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Two new 5,6-epoxysterols from calcareous marine sponge Leucetta chagosensis.
Tang, Wei-Zhuo; Yang, Zhong-Zhen; Sun, Fan; Wang, Shu-Ping; Yang, Fan; Jiao, Wei-Hua; Lin, Hou-Wen.
Afiliação
  • Tang WZ; a College of Biological and Environmental Engineering, Changsha University , Changsha , People's Republic of China.
  • Yang ZZ; b Research Center for Marine Drugs, State Key Laboratory of Oncogenes and Related Genes, Department of Pharmacy, Renji Hospital, School of Medicine, Shanghai Jiao Tong University , Shanghai , People's Republic of China.
  • Sun F; b Research Center for Marine Drugs, State Key Laboratory of Oncogenes and Related Genes, Department of Pharmacy, Renji Hospital, School of Medicine, Shanghai Jiao Tong University , Shanghai , People's Republic of China.
  • Wang SP; b Research Center for Marine Drugs, State Key Laboratory of Oncogenes and Related Genes, Department of Pharmacy, Renji Hospital, School of Medicine, Shanghai Jiao Tong University , Shanghai , People's Republic of China.
  • Yang F; b Research Center for Marine Drugs, State Key Laboratory of Oncogenes and Related Genes, Department of Pharmacy, Renji Hospital, School of Medicine, Shanghai Jiao Tong University , Shanghai , People's Republic of China.
  • Jiao WH; b Research Center for Marine Drugs, State Key Laboratory of Oncogenes and Related Genes, Department of Pharmacy, Renji Hospital, School of Medicine, Shanghai Jiao Tong University , Shanghai , People's Republic of China.
  • Lin HW; b Research Center for Marine Drugs, State Key Laboratory of Oncogenes and Related Genes, Department of Pharmacy, Renji Hospital, School of Medicine, Shanghai Jiao Tong University , Shanghai , People's Republic of China.
Nat Prod Res ; 33(20): 2970-2976, 2019 Oct.
Article em En | MEDLINE | ID: mdl-30388889
Chemical investigation on CH2Cl2 extract of the marine sponge Leucetta chagosensis, collected from the South China Sea, afforded two new 5,6-epoxysterols, 5α,6α-epoxycholesta-8(14),22(E)-diene-3ß,7α-diol (1) and (24R)-24-ethyl-5α,6α-epoxycholesta-8(14),22(E)-diene-3ß,7α-diol (2) along with ten known related steroid analogs (3-12). Their structures were elucidated on the basis of NMR spectroscopic analyses, and comparison with the literature. All isolates were tested for cytotoxicity against three tumor cell lines only known compounds 11 and 12 exhibited notable cytotoxic activity against A549 (IC50: 3.0 and 5.6 µM), PC9 (2.0 and 15.6 µM), and MCF-7 (9.4 and 11.8 µM) cell lines, respectively.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Poríferos / Esteróis / Compostos de Epóxi Limite: Animals / Humans País/Região como assunto: Asia Idioma: En Revista: Nat Prod Res Ano de publicação: 2019 Tipo de documento: Article País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Poríferos / Esteróis / Compostos de Epóxi Limite: Animals / Humans País/Região como assunto: Asia Idioma: En Revista: Nat Prod Res Ano de publicação: 2019 Tipo de documento: Article País de publicação: Reino Unido