Four new compounds having an unusual 1,7-dioxadispiro[5.1.5.2]-12-ene-11-one tricyclic ring system (1-4), their potential precursor, 5R-hydroxy-1-(4-hydroxyl-phenyl)-eicosan-3-one (5), and two known compounds, aculeatins A (6) and B (7), have been isolated from Amomum aculeatum. All compounds were characterized by spectroscopic methods and the configurations were established by 2D NOE correlations. Compounds 1-4, 6 and 7 showed cytotoxic activity against several human cancer cell lines.
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http://dx.doi.org/10.1016/j.tetlet.2007.01.017 | DOI Listing |
PLoS Negl Trop Dis
February 2014
School of Pharmaceutical Sciences, University of Geneva, University of Lausanne, Geneva, Switzerland.
Background: The silent-information regulator 2 proteins, otherwise called sirtuins, are currently considered as emerging anti-parasitic targets. Nicotinamide, a pan-sirtuin inhibitor, is known to cause kinetoplast alterations and the arrested growth of T. cruzi, the protozoan responsible for Chagas disease.
View Article and Find Full Text PDFTetrahedron Lett
March 2007
Division of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, The Ohio State University, Columbus, OH 43210, USA.
Four new compounds having an unusual 1,7-dioxadispiro[5.1.5.
View Article and Find Full Text PDFJ Nat Prod
March 2008
Division of Medicinal Chemsitry and Pharmacognosy, The Ohio State University, Columbus, Ohio 43210, USA.
Phytochemistry
August 2001
Department of Applied BioSciences, Institute of Pharmaceutical Sciences, Swiss Federal Institute of Technology (ETH), Zurich, CH-8057 Zurich, Switzerland.
A new cytotoxic 1,7-dioxa-dispiro[5.1.5.
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