Zhou B - Search Results

1

Synthesis and identification of new 4-arylidene curcumin analogues as potential anticancer agents targeting nuclear factor-κB signaling pathway.

Qiu X, Du Y, Lou B, Zuo Y, Shao W, Huo Y, Huang J, Yu Y, Zhou B, Du J, Fu H, Bu X. Qiu X, et al. Among authors: zhou b. J Med Chem. 2010 Dec 9;53(23):8260-73. doi: 10.1021/jm1004545. Epub 2010 Nov 11. J Med Chem. 2010. PMID: 21070043 Free PMC article.

2

A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds.

Liu J, Cao R, Yi W, Ma C, Wan Y, Zhou B, Ma L, Song H. Liu J, et al. Among authors: zhou b. Eur J Med Chem. 2009 Apr;44(4):1773-8. doi: 10.1016/j.ejmech.2008.04.002. Epub 2008 Apr 27. Eur J Med Chem. 2009. PMID: 18524420

3

Synthesis and biological evaluation of helicid analogues as mushroom tyrosinase inhibitors.

Yi W, Cao R, Wen H, Yan Q, Zhou B, Wan Y, Ma L, Song H. Yi W, et al. Among authors: zhou b. Bioorg Med Chem Lett. 2008 Dec 15;18(24):6490-3. doi: 10.1016/j.bmcl.2008.10.056. Epub 2008 Oct 17. Bioorg Med Chem Lett. 2008. PMID: 18996693

4

Discovery of 4-functionalized phenyl-O-beta-D-glycosides as a new class of mushroom tyrosinase inhibitors.

Yi W, Cao R, Wen H, Yan Q, Zhou B, Ma L, Song H. Yi W, et al. Among authors: zhou b. Bioorg Med Chem Lett. 2009 Nov 1;19(21):6157-60. doi: 10.1016/j.bmcl.2009.09.018. Epub 2009 Sep 10. Bioorg Med Chem Lett. 2009. PMID: 19800229

5

Synthesis and biological evaluation of novel 4-hydroxybenzaldehyde derivatives as tyrosinase inhibitors.

Yi W, Cao R, Peng W, Wen H, Yan Q, Zhou B, Ma L, Song H. Yi W, et al. Among authors: zhou b. Eur J Med Chem. 2010 Feb;45(2):639-46. doi: 10.1016/j.ejmech.2009.11.007. Epub 2009 Nov 10. Eur J Med Chem. 2010. PMID: 19932528

6

Phosphaisocoumarins as a new class of potent inhibitors for pancreatic cholesterol esterase.

Li B, Zhou B, Lu H, Ma L, Peng AY. Li B, et al. Among authors: zhou b. Eur J Med Chem. 2010 May;45(5):1955-63. doi: 10.1016/j.ejmech.2010.01.038. Epub 2010 Jan 28. Eur J Med Chem. 2010. PMID: 20149492

7

Synthesis and cytotoxicity evaluation of biaryl-based chalcones and their potential in TNFα-induced nuclear factor-κB activation inhibition.

Zuo Y, Yu Y, Wang S, Shao W, Zhou B, Lin L, Luo Z, Huang R, Du J, Bu X. Zuo Y, et al. Among authors: zhou b. Eur J Med Chem. 2012 Apr;50:393-404. doi: 10.1016/j.ejmech.2012.02.023. Epub 2012 Feb 17. Eur J Med Chem. 2012. PMID: 22386368

8

Synthesis, cytotoxicity of new 4-arylidene curcumin analogues and their multi-functions in inhibition of both NF-κB and Akt signalling.

Zuo Y, Huang J, Zhou B, Wang S, Shao W, Zhu C, Lin L, Wen G, Wang H, Du J, Bu X. Zuo Y, et al. Among authors: zhou b. Eur J Med Chem. 2012 Sep;55:346-57. doi: 10.1016/j.ejmech.2012.07.039. Epub 2012 Jul 31. Eur J Med Chem. 2012. PMID: 22889562

9

T63, a new 4-arylidene curcumin analogue, induces cell cycle arrest and apoptosis through activation of the reactive oxygen species-FOXO3a pathway in lung cancer cells.

Liu H, Zhou BH, Qiu X, Wang HS, Zhang F, Fang R, Wang XF, Cai SH, Du J, Bu XZ. Liu H, et al. Free Radic Biol Med. 2012 Dec 15;53(12):2204-17. doi: 10.1016/j.freeradbiomed.2012.10.537. Epub 2012 Oct 17. Free Radic Biol Med. 2012. PMID: 23085518

10

Epithelial-mesenchymal transition (EMT) induced by TNF-α requires AKT/GSK-3β-mediated stabilization of snail in colorectal cancer.

Wang H, Wang HS, Zhou BH, Li CL, Zhang F, Wang XF, Zhang G, Bu XZ, Cai SH, Du J. Wang H, et al. PLoS One. 2013;8(2):e56664. doi: 10.1371/journal.pone.0056664. Epub 2013 Feb 19. PLoS One. 2013. PMID: 23431386 Free PMC article.

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