Reaction Details |
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Target | Phospholipase A2, membrane associated |
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Ligand | BDBM50055429 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_156196 (CHEMBL767139) |
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IC50 | 140000±n/a nM |
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Citation | Teshirogi, I; Matsutani, S; Shirahase, K; Fujii, Y; Yoshida, T; Tanaka, K; Ohtani, M Synthesis and phospholipase A2 inhibitory activity of thielocin B3 derivatives. J Med Chem39:5183-91 (1997) [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 |
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 |
Type: | Hydrolase |
Mol. Mass.: | 16101.20 |
Organism: | Homo sapiens (Human) |
Description: | The human nps PLA2 was cloned, and expressed in E. coli. There was a refolding process in the purification. |
Residue: | 144 |
Sequence: | MKTLLLLAVIMIFGLLQAHGNLVNFHRMIKLTTGKEAALSYGFYGCHCGVGGRGSPKDAT
DRCCVTHDCCYKRLEKRGCGTKFLSYKFSNSGSRITCAKQDSCRSQLCECDKAAATCFAR
NKTTYNKKYQYYSNKHCRGSTPRC
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BDBM50055429 |
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n/a |
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Name | BDBM50055429 |
Synonyms: | 4-[[[4-[[[5-[[[[(Benzyloxycarbonyl)methyl]amino]methyl]2,4-dihydroxy-3,6-dimethylphenyl]carbonyl]oxy]-2-methoxy-3,5,6-trimethylphenyl]carbonyl]-2-methoxy-3,5,6-trimethylbenzoic acid | CHEMBL359151 |
Type | Small organic molecule |
Emp. Form. | C39H43NO12 |
Mol. Mass. | 717.7582 |
SMILES | CC1C(OC(=O)c2c(C)c(C)c(OC(=O)c3c(C)c(CNCC(=O)OCc4ccccc4)c(O)c(C)c3O)c(C)c2O)C(C)=C(C)C(C(O)=O)C1=O |t:46| |
Structure |
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