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4 similar compounds to monomer 50201479

Compile data set for download or QSAR
Wt: 254.2
BDBM50201501
Wt: 279.2
BDBM50201490
Wt: 268.2
BDBM50201492
Wt: 322.2
BDBM50201494

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50201501,50201490,50201492,50201494   
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
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50201492
PNG
(2-oxo-N-m-tolyl-2,3-dihydrobenzo[d]oxazole-4-carbo...)
Show SMILES Cc1cccc(NC(=O)c2cccc3oc(=O)[nH]c23)c1
Show InChI InChI=1S/C15H12N2O3/c1-9-4-2-5-10(8-9)16-14(18)11-6-3-7-12-13(11)17-15(19)20-12/h2-8H,1H3,(H,16,18)(H,17,19)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
109n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd

Curated by ChEMBL


Assay Description
Binding affinity to mGluR5


Bioorg Med Chem Lett 17: 1302-6 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.006
BindingDB Entry DOI: 10.7270/Q2H41R3G
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50201490
PNG
(CHEMBL391398 | N-(3-cyanophenyl)-2-oxo-2,3-dihydro...)
Show SMILES O=C(Nc1cccc(c1)C#N)c1cccc2oc(=O)[nH]c12
Show InChI InChI=1S/C15H9N3O3/c16-8-9-3-1-4-10(7-9)17-14(19)11-5-2-6-12-13(11)18-15(20)21-12/h1-7H,(H,17,19)(H,18,20)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
327n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd

Curated by ChEMBL


Assay Description
Binding affinity to mGluR5


Bioorg Med Chem Lett 17: 1302-6 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.006
BindingDB Entry DOI: 10.7270/Q2H41R3G
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50201494
PNG
(2-oxo-N-(3-(trifluoromethyl)phenyl)-2,3-dihydroben...)
Show SMILES FC(F)(F)c1cccc(NC(=O)c2cccc3oc(=O)[nH]c23)c1
Show InChI InChI=1S/C15H9F3N2O3/c16-15(17,18)8-3-1-4-9(7-8)19-13(21)10-5-2-6-11-12(10)20-14(22)23-11/h1-7H,(H,19,21)(H,20,22)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
485n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd

Curated by ChEMBL


Assay Description
Binding affinity to mGluR5


Bioorg Med Chem Lett 17: 1302-6 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.006
BindingDB Entry DOI: 10.7270/Q2H41R3G
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50201501
PNG
(2-oxo-N-phenyl-2,3-dihydrobenzo[d]oxazole-4-carbox...)
Show SMILES O=C(Nc1ccccc1)c1cccc2oc(=O)[nH]c12
Show InChI InChI=1S/C14H10N2O3/c17-13(15-9-5-2-1-3-6-9)10-7-4-8-11-12(10)16-14(18)19-11/h1-8H,(H,15,17)(H,16,18)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
2.20E+3n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd

Curated by ChEMBL


Assay Description
Binding affinity to mGluR5


Bioorg Med Chem Lett 17: 1302-6 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.006
BindingDB Entry DOI: 10.7270/Q2H41R3G
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50201492
PNG
(2-oxo-N-m-tolyl-2,3-dihydrobenzo[d]oxazole-4-carbo...)
Show SMILES Cc1cccc(NC(=O)c2cccc3oc(=O)[nH]c23)c1
Show InChI InChI=1S/C15H12N2O3/c1-9-4-2-5-10(8-9)16-14(18)11-6-3-7-12-13(11)17-15(19)20-12/h2-8H,1H3,(H,16,18)(H,17,19)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 104n/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at mGluR5 assessed as inhibition of Ca2+ efflux by FLIPR


Bioorg Med Chem Lett 17: 1302-6 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.006
BindingDB Entry DOI: 10.7270/Q2H41R3G
More data for this
Ligand-Target Pair