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Found 64 with Last Name = 'scarpi' and Initial = 'd'
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092485(4-methyl-8-chloro-1,2,5,6-tetrahydro pyrido[1,2-a]...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092492(4,8-Dimethyl-1,2,5,6-tetrahydro-pyrido[1,2-a]quino...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50057499((R)-8-Chloro-4,10b-dimethyl-1,4,4a,5,6,10b-hexahyd...)
Affinity DataKi:  9nMAssay Description:Compound was evaluated for the inhibition of human Steroid 5-alpha-reductase type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50057501((S)-7-Chloro-4a-methyl-3,4,4a,9-tetrahydro-phenant...)
Affinity DataKi:  260nMAssay Description:Compound was evaluated for the inhibition of human Steroid 5-alpha-reductase type 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50334788((17beta-(N-tert-butylcarbamoyl)-4-aza-5alpha-andro...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50072190((R)-8-Chloro-4,10b-dimethyl-1,5,6,10b-tetrahydro-2...)
Affinity DataKi:  920nMAssay Description:Compound was evaluated for the inhibition of human Steroid 5-alpha-reductase type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50057499((R)-8-Chloro-4,10b-dimethyl-1,4,4a,5,6,10b-hexahyd...)
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
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50057501((S)-7-Chloro-4a-methyl-3,4,4a,9-tetrahydro-phenant...)
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
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50072190((R)-8-Chloro-4,10b-dimethyl-1,5,6,10b-tetrahydro-2...)
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
In DepthDetails ArticlePubMed
TargetIntegrin alpha-V/beta-3(Homo sapiens (Human))
University Of Florence

Curated by ChEMBL
LigandPNGBDBM50235980(2-((2S,5R,8S,11S)-5-benzyl-11-(3-guanidinopropyl)-...)
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
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50032771((4aR,6aR,10S)-7-(1,5-Dimethyl-hexyl)-1,4a,6a,10-te...)
Affinity DataIC50:  0.5nMAssay Description:Inhibition of human Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50334788((17beta-(N-tert-butylcarbamoyl)-4-aza-5alpha-andro...)
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
In DepthDetails ArticlePubMedDrugBank

Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50334788((17beta-(N-tert-butylcarbamoyl)-4-aza-5alpha-andro...)
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 ArticlePubMedDrugBank

Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50368782(Bexlosteride | CHEMBL24955 | LY-191704)
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 ArticlePubMed
TargetIntegrin alpha-V/beta-3(Homo sapiens (Human))
University Of Florence

Curated by ChEMBL
LigandPNGBDBM50140178(CHEMBL3754350)
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
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092485(4-methyl-8-chloro-1,2,5,6-tetrahydro pyrido[1,2-a]...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50032762((4aR,10bR)-8-Chloro-4-methyl-1,4,4a,5,6,10b-hexahy...)
Affinity DataIC50:  8nMAssay Description:Inhibition of human Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092506(4,6-dimethyl-8-chloro-1,2,5,6-tetrahydro pyrido[1,...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50085567((R)-8-Chloro-6-methyl-1,2,5,6-tetrahydro-pyrido[1,...)
Affinity DataIC50:  14nMAssay Description:Inhibition of human Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092489(6-methyl-8-chloro-1,2,5,6-tetrahydro pyrido[1,2-a]...)
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 ArticlePubMed
TargetIntegrin alpha-5/beta-1(Homo sapiens (Human))
University Of Florence

Curated by ChEMBL
LigandPNGBDBM50140179(CHEMBL3753748)
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
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092500(4,5-dimethyl-8-chloro-1,2,5,6-tetrahydro pyrido[1,...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092503(4,6-dimethyl-8-methyl-1,2,5,6-tetrahydro pyrido[1,...)
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 ArticlePubMed
TargetIntegrin alpha-V/beta-3(Homo sapiens (Human))
University Of Florence

Curated by ChEMBL
LigandPNGBDBM50140177(CHEMBL3752070)
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
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092492(4,8-Dimethyl-1,2,5,6-tetrahydro-pyrido[1,2-a]quino...)
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 ArticlePubMed
TargetIntegrin alpha-5/beta-1(Homo sapiens (Human))
University Of Florence

Curated by ChEMBL
LigandPNGBDBM50140178(CHEMBL3754350)
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
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50044881(8-Chloro-4-methyl-1,4,5,6-tetrahydro-2H-benzo[f]qu...)
Affinity DataIC50:  30nMAssay Description:Inhibition of human Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin alpha-V/beta-3(Homo sapiens (Human))
University Of Florence

Curated by ChEMBL
LigandPNGBDBM50140179(CHEMBL3753748)
Affinity DataIC50:  34nMAssay 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
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092492(4,8-Dimethyl-1,2,5,6-tetrahydro-pyrido[1,2-a]quino...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092485(4-methyl-8-chloro-1,2,5,6-tetrahydro pyrido[1,2-a]...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50085564(8-Chloro-1,2,5,6-tetrahydro-pyrido[1,2-a]quinolin-...)
Affinity DataIC50:  49nMAssay Description:Inhibition of human Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50085564(8-Chloro-1,2,5,6-tetrahydro-pyrido[1,2-a]quinolin-...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50072189((7aS,8R)-7a-Methyl-2-oxo-2,3,4,7,7a,8,9,10,10a,10b...)
Affinity DataIC50:  122nMAssay Description:Compound was evaluated for the inhibition of human Steroid 5-alpha-reductase type 2 receptor from human prostate homogenates.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50072189((7aS,8R)-7a-Methyl-2-oxo-2,3,4,7,7a,8,9,10,10a,10b...)
Affinity DataIC50:  127nMAssay Description:Compound was evaluated for the inhibition of human Steroid 5-alpha-reductase type 1 from recombinant CHO cells; No inhibition up to 10 uM concentrati...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092494(4-(alpha)methyl-8-methyl-3,4,5,6-Tetrahydrobenzo[c...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092487(4-(alpha)methyl-8-chloro-3,4,5,6-Tetrahydrobenzo[c...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50032771((4aR,6aR,10S)-7-(1,5-Dimethyl-hexyl)-1,4a,6a,10-te...)
Affinity DataIC50:  154nMAssay Description:Compound was tested for inhibition against human Steroid 5-alpha-reductase type 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092504(8-methyl-3,4,5,6-Tetrahydrobenzo[c]quinolizin-3-(4...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092502(4-Methyl-1,2,5,6-tetrahydro-pyrido[1,2-a]quinolin-...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092491(6-(alpha)methyl-8-chloro-3,4,5,6-Tetrahydrobenzo[c...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50085563((4aS,6R)-8-Chloro-6-methyl-4,4a,5,6-tetrahydro-pyr...)
Affinity DataIC50:  188nMAssay Description:Inhibition of human Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092498(1-methyl-8-chloro-1,2,5,6-tetrahydro pyrido[1,2-a]...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50072191(1,2,5,6-Tetrahydro-pyrido[1,2-a]quinolin-3-one | 1...)
Affinity DataIC50:  298nMAssay Description:Inhibition of human Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50072191(1,2,5,6-Tetrahydro-pyrido[1,2-a]quinolin-3-one | 1...)
Affinity DataIC50:  298nMAssay Description:Compound was evaluated for the inhibition of human Steroid 5-alpha-reductase type 1 from recombinant CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50072191(1,2,5,6-Tetrahydro-pyrido[1,2-a]quinolin-3-one | 1...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092488(4-(beta)methyl-8-methyl-3,4,5,6-Tetrahydrobenzo[c]...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50085565((S)-8-Chloro-5-methyl-1,2,5,6-tetrahydro-pyrido[1,...)
Affinity DataIC50:  346nMAssay Description:Inhibition of human Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092497(8-Methyl-1,2,5,6-tetrahydro-pyrido[1,2-a]quinolin-...)
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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50085562((S)-8-Chloro-4,4a,5,6-tetrahydro-pyrido[1,2-a]quin...)
Affinity DataIC50:  459nMAssay Description:Inhibition of human Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50092495(8-chloro-3,4,5,6-Tetrahydrobenzo[c]quinolizin-3-(4...)
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 ArticlePubMed
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