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Terpenoids from the Sponge Sarcotragus sp. Collected in the South China Sea.
Xu, Jixiang; Wang, Mengxue; Liu, Zhaonan; Zhang, Wenjie; Ma, Junye; Li, Guoqiang; Li, Pinglin.
Afiliación
  • Xu J; Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, People's Republic of China.
  • Wang M; Laboratory of Marine Drugs and Biological Products, Pilot National Laboratory for MarineScience and Technology, Qingdao 266235, People's Republic of China.
  • Liu Z; Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, People's Republic of China.
  • Zhang W; Laboratory of Marine Drugs and Biological Products, Pilot National Laboratory for MarineScience and Technology, Qingdao 266235, People's Republic of China.
  • Ma J; Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, People's Republic of China.
  • Li G; Laboratory of Marine Drugs and Biological Products, Pilot National Laboratory for MarineScience and Technology, Qingdao 266235, People's Republic of China.
  • Li P; Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, People's Republic of China.
J Nat Prod ; 86(2): 330-339, 2023 02 24.
Article en En | MEDLINE | ID: mdl-36734533
Sarcotragusolides A-D (1-4), four new butenolide sesterterpenes featuring a rare methyl-transferred 6/6/6-tricyclic fused ring system with a butyrolactone moiety, and echinohalimane B (8), an unprecedented monocyclic diterpenoid featuring a 2,7-ring-opened halimane-type skeleton, were isolated from the sponge Sarcotragus sp. A γ-hydroxybutenolide sesterterpene derivative (5), a new scalarane sesterterpene (7), a new subersin-type diterpenoid (10), and two known terpenoids were also isolated and identified. The discovery of sarcotragusolides C and D (3 and 4) with an unprecedented inversion of configuration implied a distinct biosynthetic pathway. The structures of these compounds were elucidated based on their spectroscopic data, single-crystal X-ray diffraction, chemical derivatization, and quantum chemical calculations. Compounds 1a, 1b, and 2 presented modest cytotoxic activities against several human cancer cell lines.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Poríferos / Diterpenos / Antineoplásicos Límite: Animals / Humans Idioma: En Revista: J Nat Prod Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Poríferos / Diterpenos / Antineoplásicos Límite: Animals / Humans Idioma: En Revista: J Nat Prod Año: 2023 Tipo del documento: Article