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Journal Abstract Search

197 related items for PubMed ID: 24751157

  • 1. Design, synthesis and biological evaluation of peptidyl epoxyketone proteasome inhibitors composed of β-amino acids.
    Zhang J, Han M, Ma X, Xu L, Cao J, Zhou Y, Li J, Liu T, Hu Y.
    Chem Biol Drug Des; 2014 Nov; 84(5):497-504. PubMed ID: 24751157
    [Abstract] [Full Text] [Related]

  • 2. Design, synthesis and biological evaluation of novel tripeptidyl epoxyketone derivatives constructed from β-amino acid as proteasome inhibitors.
    Zhang J, Cao J, Xu L, Zhou Y, Liu T, Li J, Hu Y.
    Bioorg Med Chem; 2014 Jun 01; 22(11):2955-65. PubMed ID: 24767818
    [Abstract] [Full Text] [Related]

  • 3. Design, synthesis and docking studies of novel dipeptidyl boronic acid proteasome inhibitors constructed from αα- and αβ-amino acids.
    Shi J, Lei M, Wu W, Feng H, Wang J, Chen S, Zhu Y, Hu S, Liu Z, Jiang C.
    Bioorg Med Chem Lett; 2016 Apr 15; 26(8):1958-62. PubMed ID: 26965867
    [Abstract] [Full Text] [Related]

  • 4. Design, Synthesis, and Biological Activity of Isosyringolin A.
    Kitahata S, Chiba T, Yoshida T, Ri M, Iida S, Matsuda A, Ichikawa S.
    Org Lett; 2016 May 06; 18(9):2312-5. PubMed ID: 27123978
    [Abstract] [Full Text] [Related]

  • 5. Studies of C-terminal naphthoquinone dipeptides as 20S proteasome inhibitors.
    Scotti A, Trapella C, Ferretti V, Gallerani E, Gavioli R, Marastoni M.
    J Enzyme Inhib Med Chem; 2016 May 06; 31(3):456-63. PubMed ID: 25942361
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  • 7. Naphthoquinone amino acid derivatives, synthesis and biological activity as proteasome inhibitors.
    Marastoni M, Trapella C, Scotti A, Fantinati A, Ferretti V, Marzola E, Eleonora G, Gavioli R, Preti D.
    J Enzyme Inhib Med Chem; 2017 Dec 06; 32(1):865-877. PubMed ID: 28657369
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  • 9. Synthesis and biological evaluation of curcumin derivatives modified with α-amino boronic acid as proteasome inhibitors.
    Zhang W, Bai H, Han L, Zhang H, Xu B, Cui J, Wang X, Ge Z, Li R.
    Bioorg Med Chem Lett; 2018 Aug 01; 28(14):2459-2464. PubMed ID: 29886021
    [Abstract] [Full Text] [Related]

  • 10. Design, synthesis, and evaluation of cystargolide-based β-lactones as potent proteasome inhibitors.
    Niroula D, Hallada LP, Le Chapelain C, Ganegamage SK, Dotson D, Rogelj S, Groll M, Tello-Aburto R.
    Eur J Med Chem; 2018 Sep 05; 157():962-977. PubMed ID: 30165344
    [Abstract] [Full Text] [Related]

  • 11. Design and synthesis of tripeptidyl furylketones as selective inhibitors against the β5 subunit of human 20S proteasome.
    Sun Q, Zhou T, Xi D, Li X, Lü Z, Xu F, Wang C, Niu Y, Xu P.
    Eur J Med Chem; 2020 Apr 15; 192():112160. PubMed ID: 32146375
    [Abstract] [Full Text] [Related]

  • 12. Design, synthesis and biological evaluation of novel non-peptide boronic acid derivatives as proteasome inhibitors.
    Ge Y, Li A, Wu J, Feng H, Wang L, Liu H, Xu Y, Xu Q, Zhao L, Li Y.
    Eur J Med Chem; 2017 Mar 10; 128():180-191. PubMed ID: 28182990
    [Abstract] [Full Text] [Related]

  • 13. Development of novel selective peptidomimetics containing a boronic acid moiety, targeting the 20S proteasome as anticancer agents.
    Scarbaci K, Troiano V, Ettari R, Pinto A, Micale N, Di Giovanni C, Cerchia C, Schirmeister T, Novellino E, Lavecchia A, Zappalà M, Grasso S.
    ChemMedChem; 2014 Aug 10; 9(8):1801-16. PubMed ID: 24891205
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  • 15. Discovery of novel tripeptide propylene oxide proteasome inhibitors for the treatment of multiple myeloma.
    Zhang W, Wang X, Zhang H, Wen T, Yang L, Miao H, Wang J, Liu H, Yang X, Lei M, Zhu Y.
    Bioorg Med Chem; 2021 Jun 15; 40():116182. PubMed ID: 33971487
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  • 17. Total synthesis and absolute stereochemistry of the proteasome inhibitors cystargolides A and B.
    Tello-Aburto R, Hallada LP, Niroula D, Rogelj S.
    Org Biomol Chem; 2015 Oct 28; 13(40):10127-30. PubMed ID: 26400369
    [Abstract] [Full Text] [Related]

  • 18. Discovery of a novel dipeptidyl boronic acid proteasome inhibitor for the treatment of multiple myeloma and triple-negative breast cancer.
    Lei M, Feng H, Bai E, Zhou H, Wang J, Qin Y, Zhang H, Wang X, Liu Z, Hai O, Liu J, Zhu Y.
    Org Biomol Chem; 2019 Jan 16; 17(3):683-691. PubMed ID: 30601533
    [Abstract] [Full Text] [Related]

  • 19. Development of a new class of proteasome inhibitors with an epoxyketone warhead: Rational hybridization of non-peptidic belactosin derivatives and peptide epoxyketones.
    Kawamura S, Unno Y, Asai A, Arisawa M, Shuto S.
    Bioorg Med Chem; 2014 Jun 15; 22(12):3091-5. PubMed ID: 24814885
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  • 20. Design, synthesis, and biological evaluation of novel phenol ether derivatives as non-covalent proteasome inhibitors.
    Yu J, Xu L, Hong D, Zhang X, Liu J, Li D, Li J, Zhou Y, Liu T.
    Eur J Med Chem; 2019 Jan 01; 161():543-558. PubMed ID: 30391816
    [Abstract] [Full Text] [Related]

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