BDBM50088986 CHEMBL433809::{2-[2-(1-Carbamimidoyl-2-hydroxy-piperidin-3-ylcarbamoyl)-piperidin-1-yl]-1-hydroxymethyl-2-oxo-ethyl}-carbamic acid benzyl ester
SMILES: NC(=N)N1CCC[C@@H](NC(=O)[C@H]2CCCCN2C(=O)[C@@H](CO)NC(=O)OCc2ccccc2)C1O
InChI Key: InChIKey=YKKCDCXIZOOYFS-KYJJNMIMSA-N
Data: 2 IC50
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Urokinase-type plasminogen activator (Homo sapiens (Human)) | BDBM50088986 (CHEMBL433809 | {2-[2-(1-Carbamimidoyl-2-hydroxy-pi...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 101 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc. Curated by ChEMBL | Assay Description The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50 | Bioorg Med Chem Lett 10: 983-7 (2000) BindingDB Entry DOI: 10.7270/Q2765DKB | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Tissue-type plasminogen activator (Homo sapiens (Human)) | BDBM50088986 (CHEMBL433809 | {2-[2-(1-Carbamimidoyl-2-hydroxy-pi...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc. Curated by ChEMBL | Assay Description The compound was tested in vitro for its inhibitory activity against human t-PA enzyme, activity expressed as IC50 | Bioorg Med Chem Lett 10: 983-7 (2000) BindingDB Entry DOI: 10.7270/Q2765DKB | |||||||||||
More data for this Ligand-Target Pair |