Compile Data Set for Download or QSAR
Found 78 with Last Name = 'yoon' and Initial = 'hj'
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM30130(CHEMBL1201082 | CHEMBL41 | Fluoxetin | Fluoxetine ...)copy SMILEScopy InChI
Affinity DataIC50: 3.10nMAssay Description:Inhibition of serotonin reuptake at human SERT expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMedDrugBank
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM30130(CHEMBL1201082 | CHEMBL41 | Fluoxetin | Fluoxetine ...)copy SMILEScopy InChI
Affinity DataIC50: 12.6nMAssay Description:Displacement of [3H]paroxetine from SERT in rat cerebral cortexMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent noradrenaline transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325937(CHEMBL1224227 | rac-N-methyl-3-(naphthalen-2-yl)-3...)copy SMILEScopy InChI
Affinity DataIC50: 13.3nMAssay Description:Inhibition of norepinephrine reuptake at human NET expressed in MDCK cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent noradrenaline transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325936((S)-3-(5-(2H-1,2,3-triazol-2-yl)-2H-tetrazol-2-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 14.7nMAssay Description:Inhibition of norepinephrine reuptake at human NET expressed in MDCK cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent noradrenaline transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325933((S)-3-(3,4-dichlorophenyl)-N-methyl-3-(5-methyl-2H...)copy SMILEScopy InChI
Affinity DataIC50: 19.8nMAssay Description:Inhibition of norepinephrine reuptake at human NET expressed in MDCK cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325937(CHEMBL1224227 | rac-N-methyl-3-(naphthalen-2-yl)-3...)copy SMILEScopy InChI
Affinity DataIC50: 32nMAssay Description:Inhibition of serotonin reuptake at human SERT expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM82071(CAS_93413-69-5 | CAS_99300-78-4 | NSC_62923 | VENL...)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:Inhibition of serotonin reuptake at human SERT expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMedDrugBank
TargetSodium-dependent dopamine transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325933((S)-3-(3,4-dichlorophenyl)-N-methyl-3-(5-methyl-2H...)copy SMILEScopy InChI
Affinity DataIC50: 58nMAssay Description:Inhibition of dopamine reuptake at human dopamine transporter expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent noradrenaline transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325935(CHEMBL1224381 | rac-3-(3,4-dichlorophenyl)-N-methy...)copy SMILEScopy InChI
Affinity DataIC50: 69nMAssay Description:Inhibition of norepinephrine reuptake at human NET expressed in MDCK cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent noradrenaline transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50243895(1-(3,4-dichlorophenyl)-3-aza-bicyclo[3.1.0]hexane ...)copy SMILEScopy InChI
Affinity DataIC50: 72.4nMAssay Description:Inhibition of norepinephrine reuptake at human NET expressed in MDCK cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent dopamine transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325934(CHEMBL1224303 | rac-3-(3,4-dichlorophenyl)-N,N-dim...)copy SMILEScopy InChI
Affinity DataIC50: 78nMAssay Description:Inhibition of dopamine reuptake at human dopamine transporter expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent dopamine transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325936((S)-3-(5-(2H-1,2,3-triazol-2-yl)-2H-tetrazol-2-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 91.7nMAssay Description:Inhibition of dopamine reuptake at human dopamine transporter expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent dopamine transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50243895(1-(3,4-dichlorophenyl)-3-aza-bicyclo[3.1.0]hexane ...)copy SMILEScopy InChI
Affinity DataIC50: 93.8nMAssay Description:Inhibition of dopamine reuptake at human dopamine transporter expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent dopamine transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325935(CHEMBL1224381 | rac-3-(3,4-dichlorophenyl)-N-methy...)copy SMILEScopy InChI
Affinity DataIC50: 116nMAssay Description:Inhibition of dopamine reuptake at human dopamine transporter expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325932(CHEMBL1224224 | rac-N,N-dimethyl-3-(naphthalen-2-y...)copy SMILEScopy InChI
Affinity DataIC50: 138nMAssay Description:Inhibition of serotonin reuptake at human SERT expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325933((S)-3-(3,4-dichlorophenyl)-N-methyl-3-(5-methyl-2H...)copy SMILEScopy InChI
Affinity DataIC50: 143nMAssay Description:Inhibition of serotonin reuptake at human SERT expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325935(CHEMBL1224381 | rac-3-(3,4-dichlorophenyl)-N-methy...)copy SMILEScopy InChI
Affinity DataIC50: 181nMAssay Description:Inhibition of serotonin reuptake at human SERT expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50243895(1-(3,4-dichlorophenyl)-3-aza-bicyclo[3.1.0]hexane ...)copy SMILEScopy InChI
Affinity DataIC50: 215nMAssay Description:Inhibition of serotonin reuptake at human SERT expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent noradrenaline transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325934(CHEMBL1224303 | rac-3-(3,4-dichlorophenyl)-N,N-dim...)copy SMILEScopy InChI
Affinity DataIC50: 234nMAssay Description:Inhibition of norepinephrine reuptake at human NET expressed in MDCK cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent noradrenaline transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325932(CHEMBL1224224 | rac-N,N-dimethyl-3-(naphthalen-2-y...)copy SMILEScopy InChI
Affinity DataIC50: 264nMAssay Description:Inhibition of norepinephrine reuptake at human NET expressed in MDCK cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325934(CHEMBL1224303 | rac-3-(3,4-dichlorophenyl)-N,N-dim...)copy SMILEScopy InChI
Affinity DataIC50: 279nMAssay Description:Inhibition of serotonin reuptake at human SERT expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent noradrenaline transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM82071(CAS_93413-69-5 | CAS_99300-78-4 | NSC_62923 | VENL...)copy SMILEScopy InChI
Affinity DataIC50: 581nMAssay Description:Inhibition of norepinephrine reuptake at human NET expressed in MDCK cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMedDrugBank
TargetSodium-dependent dopamine transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325932(CHEMBL1224224 | rac-N,N-dimethyl-3-(naphthalen-2-y...)copy SMILEScopy InChI
Affinity DataIC50: 616nMAssay Description:Inhibition of dopamine reuptake at human dopamine transporter expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325936((S)-3-(5-(2H-1,2,3-triazol-2-yl)-2H-tetrazol-2-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 660nMAssay Description:Inhibition of serotonin reuptake at human SERT expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent dopamine transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325937(CHEMBL1224227 | rac-N-methyl-3-(naphthalen-2-yl)-3...)copy SMILEScopy InChI
Affinity DataIC50: 1.24E+3nMAssay Description:Inhibition of dopamine reuptake at human dopamine transporter expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325933((S)-3-(3,4-dichlorophenyl)-N-methyl-3-(5-methyl-2H...)copy SMILEScopy InChI
Affinity DataIC50: 6.90E+3nMAssay Description:Inhibition of CYP2D6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetSodium-dependent dopamine transporter(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM82071(CAS_93413-69-5 | CAS_99300-78-4 | NSC_62923 | VENL...)copy SMILEScopy InChI
Affinity DataIC50: 7.34E+3nMAssay Description:Inhibition of dopamine reuptake at human dopamine transporter expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMedDrugBank
TargetCytochrome P450 1A2(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325933((S)-3-(3,4-dichlorophenyl)-N-methyl-3-(5-methyl-2H...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP1A2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325933((S)-3-(3,4-dichlorophenyl)-N-methyl-3-(5-methyl-2H...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP2C9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325933((S)-3-(3,4-dichlorophenyl)-N-methyl-3-(5-methyl-2H...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP3A4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetCytochrome P450 2C19(Homo sapiens (Human))
Korea Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50325933((S)-3-(3,4-dichlorophenyl)-N-methyl-3-(5-methyl-2H...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP2C19More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24F1RQ7PubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM21015((2S)-2-{2-[(2R)-2-[(2S)-2-amino-3-(4-hydroxyphenyl...)copy SMILEScopy InChI
Affinity DataEC50:  27nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM83396(1-(4-acetamidobenzyl)-4-phenethyl-isonipecotic aci...)copy SMILEScopy InChI
Affinity DataEC50:  125nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50000507((R)-2-[(S)-2-Amino-3-(4-hydroxy-2,6-dimethyl-pheny...)copy SMILEScopy InChI
Affinity DataEC50:  1.94E+3nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554762(CHEMBL4760974)copy SMILES
Affinity DataEC50:  502nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554763(CHEMBL4758061)copy SMILES
Affinity DataEC50:  83nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554764(CHEMBL4761310)copy SMILES
Affinity DataEC50:  110nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554765(CHEMBL4781906)copy SMILES
Affinity DataEC50:  205nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554766(CHEMBL4795492)copy SMILES
Affinity DataEC50:  0.400nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554767(CHEMBL4776176)copy SMILES
Affinity DataEC50:  144nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554768(CHEMBL4783765)copy SMILES
Affinity DataEC50:  85nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554769(CHEMBL4788377)copy SMILES
Affinity DataEC50:  32nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554770(CHEMBL4783653)copy SMILES
Affinity DataEC50:  163nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554771(CHEMBL4784041)copy SMILES
Affinity DataEC50:  70nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554772(CHEMBL4793926)copy SMILES
Affinity DataEC50:  264nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554773(CHEMBL4779684)copy SMILES
Affinity DataEC50:  191nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554774(CHEMBL4755700)copy SMILES
Affinity DataEC50:  380nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554775(CHEMBL4784650)copy SMILES
Affinity DataEC50:  129nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554776(CHEMBL4751847)copy SMILES
Affinity DataEC50:  16nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50554777(CHEMBL4751491)copy SMILES
Affinity DataEC50:  4.33E+3nMAssay Description:Agonist activity at EA-fragment beta-arrestin-tagged human MOR expressed in human U2OS cell membranes assessed as stimulation of [35S]-GTPgammaS bind...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QKZPubMed
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