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Found 41 with Last Name = 'koch' and Initial = 'th'
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM17292((1S,10R,11S,14S,15S)-15-methyltetracyclo[8.7.0.0^{...)
Affinity DataIC50:  1.5nMAssay Description:Inhibition of [3H]E2 binding to estrogen receptor alpha in MCF-7 cell lysateMore data for this Ligand-Target Pair
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50474781(CHEMBL19195)
Affinity DataIC50:  5nMAssay Description:Inhibition of [3H]E2 binding to estrogen receptor alpha in MCF-7 cell lysateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50135908(4-(4,4-Dimethyl-2,5-dioxo-imidazolidin-1-yl)-2-tri...)
Affinity DataIC50:  6nMAssay Description:Inhibition of [3H]-Mibolerone binding to human Androgen receptor of PC3/AR Cell LysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50135908(4-(4,4-Dimethyl-2,5-dioxo-imidazolidin-1-yl)-2-tri...)
Affinity DataIC50:  6nMAssay Description:Inhibition of 1.0 nM [3H]mibolerone binding to human androgen receptor of PC3/AR cell lysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50135912(5,5-Dimethyl-3-(alpha,alpha,alpha-trifluoro-4-nitr...)
Affinity DataIC50:  9nMAssay Description:Inhibition of [3H]-Mibolerone binding to human Androgen receptor of PC3/AR Cell LysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50135912(5,5-Dimethyl-3-(alpha,alpha,alpha-trifluoro-4-nitr...)
Affinity DataIC50:  9nMAssay Description:Inhibition of 1.0 nM [3H]mibolerone binding to human androgen receptor of PC3/AR cell lysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

Target7-dehydrocholesterol reductase(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50411320(CHEMBL222694)
Affinity DataIC50:  30nMAssay Description:Growth inhibition of MDA-MB-231 cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target7-dehydrocholesterol reductase(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50411320(CHEMBL222694)
Affinity DataIC50:  30nMAssay Description:Growth inhibition of MCF7 cells expressing ER and antiestrogen binding sitesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target7-dehydrocholesterol reductase(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50411320(CHEMBL222694)
Affinity DataIC50:  40nMAssay Description:Growth inhibition of MDA-MB-435 cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50135914(5-{4-[3-(4-Cyano-3-trifluoromethyl-phenyl)-5,5-dim...)
Affinity DataIC50:  49nMAssay Description:Inhibition of 1.0 nM [3H]mibolerone binding to human androgen receptor of PC3/AR cell lysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50410198(CHEMBL2113036)
Affinity DataIC50:  49nMAssay Description:Inhibition of [3H]-Mibolerone binding to human Androgen receptor of PC3/AR Cell LysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target7-dehydrocholesterol reductase(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50411319(CHEMBL266892)
Affinity DataIC50:  50nMAssay Description:Growth inhibition of MDA-MB-435 cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target7-dehydrocholesterol reductase(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50411320(CHEMBL222694)
Affinity DataIC50:  60nMAssay Description:Growth inhibition of multidrug resistant MCF7/Adr cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50155877(CHEMBL386437 | Doxorubicin-Formaldehyde Conjugate)
Affinity DataIC50:  63nMAssay Description:Inhibition of [3H]-Mibolerone binding to human Androgen receptor of PC3/AR Cell LysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target7-dehydrocholesterol reductase(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50411319(CHEMBL266892)
Affinity DataIC50:  70nMAssay Description:Growth inhibition of MCF7 cells expressing ER and antiestrogen binding sitesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50135910(5-(2-{2-[3-(4-Cyano-3-trifluoromethyl-phenyl)-5,5-...)
Affinity DataIC50:  77nMAssay Description:Inhibition of 1.0 nM [3H]mibolerone binding to human androgen receptor of PC3/AR cell lysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50410197(CHEMBL2113034)
Affinity DataIC50:  77nMAssay Description:Inhibition of [3H]-Mibolerone binding to human Androgen receptor of PC3/AR Cell LysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target7-dehydrocholesterol reductase(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50411319(CHEMBL266892)
Affinity DataIC50:  80nMAssay Description:Growth inhibition of MDA-MB-231 cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50409765(CHEMBL2112885)
Affinity DataIC50:  90nMAssay Description:Inhibition of 1.0 nM [3H]mibolerone binding to human androgen receptor of PC3/AR cell lysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50155875(CHEMBL264131 | Doxorubicin-Formaldehyde Conjugate)
Affinity DataIC50:  90nMAssay Description:Inhibition of [3H]-Mibolerone binding to human Androgen receptor of PC3/AR Cell LysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50474779(CHEMBL19481)
Affinity DataIC50:  150nMAssay Description:Inhibition of [3H]E2 binding to estrogen receptor alpha in MCF-7 cell lysateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50474783(CHEMBL278308)
Affinity DataIC50:  150nMAssay Description:Inhibition of [3H]E2 binding to estrogen receptor alpha in MCF-7 cell lysateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target7-dehydrocholesterol reductase(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM22984((8S,10S)-10-{[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-me...)
Affinity DataIC50:  150nMAssay Description:Growth inhibition of MDA-MB-435 cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50131270(2-methyl-N-[4-nitro-3-(trifluoromethyl)phenyl]prop...)
Affinity DataIC50:  154nMAssay Description:Inhibition of [3H]-Mibolerone binding to human Androgen receptor of PC3/AR Cell LysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50131270(2-methyl-N-[4-nitro-3-(trifluoromethyl)phenyl]prop...)
Affinity DataIC50:  154nMAssay Description:Inhibition of 1.0 nM [3H]mibolerone binding to human androgen receptor of PC3/AR cell lysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

Target7-dehydrocholesterol reductase(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM22984((8S,10S)-10-{[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-me...)
Affinity DataIC50:  200nMAssay Description:Growth inhibition of MCF7 cells expressing ER and antiestrogen binding sitesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50474784(CHEMBL410193)
Affinity DataIC50:  200nMAssay Description:Inhibition of [3H]E2 binding to estrogen receptor alpha in MCF-7 cell lysateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50474780(CHEMBL266703)
Affinity DataIC50:  300nMAssay Description:Inhibition of [3H]E2 binding to estrogen receptor alpha in MCF-7 cell lysateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target7-dehydrocholesterol reductase(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM22984((8S,10S)-10-{[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-me...)
Affinity DataIC50:  300nMAssay Description:Growth inhibition of MDA-MB-231 cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50474782(CHEMBL19535)
Affinity DataIC50:  300nMAssay Description:Inhibition of [3H]E2 binding to estrogen receptor alpha in MCF-7 cell lysateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50474785(CHEMBL266185)
Affinity DataIC50:  300nMAssay Description:Inhibition of [3H]E2 binding to estrogen receptor alpha in MCF-7 cell lysateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50410196(CHEMBL2113032)
Affinity DataIC50:  332nMAssay Description:Inhibition of [3H]-Mibolerone binding to human Androgen receptor of PC3/AR Cell LysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50135911(5-[2-(2-{2-[3-(4-Cyano-3-trifluoromethyl-phenyl)-5...)
Affinity DataIC50:  332nMAssay Description:Inhibition of 1.0 nM [3H]mibolerone binding to human androgen receptor of PC3/AR cell lysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50135915(5-{2-[4-(2-{2-[3-(4-Cyano-3-trifluoromethyl-phenyl...)
Affinity DataIC50:  346nMAssay Description:Inhibition of [3H]-Mibolerone binding to human Androgen receptor of PC3/AR Cell LysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50135915(5-{2-[4-(2-{2-[3-(4-Cyano-3-trifluoromethyl-phenyl...)
Affinity DataIC50:  346nMAssay Description:Inhibition of 1.0 nM [3H]mibolerone binding to human androgen receptor of PC3/AR cell lysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50135909(5-[2-(4-{4-[3-(4-Cyano-3-trifluoromethyl-phenyl)-5...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibition of [3H]-Mibolerone binding to human Androgen receptor of PC3/AR Cell LysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50056900(2-Carbamoylphenol | 2-Carboxamidophenol | 2-Hydrox...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibition of 1.0 nM [3H]mibolerone binding to human androgen receptor of PC3/AR cell lysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50135909(5-[2-(4-{4-[3-(4-Cyano-3-trifluoromethyl-phenyl)-5...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibition of 1.0 nM [3H]mibolerone binding to human androgen receptor of PC3/AR cell lysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target7-dehydrocholesterol reductase(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM50411319(CHEMBL266892)
Affinity DataIC50:  2.00E+3nMAssay Description:Growth inhibition of multidrug resistant MCF7/Adr cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM20607((2-{4-[(1Z)-1,2-diphenylbut-1-en-1-yl]phenoxy}ethy...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of [3H]E2 binding to estrogen receptor alpha in MCF-7 cell lysateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target7-dehydrocholesterol reductase(Homo sapiens (Human))
University Of Colorado

Curated by ChEMBL
LigandPNGBDBM22984((8S,10S)-10-{[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-me...)
Affinity DataIC50:  1.00E+4nMAssay Description:Growth inhibition of multidrug resistant MCF7/Adr cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed