Compile Data Set for Download or QSAR
Found 85 with Last Name = 'machetti' and Initial = 'f'
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092485(4-methyl-8-chloro-1,2,5,6-tetrahydro pyrido[1,2-a]...)copy SMILEScopy InChI
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
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092492(4,8-Dimethyl-1,2,5,6-tetrahydro-pyrido[1,2-a]quino...)copy SMILEScopy InChI
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
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50334788((17beta-(N-tert-butylcarbamoyl)-4-aza-5alpha-andro...)copy SMILEScopy InChI
Affinity DataKi:  366nMAssay Description:Inhibitory activity against recombinant Steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50334788((17beta-(N-tert-butylcarbamoyl)-4-aza-5alpha-andro...)copy SMILEScopy InChI
Affinity DataIC50: 2.20nMAssay Description:Inhibitory activity against steroid 5-alpha-reductase type 2 in human prostate homogenatesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMedDrugBank
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50369335(CHEMBL1201841)copy SMILEScopy InChI
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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50368782(Bexlosteride | CHEMBL24955 | LY-191704)copy SMILEScopy InChI
Affinity DataIC50: 2.30nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type I in human scalp homogenatesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50057290((5aS,7aS,10aS,10bS)-7a-Methyl-1,5a,6,7,7a,9,10,10a...)copy SMILEScopy InChI
Affinity DataIC50: 2.40nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50057297((5aS,7aS,8S,10aS,10bS)-8-Hydroxy-7a-methyl-3,4,6,7...)copy SMILEScopy InChI
Affinity DataIC50: 2.70nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50057289((5aS,7aS,10aS,10bS,12aS)-7a-Methyl-tetradecahydro-...)copy SMILEScopy InChI
Affinity DataIC50: 2.90nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50369338(CHEMBL1237294)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50334788((17beta-(N-tert-butylcarbamoyl)-4-aza-5alpha-andro...)copy SMILEScopy InChI
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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMedDrugBank
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50057292((5aS,7aS,10aS,10bS)-7a-Methyl-3,4,5a,6,7,7a,9,10,1...)copy SMILEScopy InChI
Affinity DataIC50: 3.5nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50369336(CHEMBL1237306)copy SMILEScopy InChI
Affinity DataIC50: 4.10nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50369335(CHEMBL1201841)copy SMILEScopy InChI
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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50057295((5aS,7aS,8S,10aS,10bS)-7a-Methyl-2-oxo-2,3,4,5a,6,...)copy SMILEScopy InChI
Affinity DataIC50: 5.5nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50369335(CHEMBL1201841)copy SMILEScopy InChI
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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50369337(CHEMBL1794821)copy SMILEScopy InChI
Affinity DataIC50: 6.10nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50369334(CHEMBL1237307)copy SMILEScopy InChI
Affinity DataIC50: 6.10nMAssay Description:Inhibition against 5 alpha R-2 in human prostate homogenate relative to finasterideMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50369335(CHEMBL1201841)copy SMILEScopy InChI
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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092485(4-methyl-8-chloro-1,2,5,6-tetrahydro pyrido[1,2-a]...)copy SMILEScopy InChI
Affinity DataIC50: 7.60nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092506(4,6-dimethyl-8-chloro-1,2,5,6-tetrahydro pyrido[1,...)copy SMILEScopy InChI
Affinity DataIC50: 8.5nMAssay Description:Inhibition of recombinant Steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50369335(CHEMBL1201841)copy SMILEScopy InChI
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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092489(6-methyl-8-chloro-1,2,5,6-tetrahydro pyrido[1,2-a]...)copy SMILEScopy InChI
Affinity DataIC50: 14.4nMAssay Description:Inhibition of recombinant Steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092500(4,5-dimethyl-8-chloro-1,2,5,6-tetrahydro pyrido[1,...)copy SMILEScopy InChI
Affinity DataIC50: 15.6nMAssay Description:Inhibition of recombinant Steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092503(4,6-dimethyl-8-methyl-1,2,5,6-tetrahydro pyrido[1,...)copy SMILEScopy InChI
Affinity DataIC50: 15.8nMAssay Description:Inhibition of recombinant Steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092492(4,8-Dimethyl-1,2,5,6-tetrahydro-pyrido[1,2-a]quino...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50369335(CHEMBL1201841)copy SMILEScopy InChI
Affinity DataIC50: 37nMAssay Description:Inhibitory activity against 5-alpha Reductase-2 on human prostate homogenates from surgically derived benign hyperplastic tissue in experiment 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092485(4-methyl-8-chloro-1,2,5,6-tetrahydro pyrido[1,2-a]...)copy SMILEScopy InChI
Affinity DataIC50: 41nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type I in human scalp homogenatesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092492(4,8-Dimethyl-1,2,5,6-tetrahydro-pyrido[1,2-a]quino...)copy SMILEScopy InChI
Affinity DataIC50: 41nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type I in human scalp homogenatesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50334788((17beta-(N-tert-butylcarbamoyl)-4-aza-5alpha-andro...)copy SMILEScopy InChI
Affinity DataIC50: 42nMAssay Description:Inhibitory activity against human 5-alpha Reductase-1 expressed in DU-145 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMedDrugBank
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50085564(8-Chloro-1,2,5,6-tetrahydro-pyrido[1,2-a]quinolin-...)copy SMILEScopy InChI
Affinity DataIC50: 49nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50369335(CHEMBL1201841)copy SMILEScopy InChI
Affinity DataIC50: 122nMAssay Description:TInhibitory activity against 5-alpha Reductase-2 on human prostate homogenates from surgically derived benign hyperplastic tissue in experiment 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50369335(CHEMBL1201841)copy SMILEScopy InChI
Affinity DataIC50: 127nMAssay Description:Inhibitory activity against human 5-alpha Reductase-1 expressed in DU-145 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092494(4-(alpha)methyl-8-methyl-3,4,5,6-Tetrahydrobenzo[c...)copy SMILEScopy InChI
Affinity DataIC50: 137nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092487(4-(alpha)methyl-8-chloro-3,4,5,6-Tetrahydrobenzo[c...)copy SMILEScopy InChI
Affinity DataIC50: 141nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50369335(CHEMBL1201841)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Tested against 5 alpha R-2 on human prostate homogenate from surgically derived benign hyperplastic tissue in experiment 3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092504(8-methyl-3,4,5,6-Tetrahydrobenzo[c]quinolizin-3-(4...)copy SMILEScopy InChI
Affinity DataIC50: 176nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092502(4-Methyl-1,2,5,6-tetrahydro-pyrido[1,2-a]quinolin-...)copy SMILEScopy InChI
Affinity DataIC50: 185nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092491(6-(alpha)methyl-8-chloro-3,4,5,6-Tetrahydrobenzo[c...)copy SMILEScopy InChI
Affinity DataIC50: 188nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092498(1-methyl-8-chloro-1,2,5,6-tetrahydro pyrido[1,2-a]...)copy SMILEScopy InChI
Affinity DataIC50: 204nMAssay Description:Inhibition of recombinant Steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50369336(CHEMBL1237306)copy SMILEScopy InChI
Affinity DataIC50: 263nMAssay Description:Inhibitory activity against human 5-alpha Reductase-1 expressed in DU-145 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50072191(1,2,5,6-Tetrahydro-pyrido[1,2-a]quinolin-3-one | 1...)copy SMILEScopy InChI
Affinity DataIC50: 298nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50057292((5aS,7aS,10aS,10bS)-7a-Methyl-3,4,5a,6,7,7a,9,10,1...)copy SMILEScopy InChI
Affinity DataIC50: 299nMAssay Description:Inhibitory activity against human 5-alpha Reductase-1 expressed in DU-145 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092488(4-(beta)methyl-8-methyl-3,4,5,6-Tetrahydrobenzo[c]...)copy SMILEScopy InChI
Affinity DataIC50: 312nMAssay Description:Inhibition of recombinant Steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092497(8-Methyl-1,2,5,6-tetrahydro-pyrido[1,2-a]quinolin-...)copy SMILEScopy InChI
Affinity DataIC50: 376nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50057297((5aS,7aS,8S,10aS,10bS)-8-Hydroxy-7a-methyl-3,4,6,7...)copy SMILEScopy InChI
Affinity DataIC50: 409nMAssay Description:Inhibitory activity against human 5-alpha Reductase-1 expressed in DU-145 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092495(8-chloro-3,4,5,6-Tetrahydrobenzo[c]quinolizin-3-(4...)copy SMILEScopy InChI
Affinity DataIC50: 459nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50057295((5aS,7aS,8S,10aS,10bS)-7a-Methyl-2-oxo-2,3,4,5a,6,...)copy SMILEScopy InChI
Affinity DataIC50: 460nMAssay Description:Inhibitory activity against 5-alpha Reductase-2 on human prostate homogenates from surgically derived benign hyperplastic tissueMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50057295((5aS,7aS,8S,10aS,10bS)-7a-Methyl-2-oxo-2,3,4,5a,6,...)copy SMILEScopy InChI
Affinity DataIC50: 1.13E+3nMAssay Description:Inhibitory activity against human 5-alpha Reductase-1 expressed in DU-145 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D21Z8KPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£ di Firenze

Curated by ChEMBL
LigandPNGBDBM50092486(4-Methyl-5,6-dihydro-pyrido[1,2-a]quinolin-3-one |...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of recombinant Steroid 5-alpha-reductase type I expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B036JPubMed
Displayed 1 to 50 (of 85 total ) | Next | Last >>
Jump to: