Found 30 hits with Last Name = 'busch' and Initial = 'ae' 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 |
|---|
Solute carrier family 22 member 2
(Homo sapiens (Human)) | BDBM39687
((2E)-1-ethyl-2-[(1-ethyl-2-quinolin-1-iumyl)methyl...)Show SMILES CCN1\C(=C\c2ccc3ccccc3[n+]2CC)C=Cc2ccccc12 |c:19| Show InChI InChI=1S/C23H23N2/c1-3-24-20(15-13-18-9-5-7-11-22(18)24)17-21-16-14-19-10-6-8-12-23(19)25(21)4-2/h5-17H,3-4H2,1-2H3/q+1 | Reactome pathway
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UniProtKB/SwissProt
DrugBank
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| Purchase
CHEMBL
MCE
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 100 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Anatomisches Institut der Bayerischen Julius-Maximilians-Universit£t
Curated by ChEMBL
| Assay Description
TP_TRANSPORTER: inhibition of TEA uptake in Xenopus laevis oocytes |
DNA Cell Biol 16: 871-81 (1997)
Article DOI: 10.1089/dna.1997.16.871
BindingDB Entry DOI: 10.7270/Q2R2148R |
More data for this
Ligand-Target Pair | |
Solute carrier family 22 member 2
(Homo sapiens (Human)) | BDBM50420192
(CHEMBL2074851)Show SMILES CC[n+]1c(CC2C=C(C)N=C(N2C)c2ccccc2)ccc2ccccc12 |c:9,t:6| Show InChI InChI=1S/C24H26N3/c1-4-27-21(15-14-19-10-8-9-13-23(19)27)17-22-16-18(2)25-24(26(22)3)20-11-6-5-7-12-20/h5-16,22H,4,17H2,1-3H3/q+1 | Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
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GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| 210 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Anatomisches Institut der Bayerischen Julius-Maximilians-Universit£t
Curated by ChEMBL
| Assay Description
TP_TRANSPORTER: inhibition of TEA uptake in Xenopus laevis oocytes |
DNA Cell Biol 16: 871-81 (1997)
Article DOI: 10.1089/dna.1997.16.871
BindingDB Entry DOI: 10.7270/Q2R2148R |
More data for this
Ligand-Target Pair | |
Solute carrier family 22 member 2
(Homo sapiens (Human)) | BDBM50420181
(CHEMBL2074704)Show InChI InChI=1S/C20H44N/c1-5-9-13-17-21(18-14-10-6-2,19-15-11-7-3)20-16-12-8-4/h5-20H2,1-4H3/q+1 | Reactome pathway
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CHEMBL
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PC cid
PC sid
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PubMed
| 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Anatomisches Institut der Bayerischen Julius-Maximilians-Universit£t
Curated by ChEMBL
| Assay Description
TP_TRANSPORTER: inhibition of TEA uptake in Xenopus laevis oocytes |
DNA Cell Biol 16: 871-81 (1997)
Article DOI: 10.1089/dna.1997.16.871
BindingDB Entry DOI: 10.7270/Q2R2148R |
More data for this
Ligand-Target Pair | |
Solute carrier family 22 member 2
(Homo sapiens (Human)) | BDBM81945
(CAS_39484 | CHEMBL105891 | CHEMBL108926 | CHEMBL27...)Show InChI InChI=1S/C12H12N/c1-13-9-7-12(8-10-13)11-5-3-2-4-6-11/h2-10H,1H3/q+1 | Reactome pathway
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| Article
PubMed
| 2.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Anatomisches Institut der Bayerischen Julius-Maximilians-Universit£t
Curated by ChEMBL
| Assay Description
TP_TRANSPORTER: inhibition of TEA uptake in Xenopus laevis oocytes |
DNA Cell Biol 16: 871-81 (1997)
Article DOI: 10.1089/dna.1997.16.871
BindingDB Entry DOI: 10.7270/Q2R2148R |
More data for this
Ligand-Target Pair | |
Solute carrier family 22 member 2
(Homo sapiens (Human)) | BDBM50367247
(QUININE | Quinamm | Quinsan | cid_3034034)Show SMILES COc1ccc2nccc([C@@H](O)[C@@H]3C[C@@H]4CCN3C[C@@H]4C=C)c2c1 |THB:20:19:12.13:16.15,10:12:19.18:16.15| Show InChI InChI=1S/C20H24N2O2/c1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18/h3-6,8,11,13-14,19-20,23H,1,7,9-10,12H2,2H3/t13-,14-,19-,20+/m0/s1 | Reactome pathway
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| DrugBank
Article
PubMed
| 3.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Anatomisches Institut der Bayerischen Julius-Maximilians-Universit£t
Curated by ChEMBL
| Assay Description
TP_TRANSPORTER: inhibition of TEA uptake in Xenopus laevis oocytes |
DNA Cell Biol 16: 871-81 (1997)
Article DOI: 10.1089/dna.1997.16.871
BindingDB Entry DOI: 10.7270/Q2R2148R |
More data for this
Ligand-Target Pair | |
Solute carrier family 22 member 2
(Homo sapiens (Human)) | BDBM50420216
(MEPIPERPHENIDOL BROMIDE)Show InChI InChI=1S/C19H32NO/c1-16(2)19(17-10-6-4-7-11-17)18(21)12-15-20(3)13-8-5-9-14-20/h4,6-7,10-11,16,18-19,21H,5,8-9,12-15H2,1-3H3/q+1 | Reactome pathway
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| PC cid
PC sid
UniChem
| Article
PubMed
| 4.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Anatomisches Institut der Bayerischen Julius-Maximilians-Universit£t
Curated by ChEMBL
| Assay Description
TP_TRANSPORTER: inhibition of TEA uptake in Xenopus laevis oocytes |
DNA Cell Biol 16: 871-81 (1997)
Article DOI: 10.1089/dna.1997.16.871
BindingDB Entry DOI: 10.7270/Q2R2148R |
More data for this
Ligand-Target Pair | |
Solute carrier family 22 member 2
(Homo sapiens (Human)) | BDBM35229
(3-(10,11-dihydro-5H-dibenzo[b,f]azepin-5-yl)-N-met...)Show InChI InChI=1S/C18H22N2/c1-19-13-6-14-20-17-9-4-2-7-15(17)11-12-16-8-3-5-10-18(16)20/h2-5,7-10,19H,6,11-14H2,1H3 | Reactome pathway
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| DrugBank
Article
PubMed
| 1.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Anatomisches Institut der Bayerischen Julius-Maximilians-Universit£t
Curated by ChEMBL
| Assay Description
TP_TRANSPORTER: inhibition of TEA uptake in Xenopus laevis oocytes |
DNA Cell Biol 16: 871-81 (1997)
Article DOI: 10.1089/dna.1997.16.871
BindingDB Entry DOI: 10.7270/Q2R2148R |
More data for this
Ligand-Target Pair | |
Solute carrier family 22 member 2
(Homo sapiens (Human)) | BDBM39344
(4-amino-N-[2-(diethylamino)ethyl]benzamide;hydroch...)Show InChI InChI=1S/C13H21N3O/c1-3-16(4-2)10-9-15-13(17)11-5-7-12(14)8-6-11/h5-8H,3-4,9-10,14H2,1-2H3,(H,15,17) | Reactome pathway
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Article
PubMed
| 5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Anatomisches Institut der Bayerischen Julius-Maximilians-Universit£t
Curated by ChEMBL
| Assay Description
TP_TRANSPORTER: inhibition of TEA uptake in Xenopus laevis oocytes |
DNA Cell Biol 16: 871-81 (1997)
Article DOI: 10.1089/dna.1997.16.871
BindingDB Entry DOI: 10.7270/Q2R2148R |
More data for this
Ligand-Target Pair | |
Solute carrier family 22 member 2
(Homo sapiens (Human)) | BDBM50079455
(CHEMBL46486 | tetramethylammonium) | Reactome pathway
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| 1.80E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Anatomisches Institut der Bayerischen Julius-Maximilians-Universit£t
Curated by ChEMBL
| Assay Description
TP_TRANSPORTER: inhibition of TEA uptake in Xenopus laevis oocytes |
DNA Cell Biol 16: 871-81 (1997)
Article DOI: 10.1089/dna.1997.16.871
BindingDB Entry DOI: 10.7270/Q2R2148R |
More data for this
Ligand-Target Pair | |
Solute carrier family 22 member 2
(Homo sapiens (Human)) | BDBM50420177
(NICOTINYL METHYLAMIDE)Show InChI InChI=1S/C7H8N2O/c1-8-7(10)6-3-2-4-9-5-6/h2-5H,1H3,(H,8,10) | Reactome pathway
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| 2.66E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Anatomisches Institut der Bayerischen Julius-Maximilians-Universit£t
Curated by ChEMBL
| Assay Description
TP_TRANSPORTER: inhibition of TEA uptake in Xenopus laevis oocytes |
DNA Cell Biol 16: 871-81 (1997)
Article DOI: 10.1089/dna.1997.16.871
BindingDB Entry DOI: 10.7270/Q2R2148R |
More data for this
Ligand-Target Pair | |
Solute carrier family 22 member 2
(Homo sapiens (Human)) | BDBM50420217
(METIPRENALINE)Show InChI InChI=1S/C12H19NO3/c1-8(2)13-7-11(15)9-4-5-10(14)12(6-9)16-3/h4-6,8,11,13-15H,7H2,1-3H3 | Reactome pathway
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| 5.70E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Anatomisches Institut der Bayerischen Julius-Maximilians-Universit£t
Curated by ChEMBL
| Assay Description
TP_TRANSPORTER: inhibition of TEA uptake in Xenopus laevis oocytes |
DNA Cell Biol 16: 871-81 (1997)
Article DOI: 10.1089/dna.1997.16.871
BindingDB Entry DOI: 10.7270/Q2R2148R |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50106236
((3R,4S)-Ethanesulfonic acid (6-benzyloxy-3-hydroxy...)Show SMILES CCS(=O)(=O)N(C)[C@@H]1[C@@H](O)C(C)(C)Oc2ccc(OCc3ccccc3)cc12 Show InChI InChI=1S/C21H27NO5S/c1-5-28(24,25)22(4)19-17-13-16(26-14-15-9-7-6-8-10-15)11-12-18(17)27-21(2,3)20(19)23/h6-13,19-20,23H,5,14H2,1-4H3/t19-,20+/m0/s1 | PDB
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| CHEMBL
PC cid
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| n/a | n/a | 50 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50099582
((3R,4S)N-[3-Hydroxy-2,2-dimethyl-6-(4,4,4-trifluor...)Show SMILES CN([C@@H]1[C@@H](O)C(C)(C)Oc2ccc(OCCCC(F)(F)F)cc12)S(C)(=O)=O Show InChI InChI=1S/C17H24F3NO5S/c1-16(2)15(22)14(21(3)27(4,23)24)12-10-11(6-7-13(12)26-16)25-9-5-8-17(18,19)20/h6-7,10,14-15,22H,5,8-9H2,1-4H3/t14-,15+/m0/s1 | PDB
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CHEMBL
MCE
PC cid
PC sid
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| PubMed
| n/a | n/a | 120 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50106233
(CHEMBL124308 | N-(6-Benzyloxy-3-hydroxy-2,2-dimeth...)Show SMILES CN(C1C(O)C(C)(C)Oc2ccc(OCc3ccccc3)cc12)S(C)(=O)=O Show InChI InChI=1S/C20H25NO5S/c1-20(2)19(22)18(21(3)27(4,23)24)16-12-15(10-11-17(16)26-20)25-13-14-8-6-5-7-9-14/h5-12,18-19,22H,13H2,1-4H3 | PDB
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| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50106231
(CHEMBL340910 | N-[3-Hydroxy-2,2-dimethyl-6-(4,4,4-...)Show SMILES CN(C1C(O)C(C)(C)Oc2ccc(OCCCC(F)(F)F)cc12)S(C)(=O)=O Show InChI InChI=1S/C17H24F3NO5S/c1-16(2)15(22)14(21(3)27(4,23)24)12-10-11(6-7-13(12)26-16)25-9-5-8-17(18,19)20/h6-7,10,14-15,22H,5,8-9H2,1-4H3 | PDB
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| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 240 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50106232
(CHEMBL125307 | N-(6-Butoxy-3-hydroxy-2,2-dimethyl-...)Show SMILES CCCCOc1ccc2OC(C)(C)C(O)C(N(C)S(C)(=O)=O)c2c1 Show InChI InChI=1S/C17H27NO5S/c1-6-7-10-22-12-8-9-14-13(11-12)15(18(4)24(5,20)21)16(19)17(2,3)23-14/h8-9,11,15-16,19H,6-7,10H2,1-5H3 | PDB
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PC cid
PC sid
UniChem
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| PubMed
| n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50106237
((3S,4R)-Ethanesulfonic acid (6-benzyloxy-3-hydroxy...)Show SMILES CCS(=O)(=O)N(C)[C@H]1[C@H](O)C(C)(C)Oc2ccc(OCc3ccccc3)cc12 Show InChI InChI=1S/C21H27NO5S/c1-5-28(24,25)22(4)19-17-13-16(26-14-15-9-7-6-8-10-15)11-12-18(17)27-21(2,3)20(19)23/h6-13,19-20,23H,5,14H2,1-4H3/t19-,20+/m1/s1 | PDB
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PC sid
UniChem
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| PubMed
| n/a | n/a | 400 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50106234
((3S,4R)-(+)-N-[3-Hydroxy-2,2-dimethyl-6-(4,4,4-tri...)Show SMILES CN([C@H]1[C@H](O)C(C)(C)Oc2ccc(OCCCC(F)(F)F)cc12)S(C)(=O)=O Show InChI InChI=1S/C17H24F3NO5S/c1-16(2)15(22)14(21(3)27(4,23)24)12-10-11(6-7-13(12)26-16)25-9-5-8-17(18,19)20/h6-7,10,14-15,22H,5,8-9H2,1-4H3/t14-,15+/m1/s1 | PDB
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PC cid
PC sid
UniChem
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| PubMed
| n/a | n/a | 440 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50106228
((3R,4S)-Ethanesulfonic acid (6-fluoro-3-hydroxy-2,...)Show SMILES CCS(=O)(=O)N(C)[C@@H]1[C@@H](O)C(C)(C)Oc2ccc(F)cc12 Show InChI InChI=1S/C14H20FNO4S/c1-5-21(18,19)16(4)12-10-8-9(15)6-7-11(10)20-14(2,3)13(12)17/h6-8,12-13,17H,5H2,1-4H3/t12-,13+/m0/s1 | PDB
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| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 700 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50106235
(CHEMBL124810 | N-(3-Hydroxy-2,2-dimethyl-6-propoxy...)Show SMILES CCCOc1ccc2OC(C)(C)C(O)C(N(C)S(C)(=O)=O)c2c1 Show InChI InChI=1S/C16H25NO5S/c1-6-9-21-11-7-8-13-12(10-11)14(17(4)23(5,19)20)15(18)16(2,3)22-13/h7-8,10,14-15,18H,6,9H2,1-5H3 | PDB
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| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 900 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50106226
(CHEMBL338171 | N-(6-Chloro-3-hydroxy-2,2-dimethyl-...)Show InChI InChI=1S/C13H18ClNO4S/c1-13(2)12(16)11(15(3)20(4,17)18)9-7-8(14)5-6-10(9)19-13/h5-7,11-12,16H,1-4H3 | PDB
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| n/a | n/a | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50106229
(CHEMBL127435 | Ethanesulfonic acid (6-fluoro-3-hyd...)Show InChI InChI=1S/C14H20FNO4S/c1-5-21(18,19)16(4)12-10-8-9(15)6-7-11(10)20-14(2,3)13(12)17/h6-8,12-13,17H,5H2,1-4H3 | PDB
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| n/a | n/a | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50106223
((3S,4R)-Ethanesulfonic acid (6-fluoro-3-hydroxy-2,...)Show SMILES CCS(=O)(=O)N(C)[C@H]1[C@H](O)C(C)(C)Oc2ccc(F)cc12 Show InChI InChI=1S/C14H20FNO4S/c1-5-21(18,19)16(4)12-10-8-9(15)6-7-11(10)20-14(2,3)13(12)17/h6-8,12-13,17H,5H2,1-4H3/t12-,13+/m1/s1 | PDB
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| n/a | n/a | 2.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50106224
(CHEMBL125259 | Ethanesulfonic acid (3-hydroxy-2,2-...)Show InChI InChI=1S/C14H21NO4S/c1-5-20(17,18)15(4)12-10-8-6-7-9-11(10)19-14(2,3)13(12)16/h6-9,12-13,16H,5H2,1-4H3 | PDB
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| n/a | n/a | 3.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50099567
((3S,4R)-Ethanesulfonic acid (6-cyano-3-hydroxy-2,2...)Show SMILES CCS(=O)(=O)N(C)[C@H]1[C@H](O)C(C)(C)Oc2ccc(cc12)C#N Show InChI InChI=1S/C15H20N2O4S/c1-5-22(19,20)17(4)13-11-8-10(9-16)6-7-12(11)21-15(2,3)14(13)18/h6-8,13-14,18H,5H2,1-4H3/t13-,14+/m1/s1 | PDB
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| n/a | n/a | 5.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes,(Experiment 2) |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50106227
((3R,4S)-Ethanesulfonic acid (6-cyano-3-hydroxy-2,2...)Show SMILES CCS(=O)(=O)N(C)[C@@H]1[C@@H](O)C(C)(C)Oc2ccc(cc12)C#N Show InChI InChI=1S/C15H20N2O4S/c1-5-22(19,20)17(4)13-11-8-10(9-16)6-7-12(11)21-15(2,3)14(13)18/h6-8,13-14,18H,5H2,1-4H3/t13-,14+/m0/s1 | PDB
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| n/a | n/a | 5.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes,(Experiment 1) |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50106230
(CHEMBL338273 | Ethanesulfonic acid (6-cyano-3-hydr...)Show SMILES CCS(=O)(=O)N(C)C1C(O)C(C)(C)Oc2ccc(cc12)C#N Show InChI InChI=1S/C15H20N2O4S/c1-5-22(19,20)17(4)13-11-8-10(9-16)6-7-12(11)21-15(2,3)14(13)18/h6-8,13-14,18H,5H2,1-4H3 | PDB
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| n/a | n/a | 6.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Solute carrier family 22 member 2
(Homo sapiens (Human)) | BDBM50033369
(AMANTADINE | CHEMBL660 | SYMADINE | SYMMETREL)Show SMILES NC12CC3CC(CC(C3)C1)C2 |THB:6:5:2:8.7.9,6:7:4.5.10:2,9:7:4:10.1.2,9:1:4:8.6.7,0:1:4:8.6.7| Show InChI InChI=1S/C10H17N/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6,11H2 | Reactome pathway
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| n/a | n/a | 2.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut f£r Physiologie
Curated by ChEMBL
| Assay Description
TP_TRANSPORTER: inhibition of Dopamine uptake (Dopamine: 200 uM) in Xenopus laevis oocytes |
Mol Pharmacol 54: 342-52 (1998)
BindingDB Entry DOI: 10.7270/Q2C82BK9 |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50099567
((3S,4R)-Ethanesulfonic acid (6-cyano-3-hydroxy-2,2...)Show SMILES CCS(=O)(=O)N(C)[C@H]1[C@H](O)C(C)(C)Oc2ccc(cc12)C#N Show InChI InChI=1S/C15H20N2O4S/c1-5-22(19,20)17(4)13-11-8-10(9-16)6-7-12(11)21-15(2,3)14(13)18/h6-8,13-14,18H,5H2,1-4H3/t13-,14+/m1/s1 | PDB
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| n/a | n/a | 4.45E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes,(Experiment 1) |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
Potassium voltage-gated channel subfamily E/KQT member 1
(Homo sapiens (Human)) | BDBM50106225
(Butane-1-sulfonic acid (6-cyano-3-hydroxy-2,2-dime...)Show SMILES CCCCS(=O)(=O)N(C)C1C(O)C(C)(C)Oc2ccc(cc12)C#N Show InChI InChI=1S/C17H24N2O4S/c1-5-6-9-24(21,22)19(4)15-13-10-12(11-18)7-8-14(13)23-17(2,3)16(15)20/h7-8,10,15-16,20H,5-6,9H2,1-4H3 | PDB
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| n/a | n/a | 5.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Aventis Pharma Deutschland GmbH
Curated by ChEMBL
| Assay Description
Inhibition of human IKs-channel expressed in Xenopus oocytes |
J Med Chem 44: 3831-7 (2001)
BindingDB Entry DOI: 10.7270/Q26H4GPX |
More data for this
Ligand-Target Pair | |
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