Your browser doesn't support javascript.
loading
Sesquiterpenoids and meroterpenoids from a mangrove derived fungus Diaporthe sp. SCSIO 41011.
Luo, Xiao-Wei; Chen, Chun-Mei; Li, Kun-Long; Lin, Xiu-Ping; Gao, Cheng-Hai; Zhou, Xue-Feng; Liu, Yong-Hong.
Afiliación
  • Luo XW; Institute of Marine Drugs, Guangxi University of Chinese Medicine, Nanning, China.
  • Chen CM; CAS Key Laboratory of Tropical Marine Bio-resources and Ecology/Guangdong Key Laboratory of Marine Materia Medica/RNAM Center for Marine Microbiology, Institutions of South China Sea Ecology and Environmental Engineering, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzho
  • Li KL; University of Chinese Academy of Sciences, Beijing, China.
  • Lin XP; CAS Key Laboratory of Tropical Marine Bio-resources and Ecology/Guangdong Key Laboratory of Marine Materia Medica/RNAM Center for Marine Microbiology, Institutions of South China Sea Ecology and Environmental Engineering, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzho
  • Gao CH; University of Chinese Academy of Sciences, Beijing, China.
  • Zhou XF; CAS Key Laboratory of Tropical Marine Bio-resources and Ecology/Guangdong Key Laboratory of Marine Materia Medica/RNAM Center for Marine Microbiology, Institutions of South China Sea Ecology and Environmental Engineering, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzho
  • Liu YH; University of Chinese Academy of Sciences, Beijing, China.
Nat Prod Res ; 35(2): 282-288, 2021 Jan.
Article en En | MEDLINE | ID: mdl-31177836
ABSTRACT
One new sesquiterpenoid, 1-methoxypestabacillin B (1), along with one known sesquiterpenoid (2) and six known chrodrimanin-type meroterpenoids (3‒8) were obtained from the solid cultures of a mangrove endophytic fungus Diaporthe sp. SCSIO 41011. Their structures including the absolute configuration at C-6 of compound 1, were determined by extensive spectroscopic analyses and ECD calculations. Meanwhile, the X-ray crystal structures and absolute configurations of two previously reported chrodrimanins E (3) and H (6), are described for the first time. All the compounds were examined for HIV latency-reversal and anti-influenza A virus activities.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ascomicetos / Terpenos / Avicennia Idioma: En Revista: Nat Prod Res Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ascomicetos / Terpenos / Avicennia Idioma: En Revista: Nat Prod Res Año: 2021 Tipo del documento: Article País de afiliación: China