BDBM50246758 CHEMBL4093682
SMILES: NC(=O)CN1C[C@H](Cc2ccccc2)NC(=O)CN(C[C@H](CCC(O)=O)NC(=O)CN(C[C@H](CCC(O)=O)NC(=O)CN(C[C@H](Cc2ccccc2)NC(=O)c2ccc(CSCCC1=O)cc2)C(=O)CCC1CCCCC1)C(=O)Cc1ccc2OCOc2c1)C(=O)CCC(O)=O
InChI Key: InChIKey=OQBSFMMWTCXPMS-RWNJCICYSA-N
Data: 1 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Ephrin type-A receptor 2 (Homo sapiens (Human)) | BDBM50246758 (CHEMBL4093682) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 5.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
University of South Florida Curated by ChEMBL | Assay Description Inhibition of EphA2 autophosphorylation at Ser897 in human C13 cells after 24 hrs by Western blot method | J Med Chem 60: 9290-9298 (2017) Article DOI: 10.1021/acs.jmedchem.7b01280 BindingDB Entry DOI: 10.7270/Q20C4Z5R | |||||||||||
More data for this Ligand-Target Pair |