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Journal Abstract Search
359 related items for PubMed ID: 25942361
1. 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; 31(3):456-63. PubMed ID: 25942361 [Abstract] [Full Text] [Related]
2. 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]
3. 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 10; 32(1):865-877. PubMed ID: 28657369 [Abstract] [Full Text] [Related]
6. 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]
10. 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]
14. 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]
15. 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]
16. 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]
17. 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 05; 84(5):497-504. PubMed ID: 24751157 [Abstract] [Full Text] [Related]
20. Synthesis and antiproteasomal activity of novel O-benzyl salicylamide-based inhibitors built from leucine and phenylalanine. Jorda R, Dušek J, Řezníčková E, Pauk K, Magar PP, Imramovský A, Kryštof V. Eur J Med Chem; 2017 Jul 28; 135():142-158. PubMed ID: 28441582 [Abstract] [Full Text] [Related] Page: [Next] [New Search]