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Journal Abstract Search

178 related items for PubMed ID: 7684215

  • 1. Diarylsulfones, a new chemical class of nonnucleoside antiviral inhibitors of human immunodeficiency virus type 1 reverse transcriptase.
    McMahon JB, Gulakowski RJ, Weislow OS, Schultz RJ, Narayanan VL, Clanton DJ, Pedemonte R, Wassmundt FW, Buckheit RW, Decker WD.
    Antimicrob Agents Chemother; 1993 Apr; 37(4):754-60. PubMed ID: 7684215
    [Abstract] [Full Text] [Related]

  • 2. Oxathiin carboxanilide, a potent inhibitor of human immunodeficiency virus reproduction.
    Bader JP, McMahon JB, Schultz RJ, Narayanan VL, Pierce JB, Harrison WA, Weislow OS, Midelfort CF, Stinson SF, Boyd MR.
    Proc Natl Acad Sci U S A; 1991 Aug 01; 88(15):6740-4. PubMed ID: 1713689
    [Abstract] [Full Text] [Related]

  • 3. Biological and biochemical anti-HIV activity of the benzothiadiazine class of nonnucleoside reverse transcriptase inhibitors.
    Buckheit RW, Fliakas-Boltz V, Decker WD, Roberson JL, Pyle CA, White EL, Bowdon BJ, McMahon JB, Boyd MR, Bader JP.
    Antiviral Res; 1994 Sep 01; 25(1):43-56. PubMed ID: 7529014
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  • 5. Inhibition of reverse transcriptase of human immunodeficiency virus type 1 and chimeric enzymes of human immunodeficiency viruses types 1 and 2 by two novel non-nucleoside inhibitors.
    Rubinek T, McMahon JB, Hizi A.
    FEBS Lett; 1994 Aug 22; 350(2-3):299-303. PubMed ID: 7520874
    [Abstract] [Full Text] [Related]

  • 6. Synthesis of pyrryl aryl sulfones targeted at the HIV-1 reverse transcriptase.
    Artico M, Silvestri R, Stefancich G, Massa S, Pagnozzi E, Musu D, Scintu F, Pinna E, Tinti E, La Colla P.
    Arch Pharm (Weinheim); 1995 Mar 22; 328(3):223-9. PubMed ID: 7539250
    [Abstract] [Full Text] [Related]

  • 7. Antiviral action of oligodeoxyguanylic acids against human immunodeficiency virus type 1.
    Fujihashi T, Sakata T, Kaji A, Kaji H.
    AIDS Res Hum Retroviruses; 1995 Apr 22; 11(4):461-71. PubMed ID: 7543270
    [Abstract] [Full Text] [Related]

  • 8. T30177, an oligonucleotide stabilized by an intramolecular guanosine octet, is a potent inhibitor of laboratory strains and clinical isolates of human immunodeficiency virus type 1.
    Ojwang JO, Buckheit RW, Pommier Y, Mazumder A, De Vreese K, Esté JA, Reymen D, Pallansch LA, Lackman-Smith C, Wallace TL.
    Antimicrob Agents Chemother; 1995 Nov 22; 39(11):2426-35. PubMed ID: 8585721
    [Abstract] [Full Text] [Related]

  • 9. Potent inhibition of human immunodeficiency virus type 1 replication by template analog reverse transcriptase inhibitors derived by SELEX (systematic evolution of ligands by exponential enrichment).
    Joshi P, Prasad VR.
    J Virol; 2002 Jul 22; 76(13):6545-57. PubMed ID: 12050367
    [Abstract] [Full Text] [Related]

  • 10. New alkenyldiarylmethanes with enhanced potencies as anti-HIV agents which act as non-nucleoside reverse transcriptase inhibitors.
    Cushman M, Casimiro-Garcia A, Hejchman E, Ruell JA, Huang M, Schaeffer CA, Williamson K, Rice WG, Buckheit RW.
    J Med Chem; 1998 Jun 04; 41(12):2076-89. PubMed ID: 9622549
    [Abstract] [Full Text] [Related]

  • 11. Inhibition of HIV infection by baicalin--a flavonoid compound purified from Chinese herbal medicine.
    Li BQ, Fu T, Yan YD, Baylor NW, Ruscetti FW, Kung HF.
    Cell Mol Biol Res; 1993 Jun 04; 39(2):119-24. PubMed ID: 7693133
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  • 13. Anti-human immunodeficiency virus (HIV) activities of halogenated gomisin J derivatives, new nonnucleoside inhibitors of HIV type 1 reverse transcriptase.
    Fujihashi T, Hara H, Sakata T, Mori K, Higuchi H, Tanaka A, Kaji H, Kaji A.
    Antimicrob Agents Chemother; 1995 Sep 04; 39(9):2000-7. PubMed ID: 8540706
    [Abstract] [Full Text] [Related]

  • 14. Derivatives of 4-amino-3,6-disulfonato-1,8-naphthalimide inhibit reverse transcriptase and suppress human and feline immunodeficiency virus expression in cultured cells.
    Rideout D, Schinazi R, Pauza CD, Lovelace K, Chiang LC, Calogeropoulou T, McCarthy M, Elder JH.
    J Cell Biochem; 1993 Apr 04; 51(4):446-57. PubMed ID: 7684385
    [Abstract] [Full Text] [Related]

  • 15. The biological effects of structural variation at the meta position of the aromatic rings and at the end of the alkenyl chain in the alkenyldiarylmethane series of non-nucleoside reverse transcriptase inhibitors.
    Xu G, Micklatcher M, Silvestri MA, Hartman TL, Burrier J, Osterling MC, Wargo H, Turpin JA, Buckheit RW, Cushman M.
    J Med Chem; 2001 Nov 22; 44(24):4092-113. PubMed ID: 11708913
    [Abstract] [Full Text] [Related]

  • 16. U-90152, a potent inhibitor of human immunodeficiency virus type 1 replication.
    Dueweke TJ, Poppe SM, Romero DL, Swaney SM, So AG, Downey KM, Althaus IW, Reusser F, Busso M, Resnick L.
    Antimicrob Agents Chemother; 1993 May 22; 37(5):1127-31. PubMed ID: 7685995
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  • 18. Characteristics of a group of nonnucleoside reverse transcriptase inhibitors with structural diversity and potent anti-human immunodeficiency virus activity.
    Yang SS, Fliakas-Boltz V, Bader JP, Buckheit RW.
    Leukemia; 1995 Oct 22; 9 Suppl 1():S75-85. PubMed ID: 7475321
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  • 20. The calanolides, a novel HIV-inhibitory class of coumarin derivatives from the tropical rainforest tree, Calophyllum lanigerum.
    Kashman Y, Gustafson KR, Fuller RW, Cardellina JH, McMahon JB, Currens MJ, Buckheit RW, Hughes SH, Cragg GM, Boyd MR.
    J Med Chem; 1992 Jul 24; 35(15):2735-43. PubMed ID: 1379639
    [Abstract] [Full Text] [Related]

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