BDBM50596324 CHEMBL5179969

SMILES COc1ccc(cc1S(=O)(=O)Nc1ccc2cccc(N(C)C(=O)c3ccccc3)c2c1)-c1cccc(c1)C(=O)N(C)C

InChI Key InChIKey=MEFWUBSRJLRTEK-UHFFFAOYSA-N

Data  4 EC50

  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 4 hits for monomerid = 50596324   

TargetOrexin/Hypocretin receptor type 1(Human)
University of Tsukuba

Curated by ChEMBL
LigandPNGBDBM50596324(CHEMBL5179969)
Affinity DataEC50: >1.00E+4nMAssay Description:Agonist activity at OX1R (unknown origin) expressed in CHO cells by cell-based calcium assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/22/2023
Entry Details
PubMed
TargetOrexin receptor type 2(Human)
University of Tsukuba

Curated by ChEMBL
LigandPNGBDBM50596324(CHEMBL5179969)
Affinity DataEC50:  1.95E+3nMAssay Description:Agonist activity at OX2R (unknown origin) expressed in CHO cells by cell-based calcium assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/22/2023
Entry Details
PubMed
TargetOrexin/Hypocretin receptor type 1(Human)
University of Tsukuba

Curated by ChEMBL
LigandPNGBDBM50596324(CHEMBL5179969)
Affinity DataEC50: >1.00E+4nMAssay Description:Agonist activity at OX1R (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/22/2023
Entry Details
PubMed
TargetOrexin receptor type 2(Human)
University of Tsukuba

Curated by ChEMBL
LigandPNGBDBM50596324(CHEMBL5179969)
Affinity DataEC50:  1.95E+3nMAssay Description:Agonist activity at OX2R (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/22/2023
Entry Details
PubMed