Liang G - Search Results

1

Discovery and evaluation of asymmetrical monocarbonyl analogs of curcumin as anti-inflammatory agents.

Zhang Y, Zhao C, He W, Wang Z, Fang Q, Xiao B, Liu Z, Liang G, Yang S. Zhang Y, et al. Among authors: liang g. Drug Des Devel Ther. 2014 Apr 4;8:373-82. doi: 10.2147/DDDT.S58168. eCollection 2014. Drug Des Devel Ther. 2014. PMID: 24741294 Free PMC article.

2

Synthesis and anti-inflammatory activities of mono-carbonyl analogues of curcumin.

Liang G, Li X, Chen L, Yang S, Wu X, Studer E, Gurley E, Hylemon PB, Ye F, Li Y, Zhou H. Liang G, et al. Bioorg Med Chem Lett. 2008 Feb 15;18(4):1525-9. doi: 10.1016/j.bmcl.2007.12.068. Epub 2008 Jan 1. Bioorg Med Chem Lett. 2008. PMID: 18234497 Free PMC article.

3

Synthesis and anti-bacterial properties of mono-carbonyl analogues of curcumin.

Liang G, Yang S, Jiang L, Zhao Y, Shao L, Xiao J, Ye F, Li Y, Li X. Liang G, et al. Chem Pharm Bull (Tokyo). 2008 Feb;56(2):162-7. doi: 10.1248/cpb.56.162. Chem Pharm Bull (Tokyo). 2008. PMID: 18239300 Free article.

4

Synthesis, crystal structure and anti-inflammatory properties of curcumin analogues.

Liang G, Yang S, Zhou H, Shao L, Huang K, Xiao J, Huang Z, Li X. Liang G, et al. Eur J Med Chem. 2009 Feb;44(2):915-9. doi: 10.1016/j.ejmech.2008.01.031. Epub 2008 Feb 3. Eur J Med Chem. 2009. PMID: 18336957

5

Synthesis, structure, and bioevaluation of 2,5-bis(arylmethenyl)cyclopentanones.

Liang G, Yang SL, Shao LL, Zhao CG, Xiao J, Lv YX, Yang J, Zhao Y, Li XK. Liang G, et al. J Asian Nat Prod Res. 2008 Sep-Oct;10(9-10):957-65. doi: 10.1080/10286020802181257. J Asian Nat Prod Res. 2008. PMID: 19003615

6

Inhibition of LPS-induced production of inflammatory factors in the macrophages by mono-carbonyl analogues of curcumin.

Liang G, Zhou H, Wang Y, Gurley EC, Feng B, Chen L, Xiao J, Yang S, Li X. Liang G, et al. J Cell Mol Med. 2009 Sep;13(9B):3370-9. doi: 10.1111/j.1582-4934.2009.00711.x. Epub 2009 Feb 20. J Cell Mol Med. 2009. PMID: 19243473 Free PMC article.

7

Exploration and synthesis of curcumin analogues with improved structural stability both in vitro and in vivo as cytotoxic agents.

Liang G, Shao L, Wang Y, Zhao C, Chu Y, Xiao J, Zhao Y, Li X, Yang S. Liang G, et al. Bioorg Med Chem. 2009 Mar 15;17(6):2623-31. doi: 10.1016/j.bmc.2008.10.044. Epub 2008 Nov 1. Bioorg Med Chem. 2009. PMID: 19243951

8

Synthesis of mono-carbonyl analogues of curcumin and their effects on inhibition of cytokine release in LPS-stimulated RAW 264.7 macrophages.

Zhao C, Yang J, Wang Y, Liang D, Yang X, Li X, Wu J, Wu X, Yang S, Li X, Liang G. Zhao C, et al. Among authors: liang d, liang g. Bioorg Med Chem. 2010 Apr 1;18(7):2388-93. doi: 10.1016/j.bmc.2010.03.001. Epub 2010 Mar 6. Bioorg Med Chem. 2010. PMID: 20338767

9

Synthesis and biological analysis of a new curcumin analogue for enhanced anti-tumor activity in HepG 2 cells.

Xiao J, Chu Y, Hu K, Wan J, Huang Y, Jiang C, Liang G, Li X. Xiao J, et al. Among authors: liang g. Oncol Rep. 2010 May;23(5):1435-41. doi: 10.3892/or_00000781. Oncol Rep. 2010. PMID: 20372861

10

Synthesis and anti-inflammatory evaluation of novel mono-carbonyl analogues of curcumin in LPS-stimulated RAW 264.7 macrophages.

Zhao C, Cai Y, He X, Li J, Zhang L, Wu J, Zhao Y, Yang S, Li X, Li W, Liang G. Zhao C, et al. Among authors: liang g. Eur J Med Chem. 2010 Dec;45(12):5773-80. doi: 10.1016/j.ejmech.2010.09.037. Epub 2010 Oct 8. Eur J Med Chem. 2010. PMID: 20934787

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