Moroder L - Search Results

1

TMC-95A analogues with endocyclic biphenyl ether group as proteasome inhibitors.

Kaiser M, Milbradt AG, Siciliano C, Assfalg-Machleidt I, Machleidt W, Groll M, Renner C, Moroder L. Kaiser M, et al. Among authors: moroder l. Chem Biodivers. 2004 Jan;1(1):161-73. doi: 10.1002/cbdv.200490008. Chem Biodivers. 2004. PMID: 17191784

2

Cyclodextrins as templates for the presentation of protease inhibitors.

Schaschke N, Musiol HJ, Assfalg-Machleidt I, Machleidt W, Rudolph-Böhner S, Moroder L. Schaschke N, et al. Among authors: moroder l. FEBS Lett. 1996 Aug 12;391(3):297-301. doi: 10.1016/0014-5793(96)00752-1. FEBS Lett. 1996. PMID: 8764993 Free article.

3

E-64 analogues as inhibitors of cathepsin B. On the role of the absolute configuration of the epoxysuccinyl group.

Schaschke N, Assfalg-Machleidt I, Machleidt W, Turk D, Moroder L. Schaschke N, et al. Among authors: moroder l. Bioorg Med Chem. 1997 Sep;5(9):1789-97. doi: 10.1016/s0968-0896(97)00105-3. Bioorg Med Chem. 1997. PMID: 9354234

4

Synthesis, kinetic characterization and X-ray analysis of peptide aldehydes as inhibitors of the 20S proteasomes from Thermoplasma acidophilum and Saccharomyces cerevisiae.

Escherich A, Ditzel L, Musiol HJ, Groll M, Huber R, Moroder L. Escherich A, et al. Among authors: moroder l. Biol Chem. 1997 Aug;378(8):893-8. doi: 10.1515/bchm.1997.378.8.893. Biol Chem. 1997. PMID: 9377486

5

Substrate/propeptide-derived endo-epoxysuccinyl peptides as highly potent and selective cathepsin B inhibitors.

Schaschke N, Assfalg-Machleidt I, Machleidt W, Moroder L. Schaschke N, et al. Among authors: moroder l. FEBS Lett. 1998 Jan 2;421(1):80-2. doi: 10.1016/s0014-5793(97)01538-x. FEBS Lett. 1998. PMID: 9462845 Free article.

6

Bifunctional inhibitors of the trypsin-like activity of eukaryotic proteasomes.

Loidl G, Groll M, Musiol HJ, Ditzel L, Huber R, Moroder L. Loidl G, et al. Among authors: moroder l. Chem Biol. 1999 Apr;6(4):197-204. doi: 10.1016/S1074-5521(99)80036-2. Chem Biol. 1999. PMID: 10099130

7

Bivalency as a principle for proteasome inhibition.

Loidl G, Groll M, Musiol HJ, Huber R, Moroder L. Loidl G, et al. Among authors: moroder l. Proc Natl Acad Sci U S A. 1999 May 11;96(10):5418-22. doi: 10.1073/pnas.96.10.5418. Proc Natl Acad Sci U S A. 1999. PMID: 10318898 Free PMC article.

8

Preferred conformation of endomorphin-1 in aqueous and membrane-mimetic environments.

Fiori S, Renner C, Cramer J, Pegoraro S, Moroder L. Fiori S, et al. Among authors: moroder l. J Mol Biol. 1999 Aug 6;291(1):163-75. doi: 10.1006/jmbi.1999.2951. J Mol Biol. 1999. PMID: 10438613

9

Photomodulation of the Conformation of Cyclic Peptides with Azobenzene Moieties in the Peptide Backbone.

Behrendt R, Renner C, Schenk M, Wang F, Wachtveitl J, Oesterhelt D, Moroder L. Behrendt R, et al. Among authors: moroder l. Angew Chem Int Ed Engl. 1999 Sep;38(18):2771-2774. doi: 10.1002/(sici)1521-3773(19990917)38:18<2771::aid-anie2771>3.0.co;2-w. Angew Chem Int Ed Engl. 1999. PMID: 10508378

10

Synthesis of bivalent inhibitors of eucaryotic proteasomes.

Loidl G, Musiol HJ, Groll M, Huber R, Moroder L. Loidl G, et al. Among authors: moroder l. J Pept Sci. 2000 Jan;6(1):36-46. doi: 10.1002/(SICI)1099-1387(200001)6:1<36::AID-PSC232>3.0.CO;2-2. J Pept Sci. 2000. PMID: 10674718

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