Wang J - Search Results

1

Dipyridamole, chloroquine, montelukast sodium, candesartan, oxytetracycline, and atazanavir are not SARS-CoV-2 main protease inhibitors.

Ma C, Wang J. Ma C, et al. Among authors: wang j. Proc Natl Acad Sci U S A. 2021 Feb 23;118(8):e2024420118. doi: 10.1073/pnas.2024420118. Proc Natl Acad Sci U S A. 2021. PMID: 33568498 Free PMC article. No abstract available.

2

Exploring the size limit of templates for inhibitors of the M2 ion channel of influenza A virus.

Duque MD, Ma C, Torres E, Wang J, Naesens L, Juárez-Jiménez J, Camps P, Luque FJ, DeGrado WF, Lamb RA, Pinto LH, Vázquez S. Duque MD, et al. Among authors: wang j. J Med Chem. 2011 Apr 28;54(8):2646-57. doi: 10.1021/jm101334y. Epub 2011 Apr 5. J Med Chem. 2011. PMID: 21466220 Free PMC article.

3

Exploring the Requirements for the Hydrophobic Scaffold and Polar Amine in inhibitors of M2 from Influenza A Virus.

Wang J, Ma C, Balannik V, Pinto LH, Lamb RA, Degrado WF. Wang J, et al. ACS Med Chem Lett. 2011 Apr 14;2(4):307-312. doi: 10.1021/ml100297w. ACS Med Chem Lett. 2011. PMID: 21691418 Free PMC article.

4

Molecular dynamics simulation directed rational design of inhibitors targeting drug-resistant mutants of influenza A virus M2.

Wang J, Ma C, Fiorin G, Carnevale V, Wang T, Hu F, Lamb RA, Pinto LH, Hong M, Klein ML, DeGrado WF. Wang J, et al. Among authors: wang t. J Am Chem Soc. 2011 Aug 17;133(32):12834-41. doi: 10.1021/ja204969m. Epub 2011 Jul 21. J Am Chem Soc. 2011. PMID: 21744829 Free PMC article.

5

Exploring organosilane amines as potent inhibitors and structural probes of influenza a virus M2 proton channel.

Wang J, Ma C, Wu Y, Lamb RA, Pinto LH, DeGrado WF. Wang J, et al. J Am Chem Soc. 2011 Sep 7;133(35):13844-7. doi: 10.1021/ja2050666. Epub 2011 Aug 12. J Am Chem Soc. 2011. PMID: 21819109 Free PMC article.

6

Structure and inhibition of the drug-resistant S31N mutant of the M2 ion channel of influenza A virus.

Wang J, Wu Y, Ma C, Fiorin G, Wang J, Pinto LH, Lamb RA, Klein ML, Degrado WF. Wang J, et al. Proc Natl Acad Sci U S A. 2013 Jan 22;110(4):1315-20. doi: 10.1073/pnas.1216526110. Epub 2013 Jan 9. Proc Natl Acad Sci U S A. 2013. PMID: 23302696 Free PMC article.

7

Inhibitors of the influenza A virus M2 proton channel discovered using a high-throughput yeast growth restoration assay.

Balgi AD, Wang J, Cheng DY, Ma C, Pfeifer TA, Shimizu Y, Anderson HJ, Pinto LH, Lamb RA, DeGrado WF, Roberge M. Balgi AD, et al. Among authors: wang j. PLoS One. 2013;8(2):e55271. doi: 10.1371/journal.pone.0055271. Epub 2013 Feb 1. PLoS One. 2013. PMID: 23383318 Free PMC article.

8

Discovery of novel dual inhibitors of the wild-type and the most prevalent drug-resistant mutant, S31N, of the M2 proton channel from influenza A virus.

Wang J, Ma C, Wang J, Jo H, Canturk B, Fiorin G, Pinto LH, Lamb RA, Klein ML, DeGrado WF. Wang J, et al. J Med Chem. 2013 Apr 11;56(7):2804-12. doi: 10.1021/jm301538e. Epub 2013 Mar 27. J Med Chem. 2013. PMID: 23437766 Free PMC article.

9

Asp44 stabilizes the Trp41 gate of the M2 proton channel of influenza A virus.

Ma C, Fiorin G, Carnevale V, Wang J, Lamb RA, Klein ML, Wu Y, Pinto LH, DeGrado WF. Ma C, et al. Among authors: wang j. Structure. 2013 Nov 5;21(11):2033-41. doi: 10.1016/j.str.2013.08.029. Epub 2013 Oct 17. Structure. 2013. PMID: 24139991 Free PMC article.

10

3-Azatetracyclo[5.2.1.1(5,8).0(1,5)]undecane derivatives: from wild-type inhibitors of the M2 ion channel of influenza A virus to derivatives with potent activity against the V27A mutant.

Rey-Carrizo M, Torres E, Ma C, Barniol-Xicota M, Wang J, Wu Y, Naesens L, DeGrado WF, Lamb RA, Pinto LH, Vázquez S. Rey-Carrizo M, et al. Among authors: wang j. J Med Chem. 2013 Nov 27;56(22):9265-74. doi: 10.1021/jm401340p. Epub 2013 Nov 15. J Med Chem. 2013. PMID: 24237039 Free PMC article.

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