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Antiproliferative Illudalane Sesquiterpenes from the Marine Sediment Ascomycete Aspergillus oryzae
- Source :
- Marine Drugs, Vol 19, Iss 333, p 333 (2021), Marine Drugs, Volume 19, Issue 6
- Publication Year :
- 2021
- Publisher :
- MDPI AG, 2021.
-
Abstract
- The new asperorlactone (1), along with the known illudalane sesquiterpene echinolactone D (2), two known pyrones, 4-(hydroxymethyl)-5-hydroxy-2H-pyran-2-one (3) and its acetate 4, and 4-hydroxybenzaldehyde (5), were isolated from a culture of Aspergillus oryzae, collected from Red Sea marine sediments. The structure of asperorlactone (1) was elucidated by HR-ESIMS, 1D, and 2D NMR, and a comparison between experimental and DFT calculated electronic circular dichroism (ECD) spectra. This is the first report of illudalane sesquiterpenoids from Aspergillus fungi and, more in general, from ascomycetes. Asperorlactone (1) exhibited antiproliferative activity against human lung, liver, and breast carcinoma cell lines, with IC50 values &lt<br />100 µM. All the isolated compounds were also evaluated for their toxicity using the zebrafish embryo model.
- Subjects :
- antiproliferative activity
Circular dichroism
Aquatic Organisms
Geologic Sediments
Stereochemistry
Cell Survival
QH301-705.5
Aspergillus oryzae
zebrafish toxicity
Pharmaceutical Science
Sesquiterpene
Marine fungu
01 natural sciences
Article
Illudalane
chemistry.chemical_compound
Inhibitory Concentration 50
Ascomycota
Cell Line, Tumor
Drug Discovery
Illudalane sesquiterpene
Animals
Humans
Hydroxymethyl
Biology (General)
marine fungus
Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
Indian Ocean
Zebrafish
Cell Proliferation
Polycyclic Sesquiterpenes
Aspergillus
biology
Molecular Structure
010405 organic chemistry
Fungi
illudalane sesquiterpenes
biology.organism_classification
0104 chemical sciences
010404 medicinal & biomolecular chemistry
chemistry
Cell culture
MCF-7 Cells
Female
Two-dimensional nuclear magnetic resonance spectroscopy
Sesquiterpenes
Subjects
Details
- Language :
- English
- ISSN :
- 16603397
- Volume :
- 19
- Issue :
- 333
- Database :
- OpenAIRE
- Journal :
- Marine Drugs
- Accession number :
- edsair.doi.dedup.....96d84d91e2329c855ce22c2e9f1146b8