Found 85 hits with Last Name = 'michne' and Initial = 'wf' 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 |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030498
(CHEMBL53841 | [1-Benzyl-7-chloro-1H-quinolin-(4E)-...)Show InChI InChI=1S/C22H25ClN2/c1-2-3-4-8-14-24-21-13-15-25(17-18-9-6-5-7-10-18)22-16-19(23)11-12-20(21)22/h5-7,9-13,15-16H,2-4,8,14,17H2,1H3/b24-21+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 32 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030511
(CHEMBL293721 | [1-Benzyl-6-methoxy-1H-quinolin-(4E...)Show InChI InChI=1S/C23H28N2O/c1-3-4-5-9-15-24-22-14-16-25(18-19-10-7-6-8-11-19)23-13-12-20(26-2)17-21(22)23/h6-8,10-14,16-17H,3-5,9,15,18H2,1-2H3/b24-22+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 47 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030510
(CHEMBL299668 | [1-Benzyl-7-chloro-1H-quinolin-(4E)...)Show InChI InChI=1S/C21H23ClN2/c1-2-3-7-13-23-20-12-14-24(16-17-8-5-4-6-9-17)21-15-18(22)10-11-19(20)21/h4-6,8-12,14-15H,2-3,7,13,16H2,1H3/b23-20+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 65 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030505
(CHEMBL56589 | [7-Chloro-1-naphthalen-2-yl-1H-quino...)Show SMILES CCCCC\N=c1/ccn(-c2ccc3ccccc3c2)c2cc(Cl)ccc12 Show InChI InChI=1S/C24H23ClN2/c1-2-3-6-14-26-23-13-15-27(24-17-20(25)10-12-22(23)24)21-11-9-18-7-4-5-8-19(18)16-21/h4-5,7-13,15-17H,2-3,6,14H2,1H3/b26-23+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 75 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030495
(CHEMBL55202 | [7-Chloro-1-(4-methoxy-benzyl)-1H-qu...)Show SMILES CCCCCC\N=c1/ccn(Cc2ccc(OC)cc2)c2cc(Cl)ccc12 Show InChI InChI=1S/C23H27ClN2O/c1-3-4-5-6-14-25-22-13-15-26(23-16-19(24)9-12-21(22)23)17-18-7-10-20(27-2)11-8-18/h7-13,15-16H,3-6,14,17H2,1-2H3/b25-22+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 88 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030499
(CHEMBL56998 | [7-Chloro-1-(4-chloro-benzyl)-1H-qui...)Show SMILES CCCCCC\N=c1/ccn(Cc2ccc(Cl)cc2)c2cc(Cl)ccc12 Show InChI InChI=1S/C22H24Cl2N2/c1-2-3-4-5-13-25-21-12-14-26(16-17-6-8-18(23)9-7-17)22-15-19(24)10-11-20(21)22/h6-12,14-15H,2-5,13,16H2,1H3/b25-21+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 100 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030508
(CHEMBL54934 | [1-Benzyl-7-chloro-1H-quinolin-(4E)-...)Show InChI InChI=1S/C23H27ClN2/c1-2-3-4-5-9-15-25-22-14-16-26(18-19-10-7-6-8-11-19)23-17-20(24)12-13-21(22)23/h6-8,10-14,16-17H,2-5,9,15,18H2,1H3/b25-22+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 117 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030521
(CHEMBL56173 | [1-Benzyl-1H-quinolin-(4E)-ylidene]-...)Show InChI InChI=1S/C22H26N2/c1-2-3-4-10-16-23-21-15-17-24(18-19-11-6-5-7-12-19)22-14-9-8-13-20(21)22/h5-9,11-15,17H,2-4,10,16,18H2,1H3/b23-21+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 164 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030497
(CHEMBL298622 | [7-Chloro-1-(2-chloro-benzyl)-1H-qu...)Show InChI InChI=1S/C22H24Cl2N2/c1-2-3-4-7-13-25-21-12-14-26(16-17-8-5-6-9-20(17)24)22-15-18(23)10-11-19(21)22/h5-6,8-12,14-15H,2-4,7,13,16H2,1H3/b25-21+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 190 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030500
(CHEMBL293083 | [1-Benzyl-7-chloro-1H-quinolin-(4E)...)Show InChI InChI=1S/C20H21ClN2/c1-2-3-12-22-19-11-13-23(15-16-7-5-4-6-8-16)20-14-17(21)9-10-18(19)20/h4-11,13-14H,2-3,12,15H2,1H3/b22-19+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 198 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030528
(CHEMBL291738 | [1-Benzyl-7-chloro-1H-quinolin-(4E)...)Show InChI InChI=1S/C20H21ClN2/c1-15(2)13-22-19-10-11-23(14-16-6-4-3-5-7-16)20-12-17(21)8-9-18(19)20/h3-12,15H,13-14H2,1-2H3/b22-19+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 206 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030496
(CHEMBL416313 | [1-(4-Chloro-benzyl)-6-trifluoromet...)Show SMILES CCCCC\N=c1/ccn(Cc2ccc(Cl)cc2)c2ccc(cc12)C(F)(F)F Show InChI InChI=1S/C22H22ClF3N2/c1-2-3-4-12-27-20-11-13-28(15-16-5-8-18(23)9-6-16)21-10-7-17(14-19(20)21)22(24,25)26/h5-11,13-14H,2-4,12,15H2,1H3/b27-20+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 213 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030497
(CHEMBL298622 | [7-Chloro-1-(2-chloro-benzyl)-1H-qu...)Show InChI InChI=1S/C22H24Cl2N2/c1-2-3-4-7-13-25-21-12-14-26(16-17-8-5-6-9-20(17)24)22-15-18(23)10-11-19(21)22/h5-6,8-12,14-15H,2-4,7,13,16H2,1H3/b25-21+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 216 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030523
(CHEMBL294373 | [1-(4-Chloro-benzyl)-8-fluoro-1H-qu...)Show InChI InChI=1S/C21H22ClFN2/c1-2-3-4-13-24-20-12-14-25(15-16-8-10-17(22)11-9-16)21-18(20)6-5-7-19(21)23/h5-12,14H,2-4,13,15H2,1H3/b24-20+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 227 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030519
(CHEMBL53676 | [7-Chloro-1-(3,4-dichloro-benzyl)-1H...)Show SMILES CCCCCC\N=c1/ccn(Cc2ccc(Cl)c(Cl)c2)c2cc(Cl)ccc12 Show InChI InChI=1S/C22H23Cl3N2/c1-2-3-4-5-11-26-21-10-12-27(22-14-17(23)7-8-18(21)22)15-16-6-9-19(24)20(25)13-16/h6-10,12-14H,2-5,11,15H2,1H3/b26-21+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 231 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030502
(CHEMBL299451 | [1-(4-Chloro-benzyl)-7-trifluoromet...)Show SMILES CCCCC\N=c1/ccn(Cc2ccc(Cl)cc2)c2cc(ccc12)C(F)(F)F Show InChI InChI=1S/C22H22ClF3N2/c1-2-3-4-12-27-20-11-13-28(15-16-5-8-18(23)9-6-16)21-14-17(22(24,25)26)7-10-19(20)21/h5-11,13-14H,2-4,12,15H2,1H3/b27-20+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 239 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030515
(CHEMBL55142 | Methanesulfonate4-hexylamino-6-metho...)Show SMILES CCCCCC\[NH+]=c1/ccn(-c2ccccc2)c2c(cc(OC)cc12)-c1ccccc1 Show InChI InChI=1S/C28H30N2O/c1-3-4-5-12-18-29-27-17-19-30(23-15-10-7-11-16-23)28-25(22-13-8-6-9-14-22)20-24(31-2)21-26(27)28/h6-11,13-17,19-21H,3-5,12,18H2,1-2H3/p+1/b29-27+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 240 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030509
(CHEMBL59308 | Methanesulfonate4-hexylamino-1-methy...)Show InChI InChI=1S/C22H26N2/c1-3-4-5-9-16-23-21-15-17-24(2)22-19(13-10-14-20(21)22)18-11-7-6-8-12-18/h6-8,10-15,17H,3-5,9,16H2,1-2H3/p+1/b23-21+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 240 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030508
(CHEMBL54934 | [1-Benzyl-7-chloro-1H-quinolin-(4E)-...)Show InChI InChI=1S/C23H27ClN2/c1-2-3-4-5-9-15-25-22-14-16-26(18-19-10-7-6-8-11-19)23-17-20(24)12-13-21(22)23/h6-8,10-14,16-17H,2-5,9,15,18H2,1H3/b25-22+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 249 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030510
(CHEMBL299668 | [1-Benzyl-7-chloro-1H-quinolin-(4E)...)Show InChI InChI=1S/C21H23ClN2/c1-2-3-7-13-23-20-12-14-24(16-17-8-5-4-6-9-17)21-15-18(22)10-11-19(20)21/h4-6,8-12,14-15H,2-3,7,13,16H2,1H3/b23-20+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030516
(CHEMBL54846 | [7-Chloro-1-(2-chloro-benzyl)-1H-qui...)Show SMILES Clc1ccc(C\N=c2/ccn(Cc3ccccc3Cl)c3cc(Cl)ccc23)c(Cl)c1 Show InChI InChI=1S/C23H16Cl4N2/c24-17-6-5-15(21(27)11-17)13-28-22-9-10-29(14-16-3-1-2-4-20(16)26)23-12-18(25)7-8-19(22)23/h1-12H,13-14H2/b28-22+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 259 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030511
(CHEMBL293721 | [1-Benzyl-6-methoxy-1H-quinolin-(4E...)Show InChI InChI=1S/C23H28N2O/c1-3-4-5-9-15-24-22-14-16-25(18-19-10-7-6-8-11-19)23-13-12-20(26-2)17-21(22)23/h6-8,10-14,16-17H,3-5,9,15,18H2,1-2H3/b24-22+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 267 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030524
(CHEMBL417417 | [1-(4-Chloro-benzyl)-6-methoxy-1H-q...)Show InChI InChI=1S/C22H25ClN2O/c1-3-4-5-13-24-21-12-14-25(16-17-6-8-18(23)9-7-17)22-11-10-19(26-2)15-20(21)22/h6-12,14-15H,3-5,13,16H2,1-2H3/b24-21+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 275 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030507
(CHEMBL56590 | [7-Chloro-1-naphthalen-1-yl-1H-quino...)Show SMILES CCCCC\N=c1/ccn(-c2cccc3ccccc23)c2cc(Cl)ccc12 Show InChI InChI=1S/C24H23ClN2/c1-2-3-6-15-26-22-14-16-27(24-17-19(25)12-13-21(22)24)23-11-7-9-18-8-4-5-10-20(18)23/h4-5,7-14,16-17H,2-3,6,15H2,1H3/b26-22+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 279 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030507
(CHEMBL56590 | [7-Chloro-1-naphthalen-1-yl-1H-quino...)Show SMILES CCCCC\N=c1/ccn(-c2cccc3ccccc23)c2cc(Cl)ccc12 Show InChI InChI=1S/C24H23ClN2/c1-2-3-6-15-26-22-14-16-27(24-17-19(25)12-13-21(22)24)23-11-7-9-18-8-4-5-10-20(18)23/h4-5,7-14,16-17H,2-3,6,15H2,1H3/b26-22+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 280 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030503
(CHEMBL298608 | [1-Benzyl-7-chloro-1H-quinolin-(4E)...)Show InChI InChI=1S/C24H29ClN2/c1-2-3-4-5-6-10-16-26-23-15-17-27(19-20-11-8-7-9-12-20)24-18-21(25)13-14-22(23)24/h7-9,11-15,17-18H,2-6,10,16,19H2,1H3/b26-23+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 280 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030519
(CHEMBL53676 | [7-Chloro-1-(3,4-dichloro-benzyl)-1H...)Show SMILES CCCCCC\N=c1/ccn(Cc2ccc(Cl)c(Cl)c2)c2cc(Cl)ccc12 Show InChI InChI=1S/C22H23Cl3N2/c1-2-3-4-5-11-26-21-10-12-27(22-14-17(23)7-8-18(21)22)15-16-6-9-19(24)20(25)13-16/h6-10,12-14H,2-5,11,15H2,1H3/b26-21+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 310 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030495
(CHEMBL55202 | [7-Chloro-1-(4-methoxy-benzyl)-1H-qu...)Show SMILES CCCCCC\N=c1/ccn(Cc2ccc(OC)cc2)c2cc(Cl)ccc12 Show InChI InChI=1S/C23H27ClN2O/c1-3-4-5-6-14-25-22-13-15-26(23-16-19(24)9-12-21(22)23)17-18-7-10-20(27-2)11-8-18/h7-13,15-16H,3-6,14,17H2,1-2H3/b25-22+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 329 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030498
(CHEMBL53841 | [1-Benzyl-7-chloro-1H-quinolin-(4E)-...)Show InChI InChI=1S/C22H25ClN2/c1-2-3-4-8-14-24-21-13-15-25(17-18-9-6-5-7-10-18)22-16-19(23)11-12-20(21)22/h5-7,9-13,15-16H,2-4,8,14,17H2,1H3/b24-21+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 335 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030496
(CHEMBL416313 | [1-(4-Chloro-benzyl)-6-trifluoromet...)Show SMILES CCCCC\N=c1/ccn(Cc2ccc(Cl)cc2)c2ccc(cc12)C(F)(F)F Show InChI InChI=1S/C22H22ClF3N2/c1-2-3-4-12-27-20-11-13-28(15-16-5-8-18(23)9-6-16)21-10-7-17(14-19(20)21)22(24,25)26/h5-11,13-14H,2-4,12,15H2,1H3/b27-20+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 340 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030503
(CHEMBL298608 | [1-Benzyl-7-chloro-1H-quinolin-(4E)...)Show InChI InChI=1S/C24H29ClN2/c1-2-3-4-5-6-10-16-26-23-15-17-27(19-20-11-8-7-9-12-20)24-18-21(25)13-14-22(23)24/h7-9,11-15,17-18H,2-6,10,16,19H2,1H3/b26-23+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 351 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030505
(CHEMBL56589 | [7-Chloro-1-naphthalen-2-yl-1H-quino...)Show SMILES CCCCC\N=c1/ccn(-c2ccc3ccccc3c2)c2cc(Cl)ccc12 Show InChI InChI=1S/C24H23ClN2/c1-2-3-6-14-26-23-13-15-27(24-17-20(25)10-12-22(23)24)21-11-9-18-7-4-5-8-19(18)16-21/h4-5,7-13,15-17H,2-3,6,14H2,1H3/b26-23+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 434 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030504
(Butyl-[7-chloro-1-(3-phenyl-propyl)-1H-quinolin-(4...)Show InChI InChI=1S/C22H25ClN2/c1-2-3-14-24-21-13-16-25(22-17-19(23)11-12-20(21)22)15-7-10-18-8-5-4-6-9-18/h4-6,8-9,11-13,16-17H,2-3,7,10,14-15H2,1H3/b24-21+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 471 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030518
(CHEMBL54231 | [1-Benzyl-8-methoxy-1H-quinolin-(4E)...)Show InChI InChI=1S/C23H28N2O/c1-3-4-5-9-16-24-21-15-17-25(18-19-11-7-6-8-12-19)23-20(21)13-10-14-22(23)26-2/h6-8,10-15,17H,3-5,9,16,18H2,1-2H3/b24-21+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 475 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030522
(CHEMBL554816 | CHEMBL55791 | [1-Benzyl-7-chloro-1H...)Show InChI InChI=1S/C19H19ClN2/c1-2-11-21-18-10-12-22(14-15-6-4-3-5-7-15)19-13-16(20)8-9-17(18)19/h3-10,12-13H,2,11,14H2,1H3/b21-18+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 544 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030516
(CHEMBL54846 | [7-Chloro-1-(2-chloro-benzyl)-1H-qui...)Show SMILES Clc1ccc(C\N=c2/ccn(Cc3ccccc3Cl)c3cc(Cl)ccc23)c(Cl)c1 Show InChI InChI=1S/C23H16Cl4N2/c24-17-6-5-15(21(27)11-17)13-28-22-9-10-29(14-16-3-1-2-4-20(16)26)23-12-18(25)7-8-19(22)23/h1-12H,13-14H2/b28-22+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 550 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030509
(CHEMBL59308 | Methanesulfonate4-hexylamino-1-methy...)Show InChI InChI=1S/C22H26N2/c1-3-4-5-9-16-23-21-15-17-24(2)22-19(13-10-14-20(21)22)18-11-7-6-8-12-18/h6-8,10-15,17H,3-5,9,16H2,1-2H3/p+1/b23-21+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 602 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030506
(CHEMBL56261 | [1-Benzyl-7-chloro-1H-quinolin-(4E)-...)Show SMILES CC(C)CCCC(C)\N=c1/ccn(Cc2ccccc2)c2cc(Cl)ccc12 Show InChI InChI=1S/C24H29ClN2/c1-18(2)8-7-9-19(3)26-23-14-15-27(17-20-10-5-4-6-11-20)24-16-21(25)12-13-22(23)24/h4-6,10-16,18-19H,7-9,17H2,1-3H3/b26-23+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 817 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030526
(1-Benzyl-7-chloro-4-hexyloxy-quinolinium; bromide ...)Show InChI InChI=1S/C22H25ClNO/c1-2-3-4-8-15-25-22-13-14-24(17-18-9-6-5-7-10-18)21-16-19(23)11-12-20(21)22/h5-7,9-14,16H,2-4,8,15,17H2,1H3/q+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 828 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030529
(CHEMBL55649 | Methanesulfonate4-hexylamino-1,8-dip...)Show SMILES CCCCCC\[NH+]=c1/ccn(-c2ccccc2)c2c(cccc12)-c1ccccc1 Show InChI InChI=1S/C27H28N2/c1-2-3-4-11-20-28-26-19-21-29(23-15-9-6-10-16-23)27-24(17-12-18-25(26)27)22-13-7-5-8-14-22/h5-10,12-19,21H,2-4,11,20H2,1H3/p+1/b28-26+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 930 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030521
(CHEMBL56173 | [1-Benzyl-1H-quinolin-(4E)-ylidene]-...)Show InChI InChI=1S/C22H26N2/c1-2-3-4-10-16-23-21-15-17-24(18-19-11-6-5-7-12-19)22-14-9-8-13-20(21)22/h5-9,11-15,17H,2-4,10,16,18H2,1H3/b23-21+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 1.05E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030513
(Adamantan-1-yl-[1-benzyl-7-chloro-1H-quinolin-(4E)...)Show SMILES Clc1ccc2c(c1)n(Cc1ccccc1)cc\c2=N/C12CC3CC(CC(C3)C1)C2 |TLB:22:23:27:21.20.26,THB:22:21:27:23.28.24,24:25:20:23.28.22,24:23:20:25.27.26| Show InChI InChI=1S/C26H27ClN2/c27-22-6-7-23-24(28-26-14-19-10-20(15-26)12-21(11-19)16-26)8-9-29(25(23)13-22)17-18-4-2-1-3-5-18/h1-9,13,19-21H,10-12,14-17H2/b28-24+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 1.17E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030506
(CHEMBL56261 | [1-Benzyl-7-chloro-1H-quinolin-(4E)-...)Show SMILES CC(C)CCCC(C)\N=c1/ccn(Cc2ccccc2)c2cc(Cl)ccc12 Show InChI InChI=1S/C24H29ClN2/c1-18(2)8-7-9-19(3)26-23-14-15-27(17-20-10-5-4-6-11-20)24-16-21(25)12-13-22(23)24/h4-6,10-16,18-19H,7-9,17H2,1-3H3/b26-23+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 1.68E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030517
(CHEMBL56124 | [7-Chloro-1-indan-1-yl-1H-quinolin-(...)Show InChI InChI=1S/C23H25ClN2/c1-2-3-6-14-25-21-13-15-26(23-16-18(24)10-11-20(21)23)22-12-9-17-7-4-5-8-19(17)22/h4-5,7-8,10-11,13,15-16,22H,2-3,6,9,12,14H2,1H3/b25-21+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 2.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Concentration inhibiting [125I]-ChTX (charybdotoxin) binding to N-type potassium channel. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Protein Tat
(Human immunodeficiency virus type 1 (isolate PCV12...) | BDBM50407473
(CHEMBL3137919)Show SMILES [H][C@]12O[C@]11CC[C@@]3([H])[C@]4([H])CC[C@H](OC(C)=O)[C@@]4(C)CC[C@]3([H])[C@@]1(C)CC(C2=O)S(C)(=O)=O Show InChI InChI=1S/C22H32O6S/c1-12(23)27-17-6-5-14-13-7-10-22-19(28-22)18(24)16(29(4,25)26)11-21(22,3)15(13)8-9-20(14,17)2/h13-17,19H,5-11H2,1-4H3/t13-,14-,15-,16?,17-,19+,20-,21+,22+/m0/s1 | PDB MMDB
Reactome pathway
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 2.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sterling Winthrop Pharmaecuticals Research Division
Curated by ChEMBL
| Assay Description The compound was tested for inhibition of HIV-1 replication in SW480 cells using HIV tat assay |
J Med Chem 38: 3197-206 (1995)
BindingDB Entry DOI: 10.7270/Q27D2WBX |
More data for this Ligand-Target Pair | |
Protein Tat
(Human immunodeficiency virus type 1 (isolate PCV12...) | BDBM50045403
(Acetic acid 2-carbamoyl-3-hydroxy-10,13-dimethyl-1...)Show SMILES [H][C@@]12O[C@@]11CCC3C4CC[C@H](OC(C)=O)[C@@]4(C)CCC3[C@@]1(C)CC(C(N)=O)=C2O |c:30| Show InChI InChI=1S/C22H31NO5/c1-11(24)27-16-5-4-14-12-6-9-22-18(28-22)17(25)13(19(23)26)10-21(22,3)15(12)7-8-20(14,16)2/h12,14-16,18,25H,4-10H2,1-3H3,(H2,23,26)/t12?,14?,15?,16-,18-,20-,21+,22-/m0/s1 | PDB MMDB
Reactome pathway
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 2.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sterling Winthrop Pharmaceuticals Research Division
Curated by ChEMBL
| Assay Description Inhibition of HIV-1 nuclear regulatory protein Tat |
J Med Chem 36: 2701-2 (1993)
BindingDB Entry DOI: 10.7270/Q2NG4PP3 |
More data for this Ligand-Target Pair | |
Protein Tat
(Human immunodeficiency virus type 1 (isolate PCV12...) | BDBM50045400
(Acetic acid 2-methanesulfonyl-10,13-dimethyl-3-oxo...)Show SMILES [H][C@@]12CC[C@H](OC(C)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@]23OC2C(=O)C(C[C@]13C)S(C)(=O)=O Show InChI InChI=1S/C22H32O6S/c1-12(23)27-17-6-5-14-13-7-10-22-19(28-22)18(24)16(29(4,25)26)11-21(22,3)15(13)8-9-20(14,17)2/h13-17,19H,5-11H2,1-4H3/t13-,14-,15-,16?,17-,19?,20-,21+,22-/m0/s1 | PDB MMDB
Reactome pathway
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 2.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sterling Winthrop Pharmaceuticals Research Division
Curated by ChEMBL
| Assay Description Inhibition of HIV-1 nuclear regulatory protein Tat |
J Med Chem 36: 2701-2 (1993)
BindingDB Entry DOI: 10.7270/Q2NG4PP3 |
More data for this Ligand-Target Pair | |
Protein Tat
(Human immunodeficiency virus type 1 (isolate PCV12...) | BDBM50407474
(CHEMBL3137917)Show SMILES [H][C@]12O[C@]11CC[C@@]3([H])[C@]4([H])CC[C@H](OC(C)=O)[C@@]4(C)CC[C@]3([H])[C@@]1(C)CC(C(N)=O)C2=O Show InChI InChI=1S/C22H31NO5/c1-11(24)27-16-5-4-14-12-6-9-22-18(28-22)17(25)13(19(23)26)10-21(22,3)15(12)7-8-20(14,16)2/h12-16,18H,4-10H2,1-3H3,(H2,23,26)/t12-,13?,14-,15-,16-,18+,20-,21+,22+/m0/s1 | PDB MMDB
Reactome pathway
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 2.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sterling Winthrop Pharmaecuticals Research Division
Curated by ChEMBL
| Assay Description The compound was tested for inhibition of HIV-1 replication in SW480 cells using HIV tat assay |
J Med Chem 38: 3197-206 (1995)
BindingDB Entry DOI: 10.7270/Q27D2WBX |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily A member 3
(Homo sapiens (Human)) | BDBM50030500
(CHEMBL293083 | [1-Benzyl-7-chloro-1H-quinolin-(4E)...)Show InChI InChI=1S/C20H21ClN2/c1-2-3-12-22-19-11-13-23(15-16-7-5-4-6-8-16)20-14-17(21)9-10-18(19)20/h4-11,13-14H,2-3,12,15H2,1H3/b22-19+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 2.62E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi Winthrop Inc.
Curated by ChEMBL
| Assay Description Inhibition of outward potassium currents (IKn) in human T-lymphocyte N-type potassium channels. |
J Med Chem 38: 1877-83 (1995)
BindingDB Entry DOI: 10.7270/Q2GQ6WSJ |
More data for this Ligand-Target Pair | |
Protein Tat
(Human immunodeficiency virus type 1 (isolate PCV12...) | BDBM50407488
(CHEMBL3137916)Show SMILES [H][C@]12O[C@]11CC[C@@]3([H])[C@]4([H])CC[C@H](OC(C)=O)[C@@]4(C)CC[C@]3([H])[C@@]1(C)CC(C(=O)OC)C2=O Show InChI InChI=1S/C23H32O6/c1-12(24)28-17-6-5-15-13-7-10-23-19(29-23)18(25)14(20(26)27-4)11-22(23,3)16(13)8-9-21(15,17)2/h13-17,19H,5-11H2,1-4H3/t13-,14?,15-,16-,17-,19+,21-,22+,23+/m0/s1 | PDB MMDB
Reactome pathway
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 2.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sterling Winthrop Pharmaecuticals Research Division
Curated by ChEMBL
| Assay Description The compound was tested for inhibition of HIV-1 replication in SW480 cells using HIV tat assay |
J Med Chem 38: 3197-206 (1995)
BindingDB Entry DOI: 10.7270/Q27D2WBX |
More data for this Ligand-Target Pair | |