Reaction Details |
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Target | Phospholipase A2 |
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Ligand | BDBM50066343 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_156025 (CHEMBL763678) |
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IC50 | 500±n/a nM |
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Citation | De Rosa, M; Giordano, S; Scettri, A; Sodano, G; Soriente, A; Pastor, PG; Alcaraz, MJ; Payá, M Synthesis and comparison of the antiinflammatory activity of manoalide and cacospongionolide B analogues. J Med Chem41:3232-8 (1998) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Phospholipase A2 |
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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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BDBM50066343 |
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n/a |
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Name | BDBM50066343 |
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 |
Type | Small 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 |
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