Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10595815 | Bioorganic & Medicinal Chemistry Letters | 2013 | 4 Pages |
Abstract
27-Nor-Î4-dafachronic acid was prepared in nine steps and 14% overall yield by two sequential 2-carbon homologations from 20β-carboxyaldehyde-4-pregnen-3-one. Its activity was evaluated in vivo, where it rescued the Mig phenotype of daf-9(rh50) Caenorhabditis elegans mutants and restored their normal resistance to oxidative stress. 27-Nor-Î4-dafachronic acid was also able to directly bind and activate DAF-12 in a transactivation cell-based luciferase reporter assay, although it was less active than the corresponding 25R-and 25S dafachronic acids. The binding mode of the 27-Nor steroid was studied by molecular dynamics using a homology model of the CeDAF-12 receptor.
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Authors
Gisela A. Samaja, Olga Castro, Lautaro D. Alvarez, MarÃa V. Dansey, Daiana S. Escudero, Adriana S. Veleiro, Adalà Pecci, Gerardo Burton,