Pang LP - Search Results

1

Design and synthesis of novel 1,2,3-triazole-pyrimidine-urea hybrids as potential anticancer agents.

Ma LY, Wang B, Pang LP, Zhang M, Wang SQ, Zheng YC, Shao KP, Xue DQ, Liu HM. Ma LY, et al. Among authors: pang lp. Bioorg Med Chem Lett. 2015 Mar 1;25(5):1124-8. doi: 10.1016/j.bmcl.2014.12.087. Epub 2015 Jan 6. Bioorg Med Chem Lett. 2015. PMID: 25655718

2

Design and synthesis of novel D-ring fused steroidal heterocycles.

Zhang BL, Zhang E, Pang LP, Song LX, Li YF, Yu B, Liu HM. Zhang BL, et al. Among authors: pang lp. Steroids. 2013 Dec 11;78(12-13):1200-8. doi: 10.1016/j.steroids.2013.07.006. Epub 2013 Aug 1. Steroids. 2013. PMID: 23911850

3

Design and synthesis of novel 1,2,3-triazole-pyrimidine hybrids as potential anticancer agents.

Ma LY, Pang LP, Wang B, Zhang M, Hu B, Xue DQ, Shao KP, Zhang BL, Liu Y, Zhang E, Liu HM. Ma LY, et al. Among authors: pang lp. Eur J Med Chem. 2014 Oct 30;86:368-80. doi: 10.1016/j.ejmech.2014.08.010. Epub 2014 Aug 5. Eur J Med Chem. 2014. PMID: 25180925

4

Design, synthesis, and structure-activity relationship of novel LSD1 inhibitors based on pyrimidine-thiourea hybrids as potent, orally active antitumor agents.

Ma LY, Zheng YC, Wang SQ, Wang B, Wang ZR, Pang LP, Zhang M, Wang JW, Ding L, Li J, Wang C, Hu B, Liu Y, Zhang XD, Wang JJ, Wang ZJ, Zhao W, Liu HM. Ma LY, et al. Among authors: pang lp. J Med Chem. 2015 Feb 26;58(4):1705-16. doi: 10.1021/acs.jmedchem.5b00037. Epub 2015 Feb 6. J Med Chem. 2015. PMID: 25610955

5

LPE-1, an orally active pyrimidine derivative, inhibits growth and mobility of human esophageal cancers by targeting LSD1.

Wang B, Zhao B, Pang LP, Zhao YD, Guo Q, Wang JW, Zheng YC, Zhang XH, Liu Y, Liu GY, Guo WG, Wang C, Li ZH, Mao XJ, Yu B, Ma LY, Liu HM. Wang B, et al. Among authors: pang lp. Pharmacol Res. 2017 Aug;122:66-77. doi: 10.1016/j.phrs.2017.05.025. Epub 2017 May 30. Pharmacol Res. 2017. PMID: 28571892

6

Exploration of 1,2,3-triazole-pyrimidine hybrids as potent reversal agents against ABCB1-mediated multidrug resistance.

Wang B, Zhao B, Chen ZS, Pang LP, Zhao YD, Guo Q, Zhang XH, Liu Y, Liu GY, Hao-Zhang, Zhang XY, Ma LY, Liu HM. Wang B, et al. Among authors: pang lp. Eur J Med Chem. 2018 Jan 1;143:1535-1542. doi: 10.1016/j.ejmech.2017.10.041. Epub 2017 Oct 21. Eur J Med Chem. 2018. PMID: 29126726

7

Detailed resume of RNA m⁶A demethylases.

Shen D, Wang B, Gao Y, Zhao L, Bi Y, Zhang J, Wang N, Kang H, Pang J, Liu Y, Pang L, Chen ZS, Zheng YC, Liu HM. Shen D, et al. Acta Pharm Sin B. 2022 May;12(5):2193-2205. doi: 10.1016/j.apsb.2022.01.003. Epub 2022 Jan 11. Acta Pharm Sin B. 2022. PMID: 35646549 Free PMC article. Review.

8

Editorial: Novel anti-cancer agents targeting tumour metastasis and stemness.

Pang L, Wang B. Pang L, et al. Front Pharmacol. 2024 Oct 30;15:1504024. doi: 10.3389/fphar.2024.1504024. eCollection 2024. Front Pharmacol. 2024. PMID: 39539616 Free PMC article. No abstract available.

9

Comparative analysis of pyrimidine substituted aminoacyl-sulfamoyl nucleosides as potential inhibitors targeting class I aminoacyl-tRNA synthetases.

Nautiyal M, De Graef S, Pang L, Gadakh B, Strelkov SV, Weeks SD, Van Aerschot A. Nautiyal M, et al. Eur J Med Chem. 2019 Jul 1;173:154-166. doi: 10.1016/j.ejmech.2019.04.003. Epub 2019 Apr 5. Eur J Med Chem. 2019. PMID: 30995568

10

Synthesis and structural insights into the binding mode of the albomycin δ1 core and its analogues in complex with their target aminoacyl-tRNA synthetase.

Gadakh B, Vondenhoff G, Pang L, Nautiyal M, De Graef S, Strelkov SV, Weeks SD, Van Aerschot A. Gadakh B, et al. Bioorg Med Chem. 2020 Sep 1;28(17):115645. doi: 10.1016/j.bmc.2020.115645. Epub 2020 Jul 13. Bioorg Med Chem. 2020. PMID: 32773091

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