null
SMILES: Br.[H][C@@]12Cc3ccc(OC)cc3[C@]3(CCCCC13)CCN2C
InChI Key: InChIKey=MKXZASYAUGDDCJ-HSFDIDPMSA-N
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Delta-type opioid receptor/Kappa-type opioid receptor/Mu-type opioid receptor/Sigma non-opioid intracellular receptor 1 (Rattus norvegicus (rat)-RAT) | BDBM50225315![]() (Levomethorphan Hydrobromide) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet ![]() | PC cid PC sid UniChem Patents | PubMed | n/a | n/a | 2.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Concentration required to inhibit stereospecific [3H]- naltrexone binding by 50% in rat brain homogenate | J Med Chem 27: 1219-22 (1984) BindingDB Entry DOI: 10.7270/Q2RJ4MPW | |||||||||||
More data for this Ligand-Target Pair |