Similar articles for PMID: 22959520

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1

Biosynthesis of anti-HCV compounds using thermophilic microorganisms.

Rivero CW, De Benedetti EC, Sambeth JE, Lozano ME, Trelles JA. Rivero CW, et al. Bioorg Med Chem Lett. 2012 Oct 1;22(19):6059-62. doi: 10.1016/j.bmcl.2012.08.045. Epub 2012 Aug 21. Bioorg Med Chem Lett. 2012. PMID: 22959520 Free PMC article.

2

Suppression of subgenomic hepatitis C virus replication by 5'-O-masked analogues of 6-chloropurine-2'-deoxyriboside.

Ikejiri M, Ohshima T, Kato K, Toyama M, Murata T, Shimotohno K, Maruyama T. Ikejiri M, et al. Nucleic Acids Symp Ser (Oxf). 2007;(51):439-40. doi: 10.1093/nass/nrm220. Nucleic Acids Symp Ser (Oxf). 2007. PMID: 18029775

3

Biotransformation of 2,6-diaminopurine nucleosides by immobilized Geobacillus stearothermophilus.

De Benedetti EC, Rivero CW, Britos CN, Lozano ME, Trelles JA. De Benedetti EC, et al. Biotechnol Prog. 2012 Sep-Oct;28(5):1251-6. doi: 10.1002/btpr.1602. Epub 2012 Aug 28. Biotechnol Prog. 2012. PMID: 22837142

4

Synthesis of purine modified 2'-C-methyl nucleosides as potential anti-HCV agents.

Zhang HW, Zhou L, Coats SJ, McBrayer TR, Tharnish PM, Bondada L, Detorio M, Amichai SA, Johns MD, Whitaker T, Schinazi RF. Zhang HW, et al. Bioorg Med Chem Lett. 2011 Nov 15;21(22):6788-92. doi: 10.1016/j.bmcl.2011.09.034. Epub 2011 Sep 20. Bioorg Med Chem Lett. 2011. PMID: 21983447 Free PMC article.

5

Cytostatic 6-arylpurine nucleosides. 6. SAR in anti-HCV and cytostatic activity of extended series of 6-hetarylpurine ribonucleosides.

Hocek M, Naus P, Pohl R, Votruba I, Furman PA, Tharnish PM, Otto MJ. Hocek M, et al. J Med Chem. 2005 Sep 8;48(18):5869-73. doi: 10.1021/jm050335x. J Med Chem. 2005. PMID: 16134952

6

Synthesis and anti-hepatitis C virus (HCV) activity of 3'-C-substituted-methyl pyrimidine and purine nucleosides.

Choi WJ, Kim YM, Kim HO, Lee HW, Kim DE, Park KS, Chong Y, Jeong LS. Choi WJ, et al. Bioorg Med Chem. 2010 Jul 1;18(13):4812-20. doi: 10.1016/j.bmc.2010.05.002. Epub 2010 May 31. Bioorg Med Chem. 2010. PMID: 20627592

7

Screening of catalytically active microorganisms for the synthesis of 6-modified purine nucleosides.

Trelles JA, Valino AL, Runza V, Lewkowicz ES, Iribarren AM. Trelles JA, et al. Biotechnol Lett. 2005 Jun;27(11):759-63. doi: 10.1007/s10529-005-5628-7. Biotechnol Lett. 2005. PMID: 16086256

8

Synthesis and biological activity of 5',9-anhydro-3-purine-isonucleosides as potential anti-hepatitis C virus agents.

Chun BK, Wang P, Hassan A, Du J, Tharnish PM, Murakami E, Stuyver L, Otto MJ, Schinazi RF, Watanabe KA. Chun BK, et al. Nucleosides Nucleotides Nucleic Acids. 2007;26(1):83-97. doi: 10.1080/15257770601052307. Nucleosides Nucleotides Nucleic Acids. 2007. PMID: 17162589

9

Synthesis, cytostatic and anti-HCV activity of 6-(N-substituted aminomethyl)-, 6-(O-substituted hydroxymethyl)- and 6-(S-substituted sulfanylmethyl)purine nucleosides.

Silhár P, Hocek M, Pohl R, Votruba I, Shih IH, Mabery E, Mackman R. Silhár P, et al. Bioorg Med Chem. 2008 Mar 1;16(5):2329-66. doi: 10.1016/j.bmc.2007.11.067. Epub 2007 Nov 29. Bioorg Med Chem. 2008. PMID: 18078757

10

Synthesis and antiviral evaluation of 7-fluoro-7-deaza-2-aminopurine nucleoside derivatives.

Leroy F, Chaves D, Dukhan D, Storer R, Sommadossi JP, Loi AG, Cadeddu A, Fanti M, Boscu N, Bassetti F, Liuzzi M, Gosselin G. Leroy F, et al. Nucleic Acids Symp Ser (Oxf). 2008;(52):595-6. doi: 10.1093/nass/nrn301. Nucleic Acids Symp Ser (Oxf). 2008. PMID: 18776520

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