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Pseudocercones A-C, three new polyketide derivatives from the endophytic fungus Pseudocercospora sp. TSS-1.
Peng, Wei-Wei; Kuang, Min; Huang, Yuan-Tao; Li, Mei-Fang; Zheng, Yu-Ting; Xu, Li; Tan, Jian-Bing; Kang, Feng-Hua; Tan, Hai-Bo; Zou, Zhen-Xing.
Afiliação
  • Peng WW; Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, P. R. China.
  • Kuang M; Hunan Key Laboratory of Diagnostic and Therapeutic Drug Research for Chronic Diseases, Central South University, Changsha, P. R. China.
  • Huang YT; Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, P. R. China.
  • Li MF; Hunan Key Laboratory of Diagnostic and Therapeutic Drug Research for Chronic Diseases, Central South University, Changsha, P. R. China.
  • Zheng YT; Affiliated Haikou Hospital of Xiangya School of Medicine, Central South University, Haikou, P. R. China.
  • Xu L; Affiliated Haikou Hospital of Xiangya School of Medicine, Central South University, Haikou, P. R. China.
  • Tan JB; Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, P. R. China.
  • Kang FH; Hunan Key Laboratory of Diagnostic and Therapeutic Drug Research for Chronic Diseases, Central South University, Changsha, P. R. China.
  • Tan HB; Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, P. R. China.
  • Zou ZX; Hunan Key Laboratory of Diagnostic and Therapeutic Drug Research for Chronic Diseases, Central South University, Changsha, P. R. China.
Nat Prod Res ; : 1-8, 2022 Oct 29.
Article em En | MEDLINE | ID: mdl-36308293
Chemical investigation of an EtOAc extract of the endophytic fungus Pseudocercospora sp. TSS-1 led to the isolation of three new polyketide derivatives, including one benzophenon derivative (1), two spirocyclic polyketides (4 and 5), along with four known compounds (2, 3, 6 and 7). Their structures and the absolute configurations were characterized by means of NMR, HRESIMS, 13C NMR and theoretical electronic circular dichroism calculations. Furthermore, all compounds were evaluated for their antibacterial activity against four microbial pathogens (Staphylococcus aureus, Enterococcus faecalis, Pseudomonas aeruginosa and Escherichia coli), and compounds 1, 2, 3 and 5 displayed significant selective antibacterial activity against S. aureus with MIC values ranging from 3.9 to 7.8 µg/mL.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Prod Res Ano de publicação: 2022 Tipo de documento: Article País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Prod Res Ano de publicação: 2022 Tipo de documento: Article País de publicação: Reino Unido