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TargetPhospholipase A2
LigandBDBM50250399
Substrate/Competitorn/a
Meas. Tech.ChEMBL_156025 (CHEMBL763678)
IC50 7500±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
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  Blast E-value cutoff:
BDBM50250399
n/a
NameBDBM50250399
Synonyms:5-Hydroxy-4-{(R)-6-hydroxy-5-[(E)-4-methyl-6-(2,6,6-trimethyl-cyclohex-1-enyl)-hex-3-enyl]-3,6-dihydro-2H-pyran-2-yl}-5H-furan-2-one | 5-Hydroxy-4-{6-hydroxy-5-[(E)-4-methyl-6-(2,6,6-trimethyl-cyclohex-1-enyl)-hex-3-enyl]-3,6-dihydro-2H-pyran-2-yl}-5H-furan-2-one | CHEMBL463914 | manoalide
TypeSmall organic molecule
Emp. Form.C25H36O5
Mol. Mass.416.5503
SMILESC\C(CCC1=C(C)CCCC1(C)C)=C/CCC1=CC[C@@H](O[C@H]1O)C1=CC(=O)O[C@H]1O |r,c:4,t:17,25|
Structure
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