Zhang P - Search Results

1

Design, synthesis and antibacterial evaluation of novel 15-membered 11a-azahomoclarithromycin derivatives with the 1, 2, 3-triazole side chain.

Qin Y, Teng Y, Ma R, Bi F, Liu Z, Zhang P, Ma S. Qin Y, et al. Among authors: zhang p. Eur J Med Chem. 2019 Oct 15;180:321-339. doi: 10.1016/j.ejmech.2019.07.022. Epub 2019 Jul 11. Eur J Med Chem. 2019. PMID: 31323617

2

Discovery of 1,3,4-oxadiazol-2-one-containing benzamide derivatives targeting FtsZ as highly potent agents of killing a variety of MDR bacteria strains.

Bi F, Song D, Qin Y, Liu X, Teng Y, Zhang N, Zhang P, Zhang N, Ma S. Bi F, et al. Among authors: zhang n, zhang p. Bioorg Med Chem. 2019 Jul 15;27(14):3179-3193. doi: 10.1016/j.bmc.2019.06.010. Epub 2019 Jun 7. Bioorg Med Chem. 2019. PMID: 31200986

3

Recent development of leucyl-tRNA synthetase inhibitors as antimicrobial agents.

Zhang P, Ma S. Zhang P, et al. Medchemcomm. 2019 May 27;10(8):1329-1341. doi: 10.1039/c9md00139e. eCollection 2019 Aug 1. Medchemcomm. 2019. PMID: 31534653 Free PMC article. Review.

4

A novel series of 11-O-carbamoyl-3-O-descladinosyl clarithromycin derivatives bearing 1,2,3-triazole group: Design, synthesis and antibacterial evaluation.

Teng Y, Qin Y, Song D, Liu X, Ma Y, Zhang P, Ma S. Teng Y, et al. Among authors: zhang p. Bioorg Med Chem Lett. 2020 Jan 15;30(2):126850. doi: 10.1016/j.bmcl.2019.126850. Epub 2019 Dec 3. Bioorg Med Chem Lett. 2020. PMID: 31836439

5

Design and synthesis of aryl-substituted pyrrolidone derivatives as quorum sensing inhibitors.

Liu Z, Zhang P, Qin Y, Zhang N, Teng Y, Venter H, Ma S. Liu Z, et al. Among authors: zhang n, zhang p. Bioorg Chem. 2020 Dec;105:104376. doi: 10.1016/j.bioorg.2020.104376. Epub 2020 Oct 13. Bioorg Chem. 2020. PMID: 33099165

6

Design and structural optimization of novel 2H-benzo[h]chromene derivatives that target AcrB and reverse bacterial multidrug resistance.

Wang Y, Alenazy R, Gu X, Polyak SW, Zhang P, Sykes MJ, Zhang N, Venter H, Ma S. Wang Y, et al. Among authors: zhang n, zhang p. Eur J Med Chem. 2021 Mar 5;213:113049. doi: 10.1016/j.ejmech.2020.113049. Epub 2020 Nov 27. Eur J Med Chem. 2021. PMID: 33279291

7

Design, synthesis and evaluation of novel 9-arylalkyl-10-methylacridinium derivatives as highly potent FtsZ-targeting antibacterial agents.

Song D, Zhang N, Zhang P, Zhang N, Chen W, Zhang L, Guo T, Gu X, Ma S. Song D, et al. Among authors: zhang n, zhang l, zhang p. Eur J Med Chem. 2021 Oct 5;221:113480. doi: 10.1016/j.ejmech.2021.113480. Epub 2021 Apr 28. Eur J Med Chem. 2021. PMID: 33964649

8

Design, synthesis and structure-activity relationships of novel N11-, C12- and C13-substituted 15-membered homo-aza-clarithromycin derivatives against various resistant bacteria.

Qin Y, Song D, Teng Y, Liu X, Zhang P, Zhang N, Zhang N, Chen W, Ma S. Qin Y, et al. Among authors: zhang n, zhang p. Bioorg Chem. 2021 Aug;113:104992. doi: 10.1016/j.bioorg.2021.104992. Epub 2021 May 18. Bioorg Chem. 2021. PMID: 34051415

9

Modification of 5-methylphenanthridium from benzothiazoles to indoles as potent FtsZ inhibitors: Broadening the antibacterial spectrum toward vancomycin-resistant enterococci.

Zhang N, Song D, Chen W, Zhang S, Zhang P, Zhang N, Ma S. Zhang N, et al. Among authors: zhang s, zhang p. Eur J Med Chem. 2021 Nov 15;224:113723. doi: 10.1016/j.ejmech.2021.113723. Epub 2021 Jul 26. Eur J Med Chem. 2021. PMID: 34340044

10

Rational design and synthesis of Oreoch-2 analogues as efficient broad-spectrum antimicrobial peptides.

Zhang N, Gu X, Song D, Zhang P, Zhang N, Chen W, Ji S, Qi Y, Ma S. Zhang N, et al. Among authors: zhang p. Bioorg Chem. 2022 Feb;119:105583. doi: 10.1016/j.bioorg.2021.105583. Epub 2021 Dec 24. Bioorg Chem. 2022. PMID: 34971943

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