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Thioporidiols A and B: Two New Sulfur Compounds Discovered by Molybdenum-Catalyzed Oxidation Screening from Trichoderma polypori FKI-7382.


ABSTRACT: Two new sulfur compounds, designated thioporidiol A (1) and B (2), were discovered by the MoS-screening program from a culture broth of Trichoderma polypori FKI-7382. The structures of 1 and 2 were determined as C13 lipid structures with an N-acetylcysteine moiety. The relative configuration at the C-5 and C-6 position of 1 was determined by the derivatives of ?-methoxy-?-phenylacetic acid diesters, and the absolute configuration of the N-acetylcysteine moiety was determined by advanced Marfey's analysis. Compounds 1 and 2 were evaluated for anti-microbial, cytotoxic and anti-malarial activities. Compound 2 exhibited anti-microbial activity against Candida albicans ATCC 64548.

SUBMITTER: Matsuo H 

PROVIDER: S-EPMC7277456 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

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Thioporidiols A and B: Two New Sulfur Compounds Discovered by Molybdenum-Catalyzed Oxidation Screening from <i>Trichoderma polypori</i> FKI-7382.

Matsuo Hirotaka H   Noguchi Yoshihiko Y   Miyano Rei R   Higo Mayuka M   Nonaka Kenichi K   Sunazuka Toshiaki T   Takahashi Yōko Y   Ōmura Satoshi S   Nakashima Takuji T  

Antibiotics (Basel, Switzerland) 20200507 5


Two new sulfur compounds, designated thioporidiol A (<b>1</b>) and B (<b>2</b>), were discovered by the MoS-screening program from a culture broth of <i>Trichoderma</i> <i>polypori</i> FKI-7382. The structures of <b>1</b> and <b>2</b> were determined as C13 lipid structures with an <i>N</i>-acetylcysteine moiety. The relative configuration at the C-5 and C-6 position of <b>1</b> was determined by the derivatives of -methoxy--phenylacetic acid diesters, and the absolute configuration of the <i>  ...[more]

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