Found 92 hits with Last Name = 'af forselles' and Initial = 'k' 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 |
5-hydroxytryptamine receptor 2C
(Homo sapiens (Human)) | BDBM50161646
((1R)-8-chloro-2,3,4,5-tetrahydro-1-methyl-1H-3-ben...)Show InChI InChI=1S/C11H14ClN/c1-8-7-13-5-4-9-2-3-10(12)6-11(8)9/h2-3,6,8,13H,4-5,7H2,1H3/t8-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid PDB UniChem
Patents
Similars
| PDB Article PubMed
| 15 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Displacement of [125I]DOI from human recombinant 5HT2C receptor expressed in HEK293 cells by scintillation counting |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
5-hydroxytryptamine receptor 2C
(Homo sapiens (Human)) | BDBM50342539
(2-(3-chlorobenzyl)-6,7,8,9-tetrahydro-5H-pyrimido[...)Show InChI InChI=1S/C15H16ClN3/c16-13-3-1-2-11(8-13)9-15-18-10-12-4-6-17-7-5-14(12)19-15/h1-3,8,10,17H,4-7,9H2 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| 84 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Displacement of [3H]meselurgine from human 5HT2C receptor expressed in Swiss mouse 3T3 cells by scintillation proximity assay |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | |
5-hydroxytryptamine receptor 2C
(Homo sapiens (Human)) | BDBM50342538
(2-benzyl-6,7,8,9-tetrahydro-5H-pyrimido[5,4-d]azep...)Show InChI InChI=1S/C15H17N3/c1-2-4-12(5-3-1)10-15-17-11-13-6-8-16-9-7-14(13)18-15/h1-5,11,16H,6-10H2 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| 160 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Displacement of [3H]meselurgine from human 5HT2C receptor expressed in Swiss mouse 3T3 cells by scintillation proximity assay |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | |
5-hydroxytryptamine receptor 2C
(Homo sapiens (Human)) | BDBM50161646
((1R)-8-chloro-2,3,4,5-tetrahydro-1-methyl-1H-3-ben...)Show InChI InChI=1S/C11H14ClN/c1-8-7-13-5-4-9-2-3-10(12)6-11(8)9/h2-3,6,8,13H,4-5,7H2,1H3/t8-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid PDB UniChem
Patents
Similars
| PDB Article PubMed
| 167 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Displacement of [3H]meselurgine from human 5HT2C receptor expressed in Swiss mouse 3T3 cells by scintillation proximity assay |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
5-hydroxytryptamine receptor 2C
(Homo sapiens (Human)) | BDBM50342547
(2-(3-methylbenzyl)-6,7,8,9-tetrahydro-5H-pyrimido[...)Show InChI InChI=1S/C16H19N3/c1-12-3-2-4-13(9-12)10-16-18-11-14-5-7-17-8-6-15(14)19-16/h2-4,9,11,17H,5-8,10H2,1H3 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| 244 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Displacement of [3H]meselurgine from human 5HT2C receptor expressed in Swiss mouse 3T3 cells by scintillation proximity assay |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | |
5-hydroxytryptamine receptor 2C
(Homo sapiens (Human)) | BDBM50342548
(2-(2-methylbenzyl)-6,7,8,9-tetrahydro-5H-pyrimido[...)Show InChI InChI=1S/C16H19N3/c1-12-4-2-3-5-13(12)10-16-18-11-14-6-8-17-9-7-15(14)19-16/h2-5,11,17H,6-10H2,1H3 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| 305 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Displacement of [3H]meselurgine from human 5HT2C receptor expressed in Swiss mouse 3T3 cells by scintillation proximity assay |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | |
5-hydroxytryptamine receptor 2C
(Homo sapiens (Human)) | BDBM50342544
(2-(3-(trifluoromethyl)benzyl)-6,7,8,9-tetrahydro-5...)Show InChI InChI=1S/C16H16F3N3/c17-16(18,19)13-3-1-2-11(8-13)9-15-21-10-12-4-6-20-7-5-14(12)22-15/h1-3,8,10,20H,4-7,9H2 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| 308 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Displacement of [3H]meselurgine from human 5HT2C receptor expressed in Swiss mouse 3T3 cells by scintillation proximity assay |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | |
5-hydroxytryptamine receptor 2C
(Homo sapiens (Human)) | BDBM50342549
(2-(4-fluorobenzyl)-6,7,8,9-tetrahydro-5H-pyrimido[...)Show InChI InChI=1S/C15H16FN3/c16-13-3-1-11(2-4-13)9-15-18-10-12-5-7-17-8-6-14(12)19-15/h1-4,10,17H,5-9H2 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| 470 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Displacement of [3H]meselurgine from human 5HT2C receptor expressed in Swiss mouse 3T3 cells by scintillation proximity assay |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | |
5-hydroxytryptamine receptor 2C
(Homo sapiens (Human)) | BDBM50342545
(2-(2-chlorobenzyl)-6,7,8,9-tetrahydro-5H-pyrimido[...)Show InChI InChI=1S/C15H16ClN3/c16-13-4-2-1-3-11(13)9-15-18-10-12-5-7-17-8-6-14(12)19-15/h1-4,10,17H,5-9H2 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 1.85E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Displacement of [3H]meselurgine from human 5HT2C receptor expressed in Swiss mouse 3T3 cells by scintillation proximity assay |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50089251
(CHEMBL3576881)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cn2ccccc2n1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C24H20FN3O3/c1-16(18-8-10-20(25)11-9-18)28(14-17-5-4-6-19(13-17)24(30)31)23(29)21-15-27-12-3-2-7-22(27)26-21/h2-13,15-16H,14H2,1H3,(H,30,31)/t16-/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| >9.18E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Inhibition of dofetilide binding to human ERG |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50089248
(CHEMBL3577881)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cc2ccccn2n1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C24H20FN3O3/c1-16(18-8-10-20(25)11-9-18)27(15-17-5-4-6-19(13-17)24(30)31)23(29)22-14-21-7-2-3-12-28(21)26-22/h2-14,16H,15H2,1H3,(H,30,31)/t16-/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| >9.18E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Inhibition of dofetilide binding to human ERG |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50089252
(CHEMBL3577889)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cc2ccccc2cn1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C26H21FN2O3/c1-17(19-9-11-23(27)12-10-19)29(16-18-5-4-8-21(13-18)26(31)32)25(30)24-14-20-6-2-3-7-22(20)15-28-24/h2-15,17H,16H2,1H3,(H,31,32)/t17-/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| >9.18E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Inhibition of dofetilide binding to human ERG |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50089253
(CHEMBL3577900)Show SMILES CC[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cnc2ccccc2c1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C27H23FN2O3/c1-2-25(19-10-12-23(28)13-11-19)30(17-18-6-5-8-21(14-18)27(32)33)26(31)22-15-20-7-3-4-9-24(20)29-16-22/h3-16,25H,2,17H2,1H3,(H,32,33)/t25-/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| >1.52E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Inhibition of dofetilide binding to human ERG |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50089245
(CHEMBL3577885)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cnc2ccccc2c1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C26H21FN2O3/c1-17(19-9-11-23(27)12-10-19)29(16-18-5-4-7-21(13-18)26(31)32)25(30)22-14-20-6-2-3-8-24(20)28-15-22/h2-15,17H,16H2,1H3,(H,31,32)/t17-/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Similars
| Article PubMed
| >1.59E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Inhibition of dofetilide binding to human ERG |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089257
(CHEMBL3577904)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cc2ccccc2cn1)c1ccc(F)cc1F |r| Show InChI InChI=1S/C26H20F2N2O3/c1-16(22-10-9-21(27)13-23(22)28)30(15-17-5-4-8-19(11-17)26(32)33)25(31)24-12-18-6-2-3-7-20(18)14-29-24/h2-14,16H,15H2,1H3,(H,32,33)/t16-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 60 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089259
(CHEMBL3577902)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cnc2ccccc2c1)c1cccc(Cl)c1 |r| Show InChI InChI=1S/C26H21ClN2O3/c1-17(19-8-5-10-23(27)14-19)29(16-18-6-4-9-21(12-18)26(31)32)25(30)22-13-20-7-2-3-11-24(20)28-15-22/h2-15,17H,16H2,1H3,(H,31,32)/t17-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 62 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089252
(CHEMBL3577889)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cc2ccccc2cn1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C26H21FN2O3/c1-17(19-9-11-23(27)12-10-19)29(16-18-5-4-8-21(13-18)26(31)32)25(30)24-14-20-6-2-3-7-22(20)15-28-24/h2-15,17H,16H2,1H3,(H,31,32)/t17-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 90 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089248
(CHEMBL3577881)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cc2ccccn2n1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C24H20FN3O3/c1-16(18-8-10-20(25)11-9-18)27(15-17-5-4-6-19(13-17)24(30)31)23(29)22-14-21-7-2-3-12-28(21)26-22/h2-14,16H,15H2,1H3,(H,30,31)/t16-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 94 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089245
(CHEMBL3577885)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cnc2ccccc2c1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C26H21FN2O3/c1-17(19-9-11-23(27)12-10-19)29(16-18-5-4-7-21(13-18)26(31)32)25(30)22-14-20-6-2-3-8-24(20)28-15-22/h2-15,17H,16H2,1H3,(H,31,32)/t17-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 103 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human TRPM8 by single cell patch clamp electrophysiology |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089256
(CHEMBL3577905)Show SMILES CC[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cc2ccccn2n1)c1ccc(F)cc1F |r| Show InChI InChI=1S/C25H21F2N3O3/c1-2-23(20-10-9-18(26)13-21(20)27)29(15-16-6-5-7-17(12-16)25(32)33)24(31)22-14-19-8-3-4-11-30(19)28-22/h3-14,23H,2,15H2,1H3,(H,32,33)/t23-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 123 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089246
(CHEMBL3577883)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cc2ccccc2s1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C25H20FNO3S/c1-16(18-9-11-21(26)12-10-18)27(15-17-5-4-7-20(13-17)25(29)30)24(28)23-14-19-6-2-3-8-22(19)31-23/h2-14,16H,15H2,1H3,(H,29,30)/t16-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 145 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089245
(CHEMBL3577885)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cnc2ccccc2c1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C26H21FN2O3/c1-17(19-9-11-23(27)12-10-19)29(16-18-5-4-7-21(13-18)26(31)32)25(30)22-14-20-6-2-3-8-24(20)28-15-22/h2-15,17H,16H2,1H3,(H,31,32)/t17-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 181 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089254
(CHEMBL3577907)Show SMILES C[C@@H](N(Cc1cccc(n1)C(O)=O)C(=O)c1cc2ccccc2cn1)c1ccc(F)cc1F |r| Show InChI InChI=1S/C25H19F2N3O3/c1-15(20-10-9-18(26)12-21(20)27)30(14-19-7-4-8-22(29-19)25(32)33)24(31)23-11-16-5-2-3-6-17(16)13-28-23/h2-13,15H,14H2,1H3,(H,32,33)/t15-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 190 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089253
(CHEMBL3577900)Show SMILES CC[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cnc2ccccc2c1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C27H23FN2O3/c1-2-25(19-10-12-23(28)13-11-19)30(17-18-6-5-8-21(14-18)27(32)33)26(31)22-15-20-7-3-4-9-24(20)29-16-22/h3-16,25H,2,17H2,1H3,(H,32,33)/t25-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 202 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089255
(CHEMBL3577906)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cc2ccccn2n1)c1ccc(F)cc1F |r| Show InChI InChI=1S/C24H19F2N3O3/c1-15(20-9-8-18(25)12-21(20)26)28(14-16-5-4-6-17(11-16)24(31)32)23(30)22-13-19-7-2-3-10-29(19)27-22/h2-13,15H,14H2,1H3,(H,31,32)/t15-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 234 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089262
(CHEMBL3577898)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cnc2ccccc2c1)c1ccc(F)cc1F |r| Show InChI InChI=1S/C26H20F2N2O3/c1-16(22-10-9-21(27)13-23(22)28)30(15-17-5-4-7-19(11-17)26(32)33)25(31)20-12-18-6-2-3-8-24(18)29-14-20/h2-14,16H,15H2,1H3,(H,32,33)/t16-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 288 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Muscarinic acetylcholine receptor M1
(Homo sapiens (Human)) | BDBM50342538
(2-benzyl-6,7,8,9-tetrahydro-5H-pyrimido[5,4-d]azep...)Show InChI InChI=1S/C15H17N3/c1-2-4-12(5-3-1)10-15-17-11-13-6-8-16-9-7-14(13)18-15/h1-5,11,16H,6-10H2 | UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Binding affinity to muscarinic M1 receptor |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | |
Muscarinic acetylcholine receptor M3
(Homo sapiens (Human)) | BDBM50342538
(2-benzyl-6,7,8,9-tetrahydro-5H-pyrimido[5,4-d]azep...)Show InChI InChI=1S/C15H17N3/c1-2-4-12(5-3-1)10-15-17-11-13-6-8-16-9-7-14(13)18-15/h1-5,11,16H,6-10H2 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Binding affinity to muscarinic M3 receptor |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | |
Muscarinic acetylcholine receptor M4
(Homo sapiens (Human)) | BDBM50342538
(2-benzyl-6,7,8,9-tetrahydro-5H-pyrimido[5,4-d]azep...)Show InChI InChI=1S/C15H17N3/c1-2-4-12(5-3-1)10-15-17-11-13-6-8-16-9-7-14(13)18-15/h1-5,11,16H,6-10H2 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Binding affinity to muscarinic M4 receptor |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | |
Muscarinic acetylcholine receptor M5
(Homo sapiens (Human)) | BDBM50342538
(2-benzyl-6,7,8,9-tetrahydro-5H-pyrimido[5,4-d]azep...)Show InChI InChI=1S/C15H17N3/c1-2-4-12(5-3-1)10-15-17-11-13-6-8-16-9-7-14(13)18-15/h1-5,11,16H,6-10H2 | Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Binding affinity to muscarinic M5 receptor |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089251
(CHEMBL3576881)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cn2ccccc2n1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C24H20FN3O3/c1-16(18-8-10-20(25)11-9-18)28(14-17-5-4-6-19(13-17)24(30)31)23(29)21-15-27-12-3-2-7-22(27)26-21/h2-13,15-16H,14H2,1H3,(H,30,31)/t16-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 307 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089258
(CHEMBL3577903)Show SMILES CC[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cnc2ccccc2c1)c1ccc(C)o1 |r| Show InChI InChI=1S/C26H24N2O4/c1-3-23(24-12-11-17(2)32-24)28(16-18-7-6-9-20(13-18)26(30)31)25(29)21-14-19-8-4-5-10-22(19)27-15-21/h4-15,23H,3,16H2,1-2H3,(H,30,31)/t23-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 328 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089297
(CHEMBL3577886)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cc2ccccc2nn1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C25H20FN3O3/c1-16(18-9-11-21(26)12-10-18)29(15-17-5-4-7-20(13-17)25(31)32)24(30)23-14-19-6-2-3-8-22(19)27-28-23/h2-14,16H,15H2,1H3,(H,31,32)/t16-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 340 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089267
(CHEMBL3577893)Show SMILES C[C@@H](N(Cc1cc(ccc1F)C(O)=O)C(=O)c1cnc2ccccc2c1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C26H20F2N2O3/c1-16(17-6-9-22(27)10-7-17)30(15-21-13-19(26(32)33)8-11-23(21)28)25(31)20-12-18-4-2-3-5-24(18)29-14-20/h2-14,16H,15H2,1H3,(H,32,33)/t16-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 446 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089249
(CHEMBL3577880)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cccc(c1)-c1ccccc1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C29H24FNO3/c1-20(22-13-15-27(30)16-14-22)31(19-21-7-5-12-26(17-21)29(33)34)28(32)25-11-6-10-24(18-25)23-8-3-2-4-9-23/h2-18,20H,19H2,1H3,(H,33,34)/t20-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 837 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089247
(CHEMBL3577882)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cc2cc[nH]c2cn1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C24H20FN3O3/c1-15(17-5-7-20(25)8-6-17)28(14-16-3-2-4-19(11-16)24(30)31)23(29)21-12-18-9-10-26-22(18)13-27-21/h2-13,15,26H,14H2,1H3,(H,30,31)/t15-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 951 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089283
(CHEMBL3577890)Show SMILES C[C@@H](N(Cc1cccc(n1)C(O)=O)C(=O)c1cnc2ccccc2c1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C25H20FN3O3/c1-16(17-9-11-20(26)12-10-17)29(15-21-6-4-8-23(28-21)25(31)32)24(30)19-13-18-5-2-3-7-22(18)27-14-19/h2-14,16H,15H2,1H3,(H,31,32)/t16-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.16E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089265
(CHEMBL3577895)Show SMILES C[C@@H](N(Cc1cccc(c1)-c1nn[nH]n1)C(=O)c1cnc2ccccc2c1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C26H21FN6O/c1-17(19-9-11-23(27)12-10-19)33(16-18-5-4-7-21(13-18)25-29-31-32-30-25)26(34)22-14-20-6-2-3-8-24(20)28-15-22/h2-15,17H,16H2,1H3,(H,29,30,31,32)/t17-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.61E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
5-hydroxytryptamine receptor 6
(Homo sapiens (Human)) | BDBM50342538
(2-benzyl-6,7,8,9-tetrahydro-5H-pyrimido[5,4-d]azep...)Show InChI InChI=1S/C15H17N3/c1-2-4-12(5-3-1)10-15-17-11-13-6-8-16-9-7-14(13)18-15/h1-5,11,16H,6-10H2 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 1.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Binding affinity to 5-HT6 receptor |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | |
5-hydroxytryptamine receptor 3A
(Homo sapiens (Human)) | BDBM50342538
(2-benzyl-6,7,8,9-tetrahydro-5H-pyrimido[5,4-d]azep...)Show InChI InChI=1S/C15H17N3/c1-2-4-12(5-3-1)10-15-17-11-13-6-8-16-9-7-14(13)18-15/h1-5,11,16H,6-10H2 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 2.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Binding affinity to 5-HT3 receptor |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089266
(CHEMBL3577894)Show SMILES C[C@@H](N(Cc1cccc(CC(O)=O)c1)C(=O)c1cnc2ccccc2c1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C27H23FN2O3/c1-18(21-9-11-24(28)12-10-21)30(17-20-6-4-5-19(13-20)14-26(31)32)27(33)23-15-22-7-2-3-8-25(22)29-16-23/h2-13,15-16,18H,14,17H2,1H3,(H,31,32)/t18-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >3.25E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089274
(CHEMBL3577891)Show SMILES C[C@@H](N(Cc1ccc(F)c(c1)C(O)=O)C(=O)c1cnc2ccccc2c1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C26H20F2N2O3/c1-16(18-7-9-21(27)10-8-18)30(15-17-6-11-23(28)22(12-17)26(32)33)25(31)20-13-19-4-2-3-5-24(19)29-14-20/h2-14,16H,15H2,1H3,(H,32,33)/t16-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3.28E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089298
(CHEMBL3577884)Show SMILES CC(N(Cc1cccc(c1)C(O)=O)C(=O)c1ccc2OCCc2c1)c1ccc(F)cc1 Show InChI InChI=1S/C25H22FNO4/c1-16(18-5-8-22(26)9-6-18)27(15-17-3-2-4-21(13-17)25(29)30)24(28)20-7-10-23-19(14-20)11-12-31-23/h2-10,13-14,16H,11-12,15H2,1H3,(H,29,30) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3.62E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089294
(CHEMBL3577888)Show SMILES CC(N(Cc1cccc(c1)C(O)=O)C(=O)C1Cc2ccccc2C1)c1ccc(F)cc1 Show InChI InChI=1S/C26H24FNO3/c1-17(19-9-11-24(27)12-10-19)28(16-18-5-4-8-22(13-18)26(30)31)25(29)23-14-20-6-2-3-7-21(20)15-23/h2-13,17,23H,14-16H2,1H3,(H,30,31) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >5.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089260
(CHEMBL3577901)Show SMILES COc1ccc(cc1)C(C)N(Cc1cccc(c1)C(O)=O)C(=O)c1cnc2ccccc2c1 Show InChI InChI=1S/C27H24N2O4/c1-18(20-10-12-24(33-2)13-11-20)29(17-19-6-5-8-22(14-19)27(31)32)26(30)23-15-21-7-3-4-9-25(21)28-16-23/h3-16,18H,17H2,1-2H3,(H,31,32) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 6.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089296
(CHEMBL3577887)Show SMILES C[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1ccc(Oc2ccccc2)cc1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C29H24FNO4/c1-20(22-10-14-25(30)15-11-22)31(19-21-6-5-7-24(18-21)29(33)34)28(32)23-12-16-27(17-13-23)35-26-8-3-2-4-9-26/h2-18,20H,19H2,1H3,(H,33,34)/t20-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >6.17E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Muscarinic acetylcholine receptor M4
(Homo sapiens (Human)) | BDBM50342538
(2-benzyl-6,7,8,9-tetrahydro-5H-pyrimido[5,4-d]azep...)Show InChI InChI=1S/C15H17N3/c1-2-4-12(5-3-1)10-15-17-11-13-6-8-16-9-7-14(13)18-15/h1-5,11,16H,6-10H2 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 6.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity at human muscarinic M4 receptor |
Bioorg Med Chem Lett 21: 2715-20 (2011)
Article DOI: 10.1016/j.bmcl.2010.11.120 BindingDB Entry DOI: 10.7270/Q2HD7VZZ |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089263
(CHEMBL3577897)Show SMILES OC[C@@H](N(Cc1cccc(c1)C(O)=O)C(=O)c1cnc2ccccc2c1)c1ccccc1 |r| Show InChI InChI=1S/C26H22N2O4/c29-17-24(19-8-2-1-3-9-19)28(16-18-7-6-11-21(13-18)26(31)32)25(30)22-14-20-10-4-5-12-23(20)27-15-22/h1-15,24,29H,16-17H2,(H,31,32)/t24-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >6.86E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089273
(CHEMBL3577892)Show SMILES C[C@@H](N(Cc1ccc(C)c(c1)C(O)=O)C(=O)c1cnc2ccccc2c1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C27H23FN2O3/c1-17-7-8-19(13-24(17)27(32)33)16-30(18(2)20-9-11-23(28)12-10-20)26(31)22-14-21-5-3-4-6-25(21)29-15-22/h3-15,18H,16H2,1-2H3,(H,32,33)/t18-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >7.82E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |
Transient receptor potential cation channel subfamily M member 8
(Homo sapiens (Human)) | BDBM50089264
(CHEMBL3577896)Show SMILES OC(=O)c1cccc(CN(Cc2ccc(F)cc2)C(=O)c2cnc3ccccc3c2)c1 Show InChI InChI=1S/C25H19FN2O3/c26-22-10-8-17(9-11-22)15-28(16-18-4-3-6-20(12-18)25(30)31)24(29)21-13-19-5-1-2-7-23(19)27-14-21/h1-14H,15-16H2,(H,30,31) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >9.36E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc.
Curated by ChEMBL
| Assay Description Antagonist activity against human recombinant TRPM8 expressed in CHO T-rex cells assessed as inhibition of WS12-induced calcium response pre-incubate... |
ACS Med Chem Lett 6: 419-24 (2015)
Article DOI: 10.1021/ml500479v BindingDB Entry DOI: 10.7270/Q2FQ9ZBC |
More data for this Ligand-Target Pair | |