BDBM50101020 1-{4-[4-amino(1-methoxycarbonylimino)methylbenzylcarbamoyl]hexahydro-1-pyrazinylcarbonyloxy}-5-[4-(2-hexahydro-4-pyridinylethylcarbamoyl)hexahydro-1-pyrazinylcarbonyloxy]cyclooctane::CHEMBL42364

SMILES COC(=O)N=C(N)c1ccc(CNC(=O)N2CCN(CC2)C(=O)O[C@@H]2CCC[C@@H](CCC2)OC(=O)N2CCN(CC2)C(=O)NCCC2CCNCC2)cc1

InChI Key InChIKey=HGMFIDAVJXUGTM-QRRGNZNSSA-N

Data  4 KI

  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 4 hits for monomerid = 50101020   

TargetTryptase beta-2/delta/gamma(Homo sapiens (Human))
Axys Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50101020(1-{4-[4-amino(1-methoxycarbonylimino)methylbenzylc...)
Affinity DataKi:  41nMAssay Description:Binding affinity to 5-HT3 serotonin receptor in NG 108-15 neuroblastoma glioma cells using [3H]-GR-65,630 radioligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrypsin(Homo sapiens (Human))
Axys Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50101020(1-{4-[4-amino(1-methoxycarbonylimino)methylbenzylc...)
Affinity DataKi:  5.54E+5nMAssay Description:Binding affinity to 5-HT3 serotonin receptor in NG 108-15 neuroblastoma glioma cells using [3H]-GR-65,630 radioligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Axys Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50101020(1-{4-[4-amino(1-methoxycarbonylimino)methylbenzylc...)
Affinity DataKi:  5.61E+5nMAssay Description:Inhibition of thrombin in human mast cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Axys Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50101020(1-{4-[4-amino(1-methoxycarbonylimino)methylbenzylc...)
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition plasmin in human mast cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed