You QD - Search Results

1

Synthesis and biological evaluation of novel oxazolo[5,4-d]pyrimidines as potent VEGFR-2 inhibitors.

Deng YH, Xu D, Su YX, Cheng YJ, Yang YL, Wang XY, Zhang J, You QD, Sun LP. Deng YH, et al. Among authors: you qd. Chem Biodivers. 2015 Apr;12(4):528-37. doi: 10.1002/cbdv.201400270. Chem Biodivers. 2015. PMID: 25879498

2

Design and synthesis of 7-alkoxy-4-heteroarylamino-3-quinolinecarbonitriles as dual inhibitors of c-Src kinase and nitric oxide synthase.

Cao X, You QD, Li ZY, Guo QL, Shang J, Yan M, Chern JW, Chen ML. Cao X, et al. Among authors: you qd. Bioorg Med Chem. 2008 Jun 1;16(11):5890-8. doi: 10.1016/j.bmc.2008.04.065. Epub 2008 Apr 29. Bioorg Med Chem. 2008. PMID: 18485715

3

Design, synthesis and biological evaluation of novel compounds with conjugated structure as anti-tumor agents.

Su H, Nebbioso A, Carafa V, Chen Y, Yang B, Altucci L, You Q. Su H, et al. Bioorg Med Chem. 2008 Sep 1;16(17):7992-8002. doi: 10.1016/j.bmc.2008.07.066. Epub 2008 Jul 29. Bioorg Med Chem. 2008. PMID: 18701301

4

Recent progress of SRC family kinase inhibitors as anticancer agents.

Cao X, You QD, Li ZY, Wang XJ, Lu XY, Liu XR, Xu D, Liu B. Cao X, et al. Among authors: you qd. Mini Rev Med Chem. 2008 Sep;8(10):1053-63. doi: 10.2174/138955708785740634. Mini Rev Med Chem. 2008. PMID: 18782057 Review.

5

The design, synthesis and biological evaluation of 7-alkoxy-4-heteroarylamino-3-cyanoquinolines as dual inhibitors of c-Src and iNOS.

Cao X, You QD, Li ZY, Liu XR, Xu D, Guo QL, Shang J, Chern JW, Chen ML. Cao X, et al. Among authors: you qd. Bioorg Med Chem Lett. 2008 Dec 1;18(23):6206-9. doi: 10.1016/j.bmcl.2008.10.006. Epub 2008 Oct 5. Bioorg Med Chem Lett. 2008. PMID: 18930653

6

[Synthesis and biological evaluation of tetrahydro-beta-carline derivatives].

Ruan XQ, You QD, Yang L, Wu WT. Ruan XQ, et al. Among authors: you qd. Yao Xue Xue Bao. 2008 Aug;43(8):828-32. Yao Xue Xue Bao. 2008. PMID: 18956775 Chinese.

7

Studies on chemical structure modification and biology of a natural product, gambogic acid (I): Synthesis and biological evaluation of oxidized analogues of gambogic acid.

Wang J, Zhao L, Hu Y, Guo Q, Zhang L, Wang X, Li N, You Q. Wang J, et al. Eur J Med Chem. 2009 Jun;44(6):2611-20. doi: 10.1016/j.ejmech.2008.09.034. Epub 2008 Oct 7. Eur J Med Chem. 2009. PMID: 18996626

8

Molecular hybridization, synthesis, and biological evaluation of novel chroman I(Kr) and I(Ks) dual blockers.

Du L, Li M, Yang Q, Tang Y, You Q, Xia L. Du L, et al. Bioorg Med Chem Lett. 2009 Mar 1;19(5):1477-80. doi: 10.1016/j.bmcl.2009.01.022. Epub 2009 Jan 14. Bioorg Med Chem Lett. 2009. PMID: 19185489

9

Design, synthesis and biological evaluation of novel substituted benzoylguanidine derivatives as potent Na+/H+ exchanger inhibitors.

Xu WT, Jin N, Xu J, Xu YG, Wang QJ, You QD. Xu WT, et al. Among authors: you qd. Bioorg Med Chem Lett. 2009 Jun 15;19(12):3283-7. doi: 10.1016/j.bmcl.2009.04.079. Epub 2009 Apr 23. Bioorg Med Chem Lett. 2009. PMID: 19433354

10

[The design, synthesis and anticancer activity of 4-heteroarylamino-3-cyanoquinolines as dual inhibitors of c-Src and iNOS].

Cao X, You QD, Li ZY, Guo QL, Yang Y, Shang J, Yan M, Chen JW, Chen ML. Cao X, et al. Among authors: you qd. Yao Xue Xue Bao. 2009 Mar;44(3):288-95. Yao Xue Xue Bao. 2009. PMID: 19449526 Chinese.

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