Home
About
Info
Download
WebServices
Contact
Compile Data Set for Download or QSAR
maximum 50k data
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
(change energy unit to
kcal/mol
)
Found
13
hits in this display
Target
Prothrombin
(Bos taurus (Bovine))
TBA
Curated by
ChEMBL
Ligand
BDBM50010065
(CHEMBL563834)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4.73E+3nM
Assay Description:
Competitive reversible inhibition of bovine thrombin using alpha-N-benzoyl-DL-arginine-p-nitroanilide hydrochloride as substrate after 15 to 40 mins ...
More data for this Ligand-Target Pair
Target Info
PDB
UniProtKB/SwissProt
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Prothrombin
(Bos taurus (Bovine))
TBA
Curated by
ChEMBL
Ligand
BDBM50009967
(CHEMBL417907)
Copy SMILES
Copy InChI
Affinity Data
Ki: 7.83E+3nM
Assay Description:
Competitive reversible inhibition of bovine thrombin using alpha-N-benzoyl-DL-arginine-p-nitroanilide hydrochloride as substrate after 15 to 40 mins ...
More data for this Ligand-Target Pair
Target Info
PDB
UniProtKB/SwissProt
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Glandular kallikrein
(Sus scrofa)
TBA
Curated by
ChEMBL
Ligand
BDBM50009967
(CHEMBL417907)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.53E+4nM
Assay Description:
Competitive reversible inhibition of porcine pancreatic kallikrein using alpha-N-benzoyl-DL-arginine-p-nitroanilide hydrochloride as substrate after ...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Serine protease 1
(Homo sapiens (Human))
Axys Pharmaceuticals
Curated by
ChEMBL
Ligand
BDBM50100891
(2-Phenyl-1H-benzoimidazole-5-carboxamidine | 2-Phe...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 5.50E+4nM
Assay Description:
Compound was tested against Human Serine Protease Trypsin
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
Ligand Info
Purchase
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Urokinase-type plasminogen activator
(Homo sapiens (Human))
Axys Pharmaceuticals
Curated by
ChEMBL
Ligand
BDBM50100891
(2-Phenyl-1H-benzoimidazole-5-carboxamidine | 2-Phe...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 5.50E+4nM
Assay Description:
ComInhibition of Human Serine Protease Urokinase Plasminogen Activator (u-PA).
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Glandular kallikrein
(Sus scrofa)
TBA
Curated by
ChEMBL
Ligand
BDBM50010065
(CHEMBL563834)
Copy SMILES
Copy InChI
Affinity Data
Ki: 6.45E+4nM
Assay Description:
Competitive reversible inhibition of porcine pancreatic kallikrein using alpha-N-benzoyl-DL-arginine-p-nitroanilide hydrochloride as substrate after ...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Coagulation factor X
(Homo sapiens (Human))
Axys Pharmaceuticals
Curated by
ChEMBL
Ligand
BDBM50100891
(2-Phenyl-1H-benzoimidazole-5-carboxamidine | 2-Phe...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.25E+5nM
Assay Description:
Binding affinity against human coagulation factor X
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Prothrombin
(Homo sapiens (Human))
Axys Pharmaceuticals
Curated by
ChEMBL
Ligand
BDBM50100891
(2-Phenyl-1H-benzoimidazole-5-carboxamidine | 2-Phe...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 3.40E+5nM
Assay Description:
Inhibition of Human Serine Protease Thrombin.
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Plasminogen
(Homo sapiens (Human))
Axys Pharmaceuticals
Curated by
ChEMBL
Ligand
BDBM50100891
(2-Phenyl-1H-benzoimidazole-5-carboxamidine | 2-Phe...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 3.50E+5nM
Assay Description:
Inhibition of Human Serine Protease Plasmin.
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Tissue-type plasminogen activator
(Homo sapiens (Human))
Axys Pharmaceuticals
Curated by
ChEMBL
Ligand
BDBM50100891
(2-Phenyl-1H-benzoimidazole-5-carboxamidine | 2-Phe...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 3.81E+5nM
Assay Description:
Inhibition of Human Serine Protease tissue type Plasminogen Activator (t-PA).
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Sporulation kinase A
(Bacillus subtilis (strain 168))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
ChEMBL
Ligand
BDBM50218650
(CHEMBL2114423)
Copy SMILES
Copy InChI
Affinity Data
IC50: 8.80E+4nM
Assay Description:
Inhibition of KinA/Sp0F system two component (TCS) from Bacillus subtilis.
More data for this Ligand-Target Pair
Target Info
PDB
UniProtKB/SwissProt
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Sporulation kinase A
(Bacillus subtilis (strain 168))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
ChEMBL
Ligand
BDBM50218657
(CHEMBL289173)
Copy SMILES
Copy InChI
Affinity Data
IC50: 2.20E+5nM
Assay Description:
Inhibition of KinA/Sp0F system two component (TCS) from Bacillus subtilis.
More data for this Ligand-Target Pair
Target Info
PDB
UniProtKB/SwissProt
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Sporulation kinase A
(Bacillus subtilis (strain 168))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
ChEMBL
Ligand
BDBM50100891
(2-Phenyl-1H-benzoimidazole-5-carboxamidine | 2-Phe...)
Copy SMILES
Copy InChI
Affinity Data
IC50: >5.00E+5nM
Assay Description:
Inhibition of KinA/Sp0F system two component (TCS) from Bacillus subtilis.
More data for this Ligand-Target Pair
Target Info
PDB
UniProtKB/SwissProt
GoogleScholar
Ligand Info
Purchase
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI