Su M - Search Results

1

High-throughput screening of SARS-CoV-2 main and papain-like protease inhibitors.

Zang Y, Su M, Wang Q, Cheng X, Zhang W, Zhao Y, Chen T, Jiang Y, Shen Q, Du J, Tan Q, Wang P, Gao L, Jin Z, Zhang M, Li C, Zhu Y, Feng B, Tang B, Xie H, Wang MW, Zheng M, Pan X, Yang H, Xu Y, Wu B, Zhang L, Rao Z, Yang X, Jiang H, Xiao G, Zhao Q, Li J. Zang Y, et al. Among authors: su m. Protein Cell. 2022 Sep 28;14(1):17-27. doi: 10.1093/procel/pwac016. eCollection 2023 Jan. Protein Cell. 2022. PMID: 36726755 Free PMC article.

2

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

3

Design, synthesis and biological evaluation of colchicine derivatives as novel tubulin and histone deacetylase dual inhibitors.

Zhang X, Kong Y, Zhang J, Su M, Zhou Y, Zang Y, Li J, Chen Y, Fang Y, Zhang X, Lu W. Zhang X, et al. Among authors: su m. Eur J Med Chem. 2015 May 5;95:127-35. doi: 10.1016/j.ejmech.2015.03.035. Epub 2015 Mar 18. Eur J Med Chem. 2015. PMID: 25805446

4

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

5

Design, synthesis and biological evaluation of isoquinoline-based derivatives as novel histone deacetylase inhibitors.

Yang W, Li L, Wang Y, Wu X, Li T, Yang N, Su M, Sheng L, Zheng M, Zang Y, Li J, Liu H. Yang W, et al. Among authors: su m. Bioorg Med Chem. 2015 Sep 1;23(17):5881-90. doi: 10.1016/j.bmc.2015.06.071. Epub 2015 Jul 4. Bioorg Med Chem. 2015. PMID: 26211462

6

Design, synthesis and biological evaluation of thienopyrimidine hydroxamic acid based derivatives as structurally novel histone deacetylase (HDAC) inhibitors.

Wang J, Su M, Li T, Gao A, Yang W, Sheng L, Zang Y, Li J, Liu H. Wang J, et al. Among authors: su m. Eur J Med Chem. 2017 Mar 10;128:293-299. doi: 10.1016/j.ejmech.2017.01.035. Epub 2017 Jan 23. Eur J Med Chem. 2017. PMID: 28213282

7

5-Aminonaphthalene derivatives as selective nonnucleoside nuclear receptor binding SET domain-protein 2 (NSD2) inhibitors for the treatment of multiple myeloma.

Wang S, Yang H, Su M, Lian F, Cong Z, Wei R, Zhou Y, Li X, Zheng X, Li C, Fu X, Han X, Shi Q, Li C, Zhang N, Geng M, Liu H, Li J, Huang X, Wang J. Wang S, et al. Among authors: su m. Eur J Med Chem. 2021 Oct 15;222:113592. doi: 10.1016/j.ejmech.2021.113592. Epub 2021 Jun 5. Eur J Med Chem. 2021. PMID: 34147909

8

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

9

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

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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