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Found 58 with Last Name = 'sun' and Initial = 'cl'
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Peking University

Curated by ChEMBL
LigandPNGBDBM2198((3-(2-tert-Butyl-5-methyl-phenylsulfanyl)-4-hydrox...)
Affinity DataIC50:  1.10nMAssay Description:Inhibitory concentration against human immunodeficiency virus 1 protease in MT-4 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480563(CHEMBL561448)
Affinity DataIC50:  10nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Peking University

Curated by ChEMBL
LigandPNGBDBM50168218(4-Hydroxy-3-(2-isopropyl-phenylsulfanyl)-6-m-tolyl...)
Affinity DataIC50:  14nMAssay Description:Inhibitory concentration against human immunodeficiency virus 1 protease in MT-4 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Peking University

Curated by ChEMBL
LigandPNGBDBM50054619(4-Hydroxy-6-phenethyl-3-(1-phenyl-propyl)-6-propyl...)
Affinity DataIC50:  35nMAssay Description:Inhibitory concentration against human immunodeficiency virus 1 protease in MT-4 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480562(CHEMBL552184)
Affinity DataIC50:  40nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480561(CHEMBL551245)
Affinity DataIC50:  50nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480575(CHEMBL564613)
Affinity DataIC50:  60nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480579(CHEMBL561974)
Affinity DataIC50:  100nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480570(CHEMBL562249)
Affinity DataIC50:  100nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480583(CHEMBL549887)
Affinity DataIC50:  110nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480571(CHEMBL551852)
Affinity DataIC50:  160nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480565(CHEMBL562565)
Affinity DataIC50:  280nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480566(CHEMBL549348)
Affinity DataIC50:  350nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480567(CHEMBL560908)
Affinity DataIC50:  370nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480572(CHEMBL563346)
Affinity DataIC50:  430nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480560(CHEMBL549682)
Affinity DataIC50:  510nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480576(CHEMBL561111)
Affinity DataIC50:  570nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480569(CHEMBL556475)
Affinity DataIC50:  590nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480581(CHEMBL562049)
Affinity DataIC50:  650nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480573(CHEMBL561773)
Affinity DataIC50:  930nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480580(CHEMBL559085)
Affinity DataIC50:  980nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Peking University

Curated by ChEMBL
LigandPNGBDBM768(4-hydroxy-3-(1-phenylpropyl)-2H-chromen-2-one | CH...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory concentration against human immunodeficiency virus 1 protease in MT-4 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480574(CHEMBL551446)
Affinity DataIC50:  1.07E+3nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480578(CHEMBL560110)
Affinity DataIC50:  1.55E+3nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480559(CHEMBL563487)
Affinity DataIC50:  1.91E+3nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480584(CHEMBL555119)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480558(CHEMBL556092)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480568(CHEMBL551650)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480582(CHEMBL561110)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480577(CHEMBL551769)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetVascular cell adhesion protein 1(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50117525(CHEMBL83626 | Succinic acid mono-{2,6-di-tert-buty...)
Affinity DataIC50:  6.00E+3nMAssay Description:Inhibition of TNF-alpha inducible Vascular cell adhesion molecule-1 expression.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular cell adhesion protein 1(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50117529(3,4-Dihydroxy-butyric acid 2,6-di-tert-butyl-4-[1-...)
Affinity DataIC50:  8.00E+3nMAssay Description:Inhibition of TNF-alpha inducible Vascular cell adhesion molecule-1 expression.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular cell adhesion protein 1(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50117541(CHEMBL315559 | Pentanedioic acid mono-{2,6-di-tert...)
Affinity DataIC50:  9.00E+3nMAssay Description:Inhibition of TNF-alpha inducible Vascular cell adhesion molecule-1 expression.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480564(CHEMBL551774)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
Poniard Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50480557(CHEMBL565069)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of HSP90 in human SKBR3 cells assessed as induction of Her2 degradationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid lipoxygenase ALOX15(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50156934(6-O-{2,6-di-tert-butyl-4-[1-(3,5-di-tert-butyl-4-h...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of 15-lipoxygenase by LMB assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid lipoxygenase ALOX15(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50156942(6-O-{2,6-di-tert-butyl-4-[1-(3,5-di-tert-butyl-4-h...)
Affinity DataIC50:  1.20E+4nMAssay Description:Inhibition of 15-lipoxygenase by LMB assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid lipoxygenase ALOX15(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50007260(2,6-Di-tert-butyl-4-[1-(3,5-di-tert-butyl-4-hydrox...)
Affinity DataIC50:  1.40E+4nMAssay Description:Inhibition of 15-lipoxygenase by LMB assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid lipoxygenase ALOX15(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50156938(4-{2,6-di-tert-butyl-4-[1-(3,5-di-tert-butyl-4-hyd...)
Affinity DataIC50:  1.50E+4nMAssay Description:Inhibition of 15-lipoxygenase by LMB assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid lipoxygenase ALOX15(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50156938(4-{2,6-di-tert-butyl-4-[1-(3,5-di-tert-butyl-4-hyd...)
Affinity DataIC50:  1.70E+4nMAssay Description:Inhibition of 15-lipoxygenase by LMB assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular cell adhesion protein 1(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50117538(2,6-di(tert-butyl)-4-{1-[3,5-di(tert-butyl)-4-hydr...)
Affinity DataIC50:  1.70E+4nMAssay Description:Inhibition of TNF-alpha inducible Vascular cell adhesion molecule-1 expression.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular cell adhesion protein 1(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50117532((R)-2-Phenylacetylamino-succinic acid 4-{2,6-di-te...)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibition of TNF-alpha inducible Vascular cell adhesion molecule-1 expression.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular cell adhesion protein 1(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50117526((S)-2-Hydroxy-pentanedioic acid 1-{2,6-di-tert-but...)
Affinity DataIC50:  2.50E+4nMAssay Description:Inhibition of TNF-alpha inducible Vascular cell adhesion molecule-1 expression.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular cell adhesion protein 1(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50117527(3-Hydroxy-propionic acid 2,6-di-tert-butyl-4-[1-(3...)
Affinity DataIC50:  3.00E+4nMAssay Description:Inhibition of TNF-alpha inducible Vascular cell adhesion molecule-1 expression.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular cell adhesion protein 1(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50117536(CHEMBL86083 | Hydroxy-acetic acid 2,6-di-tert-buty...)
Affinity DataIC50:  3.00E+4nMAssay Description:Inhibition of TNF-alpha inducible Vascular cell adhesion molecule-1 expression.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular cell adhesion protein 1(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50117530(CHEMBL313980 | {2,6-Di-tert-butyl-4-[1-(3,5-di-ter...)
Affinity DataIC50:  3.70E+4nMAssay Description:Inhibition of TNF-alpha inducible Vascular cell adhesion molecule-1 expression.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular cell adhesion protein 1(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50117539(4-Hydroxy-butyric acid 2,6-di-tert-butyl-4-[1-(3,5...)
Affinity DataIC50:  4.00E+4nMAssay Description:Inhibition of TNF-alpha inducible Vascular cell adhesion molecule-1 expression.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular cell adhesion protein 1(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50117528(CHEMBL312723 | Succinic acid 2,6-di-tert-butyl-4-[...)
Affinity DataIC50:  4.00E+4nMAssay Description:Inhibition of TNF-alpha inducible Vascular cell adhesion molecule-1 expression.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular cell adhesion protein 1(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50117534(CHEMBL87881 | Octanedioic acid mono-{2,6-di-tert-b...)
Affinity DataIC50:  4.50E+4nMAssay Description:Inhibition of TNF-alpha inducible Vascular cell adhesion molecule-1 expression.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular cell adhesion protein 1(Homo sapiens (Human))
Atherogenics

Curated by ChEMBL
LigandPNGBDBM50117533(CHEMBL82014 | Oxalic acid mono-{2,6-di-tert-butyl-...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of TNF-alpha inducible Vascular cell adhesion molecule-1 expression.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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