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Compile Data Set for Download or QSAR

Found 1 hit Enz. Inhib. hit(s) with Target = 'Glutamate receptor ionotropic, NMDA 2B' and Ligand = 'BDBM521616'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/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))
BDBM521616
PNG
(US11149054, Compound 4585)
Show SMILES CO[C@H]1CC[C@](O)(CC[C@@H](C)[C@H]2CC[C@H]3[C@@H]4CC[C@H]5C[C@@](O)(CC[C@]5(C)[C@H]4CC[C@]23C)C(F)(F)F)CC1 |r,wU:18.18,26.28,14.13,20.20,24.25,11.10,5.6,29.33,wD:15.15,20.34,9.9,5.5,2.1,(9.47,-.28,;7.99,-.68,;6.9,.41,;7.3,1.9,;6.21,2.99,;4.72,2.59,;4.72,4.13,;3.21,2.27,;2.18,3.41,;.68,3.09,;-.35,4.24,;.2,1.63,;1.11,.38,;.2,-.86,;-1.26,-.39,;-2.6,-1.16,;-2.6,-2.7,;-3.93,-3.47,;-5.27,-2.7,;-6.6,-3.47,;-7.93,-2.7,;-9.02,-3.79,;-7.93,-1.16,;-6.6,-.39,;-5.27,-1.16,;-5.27,.38,;-3.93,-.39,;-3.93,1.15,;-2.6,1.92,;-1.26,1.15,;-1.1,2.68,;-9.47,-2.7,;-10.24,-1.36,;-10.24,-4.03,;-11.01,-2.7,;4.32,1.1,;5.41,.01,)|
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a 166n/an/an/an/a


TBA

Assay Description
The whole-cell patch-clamp technique was used to investigate the effects of positive allosteric modulating activity of test compounds on GlunN1/GluN2...


Citation and Details

BindingDB Entry DOI: 10.7270/Q24X5BZR
More data for this
Ligand-Target Pair