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Found 487 with Last Name = 'sullivan' and Initial = 'r'
TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171332(1-(2-Bromo-4-isopropyl-phenyl)-7-methyl-5-(1-propy...)
Affinity DataKi:  1.10nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171318(1-(4-Methoxy-phenyl)-7-methyl-5-(1-propyl-butyl)-4...)
Affinity DataKi:  2nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent noradrenaline transporter(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM35229(3-(10,11-dihydro-5H-dibenzo[b,f]azepin-5-yl)-N-met...)
Affinity DataKi:  2.10nMAssay Description:Displacement of [3H]nisoxetine from human NET expressed in MDCK-Net6 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetSodium-dependent noradrenaline transporter(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM35229(3-(10,11-dihydro-5H-dibenzo[b,f]azepin-5-yl)-N-met...)
Affinity DataKi:  2.10nMAssay Description:Displacement of [3H]nisoxetine from human NET expressed in MDCK-Net6 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50074501(Butyl-ethyl-[2,5,6-trimethyl-7-(2,4,6-trimethyl-ph...)
Affinity DataKi:  3.10nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent noradrenaline transporter(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM35229(3-(10,11-dihydro-5H-dibenzo[b,f]azepin-5-yl)-N-met...)
Affinity DataKi:  3.40nMAssay Description:Inhibition of human NET-mediated norepinephrine uptake in MDCK-Net6 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171325(2-(2,4-Dichloro-phenyl)-4-methyl-6-(1-propyl-butyl...)
Affinity DataKi:  4.5nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171322(1-(2,4-Dichloro-phenyl)-7-methyl-5-(1-propyl-butyl...)
Affinity DataKi:  5.10nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil collagenase(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130099(4-{(R)-4-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-b...)
Affinity DataKi:  6nMAssay Description:Inhibition of MMP-8More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50129204(CHEMBL65208 | N-{2-[Benzo[1,3]dioxol-5-ylmethyl-((...)
Affinity DataKi:  7nMAssay Description:In vitro inhibitory activity against procollagen C-terminal proteinase (PCP) in HT-1080 cells using synthetic peptide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50129206(CHEMBL292073 | N-{2-[Benzo[1,3]dioxol-5-ylmethyl-(...)
Affinity DataKi:  8nMAssay Description:In vitro inhibitory activity against procollagen C-terminal proteinase (PCP) in HT-1080 cells using synthetic peptide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171316(5-(1-Ethyl-propyl)-1-(4-methoxy-phenyl)-7-methyl-4...)
Affinity DataKi:  8nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil collagenase(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130108((R)-5-(4-Acetyl-piperazin-1-yl)-2-[benzo[1,3]dioxo...)
Affinity DataKi:  9nMAssay Description:Inhibition of MMP-8More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130114((R)-2-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-benz...)
Affinity DataKi:  11nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171328(1-(4-Chloro-phenyl)-7-methyl-5-(1-propyl-butyl)-4,...)
Affinity DataKi:  12nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50129212(CHEMBL294742 | N-{2-[Benzo[1,3]dioxol-5-ylmethyl-(...)
Affinity DataKi:  14nMAssay Description:In vitro inhibitory activity against procollagen C-terminal proteinase (PCP) in HT-1080 cells using synthetic peptide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171334(7-Methyl-5-(1-propyl-butyl)-1-(4-trifluoromethyl-p...)
Affinity DataKi:  17nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50129221(2-[Benzo[1,3]dioxol-5-ylmethyl-((R)-4-methoxy-benz...)
Affinity DataKi:  18nMAssay Description:In vitro inhibitory activity against procollagen C-terminal proteinase (PCP) in HT-1080 cells using synthetic peptide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130131((R)-2-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-benz...)
Affinity DataKi:  20nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171321(5-(1-Ethyl-propyl)-1-(4-methoxy-2-methyl-phenyl)-7...)
Affinity DataKi:  20nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50129209(2-[Benzo[1,3]dioxol-5-ylmethyl-((R)-4-methoxy-benz...)
Affinity DataKi:  22nMAssay Description:In vitro inhibitory activity against procollagen C-terminal proteinase (PCP) in HT-1080 cells using synthetic peptide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent dopamine transporter(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50005536(42-548 | 5-(4-Chloro-phenyl)-2,5-dihydro-3H-imidaz...)
Affinity DataKi:  22.1nMAssay Description:Displacement of [3H]-WIN-35428 from human DAT expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetSodium-dependent dopamine transporter(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50005536(42-548 | 5-(4-Chloro-phenyl)-2,5-dihydro-3H-imidaz...)
Affinity DataKi:  22.1nMAssay Description:Displacement of [3H]WIN35428 from human recombinant DAT expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171315(1-(5-Chloro-pyridin-2-yl)-7-methyl-5-(1-propyl-but...)
Affinity DataKi:  23nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50129208(2-[Benzo[1,3]dioxol-5-ylmethyl-((R)-4-methoxy-benz...)
Affinity DataKi:  28nMAssay Description:In vitro inhibitory activity against procollagen C-terminal proteinase (PCP) in HT-1080 cells using synthetic peptide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130105((R)-2-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-benz...)
Affinity DataKi:  33nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130141((R)-2-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-benz...)
Affinity DataKi:  35nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130123((R)-2-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-benz...)
Affinity DataKi:  40nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130121((R)-ethyl 4-(4-(N-(benzo[d][1,3]dioxol-5-ylmethyl)...)
Affinity DataKi:  43nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171320(1-(2-Methoxy-phenyl)-7-methyl-5-(1-propyl-butyl)-4...)
Affinity DataKi:  44nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171319(1-(4-Chloro-phenyl)-5-(1-ethyl-propyl)-7-methyl-4,...)
Affinity DataKi:  58nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171331(1-(6-Methoxy-pyridin-3-yl)-7-methyl-5-(1-propyl-bu...)
Affinity DataKi:  60nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130112((R)-5-(4-Acetyl-piperazin-1-yl)-2-[benzo[1,3]dioxo...)
Affinity DataKi:  63nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130099(4-{(R)-4-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-b...)
Affinity DataKi:  64nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50129220(5-Methyl-isoxazole-4-carboxylic acid {3-[benzo[1,3...)
Affinity DataKi:  86nMAssay Description:In vitro inhibitory activity against procollagen C-terminal proteinase (PCP) in HT-1080 cells using synthetic peptide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130132(4-{(R)-4-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-b...)
Affinity DataKi:  90nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInterstitial collagenase(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130099(4-{(R)-4-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-b...)
Affinity DataKi:  90nMAssay Description:Inhibition of matrix metalloproteinase-1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130130((R)-2-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-benz...)
Affinity DataKi:  98nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50102996(CHEMBL62908 | N-{(R)-4-[Benzo[1,3]dioxol-5-ylmethy...)
Affinity DataKi:  100nMAssay Description:In vitro inhibitory activity against procollagen C-terminal proteinase (PCP) in HT-1080 cells using synthetic peptide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130106(4-{(R)-4-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-2...)
Affinity DataKi:  100nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130136((R)-2-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-benz...)
Affinity DataKi:  100nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130128(4-{(R)-4-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-b...)
Affinity DataKi:  105nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130102((R)-2-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-2,3,...)
Affinity DataKi:  110nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInterstitial collagenase(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130108((R)-5-(4-Acetyl-piperazin-1-yl)-2-[benzo[1,3]dioxo...)
Affinity DataKi:  120nMAssay Description:Inhibition of matrix metalloproteinase-1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130103((R)-2-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-benz...)
Affinity DataKi:  120nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171314(1-(3-Methoxy-phenyl)-7-methyl-5-(1-propyl-butyl)-4...)
Affinity DataKi:  130nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171333(1-(4-Ethoxy-phenyl)-7-methyl-5-(1-propyl-butyl)-4,...)
Affinity DataKi:  140nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171336(5-(1-Methoxy-butyl)-1-(4-methoxy-phenyl)-7-methyl-...)
Affinity DataKi:  150nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBone morphogenetic protein 1(Homo sapiens (Human))
Combichem

Curated by ChEMBL
LigandPNGBDBM50130125((R)-2-[Benzo[1,3]dioxol-5-ylmethyl-(4-methoxy-benz...)
Affinity DataKi:  160nMAssay Description:Ability to inhibit procollagen C-terminal proteinase (PCP) tested in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Neurocrine Biosciences

Curated by ChEMBL
LigandPNGBDBM50171317(5-(1-Ethyl-propyl)-7-methyl-1-(4-trifluoromethyl-p...)
Affinity DataKi:  170nMAssay Description:Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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