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Found 58 with Last Name = 'huang' and Initial = 'tl'
TargetAmiloride-sensitive amine oxidase [copper-containing](Homo sapiens (Human))
Xavier University Of Louisiana

Curated by ChEMBL
LigandPNGBDBM50000999(CHEBI:81724 | DIMINAZENE)
Affinity DataKi:  13nMAssay Description:Mixed type inhibition of recombinant human DAO expressed in drosophila S2 cellsMore data for this Ligand-Target Pair
TargetCalpain small subunit 1(Sus scrofa)
University Of Tennessee Health Science Center

Curated by ChEMBL
LigandPNGBDBM50124028((S)-4-Methyl-2-(toluene-4-sulfonylamino)-pentanoic...)
Affinity DataKi:  20nMAssay Description:Compound tested for inhibition of porcine calpain IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalpain small subunit 1(Sus scrofa)
University Of Tennessee Health Science Center

Curated by ChEMBL
LigandPNGBDBM50124032(3-(Toluene-4-sulfonyl)-thiazolidine-2-carboxylic a...)
Affinity DataKi:  70nMAssay Description:Compound tested for inhibition of porcine Calpain 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B(Homo sapiens (Human))
University Of Tennessee Health Science Center

Curated by ChEMBL
LigandPNGBDBM50124028((S)-4-Methyl-2-(toluene-4-sulfonylamino)-pentanoic...)
Affinity DataKi:  70nMAssay Description:Compound tested for inhibition of human liver cathepsin BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalpain small subunit 1(Sus scrofa)
University Of Tennessee Health Science Center

Curated by ChEMBL
LigandPNGBDBM50124029(1-(Toluene-4-sulfonyl)-pyrrolidine-2-carboxylic ac...)
Affinity DataKi:  80nMAssay Description:Compound tested for inhibition of porcine Calpain 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrypsin(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189306(CHEMBL3594083)
Affinity DataKi:  192nMAssay Description:Inhibition of human trypsin using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrypsin(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189311(4,4''-(1,2-Phenylenebis(Methylene))Bis(Oxy)Dibenzi...)
Affinity DataKi:  221nMAssay Description:Inhibition of human trypsin using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrypsin(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189307(CHEMBL3594082)
Affinity DataKi:  244nMAssay Description:Inhibition of human trypsin using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalpain small subunit 1(Sus scrofa)
University Of Tennessee Health Science Center

Curated by ChEMBL
LigandPNGBDBM50124030(1-(Toluene-4-sulfonyl)-azetidine-2-carboxylic acid...)
Affinity DataKi:  250nMAssay Description:Compound tested for inhibition of porcine Calpain 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189311(4,4''-(1,2-Phenylenebis(Methylene))Bis(Oxy)Dibenzi...)
Affinity DataKi:  279nMAssay Description:Inhibition of human thrombin using Cbz-Gly-Gly-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmiloride-sensitive amine oxidase [copper-containing](Homo sapiens (Human))
Xavier University Of Louisiana

Curated by ChEMBL
LigandPNGBDBM45440(4-[5-(4-amidinophenoxy)pentoxy]benzamidine;2-hydro...)
Affinity DataKi:  290nMAssay Description:Mixed type inhibition of recombinant human DAO expressed in drosophila S2 cellsMore data for this Ligand-Target Pair
TargetTrypsin(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189310(4,4''-(1,4-Phenylenebis(Methylene))Bis(Oxy)Dibenzi...)
Affinity DataKi:  316nMAssay Description:Inhibition of human trypsin using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189306(CHEMBL3594083)
Affinity DataKi:  317nMAssay Description:Inhibition of human thrombin using Cbz-Gly-Gly-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Bos taurus)
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189310(4,4''-(1,4-Phenylenebis(Methylene))Bis(Oxy)Dibenzi...)
Affinity DataKi:  327nMAssay Description:Inhibition of bovine factor 10a using Boc-Ile-Glu-Gly-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Bos taurus)
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189307(CHEMBL3594082)
Affinity DataKi:  391nMAssay Description:Inhibition of bovine factor 10a using Boc-Ile-Glu-Gly-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189308(CHEMBL269032)
Affinity DataKi:  397nMAssay Description:Inhibition of human matriptase using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189305(CHEMBL3828410)
Affinity DataKi:  492nMAssay Description:Inhibition of human matriptase using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189307(CHEMBL3594082)
Affinity DataKi:  499nMAssay Description:Inhibition of human thrombin using Cbz-Gly-Gly-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrypsin(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189309(CHEMBL9126)
Affinity DataKi:  513nMAssay Description:Inhibition of human trypsin using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189306(CHEMBL3594083)
Affinity DataKi:  526nMAssay Description:Inhibition of human matriptase using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalpain small subunit 1(Sus scrofa)
University Of Tennessee Health Science Center

Curated by ChEMBL
LigandPNGBDBM50124031(1-(Toluene-4-sulfonyl)-piperidine-2-carboxylic aci...)
Affinity DataKi:  540nMAssay Description:Compound tested for inhibition of porcine calpain IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189307(CHEMBL3594082)
Affinity DataKi:  558nMAssay Description:Inhibition of human matriptase using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189309(CHEMBL9126)
Affinity DataKi:  719nMAssay Description:Inhibition of human matriptase using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189310(4,4''-(1,4-Phenylenebis(Methylene))Bis(Oxy)Dibenzi...)
Affinity DataKi:  816nMAssay Description:Inhibition of human matriptase using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189310(4,4''-(1,4-Phenylenebis(Methylene))Bis(Oxy)Dibenzi...)
Affinity DataKi:  1.16E+3nMAssay Description:Inhibition of human thrombin using Cbz-Gly-Gly-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransmembrane protease serine 6(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189309(CHEMBL9126)
Affinity DataKi:  1.16E+3nMAssay Description:Inhibition of human matriptase-2 transfected in HEK cells using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Bos taurus)
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189306(CHEMBL3594083)
Affinity DataKi:  1.29E+3nMAssay Description:Inhibition of bovine factor 10a using Boc-Ile-Glu-Gly-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrypsin(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189305(CHEMBL3828410)
Affinity DataKi:  1.42E+3nMAssay Description:Inhibition of human trypsin using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransmembrane protease serine 6(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189306(CHEMBL3594083)
Affinity DataKi:  1.64E+3nMAssay Description:Inhibition of human matriptase-2 transfected in HEK cells using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrypsin(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189308(CHEMBL269032)
Affinity DataKi:  1.90E+3nMAssay Description:Inhibition of human trypsin using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDiamine acetyltransferase 1(Homo sapiens (Human))
Xavier University Of Louisiana

Curated by ChEMBL
LigandPNGBDBM45440(4-[5-(4-amidinophenoxy)pentoxy]benzamidine;2-hydro...)
Affinity DataKi:  2.00E+3nMAssay Description:Inhibition of human SSAT using spermidine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189311(4,4''-(1,2-Phenylenebis(Methylene))Bis(Oxy)Dibenzi...)
Affinity DataKi:  2.28E+3nMAssay Description:Inhibition of human matriptase using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDiamine acetyltransferase 1(Homo sapiens (Human))
Xavier University Of Louisiana

Curated by ChEMBL
LigandPNGBDBM50000999(CHEBI:81724 | DIMINAZENE)
Affinity DataKi:  2.40E+3nMAssay Description:Inhibition of human SSAT using spermidine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B(Homo sapiens (Human))
University Of Tennessee Health Science Center

Curated by ChEMBL
LigandPNGBDBM50124030(1-(Toluene-4-sulfonyl)-azetidine-2-carboxylic acid...)
Affinity DataKi:  2.75E+3nMAssay Description:Compound tested for inhibition of human liver Cathepsin BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Bos taurus (Bovine))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189310(4,4''-(1,4-Phenylenebis(Methylene))Bis(Oxy)Dibenzi...)
Affinity DataKi:  3.40E+3nMAssay Description:Inhibition of bovine thrombin using BANA/BPVANA as substrate after 15 to 40 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransmembrane protease serine 6(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189307(CHEMBL3594082)
Affinity DataKi:  3.68E+3nMAssay Description:Inhibition of human matriptase-2 transfected in HEK cells using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransmembrane protease serine 6(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189308(CHEMBL269032)
Affinity DataKi:  4.39E+3nMAssay Description:Inhibition of human matriptase-2 transfected in HEK cells using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransmembrane protease serine 6(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189311(4,4''-(1,2-Phenylenebis(Methylene))Bis(Oxy)Dibenzi...)
Affinity DataKi:  5.20E+3nMAssay Description:Inhibition of human matriptase-2 transfected in HEK cells using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B(Homo sapiens (Human))
University Of Tennessee Health Science Center

Curated by ChEMBL
LigandPNGBDBM50124031(1-(Toluene-4-sulfonyl)-piperidine-2-carboxylic aci...)
Affinity DataKi:  5.26E+3nMAssay Description:Compound tested for inhibition of human liver cathepsin BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189308(CHEMBL269032)
Affinity DataKi:  5.30E+3nMAssay Description:Inhibition of human thrombin using Cbz-Gly-Gly-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransmembrane protease serine 6(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189310(4,4''-(1,4-Phenylenebis(Methylene))Bis(Oxy)Dibenzi...)
Affinity DataKi:  5.70E+3nMAssay Description:Inhibition of human matriptase-2 transfected in HEK cells using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransmembrane protease serine 6(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189305(CHEMBL3828410)
Affinity DataKi:  6.23E+3nMAssay Description:Inhibition of human matriptase-2 transfected in HEK cells using Boc-Gln-Ala-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Bos taurus)
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189308(CHEMBL269032)
Affinity DataKi:  7.83E+3nMAssay Description:Inhibition of bovine factor 10a using Boc-Ile-Glu-Gly-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189309(CHEMBL9126)
Affinity DataKi:  1.01E+4nMAssay Description:Inhibition of human thrombin using Cbz-Gly-Gly-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B(Homo sapiens (Human))
University Of Tennessee Health Science Center

Curated by ChEMBL
LigandPNGBDBM50124029(1-(Toluene-4-sulfonyl)-pyrrolidine-2-carboxylic ac...)
Affinity DataKi:  1.21E+4nMAssay Description:Compound tested for inhibition of human liver Cathepsin BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Bos taurus)
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189311(4,4''-(1,2-Phenylenebis(Methylene))Bis(Oxy)Dibenzi...)
Affinity DataKi:  1.37E+4nMAssay Description:Inhibition of bovine factor 10a using Boc-Ile-Glu-Gly-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189305(CHEMBL3828410)
Affinity DataKi:  1.58E+4nMAssay Description:Inhibition of human thrombin using Cbz-Gly-Gly-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Bos taurus)
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189309(CHEMBL9126)
Affinity DataKi:  2.00E+4nMAssay Description:Inhibition of bovine factor 10a using Boc-Ile-Glu-Gly-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Bos taurus)
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50189305(CHEMBL3828410)
Affinity DataKi:  5.23E+4nMAssay Description:Inhibition of bovine factor 10a using Boc-Ile-Glu-Gly-Arg-AMC as substrate after 20 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor ionotropic, NMDA 1/2A(Homo sapiens (Human))
Xavier University Of Louisiana

Curated by ChEMBL
LigandPNGBDBM45440(4-[5-(4-amidinophenoxy)pentoxy]benzamidine;2-hydro...)
Affinity DataIC50:  720nMpH: 7.6Assay Description:Antagonist activity at NR1/NR2A receptor (unknown origin) expressed in Xenopus laevis oocytes assessed as inhibition of glutamate/glycine-induced cur...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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