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Found 131 with Last Name = 'thai' and Initial = 'a'
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379543(CHEMBL2012752)
Affinity DataKi:  0.0400nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379542(CHEMBL2012753)
Affinity DataKi:  0.110nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50340754((S)-2-(4-fluoro-3,5-dimethylbenzyl)-6-(4-fluoroben...)
Affinity DataKi:  0.130nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379536(CHEMBL2012836)
Affinity DataKi:  0.170nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379541(CHEMBL2012832)
Affinity DataKi:  0.230nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50329265((R)-2-(4-fluoro-3,5-dimethylphenylamino)-6-(4-fluo...)
Affinity DataKi:  0.240nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379533(CHEMBL2012838)
Affinity DataKi:  0.270nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379540(CHEMBL2012750)
Affinity DataKi:  0.300nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379535(CHEMBL2010824)
Affinity DataKi:  0.310nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379544(CHEMBL2012751)
Affinity DataKi:  0.490nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50340758((S)-6-(4-fluorobenzylamino)-2-((R)-2-(4-fluorophen...)
Affinity DataKi:  0.580nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379539(CHEMBL2012834)
Affinity DataKi:  0.600nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379534(CHEMBL2012837)
Affinity DataKi:  1nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50340768((R)-2-(4-fluoro-3,5-dimethylphenoxy)-6-(4-fluorobe...)
Affinity DataKi:  1.20nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379538(CHEMBL2012833)
Affinity DataKi:  1.30nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379537(CHEMBL2012835)
Affinity DataKi:  2nMAssay Description:Inhibition of N-terminal 6-histine tagged Bacillus anthracis LF 263-C terminal catalytic domain using MCA-KKVYPYPME-Dap(Dnp)-NH2 as substrate after 4...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452691(CHEMBL4218073)
Affinity DataKi:  300nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452676(CHEMBL4206295)
Affinity DataKi:  700nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452677(CHEMBL4218072)
Affinity DataKi:  2.10E+3nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetMacrophage metalloelastase(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50340758((S)-6-(4-fluorobenzylamino)-2-((R)-2-(4-fluorophen...)
Affinity DataKi:  2.30E+3nMAssay Description:Inhibition of MMP-12 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452684(CHEMBL4217380)
Affinity DataKi:  3.70E+3nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452675(CHEMBL4211713)
Affinity DataKi:  4.60E+3nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452681(CHEMBL4209693)
Affinity DataKi:  9.40E+3nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452678(CHEMBL4211326)
Affinity DataKi:  1.09E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379533(CHEMBL2012838)
Affinity DataKi:  1.10E+4nMAssay Description:Inhibition of MMP-9 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMacrophage metalloelastase(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379533(CHEMBL2012838)
Affinity DataKi:  1.20E+4nMAssay Description:Inhibition of MMP-12 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452682(CHEMBL4210973)
Affinity DataKi:  1.47E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452683(CHEMBL4215512)
Affinity DataKi:  1.65E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50292495(((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihyd...)
Affinity DataKi:  1.84E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBotulinum neurotoxin type A(Clostridium botulinum)
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50433336(CHEMBL2376588)
Affinity DataKi:  2.10E+4nMAssay Description:Inhibition of Clostridium botulinum BoNT/A light chain (1 to 429 amino acid) using Abz-Thr-dArg-Ile-Asp-Glu-Ala-Asn-Gln-Arg-Ala-Thr-Lys-Nle-Lys(Dnp)-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50340758((S)-6-(4-fluorobenzylamino)-2-((R)-2-(4-fluorophen...)
Affinity DataKi:  2.10E+4nMAssay Description:Inhibition of MMP-9 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452693(CHEMBL4202426)
Affinity DataKi:  2.59E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452692(CHEMBL4204554)
Affinity DataKi:  2.76E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetStromelysin-1(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379533(CHEMBL2012838)
Affinity DataKi:  3.10E+4nMAssay Description:Inhibition of MMP-3 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInterstitial collagenase(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50340758((S)-6-(4-fluorobenzylamino)-2-((R)-2-(4-fluorophen...)
Affinity DataKi:  3.30E+4nMAssay Description:Inhibition of MMP-1 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452694(CHEMBL4203961)
Affinity DataKi:  3.48E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452679(CHEMBL4217046)
Affinity DataKi:  3.77E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452686(CHEMBL4217363)
Affinity DataKi:  3.89E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452697(CHEMBL4204818)
Affinity DataKi:  4.22E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetInterstitial collagenase(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379533(CHEMBL2012838)
Affinity DataKi:  4.70E+4nMAssay Description:Inhibition of MMP-1 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Hawaii Biotech

Curated by ChEMBL
LigandPNGBDBM50452689(CHEMBL4217944)
Affinity DataKi:  4.96E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-14(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379533(CHEMBL2012838)
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of MMP-14 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-14(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379534(CHEMBL2012837)
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of MMP-14 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-14(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50340768((R)-2-(4-fluoro-3,5-dimethylphenoxy)-6-(4-fluorobe...)
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of MMP-14 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-14(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379535(CHEMBL2010824)
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of MMP-14 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-14(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50340754((S)-2-(4-fluoro-3,5-dimethylbenzyl)-6-(4-fluoroben...)
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of MMP-14 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-14(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379536(CHEMBL2012836)
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of MMP-14 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-14(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50329265((R)-2-(4-fluoro-3,5-dimethylphenylamino)-6-(4-fluo...)
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of MMP-14 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMacrophage metalloelastase(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50379534(CHEMBL2012837)
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of MMP-12 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMacrophage metalloelastase(Homo sapiens (Human))
Panthera Biopharma

Curated by ChEMBL
LigandPNGBDBM50340768((R)-2-(4-fluoro-3,5-dimethylphenoxy)-6-(4-fluorobe...)
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of MMP-12 using OmniMMP as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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