Gao A - Search Results

1

3-(7-Azaindolyl)-4-indolylmaleimides as a novel class of mutant isocitrate dehydrogenase-1 inhibitors: Design, synthesis, and biological evaluation.

Hu Y, Gao A, Liao H, Zhang M, Xu G, Gao L, Xu L, Zhou Y, Gao J, Ye Q, Li J. Hu Y, et al. Among authors: gao j, gao l, gao a. Arch Pharm (Weinheim). 2018 Oct;351(10):e1800039. doi: 10.1002/ardp.201800039. Epub 2018 Aug 16. Arch Pharm (Weinheim). 2018. PMID: 30113716

2

Berberine-stimulated glucose uptake in L6 myotubes involves both AMPK and p38 MAPK.

Cheng Z, Pang T, Gu M, Gao AH, Xie CM, Li JY, Nan FJ, Li J. Cheng Z, et al. Biochim Biophys Acta. 2006 Nov;1760(11):1682-9. doi: 10.1016/j.bbagen.2006.09.007. Epub 2006 Sep 20. Biochim Biophys Acta. 2006. PMID: 17049164

3

Synthesis and biological evaluation of c7-demethyl largazole analogues.

Chen F, Gao AH, Li J, Nan FJ. Chen F, et al. ChemMedChem. 2009 Aug;4(8):1269-72. doi: 10.1002/cmdc.200900125. ChemMedChem. 2009. PMID: 19431162 No abstract available.

4

Discovery and optimization of 2,4-diaminoquinazoline derivatives as a new class of potent dengue virus inhibitors.

Chao B, Tong XK, Tang W, Li DW, He PL, Garcia JM, Zeng LM, Gao AH, Yang L, Li J, Nan FJ, Jacobs M, Altmeyer R, Zuo JP, Hu YH. Chao B, et al. J Med Chem. 2012 Apr 12;55(7):3135-43. doi: 10.1021/jm2015952. Epub 2012 Mar 26. J Med Chem. 2012. PMID: 22448770

5

Fluevirosines A-C: a biogenesis inspired example in the discovery of new bioactive scaffolds from Flueggea virosa.

Zhang H, Zhang CR, Zhu KK, Gao AH, Luo C, Li J, Yue JM. Zhang H, et al. Org Lett. 2013 Jan 4;15(1):120-3. doi: 10.1021/ol303146a. Epub 2012 Dec 17. Org Lett. 2013. PMID: 23244193

6

Berberine combined with 2-deoxy-d-glucose synergistically enhances cancer cell proliferation inhibition via energy depletion and unfolded protein response disruption.

Fan LX, Liu CM, Gao AH, Zhou YB, Li J. Fan LX, et al. Biochim Biophys Acta. 2013 Nov;1830(11):5175-83. doi: 10.1016/j.bbagen.2013.07.010. Epub 2013 Jul 18. Biochim Biophys Acta. 2013. PMID: 23872355

7

Curcusone D, a novel ubiquitin-proteasome pathway inhibitor via ROS-induced DUB inhibition, is synergistic with bortezomib against multiple myeloma cell growth.

Cao MN, Zhou YB, Gao AH, Cao JY, Gao LX, Sheng L, Xu L, Su MB, Cao XC, Han MM, Wang MK, Li J. Cao MN, et al. Biochim Biophys Acta. 2014 Jun;1840(6):2004-13. doi: 10.1016/j.bbagen.2014.02.006. Epub 2014 Feb 15. Biochim Biophys Acta. 2014. PMID: 24534329

8

Azoxystrobin, a mitochondrial complex III Qo site inhibitor, exerts beneficial metabolic effects in vivo and in vitro.

Gao AH, Fu YY, Zhang KZ, Zhang M, Jiang HW, Fan LX, Nan FJ, Yuan CG, Li J, Zhou YB, Li JY. Gao AH, et al. Biochim Biophys Acta. 2014 Jul;1840(7):2212-21. doi: 10.1016/j.bbagen.2014.04.002. Epub 2014 Apr 13. Biochim Biophys Acta. 2014. PMID: 24726979

9

Disruption of the unfolded protein response (UPR) by lead compound selectively suppresses cancer cell growth.

Huang H, Liu H, Liu C, Fan L, Zhang X, Gao A, Hu X, Zhang K, Cao X, Jiang K, Zhou Y, Hou J, Nan F, Li J. Huang H, et al. Among authors: gao a. Cancer Lett. 2015 May 1;360(2):257-68. doi: 10.1016/j.canlet.2015.02.029. Epub 2015 Feb 23. Cancer Lett. 2015. PMID: 25721085

10

Design, synthesis and biological evaluation of bisthiazole-based trifluoromethyl ketone derivatives as potent HDAC inhibitors with improved cellular efficacy.

Gong CJ, Gao AH, Zhang YM, Su MB, Chen F, Sheng L, Zhou YB, Li JY, Li J, Nan FJ. Gong CJ, et al. Eur J Med Chem. 2016 Apr 13;112:81-90. doi: 10.1016/j.ejmech.2016.02.003. Epub 2016 Feb 4. Eur J Med Chem. 2016. PMID: 26890114

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