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BDBM107263 US8598345, 205::US8598345, Table 1-49/2-9

SMILES: Fc1ccc(NC(=O)c2cc(Oc3cncnc3)ccn2)nc1

InChI Key: InChIKey=VJCZZCNDIYFAPL-UHFFFAOYSA-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 = 107263   
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))
BDBM107263
PNG
(US8598345, 205 | US8598345, Table 1-49/2-9)
Show SMILES Fc1ccc(NC(=O)c2cc(Oc3cncnc3)ccn2)nc1
Show InChI InChI=1S/C15H10FN5O2/c16-10-1-2-14(20-6-10)21-15(22)13-5-11(3-4-19-13)23-12-7-17-9-18-8-12/h1-9H,(H,20,21,22)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

US Patent
n/an/a 364n/an/an/an/an/an/a



Vanderbilt University

US Patent


Assay Description
mGluR5 activity was determined in a cell-based assay.


US Patent US8598345 (2013)


BindingDB Entry DOI: 10.7270/Q2RR1WX8
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Rattus norvegicus (Rat))
BDBM107263
PNG
(US8598345, 205 | US8598345, Table 1-49/2-9)
Show SMILES Fc1ccc(NC(=O)c2cc(Oc3cncnc3)ccn2)nc1
Show InChI InChI=1S/C15H10FN5O2/c16-10-1-2-14(20-6-10)21-15(22)13-5-11(3-4-19-13)23-12-7-17-9-18-8-12/h1-9H,(H,20,21,22)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

US Patent
n/an/a 389n/an/an/an/an/an/a



Vanderbilt University

US Patent


Assay Description
mGluR5 activity was determined in a cell-based assay.


US Patent US8598345 (2013)


BindingDB Entry DOI: 10.7270/Q2RR1WX8
More data for this
Ligand-Target Pair