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BDBM50046268 6-Bromomethylene-3-naphthalen-1-yl-tetrahydro-pyran-2-one::6-[1-Bromo-meth-(E)-ylidene]-3-naphthalen-1-yl-tetrahydro-pyran-2-one::BTNP::CHEMBL6206

SMILES: Br\C=C1/CCC(C(=O)O1)c1cccc2ccccc12

InChI Key: InChIKey=BYUCSFWXCMTYOI-ZRDIBKRKSA-N

Data: 4 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50046268   
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
Calcium-independent phospholipase A2


(Homo sapiens (Human))
BDBM50046268
PNG
(6-Bromomethylene-3-naphthalen-1-yl-tetrahydro-pyra...)
Show SMILES Br\C=C1/CCC(C(=O)O1)c1cccc2ccccc12
Show InChI InChI=1S/C16H13BrO2/c17-10-12-8-9-15(16(18)19-12)14-7-3-5-11-4-1-2-6-13(11)14/h1-7,10,15H,8-9H2/b12-10+
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n/an/a 140n/an/an/an/an/an/a



Washington University School of Medicine

Curated by ChEMBL


Assay Description
Compounds were evaluated for the inhibitory activity against canine myocardial cytosolic calcium dependent phospholipase A2 .


J Med Chem 36: 95-100 (1993)


BindingDB Entry DOI: 10.7270/Q22J69XV
More data for this
Ligand-Target Pair
Calcium-independent phospholipase A2


(Homo sapiens (Human))
BDBM50046268
PNG
(6-Bromomethylene-3-naphthalen-1-yl-tetrahydro-pyra...)
Show SMILES Br\C=C1/CCC(C(=O)O1)c1cccc2ccccc12
Show InChI InChI=1S/C16H13BrO2/c17-10-12-8-9-15(16(18)19-12)14-7-3-5-11-4-1-2-6-13(11)14/h1-7,10,15H,8-9H2/b12-10+
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PubMed
n/an/a>100n/an/an/an/an/an/a



Washington University School of Medicine

Curated by ChEMBL


Assay Description
Compounds were evaluated for the inhibitory activity against canine myocardial cytosolic calcium dependent phospholipase A2 .


J Med Chem 36: 95-100 (1993)


BindingDB Entry DOI: 10.7270/Q22J69XV
More data for this
Ligand-Target Pair
Fatty-acid amide hydrolase 1 (aa 30-579)


(Rattus norvegicus (rat))
BDBM50046268
PNG
(6-Bromomethylene-3-naphthalen-1-yl-tetrahydro-pyra...)
Show SMILES Br\C=C1/CCC(C(=O)O1)c1cccc2ccccc12
Show InChI InChI=1S/C16H13BrO2/c17-10-12-8-9-15(16(18)19-12)14-7-3-5-11-4-1-2-6-13(11)14/h1-7,10,15H,8-9H2/b12-10+
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Article
PubMed
n/an/a 800n/an/an/an/an/an/a



Johnson& Johnson Pharmaceutical Research and Development

Curated by ChEMBL


Assay Description
Inhibition of FAAH in rat brain assessed as hydrolysis of anandamide


J Med Chem 51: 7327-43 (2009)


Article DOI: 10.1021/jm800311k
BindingDB Entry DOI: 10.7270/Q2J67HT8
More data for this
Ligand-Target Pair
Fatty-acid amide hydrolase 1


(Homo sapiens (Human))
BDBM50046268
PNG
(6-Bromomethylene-3-naphthalen-1-yl-tetrahydro-pyra...)
Show SMILES Br\C=C1/CCC(C(=O)O1)c1cccc2ccccc12
Show InChI InChI=1S/C16H13BrO2/c17-10-12-8-9-15(16(18)19-12)14-7-3-5-11-4-1-2-6-13(11)14/h1-7,10,15H,8-9H2/b12-10+
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 800n/an/an/an/an/an/a



Universit£ Catholique de Louvain

Curated by ChEMBL


Assay Description
Irreversible inhibition of fatty acid amide hydrolase


J Med Chem 48: 5059-87 (2005)


Article DOI: 10.1021/jm058183t
BindingDB Entry DOI: 10.7270/Q2J96753
More data for this
Ligand-Target Pair