Related Experiment Video
Updated: Mar 6, 2026

Author Spotlight: Discovering New Alkaloids in Plants with Advanced Mass Spectrometry Techniques
Published on: March 8, 2024
Two new eudesmane-type sesquiterpenoids from Olanum lyratum
Sheng-Jun Dai1, Li Shen, Yan Ren
1School of Pharmaceutical Science, Yantai University, People's Republic of China. daishengjun_9@hotmail.com
Two novel eudesmane-type sesquiterpenoids, lyratol A-B, were isolated from Olanum lyratum. These compounds demonstrated significant cytotoxicity against P-388 and HT-29 cancer cell lines in vitro.
Area of Science:
- Natural Products Chemistry
- Medicinal Chemistry
- Pharmacology
Background:
- Olanum lyratum, a traditional medicinal plant, is a rich source of bioactive compounds.
- Sesquiterpenoids are a diverse class of natural products with a wide range of biological activities.
- Identifying novel compounds from natural sources is crucial for drug discovery.
Purpose of the Study:
- To isolate and characterize new eudesmane-type sesquiterpenoids from Olanum lyratum.
- To evaluate the in vitro cytotoxic activity of the isolated compounds against cancer cell lines.
Main Methods:
- Isolation of compounds using chromatographic techniques.
- Structure elucidation using extensive spectroscopic analyses (NMR, MS).
- In vitro cytotoxicity assays against P-388 and HT-29 cancer cells.
Main Results:
- Two new eudesmane-type sesquiterpenoids, named lyratol A (1) and lyratol B (2), were successfully isolated.
- The structures of lyratol A and B were fully elucidated.
- Both compounds exhibited significant cytotoxic effects on P-388 and HT-29 cancer cells.
Conclusions:
- Olanum lyratum yielded two novel sesquiterpenoids, lyratol A and B.
- Lyratol A and B possess notable in vitro anticancer properties.
- These findings suggest potential for developing new chemotherapeutic agents from Olanum lyratum.
Related Concept Videos
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Structure and Nomenclature of Epoxides
Base-Catalyzed Ring-Opening of Epoxides
Preparation of Epoxides
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...
α-Hydroxy Ketones via Reductive Coupling of Esters: Acyloin Condensation Overview

