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Structural and Stereochemical Studies of Five New Pregnane Steroids from the Stem Bark of Toona Ciliata Var. Pubescens

Overview
Journal Steroids
Publisher Elsevier
Specialty Biochemistry
Date 2011 Feb 26
PMID 21349279
Citations 2
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Abstract

Five new pregnane steroids, toonasterones A (1), B (2), (Z)-aglawone (3), (Z)-toonasterone C (4), and (E)-toonasterone C (5), were isolated from the stem bark of Toona ciliata var. pubescens. Their structures were elucidated by means of detailed spectroscopic (IR, MS, and 2D NMR) analysis, and the stereochemistry of 1 was secured by X-ray diffraction analysis. (Z)-aglawone (3) exhibited moderate inhibitory activity of protein tyrosine phosphatase 1B (PTP1B), a potential drug target for treatment of type-II diabetes and obesity, with an IC(50) value of 1.12 μg/mL.

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