Compile Data Set for Download or QSAR

Found 22 hits of ic50 for UniProtKB: Q12794   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Hyaluronidase-1 (Homo sapiens (Human))	BDBM81868 (N-Substituted indole-2- and 3-carboxamide derivati...) Show SMILES Fc1ccc(CNC(=O)c2cn(Cc3ccc(F)cc3)c3ccccc23)cc1 Show InChI InChI=1S/C23H18F2N2O/c24-18-9-5-16(6-10-18)13-26-23(28)21-15-27(22-4-2-1-3-20(21)22)14-17-7-11-19(25)12-8-17/h1-12,15H,13-14H2,(H,26,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.57E+4	n/a	n/a	n/a	n/a	7.0	37
TBA					Assay Description Stains-all assay were used to test inhibitors at pH of 7.				Chem Biol Drug Des 70: 547-51 (2007) Article DOI: 10.1111/j.1747-0285.2007.00590.x BindingDB Entry DOI: 10.7270/Q2FB51F7
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM81862 (N-Substituted indole-2- and 3-carboxamide derivati...) Show SMILES Fc1ccc(CNC(=O)c2cc3ccccc3n2Cc2ccccc2)cc1 Show InChI InChI=1S/C23H19FN2O/c24-20-12-10-17(11-13-20)15-25-23(27)22-14-19-8-4-5-9-21(19)26(22)16-18-6-2-1-3-7-18/h1-14H,15-16H2,(H,25,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.72E+4	n/a	n/a	n/a	n/a	7.0	37
TBA					Assay Description Stains-all assay were used to test inhibitors at pH of 7.				Chem Biol Drug Des 70: 547-51 (2007) Article DOI: 10.1111/j.1747-0285.2007.00590.x BindingDB Entry DOI: 10.7270/Q2FB51F7
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM81865 (N-Substituted indole-2- and 3-carboxamide derivati...) Show SMILES Fc1ccc(CNC(=O)c2cc3ccccc3n2Cc2ccc(F)cc2)cc1 Show InChI InChI=1S/C23H18F2N2O/c24-19-9-5-16(6-10-19)14-26-23(28)22-13-18-3-1-2-4-21(18)27(22)15-17-7-11-20(25)12-8-17/h1-13H,14-15H2,(H,26,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.99E+4	n/a	n/a	n/a	n/a	7.0	37
TBA					Assay Description Stains-all assay were used to test inhibitors at pH of 7.				Chem Biol Drug Des 70: 547-51 (2007) Article DOI: 10.1111/j.1747-0285.2007.00590.x BindingDB Entry DOI: 10.7270/Q2FB51F7
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM81866 (N-Substituted indole-2- and 3-carboxamide derivati...) Show SMILES Fc1ccc(Cn2cc(C(=O)NCc3ccccc3)c3ccccc23)cc1 Show InChI InChI=1S/C23H19FN2O/c24-19-12-10-18(11-13-19)15-26-16-21(20-8-4-5-9-22(20)26)23(27)25-14-17-6-2-1-3-7-17/h1-13,16H,14-15H2,(H,25,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.30E+4	n/a	n/a	n/a	n/a	7.0	37
TBA					Assay Description Stains-all assay were used to test inhibitors at pH of 7.				Chem Biol Drug Des 70: 547-51 (2007) Article DOI: 10.1111/j.1747-0285.2007.00590.x BindingDB Entry DOI: 10.7270/Q2FB51F7
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM81864 (N-Substituted indole-2- and 3-carboxamide derivati...) Show SMILES Fc1ccc(Cn2c(cc3ccccc23)C(=O)NCc2ccc(Cl)cc2)cc1 Show InChI InChI=1S/C23H18ClFN2O/c24-19-9-5-16(6-10-19)14-26-23(28)22-13-18-3-1-2-4-21(18)27(22)15-17-7-11-20(25)12-8-17/h1-13H,14-15H2,(H,26,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.30E+4	n/a	n/a	n/a	n/a	7.0	37
TBA					Assay Description Stains-all assay were used to test inhibitors at pH of 7.				Chem Biol Drug Des 70: 547-51 (2007) Article DOI: 10.1111/j.1747-0285.2007.00590.x BindingDB Entry DOI: 10.7270/Q2FB51F7
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM81861 (N-Substituted indole-2- and 3-carboxamide derivati...) Show SMILES Clc1ccc(CNC(=O)c2cc3ccccc3n2Cc2ccccc2)cc1 Show InChI InChI=1S/C23H19ClN2O/c24-20-12-10-17(11-13-20)15-25-23(27)22-14-19-8-4-5-9-21(19)26(22)16-18-6-2-1-3-7-18/h1-14H,15-16H2,(H,25,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.32E+4	n/a	n/a	n/a	n/a	7.0	37
TBA					Assay Description Stains-all assay were used to test inhibitors at pH of 7.				Chem Biol Drug Des 70: 547-51 (2007) Article DOI: 10.1111/j.1747-0285.2007.00590.x BindingDB Entry DOI: 10.7270/Q2FB51F7
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM81867 (N-Substituted indole-2- and 3-carboxamide derivati...) Show SMILES Fc1ccc(Cn2cc(C(=O)NCc3ccc(Cl)cc3)c3ccccc23)cc1 Show InChI InChI=1S/C23H18ClFN2O/c24-18-9-5-16(6-10-18)13-26-23(28)21-15-27(22-4-2-1-3-20(21)22)14-17-7-11-19(25)12-8-17/h1-12,15H,13-14H2,(H,26,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.37E+4	n/a	n/a	n/a	n/a	7.0	37
TBA					Assay Description Stains-all assay were used to test inhibitors at pH of 7.				Chem Biol Drug Des 70: 547-51 (2007) Article DOI: 10.1111/j.1747-0285.2007.00590.x BindingDB Entry DOI: 10.7270/Q2FB51F7
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM81860 (N-Substituted indole-2- and 3-carboxamide derivati...) Show SMILES O=C(NCc1ccccc1)c1cc2ccccc2n1Cc1ccccc1 Show InChI InChI=1S/C23H20N2O/c26-23(24-16-18-9-3-1-4-10-18)22-15-20-13-7-8-14-21(20)25(22)17-19-11-5-2-6-12-19/h1-15H,16-17H2,(H,24,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.03E+4	n/a	n/a	n/a	n/a	7.0	37
TBA					Assay Description Stains-all assay were used to test inhibitors at pH of 7.				Chem Biol Drug Des 70: 547-51 (2007) Article DOI: 10.1111/j.1747-0285.2007.00590.x BindingDB Entry DOI: 10.7270/Q2FB51F7
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM81863 (N-Substituted indole-2- and 3-carboxamide derivati...) Show SMILES Fc1ccc(Cn2c(cc3ccccc23)C(=O)NCc2ccccc2)cc1 Show InChI InChI=1S/C23H19FN2O/c24-20-12-10-18(11-13-20)16-26-21-9-5-4-8-19(21)14-22(26)23(27)25-15-17-6-2-1-3-7-17/h1-14H,15-16H2,(H,25,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.11E+4	n/a	n/a	n/a	n/a	7.0	37
TBA					Assay Description Stains-all assay were used to test inhibitors at pH of 7.				Chem Biol Drug Des 70: 547-51 (2007) Article DOI: 10.1111/j.1747-0285.2007.00590.x BindingDB Entry DOI: 10.7270/Q2FB51F7
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM81868 (N-Substituted indole-2- and 3-carboxamide derivati...) Show SMILES Fc1ccc(CNC(=O)c2cn(Cc3ccc(F)cc3)c3ccccc23)cc1 Show InChI InChI=1S/C23H18F2N2O/c24-18-9-5-16(6-10-18)13-26-23(28)21-15-27(22-4-2-1-3-20(21)22)14-17-7-11-19(25)12-8-17/h1-12,15H,13-14H2,(H,26,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.67E+4	n/a	n/a	n/a	n/a	3.5	37
TBA					Assay Description Morgan-elson assay were used to test inhibitors at pH of 3.5.				Chem Biol Drug Des 70: 547-51 (2007) Article DOI: 10.1111/j.1747-0285.2007.00590.x BindingDB Entry DOI: 10.7270/Q2FB51F7
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM81866 (N-Substituted indole-2- and 3-carboxamide derivati...) Show SMILES Fc1ccc(Cn2cc(C(=O)NCc3ccccc3)c3ccccc23)cc1 Show InChI InChI=1S/C23H19FN2O/c24-19-12-10-18(11-13-19)15-26-16-21(20-8-4-5-9-22(20)26)23(27)25-14-17-6-2-1-3-7-17/h1-13,16H,14-15H2,(H,25,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.16E+4	n/a	n/a	n/a	n/a	3.5	37
TBA					Assay Description Morgan-elson assay were used to test inhibitors at pH of 3.5.				Chem Biol Drug Des 70: 547-51 (2007) Article DOI: 10.1111/j.1747-0285.2007.00590.x BindingDB Entry DOI: 10.7270/Q2FB51F7
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM81861 (N-Substituted indole-2- and 3-carboxamide derivati...) Show SMILES Clc1ccc(CNC(=O)c2cc3ccccc3n2Cc2ccccc2)cc1 Show InChI InChI=1S/C23H19ClN2O/c24-20-12-10-17(11-13-20)15-25-23(27)22-14-19-8-4-5-9-21(19)26(22)16-18-6-2-1-3-7-18/h1-14H,15-16H2,(H,25,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.43E+4	n/a	n/a	n/a	n/a	3.5	37
TBA					Assay Description Morgan-elson assay were used to test inhibitors at pH of 3.5.				Chem Biol Drug Des 70: 547-51 (2007) Article DOI: 10.1111/j.1747-0285.2007.00590.x BindingDB Entry DOI: 10.7270/Q2FB51F7
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM81867 (N-Substituted indole-2- and 3-carboxamide derivati...) Show SMILES Fc1ccc(Cn2cc(C(=O)NCc3ccc(Cl)cc3)c3ccccc23)cc1 Show InChI InChI=1S/C23H18ClFN2O/c24-18-9-5-16(6-10-18)13-26-23(28)21-15-27(22-4-2-1-3-20(21)22)14-17-7-11-19(25)12-8-17/h1-12,15H,13-14H2,(H,26,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.29E+4	n/a	n/a	n/a	n/a	3.5	37
TBA					Assay Description Morgan-elson assay were used to test inhibitors at pH of 3.5.				Chem Biol Drug Des 70: 547-51 (2007) Article DOI: 10.1111/j.1747-0285.2007.00590.x BindingDB Entry DOI: 10.7270/Q2FB51F7
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM81860 (N-Substituted indole-2- and 3-carboxamide derivati...) Show SMILES O=C(NCc1ccccc1)c1cc2ccccc2n1Cc1ccccc1 Show InChI InChI=1S/C23H20N2O/c26-23(24-16-18-9-3-1-4-10-18)22-15-20-13-7-8-14-21(20)25(22)17-19-11-5-2-6-12-19/h1-15H,16-17H2,(H,24,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.82E+4	n/a	n/a	n/a	n/a	3.5	37
TBA					Assay Description Morgan-elson assay were used to test inhibitors at pH of 3.5.				Chem Biol Drug Des 70: 547-51 (2007) Article DOI: 10.1111/j.1747-0285.2007.00590.x BindingDB Entry DOI: 10.7270/Q2FB51F7
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM50316415 (CHEMBL1097937 | Cimicifugic acid L | cimicifugic a...) Show SMILES COc1ccc(\C=C\C(=O)O[C@H](C(O)=O)[C@](O)(Cc2ccc(O)cc2)C(O)=O)cc1OC |r| Show InChI InChI=1S/C22H22O10/c1-30-16-9-5-13(11-17(16)31-2)6-10-18(24)32-19(20(25)26)22(29,21(27)28)12-14-3-7-15(23)8-4-14/h3-11,19,23,29H,12H2,1-2H3,(H,25,26)(H,27,28)/b10-6+/t19-,22-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.02E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Shizuoka Curated by ChEMBL					Assay Description Inhibition of hyaluronidase				J Nat Prod 73: 609-12 (2010) Article DOI: 10.1021/np900752t BindingDB Entry DOI: 10.7270/Q2GF0TNW
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM50316417 (CHEMBL1094303 | Cimicifugic acid N) Show SMILES COc1ccc(\C=C/C(=O)O[C@H](C(O)=O)[C@](O)(Cc2ccc(O)c(O)c2)C(O)=O)cc1OC |r| Show InChI InChI=1S/C22H22O11/c1-31-16-7-4-12(10-17(16)32-2)5-8-18(25)33-19(20(26)27)22(30,21(28)29)11-13-3-6-14(23)15(24)9-13/h3-10,19,23-24,30H,11H2,1-2H3,(H,26,27)(H,28,29)/b8-5-/t19-,22-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.20E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Shizuoka Curated by ChEMBL					Assay Description Inhibition of hyaluronidase				J Nat Prod 73: 609-12 (2010) Article DOI: 10.1021/np900752t BindingDB Entry DOI: 10.7270/Q2GF0TNW
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM50316416 (CHEMBL1096937 | Cimicifugic acid M) Show SMILES OC(=O)[C@@H](OC(=O)\C=C\c1ccc(O)c(O)c1)[C@](O)(Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C20H18O9/c21-14-8-6-12(10-15(14)22)7-9-16(23)29-17(18(24)25)20(28,19(26)27)11-13-4-2-1-3-5-13/h1-10,17,21-22,28H,11H2,(H,24,25)(H,26,27)/b9-7+/t17-,20-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.73E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Shizuoka Curated by ChEMBL					Assay Description Inhibition of hyaluronidase				J Nat Prod 73: 609-12 (2010) Article DOI: 10.1021/np900752t BindingDB Entry DOI: 10.7270/Q2GF0TNW
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM50316414 (CHEMBL1096631 | Cimicifugic acid K) Show SMILES OC(=O)[C@@H](OC(=O)\C=C\c1ccc(O)cc1)[C@](O)(Cc1ccc(O)cc1)C(O)=O |r| Show InChI InChI=1S/C20H18O9/c21-14-6-1-12(2-7-14)5-10-16(23)29-17(18(24)25)20(28,19(26)27)11-13-3-8-15(22)9-4-13/h1-10,17,21-22,28H,11H2,(H,24,25)(H,26,27)/b10-5+/t17-,20-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.55E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Shizuoka Curated by ChEMBL					Assay Description Inhibition of hyaluronidase				J Nat Prod 73: 609-12 (2010) Article DOI: 10.1021/np900752t BindingDB Entry DOI: 10.7270/Q2GF0TNW
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM50133496 ((2R)-3-(3,4-dihydroxyphenyl)-2-[(2E)-3-(3,4-dihydr...) Show SMILES OC(=O)[C@@H](Cc1ccc(O)c(O)c1)OC(=O)\C=C\c1ccc(O)c(O)c1 |r| Show InChI InChI=1S/C18H16O8/c19-12-4-1-10(7-14(12)21)3-6-17(23)26-16(18(24)25)9-11-2-5-13(20)15(22)8-11/h1-8,16,19-22H,9H2,(H,24,25)/b6-3+/t16-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	5.45E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Shizuoka Curated by ChEMBL					Assay Description Inhibition of hyaluronidase				J Nat Prod 73: 609-12 (2010) Article DOI: 10.1021/np900752t BindingDB Entry DOI: 10.7270/Q2GF0TNW
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM4375 ((2E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid | (2...) Show SMILES OC(=O)\C=C\c1ccc(O)c(O)c1 Show InChI InChI=1S/C9H8O4/c10-7-3-1-6(5-8(7)11)2-4-9(12)13/h1-5,10-11H,(H,12,13)/b4-2+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Shizuoka Curated by ChEMBL					Assay Description Inhibition of hyaluronidase				J Nat Prod 73: 609-12 (2010) Article DOI: 10.1021/np900752t BindingDB Entry DOI: 10.7270/Q2GF0TNW
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM50214744 ((2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic aci...) Show SMILES COc1cc(\C=C\C(O)=O)ccc1O Show InChI InChI=1S/C10H10O4/c1-14-9-6-7(2-4-8(9)11)3-5-10(12)13/h2-6,11H,1H3,(H,12,13)/b5-3+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Shizuoka Curated by ChEMBL					Assay Description Inhibition of hyaluronidase				J Nat Prod 73: 609-12 (2010) Article DOI: 10.1021/np900752t BindingDB Entry DOI: 10.7270/Q2GF0TNW
					More data for this Ligand-Target Pair
Hyaluronidase-1 (Homo sapiens (Human))	BDBM50241245 ((2E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoic aci...) Show SMILES COc1ccc(\C=C\C(O)=O)cc1O Show InChI InChI=1S/C10H10O4/c1-14-9-4-2-7(6-8(9)11)3-5-10(12)13/h2-6,11H,1H3,(H,12,13)/b5-3+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Shizuoka Curated by ChEMBL					Assay Description Inhibition of hyaluronidase				J Nat Prod 73: 609-12 (2010) Article DOI: 10.1021/np900752t BindingDB Entry DOI: 10.7270/Q2GF0TNW
					More data for this Ligand-Target Pair