Guo-Chun Zhou
Affiliations: | Nanjing University of Technology |
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Publications
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Zhou GF, Li F, Xue JX, et al. (2023) Antiviral effects of the fused tricyclic derivatives of indoline and imidazolidinone on ZIKV infection and RdRp activities of ZIKV and DENV. Virus Research. 199062 |
Chen R, Francese R, Wang N, et al. (2023) Exploration of novel hexahydropyrrolo[1,2-e]imidazol-1-one derivatives as antiviral agents against ZIKV and USUV. European Journal of Medicinal Chemistry. 248: 115081 |
Qian W, Zhou GF, Ge X, et al. (2022) Discovery of dehydroandrographolide derivatives with C19 hindered ether as potent anti-ZIKV agents with inhibitory activities to MTase of ZIKV NS5. European Journal of Medicinal Chemistry. 243: 114710 |
Qian W, Xue JX, Xu J, et al. (2022) Design, synthesis, discovery and SAR of the fused tricyclic derivatives of indoline and imidazolidinone against DENV replication and infection. Bioorganic Chemistry. 120: 105639 |
Xu B, Lee EM, Medina A, et al. (2020) Inhibition of zika virus infection by fused tricyclic derivatives of 1,2,4,5-tetrahydroimidazo[1,5-a]quinolin-3(3aH)-one. Bioorganic Chemistry. 104: 104205 |
Li F, Lee EM, Sun X, et al. (2019) Design, synthesis and discovery of andrographolide derivatives against Zika virus infection. European Journal of Medicinal Chemistry. 187: 111925 |
Weng Z, Shao X, Graf D, et al. (2016) Identification of fused bicyclic derivatives of pyrrolidine and imidazolidinone as dengue virus-2 NS2B-NS3 protease inhibitors. European Journal of Medicinal Chemistry. 125: 751-759 |
Zhou GC, Weng Z, Shao X, et al. (2013) Discovery and SAR studies of methionine-proline anilides as dengue virus NS2B-NS3 protease inhibitors. Bioorganic & Medicinal Chemistry Letters. 23: 6549-54 |
Zhou GC, Liu F, Wan J, et al. (2013) Design, synthesis and evaluation of a cellular stable and detectable biotinylated fumagillin probe and investigation of cell permeability of fumagillin and its analogs to endothelial and cancer cells. European Journal of Medicinal Chemistry. 70: 631-9 |
Cheng H, Zhang L, Liu Y, et al. (2010) Design, synthesis and discovery of 5-hydroxyaurone derivatives as growth inhibitors against HUVEC and some cancer cell lines. European Journal of Medicinal Chemistry. 45: 5950-7 |