Rui-Yun Yang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Rui-Yun Yang has a total of 112 co-authors. Here are the top co-authors by number of shared publications:
Jun Li
Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), Guangxi Key Laboratory of Chemistry and Molecular Engineering of Medicinal Resources, University Engineering Research Center for Chemistry of Characteristic Medicinal Resources (Guangxi), School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin, People’s Republic of China
20 shared publicationsBen-Chao Li
State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin, P. R. China
7 shared publicationsTu-Xiang Mo
Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), Guangxi Key Laboratory of Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin, 541004, People's Republic of China
7 shared publicationsWei-Feng Xu
Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), Guangxi Key Laboratory of Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin, P. R. China
7 shared publications- Wei-Feng Xu
Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), Guangxi Key Laboratory of Chemistry and Molecular Engineering of Medicinal Resources, University Engineering Research Center for Chemistry of Characteristic Medicinal Resources (Guangxi), School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin, People’s Republic of China
7 shared publications Jia-Tong Zhou
Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), Guangxi Key Laboratory of Chemistry and Molecular Engineering of Medicinal Resources, University Engineering Research Center for Chemistry of Characteristic Medicinal Resources (Guangxi), School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin, People’s Republic of China
6 shared publications
Latest Publications
- Open Access
- 2 November 2026
- Published by Springer Nature in Natural Products and Bioprospecting
- Vol. 16 (1) , 97
Antioxidant metabolites from the endophytic fungus Aspergillus spelaeus
- 2 November 2026
- Published by Springer Nature in Natural Products and Bioprospecting
- Vol. 16 (1) , 97
Open AccessAntioxidant metabolites from the endophytic fungus Aspergillus spelaeus
- 23 July 2025
- Published by Springer Nature in Chemistry of Natural Compounds
- p. 1-3
A New Cyclopentenone Derivative from an Endophytic Fungus Aspergillus sp.
- 23 July 2025
- Published by Springer Nature in Chemistry of Natural Compounds
- p. 1-3
A New Cyclopentenone Derivative from an Endophytic Fungus Aspergillus sp.
- 2 May 2025
- Published by Elsevier in Phytochemistry
- Vol. 237, 114534
Anti-neuroinflammatory naphthol dimers from the marine-derived fungus Penicillium sp. HQ1-23
- 2 May 2025
- Published by Elsevier in Phytochemistry
- Vol. 237, 114534
Anti-neuroinflammatory naphthol dimers from the marine-derived fungus Penicillium sp. HQ1-23
- 30 March 2025
- Published by Elsevier in Phytochemistry
- Vol. 236, 114493
A series of meroterpenoids with highly oxygenated skeletons from the endophytic fungus Penicillium sp. and their anti-inflammatory activities
- 30 March 2025
- Published by Elsevier in Phytochemistry
- Vol. 236, 114493
A series of meroterpenoids with highly oxygenated skeletons from the endophytic fungus Penicillium sp. and their anti-inflammatory activities
- Open Access
- 18 October 2024
- Published by MDPI AG in Marine Drugs
- Vol. 22 (10) , 475
Talaroterpenoids A–F: Six New Seco-Terpenoids from the Marine-Derived Fungus Talaromyces aurantiacus
Six new highly oxidized seco-terpenoids, including three 3-nor-labdane type diterpenes, talaroterpenoids A–C (1–3), and three meroterpenoids containing an orthoester group, talaroterpenoids D–F (6–8), together with five known compounds (4–5 and 9–11), were isolated from the marine-derived fungus Talaromyces aurantiacus. Their chemical structures were elucidated through 1D, 2D NMR, HRESIMS, J-based configuration analysis (JBCA), computational ECD calculations, and single-crystal X-ray diffraction analysis. Compounds 1 and 2 contain an unusual 6,20-γ-lactone-bridged scaffold. Compounds 10 and 11 presented inhibitory effects on NO release in lipopolysaccharide (LPS)-induced BV-2 cells with IC50 values of 11.47 and 11.32 μM, respectively. Talaroterpenoid C (3) showed moderate antifungal activity against A. alternata and P. theae Steyaert.
- 18 October 2024
- Published by MDPI AG in Marine Drugs
- Vol. 22 (10) , 475
Open AccessTalaroterpenoids A–F: Six New Seco-Terpenoids from the Marine-Derived Fungus Talaromyces aurantiacus
Six new highly oxidized seco-terpenoids, including three 3-nor-labdane type diterpenes, talaroterpenoids A–C (1–3), and three meroterpenoids containing an orthoester group, talaroterpenoids D–F (6–8), together with five known compounds (4–5 and 9–11), were isolated from the marine-derived fungus Talaromyces aurantiacus. Their chemical structures were elucidated through 1D, 2D NMR, HRESIMS, J-based configuration analysis (JBCA), computational ECD calculations, and single-crystal X-ray diffraction analysis. Compounds 1 and 2 contain an unusual 6,20-γ-lactone-bridged scaffold. Compounds 10 and 11 presented inhibitory effects on NO release in lipopolysaccharide (LPS)-induced BV-2 cells with IC50 values of 11.47 and 11.32 μM, respectively. Talaroterpenoid C (3) showed moderate antifungal activity against A. alternata and P. theae Steyaert.
- 30 January 2024
- Published by Springer Nature in Chemistry of Natural Compounds
- Vol. 60 (1) , 189-191
Secondary Metabolites from the Endophytic Fungus Xylaria sp. GDG-102 by Osmac Strategy and Their Antibacterial Activities
- 30 January 2024
- Published by Springer Nature in Chemistry of Natural Compounds
- Vol. 60 (1) , 189-191
Secondary Metabolites from the Endophytic Fungus Xylaria sp. GDG-102 by Osmac Strategy and Their Antibacterial Activities
- 16 September 2023
- Published by Springer Nature in Chemistry of Natural Compounds
- Vol. 59 (5) , 1-3
Secondary Metabolites from the Fungus Metarhizium marquandii
- 16 September 2023
- Published by Springer Nature in Chemistry of Natural Compounds
- Vol. 59 (5) , 1-3
Secondary Metabolites from the Fungus Metarhizium marquandii
- Open Access
Triterpenoids from the Leaves of Cyclocarya paliurus and Their Glucose Uptake Activity in 3T3-L1 Adipocytes
Four new dammarane triterpenoid saponins cypaliurusides Z1–Z4 (1–4) and eight known analogs (5–12) were isolated from the leaves of Cyclocarya paliurus. The structures of the isolated compounds were determined using a comprehensive analysis of 1D and 2D NMR and HRESIMS data. The docking study demonstrated that compound 10 strongly bonded with PTP1B (a potential drug target for the treatment of type-II diabetes and obesity), hydrogen bonds, and hydrophobic interactions, verifying the importance of sugar unit. The effects of the isolates on insulin-stimulated glucose uptake in 3T3-L1 adipocytes were evaluated and three dammarane triterpenoid saponins (6, 7 and 10) were found to enhance insulin-stimulated glucose uptake in 3T3-L1 adipocytes. Furthermore, compounds 6, 7, and 10 exhibited potent abilities to promote insulin-stimulated glucose uptake in 3T3-L1 adipocytes in a dose-dependent manner. Thus, the abundant dammarane triterpenoid saponins from C. paliurus leaves exhibited stimulatory effects on glucose uptake with application potential as a antidiabetic treatment.
Open AccessTriterpenoids from the Leaves of Cyclocarya paliurus and Their Glucose Uptake Activity in 3T3-L1 Adipocytes
Four new dammarane triterpenoid saponins cypaliurusides Z1–Z4 (1–4) and eight known analogs (5–12) were isolated from the leaves of Cyclocarya paliurus. The structures of the isolated compounds were determined using a comprehensive analysis of 1D and 2D NMR and HRESIMS data. The docking study demonstrated that compound 10 strongly bonded with PTP1B (a potential drug target for the treatment of type-II diabetes and obesity), hydrogen bonds, and hydrophobic interactions, verifying the importance of sugar unit. The effects of the isolates on insulin-stimulated glucose uptake in 3T3-L1 adipocytes were evaluated and three dammarane triterpenoid saponins (6, 7 and 10) were found to enhance insulin-stimulated glucose uptake in 3T3-L1 adipocytes. Furthermore, compounds 6, 7, and 10 exhibited potent abilities to promote insulin-stimulated glucose uptake in 3T3-L1 adipocytes in a dose-dependent manner. Thus, the abundant dammarane triterpenoid saponins from C. paliurus leaves exhibited stimulatory effects on glucose uptake with application potential as a antidiabetic treatment.
- 2 March 2023
- Published by Springer Nature in Chemistry of Natural Compounds
- Vol. 59 (1) , 1-4
Cytochalasins from the Endophytic Fungus Fusarium sp. GDGJ-366
- 2 March 2023
- Published by Springer Nature in Chemistry of Natural Compounds
- Vol. 59 (1) , 1-4
Cytochalasins from the Endophytic Fungus Fusarium sp. GDGJ-366
- 1 January 2023
- Published by Springer Nature in Chemistry of Natural Compounds
- Vol. 59 (1) , 154-156
Secondary Metabolites from the Endophytic Fungus Xylaria grammica and Their Anti-Inflammatory Activities
- 1 January 2023
- Published by Springer Nature in Chemistry of Natural Compounds
- Vol. 59 (1) , 154-156
Secondary Metabolites from the Endophytic Fungus Xylaria grammica and Their Anti-Inflammatory Activities