Moroder L - Search Results

1

Design of benzamidine-type inhibitors of factor Xa.

Gabriel B, Stubbs MT, Bergner A, Hauptmann J, Bode W, Stürzebecher J, Moroder L. Gabriel B, et al. Among authors: moroder l. J Med Chem. 1998 Oct 22;41(22):4240-50. doi: 10.1021/jm980227t. J Med Chem. 1998. PMID: 9784099

2

Activation of snake venom metalloproteinases by a cysteine switch-like mechanism.

Grams F, Huber R, Kress LF, Moroder L, Bode W. Grams F, et al. Among authors: moroder l. FEBS Lett. 1993 Nov 29;335(1):76-80. doi: 10.1016/0014-5793(93)80443-x. FEBS Lett. 1993. PMID: 8243670 Free article.

3

Design and synthesis of heterotrimeric collagen peptides with a built-in cystine-knot. Models for collagen catabolism by matrix-metalloproteases.

Ottl J, Battistuta R, Pieper M, Tschesche H, Bode W, Kühn K, Moroder L. Ottl J, et al. Among authors: moroder l. FEBS Lett. 1996 Nov 25;398(1):31-6. doi: 10.1016/s0014-5793(96)01212-4. FEBS Lett. 1996. PMID: 8946948 Free article.

4

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

5

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

6

Non-peptidic cysteine derivatives as inhibitors of matrix metalloproteinases.

Müller JC, von Roedern EG, Grams F, Nagase H, Moroder L. Müller JC, et al. Among authors: moroder l. Biol Chem. 1997 Dec;378(12):1475-80. doi: 10.1515/bchm.1997.378.12.1475. Biol Chem. 1997. PMID: 9461346

7

Design and synthesis of malonic acid-based inhibitors of human neutrophil collagenase (MMP8).

Graf von Roedern E, Grams F, Brandstetter H, Moroder L. Graf von Roedern E, et al. Among authors: moroder l. J Med Chem. 1998 Jan 29;41(3):339-45. doi: 10.1021/jm9706426. J Med Chem. 1998. PMID: 9464365

8

Structure of malonic acid-based inhibitors bound to human neutrophil collagenase. A new binding mode explains apparently anomalous data.

Brandstetter H, Engh RA, Von Roedern EG, Moroder L, Huber R, Bode W, Grams F. Brandstetter H, et al. Among authors: moroder l. Protein Sci. 1998 Jun;7(6):1303-9. doi: 10.1002/pro.5560070605. Protein Sci. 1998. PMID: 9655333 Free PMC article.

9

Bis-substituted malonic acid hydroxamate derivatives as inhibitors of human neutrophil collagenase (MMP8).

Graf von Roedern E, Brandstetter H, Engh RA, Bode W, Grams F, Moroder L. Graf von Roedern E, et al. Among authors: moroder l. J Med Chem. 1998 Jul 30;41(16):3041-7. doi: 10.1021/jm980112p. J Med Chem. 1998. PMID: 9685244

10

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

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