Compile Data Set for Download or QSAR

Found 52 hits with Last Name = 'easton' and Initial = 'cj'   

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
Isoleucyl-tRNA synthetase (Rattus norvegicus)	BDBM50093001 ((4aR,6S,7R,7aS)-7-[2-((S)-2-Amino-3-methyl-butyryl...) Show SMILES CC(C)[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(O)=O |c:25| Show InChI InChI=1S/C18H29N5O8S/c1-8(2)14(19)16(27)22-32(30,31)7-13(25)21-18(17(28)29)11-6-23(3)5-10(15(20)26)9(11)4-12(18)24/h5,8-9,11-12,14,24H,4,6-7,19H2,1-3H3,(H2,20,26)(H,21,25)(H,22,27)(H,28,29)/t9-,11+,12-,14-,18+/m0/s1	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.90	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Isoleucyl-tRNA synthetase from rat liver				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Isoleucyl-tRNA synthetase (Rattus norvegicus)	BDBM50093003 ((4aR,6S,7R,7aS)-7-[2-((2S,3S)-2-Amino-3-methyl-pen...) Show SMILES CC[C@H](C)[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(O)=O |c:26| Show InChI InChI=1S/C19H31N5O8S/c1-4-9(2)15(20)17(28)23-33(31,32)8-14(26)22-19(18(29)30)12-7-24(3)6-11(16(21)27)10(12)5-13(19)25/h6,9-10,12-13,15,25H,4-5,7-8,20H2,1-3H3,(H2,21,27)(H,22,26)(H,23,28)(H,29,30)/t9-,10-,12+,13-,15-,19+/m0/s1	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	4.20	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Isoleucyl-tRNA synthetase from rat liver				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Isoleucine--tRNA ligase (Staphylococcus aureus)	BDBM50093003 ((4aR,6S,7R,7aS)-7-[2-((2S,3S)-2-Amino-3-methyl-pen...) Show SMILES CC[C@H](C)[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(O)=O |c:26| Show InChI InChI=1S/C19H31N5O8S/c1-4-9(2)15(20)17(28)23-33(31,32)8-14(26)22-19(18(29)30)12-7-24(3)6-11(16(21)27)10(12)5-13(19)25/h6,9-10,12-13,15,25H,4-5,7-8,20H2,1-3H3,(H2,21,27)(H,22,26)(H,23,28)(H,29,30)/t9-,10-,12+,13-,15-,19+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Isoleucyl-tRNA synthetase from staphylococcus aureus WCUH29				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Leucine--tRNA ligase, cytoplasmic (Homo sapiens (Human))	BDBM50093005 ((4aR,6S,7R,7aS)-7-[2-((S)-2-Amino-4-methyl-pentano...) Show SMILES CC(C)C[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(O)=O |c:26| Show InChI InChI=1S/C19H31N5O8S/c1-9(2)4-13(20)17(28)23-33(31,32)8-15(26)22-19(18(29)30)12-7-24(3)6-11(16(21)27)10(12)5-14(19)25/h6,9-10,12-14,25H,4-5,7-8,20H2,1-3H3,(H2,21,27)(H,22,26)(H,23,28)(H,29,30)/t10-,12+,13-,14-,19+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Leucyl-tRNA synthetase from staphylococcus aureus WCUH29				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Isoleucyl-tRNA synthetase (Rattus norvegicus)	BDBM50093004 ((4aR,6S,7R,7aS)-7-[2-((2S,3S)-2-Amino-3-methyl-pen...) Show SMILES CC[C@H](C)[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(=O)OC |c:26| Show InChI InChI=1S/C20H33N5O8S/c1-5-10(2)16(21)18(29)24-34(31,32)9-15(27)23-20(19(30)33-4)13-8-25(3)7-12(17(22)28)11(13)6-14(20)26/h7,10-11,13-14,16,26H,5-6,8-9,21H2,1-4H3,(H2,22,28)(H,23,27)(H,24,29)/t10-,11-,13+,14-,16-,20+/m0/s1	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Isoleucyl-tRNA synthetase from rat liver				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Isoleucyl-tRNA synthetase (Rattus norvegicus)	BDBM50093002 ((4aR,6S,7R,7aS)-7-[2-((2S,3S)-2-Amino-3-methyl-pen...) Show SMILES CC[C@H](C)[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(=O)OCc1ccccc1 |c:26| Show InChI InChI=1S/C26H37N5O8S/c1-4-15(2)22(27)24(35)30-40(37,38)14-21(33)29-26(25(36)39-13-16-8-6-5-7-9-16)19-12-31(3)11-18(23(28)34)17(19)10-20(26)32/h5-9,11,15,17,19-20,22,32H,4,10,12-14,27H2,1-3H3,(H2,28,34)(H,29,33)(H,30,35)/t15-,17-,19+,20-,22-,26+/m0/s1	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	25	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Isoleucyl-tRNA synthetase from rat liver				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Valine--tRNA ligase (Homo sapiens (Human))	BDBM50093001 ((4aR,6S,7R,7aS)-7-[2-((S)-2-Amino-3-methyl-butyryl...) Show SMILES CC(C)[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(O)=O |c:25| Show InChI InChI=1S/C18H29N5O8S/c1-8(2)14(19)16(27)22-32(30,31)7-13(25)21-18(17(28)29)11-6-23(3)5-10(15(20)26)9(11)4-12(18)24/h5,8-9,11-12,14,24H,4,6-7,19H2,1-3H3,(H2,20,26)(H,21,25)(H,22,27)(H,28,29)/t9-,11+,12-,14-,18+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against VRS (valyl tRNA synthetase) from staphylococcus aureus WCUH29				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Isoleucine--tRNA ligase (Staphylococcus aureus)	BDBM50093001 ((4aR,6S,7R,7aS)-7-[2-((S)-2-Amino-3-methyl-butyryl...) Show SMILES CC(C)[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(O)=O |c:25| Show InChI InChI=1S/C18H29N5O8S/c1-8(2)14(19)16(27)22-32(30,31)7-13(25)21-18(17(28)29)11-6-23(3)5-10(15(20)26)9(11)4-12(18)24/h5,8-9,11-12,14,24H,4,6-7,19H2,1-3H3,(H2,20,26)(H,21,25)(H,22,27)(H,28,29)/t9-,11+,12-,14-,18+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	37	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Isoleucyl-tRNA synthetase from staphylococcus aureus WCUH29				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Isoleucine--tRNA ligase (Staphylococcus aureus)	BDBM50093004 ((4aR,6S,7R,7aS)-7-[2-((2S,3S)-2-Amino-3-methyl-pen...) Show SMILES CC[C@H](C)[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(=O)OC |c:26| Show InChI InChI=1S/C20H33N5O8S/c1-5-10(2)16(21)18(29)24-34(31,32)9-15(27)23-20(19(30)33-4)13-8-25(3)7-12(17(22)28)11(13)6-14(20)26/h7,10-11,13-14,16,26H,5-6,8-9,21H2,1-4H3,(H2,22,28)(H,23,27)(H,24,29)/t10-,11-,13+,14-,16-,20+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank 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
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Isoleucyl-tRNA synthetase from staphylococcus aureus WCUH29				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Isoleucyl-tRNA synthetase (Rattus norvegicus)	BDBM50093005 ((4aR,6S,7R,7aS)-7-[2-((S)-2-Amino-4-methyl-pentano...) Show SMILES CC(C)C[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(O)=O |c:26| Show InChI InChI=1S/C19H31N5O8S/c1-9(2)4-13(20)17(28)23-33(31,32)8-15(26)22-19(18(29)30)12-7-24(3)6-11(16(21)27)10(12)5-14(19)25/h6,9-10,12-14,25H,4-5,7-8,20H2,1-3H3,(H2,21,27)(H,22,26)(H,23,28)(H,29,30)/t10-,12+,13-,14-,19+/m0/s1	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	68	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Isoleucyl-tRNA synthetase from rat liver				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Isoleucine--tRNA ligase (Staphylococcus aureus)	BDBM50093002 ((4aR,6S,7R,7aS)-7-[2-((2S,3S)-2-Amino-3-methyl-pen...) Show SMILES CC[C@H](C)[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(=O)OCc1ccccc1 |c:26| Show InChI InChI=1S/C26H37N5O8S/c1-4-15(2)22(27)24(35)30-40(37,38)14-21(33)29-26(25(36)39-13-16-8-6-5-7-9-16)19-12-31(3)11-18(23(28)34)17(19)10-20(26)32/h5-9,11,15,17,19-20,22,32H,4,10,12-14,27H2,1-3H3,(H2,28,34)(H,29,33)(H,30,35)/t15-,17-,19+,20-,22-,26+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank 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
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Isoleucyl-tRNA synthetase from staphylococcus aureus WCUH29				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Valine--tRNA ligase (Homo sapiens (Human))	BDBM50093003 ((4aR,6S,7R,7aS)-7-[2-((2S,3S)-2-Amino-3-methyl-pen...) Show SMILES CC[C@H](C)[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(O)=O |c:26| Show InChI InChI=1S/C19H31N5O8S/c1-4-9(2)15(20)17(28)23-33(31,32)8-14(26)22-19(18(29)30)12-7-24(3)6-11(16(21)27)10(12)5-13(19)25/h6,9-10,12-13,15,25H,4-5,7-8,20H2,1-3H3,(H2,21,27)(H,22,26)(H,23,28)(H,29,30)/t9-,10-,12+,13-,15-,19+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	126	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against VRS (valyl tRNA synthetase) from staphylococcus aureus WCUH29				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Valine--tRNA ligase (Homo sapiens (Human))	BDBM50093005 ((4aR,6S,7R,7aS)-7-[2-((S)-2-Amino-4-methyl-pentano...) Show SMILES CC(C)C[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(O)=O |c:26| Show InChI InChI=1S/C19H31N5O8S/c1-9(2)4-13(20)17(28)23-33(31,32)8-15(26)22-19(18(29)30)12-7-24(3)6-11(16(21)27)10(12)5-14(19)25/h6,9-10,12-14,25H,4-5,7-8,20H2,1-3H3,(H2,21,27)(H,22,26)(H,23,28)(H,29,30)/t10-,12+,13-,14-,19+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	290	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against VRS (valyl tRNA synthetase) from staphylococcus aureus WCUH29				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Isoleucyl-tRNA synthetase (Rattus norvegicus)	BDBM50093006 ((4aR,6S,7R,7aS)-6-((2S,3S)-2-Benzyloxycarbonylamin...) Show SMILES CC[C@H](C)[C@H](NC(=O)OCc1ccccc1)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@H](C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)OC(=O)[C@@H](NC(=O)OCc1ccccc1)[C@@H](C)CC)C(=O)OC |c:36| Show InChI InChI=1S/C42H56N6O13S/c1-7-25(3)34(44-40(54)59-22-27-15-11-9-12-16-27)37(51)47-62(56,57)24-33(49)46-42(39(53)58-6)31-21-48(5)20-30(36(43)50)29(31)19-32(42)61-38(52)35(26(4)8-2)45-41(55)60-23-28-17-13-10-14-18-28/h9-18,20,25-26,29,31-32,34-35H,7-8,19,21-24H2,1-6H3,(H2,43,50)(H,44,54)(H,45,55)(H,46,49)(H,47,51)/t25-,26-,29-,31+,32-,34-,35-,42+/m0/s1	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Isoleucyl-tRNA synthetase from rat liver				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Isoleucine--tRNA ligase (Staphylococcus aureus)	BDBM50093005 ((4aR,6S,7R,7aS)-7-[2-((S)-2-Amino-4-methyl-pentano...) Show SMILES CC(C)C[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(O)=O |c:26| Show InChI InChI=1S/C19H31N5O8S/c1-9(2)4-13(20)17(28)23-33(31,32)8-15(26)22-19(18(29)30)12-7-24(3)6-11(16(21)27)10(12)5-14(19)25/h6,9-10,12-14,25H,4-5,7-8,20H2,1-3H3,(H2,21,27)(H,22,26)(H,23,28)(H,29,30)/t10-,12+,13-,14-,19+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	910	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Isoleucyl-tRNA synthetase from staphylococcus aureus WCUH29				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Leucine--tRNA ligase, cytoplasmic (Homo sapiens (Human))	BDBM50093003 ((4aR,6S,7R,7aS)-7-[2-((2S,3S)-2-Amino-3-methyl-pen...) Show SMILES CC[C@H](C)[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(O)=O |c:26| Show InChI InChI=1S/C19H31N5O8S/c1-4-9(2)15(20)17(28)23-33(31,32)8-14(26)22-19(18(29)30)12-7-24(3)6-11(16(21)27)10(12)5-13(19)25/h6,9-10,12-13,15,25H,4-5,7-8,20H2,1-3H3,(H2,21,27)(H,22,26)(H,23,28)(H,29,30)/t9-,10-,12+,13-,15-,19+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.55E+3	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Leucyl-tRNA synthetase from staphylococcus aureus WCUH29				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401749 (CHEMBL2207130) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H](N)CSSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC1=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)OCC(O)=O |r| Show InChI InChI=1S/C52H73N11O15S2/c1-5-28(4)43-50(75)56-33(17-18-40(54)65)45(70)58-36(23-41(55)66)47(72)61-38(26-80-79-25-32(53)44(69)57-35(48(73)62-43)21-30-13-15-31(64)16-14-30)51(76)63-19-9-12-39(63)49(74)59-34(20-27(2)3)46(71)60-37(52(77)78-24-42(67)68)22-29-10-7-6-8-11-29/h6-8,10-11,13-16,27-28,32-39,43,64H,5,9,12,17-26,53H2,1-4H3,(H2,54,65)(H2,55,66)(H,56,75)(H,57,69)(H,58,70)(H,59,74)(H,60,71)(H,61,72)(H,62,73)(H,67,68)/t28-,32-,33-,34-,35-,36-,37-,38-,39-,43-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Leucine--tRNA ligase, cytoplasmic (Homo sapiens (Human))	BDBM50093001 ((4aR,6S,7R,7aS)-7-[2-((S)-2-Amino-3-methyl-butyryl...) Show SMILES CC(C)[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(O)=O |c:25| Show InChI InChI=1S/C18H29N5O8S/c1-8(2)14(19)16(27)22-32(30,31)7-13(25)21-18(17(28)29)11-6-23(3)5-10(15(20)26)9(11)4-12(18)24/h5,8-9,11-12,14,24H,4,6-7,19H2,1-3H3,(H2,20,26)(H,21,25)(H,22,27)(H,28,29)/t9-,11+,12-,14-,18+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Leucyl-tRNA synthetase from staphylococcus aureus WCUH29				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401751 (CHEMBL2207128) Show SMILES CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](Cc1ccccc1)C(=O)OCC(O)=O |r| Show InChI InChI=1S/C19H26N2O6/c1-12(2)9-15(20-13(3)22)18(25)21-16(19(26)27-11-17(23)24)10-14-7-5-4-6-8-14/h4-8,12,15-16H,9-11H2,1-3H3,(H,20,22)(H,21,25)(H,23,24)/t15-,16-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Isoleucine--tRNA ligase (Staphylococcus aureus)	BDBM50093008 ((4aR,6S,7R,7aS)-4-Carbamoyl-6-hydroxy-2-methyl-7-[...) Show SMILES CC[C@H](C)CC(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(O)=O |c:25| Show InChI InChI=1S/C19H30N4O8S/c1-4-10(2)5-15(25)22-32(30,31)9-16(26)21-19(18(28)29)13-8-23(3)7-12(17(20)27)11(13)6-14(19)24/h7,10-11,13-14,24H,4-6,8-9H2,1-3H3,(H2,20,27)(H,21,26)(H,22,25)(H,28,29)/t10-,11-,13+,14-,19+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.27E+3	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Isoleucyl-tRNA synthetase from staphylococcus aureus WCUH29				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401752 (CHEMBL2207127) Show SMILES CC(=O)N[C@@H](Cc1ccccc1)C(=O)OCC(O)=O |r| Show InChI InChI=1S/C13H15NO5/c1-9(15)14-11(13(18)19-8-12(16)17)7-10-5-3-2-4-6-10/h2-6,11H,7-8H2,1H3,(H,14,15)(H,16,17)/t11-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401750 (CHEMBL2207129) Show SMILES CC(C)C[C@H](NC(=O)[C@@H]1CCCN1C(C)=O)C(=O)N[C@@H](Cc1ccccc1)C(=O)OCC(O)=O |r| Show InChI InChI=1S/C24H33N3O7/c1-15(2)12-18(25-23(32)20-10-7-11-27(20)16(3)28)22(31)26-19(24(33)34-14-21(29)30)13-17-8-5-4-6-9-17/h4-6,8-9,15,18-20H,7,10-14H2,1-3H3,(H,25,32)(H,26,31)(H,29,30)/t18-,19-,20-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Isoleucyl-tRNA synthetase (Rattus norvegicus)	BDBM50093007 ((4aR,6S,7R,7aS)-4-Carbamoyl-2-methyl-6-((S)-3-meth...) Show SMILES CC[C@H](C)CC(=O)NS(=O)(=O)CC(=O)N[C@]1([C@H](C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)OC(=O)C[C@@H](C)CC)C(O)=O |c:24| Show InChI InChI=1S/C25H40N4O9S/c1-6-14(3)8-20(30)28-39(36,37)13-21(31)27-25(24(34)35)18-12-29(5)11-17(23(26)33)16(18)10-19(25)38-22(32)9-15(4)7-2/h11,14-16,18-19H,6-10,12-13H2,1-5H3,(H2,26,33)(H,27,31)(H,28,30)(H,34,35)/t14-,15-,16-,18+,19-,25+/m0/s1	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	6.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Isoleucyl-tRNA synthetase from rat liver				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401751 (CHEMBL2207128) Show SMILES CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](Cc1ccccc1)C(=O)OCC(O)=O |r| Show InChI InChI=1S/C19H26N2O6/c1-12(2)9-15(20-13(3)22)18(25)21-16(19(26)27-11-17(23)24)10-14-7-5-4-6-8-14/h4-8,12,15-16H,9-11H2,1-3H3,(H,20,22)(H,21,25)(H,23,24)/t15-,16-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of secreted PAM in human DMS53 cell culture medium using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401752 (CHEMBL2207127) Show SMILES CC(=O)N[C@@H](Cc1ccccc1)C(=O)OCC(O)=O |r| Show InChI InChI=1S/C13H15NO5/c1-9(15)14-11(13(18)19-8-12(16)17)7-10-5-3-2-4-6-10/h2-6,11H,7-8H2,1H3,(H,14,15)(H,16,17)/t11-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of secreted PAM in human DMS53 cell culture medium using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401756 (CHEMBL2207143) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H](N)CSSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC1=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)OCC(O)=O |r| Show InChI InChI=1S/C45H67N11O15S2/c1-5-23(4)37-44(69)50-27(12-13-33(47)58)40(65)52-30(17-34(48)59)41(66)54-31(21-73-72-20-26(46)38(63)51-29(42(67)55-37)16-24-8-10-25(57)11-9-24)45(70)56-14-6-7-32(56)43(68)53-28(15-22(2)3)39(64)49-18-36(62)71-19-35(60)61/h8-11,22-23,26-32,37,57H,5-7,12-21,46H2,1-4H3,(H2,47,58)(H2,48,59)(H,49,64)(H,50,69)(H,51,63)(H,52,65)(H,53,68)(H,54,66)(H,55,67)(H,60,61)/t23-,26-,27-,28-,29-,30-,31-,32-,37-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Isoleucine--tRNA ligase (Staphylococcus aureus)	BDBM50093007 ((4aR,6S,7R,7aS)-4-Carbamoyl-2-methyl-6-((S)-3-meth...) Show SMILES CC[C@H](C)CC(=O)NS(=O)(=O)CC(=O)N[C@]1([C@H](C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)OC(=O)C[C@@H](C)CC)C(O)=O |c:24| Show InChI InChI=1S/C25H40N4O9S/c1-6-14(3)8-20(30)28-39(36,37)13-21(31)27-25(24(34)35)18-12-29(5)11-17(23(26)33)16(18)10-19(25)38-22(32)9-15(4)7-2/h11,14-16,18-19H,6-10,12-13H2,1-5H3,(H2,26,33)(H,27,31)(H,28,30)(H,34,35)/t14-,15-,16-,18+,19-,25+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.46E+4	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Isoleucyl-tRNA synthetase from staphylococcus aureus WCUH29				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Isoleucyl-tRNA synthetase (Rattus norvegicus)	BDBM50093008 ((4aR,6S,7R,7aS)-4-Carbamoyl-6-hydroxy-2-methyl-7-[...) Show SMILES CC[C@H](C)CC(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(O)=O |c:25| Show InChI InChI=1S/C19H30N4O8S/c1-4-10(2)5-15(25)22-32(30,31)9-16(26)21-19(18(28)29)13-8-23(3)7-12(17(20)27)11(13)6-14(19)24/h7,10-11,13-14,24H,4-6,8-9H2,1-3H3,(H2,20,27)(H,21,26)(H,22,25)(H,28,29)/t10-,11-,13+,14-,19+/m0/s1	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.23E+4	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Isoleucyl-tRNA synthetase from rat liver				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401749 (CHEMBL2207130) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H](N)CSSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC1=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)OCC(O)=O |r| Show InChI InChI=1S/C52H73N11O15S2/c1-5-28(4)43-50(75)56-33(17-18-40(54)65)45(70)58-36(23-41(55)66)47(72)61-38(26-80-79-25-32(53)44(69)57-35(48(73)62-43)21-30-13-15-31(64)16-14-30)51(76)63-19-9-12-39(63)49(74)59-34(20-27(2)3)46(71)60-37(52(77)78-24-42(67)68)22-29-10-7-6-8-11-29/h6-8,10-11,13-16,27-28,32-39,43,64H,5,9,12,17-26,53H2,1-4H3,(H2,54,65)(H2,55,66)(H,56,75)(H,57,69)(H,58,70)(H,59,74)(H,60,71)(H,61,72)(H,62,73)(H,67,68)/t28-,32-,33-,34-,35-,36-,37-,38-,39-,43-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of secreted PAM in human DMS53 cell culture medium using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401750 (CHEMBL2207129) Show SMILES CC(C)C[C@H](NC(=O)[C@@H]1CCCN1C(C)=O)C(=O)N[C@@H](Cc1ccccc1)C(=O)OCC(O)=O |r| Show InChI InChI=1S/C24H33N3O7/c1-15(2)12-18(25-23(32)20-10-7-11-27(20)16(3)28)22(31)26-19(24(33)34-14-21(29)30)13-17-8-5-4-6-9-17/h4-6,8-9,15,18-20H,7,10-14H2,1-3H3,(H,25,32)(H,26,31)(H,29,30)/t18-,19-,20-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of secreted PAM in human DMS53 cell culture medium using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401756 (CHEMBL2207143) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H](N)CSSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC1=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)OCC(O)=O |r| Show InChI InChI=1S/C45H67N11O15S2/c1-5-23(4)37-44(69)50-27(12-13-33(47)58)40(65)52-30(17-34(48)59)41(66)54-31(21-73-72-20-26(46)38(63)51-29(42(67)55-37)16-24-8-10-25(57)11-9-24)45(70)56-14-6-7-32(56)43(68)53-28(15-22(2)3)39(64)49-18-36(62)71-19-35(60)61/h8-11,22-23,26-32,37,57H,5-7,12-21,46H2,1-4H3,(H2,47,58)(H2,48,59)(H,49,64)(H,50,69)(H,51,63)(H,52,65)(H,53,68)(H,54,66)(H,55,67)(H,60,61)/t23-,26-,27-,28-,29-,30-,31-,32-,37-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of secreted PAM in human DMS53 cell culture medium using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401757 (CHEMBL2207142) Show SMILES CC(C)C[C@H](OC(=O)[C@@H]1CCCN1C(C)=O)C(=O)NCC(=O)OCC(O)=O |r| Show InChI InChI=1S/C17H26N2O8/c1-10(2)7-13(16(24)18-8-15(23)26-9-14(21)22)27-17(25)12-5-4-6-19(12)11(3)20/h10,12-13H,4-9H2,1-3H3,(H,18,24)(H,21,22)/t12-,13-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	7.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401758 (CHEMBL2207141) Show SMILES CC(C)C[C@H](NC(C)=O)C(=O)NCC(=O)OCC(O)=O |r| Show InChI InChI=1S/C12H20N2O6/c1-7(2)4-9(14-8(3)15)12(19)13-5-11(18)20-6-10(16)17/h7,9H,4-6H2,1-3H3,(H,13,19)(H,14,15)(H,16,17)/t9-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.20E+5	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401746 (CHEMBL2207133) Show SMILES C[C@H](NC(=O)CN)C(=O)N[C@@H](Cc1ccccc1)C(=O)OCC(O)=O |r| Show InChI InChI=1S/C16H21N3O6/c1-10(18-13(20)8-17)15(23)19-12(16(24)25-9-14(21)22)7-11-5-3-2-4-6-11/h2-6,10,12H,7-9,17H2,1H3,(H,18,20)(H,19,23)(H,21,22)/t10-,12-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.60E+5	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of secreted PAM in human DMS53 cell culture medium using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401757 (CHEMBL2207142) Show SMILES CC(C)C[C@H](OC(=O)[C@@H]1CCCN1C(C)=O)C(=O)NCC(=O)OCC(O)=O |r| Show InChI InChI=1S/C17H26N2O8/c1-10(2)7-13(16(24)18-8-15(23)26-9-14(21)22)27-17(25)12-5-4-6-19(12)11(3)20/h10,12-13H,4-9H2,1-3H3,(H,18,24)(H,21,22)/t12-,13-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.80E+5	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of secreted PAM in human DMS53 cell culture medium using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Leucine--tRNA ligase, cytoplasmic (Homo sapiens (Human))	BDBM50093004 ((4aR,6S,7R,7aS)-7-[2-((2S,3S)-2-Amino-3-methyl-pen...) Show SMILES CC[C@H](C)[C@H](N)C(=O)NS(=O)(=O)CC(=O)N[C@]1([C@@H](O)C[C@@H]2[C@H]1CN(C)C=C2C(N)=O)C(=O)OC |c:26| Show InChI InChI=1S/C20H33N5O8S/c1-5-10(2)16(21)18(29)24-34(31,32)9-15(27)23-20(19(30)33-4)13-8-25(3)7-12(17(22)28)11(13)6-14(20)26/h7,10-11,13-14,16,26H,5-6,8-9,21H2,1-4H3,(H2,22,28)(H,23,27)(H,24,29)/t10-,11-,13+,14-,16-,20+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.86E+5	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against Leucyl-tRNA synthetase from staphylococcus aureus WCUH29				Bioorg Med Chem Lett 10: 2263-6 (2001) BindingDB Entry DOI: 10.7270/Q2PN94W3
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401758 (CHEMBL2207141) Show SMILES CC(C)C[C@H](NC(C)=O)C(=O)NCC(=O)OCC(O)=O |r| Show InChI InChI=1S/C12H20N2O6/c1-7(2)4-9(14-8(3)15)12(19)13-5-11(18)20-6-10(16)17/h7,9H,4-6H2,1-3H3,(H,13,19)(H,14,15)(H,16,17)/t9-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of secreted PAM in human DMS53 cell culture medium using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401759 (CHEMBL2207140) Show SMILES CC(=O)NCC(=O)OCC(O)=O Show InChI InChI=1S/C6H9NO5/c1-4(8)7-2-6(11)12-3-5(9)10/h2-3H2,1H3,(H,7,8)(H,9,10)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.10E+5	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401754 (CHEMBL2207145) Show SMILES C[C@H](N)C(=O)N1CCC[C@H]1C(=O)OCC(O)=O |r| Show InChI InChI=1S/C10H16N2O5/c1-6(11)9(15)12-4-2-3-7(12)10(16)17-5-8(13)14/h6-7H,2-5,11H2,1H3,(H,13,14)/t6-,7-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.90E+5	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of secreted PAM in human DMS53 cell culture medium using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401747 (CHEMBL2207132) Show SMILES C[C@H](N)C(=O)N[C@@H](Cc1ccccc1)C(=O)OCC(O)=O |r| Show InChI InChI=1S/C14H18N2O5/c1-9(15)13(19)16-11(14(20)21-8-12(17)18)7-10-5-3-2-4-6-10/h2-6,9,11H,7-8,15H2,1H3,(H,16,19)(H,17,18)/t9-,11-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401747 (CHEMBL2207132) Show SMILES C[C@H](N)C(=O)N[C@@H](Cc1ccccc1)C(=O)OCC(O)=O |r| Show InChI InChI=1S/C14H18N2O5/c1-9(15)13(19)16-11(14(20)21-8-12(17)18)7-10-5-3-2-4-6-10/h2-6,9,11H,7-8,15H2,1H3,(H,16,19)(H,17,18)/t9-,11-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.70E+5	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of secreted PAM in human DMS53 cell culture medium using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401754 (CHEMBL2207145) Show SMILES C[C@H](N)C(=O)N1CCC[C@H]1C(=O)OCC(O)=O |r| Show InChI InChI=1S/C10H16N2O5/c1-6(11)9(15)12-4-2-3-7(12)10(16)17-5-8(13)14/h6-7H,2-5,11H2,1H3,(H,13,14)/t6-,7-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.70E+5	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401755 (CHEMBL2207144) Show SMILES OC(=O)COC(=O)[C@@H]1CCCN1 |r| Show InChI InChI=1S/C7H11NO4/c9-6(10)4-12-7(11)5-2-1-3-8-5/h5,8H,1-4H2,(H,9,10)/t5-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of secreted PAM in human DMS53 cell culture medium using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401746 (CHEMBL2207133) Show SMILES C[C@H](NC(=O)CN)C(=O)N[C@@H](Cc1ccccc1)C(=O)OCC(O)=O |r| Show InChI InChI=1S/C16H21N3O6/c1-10(18-13(20)8-17)15(23)19-12(16(24)25-9-14(21)22)7-11-5-3-2-4-6-11/h2-6,10,12H,7-9,17H2,1H3,(H,18,20)(H,19,23)(H,21,22)/t10-,12-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.60E+5	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401755 (CHEMBL2207144) Show SMILES OC(=O)COC(=O)[C@@H]1CCCN1 |r| Show InChI InChI=1S/C7H11NO4/c9-6(10)4-12-7(11)5-2-1-3-8-5/h5,8H,1-4H2,(H,9,10)/t5-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401753 (CHEMBL2207146) Show SMILES C[C@H](NC(=O)CN)C(=O)N1CCC[C@H]1C(=O)OCC(O)=O |r| Show InChI InChI=1S/C12H19N3O6/c1-7(14-9(16)5-13)11(19)15-4-2-3-8(15)12(20)21-6-10(17)18/h7-8H,2-6,13H2,1H3,(H,14,16)(H,17,18)/t7-,8-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.80E+5	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM82195 (Substrate analogue, 13) Show SMILES CC(=O)OCC(O)=O Show InChI InChI=1S/C4H6O4/c1-3(5)8-2-4(6)7/h2H2,1H3,(H,6,7)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	1.10E+6	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM82195 (Substrate analogue, 13) Show SMILES CC(=O)OCC(O)=O Show InChI InChI=1S/C4H6O4/c1-3(5)8-2-4(6)7/h2H2,1H3,(H,6,7)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	1.10E+6	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of secreted PAM in human DMS53 cell culture medium using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401748 (CHEMBL2207131) Show SMILES N[C@@H](Cc1ccccc1)C(=O)OCC(O)=O |r| Show InChI InChI=1S/C11H13NO4/c12-9(11(15)16-7-10(13)14)6-8-4-2-1-3-5-8/h1-5,9H,6-7,12H2,(H,13,14)/t9-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.10E+6	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401753 (CHEMBL2207146) Show SMILES C[C@H](NC(=O)CN)C(=O)N1CCC[C@H]1C(=O)OCC(O)=O |r| Show InChI InChI=1S/C12H19N3O6/c1-7(14-9(16)5-13)11(19)15-4-2-3-8(15)12(20)21-6-10(17)18/h7-8H,2-6,13H2,1H3,(H,14,16)(H,17,18)/t7-,8-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.10E+6	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of secreted PAM in human DMS53 cell culture medium using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair

Displayed 1 to 50 (of 52 total )  |  Next  |  Last  >>

Jump to: