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Found 5118 with Last Name = 'fernandes' and Initial = 's'
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321606((3S,6S,9S,12S,15R,18S,21S,27R,30S)-18-((1H-imidazo...)
Affinity DataKi:  0.130nMAssay Description:Displacement of [3H]DAMGO from rat mu opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321606((3S,6S,9S,12S,15R,18S,21S,27R,30S)-18-((1H-imidazo...)
Affinity DataKi:  0.130nMAssay Description:Displacement of [3H]DAMGO from rat mu opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(3) dopamine receptor(Homo sapiens)TBA
LigandPNGBDBM50610174(CHEMBL4293814)
Affinity DataKi:  0.340nMAssay Description:Binding affinity to human D3 receptor expressed in CHO cells assessed as inhibition constant by scintillation counting methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails PubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321607((3S,6S,9S,12S,15R,18S,21S,27R,30S)-18-((1H-imidazo...)
Affinity DataKi:  0.690nMAssay Description:Displacement of [3H]DAMGO from rat mu opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(3) dopamine receptor(Homo sapiens)TBA
LigandPNGBDBM50610173(CHEMBL5280702)
Affinity DataKi:  0.700nMAssay Description:Binding affinity to human D3 receptor expressed in CHO cells assessed as inhibition constant by scintillation counting methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails PubMed
TargetD(3) dopamine receptor(Homo sapiens)TBA
LigandPNGBDBM50610180(CHEMBL5276588)
Affinity DataKi:  0.860nMAssay Description:Binding affinity to human D3 receptor expressed in CHO cells assessed as inhibition constant by scintillation counting methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails PubMed
TargetD(3) dopamine receptor(Homo sapiens)TBA
LigandPNGBDBM50610177(CHEMBL5268329)
Affinity DataKi:  0.920nMAssay Description:Inhibition of human D3 receptor expressed in CHO cells assessed as inhibition constant by scintillation counting methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails PubMed
TargetD(3) dopamine receptor(Homo sapiens)TBA
LigandPNGBDBM50610178(CHEMBL5289468)
Affinity DataKi:  0.920nMAssay Description:Binding affinity to human D3 receptor expressed in CHO cells assessed as inhibition constant by scintillation counting methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails PubMed
TargetHistamine H4 receptor(Homo sapiens (Human))
Universidade Federal De S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50121205(CHEBI:18295 | Histamine)
Affinity DataKi:  1nMAssay Description:Displacement of [3H]-Histamine from human histamine 4 receptor transfected in HEK293T cells incubated for 16 hrs by liquid scintillation counter anal...More data for this Ligand-Target Pair
TargetD(3) dopamine receptor(Homo sapiens)TBA
LigandPNGBDBM50610182(CHEMBL5287235)
Affinity DataKi:  1.40nMAssay Description:Binding affinity to human D3 receptor expressed in CHO cells assessed as inhibition constant by scintillation counting methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails PubMed
TargetCholecystokinin receptor type A(Homo sapiens (Human))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321604((3S,6S,9S,12S,15R,18S,21S,24R,27S)-18-((1H-imidazo...)
Affinity DataKi:  1.60nMAssay Description:Displacement of [125I]CCK-8(SO3) from human CCK1 receptor expressed in human HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholecystokinin receptor type A(Homo sapiens (Human))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321604((3S,6S,9S,12S,15R,18S,21S,24R,27S)-18-((1H-imidazo...)
Affinity DataKi:  1.60nMAssay Description:Displacement of [125I]CCK-8(SO3) from human CCK1 receptor expressed in human HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Universidade Federal De S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50121205(CHEBI:18295 | Histamine)
Affinity DataKi:  2.5nMAssay Description:Displacement of [3H]-Histamine from human histamine 3 receptor transfected in HEK293T cells incubated for 16 hrs by liquid scintillation counter anal...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM21123((2S)-2-{2-[(2R)-2-[(2S)-2-amino-3-(4-hydroxyphenyl...)
Affinity DataKi:  2.80nMAssay Description:Displacement of [3H]DAMGO from rat mu opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM21123((2S)-2-{2-[(2R)-2-[(2S)-2-amino-3-(4-hydroxyphenyl...)
Affinity DataKi:  2.80nMAssay Description:Displacement of [3H]DAMGO from rat mu opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(3) dopamine receptor(Homo sapiens)TBA
LigandPNGBDBM50610169(CHEMBL5270151)
Affinity DataKi:  3.10nMAssay Description:Binding affinity to human D3 receptor expressed in CHO cells assessed as inhibition constant by scintillation counting methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321605((6R,9S,12S,15R,18S,21S,24S,27S)-12-((1H-imidazol-5...)
Affinity DataKi:  3.70nMAssay Description:Displacement of [3H]DPDPE from human delta opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Universidade Federal De S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50552436(CHEMBL4749654)
Affinity DataKi:  4nMAssay Description:Displacement of [3H]-Histamine from human histamine 3 receptor transfected in HEK293T cells incubated for 16 hrs by liquid scintillation counter anal...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321605((6R,9S,12S,15R,18S,21S,24S,27S)-12-((1H-imidazol-5...)
Affinity DataKi:  4.90nMAssay Description:Displacement of [3H]DAMGO from rat mu opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321598((S)-3-((4R,7S,10S,13R,16S,22S)-16-((1H-imidazol-5-...)
Affinity DataKi:  5.90nMAssay Description:Displacement of [3H]DAMGO from rat mu opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321608((3S,6S,9S,12S,15R,18S,21S,27R,30S)-18-((1H-imidazo...)
Affinity DataKi:  6.20nMAssay Description:Displacement of [3H]DPDPE from human delta opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Universidade Federal De S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50552434(CHEMBL4747180)
Affinity DataKi:  6.30nMAssay Description:Displacement of [3H]-Histamine from human histamine 3 receptor transfected in HEK293T cells incubated for 16 hrs by liquid scintillation counter anal...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321601((2S,5R,11S,18S,21S)-2-amino-21-((S)-1-amino-1-oxo-...)
Affinity DataKi:  7.40nMAssay Description:Displacement of [3H]DAMGO from rat mu opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321599((S)-3-((4R,7S,10S,13R,16S,22S)-16-((1H-imidazol-5-...)
Affinity DataKi:  8.60nMAssay Description:Displacement of [3H]DAMGO from rat mu opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholecystokinin receptor type A(Homo sapiens (Human))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321607((3S,6S,9S,12S,15R,18S,21S,27R,30S)-18-((1H-imidazo...)
Affinity DataKi:  9nMAssay Description:Displacement of [125I]CCK-8(SO3) from human CCK1 receptor expressed in human HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholecystokinin receptor type A(Homo sapiens (Human))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321607((3S,6S,9S,12S,15R,18S,21S,27R,30S)-18-((1H-imidazo...)
Affinity DataKi:  9nMAssay Description:Displacement of [125I]CCK-8(SO3) from human CCK1 receptor expressed in human HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(3) dopamine receptor(Homo sapiens)TBA
LigandPNGBDBM50610176(CHEMBL5265920)
Affinity DataKi: >10nMAssay Description:Binding affinity to human D3 receptor expressed in CHO cells assessed as inhibition constant by scintillation counting methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails PubMed
TargetD(3) dopamine receptor(Homo sapiens)TBA
LigandPNGBDBM50610170(CHEMBL5278711)
Affinity DataKi: >10nMAssay Description:Binding affinity to human D3 receptor expressed in CHO cells assessed as inhibition constant by scintillation counting methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails PubMed
TargetD(3) dopamine receptor(Homo sapiens)TBA
LigandPNGBDBM50610179(CHEMBL5282002)
Affinity DataKi: >10nMAssay Description:Binding affinity to human D3 receptor expressed in CHO cells assessed as inhibition constant by scintillation counting methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails PubMed
TargetD(3) dopamine receptor(Homo sapiens)TBA
LigandPNGBDBM50610175(CHEMBL5283987)
Affinity DataKi: >10nMAssay Description:Binding affinity to human D3 receptor expressed in CHO cells assessed as inhibition constant by scintillation counting methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails PubMed
TargetD(3) dopamine receptor(Homo sapiens)TBA
LigandPNGBDBM50610181(CHEMBL5270288)
Affinity DataKi: >10nMAssay Description:Binding affinity to human D3 receptor expressed in CHO cells assessed as inhibition constant by scintillation counting methodMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails PubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321608((3S,6S,9S,12S,15R,18S,21S,27R,30S)-18-((1H-imidazo...)
Affinity DataKi:  14nMAssay Description:Displacement of [3H]DAMGO from rat mu opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321608((3S,6S,9S,12S,15R,18S,21S,27R,30S)-18-((1H-imidazo...)
Affinity DataKi:  14nMAssay Description:Displacement of [3H]DAMGO from rat mu opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholecystokinin receptor type A(Homo sapiens (Human))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321596((3S,6R,9S,12S,15S,18S)-3-((1H-imidazol-5-yl)methyl...)
Affinity DataKi:  15nMAssay Description:Displacement of [125I]CCK-8(SO3) from human CCK1 receptor expressed in human HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholecystokinin receptor type A(Homo sapiens (Human))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321596((3S,6R,9S,12S,15S,18S)-3-((1H-imidazol-5-yl)methyl...)
Affinity DataKi:  15nMAssay Description:Displacement of [125I]CCK-8(SO3) from human CCK1 receptor expressed in human HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Universidade Federal De S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50405713(CHEMBL4173854)
Affinity DataKi:  16nMAssay Description:Inhibition of human H3 receptor assessed as inhibition constant incubated for 90 mins by scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Universidade Federal De S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50552435(CHEMBL4756432)
Affinity DataKi:  16nMAssay Description:Displacement of [3H]-Histamine from human histamine 3 receptor transfected in HEK293T cells incubated for 16 hrs by liquid scintillation counter anal...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProteasome subunit beta type-5(Homo sapiens (Human))
S£O Paulo State University

Curated by ChEMBL
LigandPNGBDBM50516759(CHEMBL4458610)
Affinity DataKi:  17nMAssay Description:Inhibition of human chymotrypsin-like activity of 20S proteasome (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321608((3S,6S,9S,12S,15R,18S,21S,27R,30S)-18-((1H-imidazo...)
Affinity DataKi:  18nMAssay Description:Displacement of [125I]CCK-8(SO3) from human CCK2 receptor expressed in human HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321608((3S,6S,9S,12S,15R,18S,21S,27R,30S)-18-((1H-imidazo...)
Affinity DataKi:  18nMAssay Description:Displacement of [125I]CCK-8(SO3) from human CCK2 receptor expressed in human HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholecystokinin receptor type A(Homo sapiens (Human))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321606((3S,6S,9S,12S,15R,18S,21S,27R,30S)-18-((1H-imidazo...)
Affinity DataKi:  18nMAssay Description:Displacement of [125I]CCK-8(SO3) from human CCK1 receptor expressed in human HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321597((3S,6R,9S,12S,15S,18S)-3-((1H-imidazol-5-yl)methyl...)
Affinity DataKi:  18nMAssay Description:Displacement of [3H]DAMGO from rat mu opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholecystokinin receptor type A(Homo sapiens (Human))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321606((3S,6S,9S,12S,15R,18S,21S,27R,30S)-18-((1H-imidazo...)
Affinity DataKi:  18nMAssay Description:Displacement of [125I]CCK-8(SO3) from human CCK1 receptor expressed in human HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholecystokinin receptor type A(Homo sapiens (Human))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321597((3S,6R,9S,12S,15S,18S)-3-((1H-imidazol-5-yl)methyl...)
Affinity DataKi:  32nMAssay Description:Displacement of [125I]CCK-8(SO3) from human CCK1 receptor expressed in human HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Universidade Federal De S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50552430(CHEMBL4798369)
Affinity DataKi:  40nMAssay Description:Displacement of [3H]-Histamine from human histamine 3 receptor transfected in HEK293T cells incubated for 16 hrs by liquid scintillation counter anal...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
S£O Paulo State University

Curated by ChEMBL
LigandPNGBDBM50516761(CHEMBL3286879)
Affinity DataKi:  40nMAssay Description:Inhibition of bacterial beta lactamase TEM-1More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321604((3S,6S,9S,12S,15R,18S,21S,24R,27S)-18-((1H-imidazo...)
Affinity DataKi:  42nMAssay Description:Displacement of [3H]DPDPE from human delta opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321596((3S,6R,9S,12S,15S,18S)-3-((1H-imidazol-5-yl)methyl...)
Affinity DataKi:  47nMAssay Description:Displacement of [3H]DAMGO from rat mu opioid receptor expressed in mouse HN9.10 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(3) dopamine receptor(Homo sapiens)TBA
LigandPNGBDBM21398(4-[4-(4-Chloro-phenyl)-4-hydroxy-piperidin-1-yl]-1...)
Affinity DataKi:  54nMAssay Description:Binding affinity to human D3 receptor expressed in CHO cells assessed as inhibition constant by scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50321609((S)-4-((S)-1-amino-1-oxo-3-phenylpropan-2-ylamino)...)
Affinity DataKi:  61nMAssay Description:Displacement of [125I]CCK-8(SO3) from human CCK2 receptor expressed in human HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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