Zhou W - Search Results

1

Design and synthesis of α-naphthoflavone chimera derivatives able to eliminate cytochrome P450 (CYP)1B1-mediated drug resistance via targeted CYP1B1 degradation.

Zhou L, Chen W, Cao C, Shi Y, Ye W, Hu J, Wang L, Zhou W. Zhou L, et al. Among authors: zhou w. Eur J Med Chem. 2020 Mar 1;189:112028. doi: 10.1016/j.ejmech.2019.112028. Epub 2020 Jan 2. Eur J Med Chem. 2020. PMID: 31945665

2

Synthesis, structure-activity relationships, and drug resistance of beta-d-3'-fluoro-2',3'-unsaturated nucleosides as anti-HIV Agents.

Zhou W, Gumina G, Chong Y, Wang J, Schinazi RF, Chu CK. Zhou W, et al. J Med Chem. 2004 Jun 17;47(13):3399-408. doi: 10.1021/jm040027j. J Med Chem. 2004. PMID: 15189036

3

Semi-synthesis and anti-tumor activity of 5,8-O-dimethyl acylshikonin derivatives.

Zhou W, Peng Y, Li SS. Zhou W, et al. Eur J Med Chem. 2010 Dec;45(12):6005-11. doi: 10.1016/j.ejmech.2010.09.068. Epub 2010 Oct 7. Eur J Med Chem. 2010. PMID: 20970893

4

Design and Synthesis of New α-Naphthoflavones as Cytochrome P450 (CYP) 1B1 Inhibitors To Overcome Docetaxel-Resistance Associated with CYP1B1 Overexpression.

Cui J, Meng Q, Zhang X, Cui Q, Zhou W, Li S. Cui J, et al. Among authors: zhou w. J Med Chem. 2015 Apr 23;58(8):3534-47. doi: 10.1021/acs.jmedchem.5b00265. Epub 2015 Apr 1. J Med Chem. 2015. PMID: 25799264

5

Regioselective semi-synthesis of 6-isomers of 5,8-O-dimethyl ether of shikonin derivatives via an 'intramolecular ring-closing/ring-opening' strategy as potent anticancer agents.

Zhou L, Zhang X, Zhou W. Zhou L, et al. Among authors: zhou w. Chem Cent J. 2017 Aug 2;11(1):74. doi: 10.1186/s13065-017-0306-0. Chem Cent J. 2017. PMID: 29086846 Free PMC article.

6

Application of Mono- and Disaccharides in Drug Targeting and Efficacy.

Yuan SS, Li ML, Chen JS, Zhou L, Zhou W. Yuan SS, et al. Among authors: zhou w, zhou l. ChemMedChem. 2018 Apr 23;13(8):764-778. doi: 10.1002/cmdc.201700762. Epub 2018 Mar 7. ChemMedChem. 2018. PMID: 29441721 Review.

7

Design and synthesis of structurally defined heparan sulfate (HS)-FK506 conjugates as an exogenous approach to investigate biological functions of nucleus HS.

Li M, Yuan S, Chen J, Lv L, Guo S, Zhou W. Li M, et al. Among authors: zhou w. Bioorg Chem. 2018 Dec;81:203-210. doi: 10.1016/j.bioorg.2018.08.015. Epub 2018 Aug 16. Bioorg Chem. 2018. PMID: 30144633

8

Extensive protein S-nitrosylation associated with human pancreatic ductal adenocarcinoma pathogenesis.

Tan C, Li Y, Huang X, Wei M, Huang Y, Tang Z, Huang H, Zhou W, Wang Y, Hu J. Tan C, et al. Among authors: zhou w. Cell Death Dis. 2019 Dec 4;10(12):914. doi: 10.1038/s41419-019-2144-6. Cell Death Dis. 2019. PMID: 31801946 Free PMC article.

9

Antitumor activity and structure-activity relationship of heparanase inhibitors: Recent advances.

Fu K, Bai Z, Chen L, Ye W, Wang M, Hu J, Liu C, Zhou W. Fu K, et al. Among authors: zhou w. Eur J Med Chem. 2020 May 1;193:112221. doi: 10.1016/j.ejmech.2020.112221. Epub 2020 Mar 14. Eur J Med Chem. 2020. PMID: 32222663 Review.

10

Oligosaccharide-camptothecin conjugates as potential antineoplastic drugs: Design, synthesis and biological evaluation.

Li M, Ye W, Fu K, Zhou C, Shi Y, Huang W, Chen W, Hu J, Jiang Z, Zhou W. Li M, et al. Among authors: zhou w, zhou c. Eur J Med Chem. 2020 Sep 15;202:112509. doi: 10.1016/j.ejmech.2020.112509. Epub 2020 Jun 30. Eur J Med Chem. 2020. PMID: 32668379

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