Huang J - Search Results

1

Discovery of new potent inhibitors for carbonic anhydrase IX by structure-based virtual screening.

Wang L, Yang C, Lu W, Liu L, Gao R, Liao S, Zhao Z, Zhu L, Xu Y, Li H, Huang J, Zhu W. Wang L, et al. Among authors: huang j. Bioorg Med Chem Lett. 2013 Jun 15;23(12):3496-9. doi: 10.1016/j.bmcl.2013.04.048. Epub 2013 Apr 29. Bioorg Med Chem Lett. 2013. PMID: 23664215

2

2-amido-3-(1H-indol-3-yl)-N-substituted-propanamides as a new class of falcipain-2 inhibitors. 1. Design, synthesis, biological evaluation and binding model studies.

Zhu J, Chen T, Chen L, Lu W, Che P, Huang J, Li H, Li J, Jiang H. Zhu J, et al. Among authors: huang j. Molecules. 2009 Jan 21;14(1):494-508. doi: 10.3390/molecules14010494. Molecules. 2009. PMID: 19158658 Free PMC article.

3

2-(3,4-dihydro-4-oxothieno[2,3-d]pyrimidin-2-ylthio) acetamides as a new class of falcipain-2 inhibitors. 3. design, synthesis and biological evaluation.

Zhu J, Chen T, Liu J, Ma R, Lu W, Huang J, Li H, Li J, Jiang H. Zhu J, et al. Among authors: huang j. Molecules. 2009 Feb 16;14(2):785-97. doi: 10.3390/molecules14020785. Molecules. 2009. PMID: 19223827 Free PMC article.

4

Identification of novel falcipain-2 inhibitors as potential antimalarial agents through structure-based virtual screening.

Li H, Huang J, Chen L, Liu X, Chen T, Zhu J, Lu W, Shen X, Li J, Hilgenfeld R, Jiang H. Li H, et al. Among authors: huang j. J Med Chem. 2009 Aug 13;52(15):4936-40. doi: 10.1021/jm801622x. J Med Chem. 2009. PMID: 19586036

5

Discovering potent small molecule inhibitors of cyclophilin A using de novo drug design approach.

Ni S, Yuan Y, Huang J, Mao X, Lv M, Zhu J, Shen X, Pei J, Lai L, Jiang H, Li J. Ni S, et al. Among authors: huang j. J Med Chem. 2009 Sep 10;52(17):5295-8. doi: 10.1021/jm9008295. J Med Chem. 2009. PMID: 19691347

6

Discovery of potent ligands for estrogen receptor beta by structure-based virtual screening.

Shen J, Tan C, Zhang Y, Li X, Li W, Huang J, Shen X, Tang Y. Shen J, et al. Among authors: huang j. J Med Chem. 2010 Jul 22;53(14):5361-5. doi: 10.1021/jm100369g. J Med Chem. 2010. PMID: 20553023

7

HL005--a new selective PPARγ antagonist specifically inhibits the proliferation of MCF-7.

Lu W, Che P, Zhang Y, Li H, Zou S, Zhu J, Deng J, Shen X, Jiang H, Li J, Huang J. Lu W, et al. Among authors: huang j. J Steroid Biochem Mol Biol. 2011 Apr;124(3-5):112-20. doi: 10.1016/j.jsbmb.2011.01.019. Epub 2011 Feb 4. J Steroid Biochem Mol Biol. 2011. PMID: 21296151

8

SHAFTS: a hybrid approach for 3D molecular similarity calculation. 2. Prospective case study in the discovery of diverse p90 ribosomal S6 protein kinase 2 inhibitors to suppress cell migration.

Lu W, Liu X, Cao X, Xue M, Liu K, Zhao Z, Shen X, Jiang H, Xu Y, Huang J, Li H. Lu W, et al. Among authors: huang j. J Med Chem. 2011 May 26;54(10):3564-74. doi: 10.1021/jm200139j. Epub 2011 Apr 22. J Med Chem. 2011. PMID: 21488662

9

Synthesis and antimalarial activity of novel dihydro-artemisinin derivatives.

Liu Y, Cui K, Lu W, Luo W, Wang J, Huang J, Guo C. Liu Y, et al. Among authors: huang j. Molecules. 2011 May 30;16(6):4527-38. doi: 10.3390/molecules16064527. Molecules. 2011. PMID: 21629181 Free PMC article.

10

A highly selective space-folded photo-induced electron transfer fluorescent probe for carbonic anhydrase isozymes IX and its applications for biological imaging.

Zhang S, Yang C, Lu W, Huang J, Zhu W, Li H, Xu Y, Qian X. Zhang S, et al. Among authors: huang j. Chem Commun (Camb). 2011 Aug 7;47(29):8301-3. doi: 10.1039/c1cc12386f. Epub 2011 Jun 17. Chem Commun (Camb). 2011. PMID: 21681333

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