,3-dimethylbu...) Show SMILES CC(C)(C)C(CO)NCc1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C23H33NO4/c1-23(2,3)20(13-25)24-12-17-15-28-19-11-7-10-18(21(19)22(17)26)27-14-16-8-5-4-6-9-16/h7,10-11,15-16,20,24-25H,4-6,8-9,12-14H2,1-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.62E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321940 (5-(Cyclohexylmethoxy)-3-((1-hydroxy-2-methylpropan...) Show SMILES CC(C)(CO)NCc1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C21H29NO4/c1-21(2,14-23)22-11-16-13-26-18-10-6-9-17(19(18)20(16)24)25-12-15-7-4-3-5-8-15/h6,9-10,13,15,22-23H,3-5,7-8,11-12,14H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.64E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Interleukin-5 (Homo sapiens (Human))	BDBM50354850 (BUDESONIDE | US10869929, Compound Budesonide | US1...) Show SMILES CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@@]2(O1)C(=O)CO |r,c:15,t:11| Show InChI InChI=1S/C25H34O6/c1-4-5-21-30-20-11-17-16-7-6-14-10-15(27)8-9-23(14,2)22(16)18(28)12-24(17,3)25(20,31-21)19(29)13-26/h8-10,16-18,20-22,26,28H,4-7,11-13H2,1-3H3/t16-,17-,18-,20+,21?,22+,23-,24-,25+/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase DrugBank MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.68E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50356168 (CHEMBL1087472) Show SMILES CCc1ccccc1NC(N)=S Show InChI InChI=1S/C9H12N2S/c1-2-7-5-3-4-6-8(7)11-9(10)12/h3-6H,2H2,1H3,(H3,10,11,12)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.71E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase activity using L-tyrosine as substrate by spectrometric analysis				Bioorg Med Chem Lett 21: 6824-8 (2011) Article DOI: 10.1016/j.bmcl.2011.09.024 BindingDB Entry DOI: 10.7270/Q2M9093C
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321935 (5-(Cyclohexylmethoxy)-3-((4-hydroxyphenylamino)-me...) Show SMILES Oc1ccc(NCc2coc3cccc(OCC4CCCCC4)c3c2=O)cc1 Show InChI InChI=1S/C23H25NO4/c25-19-11-9-18(10-12-19)24-13-17-15-28-21-8-4-7-20(22(21)23(17)26)27-14-16-5-2-1-3-6-16/h4,7-12,15-16,24-25H,1-3,5-6,13-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.73E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321932 (5-(Cyclohexylmethoxy)-3-((4-hydroxybenzylamino)met...) Show SMILES Oc1ccc(CNCc2coc3cccc(OCC4CCCCC4)c3c2=O)cc1 Show InChI InChI=1S/C24H27NO4/c26-20-11-9-17(10-12-20)13-25-14-19-16-29-22-8-4-7-21(23(22)24(19)27)28-15-18-5-2-1-3-6-18/h4,7-12,16,18,25-26H,1-3,5-6,13-15H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.85E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50320925 ((Z)-4-(cyclohexylmethoxy)-2-(4-ethylbenzylidene)be...) Show SMILES CCc1ccc(\C=C2/Oc3cccc(OCC4CCCCC4)c3C2=O)cc1 Show InChI InChI=1S/C24H26O3/c1-2-17-11-13-18(14-12-17)15-22-24(25)23-20(9-6-10-21(23)27-22)26-16-19-7-4-3-5-8-19/h6,9-15,19H,2-5,7-8,16H2,1H3/b22-15-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50320924 (5-(Cyclohexylmethoxy)-3-(4-ethylphenyl)-4H-chromen...) Show SMILES CCc1ccc(cc1)-c1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C24H26O3/c1-2-17-11-13-19(14-12-17)20-16-27-22-10-6-9-21(23(22)24(20)25)26-15-18-7-4-3-5-8-18/h6,9-14,16,18H,2-5,7-8,15H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50320922 (5-(Cyclohexylmethoxy)-3-(4-hydroxy-3-methoxyphenyl...) Show SMILES COc1cc(ccc1O)-c1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C23H24O5/c1-26-21-12-16(10-11-18(21)24)17-14-28-20-9-5-8-19(22(20)23(17)25)27-13-15-6-3-2-4-7-15/h5,8-12,14-15,24H,2-4,6-7,13H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50320917 (5-(Cyclohexylmethoxy)-3-[4-(methoxymethoxy)phenyl]...) Show SMILES COCOc1ccc(cc1)-c1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C24H26O5/c1-26-16-29-19-12-10-18(11-13-19)20-15-28-22-9-5-8-21(23(22)24(20)25)27-14-17-6-3-2-4-7-17/h5,8-13,15,17H,2-4,6-7,14,16H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50320930 ((Z)-4-(Cyclohexylmethoxy)-2-(4-nitrobenzylidene)be...) Show SMILES [O-][N+](=O)c1ccc(\C=C2/Oc3cccc(OCC4CCCCC4)c3C2=O)cc1 Show InChI InChI=1S/C22H21NO5/c24-22-20(13-15-9-11-17(12-10-15)23(25)26)28-19-8-4-7-18(21(19)22)27-14-16-5-2-1-3-6-16/h4,7-13,16H,1-3,5-6,14H2/b20-13-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50320929 (CHEMBL1165763 | Methyl(Z)-4-[4-(cyclohexylmethoxy)...) Show SMILES COC(=O)c1ccc(\C=C2/Oc3cccc(OCC4CCCCC4)c3C2=O)cc1 Show InChI InChI=1S/C24H24O5/c1-27-24(26)18-12-10-16(11-13-18)14-21-23(25)22-19(8-5-9-20(22)29-21)28-15-17-6-3-2-4-7-17/h5,8-14,17H,2-4,6-7,15H2,1H3/b21-14-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50320928 ((Z)-4-{[4-(Cyclohexylmethoxy)-3-oxobenzofuran-2(3H...) Show SMILES O=Cc1ccc(\C=C2/Oc3cccc(OCC4CCCCC4)c3C2=O)cc1 Show InChI InChI=1S/C23H22O4/c24-14-17-11-9-16(10-12-17)13-21-23(25)22-19(7-4-8-20(22)27-21)26-15-18-5-2-1-3-6-18/h4,7-14,18H,1-3,5-6,15H2/b21-13-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50320927 ((Z)-2-(4-Chlorobenzylidene)-4-(cyclohexylmethoxy)b...) Show SMILES Clc1ccc(\C=C2/Oc3cccc(OCC4CCCCC4)c3C2=O)cc1 Show InChI InChI=1S/C22H21ClO3/c23-17-11-9-15(10-12-17)13-20-22(24)21-18(7-4-8-19(21)26-20)25-14-16-5-2-1-3-6-16/h4,7-13,16H,1-3,5-6,14H2/b20-13-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50320926 ((Z)-2-(Benzylidene)-4-(cyclohexylmethoxy)benzofura...) Show SMILES O=C1\C(Oc2cccc(OCC3CCCCC3)c12)=C\c1ccccc1 Show InChI InChI=1S/C22H22O3/c23-22-20(14-16-8-3-1-4-9-16)25-19-13-7-12-18(21(19)22)24-15-17-10-5-2-6-11-17/h1,3-4,7-9,12-14,17H,2,5-6,10-11,15H2/b20-14-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50320918 (5-(Cyclohexylmethoxy)-3-(4-methoxyphenyl)-4H-chrom...) Show SMILES COc1ccc(cc1)-c1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C23H24O4/c1-25-18-12-10-17(11-13-18)19-15-27-21-9-5-8-20(22(21)23(19)24)26-14-16-6-3-2-4-7-16/h5,8-13,15-16H,2-4,6-7,14H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321931 (5-(Cyclohexylmethoxy)-3-((4-methoxybenzylamino)-me...) Show SMILES COc1ccc(CNCc2coc3cccc(OCC4CCCCC4)c3c2=O)cc1 Show InChI InChI=1S/C25H29NO4/c1-28-21-12-10-18(11-13-21)14-26-15-20-17-30-23-9-5-8-22(24(23)25(20)27)29-16-19-6-3-2-4-7-19/h5,8-13,17,19,26H,2-4,6-7,14-16H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50320919 (5-(Cyclohexylmethoxy)-3-(3,4-dimethoxyphenyl)-4Hch...) Show SMILES COc1ccc(cc1OC)-c1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C24H26O5/c1-26-19-12-11-17(13-22(19)27-2)18-15-29-21-10-6-9-20(23(21)24(18)25)28-14-16-7-4-3-5-8-16/h6,9-13,15-16H,3-5,7-8,14H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50320920 (5-(Cyclohexylmethoxy)-3-(2,5-dimethoxyphenyl)-4Hch...) Show SMILES COc1ccc(c(OC)c1)-c1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C24H26O5/c1-26-17-11-12-18(22(13-17)27-2)19-15-29-21-10-6-9-20(23(21)24(19)25)28-14-16-7-4-3-5-8-16/h6,9-13,15-16H,3-5,7-8,14H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of IL5-mediated proliferation of mouse Y16 cells by WST1 assay				Bioorg Med Chem 18: 4441-5 (2010) Article DOI: 10.1016/j.bmc.2010.04.075 BindingDB Entry DOI: 10.7270/Q2H41SDX
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321937 (5-(Cyclohexylmethoxy)-3-((3-hydroxypropylamino)-me...) Show SMILES OCCCNCc1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C20H27NO4/c22-11-5-10-21-12-16-14-25-18-9-4-8-17(19(18)20(16)23)24-13-15-6-2-1-3-7-15/h4,8-9,14-15,21-22H,1-3,5-7,10-13H2	PDB MMDB Reactome pathway 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321936 (5-(Cyclohexylmethoxy)-3-((2-hydroxyethylamino)-met...) Show SMILES OCCNCc1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C19H25NO4/c21-10-9-20-11-15-13-24-17-8-4-7-16(18(17)19(15)22)23-12-14-5-2-1-3-6-14/h4,7-8,13-14,20-21H,1-3,5-6,9-12H2	PDB MMDB Reactome pathway 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321927 (5-(Cyclohexylmethoxy)-3-((3-hydroxy-1-phenylpropyl...) Show SMILES OCCC(NCc1coc2cccc(OCC3CCCCC3)c2c1=O)c1ccccc1 Show InChI InChI=1S/C26H31NO4/c28-15-14-22(20-10-5-2-6-11-20)27-16-21-18-31-24-13-7-12-23(25(24)26(21)29)30-17-19-8-3-1-4-9-19/h2,5-7,10-13,18-19,22,27-28H,1,3-4,8-9,14-17H2	PDB MMDB Reactome pathway 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321934 (5-(Cyclohexylmethoxy)-3-((4-methoxyphenylamino)-me...) Show SMILES COc1ccc(NCc2coc3cccc(OCC4CCCCC4)c3c2=O)cc1 Show InChI InChI=1S/C24H27NO4/c1-27-20-12-10-19(11-13-20)25-14-18-16-29-22-9-5-8-21(23(22)24(18)26)28-15-17-6-3-2-4-7-17/h5,8-13,16-17,25H,2-4,6-7,14-15H2,1H3	PDB MMDB Reactome pathway 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321933 (5-(Cyclohexylmethoxy)-3-((phenylamino)methyl)-4Hch...) Show SMILES O=c1c(CNc2ccccc2)coc2cccc(OCC3CCCCC3)c12 Show InChI InChI=1S/C23H25NO3/c25-23-18(14-24-19-10-5-2-6-11-19)16-27-21-13-7-12-20(22(21)23)26-15-17-8-3-1-4-9-17/h2,5-7,10-13,16-17,24H,1,3-4,8-9,14-15H2	PDB MMDB Reactome pathway 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321938 (5-(Cyclohexylmethoxy)-3-((5-hydroxypentylamino)-me...) Show SMILES OCCCCCNCc1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C22H31NO4/c24-13-6-2-5-12-23-14-18-16-27-20-11-7-10-19(21(20)22(18)25)26-15-17-8-3-1-4-9-17/h7,10-11,16-17,23-24H,1-6,8-9,12-15H2	PDB MMDB Reactome pathway 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321930 (3-((Benzylamino)methyl)-5-(cyclohexylmethoxy)-4Hch...) Show SMILES O=c1c(CNCc2ccccc2)coc2cccc(OCC3CCCCC3)c12 Show InChI InChI=1S/C24H27NO3/c26-24-20(15-25-14-18-8-3-1-4-9-18)17-28-22-13-7-12-21(23(22)24)27-16-19-10-5-2-6-11-19/h1,3-4,7-9,12-13,17,19,25H,2,5-6,10-11,14-16H2	PDB MMDB Reactome pathway 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Interleukin-5 (Mus musculus)	BDBM50321939 (5-(Cyclohexylmethoxy)-3-((1-hydroxypentan-2-ylamin...) Show SMILES CCCC(CO)NCc1coc2cccc(OCC3CCCCC3)c2c1=O Show InChI InChI=1S/C22H31NO4/c1-2-7-18(13-24)23-12-17-15-27-20-11-6-10-19(21(20)22(17)25)26-14-16-8-4-3-5-9-16/h6,10-11,15-16,18,23-24H,2-5,7-9,12-14H2,1H3	PDB MMDB Reactome pathway 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of interleukin-5 in mouse Y16 cells				Bioorg Med Chem 18: 4625-9 (2011) Article DOI: 10.1016/j.bmc.2010.05.028 BindingDB Entry DOI: 10.7270/Q2B8593F
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50356172 (CHEMBL1087843) Show SMILES NC(=S)NCCCc1ccccc1 Show InChI InChI=1S/C10H14N2S/c11-10(13)12-8-4-7-9-5-2-1-3-6-9/h1-3,5-6H,4,7-8H2,(H3,11,12,13)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.48E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase activity using L-tyrosine as substrate by spectrometric analysis				Bioorg Med Chem Lett 21: 6824-8 (2011) Article DOI: 10.1016/j.bmcl.2011.09.024 BindingDB Entry DOI: 10.7270/Q2M9093C
					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	7.04E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase activity using L-tyrosine as substrate by spectrometric analysis				Bioorg Med Chem Lett 21: 6824-8 (2011) Article DOI: 10.1016/j.bmcl.2011.09.024 BindingDB Entry DOI: 10.7270/Q2M9093C
					More data for this Ligand-Target Pair
Polyphenol oxidase 2 (Agaricus bisporus (Common mushroom))	BDBM50356169 (CHEMBL1094725) Show SMILES CC(C)(C)c1ccccc1NC(N)=S Show InChI InChI=1S/C11H16N2S/c1-11(2,3)8-6-4-5-7-9(8)13-10(12)14/h4-7H,1-3H3,(H3,12,13,14)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase 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
Chungnam National University Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase activity using L-tyrosine as substrate by spectrometric analysis				Bioorg Med Chem Lett 21: 6824-8 (2011) Article DOI: 10.1016/j.bmcl.2011.09.024 BindingDB Entry DOI: 10.7270/Q2M9093C
					More data for this Ligand-Target Pair

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