Found 99 hits Enz. Inhib. hit(s) with all data for entry = 50018433 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 |
Cholinesterase
(Homo sapiens (Human)) | BDBM50608244
![PNG](/data/jpeg/tenK5060/BindingDB_50608244.png) (CHEMBL5271306)Show SMILES CC(=O)Nc1nc(Cl)c2n(cnc2n1)[C@H]1O[C@H](COCc2ccccc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@@H]1OCc1ccccc1 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 50 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM10404
![PNG](/data/jpeg/tenK1/BindingDB_10404.png) ((1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetrac...)Show SMILES COc1ccc2CN(C)CC[C@@]34C=C[C@H](O)C[C@@H]3Oc1c24 |r,c:12| Show InChI InChI=1S/C17H21NO3/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11(10-18)15(16)17/h3-6,12,14,19H,7-10H2,1-2H3/t12-,14-,17-/m0/s1 | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
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CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem
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Similars
| | 500 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Homo sapiens (Human)) | BDBM10404
![PNG](/data/jpeg/tenK1/BindingDB_10404.png) ((1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetrac...)Show SMILES COc1ccc2CN(C)CC[C@@]34C=C[C@H](O)C[C@@H]3Oc1c24 |r,c:12| Show InChI InChI=1S/C17H21NO3/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11(10-18)15(16)17/h3-6,12,14,19H,7-10H2,1-2H3/t12-,14-,17-/m0/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
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CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem
Patents
Similars
| DrugBank PDB
| 500 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | ![3D 3D](/images/Docked_3d.png) 3D Structure (crystal) |
Acetylcholinesterase
(Homo sapiens (Human)) | BDBM10404
![PNG](/data/jpeg/tenK1/BindingDB_10404.png) ((1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetrac...)Show SMILES COc1ccc2CN(C)CC[C@@]34C=C[C@H](O)C[C@@H]3Oc1c24 |r,c:12| Show InChI InChI=1S/C17H21NO3/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11(10-18)15(16)17/h3-6,12,14,19H,7-10H2,1-2H3/t12-,14-,17-/m0/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
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CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem
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| DrugBank PDB
| 540 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | ![3D 3D](/images/Docked_3d.png) 3D Structure (crystal) |
Acetylcholinesterase
(Homo sapiens (Human)) | BDBM11682
![PNG](/data/jpeg/tenK1/BindingDB_11682.png) (2,3-dihydroxybutanedioic acid; 3-[(1S)-1-(dimethyl...)Show InChI InChI=1S/C14H22N2O2/c1-6-16(5)14(17)18-13-9-7-8-12(10-13)11(2)15(3)4/h7-11H,6H2,1-5H3/t11-/m0/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
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DrugBank MCE KEGG PC cid PC sid UniChem
Similars
| DrugBank
| 700 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM50608255
![PNG](/data/jpeg/tenK5060/BindingDB_50608255.png) (CHEMBL5272999)Show SMILES [H][C@@]1(O[C@@H](N=[N+]=[N-])[C@H](OC(C)=O)[C@H]1OCc1ccccc1)[C@H](OCc1ccccc1)C(=O)NCCCCCCCCCCCC |r| | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 1.73E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM50608233
![PNG](/data/jpeg/tenK5060/BindingDB_50608233.png) (CHEMBL5268833)Show SMILES OC[C@H]1O[C@@H](OCc2cn(CCCCCCn3c4ccccc4c(=O)c4ccccc34)nn2)[C@H](O)[C@@H]1O |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 1.76E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
|
More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM50608259
![PNG](/data/jpeg/tenK5060/BindingDB_50608259.png) (CHEMBL5267382)Show SMILES CCCCCCCCO[C@H]1[C@H](OC(C)=O)[C@@H](Cn2c(=O)n(C)c3ncn(C)c3c2=O)OC(OC(C)=O)[C@@H]1OC(C)=O |r| | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 3.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM50608257
![PNG](/data/jpeg/tenK5060/BindingDB_50608257.png) (CHEMBL5266593)Show SMILES [H][C@@]1(O[C@H]([C@H](OC(C)=O)[C@H]1OCc1ccccc1)n1cc(nn1)-c1ccccc1)[C@H](OCc1ccccc1)C(=O)NCCCCCCCCCCCC |r| | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 3.53E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM50608245
![PNG](/data/jpeg/tenK5060/BindingDB_50608245.png) (CHEMBL5273571)Show SMILES CO[C@H]1O[C@H](Cn2c(=O)n(C)c3ncn(C)c3c2=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 4.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM50608248
![PNG](/data/jpeg/tenK5060/BindingDB_50608248.png) (CHEMBL5273862)Show SMILES COC1O[C@H](Cn2ccc(=O)n(C[C@H]3O[C@H](OC)[C@H](OCc4ccccc4)[C@@H](OCc4ccccc4)[C@@H]3OCc3ccccc3)c2=O)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 4.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM50608248
![PNG](/data/jpeg/tenK5060/BindingDB_50608248.png) (CHEMBL5273862)Show SMILES COC1O[C@H](Cn2ccc(=O)n(C[C@H]3O[C@H](OC)[C@H](OCc4ccccc4)[C@@H](OCc4ccccc4)[C@@H]3OCc3ccccc3)c2=O)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1 |r| | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 4.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM50608245
![PNG](/data/jpeg/tenK5060/BindingDB_50608245.png) (CHEMBL5273571)Show SMILES CO[C@H]1O[C@H](Cn2c(=O)n(C)c3ncn(C)c3c2=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O |r| | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 4.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM50608259
![PNG](/data/jpeg/tenK5060/BindingDB_50608259.png) (CHEMBL5267382)Show SMILES CCCCCCCCO[C@H]1[C@H](OC(C)=O)[C@@H](Cn2c(=O)n(C)c3ncn(C)c3c2=O)OC(OC(C)=O)[C@@H]1OC(C)=O |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 5.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM50608254
![PNG](/data/jpeg/tenK5060/BindingDB_50608254.png) (CHEMBL5274058)Show SMILES CC(=O)O[C@H]1C(NS(C)(=O)=O)O[C@H](Cn2c(=O)n(C)c3ncn(C)c3c2=O)[C@@H]1OCc1ccccc1 |r| | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 6.61E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM50608246
![PNG](/data/jpeg/tenK5060/BindingDB_50608246.png) (CHEMBL5285312)Show SMILES CO[C@H]1O[C@H](Cn2cnc3c(Cl)nc(NC(C)=O)nc23)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1 |r| | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 7.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
|
More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM10404
![PNG](/data/jpeg/tenK1/BindingDB_10404.png) ((1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetrac...)Show SMILES COc1ccc2CN(C)CC[C@@]34C=C[C@H](O)C[C@@H]3Oc1c24 |r,c:12| Show InChI InChI=1S/C17H21NO3/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11(10-18)15(16)17/h3-6,12,14,19H,7-10H2,1-2H3/t12-,14-,17-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
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CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem
Patents
Similars
| DrugBank
| 9.37E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
|
More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM10404
![PNG](/data/jpeg/tenK1/BindingDB_10404.png) ((1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetrac...)Show SMILES COc1ccc2CN(C)CC[C@@]34C=C[C@H](O)C[C@@H]3Oc1c24 |r,c:12| Show InChI InChI=1S/C17H21NO3/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11(10-18)15(16)17/h3-6,12,14,19H,7-10H2,1-2H3/t12-,14-,17-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| Purchase
CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem
Patents
Similars
| DrugBank
| 9.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
|
More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM50608252
![PNG](/data/jpeg/tenK5060/BindingDB_50608252.png) (CHEMBL5271574)Show SMILES [H][C@@]1(OC([C@H](OC(C)=O)[C@H]1OC(C)=O)n1cc(nn1)-c1ccccc1)[C@H](OCc1ccccc1)C(=O)NCCCCCCCCCCCC |r| | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 9.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM50608258
![PNG](/data/jpeg/tenK5060/BindingDB_50608258.png) (CHEMBL5287680)Show SMILES [H][C@@]1(O[C@@H]([C@H](OC(C)=O)[C@H]1OCc1ccccc1)n1cc(nn1)-c1ccccc1)[C@H](OCc1ccccc1)C(=O)NCCCCCCCCCCCC |r| | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 9.69E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Homo sapiens (Human)) | BDBM50608238
![PNG](/data/jpeg/tenK5060/BindingDB_50608238.png) (CHEMBL5279849)Show SMILES CC(=O)Nc1nc(Cl)c2ncn(C3O[C@H](CC(=O)NCc4ccccc4)[C@H](OC(C)=O)[C@H]3OC(C)=O)c2n1 |r| | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 1.48E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Equus caballus (Horse)) | BDBM50608225
![PNG](/data/jpeg/tenK5060/BindingDB_50608225.png) (CHEMBL5282473)Show SMILES OC[C@H]1O[C@@H](OCCn2cnc3ccccc23)[C@H](O)[C@@H](O)[C@@H]1O |r| | PDB
UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 1.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Homo sapiens (Human)) | BDBM50608240
![PNG](/data/jpeg/tenK5060/BindingDB_50608240.png) (CHEMBL5273719)Show SMILES CC(=O)Nc1nc(Cl)c2n(cnc2n1)C1O[C@@H]([C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@H]1OC(C)=O)C(=O)NCc1ccccc1 |r| | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 1.87E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM50608247
![PNG](/data/jpeg/tenK5060/BindingDB_50608247.png) (CHEMBL5279226)Show SMILES COC1O[C@H](Cn2ccc(=O)n(C[C@H]3O[C@H](OC)[C@H](O)[C@@H](O)[C@@H]3O)c2=O)[C@@H](O)[C@H](O)[C@H]1O |r| | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 2.29E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Homo sapiens (Human)) | BDBM50608237
![PNG](/data/jpeg/tenK5060/BindingDB_50608237.png) (CHEMBL5271146)Show SMILES [H][C@]12OC([C@H](OC(C)=O)[C@@]1([H])OC(=O)[C@@H]2O)n1cnc2c(Cl)nc(NC(C)=O)nc12 |r| | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 2.37E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Equus caballus (Horse)) | BDBM50608227
![PNG](/data/jpeg/tenK5060/BindingDB_50608227.png) (CHEMBL5287005)Show SMILES OC[C@H]1O[C@@H](OCCN2CN(Cc3ccccc3)c3ccccc23)[C@H](O)[C@@H](O)[C@H]1O |r| | PDB
UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 2.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Homo sapiens (Human)) | BDBM50608243
![PNG](/data/jpeg/tenK5060/BindingDB_50608243.png) (CHEMBL5281655)Show SMILES CC(=O)Nc1nc(Cl)c2ncn(C3O[C@@H]([C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)C(O)=O)c2n1 |r| | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 2.69E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Homo sapiens (Human)) | BDBM50608241
![PNG](/data/jpeg/tenK5060/BindingDB_50608241.png) (CHEMBL5266369)Show SMILES CC(=O)Nc1nc(Cl)c2ncn(C3O[C@@H]([C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)C(=O)NCc3ccccc3)c2n1 |r| | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 3.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Homo sapiens (Human)) | BDBM50608242
![PNG](/data/jpeg/tenK5060/BindingDB_50608242.png) (CHEMBL5279509)Show SMILES CC(=O)Nc1nc(Cl)c2n(cnc2n1)C1O[C@@H]([C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@H]1OC(C)=O)C(O)=O |r| | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 3.79E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Homo sapiens (Human)) | BDBM50608239
![PNG](/data/jpeg/tenK5060/BindingDB_50608239.png) (CHEMBL5284808)Show SMILES CC(=O)Nc1nc(NCc2ccccc2)c2ncn(C3O[C@H](CC(=O)NCc4ccccc4)[C@H](OC(C)=O)[C@H]3OC(C)=O)c2n1 |r| | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 5.05E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Equus caballus (Horse)) | BDBM50608228
![PNG](/data/jpeg/tenK5060/BindingDB_50608228.png) (CHEMBL5287059)Show SMILES OC[C@H]1O[C@@H](OCCN2CN(Cc3ccccc3)c3ccccc23)[C@H](O)[C@@H](O)[C@@H]1O |r| | PDB
UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 5.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM50608260
![PNG](/data/jpeg/tenK5060/BindingDB_50608260.png) (CHEMBL5266941)Show SMILES COC1O[C@H](Cn2ccc(=O)[nH]c2=O)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | <1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM50608247
![PNG](/data/jpeg/tenK5060/BindingDB_50608247.png) (CHEMBL5279226)Show SMILES COC1O[C@H](Cn2ccc(=O)n(C[C@H]3O[C@H](OC)[C@H](O)[C@@H](O)[C@@H]3O)c2=O)[C@@H](O)[C@H](O)[C@H]1O |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | <1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM50608246
![PNG](/data/jpeg/tenK5060/BindingDB_50608246.png) (CHEMBL5285312)Show SMILES CO[C@H]1O[C@H](Cn2cnc3c(Cl)nc(NC(C)=O)nc23)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | <1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM50608256
![PNG](/data/jpeg/tenK5060/BindingDB_50608256.png) (CHEMBL5280828)Show SMILES [H][C@@]1(O[C@H](N=[N+]=[N-])[C@H](OC(C)=O)[C@H]1OCc1ccccc1)[C@H](OCc1ccccc1)C(=O)NCCCCCCCCCCCC |r| | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM50608253
![PNG](/data/jpeg/tenK5060/BindingDB_50608253.png) (CHEMBL5284047)Show SMILES [H][C@]12O[C@H](Cn3c(=O)n(C)c4ncn(C)c4c3=O)[C@H](OCc3ccccc3)[C@@]1([H])OC(C)(C)O2 |r| | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM50608251
![PNG](/data/jpeg/tenK5060/BindingDB_50608251.png) (CHEMBL5287695)Show SMILES [H][C@@]1(OC(N=[N+]=[N-])[C@H](OC(C)=O)[C@H]1OC(C)=O)[C@H](OCc1ccccc1)C(=O)NCCCCCCCCCCCC |r| | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM50608250
![PNG](/data/jpeg/tenK5060/BindingDB_50608250.png) (CHEMBL5289835)Show SMILES [H][C@@]1(OC(OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O)[C@H](OCc1ccccc1)C(=O)NCCCCCCCCCCCC |r| | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Electrophorus electricus (Electric eel)) | BDBM50608249
![PNG](/data/jpeg/tenK5060/BindingDB_50608249.png) (CHEMBL5269964)Show SMILES [H][C@@]1(OC(OC(C)=O)[C@H](OC(C)=O)[C@H]1OCc1ccccc1)[C@H](OCc1ccccc1)C(=O)NCCCCCCCCCCCC |r| | UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM50608243
![PNG](/data/jpeg/tenK5060/BindingDB_50608243.png) (CHEMBL5281655)Show SMILES CC(=O)Nc1nc(Cl)c2ncn(C3O[C@@H]([C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)C(O)=O)c2n1 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM50608242
![PNG](/data/jpeg/tenK5060/BindingDB_50608242.png) (CHEMBL5279509)Show SMILES CC(=O)Nc1nc(Cl)c2n(cnc2n1)C1O[C@@H]([C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@H]1OC(C)=O)C(O)=O |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM50608241
![PNG](/data/jpeg/tenK5060/BindingDB_50608241.png) (CHEMBL5266369)Show SMILES CC(=O)Nc1nc(Cl)c2ncn(C3O[C@@H]([C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)C(=O)NCc3ccccc3)c2n1 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM50608240
![PNG](/data/jpeg/tenK5060/BindingDB_50608240.png) (CHEMBL5273719)Show SMILES CC(=O)Nc1nc(Cl)c2n(cnc2n1)C1O[C@@H]([C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@H]1OC(C)=O)C(=O)NCc1ccccc1 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM50608239
![PNG](/data/jpeg/tenK5060/BindingDB_50608239.png) (CHEMBL5284808)Show SMILES CC(=O)Nc1nc(NCc2ccccc2)c2ncn(C3O[C@H](CC(=O)NCc4ccccc4)[C@H](OC(C)=O)[C@H]3OC(C)=O)c2n1 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM50608237
![PNG](/data/jpeg/tenK5060/BindingDB_50608237.png) (CHEMBL5271146)Show SMILES [H][C@]12OC([C@H](OC(C)=O)[C@@]1([H])OC(=O)[C@@H]2O)n1cnc2c(Cl)nc(NC(C)=O)nc12 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Homo sapiens (Human)) | BDBM50608238
![PNG](/data/jpeg/tenK5060/BindingDB_50608238.png) (CHEMBL5279849)Show SMILES CC(=O)Nc1nc(Cl)c2ncn(C3O[C@H](CC(=O)NCc4ccccc4)[C@H](OC(C)=O)[C@H]3OC(C)=O)c2n1 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Cholinesterase
(Equus caballus (Horse)) | BDBM50608226
![PNG](/data/jpeg/tenK5060/BindingDB_50608226.png) (CHEMBL5269935)Show SMILES OC[C@H]1O[C@@H](OCCn2cnc3ccccc23)[C@H](O)[C@@H](O)[C@H]1O |r| | PDB
UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | 7.82E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Mus musculus (mouse)) | BDBM8963
![PNG](/data/jpeg/tenK0/BindingDB_8963.png) (CHEMBL32823 | Homodimeric Tacrine Analog 3b | N-[7...)Show SMILES C(CCCNc1c2CCCCc2nc2ccccc12)CCCNc1c2CCCCc2nc2ccccc12 Show InChI InChI=1S/C33H40N4/c1(2-12-22-34-32-24-14-4-8-18-28(24)36-29-19-9-5-15-25(29)32)3-13-23-35-33-26-16-6-10-20-30(26)37-31-21-11-7-17-27(31)33/h4,6,8,10,14,16,18,20H,1-3,5,7,9,11-13,15,17,19,21-23H2,(H,34,36)(H,35,37) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| Purchase
CHEMBL MCE MMDB PC cid PC sid PDB UniChem
Similars
| | n/a | n/a | 1.90 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Mus musculus (mouse)) | BDBM50608266
![PNG](/data/jpeg/tenK5060/BindingDB_50608266.png) (CHEMBL5288285)Show SMILES [H][C@]12O[C@H](CNCCCCCCCCCCCNc3c4CCCCc4nc4ccccc34)[C@H](O)[C@@]1([H])OC(C)(C)O2 |r| | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | n/a | n/a | 2.20 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |
Acetylcholinesterase
(Mus musculus (mouse)) | BDBM50467898
![PNG](/data/jpeg/tenK5046/BindingDB_50467898.png) (CHEMBL4282214)Show SMILES [H][C@@]12OC(C)(C)O[C@]1([H])[C@@]1([H])OC(C)(C)O[C@@]1([H])[C@@H](CNCCCCCCCCCNc1c3CCCCc3nc3ccccc13)O2 |r| Show InChI InChI=1S/C34H51N3O5/c1-33(2)39-29-27(38-32-31(30(29)40-33)41-34(3,4)42-32)22-35-20-14-8-6-5-7-9-15-21-36-28-23-16-10-12-18-25(23)37-26-19-13-11-17-24(26)28/h10,12,16,18,27,29-32,35H,5-9,11,13-15,17,19-22H2,1-4H3,(H,36,37)/t27-,29+,30+,31-,32-/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| | n/a | n/a | 4.80 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
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Citation and Details
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More data for this Ligand-Target Pair | |