Funginocarterphenyls A–C: Thiazole-Containing <i>p</i> -Terphenyls from <i>Paulkirkia</i> sp. KT4190

Funginocarterphenyls A-C (1-3), which are thiazole-containing p-terphenyls, were identified from the fungus Paulkirkia sp. KT4190. Although structurally related p-terphenyls, such as nocarterphenyls (Wang et al. 2019) and echoside D (Deng et al. 2014), have been reported from actinomycete strains, these compounds represent the first examples isolated from filamentous fungi. The substitution pattern of the central hexasubstituted benzene ring was established via detailed HMBC (hetero multiple bond correlation) spectral analyses. This was further verified by DFT (density functional theory)-based chemical-shift calculations. Time-course analysis of compound production suggested their biosynthetic sequence.

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Publication Details

Journal
Bioscience Biotechnology and Biochemistry
Published
2026-03-21
DOI
https://doi.org/10.1093/bbb/zbag042
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00
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article

Funginocarterphenyls A–C: Thiazole-Containing p -Terphenyls from Paulkirkia sp. KT4190

H. Maeda, Masaru Hashimoto, Kazuaki Tanaka, Rui Kanehira
Bioscience Biotechnology and Biochemistry
Microbial Natural Products and Biosynthesis
article

Funginocarterphenyls A–C: Thiazole-Containing p -Terphenyls from Paulkirkia sp. KT4190

H. Maeda, Masaru Hashimoto, Kazuaki Tanaka, Rui Kanehira
article en

Abstract

Funginocarterphenyls A-C (1-3), which are thiazole-containing p-terphenyls, were identified from the fungus Paulkirkia sp. KT4190. Although structurally related p-terphenyls, such as nocarterphenyls (Wang et al. 2019) and echoside D (Deng et al. 2014), have been reported from actinomycete strains, these compounds represent the first examples isolated from filamentous fungi. The substitution pattern of the central hexasubstituted benzene ring was established via detailed HMBC (hetero multiple bond correlation) spectral analyses. This was further verified by DFT (density functional theory)-based chemical-shift calculations. Time-course analysis of compound production suggested their biosynthetic sequence.

Bioscience Biotechnology and Biochemistry
Hirosaki University (JP)
Openalex Percentile: Top 11%
Microbial Natural Products and Biosynthesis
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