Su M - Search Results

1

Design, synthesis and biological evaluation of 4-anilinothieno[2,3-d]pyrimidine-based hydroxamic acid derivatives as novel histone deacetylase inhibitors.

Yang W, Li L, Ji X, Wu X, Su M, Sheng L, Zang Y, Li J, Liu H. Yang W, et al. Among authors: su m. Bioorg Med Chem. 2014 Nov 1;22(21):6146-55. doi: 10.1016/j.bmc.2014.08.030. Epub 2014 Sep 4. Bioorg Med Chem. 2014. PMID: 25261927

2

Small molecule antagonizes autoinhibition and activates AMP-activated protein kinase in cells.

Pang T, Zhang ZS, Gu M, Qiu BY, Yu LF, Cao PR, Shao W, Su MB, Li JY, Nan FJ, Li J. Pang T, et al. Among authors: su mb. J Biol Chem. 2008 Jun 6;283(23):16051-60. doi: 10.1074/jbc.M710114200. Epub 2008 Mar 5. J Biol Chem. 2008. PMID: 18321858 Free PMC article.

3

Histone deacetylase inhibitor activity in royal jelly might facilitate caste switching in bees.

Spannhoff A, Kim YK, Raynal NJ, Gharibyan V, Su MB, Zhou YY, Li J, Castellano S, Sbardella G, Issa JP, Bedford MT. Spannhoff A, et al. Among authors: su mb. EMBO Rep. 2011 Mar;12(3):238-43. doi: 10.1038/embor.2011.9. Epub 2011 Feb 18. EMBO Rep. 2011. PMID: 21331099 Free PMC article.

4

Synthesis and biological evaluation of piperamide analogues as HDAC inhibitors.

Luo Y, Liu HM, Su MB, Sheng L, Zhou YB, Li J, Lu W. Luo Y, et al. Bioorg Med Chem Lett. 2011 Aug 15;21(16):4844-6. doi: 10.1016/j.bmcl.2011.06.046. Epub 2011 Jun 17. Bioorg Med Chem Lett. 2011. PMID: 21745740

5

Discovering novel α-aminoacyl-containing proline derivatives with potent and selective inhibitory activity against dipeptidyl peptidase IV: design, synthesis, biological evaluation, and molecular modeling.

Zhang X, Wang J, Su M, Li Z, Li J, Li J, Liu H. Zhang X, et al. Among authors: su m. Chem Biol Drug Des. 2012 Dec;80(6):843-52. doi: 10.1111/j.1747-0285.2012.01438.x. Epub 2012 Oct 12. Chem Biol Drug Des. 2012. PMID: 22726613

6

CCLab--a multi-objective genetic algorithm based combinatorial library design software and an application for histone deacetylase inhibitor design.

Fang G, Xue M, Su M, Hu D, Li Y, Xiong B, Ma L, Meng T, Chen Y, Li J, Li J, Shen J. Fang G, et al. Among authors: su m. Bioorg Med Chem Lett. 2012 Jul 15;22(14):4540-5. doi: 10.1016/j.bmcl.2012.05.123. Epub 2012 Jun 7. Bioorg Med Chem Lett. 2012. PMID: 22738629

7

Design, synthesis, structure-activity relationships, and docking studies of 1-(γ-1,2,3-triazol substituted prolyl)-(S)-3,3-difluoropyrrolidines as a novel series of potent and selective dipeptidyl peptidase-4 inhibitors.

Zhang L, Su M, Li J, Ji X, Wang J, Li Z, Li J, Liu H. Zhang L, et al. Among authors: su m. Chem Biol Drug Des. 2013 Feb;81(2):198-207. doi: 10.1111/cbdd.12058. Epub 2012 Nov 19. Chem Biol Drug Des. 2013. PMID: 22994702

8

The discovery of colchicine-SAHA hybrids as a new class of antitumor agents.

Zhang X, Zhang J, Tong L, Luo Y, Su M, Zang Y, Li J, Lu W, Chen Y. Zhang X, et al. Among authors: su m. Bioorg Med Chem. 2013 Jun 1;21(11):3240-4. doi: 10.1016/j.bmc.2013.03.049. Epub 2013 Mar 31. Bioorg Med Chem. 2013. PMID: 23602523

9

Design and synthesis of 4-(2,4,5-trifluorophenyl)butane-1,3-diamines as dipeptidyl peptidase IV inhibitors.

Zhu L, Li Y, Qiu L, Su M, Wang X, Xia C, Qu Y, Li J, Li J, Xiong B, Shen J. Zhu L, et al. Among authors: su m. ChemMedChem. 2013 Jul;8(7):1104-16. doi: 10.1002/cmdc.201300104. Epub 2013 May 13. ChemMedChem. 2013. PMID: 23671024

10

The design and synthesis of a new class of RTK/HDAC dual-targeted inhibitors.

Zhang X, Su M, Chen Y, Li J, Lu W. Zhang X, et al. Among authors: su m. Molecules. 2013 Jun 3;18(6):6491-503. doi: 10.3390/molecules18066491. Molecules. 2013. PMID: 23736786 Free PMC article.

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