BDBM50110025 CHEMBL158405::N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHYL]BENZYL}-L-ALANINAMIDE::N-[1-(4-Carbamimidoyl-benzylcarbamoyl)-ethyl]-3-hydroxy-2-phenylmethanesulfonylamino-propionamide

SMILES C[C@H](NC(=O)[C@@H](CO)NS(=O)(=O)Cc1ccccc1)C(=O)NCc1ccc(cc1)C(N)=N

InChI Key InChIKey=QJNHUFOFEMCMGR-UHFFFAOYSA-N

Data  9 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50110025   

TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  3.30nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  7.70nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  7.70nMAssay Description:Inhibition of human uPA using pyroGlu-Gly-Arg-p-NA.HCl as substrate preincubated for 15 mins prior substrate addition measured for 10 mins by spectro...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProthrombin(Human)
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50110025(N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  100nMAssay Description:Inhibition of human plasma thrombin using pyroGlu-Pro-Arg-p-NA.HCl as substrate preincubated for 15 mins prior substrate addition measured for 10 min...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProthrombin(Human)
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50110025(N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  110nMAssay Description:In vitro inhibition of thrombin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPlasminogen(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  540nMAssay Description:In vitro inhibition of Plasmin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPlasminogen(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  540nMAssay Description:Inhibition of human plasma plasmin using pyroGlu-Pro-Arg-p-NA.HCl as substrate preincubated for 15 mins prior substrate addition measured for 10 mins...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCoagulation factor X(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  2.10E+3nMAssay Description:In vitro inhibition of Coagulation factor Xa.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetTissue-type plasminogen activator(Human)
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50110025(N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  7.40E+3nMAssay Description:Inhibition of recombinant tPA using H-D-Ile-Pro-Arg-pNA.2HCl as substrate preincubated for 15 mins prior substrate addition measured for 10 mins by s...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed