Tong LJ - Search Results

1

DW09849, a selective phosphatidylinositol 3-kinase (PI3K) inhibitor, prevents PI3K signaling and preferentially inhibits proliferation of cells containing the oncogenic mutation p110α (H1047R).

Liu JL, Gao GR, Zhang X, Cao SF, Guo CL, Wang X, Tong LJ, Ding J, Duan WH, Meng LH. Liu JL, et al. Among authors: tong lj. J Pharmacol Exp Ther. 2014 Mar;348(3):432-41. doi: 10.1124/jpet.113.210724. Epub 2013 Dec 20. J Pharmacol Exp Ther. 2014. PMID: 24361696

2

Actinomycin D inhibiting K562 cell apoptosis elicited by salvicine but not decreasing its cytotoxicity.

Qing C, Miao ZH, Tong LJ, Zhang JS, Ding J. Qing C, et al. Among authors: tong lj. Acta Pharmacol Sin. 2003 May;24(5):415-21. Acta Pharmacol Sin. 2003. PMID: 12740176 Free article.

3

Characterization of salvicine-resistant lung adenocarcinoma A549/SAL cell line.

Miao ZH, Tong LJ, Zhang JS, Han JX, Ding J. Miao ZH, et al. Among authors: tong lj. Int J Cancer. 2004 Jul 10;110(5):627-32. doi: 10.1002/ijc.20026. Int J Cancer. 2004. PMID: 15146550

4

Anti-angiogenic effects of Shiraiachrome A, a compound isolated from a Chinese folk medicine used to treat rheumatoid arthritis.

Tong Y, Zhang X, Zhao W, Zhang Y, Lang J, Shi Y, Tan W, Li M, Zhang Y, Tong L, Lu H, Lin L, Ding J. Tong Y, et al. Eur J Pharmacol. 2004 Jun 28;494(2-3):101-9. doi: 10.1016/j.ejphar.2004.04.053. Eur J Pharmacol. 2004. PMID: 15212963

5

Philinopside A, a novel marine-derived compound possessing dual anti-angiogenic and anti-tumor effects.

Tong Y, Zhang X, Tian F, Yi Y, Xu Q, Li L, Tong L, Lin L, Ding J. Tong Y, et al. Int J Cancer. 2005 May 10;114(6):843-53. doi: 10.1002/ijc.20804. Int J Cancer. 2005. PMID: 15645493

6

Anti-proliferative effects, cell cycle G2/M phase arrest and blocking of chromosome segregation by probimane and MST-16 in human tumor cell lines.

Lu DY, Huang M, Xu CH, Yang WY, Hu CX, Lin LP, Tong LJ, Li MH, Lu W, Zhang XW, Ding J. Lu DY, et al. Among authors: tong lj. BMC Pharmacol. 2005 Jun 20;5:11. doi: 10.1186/1471-2210-5-11. BMC Pharmacol. 2005. PMID: 15963241 Free PMC article.

7

Pseudolarix acid B, a new tubulin-binding agent, inhibits angiogenesis by interacting with a novel binding site on tubulin.

Tong YG, Zhang XW, Geng MY, Yue JM, Xin XL, Tian F, Shen X, Tong LJ, Li MH, Zhang C, Li WH, Lin LP, Ding J. Tong YG, et al. Among authors: tong lj. Mol Pharmacol. 2006 Apr;69(4):1226-33. doi: 10.1124/mol.105.020537. Epub 2006 Jan 19. Mol Pharmacol. 2006. PMID: 16424078

8

TKI-31 inhibits angiogenesis by combined suppression signaling pathway of VEGFR2 and PDGFRbeta.

Zhong L, Guo XN, Zhang XH, Sun QM, Tong LJ, Wu ZX, Luo XM, Jiang HL, Nan FJ, Zhang XW, Lin LP, Ding J. Zhong L, et al. Among authors: tong lj. Cancer Biol Ther. 2006 Mar;5(3):323-30. doi: 10.4161/cbt.5.3.2543. Epub 2006 Mar 23. Cancer Biol Ther. 2006. PMID: 16575201 Free article.

9

BM6, a new semi-synthetic vinca alkaloid, exhibits its potent in vivo anti-tumor activities via its high binding affinity for tubulin and improved pharmacokinetic profiles.

Li W, Shao Y, Hu L, Zhang X, Chen Y, Tong L, Li C, Shen X, Ding J. Li W, et al. Cancer Biol Ther. 2007 May;6(5):787-94. doi: 10.4161/cbt.6.5.4006. Epub 2007 Feb 14. Cancer Biol Ther. 2007. PMID: 17387272 Free article.

10

Structural modification of an angiogenesis inhibitor discovered from traditional Chinese medicine and a structure-activity relationship study.

Yang SP, Cai YJ, Zhang BL, Tong LJ, Xie H, Wu Y, Lin LP, Ding J, Yue JM. Yang SP, et al. Among authors: tong lj. J Med Chem. 2008 Jan 10;51(1):77-85. doi: 10.1021/jm070906g. Epub 2007 Dec 14. J Med Chem. 2008. PMID: 18078313

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