Cui YM - Search Results

1

Specificity for inhibitors of metal-substituted methionine aminopeptidase.

Li JY, Chen LL, Cui YM, Luo QL, Li J, Nan FJ, Ye QZ. Li JY, et al. Among authors: cui ym. Biochem Biophys Res Commun. 2003 Jul 18;307(1):172-9. doi: 10.1016/s0006-291x(03)01144-6. Biochem Biophys Res Commun. 2003. PMID: 12849997

2

Mutations at the S1 sites of methionine aminopeptidases from Escherichia coli and Homo sapiens reveal the residues critical for substrate specificity.

Li JY, Cui YM, Chen LL, Gu M, Li J, Nan FJ, Ye QZ. Li JY, et al. Among authors: cui ym. J Biol Chem. 2004 May 14;279(20):21128-34. doi: 10.1074/jbc.M401679200. Epub 2004 Feb 19. J Biol Chem. 2004. PMID: 14976199 Free article.

3

Design and synthesis of chromogenic thiopeptolide substrates as MetAPs active site probes.

Cui YM, Li JY, Chen LL, Li J, Ye QZ, Nan FJ. Cui YM, et al. Bioorg Med Chem. 2004 Jun 1;12(11):2853-61. doi: 10.1016/j.bmc.2004.03.044. Bioorg Med Chem. 2004. PMID: 15142545

4

Characterization of full length and truncated type I human methionine aminopeptidases expressed from Escherichia coli.

Li JY, Chen LL, Cui YM, Luo QL, Gu M, Nan FJ, Ye QZ. Li JY, et al. Among authors: cui ym. Biochemistry. 2004 Jun 22;43(24):7892-8. doi: 10.1021/bi0360859. Biochemistry. 2004. PMID: 15196033

5

Identification of potent type I MetAP inhibitors by simple bioisosteric replacement. Part 1: Synthesis and preliminary SAR studies of thiazole-4-carboxylic acid thiazol-2-ylamide derivatives.

Cui YM, Huang QQ, Xu J, Chen LL, Li JY, Ye QZ, Li J, Nan FJ. Cui YM, et al. Bioorg Med Chem Lett. 2005 Aug 15;15(16):3732-6. doi: 10.1016/j.bmcl.2005.05.055. Bioorg Med Chem Lett. 2005. PMID: 15993057

6

Identification of potent type I MetAPs inhibitors by simple bioisosteric replacement. Part 2: SAR studies of 5-heteroalkyl substituted TCAT derivatives.

Cui YM, Huang QQ, Xu J, Chen LL, Li JY, Ye QZ, Li J, Nan FJ. Cui YM, et al. Bioorg Med Chem Lett. 2005 Sep 15;15(18):4130-5. doi: 10.1016/j.bmcl.2005.06.005. Bioorg Med Chem Lett. 2005. PMID: 16005224

7

Total synthesis of the originally proposed and revised structures of scleritodermin A.

Liu S, Cui YM, Nan FJ. Liu S, et al. Among authors: cui ym. Org Lett. 2008 Sep 4;10(17):3765-8. doi: 10.1021/ol801419m. Epub 2008 Aug 8. Org Lett. 2008. PMID: 18686965

8

The synthesis and antileukemic activity of 5-substituted thiazolyl urea derivatives.

Peng C, Sheng L, Xu GY, Qi XL, Zhou YB, Jia-Li, Cui YM. Peng C, et al. Among authors: cui ym. Bioorg Med Chem Lett. 2025 Jan 1;115:130018. doi: 10.1016/j.bmcl.2024.130018. Epub 2024 Nov 12. Bioorg Med Chem Lett. 2025. PMID: 39536837

9

Characterization of covalent binding of tyrosine kinase inhibitors to plasma proteins.

Liu X, Feng D, Zheng M, Cui Y, Zhong D. Liu X, et al. Drug Metab Pharmacokinet. 2020 Oct;35(5):456-465. doi: 10.1016/j.dmpk.2020.07.002. Epub 2020 Jul 24. Drug Metab Pharmacokinet. 2020. PMID: 32847720

10

Design, synthesis, and structure-activity relationship studies of novel tetrazole antifungal agents with potent activity, broad antifungal spectrum and high selectivity.

Qian A, Zheng Y, Wang R, Wei J, Cui Y, Cao X, Yang Y. Qian A, et al. Bioorg Med Chem Lett. 2018 Feb 1;28(3):344-350. doi: 10.1016/j.bmcl.2017.12.040. Epub 2017 Dec 20. Bioorg Med Chem Lett. 2018. PMID: 29289430

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