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Found 69 with Last Name = 'waibel' and Initial = 'm'
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM912((3S,4S)-3-hydroxy-4-[(2S)-2-[(3S,4S)-3-hydroxy-6-m...)
Affinity DataKi:  38nMAssay Description:Inhibition of HIV1 protease by Hanes methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM912((3S,4S)-3-hydroxy-4-[(2S)-2-[(3S,4S)-3-hydroxy-6-m...)
Affinity DataKi:  38nMAssay Description:Inhibition of HIV1 protease by Lineweaver-Burke methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM912((3S,4S)-3-hydroxy-4-[(2S)-2-[(3S,4S)-3-hydroxy-6-m...)
Affinity DataKi:  50nMAssay Description:Inhibition of HIV1 protease by Dixon methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480048(CHEMBL466684)
Affinity DataKi:  2.62E+4nMAssay Description:Inhibition of HIV1 protease by Lineweaver-Burke methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480048(CHEMBL466684)
Affinity DataKi:  2.62E+4nMAssay Description:Inhibition of HIV1 protease by Hanes methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480043(CHEMBL466688)
Affinity DataKi:  3.43E+4nMAssay Description:Inhibition of HIV1 protease by Lineweaver-Burke methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480043(CHEMBL466688)
Affinity DataKi:  3.43E+4nMAssay Description:Inhibition of HIV1 protease by Hanes methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480048(CHEMBL466684)
Affinity DataKi:  3.48E+4nMAssay Description:Inhibition of HIV1 protease by Dixon methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480043(CHEMBL466688)
Affinity DataKi:  4.39E+4nMAssay Description:Inhibition of HIV1 protease by Dixon methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480047(CHEMBL466502)
Affinity DataKi:  9.60E+4nMAssay Description:Inhibition of HIV1 protease by Dixon methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480047(CHEMBL466502)
Affinity DataKi:  9.60E+4nMAssay Description:Inhibition of HIV1 protease by Hanes methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480047(CHEMBL466502)
Affinity DataKi:  9.90E+4nMAssay Description:Inhibition of HIV1 protease by Lineweaver-Burke methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480044(CHEMBL471433)
Affinity DataKi:  1.38E+5nMAssay Description:Inhibition of HIV1 protease by Dixon methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480044(CHEMBL471433)
Affinity DataKi:  1.49E+5nMAssay Description:Inhibition of HIV1 protease by Hanes methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480044(CHEMBL471433)
Affinity DataKi:  1.49E+5nMAssay Description:Inhibition of HIV1 protease by Lineweaver-Burke methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480049(CHEMBL512599)
Affinity DataKi:  2.86E+5nMAssay Description:Inhibition of HIV1 protease by Dixon methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480049(CHEMBL512599)
Affinity DataKi:  2.92E+5nMAssay Description:Inhibition of HIV1 protease by Hanes methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480049(CHEMBL512599)
Affinity DataKi:  2.92E+5nMAssay Description:Inhibition of HIV1 protease by Lineweaver-Burke methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480042(CHEMBL466687)
Affinity DataKi:  4.54E+5nMAssay Description:Inhibition of HIV1 protease by Dixon methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480042(CHEMBL466687)
Affinity DataKi:  4.61E+5nMAssay Description:Inhibition of HIV1 protease by Hanes methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480042(CHEMBL466687)
Affinity DataKi:  4.61E+5nMAssay Description:Inhibition of HIV1 protease by Lineweaver-Burke methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480046(CHEMBL511210)
Affinity DataKi:  5.74E+5nMAssay Description:Inhibition of HIV1 protease by Lineweaver-Burke methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480046(CHEMBL511210)
Affinity DataKi:  5.77E+5nMAssay Description:Inhibition of HIV1 protease by Dixon methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480046(CHEMBL511210)
Affinity DataKi:  6.18E+5nMAssay Description:Inhibition of HIV1 protease by Hanes methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM912((3S,4S)-3-hydroxy-4-[(2S)-2-[(3S,4S)-3-hydroxy-6-m...)
Affinity DataIC50:  41nMAssay Description:Inhibition of HIV1 protease by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480048(CHEMBL466684)
Affinity DataIC50:  3.72E+4nMAssay Description:Inhibition of HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480043(CHEMBL466688)
Affinity DataIC50:  4.45E+4nMAssay Description:Inhibition of HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480044(CHEMBL471433)
Affinity DataIC50:  1.69E+5nMAssay Description:Inhibition of HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480047(CHEMBL466502)
Affinity DataIC50:  2.04E+5nMAssay Description:Inhibition of HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480049(CHEMBL512599)
Affinity DataIC50:  3.41E+5nMAssay Description:Inhibition of HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480042(CHEMBL466687)
Affinity DataIC50:  5.43E+5nMAssay Description:Inhibition of HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480046(CHEMBL511210)
Affinity DataIC50:  5.45E+5nMAssay Description:Inhibition of HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Universit£

Curated by ChEMBL
LigandPNGBDBM50480045(CHEMBL466085)
Affinity DataIC50: >1.00E+6nMAssay Description:Inhibition of HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50297513(6-[2-(4-Hydroxy-phenyl)-1-methyl-ethyl]-pyridin-3-...)
Affinity DataEC50:  330nMAssay Description:Activity at human ERalpha expressed in HEC1 cells cotransfected with 2ERE-pS2-Luc assessed as relative transcriptional potency by luciferase reporter...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50297514(6-[1-(4-Hydroxy-benzyl)-propyl]-pyridin-3-ol | CHE...)
Affinity DataEC50:  65nMAssay Description:Activity at human ERalpha expressed in HEC1 cells cotransfected with 2ERE-pS2-Luc assessed as relative transcriptional potency by luciferase reporter...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50297515(6-[2-(4-Hydroxy-phenyl)-propyl]-pyridin-3-ol | CHE...)
Affinity DataEC50:  440nMAssay Description:Activity at human ERalpha expressed in HEC1 cells cotransfected with 2ERE-pS2-Luc assessed as relative transcriptional potency by luciferase reporter...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50297516(CHEMBL538148 | trans-6-[1-ethyl-2-(4-hydroxy-pheny...)
Affinity DataEC50:  0.110nMAssay Description:Activity at human ERalpha expressed in HEC1 cells cotransfected with 2ERE-pS2-Luc assessed as relative transcriptional potency by luciferase reporter...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50297517(CHEMBL552019 | cis-6-[1-ethyl-2-(4-hydroxy-phenyl)...)
Affinity DataEC50:  16nMAssay Description:Activity at human ERalpha expressed in HEC1 cells cotransfected with 2ERE-pS2-Luc assessed as relative transcriptional potency by luciferase reporter...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50297518(CHEMBL556650 | trans-6-[1-ethyl-2-(4-hydroxy-pheny...)
Affinity DataEC50:  0.110nMAssay Description:Activity at human ERalpha expressed in HEC1 cells cotransfected with 2ERE-pS2-Luc assessed as relative transcriptional potency by luciferase reporter...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50297519((+/-)-1,2-Bis-(4-hydroxy-phenyl)-propane | 4,4'-(p...)
Affinity DataEC50:  6.5nMAssay Description:Activity at human ERalpha expressed in HEC1 cells cotransfected with 2ERE-pS2-Luc assessed as relative transcriptional potency by luciferase reporter...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50297513(6-[2-(4-Hydroxy-phenyl)-1-methyl-ethyl]-pyridin-3-...)
Affinity DataEC50:  60nMAssay Description:Activity at human ERbeta expressed in HEC1 cells cotransfected with 2ERE-pS2-Luc assessed as relative transcriptional potency by luciferase reporter ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50297514(6-[1-(4-Hydroxy-benzyl)-propyl]-pyridin-3-ol | CHE...)
Affinity DataEC50:  17nMAssay Description:Activity at human ERbeta expressed in HEC1 cells cotransfected with 2ERE-pS2-Luc assessed as relative transcriptional potency by luciferase reporter ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50297515(6-[2-(4-Hydroxy-phenyl)-propyl]-pyridin-3-ol | CHE...)
Affinity DataEC50:  170nMAssay Description:Activity at human ERbeta expressed in HEC1 cells cotransfected with 2ERE-pS2-Luc assessed as relative transcriptional potency by luciferase reporter ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50297516(CHEMBL538148 | trans-6-[1-ethyl-2-(4-hydroxy-pheny...)
Affinity DataEC50:  1.10nMAssay Description:Activity at human ERbeta expressed in HEC1 cells cotransfected with 2ERE-pS2-Luc assessed as relative transcriptional potency by luciferase reporter ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50297517(CHEMBL552019 | cis-6-[1-ethyl-2-(4-hydroxy-phenyl)...)
Affinity DataEC50:  26nMAssay Description:Activity at human ERbeta expressed in HEC1 cells cotransfected with 2ERE-pS2-Luc assessed as relative transcriptional potency by luciferase reporter ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50297518(CHEMBL556650 | trans-6-[1-ethyl-2-(4-hydroxy-pheny...)
Affinity DataEC50:  0.610nMAssay Description:Activity at human ERbeta expressed in HEC1 cells cotransfected with 2ERE-pS2-Luc assessed as relative transcriptional potency by luciferase reporter ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50297519((+/-)-1,2-Bis-(4-hydroxy-phenyl)-propane | 4,4'-(p...)
Affinity DataEC50:  1.20nMAssay Description:Activity at human ERbeta expressed in HEC1 cells cotransfected with 2ERE-pS2-Luc assessed as relative transcriptional potency by luciferase reporter ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50297519((+/-)-1,2-Bis-(4-hydroxy-phenyl)-propane | 4,4'-(p...)
Affinity DataEC50:  1.20nMAssay Description:Agonist activity at ERbeta expressed in human HEC1 cells assessed as transcriptional potency after 24 hrs by luciferase-beta galactosidase reporter g...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50298235(1,2-Bis-(4-hydroxy-phenyl)-2-methyl-propane | CHEM...)
Affinity DataEC50:  1.10nMAssay Description:Agonist activity at ERbeta expressed in human HEC1 cells assessed as transcriptional potency after 24 hrs by luciferase-beta galactosidase reporter g...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Illinois

Curated by ChEMBL
LigandPNGBDBM50106635((+/-)-2,3-bis(4-hydroxyphenyl)propanenitrile | 2,3...)
Affinity DataEC50:  0.850nMAssay Description:Agonist activity at ERbeta expressed in human HEC1 cells assessed as transcriptional potency after 24 hrs by luciferase-beta galactosidase reporter g...More data for this Ligand-Target Pair
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