Compile Data Set for Download or QSAR

Found 114 hits with Last Name = 'ohemeng' and Initial = 'k'   

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
Serine protease 1 (Homo sapiens (Human))	BDBM50368077 (CHEMBL3216901 | CHEMBL493336) Show SMILES Cl.Cl.NC(=N)c1ccc(OCCCCCOc2ccc(cc2[N+]([O-])=O)C(N)=N)c(c1)[N+]([O-])=O Show InChI InChI=1S/C19H22N6O6/c20-18(21)12-4-6-16(14(10-12)24(26)27)30-8-2-1-3-9-31-17-7-5-13(19(22)23)11-15(17)25(28)29/h4-7,10-11H,1-3,8-9H2,(H3,20,21)(H3,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368081 (CHEMBL3217116 | CHEMBL522538) Show SMILES Cl.Cl.NC(=N)c1cccc(OCCCOc2cccc(c2)C(N)=N)c1 Show InChI InChI=1S/C17H20N4O2/c18-16(19)12-4-1-6-14(10-12)22-8-3-9-23-15-7-2-5-13(11-15)17(20)21/h1-2,4-7,10-11H,3,8-9H2,(H3,18,19)(H3,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368096 (CHEMBL1204157) Show SMILES NC(=N)c1ccc(NCCCNc2ccc(cc2)C(N)=N)cc1 Show InChI InChI=1S/C17H22N6/c18-16(19)12-2-6-14(7-3-12)22-10-1-11-23-15-8-4-13(5-9-15)17(20)21/h2-9,22-23H,1,10-11H2,(H3,18,19)(H3,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368094 (CHEMBL3216660 | CHEMBL494405) Show SMILES Cl.Cl.COc1cc(ccc1OCCCOc1ccc(cc1OC)C(N)=N)C(N)=N Show InChI InChI=1S/C19H24N4O4/c1-24-16-10-12(18(20)21)4-6-14(16)26-8-3-9-27-15-7-5-13(19(22)23)11-17(15)25-2/h4-7,10-11H,3,8-9H2,1-2H3,(H3,20,21)(H3,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368082 (CHEMBL3216435 | CHEMBL523180) Show SMILES Cl.Cl.COc1cc(ccc1OCCCCCOc1ccc(cc1OC)C(N)=N)C(N)=N Show InChI InChI=1S/C21H28N4O4/c1-26-18-12-14(20(22)23)6-8-16(18)28-10-4-3-5-11-29-17-9-7-15(21(24)25)13-19(17)27-2/h6-9,12-13H,3-5,10-11H2,1-2H3,(H3,22,23)(H3,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368098 (CHEMBL492579) Show SMILES NC(=N)c1ccc(NCCCCCNc2ccc(cc2)C(N)=N)cc1 Show InChI InChI=1S/C19H26N6/c20-18(21)14-4-8-16(9-5-14)24-12-2-1-3-13-25-17-10-6-15(7-11-17)19(22)23/h4-11,24-25H,1-3,12-13H2,(H3,20,21)(H3,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368102 (CHEMBL3216029 | CHEMBL494850) Show SMILES Cl.Cl.NC(=N)c1ccc(OCCCCOc2ccc(cc2)C(N)=N)cc1 Show InChI InChI=1S/C18H22N4O2/c19-17(20)13-3-7-15(8-4-13)23-11-1-2-12-24-16-9-5-14(6-10-16)18(21)22/h3-10H,1-2,11-12H2,(H3,19,20)(H3,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.50E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368093 (CHEMBL1204156) Show SMILES NC(=N)c1ccc(NCCCCNc2ccc(cc2)C(N)=N)cc1 Show InChI InChI=1S/C18H24N6/c19-17(20)13-3-7-15(8-4-13)23-11-1-2-12-24-16-9-5-14(6-10-16)18(21)22/h3-10,23-24H,1-2,11-12H2,(H3,19,20)(H3,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368083 (CHEMBL3216032 | CHEMBL495206) Show SMILES Cl.Cl.NC(=N)c1cccc(OCCCCOc2cccc(c2)C(N)=N)c1 Show InChI InChI=1S/C18H22N4O2/c19-17(20)13-5-3-7-15(11-13)23-9-1-2-10-24-16-8-4-6-14(12-16)18(21)22/h3-8,11-12H,1-2,9-10H2,(H3,19,20)(H3,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368100 (CHEMBL1204159) Show SMILES NC(=N)c1ccc(OCCCCCOc2ccc(cc2N)C(N)=N)c(N)c1 Show InChI InChI=1S/C19H26N6O2/c20-14-10-12(18(22)23)4-6-16(14)26-8-2-1-3-9-27-17-7-5-13(19(24)25)11-15(17)21/h4-7,10-11H,1-3,8-9,20-21H2,(H3,22,23)(H3,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM45440 (4-[5-(4-amidinophenoxy)pentoxy]benzamidine;2-hydro...) Show SMILES NC(=N)c1ccc(OCCCCCOc2ccc(cc2)C(N)=N)cc1 Show InChI InChI=1S/C19H24N4O2/c20-18(21)14-4-8-16(9-5-14)24-12-2-1-3-13-25-17-10-6-15(7-11-17)19(22)23/h4-11H,1-3,12-13H2,(H3,20,21)(H3,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Similars	PubMed	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50015234 (4,4''[1,6-HEXANEDIYLBIS(OXY)]BISBENZENECARBOXIMIDA...) Show SMILES NC(=N)c1ccc(OCCCCCCOc2ccc(cc2)C(N)=N)cc1 Show InChI InChI=1S/C20H26N4O2/c21-19(22)15-5-9-17(10-6-15)25-13-3-1-2-4-14-26-18-11-7-16(8-12-18)20(23)24/h5-12H,1-4,13-14H2,(H3,21,22)(H3,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PubMed	2.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368092 (GNF-PF-3839 | PROPAMIDINE CHLORIDE) Show SMILES NC(=N)c1ccc(OCCCOc2ccc(cc2)C(N)=N)cc1 Show InChI InChI=1S/C17H20N4O2/c18-16(19)12-2-6-14(7-3-12)22-10-1-11-23-15-8-4-13(5-9-15)17(20)21/h2-9H,1,10-11H2,(H3,18,19)(H3,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem Similars	PubMed	3.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368087 (CHEMBL3215566 | CHEMBL493170) Show SMILES Cl.Cl.NC(=N)c1cccc(OCCCCCOc2cccc(c2)C(N)=N)c1 Show InChI InChI=1S/C19H24N4O2/c20-18(21)14-6-4-8-16(12-14)24-10-2-1-3-11-25-17-9-5-7-15(13-17)19(22)23/h4-9,12-13H,1-3,10-11H2,(H3,20,21)(H3,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	3.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368085 (CHEMBL3216215 | CHEMBL492970) Show SMILES Cl.Cl.NC(=N)c1cccc(OCCCCCCOc2cccc(c2)C(N)=N)c1 Show InChI InChI=1S/C20H26N4O2/c21-19(22)15-7-5-9-17(13-15)25-11-3-1-2-4-12-26-18-10-6-8-16(14-18)20(23)24/h5-10,13-14H,1-4,11-12H2,(H3,21,22)(H3,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368074 (CHEMBL1204155) Show SMILES NC(=N)c1ccc(NCCCNc2ccc(cc2[N+]([O-])=O)C(N)=N)c(c1)[N+]([O-])=O Show InChI InChI=1S/C17H20N8O4/c18-16(19)10-2-4-12(14(8-10)24(26)27)22-6-1-7-23-13-5-3-11(17(20)21)9-15(13)25(28)29/h2-5,8-9,22-23H,1,6-7H2,(H3,18,19)(H3,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	4.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368075 (CHEMBL1202472) Show SMILES NC(=N)c1ccc(NCCCCCNc2ccc(cc2N)C(N)=N)c(N)c1 Show InChI InChI=1S/C19H28N8/c20-14-10-12(18(22)23)4-6-16(14)26-8-2-1-3-9-27-17-7-5-13(19(24)25)11-15(17)21/h4-7,10-11,26-27H,1-3,8-9,20-21H2,(H3,22,23)(H3,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	4.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368095 (CHEMBL1204150) Show SMILES NC(=N)c1ccc(OCCOc2ccc(cc2N)C(N)=N)c(N)c1 Show InChI InChI=1S/C16H20N6O2/c17-11-7-9(15(19)20)1-3-13(11)23-5-6-24-14-4-2-10(16(21)22)8-12(14)18/h1-4,7-8H,5-6,17-18H2,(H3,19,20)(H3,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368078 (CHEMBL1204161) Show SMILES NC(=N)c1ccc(NCCCCCCNc2ccc(cc2N)C(N)=N)c(N)c1 Show InChI InChI=1S/C20H30N8/c21-15-11-13(19(23)24)5-7-17(15)27-9-3-1-2-4-10-28-18-8-6-14(20(25)26)12-16(18)22/h5-8,11-12,27-28H,1-4,9-10,21-22H2,(H3,23,24)(H3,25,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	5.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368079 (CHEMBL3216662 | CHEMBL492360) Show SMILES Cl.Cl.NC(=N)c1ccc(OCCCCOc2ccc(cc2[N+]([O-])=O)C(N)=N)c(c1)[N+]([O-])=O Show InChI InChI=1S/C18H20N6O6/c19-17(20)11-3-5-15(13(9-11)23(25)26)29-7-1-2-8-30-16-6-4-12(18(21)22)10-14(16)24(27)28/h3-6,9-10H,1-2,7-8H2,(H3,19,20)(H3,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	5.40E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368089 (CHEMBL3215570 | CHEMBL522667) Show SMILES Cl.Cl.NC(=N)c1ccc(OCCCOc2ccc(cc2N)C(N)=N)c(N)c1 Show InChI InChI=1S/C17H22N6O2/c18-12-8-10(16(20)21)2-4-14(12)24-6-1-7-25-15-5-3-11(17(22)23)9-13(15)19/h2-5,8-9H,1,6-7,18-19H2,(H3,20,21)(H3,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	5.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368097 (CHEMBL1204158) Show SMILES NC(=N)c1ccc(OCCOc2ccc(cc2)C(N)=N)cc1 Show InChI InChI=1S/C16H18N4O2/c17-15(18)11-1-5-13(6-2-11)21-9-10-22-14-7-3-12(4-8-14)16(19)20/h1-8H,9-10H2,(H3,17,18)(H3,19,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	7.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368084 (CHEMBL1204154) Show SMILES NC(=N)c1ccc(NCCCCCNc2ccc(cc2[N+]([O-])=O)C(N)=N)c(c1)[N+]([O-])=O Show InChI InChI=1S/C19H24N8O4/c20-18(21)12-4-6-14(16(10-12)26(28)29)24-8-2-1-3-9-25-15-7-5-13(19(22)23)11-17(15)27(30)31/h4-7,10-11,24-25H,1-3,8-9H2,(H3,20,21)(H3,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	8.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368076 (CHEMBL1204149) Show SMILES NC(=N)c1ccc(OCCCCOc2ccc(cc2N)C(N)=N)c(N)c1 Show InChI InChI=1S/C18H24N6O2/c19-13-9-11(17(21)22)3-5-15(13)25-7-1-2-8-26-16-6-4-12(18(23)24)10-14(16)20/h3-6,9-10H,1-2,7-8,19-20H2,(H3,21,22)(H3,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	9.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368086 (CHEMBL1204153) Show SMILES NC(=N)c1ccc(NCCCNc2ccc(cc2N)C(N)=N)c(N)c1 Show InChI InChI=1S/C17H24N8/c18-12-8-10(16(20)21)2-4-14(12)24-6-1-7-25-15-5-3-11(17(22)23)9-13(15)19/h2-5,8-9,24-25H,1,6-7,18-19H2,(H3,20,21)(H3,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.03E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368080 (CHEMBL1204152) Show SMILES NC(=N)c1ccc(NCCCCNc2ccc(cc2N)C(N)=N)c(N)c1 Show InChI InChI=1S/C18H26N8/c19-13-9-11(17(21)22)3-5-15(13)25-7-1-2-8-26-16-6-4-12(18(23)24)10-14(16)20/h3-6,9-10,25-26H,1-2,7-8,19-20H2,(H3,21,22)(H3,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.11E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368090 (CHEMBL1204160) Show SMILES NC(=N)c1ccc(NCCNc2ccc(cc2N)C(N)=N)c(N)c1 Show InChI InChI=1S/C16H22N8/c17-11-7-9(15(19)20)1-3-13(11)23-5-6-24-14-4-2-10(16(21)22)8-12(14)18/h1-4,7-8,23-24H,5-6,17-18H2,(H3,19,20)(H3,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.27E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368088 (CHEMBL1204151) Show SMILES NC(=N)c1ccc(OCCCCCCOc2ccc(cc2N)C(N)=N)c(N)c1 Show InChI InChI=1S/C20H28N6O2/c21-15-11-13(19(23)24)5-7-17(15)27-9-3-1-2-4-10-28-18-8-6-14(20(25)26)12-16(18)22/h5-8,11-12H,1-4,9-10,21-22H2,(H3,23,24)(H3,25,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.93E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50368099 (CHEMBL494956) Show SMILES C(CCOc1ccc(cc1)C1=NCCN1)CCOc1ccc(cc1)C1=NCCN1 |t:11,27| Show InChI InChI=1S/C23H28N4O2/c1(2-16-28-20-8-4-18(5-9-20)22-24-12-13-25-22)3-17-29-21-10-6-19(7-11-21)23-26-14-15-27-23/h4-11H,1-3,12-17H2,(H,24,25)(H,26,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of trypsin by amidase assay.				J Med Chem 33: 1252-7 (1990) BindingDB Entry DOI: 10.7270/Q2154HNW
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037791 (4-(Hydroxy-{1-[2-(3,4,5-trimethoxy-phenyl)-benzofu...) Show SMILES COC(=O)CCCC(=O)N(O)C(C)c1ccc2oc(cc2c1)-c1cc(OC)c(OC)c(OC)c1 Show InChI InChI=1S/C25H29NO8/c1-15(26(29)23(27)7-6-8-24(28)32-4)16-9-10-19-17(11-16)12-20(34-19)18-13-21(30-2)25(33-5)22(14-18)31-3/h9-15,29H,6-8H2,1-5H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	40	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037795 (CHEMBL120885 | Furan-2-carboxylic acid hydroxy-[1-...) Show SMILES CC(N(O)C(=O)c1ccco1)c1ccc2oc(cc2c1)-c1ccccc1 Show InChI InChI=1S/C21H17NO4/c1-14(22(24)21(23)19-8-5-11-25-19)16-9-10-18-17(12-16)13-20(26-18)15-6-3-2-4-7-15/h2-14,24H,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	40	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037807 (CHEMBL331626 | N-[1-(2-Butyl-benzofuran-5-yl)-ethy...) Show SMILES CCCCc1cc2cc(ccc2o1)C(C)N(O)C(C)=O Show InChI InChI=1S/C16H21NO3/c1-4-5-6-15-10-14-9-13(7-8-16(14)20-15)11(2)17(19)12(3)18/h7-11,19H,4-6H2,1-3H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	50	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037805 (CHEMBL121025 | N-hydroxy-N-[1-[2-(3,4,5-trimethoxy...) Show SMILES COc1cc(cc(OC)c1OC)-c1cc2cc(ccc2o1)C(C)N(O)C(N)=O Show InChI InChI=1S/C20H22N2O6/c1-11(22(24)20(21)23)12-5-6-15-13(7-12)8-16(28-15)14-9-17(25-2)19(27-4)18(10-14)26-3/h5-11,24H,1-4H3,(H2,21,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	50	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037792 (CHEMBL122955 | N-Hydroxy-N-[1-(2-phenyl-benzofuran...) Show SMILES CCOC(=O)CCC(=O)N(O)C(C)c1ccc2oc(cc2c1)-c1ccccc1 Show InChI InChI=1S/C22H23NO5/c1-3-27-22(25)12-11-21(24)23(26)15(2)17-9-10-19-18(13-17)14-20(28-19)16-7-5-4-6-8-16/h4-10,13-15,26H,3,11-12H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	50	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037803 (4-{[1-(2-Butyl-benzofuran-5-yl)-ethyl]-hydroxy-car...) Show SMILES CCCCc1cc2cc(ccc2o1)C(C)N(O)C(=O)CCCC(=O)OC Show InChI InChI=1S/C20H27NO5/c1-4-5-7-17-13-16-12-15(10-11-18(16)26-17)14(2)21(24)19(22)8-6-9-20(23)25-3/h10-14,24H,4-9H2,1-3H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	50	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037793 (4-{Hydroxy-[1-(2-phenyl-benzofuran-5-yl)-ethyl]-ca...) Show SMILES COC(=O)CCCC(=O)N(O)C(C)c1ccc2oc(cc2c1)-c1ccccc1 Show InChI InChI=1S/C22H23NO5/c1-15(23(26)21(24)9-6-10-22(25)27-2)17-11-12-19-18(13-17)14-20(28-19)16-7-4-3-5-8-16/h3-5,7-8,11-15,26H,6,9-10H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037788 (CHEMBL421255 | N-Hydroxy-N-{1-[2-(6-methoxy-naphth...) Show SMILES COc1ccc2cc(ccc2c1)-c1cc2cc(ccc2o1)C(C)N(O)C(C)=O Show InChI InChI=1S/C23H21NO4/c1-14(24(26)15(2)25)16-7-9-22-20(10-16)13-23(28-22)19-5-4-18-12-21(27-3)8-6-17(18)11-19/h4-14,26H,1-3H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	120	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037801 (4-{[1-(2-Decyl-benzofuran-5-yl)-ethyl]-hydroxy-car...) Show SMILES CCCCCCCCCCc1cc2cc(ccc2o1)C(C)N(O)C(=O)CCCC(=O)OC Show InChI InChI=1S/C26H39NO5/c1-4-5-6-7-8-9-10-11-13-23-19-22-18-21(16-17-24(22)32-23)20(2)27(30)25(28)14-12-15-26(29)31-3/h16-20,30H,4-15H2,1-3H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	150	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037796 (Acetic acid {hydroxy-[1-(2-phenyl-benzofuran-5-yl)...) Show SMILES CC(N(O)C(=O)COC(C)=O)c1ccc2oc(cc2c1)-c1ccccc1 Show InChI InChI=1S/C20H19NO5/c1-13(21(24)20(23)12-25-14(2)22)16-8-9-18-17(10-16)11-19(26-18)15-6-4-3-5-7-15/h3-11,13,24H,12H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	160	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037789 (CHEMBL332395 | N-Hydroxy-2-methoxy-N-[1-(2-phenyl-...) Show SMILES COCC(=O)N(O)C(C)c1ccc2oc(cc2c1)-c1ccccc1 Show InChI InChI=1S/C19H19NO4/c1-13(20(22)19(21)12-23-2)15-8-9-17-16(10-15)11-18(24-17)14-6-4-3-5-7-14/h3-11,13,22H,12H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	160	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037797 (CHEMBL123396 | N-Hydroxy-3,4-dimethoxy-N-[1-(2-phe...) Show SMILES COc1ccc(cc1OC)C(=O)N(O)C(C)c1ccc2oc(cc2c1)-c1ccccc1 Show InChI InChI=1S/C25H23NO5/c1-16(26(28)25(27)19-10-12-22(29-2)24(14-19)30-3)18-9-11-21-20(13-18)15-23(31-21)17-7-5-4-6-8-17/h4-16,28H,1-3H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037806 (CHEMBL123177 | Thiophene-2-carboxylic acid hydroxy...) Show SMILES CC(N(O)C(=O)c1cccs1)c1ccc2oc(cc2c1)-c1ccccc1 Show InChI InChI=1S/C21H17NO3S/c1-14(22(24)21(23)20-8-5-11-26-20)16-9-10-18-17(12-16)13-19(25-18)15-6-3-2-4-7-15/h2-14,24H,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	250	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037794 (CHEMBL331060 | N-Hydroxy-N-{1-[2-(3,4,5-trimethoxy...) Show SMILES COc1cc(cc(OC)c1OC)-c1cc2cc(ccc2o1)C(C)N(O)C(C)=O Show InChI InChI=1S/C21H23NO6/c1-12(22(24)13(2)23)14-6-7-17-15(8-14)9-18(28-17)16-10-19(25-3)21(27-5)20(11-16)26-4/h6-12,24H,1-5H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	310	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50000541 ((+-)-1-(1-Benzo[b]thien-2-ylethyl)-1-hydroxyurea |...) Show SMILES CC(N(O)C(N)=O)c1cc2ccccc2s1 Show InChI InChI=1S/C11H12N2O2S/c1-7(13(15)11(12)14)10-6-8-4-2-3-5-9(8)16-10/h2-7,15H,1H3,(H2,12,14)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	370	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50022683 (CHEMBL418304 | N-[1-(4-Benzyloxy-phenyl)-ethyl]-N-...) Show SMILES CC(N(O)C(C)=O)c1ccc(OCc2ccccc2)cc1 Show InChI InChI=1S/C17H19NO3/c1-13(18(20)14(2)19)16-8-10-17(11-9-16)21-12-15-6-4-3-5-7-15/h3-11,13,20H,12H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	370	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037799 (CHEMBL123649 | N-Hydroxy-N-[1-(4-phenethyloxy-phen...) Show SMILES CC(N(O)C(C)=O)c1ccc(OCCc2ccccc2)cc1 Show InChI InChI=1S/C18H21NO3/c1-14(19(21)15(2)20)17-8-10-18(11-9-17)22-13-12-16-6-4-3-5-7-16/h3-11,14,21H,12-13H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	410	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037798 (CHEMBL121390 | N-hydroxy-N-[1-(2-phinyl-5-benzofur...) Show SMILES CC(N(O)C(N)=O)c1ccc2oc(cc2c1)-c1ccccc1 Show InChI InChI=1S/C17H16N2O3/c1-11(19(21)17(18)20)13-7-8-15-14(9-13)10-16(22-15)12-5-3-2-4-6-12/h2-11,21H,1H3,(H2,18,20)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	410	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037790 (CHEMBL331881 | N-[1-(2-Decyl-benzofuran-5-yl)-ethy...) Show SMILES CCCCCCCCCCc1cc2cc(ccc2o1)C(C)N(O)C(C)=O Show InChI InChI=1S/C22H33NO3/c1-4-5-6-7-8-9-10-11-12-21-16-20-15-19(13-14-22(20)26-21)17(2)23(25)18(3)24/h13-17,25H,4-12H2,1-3H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	410	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50037787 (CHEMBL332814 | N-Hydroxy-N-[1-(2-phenyl-benzofuran...) Show SMILES CC(N(O)C(C)=O)c1ccc2oc(cc2c1)-c1ccccc1 Show InChI InChI=1S/C18H17NO3/c1-12(19(21)13(2)20)15-8-9-17-16(10-15)11-18(22-17)14-6-4-3-5-7-14/h3-12,21H,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	490	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Rattus norvegicus)	BDBM50022697 (CHEMBL62114 | N-Hydroxy-N-{1-[4-(1-phenyl-ethoxy)-...) Show SMILES CC(Oc1ccc(cc1)C(C)N(O)C(C)=O)c1ccccc1 Show InChI InChI=1S/C18H21NO3/c1-13(19(21)15(3)20)16-9-11-18(12-10-16)22-14(2)17-7-5-4-6-8-17/h4-14,21H,1-3H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of 5-lipoxygenase (5-HETE) derived from the 9000xg supernatant of RBL broken cell assay				J Med Chem 37: 3663-7 (1994) BindingDB Entry DOI: 10.7270/Q27943Q2
					More data for this Ligand-Target Pair

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