Li NG - Search Results

1

Design and synthesis 1H-Pyrrolo[2,3-b]pyridine derivatives as FLT3 inhibitors for the treatment of Acute myeloid Leukemia.

Wei TH, Zhou Y, Yang J, Zhang MY, Wang JJ, Tong ZJ, Wu JZ, Wang YB, Sha JK, Chen M, Ding N, Yu YC, Dai WC, Leng XJ, Xue X, Sun SL, Wang XL, Li NG, Shi ZH. Wei TH, et al. Among authors: li ng. Bioorg Med Chem. 2024 Feb 15;100:117631. doi: 10.1016/j.bmc.2024.117631. Epub 2024 Feb 2. Bioorg Med Chem. 2024. PMID: 38330848

2

Recent progress on the total synthesis of acetogenins from Annonaceae.

Li N, Shi Z, Tang Y, Chen J, Li X. Li N, et al. Beilstein J Org Chem. 2008;4:48. doi: 10.3762/bjoc.4.48. Epub 2008 Dec 5. Beilstein J Org Chem. 2008. PMID: 19190742 Free PMC article.

3

Highly efficient esterification of ferulic acid under microwave irradiation.

Li NG, Shi ZH, Tang YP, Li BQ, Duan JA. Li NG, et al. Among authors: li bq. Molecules. 2009 Jun 10;14(6):2118-26. doi: 10.3390/molecules14062118. Molecules. 2009. PMID: 19553885 Free PMC article.

4

An efficient partial synthesis of 4'-O-methylquercetin via regioselective protection and alkylation of quercetin.

Li NG, Shi ZH, Tang YP, Yang JP, Duan JA. Li NG, et al. Beilstein J Org Chem. 2009 Nov 4;5:60. doi: 10.3762/bjoc.5.60. Beilstein J Org Chem. 2009. PMID: 20300474 Free PMC article.

5

Metabolism-based synthesis, biologic evaluation and SARs analysis of O-methylated analogs of quercetin as thrombin inhibitors.

Shi ZH, Li NG, Tang YP, Wei-Li, Lian-Yin, Yang JP, Hao-Tang, Duan JA. Shi ZH, et al. Among authors: li ng. Eur J Med Chem. 2012 Aug;54:210-22. doi: 10.1016/j.ejmech.2012.04.044. Epub 2012 May 14. Eur J Med Chem. 2012. PMID: 22647223

6

Design, synthesis and biological evaluation of ferulic Acid amides as selective matrix metalloproteinase inhibitors.

Shi ZH, Li NG, Shi QP, Tang H, Tang YP, Li W, Yin L, Yang JP, Duan JA. Shi ZH, et al. Among authors: li w, li ng. Med Chem. 2013 Nov;9(7):947-54. doi: 10.2174/1573406411309070008. Med Chem. 2013. PMID: 23061601

7

Mannich bases of scutellarein as thrombin-inhibitors: design, synthesis, biological activity and solubility.

Li NG, Song SL, Shen MZ, Tang YP, Shi ZH, Tang H, Shi QP, Fu YF, Duan JA. Li NG, et al. Bioorg Med Chem. 2012 Dec 15;20(24):6919-23. doi: 10.1016/j.bmc.2012.10.015. Epub 2012 Oct 23. Bioorg Med Chem. 2012. PMID: 23131413

8

Design, synthesis and biological evaluation of glucose-containing scutellarein derivatives as neuroprotective agents based on metabolic mechanism of scutellarin in vivo.

Li NG, Shen MZ, Wang ZJ, Tang YP, Shi ZH, Fu YF, Shi QP, Tang H, Duan JA. Li NG, et al. Bioorg Med Chem Lett. 2013 Jan 1;23(1):102-6. doi: 10.1016/j.bmcl.2012.11.002. Epub 2012 Nov 10. Bioorg Med Chem Lett. 2013. PMID: 23177255

9

Synthesis and structure-activity relationship analysis of caffeic acid amides as selective matrix metalloproteinase inhibitors.

Shi ZH, Li NG, Shi QP, Tang H, Tang YP, Li W, Yin L, Yang JP, Duan JA. Shi ZH, et al. Among authors: li w, li ng. Bioorg Med Chem Lett. 2013 Mar 1;23(5):1206-11. doi: 10.1016/j.bmcl.2013.01.027. Epub 2013 Jan 16. Bioorg Med Chem Lett. 2013. PMID: 23375794

10

Biological evaluation and SAR analysis of O-methylated analogs of quercetin as inhibitors of cancer cell proliferation.

Shi ZH, Li NG, Tang YP, Shi QP, Tang H, Li W, Zhang X, Fu HA, Duan JA. Shi ZH, et al. Among authors: li w, li ng. Drug Dev Res. 2014 Nov;75(7):455-62. doi: 10.1002/ddr.21181. Epub 2014 Jun 27. Drug Dev Res. 2014. PMID: 24976071

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