Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551191 (3-(7-Chloro-1H-indazol-5-yl)-2-cyclobutyl-5-(trifl...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.00500 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551190 (3-(7-Chloro-1H-indazol-5-yl)-2-cyclopropyl-5-(trif...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.00500 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551115 (3-(7-Chloro-1H-indazol-5-yl)-5-(difluoromethyl)-2-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.00600 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551252 (2-Isopropyl-1-(7-methyl-1H-indazol-5-yl)-6-(triflu...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.00800 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551251 (7-Fluoro-5-[2-isopropyl-6-(trifluoromethyl)pyrrolo...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.00800 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551073 (3-(7-Bromo-1H-indazol-5-yl)-2-isopropyl-5-(trifluo...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0100 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551213 (7-Methyl-5-(2-methyl-6-(trifluoromethyl)-1H-pyrrol...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0100 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551218 (5-[2-(Difluoromethyl)-6-(trifluoromethyl)pyrrolo[2...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0100 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM288255 (7-Chloro-5-(2-isopropyl-6-(trifluoromethyl)pyrazol...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0100 | n/a | n/a | n/a | n/a | 7.4 | n/a |
Janssen Pharmaceutica NV US Patent | Assay Description This assay was used to test compounds for their ability to inhibit TARP γ8 dependent AMPA receptor activity. The AMPA receptor is a non-selectiv... | US Patent US10087185 (2018) BindingDB Entry DOI: 10.7270/Q2QZ2D0H | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551075 (3-(7-Bromo-1H-indazol-5-yl)-2,5-bis(trifluoromethy...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0100 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551256 (1-(7-Chloro-1H-indazol-5-yl)-2-methyl-6-(trifluoro...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0130 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551277 (5-[2-Isopropyl-6-(trifluoromethyl)pyrrolo[2,3-b]py...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0130 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM288248 (5-(2,6-Bis(trifluoromethyl)pyrazolo[1,5-a]pyridin-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0130 | n/a | n/a | n/a | n/a | 7.4 | n/a |
Janssen Pharmaceutica NV US Patent | Assay Description This assay was used to test compounds for their ability to inhibit TARP γ8 dependent AMPA receptor activity. The AMPA receptor is a non-selectiv... | US Patent US10087185 (2018) BindingDB Entry DOI: 10.7270/Q2QZ2D0H | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551083 (2-(4-Fluorophenyl)-3-(7-methyl-1H-indazol-5-yl)-5-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0130 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM288254 (5-(2-Isopropyl-6-(trifluoromethyl)pyrazolo[1,5-a]p...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0130 | n/a | n/a | n/a | n/a | 7.4 | n/a |
Janssen Pharmaceutica NV US Patent | Assay Description This assay was used to test compounds for their ability to inhibit TARP γ8 dependent AMPA receptor activity. The AMPA receptor is a non-selectiv... | US Patent US10087185 (2018) BindingDB Entry DOI: 10.7270/Q2QZ2D0H | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM288253 (5-(2-Isopropyl-6-(trifluoromethyl)pyrazolo[1,5-a]p...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0160 | n/a | n/a | n/a | n/a | 7.4 | n/a |
Janssen Pharmaceutica NV US Patent | Assay Description This assay was used to test compounds for their ability to inhibit TARP γ8 dependent AMPA receptor activity. The AMPA receptor is a non-selectiv... | US Patent US10087185 (2018) BindingDB Entry DOI: 10.7270/Q2QZ2D0H | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM288247 (5-(2,6-Bis(trifluoromethyl)pyrazolo[1,5-a]pyridin-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0160 | n/a | n/a | n/a | n/a | 7.4 | n/a |
Janssen Pharmaceutica NV US Patent | Assay Description This assay was used to test compounds for their ability to inhibit TARP γ8 dependent AMPA receptor activity. The AMPA receptor is a non-selectiv... | US Patent US10087185 (2018) BindingDB Entry DOI: 10.7270/Q2QZ2D0H | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM288246 (5-(2,6-Bis(trifluoromethyl)pyrazolo[1,5-a]pyridin-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0160 | n/a | n/a | n/a | n/a | 7.4 | n/a |
Janssen Pharmaceutica NV US Patent | Assay Description This assay was used to test compounds for their ability to inhibit TARP γ8 dependent AMPA receptor activity. The AMPA receptor is a non-selectiv... | US Patent US10087185 (2018) BindingDB Entry DOI: 10.7270/Q2QZ2D0H | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM288245 (5-(2,6-Bis(trifluoromethyl)pyrazolo[1,5-a]pyridin-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0160 | n/a | n/a | n/a | n/a | 7.4 | n/a |
Janssen Pharmaceutica NV US Patent | Assay Description This assay was used to test compounds for their ability to inhibit TARP γ8 dependent AMPA receptor activity. The AMPA receptor is a non-selectiv... | US Patent US10087185 (2018) BindingDB Entry DOI: 10.7270/Q2QZ2D0H | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM288302 (7-(7-Chloro-1H-indazol-5-yl)-6-(difluoromethyl)-2-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0160 | n/a | n/a | n/a | n/a | 7.4 | n/a |
Janssen Pharmaceutica NV US Patent | Assay Description This assay was used to test compounds for their ability to inhibit TARP γ8 dependent AMPA receptor activity. The AMPA receptor is a non-selectiv... | US Patent US10087185 (2018) BindingDB Entry DOI: 10.7270/Q2QZ2D0H | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551163 (3-(7-Bromo-1H-indazol-5-yl)-2-(difluoromethyl)-5-(...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0160 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551150 (3-(7-Chloro-1H-indazol-5-yl)-2-(1,1-difluoroethyl)...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0160 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551114 (5-(Difluoromethyl)-2-(4-fluorophenyl)-3-(7-methyl-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0160 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551217 (1-(1H-Indazol-5-yl)-2-isopropyl-6-(trifluoromethyl...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0160 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551199 (3-(7-Chloro-1H-indazol-5-yl)-2-isopropyl-5-(triflu...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0200 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551237 (6-(2-Methyl-6-(trifluoromethyl)-1H-pyrrolo[2,3-b]p...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0200 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551238 (1-(7-Chloro-1H-indazol-5-yl)-2-isopropyl-pyrrolo[2...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0200 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551153 (3-(7-Chloro-1H-indazol-5-yl)-2,5-bis(trifluorometh...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0200 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551030 (3-(7-Bromo-1H-indazol-5-yl)-2-cyclobutyl-5-(triflu...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0200 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551188 (3-(7-(Prop-1-en-2-yl)-1H-indazol-5-yl)-2,5-bis(tri...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0200 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM288250 (5-(2-Cyclopropyl-6-(trifluoromethyl)pyrazolo[1,5-a...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0200 | n/a | n/a | n/a | n/a | 7.4 | n/a |
Janssen Pharmaceutica NV US Patent | Assay Description This assay was used to test compounds for their ability to inhibit TARP γ8 dependent AMPA receptor activity. The AMPA receptor is a non-selectiv... | US Patent US10087185 (2018) BindingDB Entry DOI: 10.7270/Q2QZ2D0H | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551177 (3-(7-Methyl-1H-indazol-5-yl)-2,5-bis(trifluorometh...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0200 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM288303 (6-(Difluoromethyl)-7-(7-methyl-1H-indazol-5-yl)-2-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0250 | n/a | n/a | n/a | n/a | 7.4 | n/a |
Janssen Pharmaceutica NV US Patent | Assay Description This assay was used to test compounds for their ability to inhibit TARP γ8 dependent AMPA receptor activity. The AMPA receptor is a non-selectiv... | US Patent US10087185 (2018) BindingDB Entry DOI: 10.7270/Q2QZ2D0H | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551280 (5-[2-Cyclopropyl-6-(trifluoromethyl)pyrrolo[2,3-b]...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0250 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551249 (5-[2-Isopropyl-6-(trifluoromethyl)pyrrolo[2,3-b]py...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0250 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551197 (3-(7-Chloro-1H-indazol-5-yl)-2-ethyl-5-(trifluorom...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0320 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551239 (7-Chloro-5-(2-isopropylpyrrolo[2,3-b]pyridin-1-yl)...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0320 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551254 (1-(7-Chloro-1H-indazol-5-yl)-2-(3-fluoropropyl)-6-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0320 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551282 (5-[2-Isopropyl-6-(trifluoromethyl)pyrrolo[2,3-b]py...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0320 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551011 (2-Cyclobutyl-3-(1H-indazol-5-yl)-5-isopropyl-imida...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0320 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551136 (3-(7-Chloro-1H-indazol-5-yl)-2-(3-fluorocyclobutyl...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0320 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551141 (2-Cyclopropyl-3-(7-methyl-1H-indazol-5-yl)-5-(trif...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0320 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551152 (3-(7-Chloro-1H-indazol-5-yl)-5-(difluoromethyl)-2-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0320 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551165 (6-[2,5-Bis(trifluoromethyl)imidazo[4,5-b]pyridin-3...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0320 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551086 (2-Isopropyl-3-(7-methyl-1H-indazol-5-yl)-5-(triflu...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0320 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551209 (5-(Difluoromethyl)-3-(7-methyl-1H-indazol-5-yl)-2-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0400 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551214 (5-(2-Isopropyl-1H-pyrrolo[2,3-b]pyridin-1-yl)-7-me...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0400 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551216 (5-[6-(Difluoromethyl)-2-isopropyl-pyrrolo[2,3-b]py...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0400 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM288237 (6-(4-Fluorophenyl)-5-(7-methyl-1H-indazol-5-yl)-2-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0400 | n/a | n/a | n/a | n/a | 7.4 | n/a |
Janssen Pharmaceutica NV US Patent | Assay Description This assay was used to test compounds for their ability to inhibit TARP γ8 dependent AMPA receptor activity. The AMPA receptor is a non-selectiv... | US Patent US10087185 (2018) BindingDB Entry DOI: 10.7270/Q2QZ2D0H | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent calcium channel gamma-8 subunit (Homo sapiens (Human)) | BDBM551253 (2-(3-Fluoropropyl)-1-(7-methyl-1H-indazol-5-yl)-6-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.0400 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description An in vitro assay was used to determine the potency of test compounds as inhibitors of the glutamate response of the channel formed by GluA1o-γ8... | Citation and Details BindingDB Entry DOI: 10.7270/Q2K93BR4 | |||||||||||
More data for this Ligand-Target Pair |
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