Structure and Absolute Configuration of Methyl (3R)-Malonyl-(13S)-hydroxycheilanth-17-en-19-oate, a Sesterterpene Derivative from the Roots of Aletris farinosa
Author:
Affiliation:
1. School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane 4072, Australia
2. Integria Healthcare, Brisbane 4113, Australia
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/np400035n
Reference14 articles.
1. Pharmacological Studies. I. Aletris Farinos**From the Research Laboratories of the Lydia E. Pinkham Medicine Company, Lynn, Mass.
2. The Truth about False Unicorn (Chamaelirium luteum): Total Synthesis of 23R,24S-Chiograsterol B Defines the Structure and Stereochemistry of the Major Saponins from this Medicinal Herb
3. Structure and Absolute Configuration of Helosides A and B, New Saponins from Chamaelirium luteum
4. Structure and Bioactivity of Steroidal Saponins Isolated from the Roots of Chamaelirium luteum (False Unicorn)
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