Reaction Details |
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Target | Phospholipase A2, major isoenzyme |
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Ligand | BDBM50055287 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_156353 (CHEMBL761683) |
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IC50 | 610±n/a nM |
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Citation | Dillard, RD; Bach, NJ; Draheim, SE; Berry, DR; Carlson, DG; Chirgadze, NY; Clawson, DK; Hartley, LW; Johnson, LM; Jones, ND; McKinney, ER; Mihelich, ED; Olkowski, JL; Schevitz, RW; Smith, AC; Snyder, DW; Sommers, CD; Wery, JP Indole inhibitors of human nonpancreatic secretory phospholipase A2. 2. Indole-3-acetamides with additional functionality. J Med Chem39:5137-58 (1997) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Phospholipase A2, major isoenzyme |
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Name: | Phospholipase A2, major isoenzyme |
Synonyms: | Group IB phospholipase A2 | PA21B_PIG | PLA2G1B | Phosphatidylcholine 2-acylhydrolase | Phospholipase A2 |
Type: | Hydrolase; monomer or homodimer |
Mol. Mass.: | 16279.83 |
Organism: | Sus scrofa (pig) |
Description: | Purchased from Sigma. |
Residue: | 146 |
Sequence: | MKFLVLAVLLTVGAAQEGISSRALWQFRSMIKCAIPGSHPLMDFNNYGCYCGLGGSGTPV
DELDRCCETHDNCYRDAKNLDSCKFLVDNPYTESYSYSCSNTEITCNSKNNACEAFICNC
DRNAAICFSKAPYNKEHKNLDTKKYC
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BDBM50055287 |
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n/a |
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Name | BDBM50055287 |
Synonyms: | 4-(1-Benzyl-3-carbamoylmethyl-2-methyl-1H-indol-4-yloxy)-butyric acid | CHEMBL146572 |
Type | Small organic molecule |
Emp. Form. | C22H24N2O4 |
Mol. Mass. | 380.437 |
SMILES | Cc1c(CC(N)=O)c2c(OCCCC(O)=O)cccc2n1Cc1ccccc1 |
Structure |
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