null

SMILES CC(=O)c1cccc(c1)-c1cc(cc(-c2nc3ccc(cc3[nH]2)C(N)=N)c1O)C(CC(O)=O)C(O)=O

InChI Key InChIKey=YZJXJVFIOXDWAC-UHFFFAOYSA-N

PDB links: 4 PDB IDs contain inhibitors having a similarity of 90% to this monomer.

  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 2 hits for monomerid = 14912   

TargetPlasma kallikrein(Homo sapiens (Human))
Celera Genomics

Curated by ChEMBL
LigandPNGBDBM14912(2-[3-(5-carbamimidoyl-1H-1,3-benzodiazol-2-yl)-5-(...)copy SMILEScopy InChI
Affinity DataKi:  6nMAssay Description:Binding affinity to plasma kallikreinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2P55N3NPubMed
TargetCoagulation factor VII(Homo sapiens (Human))
Celera

LigandPNGBDBM14912(2-[3-(5-carbamimidoyl-1H-1,3-benzodiazol-2-yl)-5-(...)copy SMILEScopy InChI
Affinity DataKi:  33nM ΔG°:  -10.1kcal/molepH: 7.4 T: 2°CAssay Description:The enzyme reactions were initiated by the addition of substrate, and the color developed from the release of p-nitroanilide from each chromogenic su...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0DSZPubMed