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Two new alkaloids produced by Dothideomycetes sp. BMC-101 isolated from the Magnolia grandiflora.
Wang, Lu-Sheng; Zong, Shi-Kun; Wu, Ping-Ping; Sun, Xiao-Long; Wu, Cheng-Zhu; Wang, Hao-Tian; Zhu, Mei-Lin.
Afiliación
  • Wang LS; Faculty of Pharmacy, Bengbu Medical College, Bengbu 233030, China.
  • Zong SK; Faculty of Pharmacy, Bengbu Medical College, Bengbu 233030, China.
  • Wu PP; Faculty of Pharmacy, Bengbu Medical College, Bengbu 233030, China.
  • Sun XL; Faculty of Pharmacy, Bengbu Medical College, Bengbu 233030, China.
  • Wu CZ; Faculty of Pharmacy, Bengbu Medical College, Bengbu 233030, China.
  • Wang HT; Faculty of Pharmacy, Bengbu Medical College, Bengbu 233030, China.
  • Zhu ML; Faculty of Pharmacy, Bengbu Medical College, Bengbu 233030, China.
J Asian Nat Prod Res ; 25(8): 731-740, 2023.
Article en En | MEDLINE | ID: mdl-36448521
ABSTRACT
AbstactA total of 16 fungal strains were isolated from fresh leaves and flowers of Magnolia grandiflora and the EtOAc extracts of them were assayed for antitumor activities. Among these, the fungus Dothideomycetes sp. BMC-101 with broad spectrum inhibition was selected for further study. Four alkaloids (1-4) including two new compounds (2-(hydroxyimino)-3-phenylpropanoyl)-L-phenylalanine (1) and 8-Acetyl-bisdethiobis(methylsulfanyl)apoaranotin (4)) were isolated from Dothideomycetes sp. BMC-101. The structure of 1 was characterized with an oxime moiety formed by the condensation of two phenylalanines. To our knowledge, this is the first report on a fungal phenylalanine derivative with an oxime moiety.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Asian Nat Prod Res Asunto de la revista: BOTANICA / QUIMICA Año: 2023 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Asian Nat Prod Res Asunto de la revista: BOTANICA / QUIMICA Año: 2023 Tipo del documento: Article País de afiliación: China