Zhang Yeting, Shi Zhengyi, Zhao Chunhua, Li Lanqin, Chen Ming, Cao Yunfang, Wang Fengqing, Tao Bo, Huang Xinye, Guo Jieru, Qi Changxing, Sun Weiguang, Zhang Yonghui. Amoenucles A−F, novel nucleoside derivatives with TNF-α inhibitory activities from Aspergillus amoenus TJ507J. Chinese Journal of Natural Medicines, 2025, 23(1): 111-118. DOI: 10.1016/S1875-5364(25)60805-3
Citation: Zhang Yeting, Shi Zhengyi, Zhao Chunhua, Li Lanqin, Chen Ming, Cao Yunfang, Wang Fengqing, Tao Bo, Huang Xinye, Guo Jieru, Qi Changxing, Sun Weiguang, Zhang Yonghui. Amoenucles A−F, novel nucleoside derivatives with TNF-α inhibitory activities from Aspergillus amoenus TJ507J. Chinese Journal of Natural Medicines, 2025, 23(1): 111-118. DOI: 10.1016/S1875-5364(25)60805-3

Amoenucles A−F, novel nucleoside derivatives with TNF-α inhibitory activities from Aspergillus amoenus TJ507

  • Amoenucles A−F (1−6), six previously undescribed nucleoside derivatives, and two known analogs (7 and 8) were isolated from the culture of Aspergillus amoenus TJ507. Their structures were elucidated through spectroscopic analysis, single-crystal X-ray crystallography, and chemical reactions. Notably, 3 and 4 represent the first reported instances of nucleosides with an attached pyrrole moiety. Of particular significance, the absolute configuration of the sugar moiety of 1−4 was determined using nuclear magnetic resonance (NMR), electric circular dichroism (ECD) calculations, and a hydrolysis reaction, presenting a potentially valuable method for confirming nucleoside structures. Furthermore, 1, 2, and 5−8 exhibited potential tumor necrosis factor α (TNF-α) inhibitory activities, which may provide a novel chemical template for the development of agents targeting autoimmune and inflammatory diseases.
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