Jiang S - Search Results

1

Structure-based identification of small molecule compounds targeting cell cyclophilin A with anti-HIV-1 activity.

Chen S, Zhao X, Tan J, Lu H, Qi Z, Huang Q, Zeng X, Zhang M, Jiang S, Jiang H, Yu L. Chen S, et al. Among authors: jiang s, jiang h. Eur J Pharmacol. 2007 Jun 22;565(1-3):54-9. doi: 10.1016/j.ejphar.2007.03.023. Epub 2007 Mar 24. Eur J Pharmacol. 2007. PMID: 17449029 Free PMC article.

2

Automatic quantitation of HIV-1 mediated cell-to-cell fusion with a digital image analysis system (DIAS): application for rapid screening of HIV-1 fusion inhibitors.

Lu H, Zhao Q, Xu Z, Jiang S. Lu H, et al. Among authors: jiang s. J Virol Methods. 2003 Feb;107(2):155-61. doi: 10.1016/s0166-0934(02)00213-6. J Virol Methods. 2003. PMID: 12505629

3

Development of a cell-based enzyme-linked immunosorbent assay for high-throughput screening of HIV type 1 entry inhibitors targeting the coreceptor CXCR4.

Zhao Q, Lu H, Schols D, De Clercq E, Jiang S. Zhao Q, et al. Among authors: jiang s. AIDS Res Hum Retroviruses. 2003 Nov;19(11):947-55. doi: 10.1089/088922203322588297. AIDS Res Hum Retroviruses. 2003. PMID: 14678601

4

Rapid and automated fluorescence-linked immunosorbent assay for high-throughput screening of HIV-1 fusion inhibitors targeting gp41.

Liu S, Boyer-Chatenet L, Lu H, Jiang S. Liu S, et al. Among authors: jiang s. J Biomol Screen. 2003 Dec;8(6):685-93. doi: 10.1177/1087057103259155. J Biomol Screen. 2003. PMID: 14711394

5

Synthesis and anti-HIV-1 activity of 4-[4-(4,6-bisphenylamino-triazin-2-ylamino)-5-methoxy-2-methylphenylazo]-5-hydroxynaphthalene-2,7-disulfonic acid and its derivatives.

Naicker KP, Jiang S, Lu H, Ni J, Boyer-Chatenet L, Wang LX, Debnath AK. Naicker KP, et al. Among authors: jiang s. Bioorg Med Chem. 2004 Mar 1;12(5):1215-20. doi: 10.1016/j.bmc.2003.11.006. Bioorg Med Chem. 2004. PMID: 14980633

6

N-substituted pyrrole derivatives as novel human immunodeficiency virus type 1 entry inhibitors that interfere with the gp41 six-helix bundle formation and block virus fusion.

Jiang S, Lu H, Liu S, Zhao Q, He Y, Debnath AK. Jiang S, et al. Antimicrob Agents Chemother. 2004 Nov;48(11):4349-59. doi: 10.1128/AAC.48.11.4349-4359.2004. Antimicrob Agents Chemother. 2004. PMID: 15504864 Free PMC article.

7

Different from the HIV fusion inhibitor C34, the anti-HIV drug Fuzeon (T-20) inhibits HIV-1 entry by targeting multiple sites in gp41 and gp120.

Liu S, Lu H, Niu J, Xu Y, Wu S, Jiang S. Liu S, et al. Among authors: jiang s. J Biol Chem. 2005 Mar 25;280(12):11259-73. doi: 10.1074/jbc.M411141200. Epub 2005 Jan 7. J Biol Chem. 2005. PMID: 15640162 Free article.

8

Theaflavin derivatives in black tea and catechin derivatives in green tea inhibit HIV-1 entry by targeting gp41.

Liu S, Lu H, Zhao Q, He Y, Niu J, Debnath AK, Wu S, Jiang S. Liu S, et al. Among authors: jiang s. Biochim Biophys Acta. 2005 May 25;1723(1-3):270-81. doi: 10.1016/j.bbagen.2005.02.012. Epub 2005 Mar 24. Biochim Biophys Acta. 2005. PMID: 15823507

9

Combination of candidate microbicides cellulose acetate 1,2-benzenedicarboxylate and UC781 has synergistic and complementary effects against human immunodeficiency virus type 1 infection.

Liu S, Lu H, Neurath AR, Jiang S. Liu S, et al. Among authors: jiang s. Antimicrob Agents Chemother. 2005 May;49(5):1830-6. doi: 10.1128/AAC.49.5.1830-1836.2005. Antimicrob Agents Chemother. 2005. PMID: 15855503 Free PMC article.

10

Chemoenzymatic synthesis of HIV-1 gp41 glycopeptides: effects of glycosylation on the anti-HIV activity and alpha-helix bundle-forming ability of peptide C34.

Wang LX, Song H, Liu S, Lu H, Jiang S, Ni J, Li H. Wang LX, et al. Among authors: jiang s. Chembiochem. 2005 Jun;6(6):1068-74. doi: 10.1002/cbic.200400440. Chembiochem. 2005. PMID: 15883971

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