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
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Calcium-independent phospholipase A2 (Homo sapiens (Human)) | BDBM50046268 (6-Bromomethylene-3-naphthalen-1-yl-tetrahydro-pyra...) | Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars | PubMed | n/a | n/a | 140 | n/a | n/a | n/a | n/a | n/a | n/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 (6-Bromomethylene-3-naphthalen-1-yl-tetrahydro-pyra...) | Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars | PubMed | n/a | n/a | >100 | n/a | n/a | n/a | n/a | n/a | n/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 (6-Bromomethylene-3-naphthalen-1-yl-tetrahydro-pyra...) | PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 800 | n/a | n/a | n/a | n/a | n/a | n/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 (6-Bromomethylene-3-naphthalen-1-yl-tetrahydro-pyra...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 800 | n/a | n/a | n/a | n/a | n/a | n/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 |