null

SMILES NC(=N)c1ccccc1

InChI Key InChIKey=PXXJHWLDUBFPOL-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 35 hits for monomerid = 50038002   

TargetSerine protease 1(Bos taurus (bovine))
F. Hoffmann-La Roche Ltd.

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  31nMAssay Description:In vitro binding affinity by measuring the inhibition of bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25X29KKPubMed
TargetSerine protease 1(Bos taurus (bovine))
F. Hoffmann-La Roche Ltd.

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  31nMAssay Description:Inhibitory Activity against bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20R9Q3NPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Protherics Molecular Design

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  200nMAssay Description:Inhibitory concentration against human Coagulation factor Xa (fXa)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2319V5WPubMed
TargetProthrombin(Homo sapiens (Human))
Boehringer Ingelheim Pharma KG

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  300nMAssay Description:Inhibitory Activity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20R9Q3NPubMed
TargetProthrombin(Homo sapiens (Human))
Boehringer Ingelheim Pharma KG

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  300nMAssay Description:In vitro binding affinity by measuring the inhibition of human thrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25X29KKPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Protherics Molecular Design

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  410nMAssay Description:Binding affinity of the compound was evaluated against Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2222SX9PubMed
TargetProthrombin(Homo sapiens (Human))
Boehringer Ingelheim Pharma KG

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  1.24E+3nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q28916J7PubMed
TargetProthrombin(Homo sapiens (Human))
Boehringer Ingelheim Pharma KG

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  1.24E+3nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q28916J7PubMed
TargetAcrosin(Sus scrofa)
TBA

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  4.00E+3nMAssay Description:Reversible competitive inhibition of boar spermatozoa acrosin using BzArgOEt as substrate by Dixon plot analysisMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TT4SGNPubMed
TargetIonotropic glutamate receptor subunit Delta2(Xenopus)
State University of New York

Curated by PDSP Ki Database
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N878C5PubMed
TargetSerine protease 1(Homo sapiens (Human))
University of Parma

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  1.84E+4nMAssay Description:Binding affinity against bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q28916J7PubMed
TargetSerine protease 1(Homo sapiens (Human))
University of Parma

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  1.84E+4nMAssay Description:Binding affinity against bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q28916J7PubMed
TargetSerine protease 1(Bos taurus (bovine))
F. Hoffmann-La Roche Ltd.

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  2.00E+4nMAssay Description:Inhibitory concentration against bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2319V5WPubMed
TargetSerine protease 1(Bos taurus (bovine))
F. Hoffmann-La Roche Ltd.

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  3.20E+4nMAssay Description:Competitive inhibition of bovine beta trypsin using Bz-Arg-NH-Np as substrate at pH 7 at 30 degCMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GT5RWWPubMed
TargetSerine protease 1(Bos taurus (bovine))
F. Hoffmann-La Roche Ltd.

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  3.50E+4nMpH: 7.5Assay Description:Tested for the Inhibition of the catalytic activity of bovine trypsin at 25 degree C and pH 7.5.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29W0FZ9
TargetSerine protease 1(Bos taurus (bovine))
F. Hoffmann-La Roche Ltd.

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  3.90E+4nMAssay Description:Inhibitory activity against bovine trypsin expressed as dissociation constantMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KK99ZFPubMed
TargetCoagulation factor X(Bos taurus)
Institut für Biochemie

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  1.60E+5nMAssay Description:Inhibitory activity against bovine coagulation factor X expressed as dissociation constantMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KK99ZFPubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Institut für Biochemie

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  1.80E+5nMAssay Description:Inhibitory activity against human urokinase plasminogen activator expressed as dissociation constantMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KK99ZFPubMed
TargetProthrombin(Homo sapiens (Human))
Boehringer Ingelheim Pharma KG

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  2.20E+5nMpH: 7.5Assay Description:Tested for the Inhibition of the catalytic activity of human Thrombin at 25 degree C and pH 7.5.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29W0FZ9
TargetCoagulation factor VII/Tissue factor(Homo sapiens (Human))
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  2.40E+5nMAssay Description:Inhibition of human soluble tissue factor/factor VIIa expressed in Origami B (DE3) using D-Ile-Pro-Arg-pNA as substrate after 30 mins by spectrophoto...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28D007CPubMed
TargetProthrombin(Homo sapiens (Human))
Boehringer Ingelheim Pharma KG

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  2.58E+5nMAssay Description:Binding affinity to thrombin (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M38M6PubMed
TargetProthrombin(Homo sapiens (Human))
Boehringer Ingelheim Pharma KG

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  3.16E+5nMAssay Description:Competitive inhibition of esterase activity of human plasmin assessed as assessed as decrease in p-nitrophenol production using N-Z-L-Tyr-ONp as subs...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ST7RCQPubMed
TargetPlasminogen(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  3.50E+5nMpH: 7.5Assay Description:Tested for the Inhibition of the catalytic activity of human plasmin at 25 degree C and pH 7.5.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29W0FZ9
TargetComplement C1s subcomponent(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  3.98E+5nMAssay Description:Competitive inhibition of esterase activity of human plasmin assessed as assessed as decrease in p-nitrophenol production using N-Z-L-Tyr-ONp as subs...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ST7RCQPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Aurigene Discovery Technologies Limited

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  4.00E+5nMAssay Description:Inhibition of matriptase-SP1 (615 to 855) (unknown origin) expressed in Escherichia coli BL21(DE3) using Boc-Gln-Ala-Arg-7-amido-4-methyl coumarin hy...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1SHZPubMed
TargetPlasminogen(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  5.00E+5nMAssay Description:Competitive inhibition of esterase activity of human plasmin assessed as assessed as decrease in p-nitrophenol production using N-Z-L-Tyr-ONp as subs...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ST7RCQPubMed
TargetProthrombin(Bos taurus (Bovine))
Institut für Biochemie

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  8.90E+5nMAssay Description:Inhibitory activity against bovine thrombin expressed as dissociation constantMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KK99ZFPubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Institut für Biochemie

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  9.10E+5nMAssay Description:Inhibitory activity against human tissue-type plasminogen activator expressed as dissociation constantMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KK99ZFPubMed
TargetPlasminogen(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKi:  2.51E+6nMAssay Description:Competitive inhibition of esterase activity of human plasmin assessed as assessed as decrease in p-nitrophenol production using N-Z-L-Tyr-ONp as subs...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ST7RCQPubMed
TargetKallikrein-5(Homo sapiens (Human))
GlaxoSmithKline

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataIC50: 5.01E+5nMAssay Description:Inhibition of human recombinant 6His-Q-FLAG-tagged KLK5 expressed in baculovirus infected Sf9 insect cells using rhodamine-labelled tripeptide as sub...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571GG1PubMed
TargetSerine protease 1(Homo sapiens (Human))
University of Parma

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKd:  1.82E+4nMAssay Description:Binding affinity against trypsinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MG7S8SPubMed
TargetAnionic trypsin(Bos taurus)
Harvard University

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKd:  1.48E+7nMAssay Description:log Kd (Binding affinity against specified protein) value of the compoundMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MG7S8SPubMed
TargetCoagulation factor XI(Homo sapiens (Human))
Daiichi Asubio Medical Research Laboratories, LLC

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+5nMAssay Description:Inhibition of f11aMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6M5DPubMed
TargetProthrombin(Homo sapiens (Human))
Boehringer Ingelheim Pharma KG

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKd:  4.55E+5nMAssay Description:Binding affinity to thrombin (unknown origin) by displacement titration based isothermal titration colorimetryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M38M6PubMed
TargetProthrombin(Homo sapiens (Human))
Boehringer Ingelheim Pharma KG

Curated by ChEMBL
LigandPNGBDBM50038002(Benzamidine (Protonated) | CHEMBL20936 | CHEMBL537...)copy SMILEScopy InChI
Affinity DataKd:  3.55E+5nMAssay Description:Binding affinity to thrombin (unknown origin) by direct isothermal titration colorimetryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M38M6PubMed