Structure of a Triterpenoid with Contact Insecticidal Activity from the Entomopathogenic Fungus Akanthomyces muscarius

A method has been developed for isolating individual compounds from the mycelium of the entomopathogenic fungus Akanthomyces muscarius responsible for contact insecticidal activity against sap-sucking pests. The stereochemical structure of the main insecticidal metabolite of triterpenoid nature—(3β,5α,8α,22E)-5,8-epidioxy-ergosta-6,22-dien-3-ol—has been established using a combination of nuclear magnetic resonance (NMR) spectroscopy and X-ray diffraction (XRD) analysis.

Authors

Institutions

Publication Details

Journal
Russian Journal of General Chemistry
Published
2026-02-19
DOI
https://doi.org/10.1134/s1070363226030096
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Structure of a Triterpenoid with Contact Insecticidal Activity from the Entomopathogenic Fungus Akanthomyces muscarius

D. G. Golovanov, G. V. Mitina, O. S. Yuzikhin
Russian Journal of General Chemistry
Microbial Natural Products and Biosynthesis
article

Structure of a Triterpenoid with Contact Insecticidal Activity from the Entomopathogenic Fungus Akanthomyces muscarius

D. G. Golovanov, G. V. Mitina, O. S. Yuzikhin
article en

Abstract

A method has been developed for isolating individual compounds from the mycelium of the entomopathogenic fungus Akanthomyces muscarius responsible for contact insecticidal activity against sap-sucking pests. The stereochemical structure of the main insecticidal metabolite of triterpenoid nature—(3β,5α,8α,22E)-5,8-epidioxy-ergosta-6,22-dien-3-ol—has been established using a combination of nuclear magnetic resonance (NMR) spectroscopy and X-ray diffraction (XRD) analysis.

Russian Journal of General ChemistryVol. 96(3)
Lomonosov Moscow State University (RU), All-Russian Research Institute of Agricultural Microbiology (RU), All-Russian Institute of Plant Protection (RU)
Openalex Percentile: Top 50%
Microbial Natural Products and Biosynthesis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.