Ye XS - Search Results

1

3D-QSAR analysis of sialyltransferase inhibitors.

Wang X, Niu Y, Cao X, Zhang L, Zhang LH, Ye XS. Wang X, et al. Among authors: ye xs. Bioorg Med Chem. 2003 Sep 15;11(19):4217-24. doi: 10.1016/s0968-0896(03)00489-9. Bioorg Med Chem. 2003. PMID: 12951152

2

Recent development in the design of sialyltransferase inhibitors.

Wang X, Zhang LH, Ye XS. Wang X, et al. Among authors: ye xs. Med Res Rev. 2003 Jan;23(1):32-47. doi: 10.1002/med.10030. Med Res Rev. 2003. PMID: 12424752 Review.

3

Synthetic iminosugar derivatives as new potential immunosuppressive agents.

Ye XS, Sun F, Liu M, Li Q, Wang Y, Zhang G, Zhang LH, Zhang XL. Ye XS, et al. J Med Chem. 2005 Jun 2;48(11):3688-91. doi: 10.1021/jm050169t. J Med Chem. 2005. PMID: 15916418

4

Base-promoted rearrangement of sugar epoxides to unsaturated sugars.

Wang Y, Li Q, Cheng S, Wu Y, Guo D, Fan QH, Wang X, Zhang LH, Ye XS. Wang Y, et al. Among authors: ye xs. Org Lett. 2005 Dec 8;7(25):5577-9. doi: 10.1021/ol052128x. Org Lett. 2005. PMID: 16320995

5

An expeditious one-pot synthesis of 1,6-dideoxy-N-alkylated nojirimycin derivatives and their inhibitory effects on the secretion of IFN-gamma and IL-4.

Zhou J, Zhang Y, Zhou X, Zhou J, Zhang LH, Ye XS, Zhang XL. Zhou J, et al. Among authors: ye xs. Bioorg Med Chem. 2008 Feb 15;16(4):1605-12. doi: 10.1016/j.bmc.2007.11.036. Epub 2007 Nov 17. Bioorg Med Chem. 2008. PMID: 18060793

6

Rational design and synthesis of highly potent pharmacological chaperones for treatment of N370S mutant Gaucher disease.

Wang GN, Reinkensmeier G, Zhang SW, Zhou J, Zhang LR, Zhang LH, Butters TD, Ye XS. Wang GN, et al. Among authors: ye xs. J Med Chem. 2009 May 28;52(10):3146-9. doi: 10.1021/jm801506m. J Med Chem. 2009. PMID: 19397268

7

Development of aminoglycoside antibiotics effective against resistant bacterial strains.

Yang L, Ye XS. Yang L, et al. Among authors: ye xs. Curr Top Med Chem. 2010;10(18):1898-26. doi: 10.2174/156802610793176684. Curr Top Med Chem. 2010. PMID: 20615188 Review.

8

Rational design and synthesis of potent aminoglycoside antibiotics against resistant bacterial strains.

Yan RB, Yuan M, Wu Y, You X, Ye XS. Yan RB, et al. Among authors: ye xs. Bioorg Med Chem. 2011 Jan 1;19(1):30-40. doi: 10.1016/j.bmc.2010.11.065. Epub 2010 Dec 4. Bioorg Med Chem. 2011. PMID: 21177112

9

Synthesis and in vitro anti-hepatitis B virus activity of six-membered azanucleoside analogues.

Wang D, Li YH, Wang YP, Gao RM, Zhang LH, Ye XS. Wang D, et al. Among authors: ye xs. Bioorg Med Chem. 2011 Jan 1;19(1):41-51. doi: 10.1016/j.bmc.2010.11.063. Epub 2010 Dec 4. Bioorg Med Chem. 2011. PMID: 21183354

10

Synthesis of N-substituted ε-hexonolactams as pharmacological chaperones for the treatment of N370S mutant Gaucher disease.

Wang GN, Twigg G, Butters TD, Zhang S, Zhang L, Zhang LH, Ye XS. Wang GN, et al. Among authors: ye xs. Org Biomol Chem. 2012 Apr 21;10(15):2923-7. doi: 10.1039/c2ob06987c. Epub 2012 Jan 27. Org Biomol Chem. 2012. PMID: 22286559

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