BDBM50269784 CHEMBL4104737

SMILES: O[C@@]1(CC(=O)Nc2ccc3[nH]c(=O)oc3c2)CC[C@H](Cc2ccc(F)cc2)CC1

InChI Key: InChIKey=KQKYIUVHVBZFBO-VVONHTQRSA-N

Data: 2 IC50

Find this compound or compounds like it in BindingDB or PDB:

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50269784   

Target/Host (Institution)	Ligand	Target/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	pH	Temp °C
Glutamate receptor ionotropic, NMDA 2B (Rattus norvegicus (Rat))	BDBM50269784 (CHEMBL4104737) Show SMILES O[C@@]1(CC(=O)Nc2ccc3[nH]c(=O)oc3c2)CC[C@H](Cc2ccc(F)cc2)CC1 |r,wU:18.20,wD:1.0,(13.05,-7.68,;13.82,-9.01,;12.28,-9.01,;11.51,-10.35,;12.28,-11.68,;9.97,-10.35,;9.2,-11.68,;9.98,-13.01,;9.21,-14.34,;7.67,-14.34,;6.64,-15.49,;5.22,-14.87,;3.89,-15.64,;5.38,-13.33,;6.89,-13.01,;7.67,-11.68,;13.82,-10.55,;15.15,-11.32,;16.48,-10.55,;17.81,-11.33,;19.15,-10.56,;20.48,-11.33,;21.81,-10.57,;21.81,-9.02,;23.15,-8.25,;20.47,-8.25,;19.14,-9.02,;16.48,-9.01,;15.15,-8.24,)| Show InChI InChI=1S/C22H23FN2O4/c23-16-3-1-14(2-4-16)11-15-7-9-22(28,10-8-15)13-20(26)24-17-5-6-18-19(12-17)29-21(27)25-18/h1-6,12,15,28H,7-11,13H2,(H,24,26)(H,25,27)/t15-,22-	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	40	n/a	n/a	n/a	n/a	n/a	n/a
Medicinal Chemistry Research Laboratory, Shionogi& Co Ltd, 1-1 Futabacho, 3-chome, Toyonaka 561-0825, Japan. Electronic address: kousuke.anan@shionogi.co.jp. Curated by ChEMBL					Assay Description Displacement of [3H]-ifenprodil from NR2B in Wistar rat brain membrane after 120 mins by liquid scintillation counting analysis				Bioorg Med Chem Lett 27: 4194-4198 (2017) Article DOI: 10.1016/j.bmcl.2017.06.076 BindingDB Entry DOI: 10.7270/Q2VX0K0Q
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2B (Mus musculus)	BDBM50269784 (CHEMBL4104737) Show SMILES O[C@@]1(CC(=O)Nc2ccc3[nH]c(=O)oc3c2)CC[C@H](Cc2ccc(F)cc2)CC1 |r,wU:18.20,wD:1.0,(13.05,-7.68,;13.82,-9.01,;12.28,-9.01,;11.51,-10.35,;12.28,-11.68,;9.97,-10.35,;9.2,-11.68,;9.98,-13.01,;9.21,-14.34,;7.67,-14.34,;6.64,-15.49,;5.22,-14.87,;3.89,-15.64,;5.38,-13.33,;6.89,-13.01,;7.67,-11.68,;13.82,-10.55,;15.15,-11.32,;16.48,-10.55,;17.81,-11.33,;19.15,-10.56,;20.48,-11.33,;21.81,-10.57,;21.81,-9.02,;23.15,-8.25,;20.47,-8.25,;19.14,-9.02,;16.48,-9.01,;15.15,-8.24,)| Show InChI InChI=1S/C22H23FN2O4/c23-16-3-1-14(2-4-16)11-15-7-9-22(28,10-8-15)13-20(26)24-17-5-6-18-19(12-17)29-21(27)25-18/h1-6,12,15,28H,7-11,13H2,(H,24,26)(H,25,27)/t15-,22-	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a	n/a
Medicinal Chemistry Research Laboratory, Shionogi& Co Ltd, 1-1 Futabacho, 3-chome, Toyonaka 561-0825, Japan. Electronic address: kousuke.anan@shionogi.co.jp. Curated by ChEMBL					Assay Description Antagonist activity at mouse NR2B expressed in Hek293 cells co-expressing mouse NR1 assessed as inhibition of glutamic acid/glycine-induced intracell...				Bioorg Med Chem Lett 27: 4194-4198 (2017) Article DOI: 10.1016/j.bmcl.2017.06.076 BindingDB Entry DOI: 10.7270/Q2VX0K0Q
					More data for this Ligand-Target Pair