Related Experiment Video
Updated: Aug 13, 2026

11:04
Preparation of Enantiopure Non-Activated Aziridines and Synthesis of Biemamide B, D, and epiallo-Isomuscarine
Published on: June 13, 2022
Two new alkaloids from artabotrys uncinatus
1Graduate Institute of Natural Products, Kaohsiung Medical College, Kaohsiung 807, Taiwan.
Journal of Natural Products
|September 10, 1999
Summary
Two new compounds, artabonatine A and artabonatine B, were isolated from Artabotrys uncinatus fruits. Their structures were determined using spectroscopic methods, expanding knowledge of plant-derived alkaloids.
Area of Science:
- Natural Product Chemistry
- Phytochemistry
- Organic Chemistry
Background:
- Artabotrys uncinatus is a plant species known for its potential medicinal properties.
- Aporphine alkaloids are a class of natural products with diverse biological activities.
- Previous research has identified various compounds from the Artabotrys genus.
Purpose of the Study:
- To isolate and characterize novel compounds from the fresh unripe fruits of Artabotrys uncinatus.
- To elucidate the chemical structures of the newly discovered compounds.
- To contribute to the understanding of the phytochemical profile of Artabotrys uncinatus.
Main Methods:
- Extraction and isolation of compounds from plant material.
- Structure elucidation using spectroscopic techniques including UV, IR, NMR, and MS.
- Comparison with known compounds for identification.
Main Results:
- Isolation and characterization of a novel oxazoloaporphine, artabonatine A (1).
- Isolation and characterization of a new 7-hydroxyaporphine, artabonatine B (2).
- Identification of five known compounds from the same plant source.
Conclusions:
- Artabotrys uncinatus fruits are a source of novel aporphine alkaloids.
- The identified compounds, artabonatine A and B, represent new chemical entities.
- The structural characterization provides valuable data for further pharmacological investigations.
More Related Videos
Related Concept Videos
Drugs that Stabilize Microtubules
Microtubules are dynamic structures that undergo cycles of catastrophe and rescue. The microtubules play a central role in cell division by forming the spindle apparatus for segregating the chromosomes. This makes them ideal targets for regulating dividing cells in tumors and malignant cancer cells. Microtubule stabilizing drugs help stabilize the microtubule formation and promote its polymerization. Paclitaxel was the first microtubule stabilizing agent used as anticancer drug in chemotherapy...
Drugs that Destabilize Microtubules
Microtubules are dynamic structures and can be regulated by microtubule targeting agents (MTAs). Microtubule destabilizing drugs are a class of MTAs that destabilize and prevent microtubules' polymerization. Both natural and synthetic chemicals can be found under this class of drugs. Vincristine and vinblastine, two vinca alkaloids, and colchicine were among the first to be discovered. These drugs can affect cells in various ways, either by inducing a change in cell morphology, preventing...
Anthelminthic Agents
Anthelmintic drugs differ significantly from antiparasitic therapies targeting protozoa, primarily due to differences in parasite biology. Whereas most protozoal treatments act on proliferating cells, anthelmintics are typically directed against mature, nonproliferative helminths. The therapeutic approach considers the helminth's reliance on neuromuscular coordination, glucose metabolism, and microtubular integrity for survival, reproduction, and localization within the host. Most anthelmintics...

