| Reaction Details |
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 | Report a problem with these data |
| Target | Phospholipase A2 group V |
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| Ligand | BDBM50591715 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_2201656 (CHEMBL5114364) |
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| IC50 | 3040±n/a nM |
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| Citation |  Jiang, X; Wu, K; Bai, R; Zhang, P; Zhang, Y Functionalized quinoxalinones as privileged structures with broad-ranging pharmacological activities. Eur J Med Chem229:0 (2022) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| Phospholipase A2 group V |
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| Name: | Phospholipase A2 group V |
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| Synonyms: | PA2G5_HUMAN | PLA2G5 | Phospholipase A2 group V | Secretory phospholipase A2, group V (sPLA2-V) |
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| Type: | Protein |
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| Mol. Mass.: | 15682.61 |
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| Organism: | Homo sapiens (Human) |
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| Description: | n/a |
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| Residue: | 138 |
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| Sequence: | MKGLLPLAWFLACSVPAVQGGLLDLKSMIEKVTGKNALTNYGFYGCYCGWGGRGTPKDGT
DWCCWAHDHCYGRLEEKGCNIRTQSYKYRFAWGVVTCEPGPFCHVNLCACDRKLVYCLKR
NLRSYNPQYQYFPNILCS
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| BDBM50591715 |
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| n/a |
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| Name | BDBM50591715 |
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| Synonyms: | CHEMBL5179709 |
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| Type | Small organic molecule |
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| Emp. Form. | C17H10Cl2N2O |
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| Mol. Mass. | 329.18 |
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| SMILES | Clc1ccc(cc1Cl)-c1ccc2n1c1ccccc1[nH]c2=O |
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| Structure | 
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