TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Affinity DataKi: 2nMAssay Description:Displacement of [3H]Prazosin from human adrenergic alpha1A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 25nMAssay Description:Inhibitory activity against human carbonic anhydrase I at 0.09 uMMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Affinity DataKi: 49nMAssay Description:Displacement of [3H]GR127543 from human 5HT1D receptorMore data for this Ligand-Target Pair
Affinity DataKi: 50nMAssay Description:Inhibitory activity against human carbonic anhydrase I at 0.09 uMMore data for this Ligand-Target Pair
Affinity DataKi: 60nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 7(Homo sapiens (Human))
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Affinity DataKi: 67nMAssay Description:Displacement of [3H]LSD from human 5HT7 receptorMore data for this Ligand-Target Pair
Affinity DataKi: 90nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1B(Homo sapiens (Human))
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Affinity DataKi: 100nMAssay Description:Displacement of [3H]GR127543 from human 5HT1B receptorMore data for this Ligand-Target Pair
Affinity DataKi: 100nMAssay Description:Inhibitory activity against human carbonic anhydrase I at 0.09 uMMore data for this Ligand-Target Pair
Affinity DataKi: 120nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 120nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Co-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 130nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Co-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 130nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 140nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 140nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 140nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 150nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Co-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 170nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Co-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 170nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 180nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
TargetAlpha-2C adrenergic receptor(Homo sapiens (Human))
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Affinity DataKi: 181nMAssay Description:Displacement of [3H]Clonidine from human adrenergic Alpha-2C receptorMore data for this Ligand-Target Pair
Affinity DataKi: 190nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 200nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 220nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Co-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 240nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Co-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Affinity DataKi: 244nMAssay Description:Displacement of [3H]Citalopram from human SERTMore data for this Ligand-Target Pair
Affinity DataKi: 250nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 250nMAssay Description:Inhibitory activity against human carbonic anhydrase I at 0.09 uMMore data for this Ligand-Target Pair
Affinity DataKi: 250nMAssay Description:Inhibitory activity against human carbonic anhydrase I at 0.09 uMMore data for this Ligand-Target Pair
TargetAlpha-2B adrenergic receptor(Homo sapiens (Human))
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Affinity DataKi: 252nMAssay Description:Displacement of [3H]Clonidine from human adrenergic alpha2B receptorMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 6(Homo sapiens (Human))
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Affinity DataKi: 257nMAssay Description:Displacement of [3H]LSD from human 5HT6 receptorMore data for this Ligand-Target Pair
TargetD(4) dopamine receptor(Homo sapiens (Human))
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Affinity DataKi: 262nMAssay Description:Displacement of [3H]N-methylspiperone from human dopamine D4 receptorMore data for this Ligand-Target Pair
Affinity DataKi: 270nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 280nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 280nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Co-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
TargetD(3) dopamine receptor(Homo sapiens (Human))
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Affinity DataKi: 309nMAssay Description:Displacement of [3H]N-methylspiperone from human dopamine D3 receptorMore data for this Ligand-Target Pair
TargetAlpha-1D adrenergic receptor(Homo sapiens (Human))
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Affinity DataKi: 340nMAssay Description:Binding affinity to human adrenergic Alpha-1D receptorMore data for this Ligand-Target Pair
Affinity DataKi: 350nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 410nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 420nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Co-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 500nMAssay Description:Inhibitory constant against carbonic anhydrase IMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 2B(Homo sapiens (Human))
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Affinity DataKi: 543nMAssay Description:Displacement of [3H]LSD from human 5HT2B receptorMore data for this Ligand-Target Pair
Affinity DataKi: 600nMAssay Description:Inhibitory constant against carbonic anhydrase IMore data for this Ligand-Target Pair
Affinity DataKi: 610nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Co-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 660nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Co-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
TargetHistamine H2 receptor(Homo sapiens (Human))
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Hunter College And The Graduate Center Of The City University Of New York
Curated by ChEMBL
Affinity DataKi: 672nMAssay Description:Displacement of [3H]Tiotidine from human histamine H2 receptorMore data for this Ligand-Target Pair
Affinity DataKi: 700nMAssay Description:Inhibitory constant against carbonic anhydrase IMore data for this Ligand-Target Pair
Affinity DataKi: 740nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Co-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 740nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Co-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair
Affinity DataKi: 830nMAssay Description:Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophilaMore data for this Ligand-Target Pair