BDBM50188803 (S)-4-phenyl-8-((1R,2R)-2-phenyl-cyclohexyl)-2,8-diaza-spiro[4.5]decan-1-one::CHEMBL379860
SMILES: O=C1NC[C@@H](c2ccccc2)C11CCN(CC1)[C@@H]1CCCC[C@@H]1c1ccccc1
InChI Key: InChIKey=MMAYPVADBNWURJ-TZRRMPRUSA-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 |
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Mu-type opioid receptor (Homo sapiens (Human)) | BDBM50188803 ((S)-4-phenyl-8-((1R,2R)-2-phenyl-cyclohexyl)-2,8-d...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 3.92E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
F. Hoffmann-La Roche Ltd Curated by ChEMBL | Assay Description Displacement of [3H]naloxone from human mu opioid receptor expressed in BHK cells | Bioorg Med Chem Lett 16: 4311-5 (2006) Article DOI: 10.1016/j.bmcl.2006.05.058 BindingDB Entry DOI: 10.7270/Q2Z31Z8W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Glycine transporter 1 (Homo sapiens (Human)) | BDBM50188803 ((S)-4-phenyl-8-((1R,2R)-2-phenyl-cyclohexyl)-2,8-d...) | PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | n/a | n/a | 232 | n/a | n/a | n/a | n/a |
F. Hoffmann-La Roche Ltd Curated by ChEMBL | Assay Description Inhibition of [3H]glycine uptake at human GlyT1 by radiometric assay | Bioorg Med Chem Lett 16: 4311-5 (2006) Article DOI: 10.1016/j.bmcl.2006.05.058 BindingDB Entry DOI: 10.7270/Q2Z31Z8W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Glycine transporter 1 (Homo sapiens (Human)) | BDBM50188803 ((S)-4-phenyl-8-((1R,2R)-2-phenyl-cyclohexyl)-2,8-d...) | PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | n/a | n/a | 2.83E+3 | n/a | n/a | n/a | n/a |
F. Hoffmann-La Roche Ltd Curated by ChEMBL | Assay Description Inhibition of [3H]glycine uptake at GlyT1 | Bioorg Med Chem Lett 16: 4305-10 (2006) Article DOI: 10.1016/j.bmcl.2006.05.064 BindingDB Entry DOI: 10.7270/Q28C9VVV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Glycine transporter 1 (Homo sapiens (Human)) | BDBM50188803 ((S)-4-phenyl-8-((1R,2R)-2-phenyl-cyclohexyl)-2,8-d...) | PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | n/a | n/a | 232 | n/a | n/a | n/a | n/a |
F. Hoffmann-La Roche Ltd Curated by ChEMBL | Assay Description Inhibition of [3H]glycine uptake at human GlyT1 by radiometric assay | Bioorg Med Chem Lett 16: 4311-5 (2006) Article DOI: 10.1016/j.bmcl.2006.05.058 BindingDB Entry DOI: 10.7270/Q2Z31Z8W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Nociceptin receptor (Homo sapiens (Human)) | BDBM50188803 ((S)-4-phenyl-8-((1R,2R)-2-phenyl-cyclohexyl)-2,8-d...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
F. Hoffmann-La Roche Ltd Curated by ChEMBL | Assay Description Displacement of [3H]NOP from human NOP receptors expressed in HEK293 cells | Bioorg Med Chem Lett 16: 4311-5 (2006) Article DOI: 10.1016/j.bmcl.2006.05.058 BindingDB Entry DOI: 10.7270/Q2Z31Z8W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Glycine transporter 2 (Homo sapiens (Human)) | BDBM50188803 ((S)-4-phenyl-8-((1R,2R)-2-phenyl-cyclohexyl)-2,8-d...) | Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | n/a | n/a | 2.50E+4 | n/a | n/a | n/a | n/a |
F. Hoffmann-La Roche Ltd Curated by ChEMBL | Assay Description Inhibition of [3H]glycine uptake at human GlyT2 by radiometric assay | Bioorg Med Chem Lett 16: 4311-5 (2006) Article DOI: 10.1016/j.bmcl.2006.05.058 BindingDB Entry DOI: 10.7270/Q2Z31Z8W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human)) | BDBM50188803 ((S)-4-phenyl-8-((1R,2R)-2-phenyl-cyclohexyl)-2,8-d...) | 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 | 1.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
F. Hoffmann-La Roche Ltd Curated by ChEMBL | Assay Description Inhibition of hERG potassium channel expressed in CHO cells by whole cell patch clamp method | Bioorg Med Chem Lett 16: 4311-5 (2006) Article DOI: 10.1016/j.bmcl.2006.05.058 BindingDB Entry DOI: 10.7270/Q2Z31Z8W | |||||||||||
More data for this Ligand-Target Pair |