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PUBMED FOR HANDHELDS

Journal Abstract Search


128 related items for PubMed ID: 9875396

  • 1. Synthesis, structure and in vitro anti-human immunodeficiency virus activity of novel 3-methyl-1H,3H-thiazolo[3,4-a]benzimidazoles.
    Chimirri A, Grasso S, Monforte AM, Monforte P, Rao A, Zappalà M, Bruno G, Nicolò F, Pannecouque C, Witvrouw M, De Clercq E.
    Antivir Chem Chemother; 1998 Sep; 9(5):431-8. PubMed ID: 9875396
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  • 2. Anti-HIV agents II. Synthesis and in vitro anti-HIV activity of novel 1H,3H-thiazolo[3,4-a]benzimidazoles.
    Chimirri A, Grasso S, Monforte AM, Monforte P, Zappala M.
    Farmaco; 1991 Sep; 46(7-8):925-33. PubMed ID: 1686551
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  • 3. Anti-HIV agents. I: Synthesis and in vitro anti-HIV evaluation of novel 1H,3H-thiazolo[3,4-a]benzimidazoles.
    Chimirri A, Grasso S, Monforte AM, Monforte P, Zappalà M.
    Farmaco; 1991 Jun; 46(6):817-23. PubMed ID: 1685321
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  • 6. Anti-HIV agents. IV. Synthesis and in vitro anti-HIV activity of novel 1-(2,6-difluorophenyl)-1H,3H-thiazolo[3,4-a]benzimidazoles.
    Chimirri A, Grasso S, Molica C, Monforte AM, Monforte P, Zappalà M, Scopelliti R.
    Farmaco; 1996 Apr; 51(4):279-82. PubMed ID: 8645416
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  • 8. Synthesis and biological activity of novel nonnucleoside inhibitors of HIV-1 reverse transcriptase. 2-Aryl-substituted benzimidazoles.
    Roth T, Morningstar ML, Boyer PL, Hughes SH, Buckheit RW, Michejda CJ.
    J Med Chem; 1997 Dec 19; 40(26):4199-207. PubMed ID: 9435891
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  • 9. Anti-HIV agents. V. Synthesis, structure and in vitro anti-HIV activity of novel 1H,3H-naphtho[2',3':4,5]imidazo[1,2-c]thiazoles.
    Chimirri A, Grasso S, Monforte AM, Monforte P, Rao A, Zappalà M, Bruno G, Nicolò F, Scopelliti R.
    Farmaco; 1997 Nov 19; 52(11):673-7. PubMed ID: 9550093
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  • 11. Synthesis and biological investigations of some novel thiazolylbenzimidazoles, and benzimidazolyl-thiazolo[4,5-d]pyrimidines.
    Habib NS, Rida SM, Badawey EA, Fahmy HT, Ghozlan HA.
    Pharmazie; 1997 May 19; 52(5):346-50. PubMed ID: 9183785
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  • 14. Synthesis and in vitro anti-HIV activity of certain 2-(1H-benzimidazol-2-ylamino)pyrimidin-4(3H)-ones and related derivatives.
    Badawey el-S, Kappe T.
    Arch Pharm (Weinheim); 1997 Mar 19; 330(3):59-62. PubMed ID: 9167448
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  • 18. Design, synthesis, and antiviral evaluations of 1-(substituted benzyl)-2-substituted-5,6-dichlorobenzimidazoles as nonnucleoside analogues of 2,5,6-trichloro-1-(beta-D-ribofuranosyl)benzimidazole.
    Porcari AR, Devivar RV, Kucera LS, Drach JC, Townsend LB.
    J Med Chem; 1998 Apr 09; 41(8):1252-62. PubMed ID: 9548815
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  • 19. Synthesis of syn and anti isomers of 6-[[(hydroxyimino)phenyl]methyl]-1-[(1-methylethyl)sulfonyl]-1H-benzimidazol-2-amine. Inhibitors of rhinovirus multiplication.
    Wikel JH, Paget CJ, DeLong DC, Nelson JD, Wu CY, Paschal JW, Dinner A, Templeton RJ, Chaney MO, Jones ND, Chamberlin JW.
    J Med Chem; 1980 Apr 09; 23(4):368-72. PubMed ID: 6247489
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  • 20. Synthesis of some benzimidazole derivatives endowed with 1,2,3-triazole as potential inhibitors of hepatitis C virus.
    Youssif BG, Mohamed YA, Salim MT, Inagaki F, Mukai C, Abdu-Allah HH.
    Acta Pharm; 2016 Jun 01; 66(2):219-31. PubMed ID: 27279065
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