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1 similar compounds to monomer 60835

Wt: 279.2
BDBM50138507

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50138507   
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
Transient receptor potential cation channel subfamily V member 1


(Homo sapiens (Human))
BDBM50138507
PNG
((7-Hydroxy-naphthalen-1-yl)-carbamic acid phenyl e...)
Show SMILES Oc1ccc2cccc(NC(=O)Oc3ccccc3)c2c1
Show InChI InChI=1S/C17H13NO3/c19-13-10-9-12-5-4-8-16(15(12)11-13)18-17(20)21-14-6-2-1-3-7-14/h1-11,19H,(H,18,20)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

PubMed
>1.00E+4n/an/an/an/an/an/an/an/a



Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL


Assay Description
Dislacement of [3H]-RTX binding to human vanilloid receptor subtype 1 expressed in HEK293 cell membranes (inactive)


Citation and Details
More data for this
Ligand-Target Pair
Vanilloid receptor


(Homo sapiens (Human))
BDBM50138507
PNG
((7-Hydroxy-naphthalen-1-yl)-carbamic acid phenyl e...)
Show SMILES Oc1ccc2cccc(NC(=O)Oc3ccccc3)c2c1
Show InChI InChI=1S/C17H13NO3/c19-13-10-9-12-5-4-8-16(15(12)11-13)18-17(20)21-14-6-2-1-3-7-14/h1-11,19H,(H,18,20)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

PubMed
n/an/a 6.30E+3n/an/an/an/an/an/a



Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL


Assay Description
Binding affinity towards cloned human vanilloid receptor subtype 1 in HEK293 cell membranes using [3H]-RTX as radioligand


Citation and Details
More data for this
Ligand-Target Pair