Zhao F - Search Results

1

Design, synthesis, and biological evaluation of novel sulfamoylbenzamide derivatives as HBV capsid assembly modulators.

Wang S, Ren Y, Li Q, Wang Y, Jiang X, Xu S, Zhang X, Zhao S, Bradley DP, Woodson ME, Zhao F, Wu S, Li Y, Tian Y, Liu X, Tavis JE, Zhan P. Wang S, et al. Among authors: zhao f, zhao s. Bioorg Chem. 2022 Dec;129:106192. doi: 10.1016/j.bioorg.2022.106192. Epub 2022 Oct 13. Bioorg Chem. 2022. PMID: 36265355 Free PMC article.

2

Discovery of HCV NS5B thumb site I inhibitors: core-refining from benzimidazole to indole scaffold.

Zhao F, Liu N, Zhan P, Jiang X, Liu X. Zhao F, et al. Eur J Med Chem. 2015 Apr 13;94:218-28. doi: 10.1016/j.ejmech.2015.03.012. Epub 2015 Mar 6. Eur J Med Chem. 2015. PMID: 25768704 Review.

3

Review of small synthetic molecules targeting HBV capsid assembly.

Liu N, Zhao F, Zhan P, Liu X. Liu N, et al. Among authors: zhao f. Med Chem. 2015;11(8):710-6. doi: 10.2174/157340641108151029111243. Med Chem. 2015. PMID: 25985859 Review.

4

Repurposing of HDAC inhibitors toward anti-hepatitis C virus drug discovery: teaching an old dog new tricks.

Zhao F, Liu N, Zhan P, Liu X. Zhao F, et al. Future Med Chem. 2015;7(11):1367-71. doi: 10.4155/fmc.15.76. Future Med Chem. 2015. PMID: 26230876 No abstract available.

5

Discovery of non-peptide small molecular CXCR4 antagonists as anti-HIV agents: Recent advances and future opportunities.

Zhang H, Kang D, Huang B, Liu N, Zhao F, Zhan P, Liu X. Zhang H, et al. Among authors: zhao f. Eur J Med Chem. 2016 May 23;114:65-78. doi: 10.1016/j.ejmech.2016.02.051. Epub 2016 Feb 24. Eur J Med Chem. 2016. PMID: 26974376 Review.

6

Arylazolyl(azinyl)thioacetanilides. Part 20: Discovery of novel purinylthioacetanilides derivatives as potent HIV-1 NNRTIs via a structure-based bioisosterism approach.

Lu X, Li X, Yang J, Huang B, Kang D, Zhao F, Zhou Z, De Clercq E, Daelemans D, Pannecouque C, Zhan P, Liu X. Lu X, et al. Among authors: zhao f. Bioorg Med Chem. 2016 Sep 15;24(18):4424-4433. doi: 10.1016/j.bmc.2016.07.041. Epub 2016 Jul 21. Bioorg Med Chem. 2016. PMID: 27501911

7

Discovery of Novel Bicyclic Imidazolopyridine-Containing Human Urate Transporter 1 Inhibitors as Hypouricemic Drug Candidates with Improved Efficacy and Favorable Druggability.

Zhao T, Zhang J, Tao Y, Liao H, Zhao F, Liang R, Shi X, Zhang Z, Ji J, Wu T, Pang J, Liu X, Zhan P. Zhao T, et al. Among authors: zhao f. J Med Chem. 2022 Mar 10;65(5):4218-4237. doi: 10.1021/acs.jmedchem.1c02057. Epub 2022 Jan 27. J Med Chem. 2022. PMID: 35084182

8

Chemical space exploration around indolylarylsulfone scaffold led to a novel class of highly active HIV-1 NNRTIs with spiro structural features.

Gao S, Cheng Y, Song S, Song L, Zhao F, Xu S, Kang D, Sun L, Gao P, De Clercq E, Pannecouque C, Liu X, Zhan P. Gao S, et al. Among authors: zhao f. Eur J Med Chem. 2022 Aug 5;238:114471. doi: 10.1016/j.ejmech.2022.114471. Epub 2022 May 20. Eur J Med Chem. 2022. PMID: 35640327

9

Design, synthesis, and biological evaluation of novel double-winged galloyl derivatives as HIV-1 RNase H inhibitors.

Zhang L, Wei F, Borrego D, Zhao F, Río JMD, Frutos-Beltrán E, Zhang J, Xu S, López-Carrobles N, Gao S, Kang D, Pannecouque C, Clercq E, Liu X, Menéndez-Arias L, Zhan P. Zhang L, et al. Among authors: zhao f. Eur J Med Chem. 2022 Oct 5;240:114563. doi: 10.1016/j.ejmech.2022.114563. Epub 2022 Jun 26. Eur J Med Chem. 2022. PMID: 35780636

10

Iterative Optimization and Structure-Activity Relationship Studies of Oseltamivir Amino Derivatives as Potent and Selective Neuraminidase Inhibitors via Targeting 150-Cavity.

Ju H, Hou L, Zhao F, Zhang Y, Jia R, Guizzo L, Bonomini A, Zhang J, Gao Z, Liang R, Bertagnin C, Kong X, Ma X, Kang D, Loregian A, Huang B, Liu X, Zhan P. Ju H, et al. Among authors: zhao f. J Med Chem. 2022 Sep 8;65(17):11550-11573. doi: 10.1021/acs.jmedchem.1c01970. Epub 2022 Aug 8. J Med Chem. 2022. PMID: 35939763

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