Cladoic Acid, an Anti-<i>Trypanosoma cruzi</i> Polyketide from <i>Cladosporium</i> sp. TP-F2020

A new polyketide, cladoic acid, was isolated from a fungus of the genus <i>Cladosporium</i>. The structure of the highly oxygenated <i>trans</i>-decalin ring with an all-<i>E</i> triene side chain was elucidated by extensive spectroscopic analysis. The unique chair/twist-boat conformation of the <i>trans</i>-decalin core and the flexibility of the B-ring were demonstrated by computer-aided conformational analysis. Cladoic acid was active against <i>Trypanosoma cruzi</i> and inhibited the proliferation of amastigotes and epimastigotes with IC<sub>50</sub> values of 27 and 46 μM, respectively, but it did not show any appreciable activity against P388 murine leukemia cells, bacteria, or fungi, indicating it is a potential candidate for drug development against Chagas disease.

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Publication Details

Journal
Journal of Natural Products
Published
2024-08-05
DOI
https://doi.org/10.1021/acs.jnatprod.4c00567
Citations
3
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
1.34

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article

Cladoic Acid, an Anti-Trypanosoma cruzi Polyketide from Cladosporium sp. TP-F2020

Yasuhiro Igarashi, Keisuke Fukaya, Daisuke Urabe, Shiyang Lu et al.
3 citations
Journal of Natural Products
Microbial Natural Products and Biosynthesis
1.34
article

Cladoic Acid, an Anti-Trypanosoma cruzi Polyketide from Cladosporium sp. TP-F2020

Yasuhiro Igarashi, Keisuke Fukaya, Daisuke Urabe, Shiyang Lu, Junko Nakajima‐Shimada, Md. Masud Rana, Tatiana Ascencio Menjívar
article en
3 citations

Abstract

A new polyketide, cladoic acid, was isolated from a fungus of the genus <i>Cladosporium</i>. The structure of the highly oxygenated <i>trans</i>-decalin ring with an all-<i>E</i> triene side chain was elucidated by extensive spectroscopic analysis. The unique chair/twist-boat conformation of the <i>trans</i>-decalin core and the flexibility of the B-ring were demonstrated by computer-aided conformational analysis. Cladoic acid was active against <i>Trypanosoma cruzi</i> and inhibited the proliferation of amastigotes and epimastigotes with IC<sub>50</sub> values of 27 and 46 μM, respectively, but it did not show any appreciable activity against P388 murine leukemia cells, bacteria, or fungi, indicating it is a potential candidate for drug development against Chagas disease.

Journal of Natural ProductsVol. 87(8)
Gunma University (JP), Jose Matias Delgado University (SV), Toyama Prefectural University (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 19%
Microbial Natural Products and Biosynthesis
1.34
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