Suo FZ - Search Results

1

Discovery of tranylcypromine analogs with an acylhydrazone substituent as LSD1 inactivators: Design, synthesis and their biological evaluation.

Sun K, Peng JD, Suo FZ, Zhang T, Fu YD, Zheng YC, Liu HM. Sun K, et al. Among authors: suo fz. Bioorg Med Chem Lett. 2017 Nov 15;27(22):5036-5039. doi: 10.1016/j.bmcl.2017.10.003. Epub 2017 Oct 3. Bioorg Med Chem Lett. 2017. PMID: 29037950

2

Design, synthesis and in vitro evaluation of stilbene derivatives as novel LSD1 inhibitors for AML therapy.

Duan Y, Qin W, Suo F, Zhai X, Guan Y, Wang X, Zheng Y, Liu H. Duan Y, et al. Bioorg Med Chem. 2018 Dec 15;26(23-24):6000-6014. doi: 10.1016/j.bmc.2018.10.037. Epub 2018 Oct 29. Bioorg Med Chem. 2018. PMID: 30448189

3

Discovery of [1,2,3]Triazolo[4,5-d]pyrimidine Derivatives as Novel LSD1 Inhibitors.

Li ZH, Liu XQ, Geng PF, Suo FZ, Ma JL, Yu B, Zhao TQ, Zhou ZQ, Huang CX, Zheng YC, Liu HM. Li ZH, et al. Among authors: suo fz. ACS Med Chem Lett. 2017 Mar 6;8(4):384-389. doi: 10.1021/acsmedchemlett.6b00423. eCollection 2017 Apr 13. ACS Med Chem Lett. 2017. PMID: 28435523 Free PMC article.

4

An Overview on Screening Methods for Lysine Specific Demethylase 1 (LSD1) Inhibitors.

Zheng YC, Chang J, Zhang T, Suo FZ, Chen XB, Liu Y, Zhao B, Yu B, Liu HM. Zheng YC, et al. Among authors: suo fz. Curr Med Chem. 2017;24(23):2496-2504. doi: 10.2174/0929867324666170509114321. Curr Med Chem. 2017. PMID: 28486922 Review.

5

Lysine-specific demethylase 1 activation by vitamin B2 attenuates efficacy of apatinib for proliferation and migration of gastric cancer cell MGC-803.

Ma JL, Zhang T, Suo FZ, Chang J, Wan XB, Feng XJ, Zheng YC, Liu HM. Ma JL, et al. Among authors: suo fz. J Cell Biochem. 2018 Jun;119(6):4957-4966. doi: 10.1002/jcb.26741. Epub 2018 Mar 9. J Cell Biochem. 2018. PMID: 29384217

6

Identification of osimertinib (AZD9291) as a lysine specific demethylase 1 inhibitor.

Li ZR, Suo FZ, Hu B, Guo YJ, Fu DJ, Yu B, Zheng YC, Liu HM. Li ZR, et al. Among authors: suo fz. Bioorg Chem. 2019 Mar;84:164-169. doi: 10.1016/j.bioorg.2018.11.018. Epub 2018 Nov 16. Bioorg Chem. 2019. PMID: 30502627

7

Experience-based discovery (EBD) of aryl hydrazines as new scaffolds for the development of LSD1/KDM1A inhibitors.

Li ZR, Wang S, Yang L, Yuan XH, Suo FZ, Yu B, Liu HM. Li ZR, et al. Among authors: suo fz. Eur J Med Chem. 2019 Mar 15;166:432-444. doi: 10.1016/j.ejmech.2019.01.075. Epub 2019 Feb 2. Eur J Med Chem. 2019. PMID: 30739825

8

Synthesis, structure-activity relationship studies and biological characterization of new [1,2,4]triazolo[1,5-a]pyrimidine-based LSD1/KDM1A inhibitors.

Wang S, Li ZR, Suo FZ, Yuan XH, Yu B, Liu HM. Wang S, et al. Among authors: suo fz. Eur J Med Chem. 2019 Apr 1;167:388-401. doi: 10.1016/j.ejmech.2019.02.039. Epub 2019 Feb 13. Eur J Med Chem. 2019. PMID: 30780087

9

Sanggenon O induced apoptosis of A549 cells is counterbalanced by protective autophagy.

Li ZR, Ma T, Guo YJ, Hu B, Niu SH, Suo FZ, Du LN, You YH, Kang WT, Liu S, Mamun M, Song QM, Pang JR, Zheng YC, Liu HM. Li ZR, et al. Among authors: suo fz. Bioorg Chem. 2019 Jun;87:688-698. doi: 10.1016/j.bioorg.2019.03.072. Epub 2019 Apr 4. Bioorg Chem. 2019. PMID: 30953888

10

Discovery and synthesis of novel indole derivatives-containing 3-methylenedihydrofuran-2(3H)-one as irreversible LSD1 inhibitors.

Liu HM, Suo FZ, Li XB, You YH, Lv CT, Zheng CX, Zhang GC, Liu YJ, Kang WT, Zheng YC, Xu HW. Liu HM, et al. Among authors: suo fz. Eur J Med Chem. 2019 Aug 1;175:357-372. doi: 10.1016/j.ejmech.2019.04.065. Epub 2019 Apr 29. Eur J Med Chem. 2019. PMID: 31096156

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