Synthesis and evaluation of macrocyclic diarylether heptanoid natural products and their analogs

Bryant, V.C., Kumar, G.D.K., Nyong, A.M. and Natarajan, A. (2012) Synthesis and evaluation of macrocyclic diarylether heptanoid natural products and their analogs. Bioorganic and Medicinal Chemistry Letters, 22(1), pp. 245-248. (doi: 10.1016/j.bmcl.2011.11.025)

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Publisher's URL: http://dx.doi.org/10.1016/j.bmcl.2011.11.025

Abstract

The macrocyclic diarylether heptanoid (MDEH) natural products have been used in folk medicine for centuries. MDEHs are reported to exert anti-tumor properties by inhibiting the activation of NF-κB. Here we report the synthesis of a small MDEH library (first reported synthesis of racemic platycarynol) using a Grubbs cross metathesis/Ullmann cyclization strategy. Evaluation of the library led to the identification of MDEH 9b which sensitizes pancreatic cancer cells to gemcitabine mediated growth inhibition and apoptosis.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Gaddale Devanna, Dr Kishore Kumar
Authors: Bryant, V.C., Kumar, G.D.K., Nyong, A.M., and Natarajan, A.
College/School:College of Science and Engineering > School of Chemistry
Journal Name:Bioorganic and Medicinal Chemistry Letters
ISSN:0960-894X
ISSN (Online):1464-3405

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