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Absolute configuration of fibaruretin B
Summary
A novel furan-oditerpenoid, fibaruretin B, was isolated from Arcangelisia flava roots. Its structure and absolute configurations were determined, revealing specific molecular arrangements and hydrogen bonding in its crystal form.
Area of Science:
- Natural Product Chemistry
- Organic Chemistry
- Phytochemistry
Background:
- Arcangelisia flava is a plant species known for its potential medicinal properties.
- Diterpenoids are a class of terpenes derived from isoprene units, often exhibiting diverse biological activities.
Purpose of the Study:
- To isolate and elucidate the structure of a novel compound from Arcangelisia flava roots.
- To determine the absolute configurations and crystal structure of the isolated compound, fibaruretin B.
Main Methods:
- Isolation of fibaruretin B from the roots of Arcangelisia flava.
- Spectroscopic analysis (e.g., NMR, MS) for structural determination.
- X-ray crystallography for absolute configuration and crystal structure analysis.
Main Results:
- Identification of fibaruretin B, a furan-oditerpenoid, with the chemical formula C(20)H(24)O(7).
- Determination of the absolute configurations at eight stereocenters (2, 3, 4, 4a, 7, 9, 10a, 10b) as S, R, S, R, S, S, S, and S, respectively.
- Crystal structure analysis revealed molecular chains linked by O-H⋯O hydrogen bonds and weak C-H⋯O interactions along the c axis.
Conclusions:
- Fibaruretin B is a newly identified furan-oditerpenoid with a defined stereochemical structure.
- The crystal structure provides insights into the intermolecular interactions and solid-state arrangement of fibaruretin B.
- This study contributes to the understanding of the chemical constituents of Arcangelisia flava.

