Journal article

The design, synthesis, and anti-inflammatory evaluation of a drug-like library based on the natural product valerenic acid

FA Egbewande, N Nilsson, JM White, MJ Coster, RA Davis

Bioorganic and Medicinal Chemistry Letters | PERGAMON-ELSEVIER SCIENCE LTD | Published : 2017

Abstract

The plant natural product, valerenic acid (1) was chosen as a desirable scaffold for the generation of a novel screening library due to its drug-like physicochemical parameters (such as Log P, hydrogen bond donor/acceptor counts, and molecular weight). An 11-membered amide library (2–12) was subsequently generated using parallel solution-phase synthesis and Ghosez's reagent. The chemical structures of all semi-synthetic analogues (2–12) were elucidated following analysis of the NMR, MS, UV and IR data. The structures of compounds 8 and 11 were also confirmed by X-ray crystallographic analysis. All library members were evaluated for their ability to inhibit the release of IL-8 and TNF-α. Six ..

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University of Melbourne Researchers

Grants

Awarded by Australian Research Council


Funding Acknowledgements

This research was supported by National Health and Medical Research Council - Australia (Grant APP1024314 to R.A.D), the Australian Research Council for support towards NMR and MS equipment (Grant LE0668477 and LE0237908) and financial support (Grant LP120200339 to R.A.D.). W. Loa is acknowledged for the HRESIMS measurements. F.A.E. thanks Griffith University for Ph.D. scholarships (GUPRS and GUIPRS).