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Found 61 with Last Name = 'wnuk' and Initial = 'sf'
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50051435(5'-Dehydroadenosine | 5'-deoxy-5'-oxoadenosine | 9...)
Affinity DataKi:  39nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50051435(5'-Dehydroadenosine | 5'-deoxy-5'-oxoadenosine | 9...)
Affinity DataKi:  39nMAssay Description:concentration dependent inhibition of S-Adenosyl-homocysteine hydrolase was determined by Kitz and Wilson methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Rattus norvegicus)
University Of Kansas

Curated by ChEMBL
LigandPNGBDBM50046747(2-(6-Amino-purin-9-yl)-5-fluoromethylene-tetrahydr...)
Affinity DataKi:  39nMAssay Description:Inhibitory activity against recombinant rat liver S-adenosyl-homocysteine hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Rattus norvegicus)
University Of Kansas

Curated by ChEMBL
LigandPNGBDBM50051436((2R,3S,4R,5R)-5-(6-Amino-purin-9-yl)-3,4-dihydroxy...)
Affinity DataKi:  39nMAssay Description:Inhibitory activity against recombinant rat liver S-adenosyl-homocysteine hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Rattus norvegicus)
University Of Kansas

Curated by ChEMBL
LigandPNGBDBM50046748(2-(6-Amino-purin-9-yl)-5-fluoromethylene-tetrahydr...)
Affinity DataKi:  40nMAssay Description:Inhibitory activity against recombinant rat liver S-adenosyl-homocysteine hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50051436((2R,3S,4R,5R)-5-(6-Amino-purin-9-yl)-3,4-dihydroxy...)
Affinity DataKi:  43nMAssay Description:concentration dependent inhibition of S-Adenosyl-homocysteine hydrolase was determined by Kitz and Wilson methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Rattus norvegicus)
University Of Kansas

Curated by ChEMBL
LigandPNGBDBM50051435(5'-Dehydroadenosine | 5'-deoxy-5'-oxoadenosine | 9...)
Affinity DataKi:  43nMAssay Description:Inhibitory activity against recombinant rat liver S-adenosyl-homocysteine hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369258(CHEMBL606276)
Affinity DataKi:  95nMAssay Description:concentration dependent inhibition of S-Adenosyl-homocysteine hydrolase was determined by Kitz and Wilson methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50368896(CHEMBL608056)
Affinity DataKi:  96nMAssay Description:Tested for kinetic constant for the inhibition of recombinant human placental S-Adenosyl-L-homocysteine HydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369257(CHEMBL605902)
Affinity DataKi:  101nMAssay Description:concentration dependent inhibition of S-Adenosyl-homocysteine hydrolase was determined by Kitz and Wilson methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50407233(CHEMBL2092790)
Affinity DataKi:  110nMAssay Description:Tested for kinetic constant for the inhibition of recombinant human placental S-Adenosyl-L-homocysteine HydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369255(CHEMBL605900)
Affinity DataKi:  111nMAssay Description:concentration dependent inhibition of S-Adenosyl-homocysteine hydrolase was determined by Kitz and Wilson methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50407232(CHEMBL2092789)
Affinity DataKi:  134nMAssay Description:Tested for kinetic constant for the inhibition of recombinant human placental S-Adenosyl-L-homocysteine HydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50408149(CHEMBL2093112)
Affinity DataKi:  224nMAssay Description:concentration dependent inhibition of S-Adenosyl-homocysteine hydrolase was determined by Kitz and Wilson methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369159(CHEMBL610148)
Affinity DataKi:  320nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369158(CHEMBL612224)
Affinity DataKi:  360nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50331791((2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydr...)
Affinity DataKi:  410nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University

Curated by ChEMBL
LigandPNGBDBM50304165(CHEMBL593446 | S-(5-Deoxy-D-xylofuranos-5-yl)-L-ho...)
Affinity DataKi:  430nMAssay Description:Inhibition of Bacillus subtilis LuxS assessed as enzyme-inhibitor dissociation constantMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50370520(CHEMBL611098)
Affinity DataKi:  550nMAssay Description:Inhibition of recombinant Placental AdenosylhomocysteinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369161(CHEMBL610383)
Affinity DataKi:  570nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369156(CHEMBL608072)
Affinity DataKi:  570nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50408148(CHEMBL1288616)
Affinity DataKi:  670nMAssay Description:concentration dependent inhibition of S-Adenosyl-homocysteine hydrolase was determined by Kitz and Wilson methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50422678(CHEMBL2364569)
Affinity DataKi:  670nMAssay Description:Inhibitory potency against recombinant human placental S-Adenosyl-L-homocysteine HydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50368898(CHEMBL604208)
Affinity DataKi:  681nMAssay Description:Tested for kinetic constant for the inhibition of recombinant human placental S-Adenosyl-L-homocysteine HydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University

Curated by ChEMBL
LigandPNGBDBM50304168((2S)-2-amino-4-(((2S,3S,4S)-3-fluoro-4,5-dihydroxy...)
Affinity DataKi:  700nMAssay Description:Inhibition of Bacillus subtilis LuxS assessed as enzyme-inhibitor dissociation constantMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369162(CHEMBL610384)
Affinity DataKi:  710nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369157(CHEMBL608915)
Affinity DataKi:  770nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369393(CHEMBL608312)
Affinity DataKi:  1.10E+3nMAssay Description:Kinetic constant calculated from the pseudo-first-order rate constant(k app) for S-adenosyl-homocysteine hydrolase inactivationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50368895(CHEMBL610125)
Affinity DataKi:  1.30E+3nMAssay Description:Tested for kinetic constant for the inhibition of recombinant human placental S-Adenosyl-L-homocysteine HydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University

Curated by ChEMBL
LigandPNGBDBM50304169((2S)-2-amino-4-(((2R,3S,4S)-3-bromo-4,5-dihydroxyt...)
Affinity DataKi:  1.40E+3nMAssay Description:Inhibition of Bacillus subtilis LuxS assessed as enzyme-inhibitor dissociation constantMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369160(CHEMBL608025)
Affinity DataKi:  1.70E+3nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369392(CHEMBL608911)
Affinity DataKi:  1.70E+3nMAssay Description:Kinetic constant calculated from the pseudo-first-order rate constant(k app) for S-adenosyl-homocysteine hydrolase inactivationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50407975(CHEMBL519809)
Affinity DataKi:  1.93E+3nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50367376(CHEMBL605866)
Affinity DataKi:  2.60E+3nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University

Curated by ChEMBL
LigandPNGBDBM50304166(CHEMBL593447 | S-(3,5-Dideoxy-3-fluoro-D-xylofuran...)
Affinity DataKi:  2.80E+3nMAssay Description:Inhibition of Bacillus subtilis LuxS assessed as enzyme-inhibitor dissociation constantMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369380(CHEMBL606502)
Affinity DataKi:  3.10E+3nMAssay Description:The kinetic constant for inhibition of S-adenosyl-homocysteine hydrolase by the compoundMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369381(CHEMBL612194)
Affinity DataKi:  3.60E+3nMAssay Description:The kinetic constant for inhibition of S-adenosyl-homocysteine hydrolase by the compoundMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369394(CHEMBL608943)
Affinity DataKi:  3.80E+3nMAssay Description:Kinetic constant calculated from the pseudo-first-order rate constant(k app) for S-adenosyl-homocysteine hydrolase inactivationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369379(CHEMBL607755)
Affinity DataKi:  3.90E+3nMAssay Description:The kinetic constant for inhibition of S-adenosyl-homocysteine hydrolase by the compoundMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University

Curated by ChEMBL
LigandPNGBDBM50304165(CHEMBL593446 | S-(5-Deoxy-D-xylofuranos-5-yl)-L-ho...)
Affinity DataKi:  4.20E+3nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University

Curated by ChEMBL
LigandPNGBDBM50304166(CHEMBL593447 | S-(3,5-Dideoxy-3-fluoro-D-xylofuran...)
Affinity DataKi:  7.70E+3nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University

Curated by ChEMBL
LigandPNGBDBM50304169((2S)-2-amino-4-(((2R,3S,4S)-3-bromo-4,5-dihydroxyt...)
Affinity DataKi:  7.90E+3nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University

Curated by ChEMBL
LigandPNGBDBM50304167(CHEMBL610483 | S-(3,5-Dideoxy-3-fluoro-1-O-methyl-...)
Affinity DataKi:  8.80E+3nMAssay Description:Inhibition of Bacillus subtilis LuxS assessed as enzyme-inhibitor dissociation constantMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50370118(CHEMBL607987)
Affinity DataKi:  1.00E+4nMAssay Description:Inhibitory constant for S-adenosyl-homocysteine hydrolase, was determined using Kitz and Wilson equation {Kobs = Kinact . [I]/(Ki + [I])}.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University

Curated by ChEMBL
LigandPNGBDBM50304168((2S)-2-amino-4-(((2S,3S,4S)-3-fluoro-4,5-dihydroxy...)
Affinity DataKi:  1.06E+4nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50370119(CHEMBL604963)
Affinity DataKi:  1.37E+4nMAssay Description:Inhibitory constant for S-adenosyl-homocysteine hydrolase, was determined using Kitz and Wilson equation {Kobs = Kinact . [I]/(Ki + [I])}.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM50369155(CHEMBL609186)
Affinity DataKi:  1.98E+4nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University

Curated by ChEMBL
LigandPNGBDBM50304167(CHEMBL610483 | S-(3,5-Dideoxy-3-fluoro-1-O-methyl-...)
Affinity DataKi:  4.20E+4nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University

Curated by ChEMBL
LigandPNGBDBM50304164(CHEMBL611818 | S-(5-Deoxy-3-O-methyl-D-ribofuranos...)
Affinity DataKi:  4.20E+4nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Brigham Young University

Curated by ChEMBL
LigandPNGBDBM85777(B-NECA)
Affinity DataKi:  4.34E+4nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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