Compile Data Set for Download or QSAR
maximum 50k data
Found 2112 with Last Name = 'woods' and Initial = 'r'
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50367249(CHEMBL309601)
Affinity DataKi:  0.5nMAssay Description:Compound was evaluated for the inhibition of Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50020843(2-[(2S)-2-carboxypyrrolidin-1-yl]-1-methyl-2-oxoet...)
Affinity DataKi:  1.40nMAssay Description:Compound was evaluated for the inhibition of Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50196190(1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...)
Affinity DataKi:  25nMAssay Description:Displacement of [125I]CCK-8S from CCK2 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50196190(1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...)
Affinity DataKi:  25nMAssay Description:Displacement of [125I]CCK8S from human CCK2RMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50196191(4-[4-iodo-2-[(5-quinoxalinylsulfonyl)amino]benzoyl...)
Affinity DataKi:  32nMAssay Description:Displacement of [125I]CCK8S from human CCK2RMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50196157(1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...)
Affinity DataKi:  40nMAssay Description:Displacement of [125I]CCK8S from human CCK2RMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84465(Benzylation of mannostatin A, 1e)
Affinity DataKi:  50nM ΔG°:  -43.3kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50478086(CHEMBL261682)
Affinity DataKi:  63nMAssay Description:Displacement of [125I]CCK8S from human CCK2RMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50478090(CHEMBL259762)
Affinity DataKi:  79nMAssay Description:Displacement of [125I]CCK8S from human CCK2RMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM50078117((1R,2R,3R,4S,5R)-4-AMINO-5-(METHYLTHIO)CYCLOPENTAN...)
Affinity DataKi:  90nM ΔG°:  -41.8kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84466(Benzylation of mannostatin A, 1f)
Affinity DataKi:  100nM ΔG°:  -41.6kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84464(Benzylation of mannostatin A, 1d)
Affinity DataKi:  100nM ΔG°:  -41.6kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84462(Benzylation of mannostatin A, 1b)
Affinity DataKi:  110nM ΔG°:  -41.3kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84467(Benzylation of mannostatin A, 1g)
Affinity DataKi:  140nM ΔG°:  -40.7kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84474(Aminocyclopentitetrol, 2g)
Affinity DataKi:  160nM ΔG°:  -40.3kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84463(Benzylation of mannostatin A, 1c)
Affinity DataKi:  170nM ΔG°:  -40.2kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM50078117((1R,2R,3R,4S,5R)-4-AMINO-5-(METHYLTHIO)CYCLOPENTAN...)
Affinity DataKi:  210nM ΔG°:  -39.6kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84470(Aminocyclopentitetrol, 2c)
Affinity DataKi:  330nM ΔG°:  -38.5kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84472(Aminocyclopentitetrol, 2e)
Affinity DataKi:  330nM ΔG°:  -38.5kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50477817(CHEMBL387285)
Affinity DataKi:  398nMAssay Description:Displacement of [125I]CCK-8S from CCK2 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84469(Aminocyclopentitetrol, 2b)
Affinity DataKi:  450nM ΔG°:  -37.7kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84473(Aminocyclopentitetrol, 2f)
Affinity DataKi:  480nM ΔG°:  -37.5kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50478094(CHEMBL408452)
Affinity DataKi:  501nMAssay Description:Displacement of [125I]CCK8S from human CCK2RMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50477813(CHEMBL249469)
Affinity DataKi:  501nMAssay Description:Displacement of [125I]CCK-8S from CCK2 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50477804(CHEMBL251466)
Affinity DataKi:  501nMAssay Description:Displacement of [125I]CCK-8S from CCK2 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84465(Benzylation of mannostatin A, 1e)
Affinity DataKi:  510nM ΔG°:  -37.4kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84466(Benzylation of mannostatin A, 1f)
Affinity DataKi:  520nM ΔG°:  -37.3kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84463(Benzylation of mannostatin A, 1c)
Affinity DataKi:  530nM ΔG°:  -37.3kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50477822(CHEMBL251467)
Affinity DataKi:  631nMAssay Description:Displacement of [125I]CCK-8S from CCK2 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84471(Aminocyclopentitetrol, 2d)
Affinity DataKi:  670nM ΔG°:  -36.7kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50477819(CHEMBL251486)
Affinity DataKi:  794nMAssay Description:Displacement of [125I]CCK-8S from CCK2 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50196192(1-[4-bromo-2-[(quinolin-5-ylsulfonyl)amino]-benzoy...)
Affinity DataKi:  794nMAssay Description:Displacement of [125I]CCK8S from human CCK2RMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50478089(CHEMBL261636)
Affinity DataKi:  794nMAssay Description:Displacement of [125I]CCK8S from human CCK2RMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50478092(CHEMBL410708)
Affinity DataKi:  794nMAssay Description:Displacement of [125I]CCK8S from human CCK2RMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84462(Benzylation of mannostatin A, 1b)
Affinity DataKi:  880nM ΔG°:  -36.0kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84464(Benzylation of mannostatin A, 1d)
Affinity DataKi:  910nM ΔG°:  -35.9kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50196171(1-[2-[(2,1,3-benzooxadiazol-4-ylsulfonyl)amino]-4-...)
Affinity DataKi:  1.59E+3nMAssay Description:Displacement of [125I]CCK8S from human CCK2RMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50478085(CHEMBL259224)
Affinity DataKi:  1.59E+3nMAssay Description:Displacement of [125I]CCK8S from human CCK2RMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50477809(CHEMBL251684)
Affinity DataKi:  1.59E+3nMAssay Description:Displacement of [125I]CCK-8S from CCK2 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50477814(CHEMBL399918)
Affinity DataKi:  1.59E+3nMAssay Description:Displacement of [125I]CCK-8S from CCK2 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50477808(CHEMBL251651)
Affinity DataKi:  2.00E+3nMAssay Description:Displacement of [125I]CCK-8S from CCK2 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50478091(CHEMBL259751)
Affinity DataKi:  2.00E+3nMAssay Description:Displacement of [125I]CCK8S from human CCK2RMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50477816(CHEMBL399059)
Affinity DataKi:  2.51E+3nMAssay Description:Displacement of [125I]CCK-8S from CCK2 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50477811(CHEMBL251485)
Affinity DataKi:  3.16E+3nMAssay Description:Displacement of [125I]CCK-8S from CCK2 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50478087(CHEMBL409479)
Affinity DataKi:  3.16E+3nMAssay Description:Displacement of [125I]CCK8S from human CCK2RMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50477818(CHEMBL399919)
Affinity DataKi:  3.16E+3nMAssay Description:Displacement of [125I]CCK-8S from CCK2 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84467(Benzylation of mannostatin A, 1g)
Affinity DataKi:  3.22E+3nM ΔG°:  -32.6kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50477821(CHEMBL251655)
Affinity DataKi:  3.98E+3nMAssay Description:Displacement of [125I]CCK-8S from CCK2 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
University of Georgia

LigandPNGBDBM84474(Aminocyclopentitetrol, 2g)
Affinity DataKi:  4.40E+3nM ΔG°:  -31.8kJ/molepH: 5.6 T: 2°CMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50477812(CHEMBL400164)
Affinity DataKi:  5.01E+3nMAssay Description:Displacement of [125I]CCK-8S from CCK2 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Displayed 1 to 50 (of 2112 total ) | Next | Last >>
Jump to: