Cyclodextrins as templates for the presentation of protease inhibitors

Schaschke, Norbert; Musiol, HJ; AssfalgMachleidt, I; Machleidt, W; RudolphBohner, S; Moroder, L

Cyclodextrins as templates for the presentation of protease inhibitors

Schaschke N, Musiol HJ, AssfalgMachleidt I, Machleidt W, RudolphBohner S, Moroder L (1996)
FEBS LETTERS 391(3): 297-301.

Zeitschriftenaufsatz | Veröffentlicht | Englisch

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DOI

https://doi.org/10.1016/0014-5793(96)00752-1

Autor*in

Schaschke, Norbert^UniBi; Musiol, HJ; AssfalgMachleidt, I; Machleidt, W; RudolphBohner, S; Moroder, L

Einrichtung

Fakultät für Chemie > Organische Chemie III

Erscheinungsjahr

1996

Zeitschriftentitel

FEBS LETTERS

Band

391

Ausgabe

3

Seite(n)

297-301

ISSN

0014-5793

Page URI

https://pub.uni-bielefeld.de/record/2403889

Zitieren

Schaschke N, Musiol HJ, AssfalgMachleidt I, Machleidt W, RudolphBohner S, Moroder L. Cyclodextrins as templates for the presentation of protease inhibitors. FEBS LETTERS. 1996;391(3):297-301.

Schaschke, N., Musiol, H. J., AssfalgMachleidt, I., Machleidt, W., RudolphBohner, S., & Moroder, L. (1996). Cyclodextrins as templates for the presentation of protease inhibitors. FEBS LETTERS, 391(3), 297-301. https://doi.org/10.1016/0014-5793(96)00752-1

Schaschke, Norbert, Musiol, HJ, AssfalgMachleidt, I, Machleidt, W, RudolphBohner, S, and Moroder, L. 1996. “Cyclodextrins as templates for the presentation of protease inhibitors”. FEBS LETTERS 391 (3): 297-301.

Schaschke, N., Musiol, H. J., AssfalgMachleidt, I., Machleidt, W., RudolphBohner, S., and Moroder, L. (1996). Cyclodextrins as templates for the presentation of protease inhibitors. FEBS LETTERS 391, 297-301.

Schaschke, N., et al., 1996. Cyclodextrins as templates for the presentation of protease inhibitors. FEBS LETTERS, 391(3), p 297-301.

N. Schaschke, et al., “Cyclodextrins as templates for the presentation of protease inhibitors”, FEBS LETTERS, vol. 391, 1996, pp. 297-301.

Schaschke, N., Musiol, H.J., AssfalgMachleidt, I., Machleidt, W., RudolphBohner, S., Moroder, L.: Cyclodextrins as templates for the presentation of protease inhibitors. FEBS LETTERS. 391, 297-301 (1996).

Schaschke, Norbert, Musiol, HJ, AssfalgMachleidt, I, Machleidt, W, RudolphBohner, S, and Moroder, L. “Cyclodextrins as templates for the presentation of protease inhibitors”. FEBS LETTERS 391.3 (1996): 297-301.

8 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Carbohydrates in peptide and protein design.
Jensen KJ, Brask J., Biopolymers 80(6), 2005
PMID: 15929028

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., Biol Chem 384(3), 2003
PMID: 12715890

Bivalent inhibition of human beta-tryptase.
Schaschke N, Matschiner G, Zettl F, Marquardt U, Bergner A, Bode W, Sommerhoff CP, Moroder L., Chem Biol 8(4), 2001
PMID: 11325588

Synthesis of bivalent inhibitors of eucaryotic proteasomes.
Loidl G, Musiol HJ, Groll M, Huber R, Moroder L., J Pept Sci 6(1), 2000
PMID: 10674718

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., Bioorg Med Chem Lett 10(7), 2000
PMID: 10762052

Bifunctional inhibitors of the trypsin-like activity of eukaryotic proteasomes.
Loidl G, Groll M, Musiol HJ, Ditzel L, Huber R, Moroder L., Chem Biol 6(4), 1999
PMID: 10099130

Bivalency as a principle for proteasome inhibition.
Loidl G, Groll M, Musiol HJ, Huber R, Moroder L., Proc Natl Acad Sci U S A 96(10), 1999
PMID: 10318898

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., Biol Chem 378(8), 1997
PMID: 9377486

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