Reaction Details |
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Target | Cytosolic phospholipase A2 |
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Ligand | BDBM50185356 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_475613 (CHEMBL923246) |
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IC50 | 18±n/a nM |
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Citation | Fritsche, A; Elfringhoff, AS; Fabian, J; Lehr, M 1-(2-Carboxyindol-5-yloxy)propan-2-ones as inhibitors of human cytosolic phospholipase A2alpha: synthesis, biological activity, metabolic stability, and solubility. Bioorg Med Chem16:3489-500 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Cytosolic phospholipase A2 |
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Name: | Cytosolic phospholipase A2 |
Synonyms: | CPLA2 | Lysophospholipase | PA24A_HUMAN | PLA2G4 | PLA2G4A | Phosphatidylcholine 2-acylhydrolase | Phospholipase A2 | Phospholipase A2 group IVA |
Type: | Protein |
Mol. Mass.: | 85219.30 |
Organism: | Homo sapiens (Human) |
Description: | P47712 |
Residue: | 749 |
Sequence: | MSFIDPYQHIIVEHQYSHKFTVVVLRATKVTKGAFGDMLDTPDPYVELFISTTPDSRKRT
RHFNNDINPVWNETFEFILDPNQENVLEITLMDANYVMDETLGTATFTVSSMKVGEKKEV
PFIFNQVTEMVLEMSLEVCSCPDLRFSMALCDQEKTFRQQRKEHIRESMKKLLGPKNSEG
LHSARDVPVVAILGSGGGFRAMVGFSGVMKALYESGILDCATYVAGLSGSTWYMSTLYSH
PDFPEKGPEEINEELMKNVSHNPLLLLTPQKVKRYVESLWKKKSSGQPVTFTDIFGMLIG
ETLIHNRMNTTLSSLKEKVNTAQCPLPLFTCLHVKPDVSELMFADWVEFSPYEIGMAKYG
TFMAPDLFGSKFFMGTVVKKYEENPLHFLMGVWGSAFSILFNRVLGVSGSQSRGSTMEEE
LENITTKHIVSNDSSDSDDESHEPKGTENEDAGSDYQSDNQASWIHRMIMALVSDSALFN
TREGRAGKVHNFMLGLNLNTSYPLSPLSDFATQDSFDDDELDAAVADPDEFERIYEPLDV
KSKKIHVVDSGLTFNLPYPLILRPQRGVDLIISFDFSARPSDSSPPFKELLLAEKWAKMN
KLPFPKIDPYVFDREGLKECYVFKPKNPDMEKDCPTIIHFVLANINFRKYRAPGVPRETE
EEKEIADFDIFDDPESPFSTFNFQYPNQAFKRLHDLMHFNTLNNIDVIKEAMVESIEYRR
QNPSRCSVSLSNVEARRFFNKEFLSKPKA
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BDBM50185356 |
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n/a |
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Name | BDBM50185356 |
Synonyms: | 1-(3-(4-octylphenoxy)-2-oxopropyl)-1H-indole-5-carboxylic acid | 1-[3-(4-octylphenoxy)-2-oxopropyl]indole-5-carboxylic acid | CHEMBL205892 |
Type | Small organic molecule |
Emp. Form. | C26H31NO4 |
Mol. Mass. | 421.5286 |
SMILES | CCCCCCCCc1ccc(OCC(=O)Cn2ccc3cc(ccc23)C(O)=O)cc1 |
Structure |
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