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Number of items: 7.

Korner, M. ; Sauer, G. ; Heil, A. ; Nasu, D. ; Empting, M. ; Tietze, D. ; Voigt, S. ; Weidler, H. ; Gutmann, T. ; Avrutina, O. ; Kolmar, H. ; Ratajczyk, T. ; Buntkowsky, G. (2013):
PHIP-label: parahydrogen-induced polarization in propargylglycine-containing synthetic oligopeptides.
In: Chemical Communications, 49 (71), pp. 7839-7841. [Article]

Tischler, M. ; Nasu, D. ; Empting, M. ; Schmelz, S. ; Heinz, D. W. ; Rottmann, P. ; Kolmar, H. ; Buntkowsky, G. ; Tietze, D. ; Avrutina, O. (2012):
Braces for the Peptide Backbone: Insights into Structure-Activity Relationships of Protease Inhibitor Mimics with Locked Amide Conformations.
In: Angewandte Chemie-International Edition, 51 (15), pp. 3708-3712. [Article]

Empting, M. ; Avrutina, O. ; Meusinger, R. ; Fabritz, S. ; Reinwarth, M. ; Biesalski, M. ; Voigt, S. ; Buntkowsky, G. ; Kolmar, H. (2011):
"Triazole Bridge": Disulfide-Bond Replacement by Ruthenium-Catalyzed Formation of 1,5-Disubstituted 1,2,3-Triazoles.
In: Angewandte Chemie-International Edition, 50 (22), pp. 5207-5211. [Article]

Niemann, H. H. ; Schmoldt, H.-U. ; Wentzel, A. ; Kolmar, H. ; Heinz, D. W. (2006):
Barnase fusion as a tool to determine the crystal structure of the small disulfide-rich protein McoEeTI.
In: Journal of Molecular Biology, 356, pp. 1-8. [Article]

Reiss, S. ; Sieber, M. ; Oberle, V. ; Wentzel, A. ; Spangenberg, P. ; Claus, R. ; Kolmar, H. ; Lösche, W. (2006):
Inhibition of platelet aggregation by grafting RGD and KGD sequences on the structural scaffold of small disulfide-rich proteins.
In: Platelets, 17, pp. 153-157. [Article]

Hagelueken, G. ; Adams, T. M. ; Wiehlmann, L. ; Widow, U. ; Kolmar, H. ; Tümmler, B. ; Heinz, D. W. ; Schubert, W. D. (2006):
The crystal structure of SdsA1, an alkylsulfatase from Pseudomonas aeruginosa, defines a third class of sulfatases.
In: Proceedings of the National Academy of Sciences U.S. A. PNAS, 103, pp. 7631-7634. [Article]

Werle, M. ; Schmitz, T. ; Huang, H.-L. ; Wentzel, A. ; Kolmar, H. ; Bernkop-Schnürch, A. (2006):
The potential of cystine-knot microproteins as novel pharmacophoric scaffolds in oral peptide drug delivery.
In: Journal of Drug Targeting, 14, pp. 137-146. [Article]

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