Found 56 hits of ki for UniProtKB: Q01782 Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
Pteridine reductase 1
(Leishmania major) | BDBM50398391
(CHEMBL2178602)Show SMILES COC(=O)C1CCN(CC1)C(=O)c1ccc(cc1)N(CCO)Cc1cnc2nc(N)nc(N)c2n1 Show InChI InChI=1S/C23H28N8O4/c1-35-22(34)15-6-8-30(9-7-15)21(33)14-2-4-17(5-3-14)31(10-11-32)13-16-12-26-20-18(27-16)19(24)28-23(25)29-20/h2-5,12,15,32H,6-11,13H2,1H3,(H4,24,25,26,28,29) | PDB MMDB
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UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
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Similars
| Article PubMed
| 30 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita` degli Studi di Sassari
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by spectrophotometric assay |
J Med Chem 55: 8318-29 (2012)
Article DOI: 10.1021/jm300563f BindingDB Entry DOI: 10.7270/Q2R49RXF |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50398394
(CHEMBL1232702)Show SMILES COC(=O)C1CCN(CC1)C(=O)c1ccc(cc1)N(C)Cc1cnc2nc(N)nc(N)c2n1 Show InChI InChI=1S/C22H26N8O3/c1-29(12-15-11-25-19-17(26-15)18(23)27-22(24)28-19)16-5-3-13(4-6-16)20(31)30-9-7-14(8-10-30)21(32)33-2/h3-6,11,14H,7-10,12H2,1-2H3,(H4,23,24,25,27,28) | PDB MMDB
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UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
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Similars
| MMDB PDB Article PubMed
| 37 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita` degli Studi di Sassari
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by spectrophotometric assay |
J Med Chem 55: 8318-29 (2012)
Article DOI: 10.1021/jm300563f BindingDB Entry DOI: 10.7270/Q2R49RXF |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Pteridine reductase 1
(Leishmania major) | BDBM18050
(2-[(4-{[(2,4-diaminopteridin-6-yl)methyl](methyl)a...)Show SMILES CN(Cc1cnc2nc(N)nc(N)c2n1)c1ccc(cc1)C(=O)N[C@@H](CCC(O)=O)C(O)=O |r| Show InChI InChI=1S/C20H22N8O5/c1-28(9-11-8-23-17-15(24-11)16(21)26-20(22)27-17)12-4-2-10(3-5-12)18(31)25-13(19(32)33)6-7-14(29)30/h2-5,8,13H,6-7,9H2,1H3,(H,25,31)(H,29,30)(H,32,33)(H4,21,22,23,26,27)/t13-/m0/s1 | PDB MMDB
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| 39 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Pteridine reductase 1
(Leishmania major) | BDBM50398392
(CHEMBL2178603)Show SMILES CCc1ccc(NCc2cnc3nc(N)nc(N)c3n2)cc1C(=O)N1CCC(CC1)C(=O)OC Show InChI InChI=1S/C23H28N8O3/c1-3-13-4-5-15(10-17(13)21(32)31-8-6-14(7-9-31)22(33)34-2)26-11-16-12-27-20-18(28-16)19(24)29-23(25)30-20/h4-5,10,12,14,26H,3,6-9,11H2,1-2H3,(H4,24,25,27,29,30) | PDB MMDB
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UniProtKB/SwissProt
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Similars
| Article PubMed
| 60 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita` degli Studi di Sassari
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by spectrophotometric assay |
J Med Chem 55: 8318-29 (2012)
Article DOI: 10.1021/jm300563f BindingDB Entry DOI: 10.7270/Q2R49RXF |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50398390
(CHEMBL2177120)Show SMILES CCc1cc(ccc1NCc1cnc2nc(N)nc(N)c2n1)C(=O)N1CCC(CC1)C(=O)OC Show InChI InChI=1S/C23H28N8O3/c1-3-13-10-15(21(32)31-8-6-14(7-9-31)22(33)34-2)4-5-17(13)26-11-16-12-27-20-18(28-16)19(24)29-23(25)30-20/h4-5,10,12,14,26H,3,6-9,11H2,1-2H3,(H4,24,25,27,29,30) | PDB MMDB
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UniProtKB/SwissProt
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| Article PubMed
| 78 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita` degli Studi di Sassari
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by spectrophotometric assay |
J Med Chem 55: 8318-29 (2012)
Article DOI: 10.1021/jm300563f BindingDB Entry DOI: 10.7270/Q2R49RXF |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50398389
(CHEMBL2178601)Show SMILES CCOC(=O)CN(Cc1cnc2nc(N)nc(N)c2n1)c1ccc(cc1)C(=O)N1CCC(CC1)C(=O)OC Show InChI InChI=1S/C25H30N8O5/c1-3-38-19(34)14-33(13-17-12-28-22-20(29-17)21(26)30-25(27)31-22)18-6-4-15(5-7-18)23(35)32-10-8-16(9-11-32)24(36)37-2/h4-7,12,16H,3,8-11,13-14H2,1-2H3,(H4,26,27,28,30,31) | PDB MMDB
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UniProtKB/SwissProt
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Similars
| Article PubMed
| 100 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita` degli Studi di Sassari
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by spectrophotometric assay |
J Med Chem 55: 8318-29 (2012)
Article DOI: 10.1021/jm300563f BindingDB Entry DOI: 10.7270/Q2R49RXF |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50398395
(CHEMBL1232399)Show SMILES COC(=O)C1CCN(CC1)C(=O)c1ccc(NCc2cnc3nc(N)nc(N)c3n2)cc1 Show InChI InChI=1S/C21H24N8O3/c1-32-20(31)13-6-8-29(9-7-13)19(30)12-2-4-14(5-3-12)24-10-15-11-25-18-16(26-15)17(22)27-21(23)28-18/h2-5,11,13,24H,6-10H2,1H3,(H4,22,23,25,27,28) | PDB MMDB
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UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
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Similars
| MMDB PDB Article PubMed
| 100 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita` degli Studi di Sassari
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by spectrophotometric assay |
J Med Chem 55: 8318-29 (2012)
Article DOI: 10.1021/jm300563f BindingDB Entry DOI: 10.7270/Q2R49RXF |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Pteridine reductase 1
(Leishmania major) | BDBM18050
(2-[(4-{[(2,4-diaminopteridin-6-yl)methyl](methyl)a...)Show SMILES CN(Cc1cnc2nc(N)nc(N)c2n1)c1ccc(cc1)C(=O)N[C@@H](CCC(O)=O)C(O)=O |r| Show InChI InChI=1S/C20H22N8O5/c1-28(9-11-8-23-17-15(24-11)16(21)26-20(22)27-17)12-4-2-10(3-5-12)18(31)25-13(19(32)33)6-7-14(29)30/h2-5,8,13H,6-7,9H2,1H3,(H,25,31)(H,29,30)(H,32,33)(H4,21,22,23,26,27)/t13-/m0/s1 | PDB MMDB
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| PDB Article PubMed
| 180 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita` degli Studi di Sassari
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by spectrophotometric assay |
J Med Chem 55: 8318-29 (2012)
Article DOI: 10.1021/jm300563f BindingDB Entry DOI: 10.7270/Q2R49RXF |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Pteridine reductase 1
(Leishmania major) | BDBM50398396
(CHEMBL2178600)Show SMILES COC(=O)C1CCN(CC1)C(=O)c1ccc(NCc2cnc3nc(N)nc(N)c3n2)cn1 Show InChI InChI=1S/C20H23N9O3/c1-32-19(31)11-4-6-29(7-5-11)18(30)14-3-2-12(8-24-14)23-9-13-10-25-17-15(26-13)16(21)27-20(22)28-17/h2-3,8,10-11,23H,4-7,9H2,1H3,(H4,21,22,25,27,28) | PDB MMDB
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| Article PubMed
| 210 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita` degli Studi di Sassari
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by spectrophotometric assay |
J Med Chem 55: 8318-29 (2012)
Article DOI: 10.1021/jm300563f BindingDB Entry DOI: 10.7270/Q2R49RXF |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303504
(2,4-diamino-6,7-diisopropylpteridin-1-ium | 6,7-bi...)Show InChI InChI=1S/C12H18N6/c1-5(2)7-8(6(3)4)16-11-9(15-7)10(13)17-12(14)18-11/h5-6H,1-4H3,(H4,13,14,16,17,18) | PDB MMDB
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| 240 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50398393
(CHEMBL2178599)Show SMILES NC(=O)C1CCN(CC1)C(=O)c1ccc(NCc2cnc3nc(N)nc(N)c3n2)cc1 Show InChI InChI=1S/C20H23N9O2/c21-16-15-18(28-20(23)27-16)25-10-14(26-15)9-24-13-3-1-12(2-4-13)19(31)29-7-5-11(6-8-29)17(22)30/h1-4,10-11,24H,5-9H2,(H2,22,30)(H4,21,23,25,27,28) | PDB MMDB
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UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
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| Article PubMed
| 390 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita` degli Studi di Sassari
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by spectrophotometric assay |
J Med Chem 55: 8318-29 (2012)
Article DOI: 10.1021/jm300563f BindingDB Entry DOI: 10.7270/Q2R49RXF |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303518
(2,4-diamino-6-(benzylthio)pyrimidin-1-ium | 6-(ben...)Show InChI InChI=1S/C11H12N4S/c12-9-6-10(15-11(13)14-9)16-7-8-4-2-1-3-5-8/h1-6H,7H2,(H4,12,13,14,15) | PDB MMDB
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UniProtKB/SwissProt
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Similars
| Article PubMed
| 600 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50335104
(3-(5-Amino-[1,3,4]thiadiazol-2-yl)-1-(thiophen-2-y...)Show InChI InChI=1S/C9H9N3OS2/c10-9-12-11-8(15-9)4-3-6(13)7-2-1-5-14-7/h1-2,5H,3-4H2,(H2,10,12) | PDB MMDB
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UniProtKB/SwissProt
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| Article PubMed
| 2.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Rutgers University
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysis |
J Agric Food Chem 59: 56-61 (2011)
Article DOI: 10.1021/jf103164r BindingDB Entry DOI: 10.7270/Q27W6D6P |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50335105
(2-(5-Amino-[1,3,4]thiadiazol-2-yl)-4H-chromen-4-on...)Show InChI InChI=1S/C11H7N3O2S/c12-11-14-13-10(17-11)9-5-7(15)6-3-1-2-4-8(6)16-9/h1-5H,(H2,12,14) | PDB MMDB
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| Article PubMed
| 2.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Rutgers University
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysis |
J Agric Food Chem 59: 56-61 (2011)
Article DOI: 10.1021/jf103164r BindingDB Entry DOI: 10.7270/Q27W6D6P |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50335107
(5-(4-aminopyridin-3-yl)-1,3,4-thiadiazol-2-amine |...)Show InChI InChI=1S/C7H7N5S/c8-5-1-2-10-3-4(5)6-11-12-7(9)13-6/h1-3H,(H2,8,10)(H2,9,12) | PDB MMDB
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UniProtKB/SwissProt
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| Article PubMed
| 2.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Rutgers University
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysis |
J Agric Food Chem 59: 56-61 (2011)
Article DOI: 10.1021/jf103164r BindingDB Entry DOI: 10.7270/Q27W6D6P |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303514
(2-amino-6-(1,3-benzodioxol-5-yl)-4-oxo-4,7-dihydro...)Show SMILES Nc1nc2[nH]c(c(C#N)c2c(=O)[nH]1)-c1ccc2OCOc2c1 Show InChI InChI=1S/C14H9N5O3/c15-4-7-10-12(18-14(16)19-13(10)20)17-11(7)6-1-2-8-9(3-6)22-5-21-8/h1-3H,5H2,(H4,16,17,18,19,20) | PDB MMDB
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| Article PubMed
| 2.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303519
(6-[(4'-Methoxybenzyl)sulfanyl]-2,4-pyrimidinediami...)Show InChI InChI=1S/C12H14N4OS/c1-17-9-4-2-8(3-5-9)7-18-11-6-10(13)15-12(14)16-11/h2-6H,7H2,1H3,(H4,13,14,15,16) | PDB MMDB
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| 2.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50335098
(6-Nitro-benzothiazol-2-ylamine | 6-nitrobenzo[d]th...)Show InChI InChI=1S/C7H5N3O2S/c8-7-9-5-2-1-4(10(11)12)3-6(5)13-7/h1-3H,(H2,8,9) | PDB MMDB
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| 3.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Rutgers University
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysis |
J Agric Food Chem 59: 56-61 (2011)
Article DOI: 10.1021/jf103164r BindingDB Entry DOI: 10.7270/Q27W6D6P |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303512
(2-amino-6-(4-methoxyphenyl)-4-oxo-4,7-dihydro-3H-p...)Show InChI InChI=1S/C14H11N5O2/c1-21-8-4-2-7(3-5-8)11-9(6-15)10-12(17-11)18-14(16)19-13(10)20/h2-5H,1H3,(H4,16,17,18,19,20) | PDB MMDB
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| 3.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM6644
(6‐phenylpteridine‐2,4,7‐triamine...)Show InChI InChI=1S/C12H11N7/c13-9-7(6-4-2-1-3-5-6)16-8-10(14)18-12(15)19-11(8)17-9/h1-5H,(H6,13,14,15,17,18,19) | PDB MMDB
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| 3.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM30705
(CHEMBL744 | MLS000069369 | RILUZOLE | SMR000058231...)Show InChI InChI=1S/C8H5F3N2OS/c9-8(10,11)14-4-1-2-5-6(3-4)15-7(12)13-5/h1-3H,(H2,12,13) | PDB MMDB
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| Article PubMed
| 4.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Rutgers University
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysis |
J Agric Food Chem 59: 56-61 (2011)
Article DOI: 10.1021/jf103164r BindingDB Entry DOI: 10.7270/Q27W6D6P |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50398388
(CHEMBL2178604)Show SMILES Nc1nc(N)c2nc(CNc3ccc(cc3)C(=O)N3CCC(CC3)C(O)=O)cnc2n1 Show InChI InChI=1S/C20H22N8O3/c21-16-15-17(27-20(22)26-16)24-10-14(25-15)9-23-13-3-1-11(2-4-13)18(29)28-7-5-12(6-8-28)19(30)31/h1-4,10,12,23H,5-9H2,(H,30,31)(H4,21,22,24,26,27) | PDB MMDB
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Similars
| Article PubMed
| 4.17E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita` degli Studi di Sassari
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by spectrophotometric assay |
J Med Chem 55: 8318-29 (2012)
Article DOI: 10.1021/jm300563f BindingDB Entry DOI: 10.7270/Q2R49RXF |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303513
(2-amino-6-(3-formylphenyl)-4-oxo-4,7-dihydro-3H-py...)Show SMILES Nc1nc2[nH]c(c(C#N)c2c(=O)[nH]1)-c1cccc(C=O)c1 Show InChI InChI=1S/C14H9N5O2/c15-5-9-10-12(18-14(16)19-13(10)21)17-11(9)8-3-1-2-7(4-8)6-20/h1-4,6H,(H4,16,17,18,19,21) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 4.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50551183
(CHEMBL4747846)Show SMILES Oc1ccc(cc1)-c1ccc(-c2cc(O)cc(O)c2)c(c1)-c1ccccc1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| 5.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of Leishmania major PTR1 using H2B as substrate preincubated for 10 mins followed by NADPH addition and measured up to 50 mins relative to... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2020.112047 BindingDB Entry DOI: 10.7270/Q2F47SSH |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50335102
(3-Chloro-N-[5-(2-chloroethyl)-[1,3,4]thiadiazol-2-...)Show InChI InChI=1S/C7H9Cl2N3OS/c8-3-1-5(13)10-7-12-11-6(14-7)2-4-9/h1-4H2,(H,10,12,13) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 7.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Rutgers University
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysis |
J Agric Food Chem 59: 56-61 (2011)
Article DOI: 10.1021/jf103164r BindingDB Entry DOI: 10.7270/Q27W6D6P |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50335103
(3-(5-Amino-[1,3,4]thiadiazol-2-yl)-1-(4-chlorophen...)Show InChI InChI=1S/C11H10ClN3OS/c12-8-3-1-7(2-4-8)9(16)5-6-10-14-15-11(13)17-10/h1-4H,5-6H2,(H2,13,15) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| 7.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Rutgers University
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysis |
J Agric Food Chem 59: 56-61 (2011)
Article DOI: 10.1021/jf103164r BindingDB Entry DOI: 10.7270/Q27W6D6P |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50335101
(2-(1,3-Dioxoisoindolin-2-yl)-N-5-(1,3-dioxoisoindo...)Show SMILES O=C(CN1C(=O)c2ccccc2C1=O)Nc1nnc(CN2C(=O)c3ccccc3C2=O)s1 Show InChI InChI=1S/C21H13N5O5S/c27-15(9-25-17(28)11-5-1-2-6-12(11)18(25)29)22-21-24-23-16(32-21)10-26-19(30)13-7-3-4-8-14(13)20(26)31/h1-8H,9-10H2,(H,22,24,27) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| 9.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Rutgers University
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysis |
J Agric Food Chem 59: 56-61 (2011)
Article DOI: 10.1021/jf103164r BindingDB Entry DOI: 10.7270/Q27W6D6P |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50551184
(CHEMBL4797185) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| 1.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of Leishmania major PTR1 using H2B as substrate preincubated for 10 mins followed by NADPH addition and measured up to 50 mins relative to... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2020.112047 BindingDB Entry DOI: 10.7270/Q2F47SSH |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303505
(6,7,7-trimethyl-7,8-dihydropteridine-2,4-diamine |...)Show InChI InChI=1S/C9H14N6/c1-4-9(2,3)15-7-5(12-4)6(10)13-8(11)14-7/h1-3H3,(H5,10,11,13,14,15) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid PDB UniChem
| Article PubMed
| 1.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50551180
(CHEMBL4760251)Show SMILES O=C1CCCCCNCc2ccc(Cc3ccc(CNCCCCCC(=O)N(Cc4ccccc4)CCCCCCCCN1Cc1ccccc1)cc3)cc2 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| 1.48E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of Leishmania major PTR1 using H2B as substrate preincubated for 10 mins followed by NADPH addition and measured up to 50 mins relative to... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2020.112047 BindingDB Entry DOI: 10.7270/Q2F47SSH |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50551177
(CHEMBL4762279) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| 1.53E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of Leishmania major PTR1 using H2B as substrate preincubated for 10 mins followed by NADPH addition and measured up to 50 mins relative to... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2020.112047 BindingDB Entry DOI: 10.7270/Q2F47SSH |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50335097
(6-(methylsulfonyl)benzo[d]thiazol-2-amine | 6-Meth...)Show InChI InChI=1S/C8H8N2O2S2/c1-14(11,12)5-2-3-6-7(4-5)13-8(9)10-6/h2-4H,1H3,(H2,9,10) | PDB MMDB
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Patents
Similars
| Article PubMed
| 1.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Rutgers University
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysis |
J Agric Food Chem 59: 56-61 (2011)
Article DOI: 10.1021/jf103164r BindingDB Entry DOI: 10.7270/Q27W6D6P |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303511
(2-amino-6-(4-ethylphenyl)-4-oxo-4,7-dihydro-3H-pyr...)Show InChI InChI=1S/C15H13N5O/c1-2-8-3-5-9(6-4-8)12-10(7-16)11-13(18-12)19-15(17)20-14(11)21/h3-6H,2H2,1H3,(H4,17,18,19,20,21) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 1.64E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50551178
(CHEMBL4785591)Show SMILES O=C1CCCCCNCc2ccc(cc2)-c2ccc(CNCCCCCC(=O)N(Cc3ccccc3)CCCCCCCCN1Cc1ccccc1)cc2 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| 1.92E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of Leishmania major PTR1 using H2B as substrate preincubated for 10 mins followed by NADPH addition and measured up to 50 mins relative to... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2020.112047 BindingDB Entry DOI: 10.7270/Q2F47SSH |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50335106
(5-(1H-benzo[d][1,2,3]triazol-5-yl)-[1,3,4]thiadiaz...)Show InChI InChI=1S/C8H6N6S/c9-8-13-12-7(15-8)4-1-2-5-6(3-4)11-14-10-5/h1-3H,(H2,9,13)(H,10,11,14) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid PDB UniChem
| Article PubMed
| 2.40E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Rutgers University
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysis |
J Agric Food Chem 59: 56-61 (2011)
Article DOI: 10.1021/jf103164r BindingDB Entry DOI: 10.7270/Q27W6D6P |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50028122
(2-Amino-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one ...)Show InChI InChI=1S/C6H6N4O/c7-6-9-4-3(1-2-8-4)5(11)10-6/h1-2H,(H4,7,8,9,10,11) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| Purchase
MMDB PC cid PC sid PDB UniChem
Patents
| Article PubMed
| >2.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303506
(2-amino-3H-pyrrolo[2,3-d]pyrimidine-4(7H)-thione |...)Show InChI InChI=1S/C6H6N4S/c7-6-9-4-3(1-2-8-4)5(11)10-6/h1-2H,(H4,7,8,9,10,11) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
| Article PubMed
| >2.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303507
(2-amino-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimid...)Show InChI InChI=1S/C7H5N5O/c8-1-3-2-10-5-4(3)6(13)12-7(9)11-5/h2H,(H4,9,10,11,12,13) | PDB MMDB
KEGG
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CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem
| Article PubMed
| >2.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303508
(2-amino-5-(2-phenylethyl)-3,7-dihydro-4H-pyrrolo[2...)Show InChI InChI=1S/C14H14N4O/c15-14-17-12-11(13(19)18-14)10(8-16-12)7-6-9-4-2-1-3-5-9/h1-5,8H,6-7H2,(H4,15,16,17,18,19) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL MMDB PC cid PC sid PDB UniChem
| Article PubMed
| >2.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303509
(2-amino-6-bromo-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d...)Show InChI InChI=1S/C7H4BrN5O/c8-4-2(1-9)3-5(11-4)12-7(10)13-6(3)14/h(H4,10,11,12,13,14) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL MMDB PC cid PC sid PDB UniChem
| Article PubMed
| >2.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303510
(2-amino-4-oxo-6-phenyl-4,7-dihydro-3H-pyrrolo[2,3-...)Show InChI InChI=1S/C13H9N5O/c14-6-8-9-11(17-13(15)18-12(9)19)16-10(8)7-4-2-1-3-5-7/h1-5H,(H4,15,16,17,18,19) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL MMDB PC cid PC sid PDB UniChem
Similars
| Article PubMed
| >2.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303515
(2,4,6-triaminopyrimidin-1-ium | CHEMBL571518 | PYR...)Show InChI InChI=1S/C4H7N5/c5-2-1-3(6)9-4(7)8-2/h1H,(H6,5,6,7,8,9) | PDB MMDB
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UniProtKB/SwissProt
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CHEMBL MCE MMDB PC cid PC sid PDB UniChem
Patents
| Article PubMed
| >2.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303517
(2,4-diamino-6-(p-tolylthio)pyrimidin-1-ium | 6-[(4...)Show InChI InChI=1S/C11H12N4S/c1-7-2-4-8(5-3-7)16-10-6-9(12)14-11(13)15-10/h2-6H,1H3,(H4,12,13,14,15) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL MMDB PC cid PC sid PDB UniChem
| Article PubMed
| 2.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50303516
(2,4-diamino-6-(cyclopropylamino)pyrimidin-1-ium | ...)Show InChI InChI=1S/C7H11N5/c8-5-3-6(10-4-1-2-4)12-7(9)11-5/h3-4H,1-2H2,(H5,8,9,10,11,12) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| >2.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Dundee
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major recombinant PTR1 |
J Med Chem 53: 221-9 (2010)
Article DOI: 10.1021/jm901059x BindingDB Entry DOI: 10.7270/Q2H132XP |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50551181
(CHEMBL54725)Show SMILES COc1ccccc1CNCc1ccc(CNCCCCCCCCCCCCNCc2ccc(CNCc3ccccc3OC)cc2)cc1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| 3.72E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of Leishmania major PTR1 using H2B as substrate preincubated for 10 mins followed by NADPH addition and measured up to 50 mins relative to... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2020.112047 BindingDB Entry DOI: 10.7270/Q2F47SSH |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50335099
(4-chlorobenzo[d]thiazol-2-amine | CHEMBL1413383 | ...)Show InChI InChI=1S/C7H5ClN2S/c8-4-2-1-3-5-6(4)10-7(9)11-5/h1-3H,(H2,9,10) | PDB MMDB
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CHEMBL MCE PC cid PC sid PDB UniChem
Patents
| Article PubMed
| 7.90E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Rutgers University
Curated by ChEMBL
| Assay Description Inhibition of Leishmania major PTR1 by Lineweaver-Burk analysis |
J Agric Food Chem 59: 56-61 (2011)
Article DOI: 10.1021/jf103164r BindingDB Entry DOI: 10.7270/Q27W6D6P |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50551176
(CHEMBL4748094) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of Leishmania major PTR1 using H2B as substrate preincubated for 10 mins followed by NADPH addition and measured up to 50 mins relative to... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2020.112047 BindingDB Entry DOI: 10.7270/Q2F47SSH |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50062821
(6-Benzyloxy-pyrimidine-2,4-diamine | CHEMBL121445)Show InChI InChI=1S/C11H12N4O/c12-9-6-10(15-11(13)14-9)16-7-8-4-2-1-3-5-8/h1-6H,7H2,(H4,12,13,14,15) | PDB MMDB
KEGG
UniProtKB/SwissProt
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CHEMBL PC cid PC sid UniChem
Patents
| Article PubMed
| >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of Leishmania major PTR1 using H2B as substrate preincubated for 10 mins followed by NADPH addition and measured up to 50 mins relative to... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2020.112047 BindingDB Entry DOI: 10.7270/Q2F47SSH |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50551173
(CHEMBL4753331) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of Leishmania major PTR1 using H2B as substrate preincubated for 10 mins followed by NADPH addition and measured up to 50 mins relative to... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2020.112047 BindingDB Entry DOI: 10.7270/Q2F47SSH |
More data for this Ligand-Target Pair | |
Pteridine reductase 1
(Leishmania major) | BDBM50551175
(CHEMBL1993081) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of Leishmania major PTR1 using H2B as substrate preincubated for 10 mins followed by NADPH addition and measured up to 50 mins relative to... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2020.112047 BindingDB Entry DOI: 10.7270/Q2F47SSH |
More data for this Ligand-Target Pair | |