Zhong W - Search Results

1

Selective substitution of 31/42-OH in rapamycin guided by an in situ IR technique.

Cao S, Zhou X, Yang Y, Zhong W, Sun T. Cao S, et al. Among authors: zhong w. Molecules. 2014 Jun 10;19(6):7770-84. doi: 10.3390/molecules19067770. Molecules. 2014. PMID: 24918544 Free PMC article.

2

(S)-3-(4-(2-(5-Methyl-2-phenyloxazol-4-yl)ethoxy)phenyl)-2-(piperazin-1-yl) propanoic acid compounds: synthesis and biological evaluation of dual PPARalpha/gamma agonists.

Zhou X, Chen W, Xu C, Fan S, Xie Y, Zhong W, Wang L, Li S. Zhou X, et al. Among authors: zhong w. Bioorg Med Chem Lett. 2010 Apr 15;20(8):2605-8. doi: 10.1016/j.bmcl.2010.02.071. Epub 2010 Mar 1. Bioorg Med Chem Lett. 2010. PMID: 20299214

3

(3S,4R,4aS,7aR,12bS)-3-Cyclo-propyl-meth-yl-4a,9-dihy-droxy-3-methyl-7-oxo-2,3,4,4a,5,6,7,7a-octa-hydro-1H-4,12-methano-1-benzofuro[3,2-e]isoquinolin-3-ium 2,2,2-trifluoro-acetate methanol solvate.

Cai X, Zhou X, Zheng Z, Zhong W, Li S. Cai X, et al. Among authors: zhong w. Acta Crystallogr Sect E Struct Rep Online. 2010 Oct 20;66(Pt 11):o2868. doi: 10.1107/S1600536810041164. Acta Crystallogr Sect E Struct Rep Online. 2010. PMID: 21589050 Free PMC article.

4

Synthesis of potent inhibitors of β-ketoacyl-acyl carrier protein synthase III as potential antimicrobial agents.

Liu Y, Zhong W, Li RJ, Li S. Liu Y, et al. Among authors: zhong w. Molecules. 2012 Apr 25;17(5):4770-81. doi: 10.3390/molecules17054770. Molecules. 2012. PMID: 22534662 Free PMC article.

5

Novel substituted heteroaromatic piperazine and piperidine derivatives as inhibitors of human enterovirus 71 and coxsackievirus a16.

Zhang X, Wang H, Li Y, Cao R, Zhong W, Zheng Z, Wang G, Xiao J, Li S. Zhang X, et al. Among authors: zhong w. Molecules. 2013 Apr 29;18(5):5059-71. doi: 10.3390/molecules18055059. Molecules. 2013. PMID: 23629759 Free PMC article.

6

Novel cross-link breaker based on zwitterion structure: synthesis, structure and druggability studies.

Cao S, Zhou XB, Zhang H, Li S, Zhong W. Cao S, et al. Among authors: zhong w. Eur J Med Chem. 2013 Oct;68:89-95. doi: 10.1016/j.ejmech.2013.07.033. Epub 2013 Aug 9. Eur J Med Chem. 2013. PMID: 23973820 Free article.

7

Synthesis and biological evaluation of Chromenylurea and Chromanylurea derivatives as anti-TNF-α agents that target the p38 MAPK pathway.

Li X, Zhou X, Zhang J, Wang L, Long L, Zheng Z, Li S, Zhong W. Li X, et al. Among authors: zhong w. Molecules. 2014 Feb 13;19(2):2004-28. doi: 10.3390/molecules19022004. Molecules. 2014. PMID: 24531217 Free PMC article.

8

Design, Synthesis and Biological Evaluation of Novel Substituted N,N'-Diaryl ureas as Potent p38 Inhibitors.

Zhu D, Li X, Zhong W, Zhao D. Zhu D, et al. Among authors: zhong w. Molecules. 2015 Sep 11;20(9):16604-19. doi: 10.3390/molecules200916604. Molecules. 2015. PMID: 26378516 Free PMC article.

9

Asymmetric Synthesis and Absolute Configuration Assignment of a New Type of Bedaquiline Analogue.

Qiao CJ, Wang XK, Xie F, Zhong W, Li S. Qiao CJ, et al. Among authors: zhong w. Molecules. 2015 Dec 11;20(12):22272-85. doi: 10.3390/molecules201219846. Molecules. 2015. PMID: 26690407 Free PMC article.

10

Synthesis and p38 Inhibitory Activity of Some Novel Substituted N,N'-Diarylurea Derivatives.

Zhu D, Xing Q, Cao R, Zhao D, Zhong W. Zhu D, et al. Among authors: zhong w. Molecules. 2016 May 23;21(5):677. doi: 10.3390/molecules21050677. Molecules. 2016. PMID: 27223276 Free PMC article.

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