Machleidt W - 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: machleidt w. Chem Biodivers. 2004 Jan;1(1):161-73. doi: 10.1002/cbdv.200490008. Chem Biodivers. 2004. PMID: 17191784

2

Inhibition of human mu-calpain by conformationally constrained calpastatin peptides.

Pfizer J, Assfalg-Machleidt I, Machleidt W, Schaschke N. Pfizer J, et al. Among authors: machleidt w. Biol Chem. 2008 Jan;389(1):83-90. doi: 10.1515/BC.2008.004. Biol Chem. 2008. PMID: 18095873

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: machleidt w. Bioorg Med Chem. 1997 Sep;5(9):1789-97. doi: 10.1016/s0968-0896(97)00105-3. Bioorg Med Chem. 1997. PMID: 9354234

4

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: machleidt w. FEBS Lett. 1998 Jan 2;421(1):80-2. doi: 10.1016/s0014-5793(97)01538-x. FEBS Lett. 1998. PMID: 9462845 Free article.

5

Epoxysuccinyl peptide-derived cathepsin B inhibitors: modulating membrane permeability by conjugation with the C-terminal heptapeptide segment of penetratin.

Schaschke N, Deluca D, Assfalg-Machleidt I, Höhneke C, Sommerhoff CP, Machleidt W. Schaschke N, et al. Among authors: machleidt w. Biol Chem. 2002 May;383(5):849-52. doi: 10.1515/BC.2002.090. Biol Chem. 2002. PMID: 12108551

6

Calpastatin exon 1B-derived peptide, a selective inhibitor of calpain: enhancing cell permeability by conjugation with penetratin.

Gil-Parrado S, Assfalg-Machleidt I, Fiorino F, Deluca D, Pfeiler D, Schaschke N, Moroder L, Machleidt W. Gil-Parrado S, et al. Among authors: machleidt w. Biol Chem. 2003 Mar;384(3):395-402. doi: 10.1515/BC.2003.045. Biol Chem. 2003. PMID: 12715890 Free article.

7

A new cell-permeable calpain inhibitor.

Fiorino F, Gil-Parrado S, Assfalg-Machleidt I, Machleidt W, Moroder L. Fiorino F, et al. Among authors: machleidt w. J Pept Sci. 2007 Jan;13(1):70-3. doi: 10.1002/psc.790. J Pept Sci. 2007. PMID: 17019744

8

Beta-cyclodextrin/epoxysuccinyl peptide conjugates: a new drug targeting system for tumor cells.

Schaschke N, Assfalg-Machleidt I, Machleidt W, Lassleben T, Sommerhoff CP, Moroder L. Schaschke N, et al. Among authors: machleidt w. Bioorg Med Chem Lett. 2000 Apr 3;10(7):677-80. doi: 10.1016/s0960-894x(00)00078-0. Bioorg Med Chem Lett. 2000. PMID: 10762052

9

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: machleidt w. FEBS Lett. 1996 Aug 12;391(3):297-301. doi: 10.1016/0014-5793(96)00752-1. FEBS Lett. 1996. PMID: 8764993 Free article.

10

Rapid enzymatic test for phenotypic HIV protease drug resistance.

Hoffmann D, Assfalg-Machleidt I, Nitschko H, von der Helm K, Koszinowski U, Machleidt W. Hoffmann D, et al. Among authors: machleidt w. Biol Chem. 2003 Jul;384(7):1109-17. doi: 10.1515/BC.2003.124. Biol Chem. 2003. PMID: 12956428

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