Compile Data Set for Download or QSAR
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Found 5 of ic50 for monomerid = 50001000
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Center For Neurologic Study

US Patent
LigandPNGBDBM50001000(CHEBI:29133 | DEXTRORPHAN | US11535596, Compound D...)
Affinity DataIC50:  259nMAssay Description:In vitro binding assays for the phencyclidine site of NMDA-type glutamate receptors, and for sigma-1 receptors, both of which are known to be bound b...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetGlutamate receptor ionotropic, NMDA 1/2A(Homo sapiens (Human))
Xavier University Of Louisiana

Curated by ChEMBL
LigandPNGBDBM50001000(CHEBI:29133 | DEXTRORPHAN | US11535596, Compound D...)
Affinity DataIC50:  1.30E+3nMpH: 7.6Assay Description:Antagonist activity at NR1/NR2A receptor (unknown origin) expressed in Xenopus laevis oocytes assessed as inhibition of glutamate/glycine-induced cur...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor ionotropic, NMDA 1(Homo sapiens (Human))
Center For Neurologic Study

US Patent
LigandPNGBDBM50001000(CHEBI:29133 | DEXTRORPHAN | US11535596, Compound D...)
Affinity DataIC50:  1.53E+3nMAssay Description:In vitro binding assays for the phencyclidine site of NMDA-type glutamate receptors, and for sigma-1 receptors, both of which are known to be bound b...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetSolute carrier family 22 member 1(Homo sapiens (Human))
University Medicine Greifswald

Curated by ChEMBL
LigandPNGBDBM50001000(CHEBI:29133 | DEXTRORPHAN | US11535596, Compound D...)
Affinity DataIC50:  6.00E+3nMAssay Description:Inhibition of human OCT1 expressed in HEK293 cells assessed as reduction in ASP+ substrate uptake by microplate reader based analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium channel protein type 1/2/3 subunit alpha(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50001000(CHEBI:29133 | DEXTRORPHAN | US11535596, Compound D...)
Affinity DataIC50:  1.80E+4nMAssay Description:Inhibition of binding of Batrachotoxinin [3H]BTX-B to high affinity sites on voltage dependent sodium channels in a vesicular preparation from guinea...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed