Wang Q - Search Results

1

Development of oleanane-type triterpenes as a new class of HCV entry inhibitors.

Yu F, Wang Q, Zhang Z, Peng Y, Qiu Y, Shi Y, Zheng Y, Xiao S, Wang H, Huang X, Zhu L, Chen K, Zhao C, Zhang C, Yu M, Sun D, Zhang L, Zhou D. Yu F, et al. Among authors: wang h, wang q. J Med Chem. 2013 Jun 13;56(11):4300-19. doi: 10.1021/jm301910a. Epub 2013 May 28. J Med Chem. 2013. PMID: 23662817

2

Conjugation of cyclodextrin with fullerene as a new class of HCV entry inhibitors.

Xiao SL, Wang Q, Yu F, Peng YY, Yang M, Sollogoub M, Sinaÿ P, Zhang YM, Zhang LH, Zhou DM. Xiao SL, et al. Among authors: wang q. Bioorg Med Chem. 2012 Sep 15;20(18):5616-22. doi: 10.1016/j.bmc.2012.07.029. Epub 2012 Jul 23. Bioorg Med Chem. 2012. PMID: 22884577

3

Elucidation of the pharmacophore of echinocystic acid, a new lead for blocking HCV entry.

Wang H, Wang Q, Xiao SL, Yu F, Ye M, Zheng YX, Zhao CK, Sun DA, Zhang LH, Zhou DM. Wang H, et al. Among authors: wang q. Eur J Med Chem. 2013 Jun;64:160-8. doi: 10.1016/j.ejmech.2013.03.041. Epub 2013 Apr 3. Eur J Med Chem. 2013. PMID: 23644199

4

Synthesis and anti-HCV entry activity studies of β-cyclodextrin-pentacyclic triterpene conjugates.

Xiao S, Wang Q, Si L, Shi Y, Wang H, Yu F, Zhang Y, Li Y, Zheng Y, Zhang C, Wang C, Zhang L, Zhou D. Xiao S, et al. Among authors: wang h, wang c, wang q. ChemMedChem. 2014 May;9(5):1060-70. doi: 10.1002/cmdc.201300545. Epub 2014 Mar 12. ChemMedChem. 2014. PMID: 24623716

5

Development of bivalent oleanane-type triterpenes as potent HCV entry inhibitors.

Yu F, Peng Y, Wang Q, Shi Y, Si L, Wang H, Zheng Y, Lee E, Xiao S, Yu M, Li Y, Zhang C, Tang H, Wang C, Zhang L, Zhou D. Yu F, et al. Among authors: wang h, wang c, wang q. Eur J Med Chem. 2014 Apr 22;77:258-68. doi: 10.1016/j.ejmech.2014.03.017. Epub 2014 Mar 7. Eur J Med Chem. 2014. PMID: 24650713

6

Synthesis and biological evaluation of ring A and/or C expansion and opening echinocystic acid derivatives for anti-HCV entry inhibitors.

Wang H, Yu F, Peng Y, Wang Q, Han X, Xu R, Zhou X, Wan C, Fan Z, Jiao P, Zhang Y, Zhang L, Zhou D, Xiao S. Wang H, et al. Among authors: wang q. Eur J Med Chem. 2015 Sep 18;102:594-9. doi: 10.1016/j.ejmech.2015.08.034. Epub 2015 Aug 18. Eur J Med Chem. 2015. PMID: 26318066

7

Synthesis and evaluation of novel neamine derivatives effectively targeting to RNA.

Xu Y, Jin H, Yang Z, Zhang L, Wang Q, Li M, Zhang L. Xu Y, et al. Among authors: wang q. Bioorg Med Chem Lett. 2009 Apr 15;19(8):2103-6. doi: 10.1016/j.bmcl.2009.03.021. Epub 2009 Mar 13. Bioorg Med Chem Lett. 2009. PMID: 19327991

8

Broadening the versatility of lentiviral vectors as a tool in nucleic acid research via genetic code expansion.

Zheng Y, Yu F, Wu Y, Si L, Xu H, Zhang C, Xia Q, Xiao S, Wang Q, He Q, Chen P, Wang J, Taira K, Zhang L, Zhou D. Zheng Y, et al. Among authors: wang j, wang q. Nucleic Acids Res. 2015 Jun 23;43(11):e73. doi: 10.1093/nar/gkv202. Epub 2015 Mar 12. Nucleic Acids Res. 2015. PMID: 25765642 Free PMC article.

9

Fragment-based drug discovery of 2-thiazolidinones as BRD4 inhibitors: 2. Structure-based optimization.

Zhao L, Wang Y, Cao D, Chen T, Wang Q, Li Y, Xu Y, Zhang N, Wang X, Chen D, Chen L, Chen YL, Xia G, Shi Z, Liu YC, Lin Y, Miao Z, Shen J, Xiong B. Zhao L, et al. Among authors: wang x, wang y, wang q. J Med Chem. 2015 Feb 12;58(3):1281-97. doi: 10.1021/jm501504k. Epub 2015 Jan 14. J Med Chem. 2015. PMID: 25559428

10

Structural Modification of Sylibin to Derivatives of Sylibin/Hydnocarpin D/Silandrin, and Evaluation of their Cytotoxicity against Cancer Cells.

Maihesuti L, Gao H, Wang Q, Cao J, Aisa HA, Huang G. Maihesuti L, et al. Among authors: wang q. Curr Top Med Chem. 2021;21(15):1398-1417. doi: 10.2174/1568026621666210701142826. Curr Top Med Chem. 2021. PMID: 34218782

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