Benzaldehyde and azaphilone derivatives from the marine-derived fungus <i>Penicillium sclerotiorum</i> PSU-AMF89

Two new compounds including one benzaldehyde (<b>1</b>) and one azaphilone (<b>2</b>) were isolated from the marine-derived fungus <i>Penicillium sclerotiorum</i> PSU-AMF89 together with nine known compounds (<b>3</b>-<b>11</b>). Their structures were determined by spectroscopic evidences. The absolute configuration of <b>2</b> was established by comparison of the ECD data with those of the previously reported data of compound <b>7</b> as well as the biosynthetic consideration. Compound <b>1</b> displayed potent cytotoxic activity against MCF-7 cells with an IC<sub>50</sub> value of 9 <i>µ</i>M, compared with the standard drugs, tamoxifen and doxorubicin, whereas compounds <b>3</b> and <b>8</b> were moderately active against <i>Cryptococcus neoformans</i> and methicillin-resistant <i>Staphylococcus aureus</i>, respectively, with equal MIC values of 64 <i>µ</i>g/mL. In addition, they were non-cytotoxic to noncancerous Vero cells.

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Publication Details

Journal
Natural Product Research
Published
2024-12-26
DOI
https://doi.org/10.1080/14786419.2024.2442101
Citations
1
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.45
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article

Benzaldehyde and azaphilone derivatives from the marine-derived fungus Penicillium sclerotiorum PSU-AMF89

Jariya Sakayaroj, Saowanit Saithong, Souwalak Phongpaichit, Praphatsorn Saetang et al.
1 citations
Natural Product Research
Microbial Natural Products and Biosynthesis
0.45
article

Benzaldehyde and azaphilone derivatives from the marine-derived fungus Penicillium sclerotiorum PSU-AMF89

Jariya Sakayaroj, Saowanit Saithong, Souwalak Phongpaichit, Praphatsorn Saetang, Vatcharin Rukachaisirikul, Sita Preedanon
article en
1 citations

Abstract

Two new compounds including one benzaldehyde (<b>1</b>) and one azaphilone (<b>2</b>) were isolated from the marine-derived fungus <i>Penicillium sclerotiorum</i> PSU-AMF89 together with nine known compounds (<b>3</b>-<b>11</b>). Their structures were determined by spectroscopic evidences. The absolute configuration of <b>2</b> was established by comparison of the ECD data with those of the previously reported data of compound <b>7</b> as well as the biosynthetic consideration. Compound <b>1</b> displayed potent cytotoxic activity against MCF-7 cells with an IC<sub>50</sub> value of 9 <i>µ</i>M, compared with the standard drugs, tamoxifen and doxorubicin, whereas compounds <b>3</b> and <b>8</b> were moderately active against <i>Cryptococcus neoformans</i> and methicillin-resistant <i>Staphylococcus aureus</i>, respectively, with equal MIC values of 64 <i>µ</i>g/mL. In addition, they were non-cytotoxic to noncancerous Vero cells.

Natural Product ResearchVol. 40(7)
Prince of Songkla University (TH), National Science and Technology Development Agency (TH), Walailak University (TH)
Life below water
Openalex Percentile: Top 29%
Microbial Natural Products and Biosynthesis
0.45
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Benzaldehyde and azaphilone derivatives from the marine-derived fungus <i>Penicillium sclerotiorum</i> PSU-AMF89 — Jariya Sakayaroj, Saowanit Saithong, et al. · Natural Product Research (2024) | TGRS Research Map | TGRS