Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataKd: 1nMAssay Description:Binding affinity towards antiestrogen binding site AEBSMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 0.100nMAssay Description:Inhibition of DHCR7 (unknown origin)More data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 2.30nMAssay Description:Inhibition of 7-dehydroxycholesterol reductase-mediated cholesterol biosynthesis in human HL60 cells assessed as inhibition of 2-[13C]acetate after 2...More data for this Ligand-Target Pair
Target3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase/7-dehydrocholesterol reductase(Human)
University of Georgia
Curated by ChEMBL
University of Georgia
Curated by ChEMBL
Affinity DataIC50: 12nMAssay Description:Displacement of [3H]tamoxifen from antiestrogen binding site (AEBS)More data for this Ligand-Target Pair
Target3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase/7-dehydrocholesterol reductase(Human)
University of Georgia
Curated by ChEMBL
University of Georgia
Curated by ChEMBL
Affinity DataIC50: 22nMAssay Description:Displacement of [3H]tamoxifen from antiestrogen binding site (AEBS)More data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 30nMAssay Description:Inhibition of DHCR7 (unknown origin)More data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 30nMAssay Description:Growth inhibition of MDA-MB-231 cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 30nMAssay Description:Growth inhibition of MCF7 cells expressing ER and antiestrogen binding sitesMore data for this Ligand-Target Pair
Target3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase/7-dehydrocholesterol reductase(Human)
University of Georgia
Curated by ChEMBL
University of Georgia
Curated by ChEMBL
Affinity DataIC50: 32nMAssay Description:Displacement of [3H]tamoxifen from antiestrogen binding site (AEBS)More data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 40nMAssay Description:Growth inhibition of MDA-MB-435 cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 50nMAssay Description:Growth inhibition of MDA-MB-435 cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 60nMAssay Description:Growth inhibition of multidrug resistant MCF7/Adr cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 70nMAssay Description:Growth inhibition of MCF7 cells expressing ER and antiestrogen binding sitesMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 80nMAssay Description:Growth inhibition of MDA-MB-231 cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 120nMAssay Description:Inhibition of 7-dehydroxycholesterol reductase-mediated cholesterol biosynthesis in human HL60 cells assessed as inhibition of 2-[13C]acetate after 2...More data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 150nMAssay Description:Growth inhibition of MDA-MB-435 cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 200nMAssay Description:Growth inhibition of MCF7 cells expressing ER and antiestrogen binding sitesMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 300nMAssay Description:Growth inhibition of MDA-MB-231 cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 400nMAssay Description:Displacement of [3H]tamoxifen from antiestrogen binding site in Sprague-Dawley rat liver by liquid scintillation countingMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 500nMAssay Description:Inhibition of 7-dehydroxycholesterol reductase-mediated cholesterol biosynthesis in human HL60 cells assessed as inhibition of 2-[13C]acetate after 2...More data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 600nMAssay Description:Displacement of [3H]tamoxifen from antiestrogen binding site in Sprague-Dawley rat liver by liquid scintillation countingMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 600nMAssay Description:Displacement of [3H]tamoxifen from antiestrogen binding site in Sprague-Dawley rat liver by liquid scintillation countingMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 1.07E+3nMAssay Description:Inhibition of DHCR7 (unknown origin)More data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 1.39E+3nMAssay Description:Inhibition of DHCR7 (unknown origin)More data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 2.00E+3nMAssay Description:Growth inhibition of multidrug resistant MCF7/Adr cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 2.04E+3nMAssay Description:Inhibition of DHCR7 (unknown origin)More data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 2.80E+3nMAssay Description:Displacement of [3H]tamoxifen from antiestrogen binding site in Sprague-Dawley rat liver by liquid scintillation countingMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 3.50E+3nMAssay Description:Displacement of [3H]tamoxifen from antiestrogen binding site in Sprague-Dawley rat liver by liquid scintillation countingMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 6.80E+3nMAssay Description:Displacement of [3H]tamoxifen from antiestrogen binding site in Sprague-Dawley rat liver by liquid scintillation countingMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 7.30E+3nMAssay Description:Inhibition of 7-dehydroxycholesterol reductase-mediated cholesterol biosynthesis in human HL60 cells assessed as inhibition of 2-[13C]acetate after 2...More data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 7.40E+3nMAssay Description:Displacement of [3H]tamoxifen from antiestrogen binding site in Sprague-Dawley rat liver by liquid scintillation countingMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 8.00E+3nMAssay Description:Displacement of [3H]tamoxifen from antiestrogen binding site in Sprague-Dawley rat liver by liquid scintillation countingMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 1.00E+4nMAssay Description:Growth inhibition of multidrug resistant MCF7/Adr cells containing antiestrogen binding sitesMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 2.00E+4nMAssay Description:Displacement of [3H]tamoxifen from antiestrogen binding site in Sprague-Dawley rat liver by liquid scintillation countingMore data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of DHCR7 (unknown origin)More data for this Ligand-Target Pair
Target7-dehydrocholesterol reductase(Human)
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
The Feinberg School of Medicine of Northwestern University
Curated by ChEMBL
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of DHCR7 (unknown origin)More data for this Ligand-Target Pair
