Related Experiment Video
Updated: Jul 7, 2026
![Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60786.jpg&w=3840&q=50)
Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions
Published on: July 17, 2020
New phenantrene alkaloids from Cryptocarya crassinervia
Khalijah Awang1, A Hamid A Hadi, Nurdin Saidi
1Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur, Malaysia. khalijah@um.edu.my
Two new phenanthrene alkaloids, 2-hydroxyatherosperminine and N-demethyl-2-methoxyatherosperminine, were identified from the bark of Cryptocarya crassinervia. This discovery expands the known chemical diversity of this plant species.
Area of Science:
- Phytochemistry
- Natural Product Chemistry
- Organic Chemistry
Background:
- Cryptocarya crassinervia is a plant species known for its potential medicinal properties.
- The chemical constituents of plants are a rich source of novel compounds with diverse biological activities.
Purpose of the Study:
- To isolate and characterize new chemical compounds from the bark of Cryptocarya crassinervia.
- To contribute to the understanding of the phytochemical profile of this plant species.
Main Methods:
- Phytochemical investigation of Cryptocarya crassinervia bark.
- Isolation and purification of alkaloid compounds using chromatographic techniques.
- Structure elucidation of isolated compounds using spectroscopic methods (e.g., NMR, MS).
Main Results:
- Two new phenanthrene alkaloids were successfully isolated and identified.
- The new compounds were named 2-hydroxyatherosperminine (1) and N-demethyl-2-methoxyatherosperminine (2).
- The structures were confirmed through comprehensive spectroscopic analysis.
Conclusions:
- The bark of Cryptocarya crassinervia is a source of novel phenanthrene alkaloids.
- The identification of these new compounds adds to the known chemical diversity of Cryptocarya species.
- Further research may explore the biological activities of these newly discovered alkaloids.
More Related Videos
07:30A Direct, Regioselective and Atom-Economical Synthesis of 3-Aroyl-N-hydroxy-5-nitroindoles by Cycloaddition of 4-Nitronitrosobenzene with Alkynones
Published on: January 21, 2020
09:36Applications of Liquid-Chromatography Tandem Mass Spectrometry in Natural Products Research: Tropane Alkaloids as a Case Study
Published on: March 8, 2024
Related Concept Videos
Adrenergic Agonists: Chemistry and Structure-Activity Relationship
Aromatic ring substitutions: Substituting the aromatic ring with –OH groups at positions 3 and 4 yields catecholamines (e.g., epinephrine), which have a high affinity for adrenoceptors. Hydrogen bonding between –OH groups and receptors enhances adrenergic activity.
Separation of the aromatic...
Antifungal Agents
Preparation of 1° Amines: Hofmann and Curtius Rearrangement Overview
Drugs Affecting Neurotransmitter Release or Uptake
Aldehydes and Ketones with HCN: Cyanohydrin Formation Overview
Nomenclature of Aryl and Heterocyclic Amines