Compile Data Set for Download or QSAR

Found 31 hits Enz. Inhib. hit(s) with all data for entry = 50044489   

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
Acrosin (Homo sapiens (Human))	BDBM50018974 (CHEMBL3287446) Show SMILES Cl.COc1ccc(NC(=O)c2cc(on2)-c2ccc(NC(N)=N)cc2)c(OC)c1 Show InChI InChI=1S/C19H19N5O4.ClH/c1-26-13-7-8-14(17(9-13)27-2)23-18(25)15-10-16(28-24-15)11-3-5-12(6-4-11)22-19(20)21;/h3-10H,1-2H3,(H,23,25)(H4,20,21,22);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL 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
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018973 (CHEMBL3287445) Show SMILES Cl.COc1ccc(OC)c(NC(=O)c2cc(on2)-c2ccc(NC(N)=N)cc2)c1 Show InChI InChI=1S/C19H19N5O4.ClH/c1-26-13-7-8-16(27-2)14(9-13)23-18(25)15-10-17(28-24-15)11-3-5-12(6-4-11)22-19(20)21;/h3-10H,1-2H3,(H,23,25)(H4,20,21,22);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018978 (CHEMBL3287450) Show SMILES Cl.Cc1cccc(C)c1NC(=O)c1cc(on1)-c1ccc(NC(N)=N)cc1 Show InChI InChI=1S/C19H19N5O2.ClH/c1-11-4-3-5-12(2)17(11)23-18(25)15-10-16(26-24-15)13-6-8-14(9-7-13)22-19(20)21;/h3-10H,1-2H3,(H,23,25)(H4,20,21,22);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018983 (CHEMBL3287455) Show SMILES Cl.CCOc1ccc(NC(=O)c2cc(on2)-c2ccc(NC(N)=N)cc2)cc1 Show InChI InChI=1S/C19H19N5O3.ClH/c1-2-26-15-9-7-13(8-10-15)22-18(25)16-11-17(27-24-16)12-3-5-14(6-4-12)23-19(20)21;/h3-11H,2H2,1H3,(H,22,25)(H4,20,21,23);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018988 (CHEMBL3287459) Show SMILES Cl.COc1cccc(NC(=O)c2cc(on2)-c2ccc(NC(N)=N)cc2)c1 Show InChI InChI=1S/C18H17N5O3.ClH/c1-25-14-4-2-3-13(9-14)21-17(24)15-10-16(26-23-15)11-5-7-12(8-6-11)22-18(19)20;/h2-10H,1H3,(H,21,24)(H4,19,20,22);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018976 (CHEMBL3287448) Show SMILES Cl.CC(C)(C)c1ccc(NC(=O)c2cc(on2)-c2ccc(NC(N)=N)cc2)cc1 Show InChI InChI=1S/C21H23N5O2.ClH/c1-21(2,3)14-6-10-15(11-7-14)24-19(27)17-12-18(28-26-17)13-4-8-16(9-5-13)25-20(22)23;/h4-12H,1-3H3,(H,24,27)(H4,22,23,25);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018987 (CHEMBL3287458) Show SMILES Cl.COc1ccccc1NC(=O)c1cc(on1)-c1ccc(NC(N)=N)cc1 Show InChI InChI=1S/C18H17N5O3.ClH/c1-25-15-5-3-2-4-13(15)22-17(24)14-10-16(26-23-14)11-6-8-12(9-7-11)21-18(19)20;/h2-10H,1H3,(H,22,24)(H4,19,20,21);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018975 (CHEMBL3287447) Show SMILES Cl.CCOC(=O)c1ccc(NC(=O)c2cc(on2)-c2ccc(NC(N)=N)cc2)cc1 Show InChI InChI=1S/C20H19N5O4.ClH/c1-2-28-19(27)13-5-9-14(10-6-13)23-18(26)16-11-17(29-25-16)12-3-7-15(8-4-12)24-20(21)22;/h3-11H,2H2,1H3,(H,23,26)(H4,21,22,24);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018992 (CHEMBL3287462) Show SMILES Cl.Cc1cccc(NC(=O)c2cc(on2)-c2ccc(NC(N)=N)cc2)c1 Show InChI InChI=1S/C18H17N5O2.ClH/c1-11-3-2-4-14(9-11)21-17(24)15-10-16(25-23-15)12-5-7-13(8-6-12)22-18(19)20;/h2-10H,1H3,(H,21,24)(H4,19,20,22);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	9.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018977 (CHEMBL3287449) Show SMILES Cl.Cc1ccc(NC(=O)c2cc(on2)-c2ccc(NC(N)=N)cc2)cc1 Show InChI InChI=1S/C18H17N5O2.ClH/c1-11-2-6-13(7-3-11)21-17(24)15-10-16(25-23-15)12-4-8-14(9-5-12)22-18(19)20;/h2-10H,1H3,(H,21,24)(H4,19,20,22);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.01E+4	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018994 (CHEMBL3287464) Show SMILES Cl.Cc1cccc(NC(=O)c2cc(on2)-c2ccc(NC(N)=N)cc2)c1C Show InChI InChI=1S/C19H19N5O2.ClH/c1-11-4-3-5-15(12(11)2)23-18(25)16-10-17(26-24-16)13-6-8-14(9-7-13)22-19(20)21;/h3-10H,1-2H3,(H,23,25)(H4,20,21,22);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.15E+4	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018980 (CHEMBL3287452) Show SMILES Cl.Cc1cc(C)cc(NC(=O)c2cc(on2)-c2ccc(NC(N)=N)cc2)c1 Show InChI InChI=1S/C19H19N5O2.ClH/c1-11-7-12(2)9-15(8-11)22-18(25)16-10-17(26-24-16)13-3-5-14(6-4-13)23-19(20)21;/h3-10H,1-2H3,(H,22,25)(H4,20,21,23);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.21E+4	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018982 (CHEMBL3287454) Show SMILES Cl.Cc1ccccc1NC(=O)c1cc(on1)-c1ccc(NC(N)=N)cc1 Show InChI InChI=1S/C18H17N5O2.ClH/c1-11-4-2-3-5-14(11)22-17(24)15-10-16(25-23-15)12-6-8-13(9-7-12)21-18(19)20;/h2-10H,1H3,(H,22,24)(H4,19,20,21);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.44E+4	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018981 (CHEMBL3287453) Show SMILES Cl.NC(=N)Nc1ccc(cc1)-c1cc(no1)C(=O)Nc1cccc(Br)c1 Show InChI InChI=1S/C17H14BrN5O2.ClH/c18-11-2-1-3-13(8-11)21-16(24)14-9-15(25-23-14)10-4-6-12(7-5-10)22-17(19)20;/h1-9H,(H,21,24)(H4,19,20,22);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.44E+4	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018984 (CHEMBL3287456) Show SMILES Cl.NC(=N)Nc1ccc(cc1)-c1cc(no1)C(=O)Nc1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C18H14F3N5O2.ClH/c19-18(20,21)11-3-7-12(8-4-11)24-16(27)14-9-15(28-26-14)10-1-5-13(6-2-10)25-17(22)23;/h1-9H,(H,24,27)(H4,22,23,25);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.03E+4	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018995 (CHEMBL3287465) Show SMILES Cl.NC(=N)Nc1ccc(cc1)-c1cc(no1)C(=O)Nc1ccc(F)cc1 Show InChI InChI=1S/C17H14FN5O2.ClH/c18-11-3-7-12(8-4-11)21-16(24)14-9-15(25-23-14)10-1-5-13(6-2-10)22-17(19)20;/h1-9H,(H,21,24)(H4,19,20,22);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.05E+4	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018972 (CHEMBL3287444) Show SMILES Cl.Cc1ccnc(NC(=O)c2cc(on2)-c2ccc(NC(N)=N)cc2)c1 Show InChI InChI=1S/C17H16N6O2.ClH/c1-10-6-7-20-15(8-10)22-16(24)13-9-14(25-23-13)11-2-4-12(5-3-11)21-17(18)19;/h2-9H,1H3,(H4,18,19,21)(H,20,22,24);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.14E+4	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018993 (CHEMBL3287463) Show SMILES Cl.NC(=N)Nc1ccc(cc1)-c1cc(no1)C(=O)Nc1ccc(cc1)C#N Show InChI InChI=1S/C18H14N6O2.ClH/c19-10-11-1-5-13(6-2-11)22-17(25)15-9-16(26-24-15)12-3-7-14(8-4-12)23-18(20)21;/h1-9H,(H,22,25)(H4,20,21,23);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia 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
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018971 (CHEMBL3287443) Show SMILES Cl.NC(=N)Nc1ccc(cc1)-c1cc(no1)C(=O)Nc1ccccc1 Show InChI InChI=1S/C17H15N5O2.ClH/c18-17(19)21-13-8-6-11(7-9-13)15-10-14(22-24-15)16(23)20-12-4-2-1-3-5-12;/h1-10H,(H,20,23)(H4,18,19,21);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.46E+4	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018979 (CHEMBL3287451) Show SMILES Cl.NC(=N)Nc1ccc(cc1)-c1cc(no1)C(=O)Nc1cccc(Cl)c1 Show InChI InChI=1S/C17H14ClN5O2.ClH/c18-11-2-1-3-13(8-11)21-16(24)14-9-15(25-23-14)10-4-6-12(7-5-10)22-17(19)20;/h1-9H,(H,21,24)(H4,19,20,22);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL 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
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018986 (CHEMBL3287457) Show SMILES Cl.NC(=N)Nc1ccc(cc1)-c1cc(no1)C(=O)Nc1ccc(Cl)cc1 Show InChI InChI=1S/C17H14ClN5O2.ClH/c18-11-3-7-12(8-4-11)21-16(24)14-9-15(25-23-14)10-1-5-13(6-2-10)22-17(19)20;/h1-9H,(H,21,24)(H4,19,20,22);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL 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
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018989 (CHEMBL3287460) Show SMILES Cl.NC(=N)Nc1ccc(cc1)-c1cc(no1)C(=O)Nc1ccccc1Br Show InChI InChI=1S/C17H14BrN5O2.ClH/c18-12-3-1-2-4-13(12)22-16(24)14-9-15(25-23-14)10-5-7-11(8-6-10)21-17(19)20;/h1-9H,(H,22,24)(H4,19,20,21);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.79E+4	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018990 (CHEMBL3287461) Show SMILES Cl.NC(=N)Nc1ccc(cc1)-c1cc(no1)C(=O)Nc1cccc2ccccc12 Show InChI InChI=1S/C21H17N5O2.ClH/c22-21(23)24-15-10-8-14(9-11-15)19-12-18(26-28-19)20(27)25-17-7-3-5-13-4-1-2-6-16(13)17;/h1-12H,(H,25,27)(H4,22,23,24);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.99E+4	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018965 (CHEMBL3287437) Show SMILES CCOC(=O)c1cc(on1)-c1ccc(NC(=O)c2ccccc2Cl)cc1 Show InChI InChI=1S/C19H15ClN2O4/c1-2-25-19(24)16-11-17(26-22-16)12-7-9-13(10-8-12)21-18(23)14-5-3-4-6-15(14)20/h3-11H,2H2,1H3,(H,21,23)	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018970 (CHEMBL3287442) Show SMILES Cl.CC(CO)NC(=O)c1cc(on1)-c1ccc(NC(N)=N)cc1 Show InChI InChI=1S/C14H17N5O3.ClH/c1-8(7-20)17-13(21)11-6-12(22-19-11)9-2-4-10(5-3-9)18-14(15)16;/h2-6,8,20H,7H2,1H3,(H,17,21)(H4,15,16,18);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018969 (CHEMBL3287441) Show SMILES Cl.CC(C)NC(=O)c1cc(on1)-c1ccc(NC(N)=N)cc1 Show InChI InChI=1S/C14H17N5O2.ClH/c1-8(2)17-13(20)11-7-12(21-19-11)9-3-5-10(6-4-9)18-14(15)16;/h3-8H,1-2H3,(H,17,20)(H4,15,16,18);1H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018966 (CHEMBL3287438) Show SMILES CCOC(=O)c1cc(on1)-c1ccc(NC(=O)c2ccc(F)cc2)cc1 Show InChI InChI=1S/C19H15FN2O4/c1-2-25-19(24)16-11-17(26-22-16)12-5-9-15(10-6-12)21-18(23)13-3-7-14(20)8-4-13/h3-11H,2H2,1H3,(H,21,23)	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.40E+5	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018967 (CHEMBL3287439) Show SMILES CCOC(=O)c1cc(on1)-c1ccc(NC(=O)c2ccc(Cl)c(Cl)c2)cc1 Show InChI InChI=1S/C19H14Cl2N2O4/c1-2-26-19(25)16-10-17(27-23-16)11-3-6-13(7-4-11)22-18(24)12-5-8-14(20)15(21)9-12/h3-10H,2H2,1H3,(H,22,24)	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.40E+5	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018968 (CHEMBL3287440) Show SMILES CCOC(=O)c1cc(on1)-c1ccc(NC(=O)c2ccc(Cl)cc2)cc1 Show InChI InChI=1S/C19H15ClN2O4/c1-2-25-19(24)16-11-17(26-22-16)12-5-9-15(10-6-12)21-18(23)13-3-7-14(20)8-4-13/h3-11H,2H2,1H3,(H,21,23)	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.80E+5	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50382109 (CHEMBL2023319) Show SMILES Clc1ccc(-c2cc(C=O)no2)c(Cl)c1 Show InChI InChI=1S/C10H5Cl2NO2/c11-6-1-2-8(9(12)3-6)10-4-7(5-14)13-15-10/h1-5H	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.90E+5	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair
Acrosin (Homo sapiens (Human))	BDBM50018964 (CHEMBL3287436) Show SMILES CCOC(=O)c1cc(on1)-c1ccc(NC(=O)c2ccccc2)cc1 Show InChI InChI=1S/C19H16N2O4/c1-2-24-19(23)16-12-17(25-21-16)13-8-10-15(11-9-13)20-18(22)14-6-4-3-5-7-14/h3-12H,2H2,1H3,(H,20,22)	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.60E+5	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometry				Bioorg Med Chem Lett 24: 2802-6 (2014) Article DOI: 10.1016/j.bmcl.2014.04.118 BindingDB Entry DOI: 10.7270/Q2J38V4S
					More data for this Ligand-Target Pair