Compile Data Set for Download or QSAR
maximum 50k data
Found 60 Enz. Inhib. hit(s) with all data for entry = 50037197
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM82551(C18130 | CAS_105618-26-6 | NOR-BNI (HCI)2 | NORBNI)
Affinity DataKi:  0.200nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122859(22-cyclopropylmethyl-7-[2-(1-iminobutylamino)ethyl...)
Affinity DataKi:  0.25nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122869(22-cyclopropylmethyl-7-[2-(1-iminopropylamino)ethy...)
Affinity DataKi:  0.280nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122862(22-cyclopropylmethyl-7-[2-(1-iminoethylamino)ethyl...)
Affinity DataKi:  0.290nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122863(22-cyclopropylmethyl-7-[2-(1-iminopentylamino)ethy...)
Affinity DataKi:  0.300nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122855(1N-{2-[22-cyclopropylmethyl-2,16-dihydroxy-14-oxa-...)
Affinity DataKi:  0.680nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122852(1N-{2-[22-cyclopropylmethyl-2,16-dihydroxy-14-oxa-...)
Affinity DataKi:  0.850nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122865(22-cyclopropylmethyl-7-[2-(1-imino-3-methylbutylam...)
Affinity DataKi:  1.40nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122856(22-cyclopropylmethyl-7-(2-imino-2-pentylaminoethyl...)
Affinity DataKi:  1.40nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122860(1N-{2-[22-cyclopropylmethyl-2,16-dihydroxy-14-oxa-...)
Affinity DataKi:  1.60nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122864(22-cyclopropylmethyl-7-(2-imino-2-propylaminoethyl...)
Affinity DataKi:  1.60nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122851(7N-(4-methoxybenzyl)-22-cyclopropylmethyl-2,16-dih...)
Affinity DataKi:  2.10nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122853(7N-phenethyl-22-cyclopropylmethyl-2,16-dihydroxy-1...)
Affinity DataKi:  2.20nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122857(22-cyclopropylmethyl-7-(6-hexylaminocarbonylaminoe...)
Affinity DataKi:  2.30nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122861(22-cyclopropylmethyl-7-(2-ethylaminocarbonylaminoe...)
Affinity DataKi:  2.40nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122866(22-cyclopropylmethyl-7-(4-butylaminocarbonylaminoe...)
Affinity DataKi:  2.60nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122860(1N-{2-[22-cyclopropylmethyl-2,16-dihydroxy-14-oxa-...)
Affinity DataKi:  3.10nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122853(7N-phenethyl-22-cyclopropylmethyl-2,16-dihydroxy-1...)
Affinity DataKi:  3.5nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122852(1N-{2-[22-cyclopropylmethyl-2,16-dihydroxy-14-oxa-...)
Affinity DataKi:  3.70nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122851(7N-(4-methoxybenzyl)-22-cyclopropylmethyl-2,16-dih...)
Affinity DataKi:  4.60nMAssay Description:Ability to displace [3H]DAMGO from human recombinant Opioid receptor mu 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122866(22-cyclopropylmethyl-7-(4-butylaminocarbonylaminoe...)
Affinity DataKi:  4.80nMAssay Description:Ability to displace [3H]DAMGO from human recombinant Opioid receptor mu 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122864(22-cyclopropylmethyl-7-(2-imino-2-propylaminoethyl...)
Affinity DataKi:  5.30nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122858(22-cyclopropylmethyl-7-(2-heptylamino-2-iminoethyl...)
Affinity DataKi:  5.60nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM82551(C18130 | CAS_105618-26-6 | NOR-BNI (HCI)2 | NORBNI)
Affinity DataKi:  5.70nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122867(7N-(4-phenylbutyl)-22-cyclopropylmethyl-2,16-dihyd...)
Affinity DataKi:  6.20nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122866(22-cyclopropylmethyl-7-(4-butylaminocarbonylaminoe...)
Affinity DataKi:  6.30nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122858(22-cyclopropylmethyl-7-(2-heptylamino-2-iminoethyl...)
Affinity DataKi:  7.30nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122851(7N-(4-methoxybenzyl)-22-cyclopropylmethyl-2,16-dih...)
Affinity DataKi:  7.40nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122855(1N-{2-[22-cyclopropylmethyl-2,16-dihydroxy-14-oxa-...)
Affinity DataKi:  7.70nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122857(22-cyclopropylmethyl-7-(6-hexylaminocarbonylaminoe...)
Affinity DataKi:  8.10nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122868(7N-benzyl-22-cyclopropylmethyl-2,16-dihydroxy-14-o...)
Affinity DataKi:  10nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122868(7N-benzyl-22-cyclopropylmethyl-2,16-dihydroxy-14-o...)
Affinity DataKi:  11nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122861(22-cyclopropylmethyl-7-(2-ethylaminocarbonylaminoe...)
Affinity DataKi:  12nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122864(22-cyclopropylmethyl-7-(2-imino-2-propylaminoethyl...)
Affinity DataKi:  13nMAssay Description:Ability to displace [3H]DAMGO from human recombinant Opioid receptor mu 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122857(22-cyclopropylmethyl-7-(6-hexylaminocarbonylaminoe...)
Affinity DataKi:  14nMAssay Description:Ability to displace [3H]DAMGO from human recombinant Opioid receptor mu 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122856(22-cyclopropylmethyl-7-(2-imino-2-pentylaminoethyl...)
Affinity DataKi:  17nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122865(22-cyclopropylmethyl-7-[2-(1-imino-3-methylbutylam...)
Affinity DataKi:  20nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122862(22-cyclopropylmethyl-7-[2-(1-iminoethylamino)ethyl...)
Affinity DataKi:  21nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM82551(C18130 | CAS_105618-26-6 | NOR-BNI (HCI)2 | NORBNI)
Affinity DataKi:  21nMAssay Description:Ability to displace [3H]DAMGO from human recombinant Opioid receptor mu 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122862(22-cyclopropylmethyl-7-[2-(1-iminoethylamino)ethyl...)
Affinity DataKi:  22nMAssay Description:Ability to displace [3H]DAMGO from human recombinant Opioid receptor mu 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122854(7N-heptyl-22-cyclopropylmethyl-2,16-dihydroxy-14-o...)
Affinity DataKi:  22nMAssay Description:Ability to displace [3H]U-69593 from human recombinant Opioid receptor kappa 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122869(22-cyclopropylmethyl-7-[2-(1-iminopropylamino)ethy...)
Affinity DataKi:  22nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122860(1N-{2-[22-cyclopropylmethyl-2,16-dihydroxy-14-oxa-...)
Affinity DataKi:  23nMAssay Description:Ability to displace [3H]DAMGO from human recombinant Opioid receptor mu 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122853(7N-phenethyl-22-cyclopropylmethyl-2,16-dihydroxy-1...)
Affinity DataKi:  24nMAssay Description:Ability to displace [3H]DAMGO from human recombinant Opioid receptor mu 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122856(22-cyclopropylmethyl-7-(2-imino-2-pentylaminoethyl...)
Affinity DataKi:  25nMAssay Description:Ability to displace [3H]DAMGO from human recombinant Opioid receptor mu 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122869(22-cyclopropylmethyl-7-[2-(1-iminopropylamino)ethy...)
Affinity DataKi:  26nMAssay Description:Ability to displace [3H]DAMGO from human recombinant Opioid receptor mu 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122859(22-cyclopropylmethyl-7-[2-(1-iminobutylamino)ethyl...)
Affinity DataKi:  28nMAssay Description:Ability to displace [3H]DPDPE from human recombinant Opioid receptor delta 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122852(1N-{2-[22-cyclopropylmethyl-2,16-dihydroxy-14-oxa-...)
Affinity DataKi:  31nMAssay Description:Ability to displace [3H]DAMGO from human recombinant Opioid receptor mu 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122855(1N-{2-[22-cyclopropylmethyl-2,16-dihydroxy-14-oxa-...)
Affinity DataKi:  32nMAssay Description:Ability to displace [3H]DAMGO from human recombinant Opioid receptor mu 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50122867(7N-(4-phenylbutyl)-22-cyclopropylmethyl-2,16-dihyd...)
Affinity DataKi:  37nMAssay Description:Ability to displace [3H]DAMGO from human recombinant Opioid receptor mu 1 in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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