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Found 153 with Last Name = 'woster' and Initial = 'pm'
TargetPlasmepsin II(Plasmodium falciparum)
Wayne State University

Curated by ChEMBL
LigandPNGBDBM7977((3S,4S)-5-[(4-bromophenyl)methoxy]-N-[(1S)-1-{[(1S...)
Affinity DataKi:  0.5nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin 2More data for this Ligand-Target Pair
TargetPlasmepsin II(Plasmodium falciparum)
Wayne State University

Curated by ChEMBL
LigandPNGBDBM7974((3S,4S)-N-[(1S)-1-{[(1S)-1-carbamoyl-3-methylbutyl...)
Affinity DataKi:  0.560nMAssay Description:Inhibition of Plasmodium falciparum recombinant plasmepsin 2 expressed in Escherichia coli BL21 (DE3)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Medical University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50346873(CHEMBL1797652)
Affinity DataKi:  4.40nMAssay Description:Inhibition of recombinant LSD1 (178 to 831) (unknown origin) expressed in baculovirus infected insect Sf9 cells using diMeK4H3-21 as substrate by per...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Medical University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50446141(CHEMBL3108901)
Affinity DataKi:  5nMAssay Description:Inhibition of human recombinant LSD1 using di-methylated H3-K4 peptide as substrate assessed as release of H2O2 preincubated for 15 mins followed by ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Medical University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM101302(CHEMBL3108900 | US8524717, 57)
Affinity DataKi:  9nMAssay Description:Inhibition of human recombinant LSD1 using di-methylated H3-K4 peptide as substrate assessed as release of H2O2 preincubated for 15 mins followed by ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasmepsin II(Plasmodium falciparum)
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50316596(CHEMBL1098668 | N-((S)-1-((2S,3S)-5-((R)-1-((S)-1-...)
Affinity DataKi:  35.7nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin 2 expressed in Escherichia coli BL21 (DE3) after 40 mins by Kitz-Wilson plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Medical University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50346870(CHEMBL1797647)
Affinity DataKi:  40nMAssay Description:Inhibition of recombinant human LSD1 expressed in Escherichia coli using methylated H3-K4 peptide as substrate by peroxidase-coupled assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetREST corepressor 1(Homo sapiens (Human))
Medical University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50458057(CHEMBL4210908)
Affinity DataKi:  40nMAssay Description:Inhibition of LSD1/CoREST (unknown origin)More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A/REST corepressor 1 [4-485](Homo sapiens (Human))
Medical University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50346870(CHEMBL1797647)
Affinity DataKi:  50nMAssay Description:Inhibition of recombinant human LSD1/CoREST complex expressed in Escherichia coli using methylated H3-K4 peptide as substrate by peroxidase-coupled a...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Medical University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50346875(CHEMBL1797648)
Affinity DataKi:  107nMAssay Description:Inhibition of recombinant LSD1 (178 to 831) (unknown origin) expressed in baculovirus infected insect Sf9 cells using diMeK4H3-21 as substrate by per...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Medical University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50446142(CHEMBL3108892)
Affinity DataKi:  120nMAssay Description:Inhibition of recombinant LSD1 (unknown origin) using di-methylated H3-K4 peptide as substrate incubated for 5 mins prior to substrate addition by fl...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasmepsin II(Plasmodium falciparum)
Wayne State University

Curated by ChEMBL
LigandPNGBDBM8027((2S)-N-[(2S,3S)-4-{[(1S)-1-carbamoyl-2-[4-(4-methy...)
Affinity DataKi:  121nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasmepsin II(Plasmodium falciparum)
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50316598(CHEMBL1098670 | N-((S)-1-((2S,3S)-5-((S)-1-((S)-1-...)
Affinity DataKi:  333nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin 2 expressed in Escherichia coli BL21 (DE3) after 40 mins by Kitz-Wilson plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasmepsin II(Plasmodium falciparum)
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50119879((S)-N-((4S,6S,7S)-7-(2-(2,6-dimethylphenoxy)acetam...)
Affinity DataKi:  357nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Medical University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50446143(CHEMBL3108897)
Affinity DataKi:  385nMAssay Description:Competitive inhibition of recombinant LSD1 (unknown origin) using H3K4Me2 peptide as substrate preincubated for 30 mins followed by substrate additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-adenosylmethionine decarboxylase proenzyme(Rattus norvegicus)
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50369827(CHEMBL611536)
Affinity DataKi:  560nMAssay Description:Inhibition of rat liver form of S-adenosyl-methionine decarboxylase enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50046201((2E)-2-((2E)-2-{[(E)-amino(imino)methyl]hydrazono}...)
Affinity DataKi: >1.00E+3nMAssay Description:Inhibition of rat liver form of S-adenosyl-methionine decarboxylase enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Medical University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50346869(CHEMBL1797646)
Affinity DataKi:  1.80E+3nMAssay Description:Competitive inhibition of recombinant LSD1 (unknown origin) expressed in Escherichia coli BL21 (DE3) cells using H3K4 peptide as substrate by Dixon p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Medical University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50464671(CHEMBL3621615)
Affinity DataKi:  2.20E+3nMAssay Description:Competitive inhibition of LSD1 (unknown origin) incubated for 30 mins using H3K4me2 substrate by fluorescence based assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Medical University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50065386(CHEMBL3401327)
Affinity DataKi:  2.40E+3nMAssay Description:Competitive inhibition of human recombinant LSD1 by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50403124(CHEMBL2115571)
Affinity DataKi:  3.80E+3nMAssay Description:Compound was evaluated to inactivate the bacterial AdoMet-DC; value ranges from 3.8 to 39.6 uMMore data for this Ligand-Target Pair
In DepthDetails Article
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50281293(2-amino-5-({[(2S,3S,4R)-5-(6-amino-9H-purin-9-yl)-...)
Affinity DataKi:  7.20E+3nMAssay Description:Compound was evaluated to inactivate the human AdoMet-DCMore data for this Ligand-Target Pair
In DepthDetails Article
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50403124(CHEMBL2115571)
Affinity DataKi:  1.07E+4nMAssay Description:Compound was evaluated to inactivate the bacterial AdoMet-DC; value ranges from 3.8 to 39.6 uMMore data for this Ligand-Target Pair
In DepthDetails Article
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50403124(CHEMBL2115571)
Affinity DataKi:  1.07E+4nMAssay Description:Compound was evaluated to inactivate the human AdoMet-DC; value ranges from 10.7 to 62.7 uMMore data for this Ligand-Target Pair
In DepthDetails Article
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Medical University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50318565(CHEMBL1086217)
Affinity DataKi:  1.66E+4nMAssay Description:Time-dependent inhibition of recombinant LSD1 catalytic domain (178 to 831 amino acids) (unknown origin) expressed in baculovirus infected insect Sf9...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Medical University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50318565(CHEMBL1086217)
Affinity DataKi:  1.66E+4nMAssay Description:Inhibition of LSD1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50366321(CHEMBL3392203 | CHEMBL606101)
Affinity DataKi:  1.80E+4nMAssay Description:Tested for irreversible inhibitory activity against AdoMet-DC (S-adenosyl-methionine decarboxylase-) isolated from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails Article
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50034925(CHEMBL299398 | O-{(1S,4S)-4-[6-(6-Amino-purin-9-yl...)
Affinity DataKi:  2.12E+4nMAssay Description:compound was evaluated for the inhibitor constant against Escherichia coli S-adenosyl-L-methionine decarboxylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50368997(CHEMBL1791422)
Affinity DataKi:  2.12E+4nMAssay Description:compound was evaluated for the inhibitor constant against human S-adenosyl-L-methionine decarboxylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50034925(CHEMBL299398 | O-{(1S,4S)-4-[6-(6-Amino-purin-9-yl...)
Affinity DataKi:  2.12E+4nMAssay Description:compound was evaluated for the inhibitor constant against Escherichia coli S-adenosyl-L-methionine decarboxylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50368997(CHEMBL1791422)
Affinity DataKi:  2.15E+4nMAssay Description:compound was evaluated for the inhibitor constant against Escherichia coli S-adenosyl-L-methionine decarboxylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50368996(CHEMBL1791421)
Affinity DataKi:  2.37E+4nMAssay Description:Compound was evaluated for the inhibitor constant against Escherichia coli S-adenosyl-L-methionine decarboxylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50368996(CHEMBL1791421)
Affinity DataKi:  2.37E+4nMAssay Description:Compound was evaluated for the inhibitor constant against Escherichia coli S-adenosyl-L-methionine decarboxylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50281292(2-amino-4-({[(2S,3S,4R)-5-(6-amino-9H-purin-9-yl)-...)
Affinity DataKi:  3.11E+4nMAssay Description:Compound was evaluated to inactivate the bacterial AdoMet-DCMore data for this Ligand-Target Pair
In DepthDetails Article
TargetDiamine acetyltransferase 1(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50095444(CHEMBL315330 | Methyl-phosphonic acid mono-{3-[3-(...)
Affinity DataKi:  5.00E+4nMAssay Description:Inhibitory activity against human SSATMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50034927(CHEMBL48973 | O-{(1R,4R)-4-[6-(6-Amino-purin-9-yl)...)
Affinity DataKi:  9.52E+4nMAssay Description:compound was evaluated for the inhibitory constant against human S-adenosyl-L-methionine decarboxylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50034927(CHEMBL48973 | O-{(1R,4R)-4-[6-(6-Amino-purin-9-yl)...)
Affinity DataKi:  9.52E+4nMAssay Description:compound was evaluated for the inhibitory constant against human S-adenosyl-L-methionine decarboxylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50281292(2-amino-4-({[(2S,3S,4R)-5-(6-amino-9H-purin-9-yl)-...)
Affinity DataKi:  2.47E+5nMAssay Description:Compound was evaluated to inactivate the human AdoMet-DCMore data for this Ligand-Target Pair
In DepthDetails Article
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50366318(CHEMBL3392208 | CHEMBL605698)
Affinity DataKi:  4.15E+5nMAssay Description:Tested for irreversible inhibitory activity against AdoMet-DC (S-adenosyl-methionine decarboxylase-) isolated from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails Article
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50366320(CHEMBL3392206 | CHEMBL605899)
Affinity DataKi:  4.78E+5nMAssay Description:Tested for irreversible inhibitory activity against AdoMet-DC (S-adenosyl-methionine decarboxylase-) isolated from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails Article
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50366317(CHEMBL3392204 | CHEMBL606102)
Affinity DataKi:  6.69E+5nMAssay Description:Tested for irreversible inhibitory activity against AdoMet-DC (S-adenosyl-methionine decarboxylase-) isolated from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails Article
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50366316(CHEMBL3392209 | CHEMBL605267)
Affinity DataKi:  9.60E+5nMAssay Description:Tested for irreversible inhibitory activity against AdoMet-DC (S-adenosyl-methionine decarboxylase-) isolated from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails Article
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50366319(CHEMBL1791405 | CHEMBL3392205)
Affinity DataKi:  1.07E+6nMAssay Description:Tested for irreversible inhibitory activity against AdoMet-DC (S-adenosyl-methionine decarboxylase-) isolated from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails Article
TargetS-adenosylmethionine decarboxylase proenzyme(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50366319(CHEMBL1791405 | CHEMBL3392205)
Affinity DataKi:  1.07E+6nMAssay Description:Tested for irreversible inhibitory activity against AdoMet-DC (S-adenosyl-methionine decarboxylase-) isolated from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails Article
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50119879((S)-N-((4S,6S,7S)-7-(2-(2,6-dimethylphenoxy)acetam...)
Affinity DataIC50:  2.10nMAssay Description:Inhibition of HIV-1 NL4-3 wild type protease expressed in Escherichia coli preincubated for 20 mins by FRET analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50180655(A-157378-0 | A-157378.0 | ABT-378 | CHEBI:31781 | ...)
Affinity DataIC50:  2.5nMAssay Description:Inhibition of HIV-1 NL4-3 wild type protease expressed in Escherichia coli preincubated for 20 mins by FRET analysisMore data for this Ligand-Target Pair
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50494545(CHEMBL3093183)
Affinity DataIC50:  2.60nMAssay Description:Inhibition of HIV-1 NL4-3 wild type protease expressed in Escherichia coli preincubated for 20 mins by FRET analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Medical University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  14nMAssay Description:Inhibition of human recombinant HDAC1 by microplate reader assayMore data for this Ligand-Target Pair
TargetSpermine synthase(Homo sapiens (Human))
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50095449(2-[1-(2-Amino-ethyl)-6-(3-amino-propylamino)-hexyl...)
Affinity DataIC50:  20nMAssay Description:Inhibitory activity against spermine synthaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasmepsin II(Plasmodium falciparum)
Wayne State University

Curated by ChEMBL
LigandPNGBDBM50316597(CHEMBL1098671 | N-((S)-1-((2S,3S)-3-hydroxy-5-oxo-...)
Affinity DataIC50:  22nMAssay Description:Competitive inhibition of Plasmodium falciparum plasmepsin 2 expressed in Escherichia coli BL21 (DE3) after 30 mins by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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