Sang YL - Search Results

1

Sulfonamides containing coumarin moieties selectively and potently inhibit carbonic anhydrases II and IX: design, synthesis, inhibitory activity and 3D-QSAR analysis.

Wang ZC, Qin YJ, Wang PF, Yang YA, Wen Q, Zhang X, Qiu HY, Duan YT, Wang YT, Sang YL, Zhu HL. Wang ZC, et al. Among authors: sang yl. Eur J Med Chem. 2013 Aug;66:1-11. doi: 10.1016/j.ejmech.2013.04.035. Epub 2013 May 9. Eur J Med Chem. 2013. PMID: 23777898

2

Potentiating 1-(2-hydroxypropyl)-2-styryl-5-nitroimidazole derivatives against antibacterial agents: design, synthesis and biology analysis.

Wang ZC, Duan YT, Qin YJ, Wang PF, Luo Y, Wen Q, Yang YA, Sun J, Hu Y, Sang YL, Zhu HL. Wang ZC, et al. Among authors: sang yl. Eur J Med Chem. 2013 Jul;65:456-63. doi: 10.1016/j.ejmech.2013.05.004. Epub 2013 May 15. Eur J Med Chem. 2013. PMID: 23770447

3

Exploration of structure-based on imidazole core as antibacterial agents.

Duan YT, Wang ZC, Sang YL, Tao XX, Zhu HL. Duan YT, et al. Among authors: sang yl. Curr Top Med Chem. 2013;13(24):3118-30. doi: 10.2174/15680266113136660222. Curr Top Med Chem. 2013. PMID: 24200359 Review.

4

Design and synthesis of 2-styryl of 5-Nitroimidazole derivatives and antimicrobial activities as FabH inhibitors.

Duan YT, Wang ZC, Sang YL, Tao XX, Teraiya SB, Wang PF, Wen Q, Zhou XJ, Ding L, Yang YH, Zhu HL. Duan YT, et al. Among authors: sang yl. Eur J Med Chem. 2014 Apr 9;76:387-96. doi: 10.1016/j.ejmech.2014.02.004. Epub 2014 Feb 15. Eur J Med Chem. 2014. PMID: 24594526

5

Discovery and molecular modeling of novel 1-indolyl acetate--5-nitroimidazole targeting tubulin polymerization as antiproliferative agents.

Duan YT, Sang YL, Makawana JA, Teraiya SB, Yao YF, Tang DJ, Tao XX, Zhu HL. Duan YT, et al. Among authors: sang yl. Eur J Med Chem. 2014 Oct 6;85:341-51. doi: 10.1016/j.ejmech.2014.07.082. Epub 2014 Jul 30. Eur J Med Chem. 2014. PMID: 25105922

6

Indole-based, Antiproliferative Agents Targeting Tubulin Polymerization.

Sang YL, Zhang WM, Lv PC, Zhu HL. Sang YL, et al. Curr Top Med Chem. 2017;17(2):120-137. doi: 10.2174/1568026616666160530154812. Curr Top Med Chem. 2017. PMID: 27237326 Review.

7

Design and synthesis of a novel series of non-nucleoside HIV-1 inhibitors bearing pyrimidine and N-substituted aromatic piperazine.

Jin K, Sang Y, De Clercq E, Pannecouque C, Meng G. Jin K, et al. Bioorg Med Chem Lett. 2018 Dec 1;28(22):3491-3495. doi: 10.1016/j.bmcl.2018.10.010. Epub 2018 Oct 9. Bioorg Med Chem Lett. 2018. PMID: 30318436

8

Conformational restriction design of thiophene-biphenyl-DAPY HIV-1 non-nucleoside reverse transcriptase inhibitors.

Sang Y, Han S, Pannecouque C, De Clercq E, Zhuang C, Chen F. Sang Y, et al. Eur J Med Chem. 2019 Nov 15;182:111603. doi: 10.1016/j.ejmech.2019.111603. Epub 2019 Aug 8. Eur J Med Chem. 2019. PMID: 31421633

9

Ligand-Based Design of Nondimethylphenyl-Diarylpyrimidines with Improved Metabolic Stability, Safety, and Oral Pharmacokinetic Profiles.

Sang Y, Han S, Pannecouque C, De Clercq E, Zhuang C, Chen F. Sang Y, et al. J Med Chem. 2019 Dec 26;62(24):11430-11436. doi: 10.1021/acs.jmedchem.9b01446. Epub 2019 Dec 16. J Med Chem. 2019. PMID: 31714780

10

Fragment hopping-based discovery of novel sulfinylacetamide-diarylpyrimidines (DAPYs) as HIV-1 nonnucleoside reverse transcriptase inhibitors.

Han S, Sang Y, Wu Y, Tao Y, Pannecouque C, De Clercq E, Zhuang C, Chen FE. Han S, et al. Eur J Med Chem. 2020 Jan 1;185:111874. doi: 10.1016/j.ejmech.2019.111874. Epub 2019 Nov 10. Eur J Med Chem. 2020. PMID: 31735575

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