Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetPhospholipase A2
LigandBDBM50066343
Substrate/Competitorn/a
Meas. Tech.ChEMBL_156025 (CHEMBL763678)
IC50 500±n/a nM
Citation De Rosa, MGiordano, SScettri, ASodano, GSoriente, APastor, PGAlcaraz, MJPayá, M Synthesis and comparison of the antiinflammatory activity of manoalide and cacospongionolide B analogues. J Med Chem41:3232-8 (1998) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Phospholipase A2
Name:Phospholipase A2
Synonyms:Allergen Api m I | Allergen=Api m 1 | PA2_APIME | Phosphatidylcholine 2-acylhydrolase | Phospholipase A2 (Bee)
Type:PROTEIN
Mol. Mass.:19061.47
Organism:Apis mellifera
Description:ChEMBL_1277435
Residue:167
Sequence:
MQVVLGSLFLLLLSTSHGWQIRDRIGDNELEERIIYPGTLWCGHGNKSSGPNELGRFKHT
DACCRTHDMCPDVMSAGESKHGLTNTASHTRLSCDCDDKFYDCLKNSADTISSYFVGKMY
FNLIDTKCYKLEHPVTGCGERTEGRCLHYTVDKSKPKVYQWFDLRKY
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50066343
n/a
NameBDBM50066343
Synonyms:5-Hydroxy-4-[6-hydroxy-5-((2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl)-3,6-dihydro-2H-pyran-2-yl]-5H-furan-2-one | CHEMBL109073
TypeSmall organic molecule
Emp. Form.C24H34O5
Mol. Mass.402.5238
SMILES[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]-1=[#6]-[#6]-[#6](-[#8]-[#6]-1-[#8])-[#6]-1=[#6]-[#6](=O)-[#8]-[#6]-1-[#8] |t:15,23|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: