BDBM535943 US11242337, Example 50

SMILES CN(C)[C@H]1Cc2c(cc(Cl)cc2C#N)[C@@H]1Oc1ccc(cc1C)S(=O)(=O)N1CC[C@H](COc2ccnc(CNC(=O)NCCCCNC(=O)NCc3cc(OC[C@H]4CCN(C4)S(=O)(=O)c4ccc(O[C@@H]5[C@H](Cc6c5cc(Cl)cc6C#N)N(C)C)c(C)c4)ccn3)c2)C1

InChI Key InChIKey=MNTQGKROTBWSCZ-UHFFFAOYSA-N

Data  2 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 2 hits for monomerid = 535943   

TargetSodium/hydrogen exchanger 3(Human)
Ardelyx

US Patent
LigandPNGBDBM535943(US11242337, Example 50)
Affinity DataIC50: 100nMAssay Description:Rat and human NHE-3-mediated Na+-dependent H+ antiport was measured using a modification of the pH sensitive dye method originally reported by Paradi...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/10/2022
Entry Details
Go to US Patent

TargetSodium/hydrogen exchanger 3(Human)
Ardelyx

US Patent
LigandPNGBDBM535943(US11242337, Example 50)
Affinity DataIC50: 100nMAssay Description:The ability of compounds to inhibit human and rat NHE-3-mediated Na+ dependent H+ antiport after application and washout was measured using a modific...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/10/2022
Entry Details
Go to US Patent