A Novel Lactam and Two Rare Mycophenolic Acid Derivatives from the Fungus <i>Penicillium Sclerotiorum</i> JBHL321

A novel lactam penicillactam (1), two rare mycophenolic acid (MPA) derivatives penimycophens A and B (2 and 3), together with two known biogenetically related MPA derivatives (4 and 5) and a known alkaloid (6) were isolated from the Penicillium sclerotiorum JBHL321. The structures of these compounds were determined by comprehensive spectroscopic analyses. The absolute configuration of 1 was confirmed by electronic circular dichroism (ECD) calculations. Compound 1 represent the rare example of a oxygen bridge-linked lactam from natural products. Structurally, compounds 2 and 3 were rare MPA derivatives featuring a methoxy group at C-3. The inhibitory activity of compounds 1-6 against two phytopathogenic fungi, three phytopathogenic bacteria and four cancer cell lines were evaluated. Compounds 2-5 exhibited significant cytotoxic activity against HeLa, MCF-7, A549 and MGC-803 cells with IC<sub>50</sub> values in the low micromolar to nanomolar. Compound 3 exhibited especially cytotoxic activity against four different cell lines with IC<sub>50</sub> values ranging from 0.06-0.14 μM, compared to IC<sub>50</sub> values ranging from 0.62-2.51 μM for epirubicin.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2024-10-05
DOI
https://doi.org/10.1002/cbdv.202401962
Citations
2
Primary Topic
Antifungal resistance and susceptibility
Type
article
Field-Weighted Citation Impact
0.78
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article

A Novel Lactam and Two Rare Mycophenolic Acid Derivatives from the Fungus Penicillium Sclerotiorum JBHL321

Xue‐Ming Zhou, Yue Wang, Xin‐Ming Song, Jin-feng Du et al.
2 citations
Chemistry & Biodiversity
Antifungal resistance and susceptibility
0.78
article

A Novel Lactam and Two Rare Mycophenolic Acid Derivatives from the Fungus Penicillium Sclerotiorum JBHL321

Xue‐Ming Zhou, Yue Wang, Xin‐Ming Song, Jin-feng Du, Xue Feng Xu
article en
2 citations

Abstract

A novel lactam penicillactam (1), two rare mycophenolic acid (MPA) derivatives penimycophens A and B (2 and 3), together with two known biogenetically related MPA derivatives (4 and 5) and a known alkaloid (6) were isolated from the Penicillium sclerotiorum JBHL321. The structures of these compounds were determined by comprehensive spectroscopic analyses. The absolute configuration of 1 was confirmed by electronic circular dichroism (ECD) calculations. Compound 1 represent the rare example of a oxygen bridge-linked lactam from natural products. Structurally, compounds 2 and 3 were rare MPA derivatives featuring a methoxy group at C-3. The inhibitory activity of compounds 1-6 against two phytopathogenic fungi, three phytopathogenic bacteria and four cancer cell lines were evaluated. Compounds 2-5 exhibited significant cytotoxic activity against HeLa, MCF-7, A549 and MGC-803 cells with IC<sub>50</sub> values in the low micromolar to nanomolar. Compound 3 exhibited especially cytotoxic activity against four different cell lines with IC<sub>50</sub> values ranging from 0.06-0.14 μM, compared to IC<sub>50</sub> values ranging from 0.62-2.51 μM for epirubicin.

Chemistry & BiodiversityVol. 22(2)
University of Science and Technology (YE), Hainan Normal University (CN), Hainan University (CN)
Openalex Percentile: Top 27%
Antifungal resistance and susceptibility
0.78
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