Related Experiment Video
Updated: Apr 23, 2026

07:59
A Customizable Approach for the Enzymatic Production and Purification of Diterpenoid Natural Products
Published on: October 4, 2019
11.9K
Two new diterpenoids from Leonotis leonurus R. Br
Yuji Narukawa1, Miyuki Komori, Akiko Niimura
1Faculty of Pharmacy, Keio University, 1-5-30 Shibakoen, Minato-Ku, Tokyo, 105-8512, Japan.
Journal of Natural Medicines
|September 17, 2014
Summary
Researchers isolated two new diterpenoids and six known compounds from Leonotis leonurus. Some compounds exhibited estrogen sulfotransferase inhibitory activity, suggesting potential therapeutic applications.
Area of Science:
- Natural Products Chemistry
- Pharmacology
Background:
- Leonotis leonurus, commonly known as Lion's Tail, is a plant traditionally used in herbal medicine.
- Diterpenoids are a class of naturally occurring compounds with diverse biological activities.
Purpose of the Study:
- To isolate and characterize chemical constituents from the aerial parts of Leonotis leonurus.
- To evaluate the isolated compounds for estrogen sulfotransferase inhibitory activity.
Main Methods:
- Phytochemical investigation involving extraction and isolation techniques.
- Structure elucidation using comprehensive spectroscopic analyses (e.g., NMR, MS).
- In vitro assay to determine estrogen sulfotransferase inhibitory activity.
Main Results:
- Two novel diterpenoids, 14α-hydroxy-9α,13α-epoxylabd-5(6)-en-7-on-16,15-olide and 13ξ-hydroxylabd-5(6),8(9)-dien-7-on-16,15-olide, were identified.
- Six known diterpenoids were also isolated and characterized.
- Several isolated compounds demonstrated weak to moderate inhibition of estrogen sulfotransferase.
Conclusions:
- The chemical investigation of Leonotis leonurus yielded new diterpenoid structures.
- The identified compounds possess potential estrogen sulfotransferase inhibitory properties, warranting further investigation for therapeutic development.
Related Concept Videos
Antiasthma Drugs: Leukotriene Modifiers
2.2K
Leukotriene modifiers, or cysteinyl leukotriene receptor antagonists, are medications used to manage chronic asthma. These agents target specific inflammatory mediators produced during arachidonic acid metabolism, an essential process in generating inflammation in the body.
Leukotriene modifiers work through two distinct mechanisms:
Leukotriene modifiers work through two distinct mechanisms:
2.2K
Aromatic Hydrocarbon Cations: Structural Overview
3.4K
Cycloheptatriene is a neutral monocyclic unsaturated hydrocarbon that consists of an odd number of carbon atoms and an intervening sp3 carbon in the ring. The three double bonds in the ring correspond to 6 π electrons, which is a Huckel number, and therefore satisfies the criteria of 4n + 2 π electrons. However, the intervening sp3 carbon disrupts the continuous overlap of p orbitals. As a result, cycloheptatriene is not aromatic.
Removing one hydrogen from the intervening CH2 group...
Removing one hydrogen from the intervening CH2 group...
3.4K

