Chen BQ - Search Results

1

A selective cascade reaction-based probe for colorimetric and ratiometric fluorescence detection of benzoyl peroxide in food and living cells.

Wu X, Zeng L, Chen BQ, Zhang M, Rodrigues J, Sheng R, Bao GM. Wu X, et al. Among authors: chen bq. J Mater Chem B. 2019 Oct 14;7(38):5775-5781. doi: 10.1039/c9tb00889f. Epub 2019 Sep 11. J Mater Chem B. 2019. PMID: 31508649

2

A distinctive mitochondrion-targeting, in situ-activatable near-infrared fluorescent probe for visualizing sulfur dioxide derivatives and their fluctuations in vivo.

Zeng L, Chen T, Chen BQ, Yuan HQ, Sheng R, Bao GM. Zeng L, et al. Among authors: chen bq, chen t. J Mater Chem B. 2020 Mar 4;8(9):1914-1921. doi: 10.1039/c9tb02593f. J Mater Chem B. 2020. PMID: 32048683

3

Synthesis and antitumor-evaluation of 1,3,4-thiadiazole-containing benzisoselenazolone derivatives.

Luo Z, Chen B, He S, Shi Y, Liu Y, Li C. Luo Z, et al. Bioorg Med Chem Lett. 2012 May 1;22(9):3191-3. doi: 10.1016/j.bmcl.2012.03.043. Epub 2012 Mar 21. Bioorg Med Chem Lett. 2012. PMID: 22483583

4

Synthesis and antitumor-evaluation of 1,3-selenazole-containing 1,3,4-thiadiazole derivatives.

Zhao HC, Shi YP, Liu YM, Li CW, Xuan LN, Wang P, Zhang K, Chen BQ. Zhao HC, et al. Among authors: chen bq. Bioorg Med Chem Lett. 2013 Dec 15;23(24):6577-9. doi: 10.1016/j.bmcl.2013.10.062. Epub 2013 Nov 6. Bioorg Med Chem Lett. 2013. PMID: 24239016

5

Design, Synthesis and Antiproliferative Evaluation of Novel Disulfides Containing 1,3,4-Thiadiazole Moiety.

Zhang S, Liu XJ, Tang R, Wang HX, Liu HY, Liu YM, Chen BQ. Zhang S, et al. Among authors: chen bq. Chem Pharm Bull (Tokyo). 2017;65(10):950-958. doi: 10.1248/cpb.c17-00485. Chem Pharm Bull (Tokyo). 2017. PMID: 28966280 Free article.

6

Synthesis and in vitro antiproliferative evaluation of novel nonsymmetrical disulfides bearing 1,3,4-oxadiazole moiety.

Zhao JJ, Wang XF, Li BL, Zhang RL, Li B, Liu YM, Li CW, Liu JB, Chen BQ. Zhao JJ, et al. Among authors: chen bq. Bioorg Med Chem Lett. 2016 Sep 15;26(18):4414-4416. doi: 10.1016/j.bmcl.2016.08.014. Epub 2016 Aug 6. Bioorg Med Chem Lett. 2016. PMID: 27542307

7

Synthesis and antiproliferative evaluation of novel 1,2,4-triazole derivatives incorporating benzisoselenazolone scaffold.

Li BL, Li B, Zhang RL, Zhao JJ, Wang XF, Liu YM, Shi YP, Liu JB, Chen BQ. Li BL, et al. Among authors: chen bq. Bioorg Med Chem Lett. 2016 Feb 15;26(4):1279-81. doi: 10.1016/j.bmcl.2016.01.017. Epub 2016 Jan 8. Bioorg Med Chem Lett. 2016. PMID: 26786698

8

Synthesis and in vitro antiproliferative evaluation of novel hybrids from 1,3,4-thiadiazole and benzisoselenazolone.

Jing F, Fu X, Li S, Li B, Zhao J, Wang X, Liu Y, Chen B. Jing F, et al. Chem Pharm Bull (Tokyo). 2015;63(6):431-7. doi: 10.1248/cpb.c15-00014. Chem Pharm Bull (Tokyo). 2015. PMID: 26027467 Free article.

9

Synthesis and Biological Evaluation of Novel 1,3,4-thiadiazole Derivatives Incorporating Benzisoselenazolone Scaffold as Potential Antitumor Agents.

Fu X, Li S, Jing F, Wang X, Li B, Zhao J, Liu Y, Chen B. Fu X, et al. Med Chem. 2016;12(7):631-639. doi: 10.2174/1573406412666160201120806. Med Chem. 2016. PMID: 26833076

10

Synthesis and antitumor activities of novel hybrid molecules containing 1,3,4-oxadiazole and 1,3,4-thiadiazole bearing Schiff base moiety.

Zhang K, Wang P, Xuan LN, Fu XY, Jing F, Li S, Liu YM, Chen BQ. Zhang K, et al. Among authors: chen bq. Bioorg Med Chem Lett. 2014 Nov 15;24(22):5154-6. doi: 10.1016/j.bmcl.2014.09.086. Epub 2014 Oct 5. Bioorg Med Chem Lett. 2014. PMID: 25442303

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