Ma Y - Search Results

1

Design, synthesis, biological evaluation, and structure-activity relationship (SAR) discussion of dipeptidyl boronate proteasome inhibitors, part I: comprehensive understanding of the SAR of alpha-amino acid boronates.

Zhu Y, Zhao X, Zhu X, Wu G, Li Y, Ma Y, Yuan Y, Yang J, Hu Y, Ai L, Gao Q. Zhu Y, et al. Among authors: ma y. J Med Chem. 2009 Jul 23;52(14):4192-9. doi: 10.1021/jm9005093. J Med Chem. 2009. PMID: 19537716

2

Synthesis, in vitro and in vivo biological evaluation, docking studies, and structure--activity relationship (SAR) discussion of dipeptidyl boronic acid proteasome inhibitors composed of beta-amino acids.

Zhu Y, Zhu X, Wu G, Ma Y, Li Y, Zhao X, Yuan Y, Yang J, Yu S, Shao F, Li R, Ke Y, Lu A, Liu Z, Zhang L. Zhu Y, et al. Among authors: ma y. J Med Chem. 2010 Mar 11;53(5):1990-9. doi: 10.1021/jm901407s. J Med Chem. 2010. PMID: 20158184

3

Synthesis, in vitro and in vivo biological evaluation, and comprehensive understanding of structure-activity relationships of dipeptidyl boronic acid proteasome inhibitors constructed from β-amino acids.

Zhu Y, Wu G, Zhu X, Ma Y, Zhao X, Li Y, Yuan Y, Yang J, Yu S, Shao F, Lei M. Zhu Y, et al. Among authors: ma y. J Med Chem. 2010 Dec 23;53(24):8619-26. doi: 10.1021/jm1009742. Epub 2010 Nov 15. J Med Chem. 2010. PMID: 21077681

4

Synthesis of salinosporamide A and its analogs as 20S proteasome inhibitors and SAR summarization.

Ma Y, Qu L, Liu Z, Zhang L, Yang Z, Zhang L. Ma Y, et al. Curr Top Med Chem. 2011 Dec;11(23):2906-22. doi: 10.2174/156802611798281302. Curr Top Med Chem. 2011. PMID: 21824108 Review.

5

Synthesis and SAR study of novel peptide aldehydes as inhibitors of 20S proteasome.

Ma Y, Xu B, Fang Y, Yang Z, Cui J, Zhang L, Zhang L. Ma Y, et al. Molecules. 2011 Sep 5;16(9):7551-64. doi: 10.3390/molecules16097551. Molecules. 2011. PMID: 21894088 Free PMC article.

6

[Design, synthesis and biological assay of novel tripeptidic tetrazoles as inhibitors of 20S proteasome].

Ma YH, Xu B, Cui JR, Yang ZJ, Zhang LR, Zhang LH. Ma YH, et al. Yao Xue Xue Bao. 2012 Apr;47(4):472-8. Yao Xue Xue Bao. 2012. PMID: 22799029 Chinese.

7

Design of coiled-coil N-peptides against HIV-1 based on a CADD strategy.

Huang Y, Luo H, Jin Y, Ma Y, Zhao Y, Gao X, Zhao Y, Qi X, Liang G, Ga L, Li G, Yang J. Huang Y, et al. Among authors: ma y. Org Biomol Chem. 2024 Dec 18;23(1):157-166. doi: 10.1039/d4ob01620c. Org Biomol Chem. 2024. PMID: 39523986

8

Structure and Function of the SARS-CoV-2 6-HB Fusion Core and Peptide-Based Fusion Inhibitors: A Review.

Liang G, Li Y, Li R, Ma Y, Na H. Liang G, et al. Among authors: ma y. Curr Med Chem. 2023 Nov 24. doi: 10.2174/0109298673265694231113061842. Online ahead of print. Curr Med Chem. 2023. PMID: 38018192

9

An N-terminal heptad repeat trimer-based peptide fusion inhibitor exhibits potent anti-H1N1 activity.

Na H, Luo H, Wang J, Sun L, Gao X, Liang G, Ma Y, Meng Z. Na H, et al. Among authors: ma y. Bioorg Med Chem. 2024 Sep 1;111:117865. doi: 10.1016/j.bmc.2024.117865. Epub 2024 Jul 31. Bioorg Med Chem. 2024. PMID: 39098126

10

Structural Basis of HIV-1 gp41 N-trimer for Designing Bifunctional Peptide-based Fusion Inhibitors.

Wang J, Li P, Li R, Liang G, Ma Y, Na H. Wang J, et al. Among authors: ma y. Curr Med Chem. 2024 Apr 3. doi: 10.2174/0109298673291459240328074404. Online ahead of print. Curr Med Chem. 2024. PMID: 38584558

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