BDBM50666512 CHEMBL6170631

SMILES C=C(C)[C@@H]1CCC(C)=C[C@H]1c1c(O)cc(CCCCC)cc1OCCCCCCCCCCCCOc1cc(CCCCC)cc(O)c1[C@@H]1C=C(C)CC[C@H]1C(=C)C

InChI Key InChIKey=XGTQJSDHTXYZSP-UHFFFAOYSA-N

Data  3 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50666512   

TargetKappa-type opioid receptor(Human)
University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666512BDBM50666512(CHEMBL6170631)
Affinity DataKi:  1.70E+3nMAssay Description:Displacement of [3H]-U69593 human KOR receptor at 10 uM by cell-based radioligand binding assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
Target5-hydroxytryptamine receptor 2B(Human)
University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666512BDBM50666512(CHEMBL6170631)
Affinity DataKi:  2.40E+3nMAssay Description:Displacement of [3H]-LSD from human 5-HT2B receptor at 10 uM by cell-based radioligand binding assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetD(2) dopamine receptor(Human)
University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666512BDBM50666512(CHEMBL6170631)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]-N-Methylspiperone from human D2 receptor at 10 uM by cell-based radioligand binding assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed