{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Dockendorff C"],"funding":["NHLBI NIH HHS","NHGRI NIH HHS"],"pagination":["2594-8"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC4469081"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["25(12)"],"pubmed_abstract":["A new series of potent inhibitors of cellular lipid uptake from HDL particles mediated by scavenger receptor, class B, type I (SR-BI) was identified. The series was identified via a high-throughput screen of the National Institutes of Health Molecular Libraries Small Molecule Repository (NIH MLSMR) that measured the transfer of the fluorescent lipid DiI from HDL particles to CHO cells overexpressing SR-BI. The series is characterized by a linear peptidomimetic scaffold with two adjacent amide groups, as well as an aryl-substituted heterocycle. Analogs of the initial hit were rapidly prepared via Ugi 4-component reaction, and select enantiopure compounds were prepared via a stepwise sequence. Structure-activity relationship (SAR) studies suggest an oxygenated arene is preferred at the weste"],"journal":["Bioorganic & medicinal chemistry letters"],"pubmed_title":["Discovery of bisamide-heterocycles as inhibitors of scavenger receptor BI (SR-BI)-mediated lipid uptake."],"pmcid":["PMC4469081"],"funding_grant_id":["P01 HL066105","U54 HG005032","R01 HL052212"],"pubmed_authors":["Yu M","Dockendorff C","Nieland TJ","Faloon PW","Bennion M","Krieger M","Nag PP","Palmer MA","Germain A","Schreiber SL","Perez JR","Penman M","Youngsaye W","Munoz B","Dandapani S"],"additional_accession":[]},"is_claimable":false,"name":"Discovery of bisamide-heterocycles as inhibitors of scavenger receptor BI (SR-BI)-mediated lipid uptake.","description":"A new series of potent inhibitors of cellular lipid uptake from HDL particles mediated by scavenger receptor, class B, type I (SR-BI) was identified. The series was identified via a high-throughput screen of the National Institutes of Health Molecular Libraries Small Molecule Repository (NIH MLSMR) that measured the transfer of the fluorescent lipid DiI from HDL particles to CHO cells overexpressing SR-BI. The series is characterized by a linear peptidomimetic scaffold with two adjacent amide groups, as well as an aryl-substituted heterocycle. Analogs of the initial hit were rapidly prepared via Ugi 4-component reaction, and select enantiopure compounds were prepared via a stepwise sequence. Structure-activity relationship (SAR) studies suggest an oxygenated arene is preferred at the weste","dates":{"release":"2015-01-01T00:00:00Z","publication":"2015 Jun","modification":"2025-04-04T11:08:23.675Z","creation":"2019-03-27T01:53:31Z"},"accession":"S-EPMC4469081","cross_references":{"pubmed":["25958245"],"doi":["10.1016/j.bmcl.2015.03.074"]}}