Reaction Details |
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Target | Lipoprotein lipase |
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Ligand | BDBM50254341 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_559993 (CHEMBL1018743) |
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IC50 | 320±n/a nM |
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Citation | Goodman, KB; Bury, MJ; Cheung, M; Cichy-Knight, MA; Dowdell, SE; Dunn, AK; Lee, D; Lieby, JA; Moore, ML; Scherzer, DA; Sha, D; Suarez, DP; Murphy, DJ; Harpel, MR; Manas, ES; McNulty, DE; Annan, RS; Matico, RE; Schwartz, BK; Trill, JJ; Sweitzer, TD; Wang, DY; Keller, PM; Krawiec, JA; Jaye, MC Discovery of potent, selective sulfonylfuran urea endothelial lipase inhibitors. Bioorg Med Chem Lett19:27-30 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Lipoprotein lipase |
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Name: | Lipoprotein lipase |
Synonyms: | LIPL_RAT | Lpl |
Type: | PROTEIN |
Mol. Mass.: | 53093.31 |
Organism: | Rattus norvegicus |
Description: | ChEMBL_559993 |
Residue: | 474 |
Sequence: | MESKALLLVALGVWLQSLTAFRGGVAAADGGRDFSDIESKFALRTPEDTAEDTCHLIPGL
ADSVSNCHFNHSSKTFVVIHGWTVTGMYESWVPKLVAALYKREPDSNVIVVDWLYRAQQH
YPVSAGYTKLVGNDVARFINWLEEEFNYPLDNVHLLGYSLGAHAAGVAGSLTNKKVNRIT
GLDPAGPNFEYAEAPSRLSPDDADFVDVLHTFTRGSPGRSIGIQKPVGHVDIYPNGGTFQ
PGCNIGEAIRVIAEKGLGDVDQLVKCSHERSIHLFIDSLLNEENPSKAYRCNSKEAFEKG
LCLSCRKNRCNNVGYEINKVRAKRSSKMYLKTRSQMPYKVFHYQVKIHFSGTENDKQNNQ
AFEISLYGTVAESENIPFTLPEVATNKTYSFLIYTEVDIGELLMMKLKWKNDSYFRWSDW
WSSPSFVIEKIRVKAGETQKKVIFCAREKVSHLQKGKDAAVFVKCHDKSLKKSG
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BDBM50254341 |
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n/a |
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Name | BDBM50254341 |
Synonyms: | 1-(2-chlorophenyl)-3-(2-methyl-5-(piperidin-1-ylsulfonyl)furan-3-yl)urea | CHEMBL451911 |
Type | Small organic molecule |
Emp. Form. | C17H20ClN3O4S |
Mol. Mass. | 397.876 |
SMILES | Cc1oc(cc1NC(=O)Nc1ccccc1Cl)S(=O)(=O)N1CCCCC1 |
Structure |
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