Reaction Details |
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Target | Endothelial lipase |
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Ligand | BDBM50521232 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1883780 (CHEMBL4385279) |
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IC50 | 53±n/a nM |
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Citation | Johnson, JA; Tora, G; Pi, Z; Phillips, M; Yin, X; Yang, R; Zhao, L; Chen, AY; Taylor, DS; Basso, M; Rose, A; Behnia, K; Onorato, J; Chen, XQ; Abell, LM; Lu, H; Locke, G; Caporuscio, C; Galella, M; Adam, LP; Gordon, D; Wexler, RR; Finlay, HJ Sulfonylated Benzothiazoles as Inhibitors of Endothelial Lipase. ACS Med Chem Lett9:1263-1268 (2018) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Endothelial lipase |
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Name: | Endothelial lipase |
Synonyms: | EDL | EL | Endothelial cell-derived lipase | LIPE_HUMAN | LIPG |
Type: | Protein |
Mol. Mass.: | 56805.62 |
Organism: | Homo sapiens (Human) |
Description: | Q9Y5X9 |
Residue: | 500 |
Sequence: | MSNSVPLLCFWSLCYCFAAGSPVPFGPEGRLEDKLHKPKATQTEVKPSVRFNLRTSKDPE
HEGCYLSVGHSQPLEDCSFNMTAKTFFIIHGWTMSGIFENWLHKLVSALHTREKDANVVV
VDWLPLAHQLYTDAVNNTRVVGHSIARMLDWLQEKDDFSLGNVHLIGYSLGAHVAGYAGN
FVKGTVGRITGLDPAGPMFEGADIHKRLSPDDADFVDVLHTYTRSFGLSIGIQMPVGHID
IYPNGGDFQPGCGLNDVLGSIAYGTITEVVKCEHERAVHLFVDSLVNQDKPSFAFQCTDS
NRFKKGICLSCRKNRCNSIGYNAKKMRNKRNSKMYLKTRAGMPFRVYHYQMKIHVFSYKN
MGEIEPTFYVTLYGTNADSQTLPLEIVERIEQNATNTFLVYTEEDLGDLLKIQLTWEGAS
QSWYNLWKEFRSYLSQPRNPGRELNIRRIRVKSGETQRKLTFCTEDPENTSISPGRELWF
RKCRDGWRMKNETSPTVELP
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BDBM50521232 |
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n/a |
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Name | BDBM50521232 |
Synonyms: | CHEMBL4567596 |
Type | Small organic molecule |
Emp. Form. | C24H20ClN5O5S3 |
Mol. Mass. | 590.094 |
SMILES | NS(=O)(=O)NCc1nnc(o1)C(c1nc2ccc(cc2s1)-c1cccc(Cl)c1)S(=O)(=O)Cc1ccccc1 |
Structure |
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