1. Wu, H. R.;# Zhang, C. N.;# Dou, B. Q.; Chen, N. Y.; Gao, D. F.; Zou, P. S.; Pan, C. X.; Gu, J. H.;* Mo, D. L.;* Su, J. C.* Identification of O-Arylated Huperzinines as Novel Cholinergic Anti-Inflammatory Pathway Agonists against Gout Arthritis. Bioorg. Chem. 2024, 152, 107716. (TOP期刊,JCR Q1区)
2. Li, X. W.; Fang, S. J.; Li, Y. Z.; Qin, L. Q.; Chen, N. Y.; Zheng, B.; Mo, D. L.; Su, G. F.; Su, J. C.;* Pan, C. X.* Design and Synthesis of Luotonin A-Derived Topoisomerase Targeting Scaffold with Potent Antitumor Effect and Low Genotoxicity. Bioorg. Chem. 2024, 143, 107015. (TOP期刊,JCR Q1区)
3. Zhou, C.; Feng, K.; Wang, L. F.; Chen, N. Y.; Wang, J. W.; Wang, C. Y.; Zhang, X. Y.; Su, J. C.;* Wang, G. X.;* Kong, X. F.* Synthesis of Quinazolinone Derivatives with a Seven-Membered Ring Using Borrowing Hydrogen Methodology. Tetrahedron Lett. 2024, 145, 155156. (JCR Q2区)
4. Zhang, X.; Wei, M. Y.; Su, J. C.;* Liang, C.; Pan, C. X.; Su, G. F.;* Mo, D. L.* Synthesis of 4 (Trichloromethyl)Pyrido[2′,1′:3,4]Pyrazino[2,1-b]Quinazolinones through a Cyclized Dearomatization and Trichloromethylation Cascade Strategy. Org. Biomol. Chem. 2024, 22, 1386-1390. (JCR Q2区)
5. Li, S. H.;# Li, M. Y.;# Yuan, T. T.;# Wang, G. W.; Zeng, J. B.; Shi, Z.;* Liu, J. H.;* Su, J. C.* Osthole Activates the Cholinergic Anti‐Inflammatory Pathway via α7nAChR Upregulation to Alleviate Inflammatory Responses. Chem. Biodiversity 2024, e202400290. (JCR Q2区)
6. Cai, Q.;# Zha, H. J.;# Yuan, S. Y.;# Sun, X.;# Lin, X.; Zheng, X. Y.; Qian, Y. X.; Xia, R. F.; Luo, Y. S.; Shi, Z.; Su, J. C.;* Wan, L. S.* Diterpenoids from Euphorbia fischeriana with Kv1.3 Inhibitory Activity. J. Nat. Prod. 2023, 86, 2379-2390. (TOP期刊,JCR Q1区)
7. Qin, L. Q.; Sun, J. Y.; Chen, N. Y.; Li, X. W.; Gao, D. F.; Wang, W.; Mo, D. L.; Su, J. C.;* Su, G. F.;* Pan, C. X.* Design and Synthesis of Pseudo-Rutaecarpines as Potent Anti-Inflammatory Agents via Regulating MAPK/NF-κB Pathways to Relieve Inflammation-Induced Acute Liver Injury in Mice. Bioorg. Chem. 2023, 138, 106611. (TOP期刊,JCR Q1区)
8. Pang, L.;# Fang, S. J.;# Zou, P. S.; Wang, W.; Su, J. C.;* Liu, X. Q.; Pan, C. X.; Mo, D. L.;* Su, G. F.* Synthesis of Biologically Active [1,5]Diazocino[2,1-b]Quinazolinones through [4+4] Cycloaddition of 2-Alkynyl Quinazolinones with Aza-Ortho-Quinone Methides. Org. Chem. Front. 2023, 10, 1780–1787. (JCR Q1区)
9. Xia, R. F.;# Su, J. C.;# Yu, J.;# Zha, H. J.; Wu, J. L.; Fu, X. N.; Cai, Q.; Wan, L. S.* Anti-Inflammatory Lanostane Triterpenoids with Rearranged Spirobi[indene] Scaffold and Their Biogenetically Related Analogues from Euphorbia maculata. Phytochemistry 2023, 211, 113682. (JCR Q1区)
10. Yang, B.;# Su, J. C.;# Huang, L; Lin, S.; Jin, X.; Lei, X.; Hu, Z.;* Zhang, Y.* Hyperispirones A and B, Spiro-Bridged Polycyclic Polyprenylated Acylphloroglucinols with Anti-angiogenesis Activity from Hypericum beanii. Org. Chem. Front. 2022, 9, 3460−3466. (TOP期刊,JCR Q1区,Hot off the Press)
11. Wei, X.;# Su, J. C.;# Hu, J. S.; He, X. X.; Lin, S. J.; Zhang, D. M.; Ye, W. C.; Chen, M. F.;* Lin, H. W.;* Zhang, C. X.* Probing Indole Diketopiperazine-Based Hybrids as Environmental-Induced Products from Aspergillus sp. EGF 15-0-3. Org. Lett. 2022, 24, 158−163. (TOP期刊,JCR Q1区,Hot off the Press)
12. Su, J. C.; Pan, Q.; Xu, X.; Wei, X., Lei, X.;* Zhang, P.* Structurally Diverse Steroids from an Endophyte of Aspergillus tennesseensis 1022LEF Attenuates LPS-induced Inflammatory Response through the Cholinergic Anti-inflammatory Pathway. Chem.-Biol. Interact. 2022, 362, 109998. (JCR Q1区)
13. Hu, Z. F.;# Su, J. C.;# Sun, X.;# Xia, R. F.; Wu, J. L.; Fu, X. N.; Zhang, B. Z.;* Chen, J. C.;* Wan, L. S.* Brujavanoids A-U, Structurally Diverse Apotirucallane-Type Triterpenoids from Brucea javanica and Their Anti-Inflammatory Effects. Bioorg. Chem. 2022, 127, 106012. (TOP期刊,JCR Q1区)
14. Xiang, Z. N.;# Tong, Q. L.;# Su, J. C.;# Hu, Z. F.;# Zhao, N.; Xia, R. F.; Wu, J. L.; Chen, C.; Chen, J. C.;* Wan, L. S.* Diterpenoids with Rearranged 9(10→11)-Abeo-10,12-Cyclojatrophane Skeleton and the First (15S)-Jatrophane from Euphorbia helioscopia: Structural Elucidation, Biomimetic Conversion, and Their Immunosuppressive Effects. Org. Lett. 2022, 24, 697−701. (TOP期刊,JCR Q1区, Hot off the Press)
15. Zhou, C. G.; Xiang, Z. N.; Zhao, N.; Sun, X.; Hu, Z. F.; Wu, J. L.; Xia, R. F.; Chen, C.; Su, J. C.;* Chen, J.;* Wan, L. S.* Jatrophane Diterpenoids with Kv1.3 Inhibitory Effect from Euphorbia helioscopia. J. Nat. Prod. 2022, 85, 815−827. (JCR Q1区)
16. Lv, L. X.;# Wu, Y.;# He, H. X.; Li, N. P.; Zhao, W.; Fan, Y. Q.; Wei, X.; Su, J. C.;* Wang, Q.;* Gu, J. H.* Acronyrones A−C, unusual prenylated acetophenones from Acronychia pedunculata. Fitoterapia 2022, 105303. (JCR Q2区)
17. Li, X.D.;# Su, J. C.;# Jiang, B.Z.; Li, Y. L.; Guo, Y. Q.;* Zhang, P.* Janthinoid A, an Unprecedented Tri-nor-Meroterpenoid with Highly Modified Bridged 4a,1-(Epoxymethano)Phenanthrene Scaffold, Produced by the Endophyte of Penicillium janthinellum TE-43. Org. Chem. Front. 2021, 8, 6196−6202. (TOP期刊,JCR Q1区,2021 OCF Hot article)
18. Pan, J.;# Su, J. C.;# Liu, Y. H.; Deng, B.; Hu, Z. F.; Wu, J. L.; Xia, R. F.; Chen, C.; He, Q.; Chen, J. C.;* Wan, L. S.* Stelleranoids A-M, Guaiane-Type Sesquiterpenoids Based on [5,7] Bicyclic System from Stellera chamaejasme and Their Cytotoxic Activity. Bioorg. Chem. 2021, 115, 105251. (TOP期刊,JCR Q1区)
19. Xiang, Z. N.;# Su, J. C.;# Liu, Y. H.; Deng, B.; Zhao, N.; Pan, J.; Hu, Z. F.; Chen, F. H.; Cheng, B. Y.; Chen, J. C.;* Wan, L. S.* Structurally Diverse Alkaloids from Buxus sempervirens with Cardioprotective Activity. Bioorg. Chem. 2021, 109, 104753. (TOP期刊,JCR Q1区)
20. Song, J. G.;# Su, J. C.;# Song, Q. Y.; Huang, R. L.; Tang, W.; Hu, L. J.; Huang, X. J.; Jiang, R. W.; Li, Y. L.; Ye, W. C.;* Wang, Y.* Cleistocaltones A and B, Antiviral Phloroglucinol-Terpenoid Adducts from Cleistocalyx operculatus. Org. Lett. 2019, 21, 9579−9583. (TOP期刊,JCR Q1区)
21. Su, J. C.;# Cheng, W.;# Song, J. G.; Zhong, Y. L.; Huang, X. J.; Jiang, R. W.; Li, Y. L.; Li, M. M.;* Ye, W. C.;* Wang, Y.* Macrocyclic Diterpenoids from Euphorbia helioscopia and Their Potential Anti-Inflammatory Activity. J. Nat. Prod. 2019, 82, 2818−2827. (TOP期刊,JCR Q1区,封面文章)
22. Su, J. C.;# Wang, S.;# Cheng, W.; Huang, X. J.; Li, M. M.; Jiang, R. W.; Li, Y. L.; Wang, L.; Ye, W. C.;* Wang, Y.* Phloroglucinol Derivatives with Unusual Skeletons from Cleistocalyx operculatus and Their in Vitro Antiviral Activity. J. Org. Chem. 2018, 83, 8522−8532. (TOP期刊,JCR Q1区,Hot off the Press,2018年中国天然产物研究亮点)
23. Yang, J.;# Su, J. C.;# Lei, X. P.; Huang, X. J.; Zhang, D. M.; Ye, W. C.;* Wang, Y.* Acylphloroglucinol Derivatives from the Leaves of Syzygium samarangense and Their Cytotoxic Activities. Fitoterapia 2018, 129, 1−6. (JCR Q2区)