Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/59379
Title: Semisynthesis and biological activity of stemofoline alkaloids
Authors: Morwenna C. Baird
Stephen G. Pyne
Alison T. Ung
Wilford Lie
Thanapat Sastraruji
Araya Jatisatienr
Chaiwat Jatisatienr
Srisulak Dheeranupattana
Jaturong Lowlam
Sukanya Boonchalermkit
Keywords: Biochemistry, Genetics and Molecular Biology
Chemistry
Medicine
Pharmacology, Toxicology and Pharmaceutics
Issue Date: 24-Apr-2009
Abstract: The semisynthesis of the Stemona alkaloids (3′R)-stemofolenol (1), (3′S)-stemofolenol (2), methylstemofoline (3), and (3′S)- hydroxystemofoline (5) and the unnatural analogues (11E)-methylstemofoline (15) and 3′R-hydroxystemofoline (11) has been achieved starting from (11Z)-1′,2′-didehydrostemofoline (4). This synthesis allowed, for the first time, access to diastereomerically enriched samples of 1 and 2 and the assignment of their absolute configurations at C-3′. These compounds were obtained in sufficient quantities to allow for their biological testing. In a quantitative assay as AChE inhibitors, (11Z)-1′,2′- didehydrostemofoline (4) and (3′S)-hydroxystemofoline (5) were found to be the most active. © 2009 American Chemical Society and American Society of Pharmacognosy.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=65649116635&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/59379
ISSN: 01633864
Appears in Collections:CMUL: Journal Articles

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