BDBM688323 4-chloro-N-[2-(2-chlorophenyl)-3-(4-chlorophenyl)-5,6,7,8-tetrahydrooxepino[3,2-c]pyrazol-8-yl]benzenesulfonamide::US20240189287, Compound BNS808

SMILES Clc1ccc(cc1)-c1c2OCCCC(NS(=O)(=O)c3ccc(Cl)cc3)c2nn1-c1ccccc1Cl

InChI Key InChIKey=VSSQVUBXWXIWJG-UHFFFAOYSA-N

Data  2 KI  1 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 688323   

TargetCannabinoid receptor 1(Mouse)
Bionanosim (Bns

US Patent
LigandPNGBDBM688323(US20240189287, Compound BNS808 | 4-chloro-N-[2-(2-...)
Affinity DataKi:  0.600nMAssay Description:Mouse brain membranes were used as the source material for CB1 receptors. The displacement of specifically bound tritiated CP-55.940 from these membr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/8/2024
Entry Details
US Patent

TargetCannabinoid receptor 2(Human)
Bionanosim (Bns

US Patent
LigandPNGBDBM688323(US20240189287, Compound BNS808 | 4-chloro-N-[2-(2-...)
Affinity DataKi:  1.93E+3nMAssay Description:Human kidney membranes were used as the source material for CB2 receptors. The displacement of specifically bound tritiated CP-55,940 from these memb...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/8/2024
Entry Details
US Patent

TargetPotassium voltage-gated channel subfamily H member 2(Human)
Bionanosim (Bns

US Patent
LigandPNGBDBM688323(US20240189287, Compound BNS808 | 4-chloro-N-[2-(2-...)
Affinity DataIC50: 5.39E+3nMAssay Description:Cardiotoxicity potential of BNS808 and BNS822 on the hERG potassium channels was evaluated using the automated patch clamp method (SyncroPatch 384PE)...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/8/2024
Entry Details
US Patent