Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataKi: 2.70nMAssay Description:Inhibition constant against recombinant Steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataKi: 5.80nMAssay Description:Inhibition constant against recombinant Steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataKi: 9nMAssay Description:Compound was evaluated for the inhibition of human Steroid 5-alpha-reductase type 1More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataKi: 260nMAssay Description:Compound was evaluated for the inhibition of human Steroid 5-alpha-reductase type 2More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataKi: 366nMAssay Description:Inhibitory activity against recombinant Steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataKi: 920nMAssay Description:Compound was evaluated for the inhibition of human Steroid 5-alpha-reductase type 1More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataKi: >1.00E+3nMAssay Description:Compound was evaluated for the inhibition of human Steroid 5-alpha-reductase type 2More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataKi: 1.20E+3nMAssay Description:Compound was evaluated for the inhibition of human Steroid 5-alpha-reductase type 1More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataKi: 2.00E+4nMAssay Description:Compound was evaluated for the inhibition of human Steroid 5-alpha-reductase type 2More data for this Ligand-Target Pair
Affinity DataIC50: 0.400nMAssay Description:Binding affinity to integrin alphav/beta3 heterodimer in human M21 cells assessed as inhibition of integrin-mediated human M21 cell adhesion to vitro...More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 0.5nMAssay Description:Inhibition of human Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 1.20nMAssay Description:Compound was evaluated for the inhibition of human Steroid 5-alpha-reductase type 2 receptor from human prostate homogenatesMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 2.20nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate compared with finasteride in experiment 1More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 2.20nMAssay Description:Inhibitory activity against steroid 5-alpha-reductase type 2 in human prostate homogenatesMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 2.30nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type I in human scalp homogenatesMore data for this Ligand-Target Pair
Affinity DataIC50: 2.40nMAssay Description:Binding affinity to integrin alphav/beta3 heterodimer in human M21 cells assessed as inhibition of integrin-mediated human M21 cell adhesion to vitro...More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 2.40nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 2.70nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 2.90nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 3nMAssay Description:Inhibitory activity against 5-alpha Reductase-2 on human prostate homogenates from surgically derived benign hyperplastic tissueMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 3nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 3.5nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 4.10nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 4.30nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate compared with finasteride in experiment 3More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 5.5nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 5.70nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate compared with finasteride in experiment 2More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 5.80nMAssay Description:Inhibitory concentration against human recombinant steroid 5-alpha-reductase type I in stably transfected chinese hamster ovary (CHO) 1827 cells usin...More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 6.10nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 6.10nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 7.30nMAssay Description:Tested against 5 alpha R-2 on human prostate homogenate from surgically derived benign hyperplastic tissue in experiment 2More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 7.60nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 8nMAssay Description:Inhibition of human Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 8.10nMAssay Description:Inhibitory concentration against human recombinant steroid 5-alpha-reductase type I in stably transfected chinese hamster ovary (CHO) 1827 cells usin...More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 8.5nMAssay Description:Inhibition of recombinant Steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 8.75nMAssay Description:Inhibitory concentration against human recombinant steroid 5-alpha-reductase type I in stably transfected chinese hamster ovary (CHO) 1827 cells usin...More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 10nMAssay Description:Tested against 5 alpha R-2 on human prostate homogenate from surgically derived benign hyperplastic tissue in experiment 1More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 14nMAssay Description:Inhibition of human Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 14nMAssay Description:Inhibitory concentration against human recombinant steroid 5-alpha-reductase type I in stably transfected chinese hamster ovary (CHO) 1827 cells usin...More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 14.2nMAssay Description:Inhibitory concentration against human recombinant steroid 5-alpha-reductase type I in stably transfected chinese hamster ovary (CHO) 1827 cells usin...More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 14.4nMAssay Description:Inhibition of recombinant Steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 15nMAssay Description:Binding affinity to integrin alpha5/beta1 heterodimer in human K562 cells assessed as inhibition of integrin-mediated human K562 cell adhesion to fib...More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 15.6nMAssay Description:Inhibition of recombinant Steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 15.8nMAssay Description:Inhibition of recombinant Steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 20nMAssay Description:Inhibitory concentration against human recombinant steroid 5-alpha-reductase type I in stably transfected chinese hamster ovary (CHO) 1827 cells usin...More data for this Ligand-Target Pair
Affinity DataIC50: 20nMAssay Description:Binding affinity to integrin alphav/beta3 heterodimer (unknown origin) assessed as inhibition of integrin-mediated cell adhesion to vitronectinMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 20nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 21nMAssay Description:Inhibitory concentration against human recombinant steroid 5-alpha-reductase type 2 in stably transfected chinese hamster ovary 1827 cells using [3H]...More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 21.6nMAssay Description:Inhibitory concentration against human recombinant steroid 5-alpha-reductase type I in stably transfected chinese hamster ovary (CHO) 1827 cells usin...More data for this Ligand-Target Pair
Affinity DataIC50: 26nMAssay Description:Binding affinity to integrin alpha5/beta1 heterodimer in human K562 cells assessed as inhibition of integrin-mediated human K562 cell adhesion to fib...More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze
Curated by ChEMBL
Universit£ di Firenze
Curated by ChEMBL
Affinity DataIC50: 30nMAssay Description:Inhibition of human Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
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