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Journal Abstract Search

170 related items for PubMed ID: 12790579

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  • 3. Small dipeptide-based HIV protease inhibitors containing the hydroxymethylcarbonyl isostere as an ideal transition-state mimic.
    Kiso Y, Matsumoto H, Mizumoto S, Kimura T, Fujiwara Y, Akaji K.
    Biopolymers; 1999; 51(1):59-68. PubMed ID: 10380353
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  • 7. Synthesis of a new hydroxyethylene dipeptide isostere Phe psi [CH2CH (OH)]Phe as HIV-1 protease inhibitor.
    Chen HG, Sawyer TK, Wuts PG.
    Zhongguo Yao Li Xue Bao; 1994 Jan; 15(1):33-5. PubMed ID: 8010081
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  • 8. Structure-based design: synthesis and biological evaluation of a series of novel cycloamide-derived HIV-1 protease inhibitors.
    Ghosh AK, Swanson LM, Cho H, Leshchenko S, Hussain KA, Kay S, Walters DE, Koh Y, Mitsuya H.
    J Med Chem; 2005 May 19; 48(10):3576-85. PubMed ID: 15887965
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  • 11. Solid-phase syntheses of olefin-containing inhibitors for HTLV-1 protease using the Horner-Emmons reaction.
    Bang JK, Naka H, Teruya K, Aimoto S, Konno H, Nosaka K, Tatsumi T, Akaji K.
    J Org Chem; 2005 Dec 09; 70(25):10596-9. PubMed ID: 16323881
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  • 12. Identification of peptidomimetic HTLV-I protease inhibitors containing hydroxymethylcarbonyl (HMC) isostere as the transition-state mimic.
    Maegawa H, Kimura T, Arii Y, Matsui Y, Kasai S, Hayashi Y, Kiso Y.
    Bioorg Med Chem Lett; 2004 Dec 06; 14(23):5925-9. PubMed ID: 15501070
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  • 13. Stereocontrolled synthesis and biological activity of two diastereoisomers of the potent HIV-1 protease inhibitor saquinavir.
    Righi G, Ciambrone S, Bonini C, Campaner P.
    Bioorg Med Chem; 2008 Jan 15; 16(2):902-8. PubMed ID: 17964171
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  • 16. Synthesis of a Gln-Phe hydroxy-ethylene dipeptide isostere.
    Haug BE, Rich DH.
    Org Lett; 2004 Dec 09; 6(25):4783-6. PubMed ID: 15575685
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  • 17. Novel HIV-protease inhibitors containing beta-hydroxyether and -thioether dipeptide isostere surrogates: modification of the P3 ligand.
    Patel NM, Bennett F, Girijavallabhan VM, Dasmahapatra B, Butkiewicz N, Hart A.
    Bioorg Med Chem Lett; 1998 Apr 21; 8(8):931-4. PubMed ID: 9871514
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  • 18. Design and synthesis of potent inhibitors of the malaria aspartyl proteases plasmepsin I and II. Use of solid-phase synthesis to explore novel statine motifs.
    Johansson PO, Chen Y, Belfrage AK, Blackman MJ, Kvarnström I, Jansson K, Vrang L, Hamelink E, Hallberg A, Rosenquist A, Samuelsson B.
    J Med Chem; 2004 Jun 17; 47(13):3353-66. PubMed ID: 15189032
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