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Perylenequinone derivatives from the endolichenic fungus Phialocephala fortinii.
Song, Jintong; Xie, Fei; Luan, Xiaoyi; Xu, Ke; Qian, Lilin; Lu, Jinghui; Chang, Wenqiang; Wang, Xiaoning; Lou, Hongxiang.
Afiliação
  • Song J; Department of Natural Product Chemistry, Key Lab of Chemical Biology of Ministry of Education, School of Pharmaceutical Sciences, Shandong University, Jinan, P.R. China.
  • Xie F; Department of Natural Product Chemistry, Key Lab of Chemical Biology of Ministry of Education, School of Pharmaceutical Sciences, Shandong University, Jinan, P.R. China.
  • Luan X; Department of Pharmacy, Qilu Hospital of Shandong University, Jinan, P.R. China.
  • Xu K; Department of Natural Product Chemistry, Key Lab of Chemical Biology of Ministry of Education, School of Pharmaceutical Sciences, Shandong University, Jinan, P.R. China.
  • Qian L; Department of Natural Product Chemistry, Key Lab of Chemical Biology of Ministry of Education, School of Pharmaceutical Sciences, Shandong University, Jinan, P.R. China.
  • Lu J; The Second Hospital of Shandong University, Jinan, P.R. China.
  • Chang W; Department of Natural Product Chemistry, Key Lab of Chemical Biology of Ministry of Education, School of Pharmaceutical Sciences, Shandong University, Jinan, P.R. China.
  • Wang X; Department of Natural Product Chemistry, Key Lab of Chemical Biology of Ministry of Education, School of Pharmaceutical Sciences, Shandong University, Jinan, P.R. China.
  • Lou H; Department of Natural Product Chemistry, Key Lab of Chemical Biology of Ministry of Education, School of Pharmaceutical Sciences, Shandong University, Jinan, P.R. China.
Nat Prod Res ; 37(9): 1527-1535, 2023 May.
Article em En | MEDLINE | ID: mdl-35007177
ABSTRACT
Five undescribed perylenequinone derivatives (PQDs) phialocephalarins H - L (1 - 5), together with two known PQDs phialocephalarins A - B (6, 7) and one known spirobisnaphthalene palmarumycin P3 (8) were isolated from the endolichenic fungus Phialocephala fortinii. Their structures were elucidated on the basis of NMR and HRESIMS data as well as electronic circular dichroism (ECD) calculations. Compounds 1, 2, 4, and 6 - 8 were evaluated for cytotoxic activities against NCI-H460, NCI-H446, PC3, and EC109 cell lines. The results showed that compounds 1, 2, 6, and 8 showed cytotoxic activities against EC109 cells with IC50 values ranging from 24.5 to 33.3 µM.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ascomicetos / Antineoplásicos Idioma: En Revista: Nat Prod Res Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ascomicetos / Antineoplásicos Idioma: En Revista: Nat Prod Res Ano de publicação: 2023 Tipo de documento: Article