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1. Liu X.J. #; Su, H.G. #; Peng, X. R.; Bi, H.C.*; Qiu, M. H.*, An updated review of the genus Rhododendron since 2010: Traditional uses, phytochemistry, and pharmacology. Phytochemistry 2024, 217, 113899. £¨ÖпÆÔº2Çø£©
2. Su, H.G.; Liang, H.F.; Hu, G.L.; Zhou, L., Peng, X. R.*; Bi, H.C.*; Qiu, M. H.*, Applanoids A?E as the first examples of C-15/C-20 Michael adducts in Ganoderma triterpenoids and their PXR agonistic activity. Chinese journal of Chemistry, 2022, 40(22), 2633-2641. £¨Cover Story, ÖпÆÔº2Çø£©
3. Su, H.-G.#; Wang, Q. #; Zhou, L.; Peng, X.-R.*; Xiong, W.-Y.*; Qiu, M.-H.*, Functional triterpenoids from medicinal fungi Ganoderma applanatum: a continuous search for antiadipogenic agents. Bioorganic Chemistry, 2021,112, 104977.£¨ÖпÆÔº1Çø£©
4. Peng X.-R.#; Su, H.-G.#; Wang, H.-R.; Hu, G.-L.; Hu, K.; Zhou, L.; Qiu, M.-H.*, Applanmerotic acids A and B, two meroterpenoid dimers with an unprecedented polycyclic skeleton from Ganoderma applanatum that inhibit formyl peptide receptor 2. Organic Chemistry Frontiers, 2021,8(13),3381-3389. £¨ÖпÆÔº1Çø£©
5. Su, H.-G.#; Wang, Q. #; Zhou, L.; Peng, X.-R.*; Xiong, W.-Y.*; Qiu, M.-H.*, Highly oxygenated lanostane triterpenoids from Ganoderma applanatum as a class of agents for inhibiting lipid accumulation in adipocytes. Bioorganic Chemistry 2020, 104, 104263. £¨ÖпÆÔº1Çø£©
6. Su, H.-G.; Peng, X.-R.; Shi, Q.-Q.; Huang, Y.-J.; Zhou, L.; Qiu, M.-H.*, Lanostane triterpenoids with anti-inflammatory activities from Ganoderma lucidum. Phytochemistry 2020, 173, 112256. £¨ÖпÆÔº2Çø£©
7. Su, H.-G.; Zhou, Q.-M.; Guo, L.; Huang, Y.-J.; Peng, C.; Xiong, L.*, Lanostane triterpenoids from Ganoderma luteomarginatum and their cytotoxicity against four human cancer cell lines. Phytochemistry 2018, 156, 89-95. £¨ÖпÆÔº2Çø£©