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BDBM238861 US10052306, 300::rac-4-(2-((3aR,6aS)-5- benzylhexahydrocyclo- penta[c]pyrrol-2(1H)- yl)-1-hydroxyethyl) phenol

SMILES: OC(CN1C[C@@H]2CC(Cc3ccccc3)C[C@@H]2C1)c1ccc(O)cc1

InChI Key: InChIKey=HCJJHOOZJPOUQO-HGBKABEASA-N

Data: 1 IC50

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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 238861   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Glutamate receptor ionotropic, NMDA 2B


(Homo sapiens (Human))
BDBM238861
PNG
(US10052306, 300 | rac-4-(2-((3aR,6aS)-5- benzylhex...)
Show SMILES OC(CN1C[C@@H]2CC(Cc3ccccc3)C[C@@H]2C1)c1ccc(O)cc1 |r,w:1.0,7.7|
Show InChI InChI=1S/C22H27NO2/c24-21-8-6-18(7-9-21)22(25)15-23-13-19-11-17(12-20(19)14-23)10-16-4-2-1-3-5-16/h1-9,17,19-20,22,24-25H,10-15H2/t17?,19-,20+,22?
PDB
MMDB

NCI pathway
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KEGG

UniProtKB/SwissProt

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PC cid
PC sid
UniChem
US Patent
n/an/a 13.9n/an/an/an/an/an/a



CADENT THERAPEUTICS, INC.

US Patent


Assay Description
To each well of the plate, 10 μL test compound, control (MK801) or HHnoCa buffer was added to a final concentration of 10 μM with a final c...


US Patent US10052306 (2018)


BindingDB Entry DOI: 10.7270/Q20R9RD3
More data for this
Ligand-Target Pair