| Reaction Details |
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 | Report a problem with these data |
| Target | Phospholipase A2, membrane associated |
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| Ligand | BDBM50066343 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_156206 (CHEMBL767149) |
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| IC50 | 900±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, membrane associated |
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| Name: | Phospholipase A2, membrane associated |
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| Synonyms: | GIIC sPLA2 | Group IIA phospholipase A2 | NPS-PLA2 | Non-Pancreatic Secretory Phospholipase A2 | Non-pancreatic secretory phospholipase A2 (hnps-PLA2) | PA2GA_HUMAN | PLA2B | PLA2G2A | PLA2L | Phosphatidylcholine 2-acylhydrolase | Phospholipase A2 group IIA | RASF-A |
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| Type: | Hydrolase |
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| Mol. Mass.: | 16101.20 |
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| Organism: | Homo sapiens (Human) |
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| Description: | The human nps PLA2 was cloned, and expressed in E. coli. There was a refolding process in the purification. |
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| Residue: | 144 |
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| Sequence: | MKTLLLLAVIMIFGLLQAHGNLVNFHRMIKLTTGKEAALSYGFYGCHCGVGGRGSPKDAT
DRCCVTHDCCYKRLEKRGCGTKFLSYKFSNSGSRITCAKQDSCRSQLCECDKAAATCFAR
NKTTYNKKYQYYSNKHCRGSTPRC
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| BDBM50066343 |
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| n/a |
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| Name | BDBM50066343 |
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| 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 |
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| Type | Small organic molecule |
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| Emp. Form. | C24H34O5 |
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| Mol. Mass. | 402.5238 |
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| 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| |
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| Structure | 
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