Huang S - Search Results

1

Synthesis and biological evaluation of benzophenone derivatives as potential HIV-1 inhibitors.

Song Z, Wang P, Huang S, Wang C, Wang R, Yang L, Zhen Y, Liu K, Zheng Y, Ma X. Song Z, et al. Among authors: huang s. Med Chem. 2016 Nov 11. Online ahead of print. Med Chem. 2016. PMID: 27834135

2

Synthesis and biological evaluation of morpholine-substituted diphenylpyrimidine derivatives (Mor-DPPYs) as potent EGFR T790M inhibitors with improved activity toward the gefitinib-resistant non-small cell lung cancers (NSCLC).

Song Z, Huang S, Yu H, Jiang Y, Wang C, Meng Q, Shu X, Sun H, Liu K, Li Y, Ma X. Song Z, et al. Among authors: huang s. Eur J Med Chem. 2017 Jun 16;133:329-339. doi: 10.1016/j.ejmech.2017.03.083. Epub 2017 Apr 2. Eur J Med Chem. 2017. PMID: 28395219

3

Novel 4-anilinoquinazoline derivatives featuring an 1-adamantyl moiety as potent EGFR inhibitors with enhanced activity against NSCLC cell lines.

Yu H, Li Y, Ge Y, Song Z, Wang C, Huang S, Jin Y, Han X, Zhen Y, Liu K, Zhou Y, Ma X. Yu H, et al. Among authors: huang s. Eur J Med Chem. 2016 Mar 3;110:195-203. doi: 10.1016/j.ejmech.2016.01.045. Epub 2016 Jan 26. Eur J Med Chem. 2016. PMID: 26829280

4

Challenges and Perspectives on the Development of Small-Molecule EGFR Inhibitors against T790M-Mediated Resistance in Non-Small-Cell Lung Cancer.

Song Z, Ge Y, Wang C, Huang S, Shu X, Liu K, Zhou Y, Ma X. Song Z, et al. Among authors: huang s. J Med Chem. 2016 Jul 28;59(14):6580-94. doi: 10.1021/acs.jmedchem.5b00840. Epub 2016 Feb 26. J Med Chem. 2016. PMID: 26882288

5

Structural optimization of diphenylpyrimidine derivatives (DPPYs) as potent Bruton's tyrosine kinase (BTK) inhibitors with improved activity toward B leukemia cell lines.

Zhao D, Huang S, Qu M, Wang C, Liu Z, Li Z, Peng J, Liu K, Li Y, Ma X, Shu X. Zhao D, et al. Among authors: huang s. Eur J Med Chem. 2017 Jan 27;126:444-455. doi: 10.1016/j.ejmech.2016.11.047. Epub 2016 Nov 23. Eur J Med Chem. 2017. PMID: 27912175

6

Structural optimization of diphenylpyrimidine scaffold as potent and selective epidermal growth factor receptor inhibitors against L858R/T790M resistance mutation in nonsmall cell lung cancer.

Yi Y, Wang L, Zhao D, Huang S, Wang C, Liu Z, Sun H, Liu K, Ma X, Li Y. Yi Y, et al. Among authors: huang s. Chem Biol Drug Des. 2018 Dec;92(6):1988-1997. doi: 10.1111/cbdd.13370. Epub 2018 Aug 26. Chem Biol Drug Des. 2018. PMID: 30030903

7

Bioactive metabolites of Schisanlactone E transformed by Cunninghamella blakesleana AS 3.970.

Mai ZP, Wang C, Wang Y, Zhang HL, Zhang BJ, Wang W, Huo XK, Huang SS, Wang CY, Liu KX, Ma XC, Wang XB. Mai ZP, et al. Fitoterapia. 2014 Dec;99:352-61. doi: 10.1016/j.fitote.2014.10.016. Epub 2014 Oct 30. Fitoterapia. 2014. PMID: 25451796

8

7-O-geranylquercetin contributes to reverse P-gp-mediated adriamycin resistance in breast cancer.

Zhang E, Liu J, Shi L, Guo X, Liang Z, Zuo J, Xu H, Wang H, Shu X, Huang S, Zhang S, Kang X, Zhen Y. Zhang E, et al. Among authors: huang s. Life Sci. 2019 Dec 1;238:116938. doi: 10.1016/j.lfs.2019.116938. Epub 2019 Oct 5. Life Sci. 2019. PMID: 31593704

9

Inhibitory Effects of Highly Oxygenated Lanostane Derivatives from the Fungus Ganoderma lucidum on P-Glycoprotein and α-Glucosidase.

Zhao XR, Huo XK, Dong PP, Wang C, Huang SS, Zhang BJ, Zhang HL, Deng S, Liu KX, Ma XC. Zhao XR, et al. Among authors: huang ss. J Nat Prod. 2015 Aug 28;78(8):1868-76. doi: 10.1021/acs.jnatprod.5b00132. Epub 2015 Jul 29. J Nat Prod. 2015. PMID: 26222905

10

Combination of 7-O-geranylquercetin and microRNA-451 enhances antitumor effect of Adriamycin by reserving P-gp-mediated drug resistance in breast cancer.

Chen Y, Li X, Shi L, Ma P, Wang W, Wu N, Gan Y, Han X, Huang S, Kang X, Liu S, Zhen Y. Chen Y, et al. Among authors: huang s. Aging (Albany NY). 2022 Sep 14;14(17):7156-7169. doi: 10.18632/aging.204287. Epub 2022 Sep 14. Aging (Albany NY). 2022. PMID: 36107024 Free PMC article.

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