Your browser doesn't support javascript.
loading
New Indole Alkaloids from the Fungus Talaromyces assiutensis JTY2.
Zhu, Hong-Quan; Feng, Shuo; Xie, Rong-Kun; Zhu, Zheng-Tian; Lou, Yong-Hao; Zhou, Xue-Ming; Song, Xin-Ming.
  • Zhu HQ; Key Laboratory of Tropical Medicinal Resource Chemistry of Ministry of Education Hainan, Normal University, Haikou, Hainan, 571158, China Tel.
  • Feng S; Key Laboratory of Tropical Medicinal Plant Chemistry of Hainan Province, College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou, Hainan, 571158, China.
  • Xie RK; Key Laboratory of Tropical Medicinal Resource Chemistry of Ministry of Education Hainan, Normal University, Haikou, Hainan, 571158, China Tel.
  • Zhu ZT; Key Laboratory of Tropical Medicinal Plant Chemistry of Hainan Province, College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou, Hainan, 571158, China.
  • Lou YH; Key Laboratory of Tropical Medicinal Resource Chemistry of Ministry of Education Hainan, Normal University, Haikou, Hainan, 571158, China Tel.
  • Zhou XM; Key Laboratory of Tropical Medicinal Plant Chemistry of Hainan Province, College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou, Hainan, 571158, China.
  • Song XM; Key Laboratory of Tropical Medicinal Resource Chemistry of Ministry of Education Hainan, Normal University, Haikou, Hainan, 571158, China Tel.
Chem Biodivers ; : e202400937, 2024 Apr 29.
Article en En | MEDLINE | ID: mdl-38682724
ABSTRACT
Three new indole alkaloids, named talatensindoids A-C (1-3), together with two known biogenetically related indole alkaloids tryptamine (4) and L-tryptophan (5) were isolated from the Talaromyces assiutensis JTY2 based on the guidance of OSMAC approach. The structures of these indole alkaloids were determined by comprehensive spectroscopic analyses. The absolute configuration of 3 was confirmed by X-ray crystallographic analysis. Compound 1 represent the rare example of a chlorine-substituted indole alkaloid from natural products. The inhibitory activity of compounds 1-5 against two phytopathogenic fungi and three phytopathogenic bacteria was evaluated. Compound 1 exhibited broad spectrum antibacterial activities.
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article