Compile Data Set for Download or QSAR
Found 117 with Last Name = 'tashiro' and Initial = 'k'
TargetCoagulation factor X(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127501(3-(4-Carbamimidoyl-2-{2-[4-(pyrrolidine-1-carbonyl...)copy SMILEScopy InChI
Affinity DataKi:  3nMAssay Description:Inhibitory activity against Coagulation factor X (fXa)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127492(4-[5-Carbamimidoyl-2-(2-carboxy-2-oxo-ethyl)-pheno...)copy SMILEScopy InChI
Affinity DataKi:  11nMAssay Description:Inhibitory activity against Coagulation factor X (fXa)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127502(4-[5-Carbamimidoyl-2-(2-carboxy-2-oxo-ethyl)-pheno...)copy SMILEScopy InChI
Affinity DataKi:  18nMAssay Description:Inhibitory activity against Coagulation factor X (fXa)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127504(CHEMBL55770 | N-[2-(3-Carbamimidoyl-phenoxy)-ethyl...)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Inhibitory activity against Coagulation factor X (fXa)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127495(3-[4-Carbamimidoyl-2-(2-{4-[1-(1-imino-ethyl)-pipe...)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Inhibitory activity against Coagulation factor X (fXa)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127494(3-(4-Carbamimidoyl-2-{2-[(3,4,5,6-tetrahydro-2H-[1...)copy SMILEScopy InChI
Affinity DataKi:  21nMAssay Description:Inhibitory activity against Coagulation factor X (fXa)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127498(3-{4-Carbamimidoyl-2-[2-(4-carbamimidoyl-benzoylam...)copy SMILEScopy InChI
Affinity DataKi:  26nMAssay Description:Inhibitory activity against Coagulation factor X (fXa)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127503(3-(4-Carbamimidoyl-benzoylamino)-4-(3-carbamimidoy...)copy SMILEScopy InChI
Affinity DataKi:  28nMAssay Description:Inhibitory activity against Coagulation factor X (fXa)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127493(3-(4-Carbamimidoyl-2-{2-[(3,4,5,6-tetrahydro-2H-[1...)copy SMILEScopy InChI
Affinity DataKi:  43nMAssay Description:Inhibitory activity against Coagulation factor X (fXa)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288745(CHEMBL4159810)copy SMILEScopy InChI
Affinity DataKi:  84nMAssay Description:Displacement of [3H]-diprenorphine from human DOR expressed in CHO cell membranes after 80 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288740(CHEMBL4167726)copy SMILEScopy InChI
Affinity DataKi:  98nMAssay Description:Displacement of [3H]-diprenorphine from human DOR expressed in CHO cell membranes after 80 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288741(CHEMBL4174926)copy SMILEScopy InChI
Affinity DataKi:  120nMAssay Description:Displacement of [3H]-diprenorphine from human DOR expressed in CHO cell membranes after 80 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetCoagulation factor X(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127496(CHEMBL51796 | N-[2-(3-Carbamimidoyl-phenoxy)-ethyl...)copy SMILEScopy InChI
Affinity DataKi:  170nMAssay Description:Inhibitory activity against Coagulation factor X (fXa)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127506(3-(4-Carbamimidoyl-benzoylamino)-4-(3-carbamimidoy...)copy SMILEScopy InChI
Affinity DataKi:  170nMAssay Description:Inhibitory activity against Coagulation factor X (fXa)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127497(4-Carbamimidoyl-N-[2-(3-carbamimidoyl-phenoxy)-eth...)copy SMILEScopy InChI
Affinity DataKi:  220nMAssay Description:Inhibitory activity against Coagulation factor X (fXa)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288744(CHEMBL4163178)copy SMILEScopy InChI
Affinity DataKi:  230nMAssay Description:Displacement of [3H]-diprenorphine from human DOR expressed in CHO cell membranes after 80 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288746(CHEMBL4166622)copy SMILEScopy InChI
Affinity DataKi:  230nMAssay Description:Displacement of [3H]-diprenorphine from human DOR expressed in CHO cell membranes after 80 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288788(CHEMBL4174537)copy SMILEScopy InChI
Affinity DataKi:  250nMAssay Description:Displacement of [3H]-diprenorphine from human DOR expressed in CHO cell membranes after 80 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288742(CHEMBL4164277)copy SMILEScopy InChI
Affinity DataKi:  270nMAssay Description:Displacement of [3H]-diprenorphine from human DOR expressed in CHO cell membranes after 80 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288743(CHEMBL4171099)copy SMILEScopy InChI
Affinity DataKi:  290nMAssay Description:Displacement of [3H]-diprenorphine from human DOR expressed in CHO cell membranes after 80 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetCoagulation factor X(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127500(3,4,5,6-Tetrahydro-2H-[1,4']bipyridinyl-4-carboxyl...)copy SMILEScopy InChI
Affinity DataKi:  290nMAssay Description:Inhibitory activity against Coagulation factor X (fXa)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127499(3-[4-Carbamimidoyl-2-(2-{4-[1-(1-imino-ethyl)-pipe...)copy SMILEScopy InChI
Affinity DataKi:  330nMAssay Description:Inhibitory activity against Coagulation factor X (fXa)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288740(CHEMBL4167726)copy SMILEScopy InChI
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]-diprenorphine from human MOR expressed in CHO cell membranes after 80 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288743(CHEMBL4171099)copy SMILEScopy InChI
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]-diprenorphine from human MOR expressed in CHO cell membranes after 80 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288744(CHEMBL4163178)copy SMILEScopy InChI
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]-diprenorphine from human MOR expressed in CHO cell membranes after 80 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50203825(CHEMBL375070 | Tyr-Pro-Phe-D-2-Nal-NH2)copy SMILEScopy InChI
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]-diprenorphine from human MOR expressed in CHO cell membranes after 80 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288741(CHEMBL4174926)copy SMILEScopy InChI
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]-diprenorphine from human MOR expressed in CHO cell membranes after 80 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288745(CHEMBL4159810)copy SMILEScopy InChI
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]-diprenorphine from human MOR expressed in CHO cell membranes after 80 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288742(CHEMBL4164277)copy SMILEScopy InChI
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]-diprenorphine from human MOR expressed in CHO cell membranes after 80 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetCoagulation factor X(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127505(CHEMBL55364 | N-[2-(3-Carbamimidoyl-phenoxy)-ethyl...)copy SMILEScopy InChI
Affinity DataKi:  2.80E+3nMAssay Description:Inhibitory activity against Coagulation factor X (fXa)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetProthrombin(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127501(3-(4-Carbamimidoyl-2-{2-[4-(pyrrolidine-1-carbonyl...)copy SMILEScopy InChI
Affinity DataKi:  2.40E+4nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetProthrombin(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127498(3-{4-Carbamimidoyl-2-[2-(4-carbamimidoyl-benzoylam...)copy SMILEScopy InChI
Affinity DataKi:  3.80E+4nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetProthrombin(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127495(3-[4-Carbamimidoyl-2-(2-{4-[1-(1-imino-ethyl)-pipe...)copy SMILEScopy InChI
Affinity DataKi:  5.30E+4nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetProthrombin(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127504(CHEMBL55770 | N-[2-(3-Carbamimidoyl-phenoxy)-ethyl...)copy SMILEScopy InChI
Affinity DataKi:  1.10E+5nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetProthrombin(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127494(3-(4-Carbamimidoyl-2-{2-[(3,4,5,6-tetrahydro-2H-[1...)copy SMILEScopy InChI
Affinity DataKi:  1.40E+5nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetProthrombin(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127496(CHEMBL51796 | N-[2-(3-Carbamimidoyl-phenoxy)-ethyl...)copy SMILEScopy InChI
Affinity DataKi:  4.40E+5nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetProthrombin(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127492(4-[5-Carbamimidoyl-2-(2-carboxy-2-oxo-ethyl)-pheno...)copy SMILEScopy InChI
Affinity DataKi:  5.40E+5nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetProthrombin(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127502(4-[5-Carbamimidoyl-2-(2-carboxy-2-oxo-ethyl)-pheno...)copy SMILEScopy InChI
Affinity DataKi:  6.80E+5nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetProthrombin(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127497(4-Carbamimidoyl-N-[2-(3-carbamimidoyl-phenoxy)-eth...)copy SMILEScopy InChI
Affinity DataKi:  7.10E+5nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetProthrombin(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127505(CHEMBL55364 | N-[2-(3-Carbamimidoyl-phenoxy)-ethyl...)copy SMILEScopy InChI
Affinity DataKi:  8.00E+5nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetProthrombin(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127500(3,4,5,6-Tetrahydro-2H-[1,4']bipyridinyl-4-carboxyl...)copy SMILEScopy InChI
Affinity DataKi:  1.00E+6nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetProthrombin(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127503(3-(4-Carbamimidoyl-benzoylamino)-4-(3-carbamimidoy...)copy SMILEScopy InChI
Affinity DataKi: >1.50E+6nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetProthrombin(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127506(3-(4-Carbamimidoyl-benzoylamino)-4-(3-carbamimidoy...)copy SMILEScopy InChI
Affinity DataKi: >1.50E+6nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetProthrombin(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127493(3-(4-Carbamimidoyl-2-{2-[(3,4,5,6-tetrahydro-2H-[1...)copy SMILEScopy InChI
Affinity DataKi: >1.50E+6nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetProthrombin(Homo sapiens (Human))
Ajinomoto Company Inc.

Curated by ChEMBL
LigandPNGBDBM50127499(3-[4-Carbamimidoyl-2-(2-{4-[1-(1-imino-ethyl)-pipe...)copy SMILEScopy InChI
Affinity DataKi: >1.50E+6nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ586CPubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM82551(C18130 | CAS_105618-26-6 | NOR-BNI (HCI)2 | NORBNI)copy SMILEScopy InChI
Affinity DataIC50: 9.30nMAssay Description:Antagonist activity at human KOR expressed in CHO cell membranes assessed as inhibition of U50488-induced [35S]-GTPgammaS binding preincubated for 5 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288742(CHEMBL4164277)copy SMILEScopy InChI
Affinity DataIC50: 58nMAssay Description:Antagonist activity at human DOR expressed in CHO cell membranes assessed as inhibition of CYM51010-induced [35S]-GTPgammaS binding preincubated for ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288741(CHEMBL4174926)copy SMILEScopy InChI
Affinity DataIC50: 58nMAssay Description:Antagonist activity at human DOR expressed in CHO cell membranes assessed as inhibition of CYM51010-induced [35S]-GTPgammaS binding preincubated for ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288740(CHEMBL4167726)copy SMILEScopy InChI
Affinity DataIC50: 68nMAssay Description:Antagonist activity at human DOR expressed in CHO cell membranes assessed as inhibition of CYM51010-induced [35S]-GTPgammaS binding preincubated for ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50288745(CHEMBL4159810)copy SMILEScopy InChI
Affinity DataIC50: 76nMAssay Description:Antagonist activity at human DOR expressed in CHO cell membranes assessed as inhibition of CYM51010-induced [35S]-GTPgammaS binding preincubated for ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B0514PubMed
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