Liu J - Search Results

1

Ethynylflavones, highly potent, and selective inhibitors of cytochrome P450 1A1.

Goyal N, Liu J, Lovings L, Dupart P, Taylor S, Bellow S, Mensah L, McClain E, Dotson B, Sridhar J, Zhang X, Zhao M, Foroozesh M. Goyal N, et al. Among authors: liu j. Chem Res Toxicol. 2014 Aug 18;27(8):1431-9. doi: 10.1021/tx5001865. Epub 2014 Jul 29. Chem Res Toxicol. 2014. PMID: 25033111 Free PMC article.

2

Methyl (11aS)-1,2,3,5,11,11a-hexahydro-3,3-dimethyl-1-oxo-6H-imidazo-[3',4':1,2]pyridin[3,4-b]indol-2-substituted acetates: synthesis and three-dimensional quantitative structure-activity relationship investigation as a class of novel vasodilators.

Liu J, Zhao M, Cui G, Zhang X, Wang J, Peng S. Liu J, et al. J Med Chem. 2008 Aug 14;51(15):4715-23. doi: 10.1021/jm800249j. Epub 2008 Jul 11. J Med Chem. 2008. PMID: 18616237

3

Design, synthesis, and biological activity of a family of novel ceramide analogues in chemoresistant breast cancer cells.

Antoon JW, Liu J, Gestaut MM, Burow ME, Beckman BS, Foroozesh M. Antoon JW, et al. Among authors: liu j. J Med Chem. 2009 Sep 24;52(18):5748-52. doi: 10.1021/jm9009668. J Med Chem. 2009. PMID: 19694470

4

In silico studies of polyaromatic hydrocarbon inhibitors of cytochrome P450 enzymes 1A1, 1A2, 2A6, and 2B1.

Sridhar J, Jin P, Liu J, Foroozesh M, Stevens CL. Sridhar J, et al. Among authors: liu j. Chem Res Toxicol. 2010 Mar 15;23(3):600-7. doi: 10.1021/tx900348v. Chem Res Toxicol. 2010. PMID: 20078084 Free PMC article.

5

Novel D: -erythro N-octanoyl sphingosine analogs as chemo- and endocrine-resistant breast cancer therapeutics.

Antoon JW, Liu J, Ponnapakkam AP, Gestaut MM, Foroozesh M, Beckman BS. Antoon JW, et al. Among authors: liu j. Cancer Chemother Pharmacol. 2010 May;65(6):1191-5. doi: 10.1007/s00280-009-1233-0. Epub 2010 Feb 14. Cancer Chemother Pharmacol. 2010. PMID: 20155475

6

Benzyl 1,2,3,5,11,11a-hexahydro-3,3-dimethyl-1-oxo-6H-imidazo[3',4':1,2]pyridin[3,4-b]indole-2-substituted acetates: One-pot-preparation, anti-tumor activity, docking toward DNA and 3D QSAR analysis.

Liu J, Zhao M, Qian K, Zhang X, Lee KH, Wu J, Liu YN, Peng S. Liu J, et al. Among authors: liu yn. Bioorg Med Chem. 2010 Mar 1;18(5):1910-7. doi: 10.1016/j.bmc.2010.01.038. Epub 2010 Jan 25. Bioorg Med Chem. 2010. PMID: 20171109

7

Ethynyl and Propynylpyrene Inhibitors of Cytochrome P450.

Zhu N, Lightsey D, Liu J, Foroozesh M, Morgan KM, Stevens ED, Klein Stevens CL. Zhu N, et al. Among authors: liu j. J Chem Crystallogr. 2010 Apr 1;40(4):343-352. doi: 10.1007/s10870-009-9659-0. J Chem Crystallogr. 2010. PMID: 20473363 Free PMC article.

8

Lead detoxification activity and ADMET hepatotoxicity of N-(alpha-L-arabino-furanos-1-yl)-L-cysteine.

Zhao M, Wang Y, Huo C, Liu J, Li C, Zhang X, Peng L, Peng S. Zhao M, et al. Among authors: liu j. Chem Res Toxicol. 2010 Jul 19;23(7):1282-5. doi: 10.1021/tx100155r. Chem Res Toxicol. 2010. PMID: 20540575

9

Novel anti-viability ceramide analogs: design, synthesis, and structure-activity relationship studies of substituted (S)-2-(benzylideneamino)-3-hydroxy-N-tetradecylpropanamides.

Liu J, Antoon JW, Ponnapakkam A, Beckman BS, Foroozesh M. Liu J, et al. Bioorg Med Chem. 2010 Jul 15;18(14):5316-22. doi: 10.1016/j.bmc.2010.05.044. Epub 2010 Jun 8. Bioorg Med Chem. 2010. PMID: 20639111

10

2-Substituted (S)-2-(3,3-dimethyl-1-oxo-10,10a-dihydroimidazo[1,5-b]isoquinolin-2(1H,3H,5H)-yl)acetic acids: Conformational prediction, synthesis, anti-thrombotic and vasodilative evaluation.

Wang H, Peng L, Zhao M, Liu J, Zhang X, Wang Y, Wu J, Li L, Peng S. Wang H, et al. Among authors: liu j. Bioorg Med Chem. 2011 Jan 15;19(2):871-82. doi: 10.1016/j.bmc.2010.12.005. Epub 2010 Dec 5. Bioorg Med Chem. 2011. PMID: 21193315

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