Compile Data Set for Download or QSAR

Found 39 hits with Last Name = 'tatsumi' and Initial = 't'   

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
Nitric oxide synthase, inducible (Mus musculus (mouse))	BDBM50116666 (4-Methyl-3,6-dihydro-1H-pyridin-(2Z)-ylideneamine ...) Show SMILES CC1=CC(N)=NCC1 |c:4,t:1| Show InChI InChI=1S/C6H10N2/c1-5-2-3-8-6(7)4-5/h4H,2-3H2,1H3,(H2,7,8)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	22	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description The concentration required for inhibition of Inducible nitric oxide synthase in mouse				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, inducible (Mus musculus (mouse))	BDBM50116674 (6-Allyl-4-methyl-5,6-dihydro-1H-pyridin-(2Z)-ylide...) Show SMILES CC1=CC(N)=NC(CC=C)C1 |c:4,t:1| Show InChI InChI=1S/C9H14N2/c1-3-4-8-5-7(2)6-9(10)11-8/h3,6,8H,1,4-5H2,2H3,(H2,10,11)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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
Fukui Research Institute Curated by ChEMBL					Assay Description The concentration required for inhibition of Inducible nitric oxide synthase in mouse				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, inducible (Homo sapiens (Human))	BDBM50116674 (6-Allyl-4-methyl-5,6-dihydro-1H-pyridin-(2Z)-ylide...) Show SMILES CC1=CC(N)=NC(CC=C)C1 |c:4,t:1| Show InChI InChI=1S/C9H14N2/c1-3-4-8-5-7(2)6-9(10)11-8/h3,6,8H,1,4-5H2,2H3,(H2,10,11)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia 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
Fukui Research Institute Curated by ChEMBL					Assay Description Concentration required to inhibit human Inducible nitric oxide synthase over expressed in A549 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, inducible (Homo sapiens (Human))	BDBM50116668 (4-Methyl-6-propyl-5,6-dihydro-1H-pyridin-(2Z)-ylid...) Show SMILES CCCC1CC(C)=CC(N)=N1 |c:6,9| Show InChI InChI=1S/C9H16N2/c1-3-4-8-5-7(2)6-9(10)11-8/h6,8H,3-5H2,1-2H3,(H2,10,11)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia 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
Fukui Research Institute Curated by ChEMBL					Assay Description Concentration required to inhibit human Inducible nitric oxide synthase over expressed in A549 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, inducible (Mus musculus (mouse))	BDBM50116668 (4-Methyl-6-propyl-5,6-dihydro-1H-pyridin-(2Z)-ylid...) Show SMILES CCCC1CC(C)=CC(N)=N1 |c:6,9| Show InChI InChI=1S/C9H16N2/c1-3-4-8-5-7(2)6-9(10)11-8/h6,8H,3-5H2,1-2H3,(H2,10,11)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	100	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description The concentration required for inhibition of Inducible nitric oxide synthase in mouse				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, inducible (Mus musculus (mouse))	BDBM50116667 (4,5,5-Trimethyl-5,6-dihydro-1H-pyridin-(2Z)-yliden...) Show SMILES CC1=CC(N)=NCC1(C)C |c:4,t:1| Show InChI InChI=1S/C8H14N2/c1-6-4-7(9)10-5-8(6,2)3/h4H,5H2,1-3H3,(H2,9,10)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	100	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description The concentration required for inhibition of Inducible nitric oxide synthase in mouse				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, inducible (Homo sapiens (Human))	BDBM50116670 ((4aR,7aR)-4-Methyl-1,4a,5,6,7,7a-hexahydro-[1]pyri...) Show SMILES CC1=CC(N)=N[C@@H]2CCC[C@H]12 |c:4,t:1| Show InChI InChI=1S/C9H14N2/c1-6-5-9(10)11-8-4-2-3-7(6)8/h5,7-8H,2-4H2,1H3,(H2,10,11)/t7-,8-/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	170	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Concentration required to inhibit human Inducible nitric oxide synthase over expressed in A549 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, inducible (Homo sapiens (Human))	BDBM50116676 (4,6-Dimethyl-5,6-dihydro-1H-pyridin-(2Z)-ylideneam...) Show SMILES CC1CC(C)=CC(N)=N1 |c:4,7| Show InChI InChI=1S/C7H12N2/c1-5-3-6(2)9-7(8)4-5/h4,6H,3H2,1-2H3,(H2,8,9)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	180	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Concentration required to inhibit Inducible nitric oxide synthase over expressed in A549 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, inducible (Homo sapiens (Human))	BDBM50116666 (4-Methyl-3,6-dihydro-1H-pyridin-(2Z)-ylideneamine ...) Show SMILES CC1=CC(N)=NCC1 |c:4,t:1| Show InChI InChI=1S/C6H10N2/c1-5-2-3-8-6(7)4-5/h4H,2-3H2,1H3,(H2,7,8)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase 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
Fukui Research Institute Curated by ChEMBL					Assay Description Inhibition of human endothelial Nitric Oxide Synthase expressed in Sf-21 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, endothelial (Homo sapiens (Human))	BDBM50116666 (4-Methyl-3,6-dihydro-1H-pyridin-(2Z)-ylideneamine ...) Show SMILES CC1=CC(N)=NCC1 |c:4,t:1| Show InChI InChI=1S/C6H10N2/c1-5-2-3-8-6(7)4-5/h4H,2-3H2,1H3,(H2,7,8)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	230	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Concentration required to inhibit human Inducible nitric oxide synthase over expressed in A549 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, endothelial (Homo sapiens (Human))	BDBM50116676 (4,6-Dimethyl-5,6-dihydro-1H-pyridin-(2Z)-ylideneam...) Show SMILES CC1CC(C)=CC(N)=N1 |c:4,7| Show InChI InChI=1S/C7H12N2/c1-5-3-6(2)9-7(8)4-5/h4,6H,3H2,1-2H3,(H2,8,9)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	240	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Inhibition of human endothelial Nitric Oxide Synthase expressed in Sf-21 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, inducible (Homo sapiens (Human))	BDBM50116673 (3,4-Dimethyl-5,6-dihydro-1H-pyridin-(2Z)-ylideneam...) Show SMILES CC1=C(C)C(N)=NCC1 |c:1,5| Show InChI InChI=1S/C7H12N2/c1-5-3-4-9-7(8)6(5)2/h3-4H2,1-2H3,(H2,8,9)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia 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
Fukui Research Institute Curated by ChEMBL					Assay Description Concentration required to inhibit human Inducible nitric oxide synthase over expressed in A549 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, endothelial (Homo sapiens (Human))	BDBM50116673 (3,4-Dimethyl-5,6-dihydro-1H-pyridin-(2Z)-ylideneam...) Show SMILES CC1=C(C)C(N)=NCC1 |c:1,5| Show InChI InChI=1S/C7H12N2/c1-5-3-4-9-7(8)6(5)2/h3-4H2,1-2H3,(H2,8,9)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	320	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Inhibition of human endothelial Nitric Oxide Synthase expressed in Sf-21 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, endothelial (Homo sapiens (Human))	BDBM50116674 (6-Allyl-4-methyl-5,6-dihydro-1H-pyridin-(2Z)-ylide...) Show SMILES CC1=CC(N)=NC(CC=C)C1 |c:4,t:1| Show InChI InChI=1S/C9H14N2/c1-3-4-8-5-7(2)6-9(10)11-8/h3,6,8H,1,4-5H2,2H3,(H2,10,11)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	360	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Inhibition of human endothelial Nitric Oxide Synthase expressed in Sf-21 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, inducible (Homo sapiens (Human))	BDBM50116667 (4,5,5-Trimethyl-5,6-dihydro-1H-pyridin-(2Z)-yliden...) Show SMILES CC1=CC(N)=NCC1(C)C |c:4,t:1| Show InChI InChI=1S/C8H14N2/c1-6-4-7(9)10-5-8(6,2)3/h4H,5H2,1-3H3,(H2,9,10)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	420	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Concentration required to inhibit human Inducible nitric oxide synthase over expressed in A549 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, endothelial (Homo sapiens (Human))	BDBM50116666 (4-Methyl-3,6-dihydro-1H-pyridin-(2Z)-ylideneamine ...) Show SMILES CC1=CC(N)=NCC1 |c:4,t:1| Show InChI InChI=1S/C6H10N2/c1-5-2-3-8-6(7)4-5/h4H,2-3H2,1H3,(H2,7,8)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	440	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Inhibition of human endothelial Nitric Oxide Synthase expressed in Sf-21 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, endothelial (Homo sapiens (Human))	BDBM50116670 ((4aR,7aR)-4-Methyl-1,4a,5,6,7,7a-hexahydro-[1]pyri...) Show SMILES CC1=CC(N)=N[C@@H]2CCC[C@H]12 |c:4,t:1| Show InChI InChI=1S/C9H14N2/c1-6-5-9(10)11-8-4-2-3-7(6)8/h5,7-8H,2-4H2,1H3,(H2,10,11)/t7-,8-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	510	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Inhibition of human endothelial Nitric Oxide Synthase expressed in Sf-21 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, inducible (Homo sapiens (Human))	BDBM50116675 (4,5-Dimethyl-5,6-dihydro-1H-pyridin-(2Z)-ylideneam...) Show SMILES CC1CN=C(N)C=C1C |c:6,t:3| Show InChI InChI=1S/C7H12N2/c1-5-3-7(8)9-4-6(5)2/h3,6H,4H2,1-2H3,(H2,8,9)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	510	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Concentration required to inhibit Inducible nitric oxide synthase over expressed in A549 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, endothelial (Homo sapiens (Human))	BDBM50116675 (4,5-Dimethyl-5,6-dihydro-1H-pyridin-(2Z)-ylideneam...) Show SMILES CC1CN=C(N)C=C1C |c:6,t:3| Show InChI InChI=1S/C7H12N2/c1-5-3-7(8)9-4-6(5)2/h3,6H,4H2,1-2H3,(H2,8,9)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	520	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Inhibition of human endothelial Nitric Oxide Synthase expressed in Sf-21 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, endothelial (Homo sapiens (Human))	BDBM50116668 (4-Methyl-6-propyl-5,6-dihydro-1H-pyridin-(2Z)-ylid...) Show SMILES CCCC1CC(C)=CC(N)=N1 |c:6,9| Show InChI InChI=1S/C9H16N2/c1-3-4-8-5-7(2)6-9(10)11-8/h6,8H,3-5H2,1-2H3,(H2,10,11)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	580	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Inhibition of human endothelial Nitric Oxide Synthase expressed in Sf-21 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, inducible (Homo sapiens (Human))	BDBM50116666 (4-Methyl-3,6-dihydro-1H-pyridin-(2Z)-ylideneamine ...) Show SMILES CC1=CC(N)=NCC1 |c:4,t:1| Show InChI InChI=1S/C6H10N2/c1-5-2-3-8-6(7)4-5/h4H,2-3H2,1H3,(H2,7,8)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	700	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Concentration required to inhibit human Inducible nitric oxide synthase over expressed in A549 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, inducible (Homo sapiens (Human))	BDBM50237936 (4-Ethyl-5,6-dihydro-1H-pyridin-(2Z)-ylideneamine |...) Show SMILES CCC1=CC(N)=NCC1 |c:5,t:2| Show InChI InChI=1S/C7H12N2/c1-2-6-3-4-9-7(8)5-6/h5H,2-4H2,1H3,(H2,8,9)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Concentration required to inhibit human Inducible nitric oxide synthase over expressed in A549 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, inducible (Homo sapiens (Human))	BDBM50116677 ((4aR,8aR)-4-Methyl-4a,5,6,7,8,8a-hexahydro-1H-quin...) Show SMILES CC1=CC(N)=N[C@@H]2CCCC[C@H]12 |c:4,t:1| Show InChI InChI=1S/C10H16N2/c1-7-6-10(11)12-9-5-3-2-4-8(7)9/h6,8-9H,2-5H2,1H3,(H2,11,12)/t8-,9-/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Concentration required to inhibit human Inducible nitric oxide synthase over expressed in A549 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, endothelial (Homo sapiens (Human))	BDBM50237936 (4-Ethyl-5,6-dihydro-1H-pyridin-(2Z)-ylideneamine |...) Show SMILES CCC1=CC(N)=NCC1 |c:5,t:2| Show InChI InChI=1S/C7H12N2/c1-2-6-3-4-9-7(8)5-6/h5H,2-4H2,1H3,(H2,8,9)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Inhibition of human endothelial Nitric Oxide Synthase expressed in Sf-21 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, endothelial (Homo sapiens (Human))	BDBM50116667 (4,5,5-Trimethyl-5,6-dihydro-1H-pyridin-(2Z)-yliden...) Show SMILES CC1=CC(N)=NCC1(C)C |c:4,t:1| Show InChI InChI=1S/C8H14N2/c1-6-4-7(9)10-5-8(6,2)3/h4H,5H2,1-3H3,(H2,9,10)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Inhibition of human endothelial Nitric Oxide Synthase expressed in Sf-21 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, inducible (Homo sapiens (Human))	BDBM50116669 (5,5-Dimethyl-5,6-dihydro-1H-pyridin-(2Z)-ylideneam...) Show SMILES CC1(C)CN=C(N)C=C1 |c:7,t:4| Show InChI InChI=1S/C7H12N2/c1-7(2)4-3-6(8)9-5-7/h3-4H,5H2,1-2H3,(H2,8,9)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	2.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Concentration required to inhibit human Inducible nitric oxide synthase over expressed in A549 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, endothelial (Homo sapiens (Human))	BDBM50116677 ((4aR,8aR)-4-Methyl-4a,5,6,7,8,8a-hexahydro-1H-quin...) Show SMILES CC1=CC(N)=N[C@@H]2CCCC[C@H]12 |c:4,t:1| Show InChI InChI=1S/C10H16N2/c1-7-6-10(11)12-9-5-3-2-4-8(7)9/h6,8-9H,2-5H2,1H3,(H2,11,12)/t8-,9-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Inhibition of human endothelial Nitric Oxide Synthase expressed in Sf-21 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Nitric oxide synthase, endothelial (Homo sapiens (Human))	BDBM50116669 (5,5-Dimethyl-5,6-dihydro-1H-pyridin-(2Z)-ylideneam...) Show SMILES CC1(C)CN=C(N)C=C1 |c:7,t:4| Show InChI InChI=1S/C7H12N2/c1-7(2)4-3-6(8)9-5-7/h3-4H,5H2,1-2H3,(H2,8,9)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	3.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Fukui Research Institute Curated by ChEMBL					Assay Description Inhibition of human endothelial Nitric Oxide Synthase expressed in Sf-21 cells				Bioorg Med Chem Lett 12: 2291-4 (2002) BindingDB Entry DOI: 10.7270/Q2M32V3P
					More data for this Ligand-Target Pair
Protease (Human T-cell leukemia virus type I)	BDBM50496969 (CHEMBL3237161) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](CC(C)C)[C@H](O)C[C@H]1CCCN1C(=O)[C@H](NC(C)=O)[C@H](C)CC)C(=O)N[C@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N1CCC[C@@H]1C(N)=O |r| Show InChI InChI=1S/C41H71N7O8/c1-10-25(7)34(38(53)44-33(24(5)6)40(55)48-20-14-17-31(48)39(54)47-19-13-16-30(47)36(42)51)45-37(52)29(21-23(3)4)32(50)22-28-15-12-18-46(28)41(56)35(26(8)11-2)43-27(9)49/h23-26,28-35,50H,10-22H2,1-9H3,(H2,42,51)(H,43,49)(H,44,53)(H,45,52)/t25-,26-,28-,29+,30-,31-,32-,33-,34-,35-/m1/s1	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.10E+5	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto Prefectural University of Medicine Curated by ChEMBL					Assay Description Inhibition of HTLV-1 protease L40I/C90A/C109A mutant using dodecapeptide as substrate by HPLC analysis				Bioorg Med Chem 22: 2482-8 (2014) Article DOI: 10.1016/j.bmc.2014.02.050 BindingDB Entry DOI: 10.7270/Q2FJ2KS8
					More data for this Ligand-Target Pair
Protease (Human T-cell leukemia virus type I)	BDBM50496966 (CHEMBL1091002) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](CC(C)C)[C@H](O)C[C@H]1CCCN1C(=O)NCc1ccccc1)C(=O)N[C@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N1CCC[C@@H]1C(N)=O |r| Show InChI InChI=1S/C41H65N7O7/c1-7-27(6)35(38(52)44-34(26(4)5)40(54)48-21-13-18-32(48)39(53)47-20-12-17-31(47)36(42)50)45-37(51)30(22-25(2)3)33(49)23-29-16-11-19-46(29)41(55)43-24-28-14-9-8-10-15-28/h8-10,14-15,25-27,29-35,49H,7,11-13,16-24H2,1-6H3,(H2,42,50)(H,43,55)(H,44,52)(H,45,51)/t27-,29-,30+,31-,32-,33-,34-,35-/m1/s1	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.60E+5	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto Prefectural University of Medicine Curated by ChEMBL					Assay Description Inhibition of HTLV-1 protease L40I/C90A/C109A mutant using dodecapeptide as substrate by HPLC analysis				Bioorg Med Chem 22: 2482-8 (2014) Article DOI: 10.1016/j.bmc.2014.02.050 BindingDB Entry DOI: 10.7270/Q2FJ2KS8
					More data for this Ligand-Target Pair
Protease (Human T-cell leukemia virus type I)	BDBM50496960 (CHEMBL3237157) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](CC(C)C)[C@H](O)C[C@H]1CCCN1C(=O)CCc1ccccc1)C(=O)N[C@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N1CCC[C@@H]1C(N)=O |r| Show InChI InChI=1S/C42H66N6O7/c1-7-28(6)37(40(53)44-36(27(4)5)42(55)48-23-13-18-33(48)41(54)47-22-12-17-32(47)38(43)51)45-39(52)31(24-26(2)3)34(49)25-30-16-11-21-46(30)35(50)20-19-29-14-9-8-10-15-29/h8-10,14-15,26-28,30-34,36-37,49H,7,11-13,16-25H2,1-6H3,(H2,43,51)(H,44,53)(H,45,52)/t28-,30-,31+,32-,33-,34-,36-,37-/m1/s1	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.60E+5	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto Prefectural University of Medicine Curated by ChEMBL					Assay Description Inhibition of HTLV-1 protease L40I/C90A/C109A mutant using dodecapeptide as substrate by HPLC analysis				Bioorg Med Chem 22: 2482-8 (2014) Article DOI: 10.1016/j.bmc.2014.02.050 BindingDB Entry DOI: 10.7270/Q2FJ2KS8
					More data for this Ligand-Target Pair
Protease (Human T-cell leukemia virus type I)	BDBM50496964 (CHEMBL3237156) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](CC(C)C)[C@H](O)C[C@H]1CCCN1C(=O)\C=C\c1ccccc1)C(=O)N[C@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N1CCC[C@@H]1C(N)=O |r| Show InChI InChI=1S/C42H64N6O7/c1-7-28(6)37(40(53)44-36(27(4)5)42(55)48-23-13-18-33(48)41(54)47-22-12-17-32(47)38(43)51)45-39(52)31(24-26(2)3)34(49)25-30-16-11-21-46(30)35(50)20-19-29-14-9-8-10-15-29/h8-10,14-15,19-20,26-28,30-34,36-37,49H,7,11-13,16-18,21-25H2,1-6H3,(H2,43,51)(H,44,53)(H,45,52)/b20-19+/t28-,30-,31+,32-,33-,34-,36-,37-/m1/s1	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.90E+5	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto Prefectural University of Medicine Curated by ChEMBL					Assay Description Inhibition of HTLV-1 protease L40I/C90A/C109A mutant using dodecapeptide as substrate by HPLC analysis				Bioorg Med Chem 22: 2482-8 (2014) Article DOI: 10.1016/j.bmc.2014.02.050 BindingDB Entry DOI: 10.7270/Q2FJ2KS8
					More data for this Ligand-Target Pair
Protease (Human T-cell leukemia virus type I)	BDBM50496967 (CHEMBL3237155) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](CC(C)C)[C@H](O)C[C@H]1CCCN1C(=O)OCc1ccccc1)C(=O)N[C@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N1CCC[C@@H]1C(N)=O |r| Show InChI InChI=1S/C41H64N6O8/c1-7-27(6)35(38(51)43-34(26(4)5)40(53)47-21-13-18-32(47)39(52)46-20-12-17-31(46)36(42)49)44-37(50)30(22-25(2)3)33(48)23-29-16-11-19-45(29)41(54)55-24-28-14-9-8-10-15-28/h8-10,14-15,25-27,29-35,48H,7,11-13,16-24H2,1-6H3,(H2,42,49)(H,43,51)(H,44,50)/t27-,29-,30+,31-,32-,33-,34-,35-/m1/s1	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.80E+5	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto Prefectural University of Medicine Curated by ChEMBL					Assay Description Inhibition of HTLV-1 protease L40I/C90A/C109A mutant using dodecapeptide as substrate by HPLC analysis				Bioorg Med Chem 22: 2482-8 (2014) Article DOI: 10.1016/j.bmc.2014.02.050 BindingDB Entry DOI: 10.7270/Q2FJ2KS8
					More data for this Ligand-Target Pair
Protease (Human T-cell leukemia virus type I)	BDBM50496959 (CHEMBL3237159) Show SMILES CCCC(CCC)C(=O)N1CCC[C@@H]1C[C@@H](O)[C@H](CC(C)C)C(=O)N[C@H]([C@H](C)CC)C(=O)N[C@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N1CCC[C@@H]1C(N)=O |r| Show InChI InChI=1S/C41H72N6O7/c1-9-15-28(16-10-2)39(52)45-20-12-17-29(45)24-33(48)30(23-25(4)5)37(50)44-35(27(8)11-3)38(51)43-34(26(6)7)41(54)47-22-14-19-32(47)40(53)46-21-13-18-31(46)36(42)49/h25-35,48H,9-24H2,1-8H3,(H2,42,49)(H,43,51)(H,44,50)/t27-,29-,30+,31-,32-,33-,34-,35-/m1/s1	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.20E+5	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto Prefectural University of Medicine Curated by ChEMBL					Assay Description Inhibition of HTLV-1 protease L40I/C90A/C109A mutant using dodecapeptide as substrate by HPLC analysis				Bioorg Med Chem 22: 2482-8 (2014) Article DOI: 10.1016/j.bmc.2014.02.050 BindingDB Entry DOI: 10.7270/Q2FJ2KS8
					More data for this Ligand-Target Pair
Protease (Human T-cell leukemia virus type I)	BDBM50496961 (CHEMBL3237158) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](CC(C)C)[C@H](O)C[C@H]1CCCN1C(=O)CCC(C)C)C(=O)N[C@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N1CCC[C@@H]1C(N)=O |r| Show InChI InChI=1S/C39H68N6O7/c1-9-26(8)34(42-36(49)28(21-24(4)5)31(46)22-27-13-10-18-43(27)32(47)17-16-23(2)3)37(50)41-33(25(6)7)39(52)45-20-12-15-30(45)38(51)44-19-11-14-29(44)35(40)48/h23-31,33-34,46H,9-22H2,1-8H3,(H2,40,48)(H,41,50)(H,42,49)/t26-,27-,28+,29-,30-,31-,33-,34-/m1/s1	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.20E+5	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto Prefectural University of Medicine Curated by ChEMBL					Assay Description Inhibition of HTLV-1 protease L40I/C90A/C109A mutant using dodecapeptide as substrate by HPLC analysis				Bioorg Med Chem 22: 2482-8 (2014) Article DOI: 10.1016/j.bmc.2014.02.050 BindingDB Entry DOI: 10.7270/Q2FJ2KS8
					More data for this Ligand-Target Pair
Protease (Human T-cell leukemia virus type I)	BDBM50496965 (CHEMBL3233054) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](CC(C)C)[C@H](O)C[C@H]1CCCN1C(=O)C(C)(C)C)C(=O)N[C@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N1CCC[C@@H]1C(N)=O |r| Show InChI InChI=1S/C38H66N6O7/c1-10-24(6)31(41-33(47)26(20-22(2)3)29(45)21-25-14-11-17-42(25)37(51)38(7,8)9)34(48)40-30(23(4)5)36(50)44-19-13-16-28(44)35(49)43-18-12-15-27(43)32(39)46/h22-31,45H,10-21H2,1-9H3,(H2,39,46)(H,40,48)(H,41,47)/t24-,25-,26+,27-,28-,29-,30-,31-/m1/s1	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto Prefectural University of Medicine Curated by ChEMBL					Assay Description Inhibition of HTLV-1 protease L40I/C90A/C109A mutant using dodecapeptide as substrate by HPLC analysis				Bioorg Med Chem 22: 2482-8 (2014) Article DOI: 10.1016/j.bmc.2014.02.050 BindingDB Entry DOI: 10.7270/Q2FJ2KS8
					More data for this Ligand-Target Pair
Protease (Human T-cell leukemia virus type I)	BDBM50496968 (CHEMBL3237154) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](CC(C)C)[C@H](O)C[C@H]1CCCN1C(=O)c1ccccc1)C(=O)N[C@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N1CCC[C@@H]1C(N)=O |r| Show InChI InChI=1S/C40H62N6O7/c1-7-26(6)34(37(50)42-33(25(4)5)40(53)46-21-13-18-31(46)39(52)45-20-12-17-30(45)35(41)48)43-36(49)29(22-24(2)3)32(47)23-28-16-11-19-44(28)38(51)27-14-9-8-10-15-27/h8-10,14-15,24-26,28-34,47H,7,11-13,16-23H2,1-6H3,(H2,41,48)(H,42,50)(H,43,49)/t26-,28-,29+,30-,31-,32-,33-,34-/m1/s1	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	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
Kyoto Prefectural University of Medicine Curated by ChEMBL					Assay Description Inhibition of HTLV-1 protease L40I/C90A/C109A mutant using dodecapeptide as substrate by HPLC analysis				Bioorg Med Chem 22: 2482-8 (2014) Article DOI: 10.1016/j.bmc.2014.02.050 BindingDB Entry DOI: 10.7270/Q2FJ2KS8
					More data for this Ligand-Target Pair
Protease (Human T-cell leukemia virus type I)	BDBM50496962 (CHEMBL3237160) Show SMILES CC[C@@H](C)[C@@H](N)C(=O)N1CCC[C@@H]1C[C@@H](O)[C@H](CC(C)C)C(=O)N[C@H]([C@H](C)CC)C(=O)N[C@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N1CCC[C@@H]1C(N)=O |r| Show InChI InChI=1S/C39H69N7O7/c1-9-24(7)31(40)38(52)44-17-11-14-26(44)21-30(47)27(20-22(3)4)35(49)43-33(25(8)10-2)36(50)42-32(23(5)6)39(53)46-19-13-16-29(46)37(51)45-18-12-15-28(45)34(41)48/h22-33,47H,9-21,40H2,1-8H3,(H2,41,48)(H,42,50)(H,43,49)/t24-,25-,26-,27+,28-,29-,30-,31-,32-,33-/m1/s1	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.50E+6	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto Prefectural University of Medicine Curated by ChEMBL					Assay Description Inhibition of HTLV-1 protease L40I/C90A/C109A mutant using dodecapeptide as substrate by HPLC analysis				Bioorg Med Chem 22: 2482-8 (2014) Article DOI: 10.1016/j.bmc.2014.02.050 BindingDB Entry DOI: 10.7270/Q2FJ2KS8
					More data for this Ligand-Target Pair
Protease (Human T-cell leukemia virus type I)	BDBM50496963 (CHEMBL3237162) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H](CC(C)C)[C@H](O)C[C@H]1CCCN1C(=O)[C@H](NC(=O)[C@H](N)CCC(N)=O)[C@H](C)CC)C(=O)N[C@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N1CCC[C@@H]1C(N)=O |r| Show InChI InChI=1S/C44H77N9O9/c1-9-26(7)36(41(59)48-35(25(5)6)43(61)53-21-13-16-32(53)42(60)52-20-12-15-31(52)38(47)56)49-39(57)29(22-24(3)4)33(54)23-28-14-11-19-51(28)44(62)37(27(8)10-2)50-40(58)30(45)17-18-34(46)55/h24-33,35-37,54H,9-23,45H2,1-8H3,(H2,46,55)(H2,47,56)(H,48,59)(H,49,57)(H,50,58)/t26-,27-,28-,29+,30-,31-,32-,33-,35-,36-,37-/m1/s1	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto Prefectural University of Medicine Curated by ChEMBL					Assay Description Inhibition of HTLV-1 protease L40I/C90A/C109A mutant using dodecapeptide as substrate by HPLC analysis				Bioorg Med Chem 22: 2482-8 (2014) Article DOI: 10.1016/j.bmc.2014.02.050 BindingDB Entry DOI: 10.7270/Q2FJ2KS8
					More data for this Ligand-Target Pair