Found 39 hits of Enzyme Inhibition Constant Data 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 |
|---|
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272907
((R)-1-(2-methylcyclohexylidene)-2-(4-(4-nitropheny...)Show SMILES C[C@@H]1CCCCC1=NNc1nc(cs1)-c1ccc(cc1)[N+]([O-])=O |r,w:7.8| Show InChI InChI=1S/C16H18N4O2S/c1-11-4-2-3-5-14(11)18-19-16-17-15(10-23-16)12-6-8-13(9-7-12)20(21)22/h6-11H,2-5H2,1H3,(H,17,19)/t11-/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia
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AffyNet 
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 9.80 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272829
((+/-)-1-(4-(2,4-difluorophenyl)thiazol-2-yl)-2-(2-...)Show InChI InChI=1S/C16H17F2N3S/c1-10-4-2-3-5-14(10)20-21-16-19-15(9-22-16)12-7-6-11(17)8-13(12)18/h6-10H,2-5H2,1H3,(H,19,21) | PDB
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antibodypedia
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| CHEMBL
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| Article
PubMed
| n/a | n/a | 14.2 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272867
((S)-1-(2-methylcyclohexylidene)-2-(4-(4-nitropheny...)Show SMILES C[C@H]1CCCCC1=NNc1nc(cs1)-c1ccc(cc1)[N+]([O-])=O |r,w:7.8| Show InChI InChI=1S/C16H18N4O2S/c1-11-4-2-3-5-14(11)18-19-16-17-15(10-23-16)12-6-8-13(9-7-12)20(21)22/h6-11H,2-5H2,1H3,(H,17,19)/t11-/m0/s1 | PDB
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| n/a | n/a | 16.6 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM15579
(CHEMBL972 | DEPRENYL | L-Deprenyl | N-methyl-N-[(2...)Show InChI InChI=1S/C13H17N/c1-4-10-14(3)12(2)11-13-8-6-5-7-9-13/h1,5-9,12H,10-11H2,2-3H3/t12-/m1/s1 | PDB
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| n/a | n/a | 19.6 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272864
((R)-1-(4-(4-fluorophenyl)thiazol-2-yl)-2-(2-methyl...)Show SMILES C[C@@H]1CCCCC1=NNc1nc(cs1)-c1ccc(F)cc1 |r,w:7.8| Show InChI InChI=1S/C16H18FN3S/c1-11-4-2-3-5-14(11)19-20-16-18-15(10-21-16)12-6-8-13(17)9-7-12/h6-11H,2-5H2,1H3,(H,18,20)/t11-/m1/s1 | PDB
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| n/a | n/a | 22.0 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272832
((+/-)-4-(2-{N'-[2-Methyl-cyclohexylidene]-hydrazin...)Show SMILES CC1CCCCC1=NNc1nc(cs1)-c1ccc(cc1)C#N |w:7.8| Show InChI InChI=1S/C17H18N4S/c1-12-4-2-3-5-15(12)20-21-17-19-16(11-22-17)14-8-6-13(10-18)7-9-14/h6-9,11-12H,2-5H2,1H3,(H,19,21) | PDB
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| n/a | n/a | 26.2 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272866
(1-(4-(2,4-difluorophenyl)thiazol-2-yl)-2-((R)-2-me...)Show SMILES C[C@@H]1CCCCC1=NNc1nc(cs1)-c1ccc(F)cc1F |r,w:7.8| Show InChI InChI=1S/C16H17F2N3S/c1-10-4-2-3-5-14(10)20-21-16-19-15(9-22-16)12-7-6-11(17)8-13(12)18/h6-10H,2-5H2,1H3,(H,19,21)/t10-/m1/s1 | PDB
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| CHEMBL
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| n/a | n/a | 30.1 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272831
((+/-)-1-(2-methylcyclohexylidene)-2-(4-(4-nitrophe...)Show SMILES CC1CCCCC1=NNc1nc(cs1)-c1ccc(cc1)[N+]([O-])=O |w:7.8| Show InChI InChI=1S/C16H18N4O2S/c1-11-4-2-3-5-14(11)18-19-16-17-15(10-23-16)12-6-8-13(9-7-12)20(21)22/h6-11H,2-5H2,1H3,(H,17,19) | PDB
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| n/a | n/a | 32.3 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272909
(4-(2-{N'-[(R)-2-Methyl-cyclohexylidene]-hydrazino}...)Show SMILES C[C@@H]1CCCCC1=NNc1nc(cs1)-c1ccc(cc1)C#N |r,w:7.8| Show InChI InChI=1S/C17H18N4S/c1-12-4-2-3-5-15(12)20-21-17-19-16(11-22-17)14-8-6-13(10-18)7-9-14/h6-9,11-12H,2-5H2,1H3,(H,19,21)/t12-/m1/s1 | PDB
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| n/a | n/a | 32.5 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272865
(1-(4-(2,4-difluorophenyl)thiazol-2-yl)-2-((S)-2-me...)Show SMILES C[C@H]1CCCCC1=NNc1nc(cs1)-c1ccc(F)cc1F |r,w:7.8| Show InChI InChI=1S/C16H17F2N3S/c1-10-4-2-3-5-14(10)20-21-16-19-15(9-22-16)12-7-6-11(17)8-13(12)18/h6-10H,2-5H2,1H3,(H,19,21)/t10-/m0/s1 | PDB
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| n/a | n/a | 36.1 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272863
((S)-1-(4-(4-fluorophenyl)thiazol-2-yl)-2-(2-methyl...)Show SMILES C[C@H]1CCCCC1=NNc1nc(cs1)-c1ccc(F)cc1 |r,w:7.8| Show InChI InChI=1S/C16H18FN3S/c1-11-4-2-3-5-14(11)19-20-16-18-15(10-21-16)12-6-8-13(17)9-7-12/h6-11H,2-5H2,1H3,(H,18,20)/t11-/m0/s1 | PDB
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| n/a | n/a | 47.2 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272908
(4-(2-{N'-[(S)-2-Methyl-cyclohexylidene]-hydrazino}...)Show SMILES C[C@H]1CCCCC1=NNc1nc(cs1)-c1ccc(cc1)C#N |r,w:7.8| Show InChI InChI=1S/C17H18N4S/c1-12-4-2-3-5-15(12)20-21-17-19-16(11-22-17)14-8-6-13(10-18)7-9-14/h6-9,11-12H,2-5H2,1H3,(H,19,21)/t12-/m0/s1 | PDB
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| n/a | n/a | 63.0 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272830
((+/-)-1-(2-methylcyclohexylidene)-2-(4-p-tolylthia...)Show InChI InChI=1S/C17H21N3S/c1-12-7-9-14(10-8-12)16-11-21-17(18-16)20-19-15-6-4-3-5-13(15)2/h7-11,13H,3-6H2,1-2H3,(H,18,20) | PDB
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| n/a | n/a | 143 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272794
((+/-)-1-(4-(4-fluorophenyl)thiazol-2-yl)-2-(2-meth...)Show InChI InChI=1S/C16H18FN3S/c1-11-4-2-3-5-14(11)19-20-16-18-15(10-21-16)12-6-8-13(17)9-7-12/h6-11H,2-5H2,1H3,(H,18,20) | PDB
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| n/a | n/a | 204 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272792
((+/-)-1-(2-methylcyclohexylidene)-2-(4-phenylthiaz...)Show InChI InChI=1S/C16H19N3S/c1-12-7-5-6-10-14(12)18-19-16-17-15(11-20-16)13-8-3-2-4-9-13/h2-4,8-9,11-12H,5-7,10H2,1H3,(H,17,19) | PDB
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| n/a | n/a | 711 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50265779
((+/-)-1-(4-(4-methoxyphenyl)thiazol-2-yl)-2-(2-met...)Show SMILES COc1ccc(cc1)-c1csc(NN=C2CCCCC2C)n1 |w:13.13| Show InChI InChI=1S/C17H21N3OS/c1-12-5-3-4-6-15(12)19-20-17-18-16(11-22-17)13-7-9-14(21-2)10-8-13/h7-12H,3-6H2,1-2H3,(H,18,20) | PDB
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| n/a | n/a | 2.37E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM50265779
((+/-)-1-(4-(4-methoxyphenyl)thiazol-2-yl)-2-(2-met...)Show SMILES COc1ccc(cc1)-c1csc(NN=C2CCCCC2C)n1 |w:13.13| Show InChI InChI=1S/C17H21N3OS/c1-12-5-3-4-6-15(12)19-20-17-18-16(11-22-17)13-7-9-14(21-2)10-8-13/h7-12H,3-6H2,1-2H3,(H,18,20) | PDB
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| n/a | n/a | 2.76E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM50272864
((R)-1-(4-(4-fluorophenyl)thiazol-2-yl)-2-(2-methyl...)Show SMILES C[C@@H]1CCCCC1=NNc1nc(cs1)-c1ccc(F)cc1 |r,w:7.8| Show InChI InChI=1S/C16H18FN3S/c1-11-4-2-3-5-14(11)19-20-16-18-15(10-21-16)12-6-8-13(17)9-7-12/h6-11H,2-5H2,1H3,(H,18,20)/t11-/m1/s1 | PDB
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| n/a | n/a | 3.53E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM15581
(CHEMBL8706 | CLG | CLORGILINE | Clorgyline | N-[3-...)Show InChI InChI=1S/C13H15Cl2NO/c1-3-7-16(2)8-4-9-17-13-6-5-11(14)10-12(13)15/h1,5-6,10H,4,7-9H2,2H3 | PDB
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Article
PubMed
| n/a | n/a | 4.46E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | 
3D Structure (crystal) |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM50272865
(1-(4-(2,4-difluorophenyl)thiazol-2-yl)-2-((S)-2-me...)Show SMILES C[C@H]1CCCCC1=NNc1nc(cs1)-c1ccc(F)cc1F |r,w:7.8| Show InChI InChI=1S/C16H17F2N3S/c1-10-4-2-3-5-14(10)20-21-16-19-15(9-22-16)12-7-6-11(17)8-13(12)18/h6-10H,2-5H2,1H3,(H,19,21)/t10-/m0/s1 | PDB
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| CHEMBL
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| Article
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| n/a | n/a | 4.81E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM50272863
((S)-1-(4-(4-fluorophenyl)thiazol-2-yl)-2-(2-methyl...)Show SMILES C[C@H]1CCCCC1=NNc1nc(cs1)-c1ccc(F)cc1 |r,w:7.8| Show InChI InChI=1S/C16H18FN3S/c1-11-4-2-3-5-14(11)19-20-16-18-15(10-21-16)12-6-8-13(17)9-7-12/h6-11H,2-5H2,1H3,(H,18,20)/t11-/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia
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| CHEMBL
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UniChem
Similars
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PubMed
| n/a | n/a | 4.94E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM50272909
(4-(2-{N'-[(R)-2-Methyl-cyclohexylidene]-hydrazino}...)Show SMILES C[C@@H]1CCCCC1=NNc1nc(cs1)-c1ccc(cc1)C#N |r,w:7.8| Show InChI InChI=1S/C17H18N4S/c1-12-4-2-3-5-15(12)20-21-17-19-16(11-22-17)14-8-6-13(10-18)7-9-14/h6-9,11-12H,2-5H2,1H3,(H,19,21)/t12-/m1/s1 | PDB
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| n/a | n/a | 5.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM29136
(CHEMBL92401 | Euphozid | Iprazid | Iproniazid)Show InChI InChI=1S/C9H13N3O/c1-7(2)11-12-9(13)8-3-5-10-6-4-8/h3-7,11H,1-2H3,(H,12,13) | PDB
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| n/a | n/a | 6.56E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM50272866
(1-(4-(2,4-difluorophenyl)thiazol-2-yl)-2-((R)-2-me...)Show SMILES C[C@@H]1CCCCC1=NNc1nc(cs1)-c1ccc(F)cc1F |r,w:7.8| Show InChI InChI=1S/C16H17F2N3S/c1-10-4-2-3-5-14(10)20-21-16-19-15(9-22-16)12-7-6-11(17)8-13(12)18/h6-10H,2-5H2,1H3,(H,19,21)/t10-/m1/s1 | PDB
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| n/a | n/a | 6.83E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM50272908
(4-(2-{N'-[(S)-2-Methyl-cyclohexylidene]-hydrazino}...)Show SMILES C[C@H]1CCCCC1=NNc1nc(cs1)-c1ccc(cc1)C#N |r,w:7.8| Show InChI InChI=1S/C17H18N4S/c1-12-4-2-3-5-15(12)20-21-17-19-16(11-22-17)14-8-6-13(10-18)7-9-14/h6-9,11-12H,2-5H2,1H3,(H,19,21)/t12-/m0/s1 | PDB
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| n/a | n/a | 7.22E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM29136
(CHEMBL92401 | Euphozid | Iprazid | Iproniazid)Show InChI InChI=1S/C9H13N3O/c1-7(2)11-12-9(13)8-3-5-10-6-4-8/h3-7,11H,1-2H3,(H,12,13) | PDB
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| n/a | n/a | 7.54E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272793
((+/-)-1-(4-(4-chlorophenyl)thiazol-2-yl)-2-(2-meth...)Show InChI InChI=1S/C16H18ClN3S/c1-11-4-2-3-5-14(11)19-20-16-18-15(10-21-16)12-6-8-13(17)9-7-12/h6-11H,2-5H2,1H3,(H,18,20) | PDB
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| n/a | n/a | 1.31E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM50272795
((+/-)-1-(4-(2,4-dichlorophenyl)thiazol-2-yl)-2-(2-...)Show SMILES CC1CCCCC1=NNc1nc(cs1)-c1ccc(Cl)cc1Cl |w:7.8| Show InChI InChI=1S/C16H17Cl2N3S/c1-10-4-2-3-5-14(10)20-21-16-19-15(9-22-16)12-7-6-11(17)8-13(12)18/h6-10H,2-5H2,1H3,(H,19,21) | PDB
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| n/a | n/a | 2.68E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM50272832
((+/-)-4-(2-{N'-[2-Methyl-cyclohexylidene]-hydrazin...)Show SMILES CC1CCCCC1=NNc1nc(cs1)-c1ccc(cc1)C#N |w:7.8| Show InChI InChI=1S/C17H18N4S/c1-12-4-2-3-5-15(12)20-21-17-19-16(11-22-17)14-8-6-13(10-18)7-9-14/h6-9,11-12H,2-5H2,1H3,(H,19,21) | PDB
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| n/a | n/a | 3.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM50272793
((+/-)-1-(4-(4-chlorophenyl)thiazol-2-yl)-2-(2-meth...)Show InChI InChI=1S/C16H18ClN3S/c1-11-4-2-3-5-14(11)19-20-16-18-15(10-21-16)12-6-8-13(17)9-7-12/h6-11H,2-5H2,1H3,(H,18,20) | PDB
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| n/a | n/a | 3.52E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM50272829
((+/-)-1-(4-(2,4-difluorophenyl)thiazol-2-yl)-2-(2-...)Show InChI InChI=1S/C16H17F2N3S/c1-10-4-2-3-5-14(10)20-21-16-19-15(9-22-16)12-7-6-11(17)8-13(12)18/h6-10H,2-5H2,1H3,(H,19,21) | PDB
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| n/a | n/a | 3.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM50272792
((+/-)-1-(2-methylcyclohexylidene)-2-(4-phenylthiaz...)Show InChI InChI=1S/C16H19N3S/c1-12-7-5-6-10-14(12)18-19-16-17-15(11-20-16)13-8-3-2-4-9-13/h2-4,8-9,11-12H,5-7,10H2,1H3,(H,17,19) | PDB
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| n/a | n/a | 4.12E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM50272867
((S)-1-(2-methylcyclohexylidene)-2-(4-(4-nitropheny...)Show SMILES C[C@H]1CCCCC1=NNc1nc(cs1)-c1ccc(cc1)[N+]([O-])=O |r,w:7.8| Show InChI InChI=1S/C16H18N4O2S/c1-11-4-2-3-5-14(11)18-19-16-17-15(10-23-16)12-6-8-13(9-7-12)20(21)22/h6-11H,2-5H2,1H3,(H,17,19)/t11-/m0/s1 | PDB
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| n/a | n/a | 4.23E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM50272794
((+/-)-1-(4-(4-fluorophenyl)thiazol-2-yl)-2-(2-meth...)Show InChI InChI=1S/C16H18FN3S/c1-11-4-2-3-5-14(11)19-20-16-18-15(10-21-16)12-6-8-13(17)9-7-12/h6-11H,2-5H2,1H3,(H,18,20) | PDB
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| n/a | n/a | 4.36E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM50272907
((R)-1-(2-methylcyclohexylidene)-2-(4-(4-nitropheny...)Show SMILES C[C@@H]1CCCCC1=NNc1nc(cs1)-c1ccc(cc1)[N+]([O-])=O |r,w:7.8| Show InChI InChI=1S/C16H18N4O2S/c1-11-4-2-3-5-14(11)18-19-16-17-15(10-23-16)12-6-8-13(9-7-12)20(21)22/h6-11H,2-5H2,1H3,(H,17,19)/t11-/m1/s1 | PDB
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| n/a | n/a | 4.40E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM50272795
((+/-)-1-(4-(2,4-dichlorophenyl)thiazol-2-yl)-2-(2-...)Show SMILES CC1CCCCC1=NNc1nc(cs1)-c1ccc(Cl)cc1Cl |w:7.8| Show InChI InChI=1S/C16H17Cl2N3S/c1-10-4-2-3-5-14(10)20-21-16-19-15(9-22-16)12-7-6-11(17)8-13(12)18/h6-10H,2-5H2,1H3,(H,19,21) | PDB
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| n/a | n/a | 4.47E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] B
(Homo sapiens (Human)) | BDBM15581
(CHEMBL8706 | CLG | CLORGILINE | Clorgyline | N-[3-...)Show InChI InChI=1S/C13H15Cl2NO/c1-3-7-16(2)8-4-9-17-13-6-5-11(14)10-12(13)15/h1,5-6,10H,4,7-9H2,2H3 | PDB
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| n/a | n/a | 6.14E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOB |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM15579
(CHEMBL972 | DEPRENYL | L-Deprenyl | N-methyl-N-[(2...)Show InChI InChI=1S/C13H17N/c1-4-10-14(3)12(2)11-13-8-6-5-7-9-13/h1,5-9,12H,10-11H2,2-3H3/t12-/m1/s1 | PDB
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| n/a | n/a | 6.73E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
Amine oxidase [flavin-containing] A
(Homo sapiens (Human)) | BDBM15613
(4-chloro-N-(2-morpholin-4-ylethyl)benzamide | 4-ch...)Show InChI InChI=1S/C13H17ClN2O2/c14-12-3-1-11(2-4-12)13(17)15-5-6-16-7-9-18-10-8-16/h1-4H,5-10H2,(H,15,17) | PDB
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| n/a | n/a | 3.61E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Roma La Sapienza
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant MAOA |
J Med Chem 51: 4874-80 (2008)
Article DOI: 10.1021/jm800132g
BindingDB Entry DOI: 10.7270/Q27P8Z5J |
More data for this
Ligand-Target Pair | |
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