Wang L - Search Results

1

Novel 4 beta-anilino-podophyllotoxin derivatives: design synthesis and biological evaluation as potent DNA-topoisomerase II poisons and anti-MDR agents.

Hu C, Xu D, Du W, Qian S, Wang L, Lou J, He Q, Yang B, Hu Y. Hu C, et al. Among authors: wang l. Mol Biosyst. 2010 Feb;6(2):410-20. doi: 10.1039/b912336a. Epub 2009 Dec 1. Mol Biosyst. 2010. PMID: 20094661

2

Synthesis and biological evaluation of new 4β-anilino-4'-O-demethyl-4-desoxypodophyllotoxin derivatives as potential antitumor agents.

Wang L, Yang F, Yang X, Guan X, Hu C, Liu T, He Q, Yang B, Hu Y. Wang L, et al. Eur J Med Chem. 2011 Jan;46(1):285-96. doi: 10.1016/j.ejmech.2010.11.016. Epub 2010 Nov 19. Eur J Med Chem. 2011. PMID: 21145139

3

Pharmacophore identification, synthesis, and biological evaluation of carboxylated chalcone derivatives as CysLT1 antagonists.

Dong X, Wang L, Huang X, Liu T, Wei E, Du L, Yang B, Hu Y. Dong X, et al. Among authors: wang l. Bioorg Med Chem. 2010 Aug 1;18(15):5519-27. doi: 10.1016/j.bmc.2010.06.047. Epub 2010 Jun 20. Bioorg Med Chem. 2010. PMID: 20621485

4

GL3, a Novel 4β-Anilino-4'-O-Demethyl-4-Desoxypodophyllotoxin Analog, Traps Topoisomerase II Cleavage Complexes and Exerts Anticancer Activities.

Yang XC, Qian SJ, Wang L, Liao SD, Cao J, Hu YZ, He QJ, Zhu H, Yang B. Yang XC, et al. Among authors: wang l. Transl Oncol. 2013 Feb;6(1):75-82. doi: 10.1593/tlo.12343. Epub 2013 Feb 1. Transl Oncol. 2013. PMID: 23418619 Free PMC article.

5

Facile and efficient synthesis and biological evaluation of 4-anilinoquinazoline derivatives as EGFR inhibitors.

Wang Z, Wu X, Wang L, Zhang J, Liu J, Song Z, Tang Z. Wang Z, et al. Among authors: wang l. Bioorg Med Chem Lett. 2016 Jun 1;26(11):2589-93. doi: 10.1016/j.bmcl.2016.04.032. Epub 2016 Apr 13. Bioorg Med Chem Lett. 2016. PMID: 27118497

6

Design, synthesis and biological evaluation of hydroxamic acid derivatives as potential high density lipoprotein (HDL) receptor CLA-1 up-regulating agents.

Chen X, Wang L, Du Y, Wu Y, Jia X, Yang Y, Hong B. Chen X, et al. Among authors: wang l. Molecules. 2011 Nov 2;16(11):9178-93. doi: 10.3390/molecules16119178. Molecules. 2011. PMID: 22048700 Free PMC article.

7

Synthesis and structure-activity relationship of N-(2-arylethyl) isoquinoline derivatives as human scavenger receptor CD36 antagonists.

Wang YX, Wang L, Xu YN, Li YH, Jiang JD, Si SY, Li YB, Ren G, Shan YQ, Hong B, Song DQ. Wang YX, et al. Among authors: wang l. Eur J Med Chem. 2011 Apr;46(4):1066-73. doi: 10.1016/j.ejmech.2011.01.022. Epub 2011 Jan 21. Eur J Med Chem. 2011. PMID: 21295889

8

[Synthesis and structure-activity relationship of 13-hexylberberine analogues as CD36 antagonists].

Li YH, Wang L, Hong B, Xu YN, Si SY, Jiang JD, Song DQ. Li YH, et al. Among authors: wang l. Yao Xue Xue Bao. 2010 Sep;45(9):1128-33. Yao Xue Xue Bao. 2010. PMID: 21351569 Chinese.

9

Structure-activity relationship and biological evaluation of berberine derivatives as PCSK9 down-regulating agents.

Fan TY, Yang YX, Zeng QX, Wang XL, Wei W, Guo XX, Zhao LP, Song DQ, Wang YX, Wang L, Hong B. Fan TY, et al. Among authors: wang l, wang yx, wang xl. Bioorg Chem. 2021 Aug;113:104994. doi: 10.1016/j.bioorg.2021.104994. Epub 2021 May 18. Bioorg Chem. 2021. PMID: 34052738

10

Identification of trichostatin A as a novel transcriptional up-regulator of scavenger receptor BI both in HepG2 and RAW 264.7 cells.

Bao Y, Yang Y, Wang L, Gao L, Jiang W, Wang L, Si S, Hong B. Bao Y, et al. Among authors: wang l. Atherosclerosis. 2009 May;204(1):127-35. doi: 10.1016/j.atherosclerosis.2008.08.041. Epub 2008 Sep 11. Atherosclerosis. 2009. PMID: 18930459

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