BDBM50148534 2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoylmethyl]-3-(4-fluoro-phenyl)-acrylic acid::CHEMBL119055::CHEMBL119723
SMILES: OC(=O)C(Cc1ccc(F)cc1)CP(O)(=O)C(=N)CC1CCCCC1
InChI Key: InChIKey=QMNSNNIDXYDZAS-UHFFFAOYSA-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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Renal dipeptidase (Homo sapiens (Human)) | BDBM50148534 (2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Curated by ChEMBL | Assay Description Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancer | Bioorg Med Chem Lett 14: 3531-3 (2004) Article DOI: 10.1016/j.bmcl.2004.04.057 BindingDB Entry DOI: 10.7270/Q2GX4B1C | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dehydropeptidase-I (DHP-1) (Homo sapiens (Human)) | BDBM50148534 (2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 15 | n/a | n/a | n/a | n/a | n/a | n/a |
The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Curated by ChEMBL | Assay Description Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancer | Bioorg Med Chem Lett 14: 3531-3 (2004) Article DOI: 10.1016/j.bmcl.2004.04.057 BindingDB Entry DOI: 10.7270/Q2GX4B1C | |||||||||||
More data for this Ligand-Target Pair |