Carpensterol: a new steroid from the ethyl acetate fraction of the fruits of <i>Solanum aculeastrum</i> Dunal (Solanaceae) with antimicrobial activities

From the ethyl acetate soluble fraction obtained by liquid-liquid partitioning of the hydro-ethanolic crude extract of <i>Solanum aculeastrum</i> fruits (Solanaceae), one new steroid (carpensterol, <b>1</b>) and five other well known (<b>2-6</b>) were isolated. Their structures were elucidated by analysis spectroscopic and spectrometric data as well as comparison to data reported in the literature. The evaluation of their antimicrobial activities using the broth microdilution method revealed that, compound <b>4</b> (MIC = 4.8 µg/mL) exhibited the greatest activity against <i>Escherichia coli</i>, with an MIC value lower than that of the reference drug, ciprofloxacin (MIC = 256 µg/mL). Additionally, compounds <b>1</b> and <b>4</b> exhibited moderate activity against <i>Staphylococcus aureus</i> and <i>Salmonella thyphi</i> (MIC = 78.125 μg/mL). These results provide baseline information for the potential use of the isolated steroids.

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Publication Details

Journal
Natural Product Research
Published
2025-12-08
DOI
https://doi.org/10.1080/14786419.2025.2598831
Primary Topic
Phytochemical Studies and Bioactivities
Type
article
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article

Carpensterol: a new steroid from the ethyl acetate fraction of the fruits of Solanum aculeastrum Dunal (Solanaceae) with antimicrobial activities

Emmanuel Talla, Christian Damblon, Siméon Pierre Chegaing Fodouop, Cyrille Ngoufack Tagousop et al.
Natural Product Research
Phytochemical Studies and Bioactivities
article

Carpensterol: a new steroid from the ethyl acetate fraction of the fruits of Solanum aculeastrum Dunal (Solanaceae) with antimicrobial activities

Emmanuel Talla, Christian Damblon, Siméon Pierre Chegaing Fodouop, Cyrille Ngoufack Tagousop, Jean Momeni, Donald Léonel Feugap Tsamo, Janvier Hinmara Tina, Olivier Sopkika Daouda
article en

Abstract

From the ethyl acetate soluble fraction obtained by liquid-liquid partitioning of the hydro-ethanolic crude extract of <i>Solanum aculeastrum</i> fruits (Solanaceae), one new steroid (carpensterol, <b>1</b>) and five other well known (<b>2-6</b>) were isolated. Their structures were elucidated by analysis spectroscopic and spectrometric data as well as comparison to data reported in the literature. The evaluation of their antimicrobial activities using the broth microdilution method revealed that, compound <b>4</b> (MIC = 4.8 µg/mL) exhibited the greatest activity against <i>Escherichia coli</i>, with an MIC value lower than that of the reference drug, ciprofloxacin (MIC = 256 µg/mL). Additionally, compounds <b>1</b> and <b>4</b> exhibited moderate activity against <i>Staphylococcus aureus</i> and <i>Salmonella thyphi</i> (MIC = 78.125 μg/mL). These results provide baseline information for the potential use of the isolated steroids.

Natural Product Research
Université de Yaoundé I (CM), University of Liège (BE), Sunshine Hospital (AU), University of Ngaoundéré (CM)
Openalex Percentile: Top 64%
Phytochemical Studies and Bioactivities
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