Reaction Details |
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Target | Endothelial lipase |
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Ligand | BDBM50506501 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1825986 (CHEMBL4325750) |
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IC50 | 0.900000±n/a nM |
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Citation | Tora, G; Kim, SH; Pi, Z; Johnson, JA; Jiang, J; Phillips, M; Lloyd, J; Abell, LM; Lu, H; Locke, G; Adam, LP; Taylor, DS; Yin, X; Behnia, K; Zhao, L; Yang, R; Basso, M; Caporuscio, C; Chen, AY; Liu, E; Kirshgessner, T; Onorato, JM; Ryan, C; Traeger, SC; Gordon, D; Wexler, RR; Finlay, HJ Identification of Reversible Small Molecule Inhibitors of Endothelial Lipase (EL) That Demonstrate HDL-C Increase In Vivo. J Med Chem63:1660-1670 (2020) [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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BDBM50506501 |
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n/a |
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Name | BDBM50506501 |
Synonyms: | CHEMBL4563019 |
Type | Small organic molecule |
Emp. Form. | C22H18F2N6O6S2 |
Mol. Mass. | 564.542 |
SMILES | NS(=O)(=O)NCc1nnc(o1)C(=O)c1nc2cc(F)c(cc2s1)-c1ccc(C(=O)N2CCOCC2)c(F)c1 |
Structure |
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