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Pyranone Derivatives With Antitumor Activities, From the Endophytic Fungus Phoma sp. YN02-P-3.
Yu, Chong; Nian, Yin; Chen, Huanhua; Liang, Shuwen; Sun, Mengyang; Pei, Yuehu; Wang, Haifeng.
Affiliation
  • Yu C; School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.
  • Nian Y; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, China.
  • Chen H; School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.
  • Liang S; School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.
  • Sun M; School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.
  • Pei Y; School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.
  • Wang H; Department of Medicinal Chemistry and Natural Medicine Chemistry, College of Pharmacy, Harbin Medical University, HarBin, China.
Front Chem ; 10: 950726, 2022.
Article in En | MEDLINE | ID: mdl-35873041
Two new pyranone derivatives phomapyrone A (2) and phomapyrone B (3), one new coumarin 11S, 13R-(+)-phomacumarin A (1), three known pyranones (4-6), together with three known amide alkaloids fuscoatramides A-C (7-9), as well as 9S, 11R-(+)-ascosalitoxin (10) were isolated from the endophytic fungus Phoma sp. YN02-P-3, which was isolated from the healthy leaf tissue of a Paulownia tree in Yunnan Province, China. Their structures were elucidated using extensive NMR spectroscopic and HRESIMS data and by comparing the information with literature data. In addition, all compounds were tested for their cytotoxicity activity against human tumor cell lines, and the results showed that new compounds 1-3 showed moderate inhibitory activity against the HL-60 cell line with IC50 values of 31.02, 34.62, and 27.90 µM, respectively.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Chem Year: 2022 Document type: Article Affiliation country: China Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Chem Year: 2022 Document type: Article Affiliation country: China Country of publication: Switzerland