Compile Data Set for Download or QSAR
Found 255 with Last Name = 'marinelli' and Initial = 'b'
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50454459(CHEMBL4215036)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of Clostridium difficile toxin B transfected in CHO cells assessed as reduction in caspase 3/7 activation pre-incubated for 1 hr before Tc...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetLIM domain kinase 2(Homo sapiens (Human))
Lexicon Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50044006(CHEMBL3356431)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human full-length LIMK2 assessed as incorporation of P33 from ATP into biotinylated-cofilin substrate by scintillation counting analysi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q218384XPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50454459(CHEMBL4215036)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B catalytic fragment (Met1 to Leu543 residues) assessed as reduction in...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QR50RGPubMed
TargetLIM domain kinase 2(Homo sapiens (Human))
Lexicon Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50299586((S)-3-(2-methyl-4-(5-methyl-7H-pyrrolo[2,3-d]pyrim...)copy SMILEScopy InChI
Affinity DataIC50: 1.20nMAssay Description:Inhibition of human full-length LIMK2 assessed as incorporation of P33 from ATP into biotinylated-cofilin substrate by scintillation counting analysi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q218384XPubMed
TargetLIM domain kinase 2(Homo sapiens (Human))
Lexicon Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50044086(CHEMBL3356064)copy SMILES
Affinity DataIC50: 1.20nMAssay Description:Inhibition of human full-length LIMK2 assessed as incorporation of P33 from ATP into biotinylated-cofilin substrate by scintillation counting analysi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q218384XPubMed
TargetLIM domain kinase 2(Homo sapiens (Human))
Lexicon Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50044012(CHEMBL3356424)copy SMILEScopy InChI
Affinity DataIC50: 1.90nMAssay Description:Inhibition of human full-length LIMK2 assessed as incorporation of P33 from ATP into biotinylated-cofilin substrate by scintillation counting analysi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q218384XPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507130(CHEMBL4452983)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetLIM domain kinase 2(Homo sapiens (Human))
Lexicon Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50044010(CHEMBL3356426)copy SMILEScopy InChI
Affinity DataIC50: 2.20nMAssay Description:Inhibition of human full-length LIMK2 assessed as incorporation of P33 from ATP into biotinylated-cofilin substrate by scintillation counting analysi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q218384XPubMed
TargetLIM domain kinase 2(Homo sapiens (Human))
Lexicon Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50044087(CHEMBL3356063)copy SMILES
Affinity DataIC50: 2.70nMAssay Description:Inhibition of human full-length LIMK2 assessed as incorporation of P33 from ATP into biotinylated-cofilin substrate by scintillation counting analysi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q218384XPubMed
TargetLIM domain kinase 2(Homo sapiens (Human))
Lexicon Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50044003(CHEMBL3356430)copy SMILEScopy InChI
Affinity DataIC50: 2.70nMAssay Description:Inhibition of human full-length LIMK2 assessed as incorporation of P33 from ATP into biotinylated-cofilin substrate by scintillation counting analysi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q218384XPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50454497(CHEMBL4214079)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of Clostridium difficile toxin B transfected in CHO cells assessed as reduction in caspase 3/7 activation pre-incubated for 1 hr before Tc...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507108(CHEMBL4529863)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50454498(CHEMBL4215657)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B catalytic fragment (Met1 to Leu543 residues) assessed as reduction in...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QR50RGPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50454500(CHEMBL4212258)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B catalytic fragment (Met1 to Leu543 residues) assessed as reduction in...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QR50RGPubMed
TargetLIM domain kinase 2(Homo sapiens (Human))
Lexicon Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50044011(CHEMBL3356425)copy SMILEScopy InChI
Affinity DataIC50: 3.20nMAssay Description:Inhibition of human full-length LIMK2 assessed as incorporation of P33 from ATP into biotinylated-cofilin substrate by scintillation counting analysi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q218384XPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507115(CHEMBL4520413)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507128(CHEMBL4451752)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507135(CHEMBL4470638)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507134(CHEMBL4444965)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507107(CHEMBL4473557)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetLIM domain kinase 2(Homo sapiens (Human))
Lexicon Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50044004(CHEMBL3356433)copy SMILEScopy InChI
Affinity DataIC50: 4.30nMAssay Description:Inhibition of human full-length LIMK2 assessed as incorporation of P33 from ATP into biotinylated-cofilin substrate by scintillation counting analysi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q218384XPubMed
TargetLIM domain kinase 2(Homo sapiens (Human))
Lexicon Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50044009(CHEMBL3356427)copy SMILEScopy InChI
Affinity DataIC50: 4.80nMAssay Description:Inhibition of human full-length LIMK2 assessed as incorporation of P33 from ATP into biotinylated-cofilin substrate by scintillation counting analysi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q218384XPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507120(CHEMBL4473443)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507105(CHEMBL4557223)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507127(CHEMBL4476228)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetLIM domain kinase 2(Homo sapiens (Human))
Lexicon Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50044007(CHEMBL3356429)copy SMILEScopy InChI
Affinity DataIC50: 5.10nMAssay Description:Inhibition of human full-length LIMK2 assessed as incorporation of P33 from ATP into biotinylated-cofilin substrate by scintillation counting analysi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q218384XPubMed
TargetLIM domain kinase 2(Homo sapiens (Human))
Lexicon Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50299618((S)-N-(3-(isopropylcarbamoyl)phenyl)-2-methyl-4-(5...)copy SMILEScopy InChI
Affinity DataIC50: 5.5nMAssay Description:Inhibition of human full-length LIMK2 assessed as incorporation of P33 from ATP into biotinylated-cofilin substrate by scintillation counting analysi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q218384XPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507133(CHEMBL4461315)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507136(CHEMBL4454294)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50454497(CHEMBL4214079)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B catalytic fragment (Met1 to Leu543 residues) assessed as reduction in...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QR50RGPubMed
TargetTryptophan 5-hydroxylase 1(Homo sapiens (Human))
Princ

Curated by ChEMBL
LigandPNGBDBM50300929((S)-2-amino-3-(4-(4-amino-6-(biphenyl-2-ylmethylam...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibition of human recombinant TPH1 by continuous fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MS3SV0PubMed
TargetLIM domain kinase 2(Homo sapiens (Human))
Lexicon Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50044005(CHEMBL3356432)copy SMILEScopy InChI
Affinity DataIC50: 7.30nMAssay Description:Inhibition of human full-length LIMK2 assessed as incorporation of P33 from ATP into biotinylated-cofilin substrate by scintillation counting analysi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q218384XPubMed
TargetLIM domain kinase 2(Homo sapiens (Human))
Lexicon Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50044004(CHEMBL3356433)copy SMILEScopy InChI
Affinity DataIC50: 7.5nMAssay Description:Inhibition of human full-length LIMK2 assessed as incorporation of P33 from ATP into biotinylated-cofilin substrate by scintillation counting analysi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q218384XPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507113(CHEMBL4436890)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507126(CHEMBL4483028)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507114(CHEMBL4553525)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507116(CHEMBL4452876)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507119(CHEMBL4441033)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50454486(CHEMBL4203819)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B catalytic fragment (Met1 to Leu543 residues) assessed as reduction in...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QR50RGPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Harvard Medical School

Curated by ChEMBL
LigandPNGBDBM50358130(CHEMBL1923808)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Inhibition of human recombinant full-length HDAC1 using fluorophore conjugated substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JW8F90PubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Harvard Medical School

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 9.70nMAssay Description:Inhibition of human recombinant full-length HDAC1 using fluorophore conjugated substrate by fluorescence assayMore data for this Ligand-Target Pair
TargetLIM domain kinase 2(Homo sapiens (Human))
Lexicon Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50044083(CHEMBL3352853)copy SMILES
Affinity DataIC50: 9.90nMAssay Description:Inhibition of human full-length LIMK2 assessed as incorporation of P33 from ATP into biotinylated-cofilin substrate by scintillation counting analysi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q218384XPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507106(CHEMBL4472977)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Harvard Medical School

Curated by ChEMBL
LigandPNGBDBM50358130(CHEMBL1923808)copy SMILEScopy InChI
Affinity DataIC50: 12.7nMAssay Description:Inhibition of human recombinant full-length HDAC2 using fluorophore conjugated substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JW8F90PubMed
TargetTryptophan 5-hydroxylase 1(Homo sapiens (Human))
Princ

Curated by ChEMBL
LigandPNGBDBM50243565((S)-2-amino-3-(4-(5-(naphthalen-2-ylmethylamino)py...)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Inhibition of TPH1 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PK0FZMPubMed
TargetTryptophan 5-hydroxylase 1(Homo sapiens (Human))
Princ

Curated by ChEMBL
LigandPNGBDBM50300932((S)-2-amino-3-(4-(4-amino-6-((4'-methylbiphenyl-4-...)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:Inhibition of human recombinant TPH1 by continuous fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MS3SV0PubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507129(CHEMBL4456814)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Harvard Medical School

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:Inhibition of human recombinant full-length HDAC2 using fluorophore conjugated substrate by fluorescence assayMore data for this Ligand-Target Pair
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50454504(CHEMBL4210388)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B catalytic fragment (Met1 to Leu543 residues) assessed as reduction in...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QR50RGPubMed
TargetToxin B(Peptoclostridium difficile)
Venenum Biodesign

Curated by ChEMBL
LigandPNGBDBM50507112(CHEMBL4547929)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:Inhibition of C-terminal 6-His tagged recombinant Clostridium difficile toxin B glucosyltransferase domain assessed as reduction in UDP-glucose hydro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85FQPubMed
Displayed 1 to 50 (of 255 total ) | Next | Last >>
Jump to: