| Literature DB >> 16697191 |
John S Schneekloth1, John L Sanders, John Hines, Craig M Crews.
Abstract
A combination of solid phase and solution phase synthetic methods have been used to complete the total synthesis of the neurotrophic lipopeptide aldehyde fellutamide B (2). The beta-hydroxy aliphatic tail was prepared by regioselective reductive opening of a cyclic sulfate, and later coupled to a solid phase resin. The synthetic compound was then examined in cytotoxicity and nerve growth factor (NGF) induction assays. A simplified analog of fellutamide B also showed activity.Entities:
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Year: 2006 PMID: 16697191 PMCID: PMC2507734 DOI: 10.1016/j.bmcl.2006.04.029
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823