Ziwei Huang
Affiliations: | University of Illinois, Urbana-Champaign, Urbana-Champaign, IL |
Area:
Biochemistry, Physiology BiologyGoogle:
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Publications
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Meng Q, Zhu R, Mao Y, et al. (2023) Biological and mutational analyses of CXCR4-antagonist interactions and design of new antagonistic analogs. Bioscience Reports. 43 |
Zhu R, Sang X, Zhou J, et al. (2023) CXCR4 Recognition by L- and D-Peptides Containing the Full-Length V3 Loop of HIV-1 gp120. Viruses. 15 |
Zhu R, Meng Q, Zhang H, et al. (2022) IV-1 gp120-CXCR4 recognition probed with synthetic nanomolar affinity D-peptides containing fragments of gp120 V3 loop. European Journal of Medicinal Chemistry. 244: 114797 |
Fan T, Liang B, Nie L, et al. (2022) A synthetic bivalent peptide ligand of EphB4 with potent agonistic activity. European Journal of Medicinal Chemistry. 244: 114804 |
Fang X, Meng Q, Zhang H, et al. (2022) A fragment integrational approach to GPCR inhibition: Identification of a high affinity small molecule CXCR4 antagonist. European Journal of Medicinal Chemistry. 231: 114150 |
Fang X, Meng Q, Zhang H, et al. (2020) Design, synthesis, and biological characterization of a new class of symmetrical polyamine-based small molecule CXCR4 antagonists. European Journal of Medicinal Chemistry. 200: 112410 |
Zhang C, Zhu R, Cao Q, et al. (2020) Discoveries and developments of CXCR4-targeted HIV-1 entry inhibitors. Experimental Biology and Medicine (Maywood, N.J.). 1535370220901498 |
Zhu S, Meng Q, Schooley RT, et al. (2019) Structural and Biological Characterizations of Novel High-Affinity Fluorescent Probes with Overlapped and Distinctive Binding Regions on CXCR4. Molecules (Basel, Switzerland). 24 |
Yang S, Mao Y, Zhang H, et al. (2019) The chemical biology of apoptosis: Revisited after 17 years. European Journal of Medicinal Chemistry. 177: 63-75 |
Zhang C, Huang LS, Zhu R, et al. (2019) High affinity CXCR4 inhibitors generated by linking low affinity peptides. European Journal of Medicinal Chemistry. 172: 174-185 |