Anthranilic acid, the new player in the ensemble of aromatic residue labeling precursor compounds. Schörghuber J, Geist L, Bisaccia M, Weber F, Konrat R, Lichtenecker RJ* J Biomol NMR 2017, open access

doi.org/10.1007/s10858-017-0129-2

 

Highly selective stable isotope labeling of histidine residues using a novel precursor in E. coli-based overexpression systems. Schörghuber J, Geist L, Platzer G, Konrat R, Lichtenecker RJ* ChemBioChem 2017, 18, 1487–1491.

onlinelibrary.wiley.com/doi/10.1002/cbic.201700192/full

 

Bioactivity of topologically confined gramicidin A dimers. Jadhav KB, Stein C, Makarewicz O, Pradel G, Lichtenecker RJ, Sack H, Heinemann SH, Arndt H-D* Bioorg. Med. Chem. 2017, 25, 261-268.

www.sciencedirect.com/science/article/pii/S0968089616310781

 

Synthesis of Metabolic Amino acid Precursors: Tools for Selective Isotope Labeling in Cell-Based Protein Overexpression. Lichtenecker RJ*, Schörghuber J, Bisaccia M Synlett 2015, 26, 2611-2616.

www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0034-1378878

 

Novel approaches in selective tryptophan isotope labeling using Escherichia coli overexpression media. Schörghuber J, Sara T, Bisaccia M, Schmid W, Konrat R, Lichtenecker RJ* ChemBioChem 2015, 16, 5, 746-751.

onlinelibrary.wiley.com/doi/10.1002/cbic.201402677/full

 

Dynamic combinatorial enrichment of polyconformational D-/L peptide dimers. Jadhav KBǂ, Lichtenecker RJǂ, Bullach A, Bhubaneswar M, Arndt H-D* Chem. Eur. J. 2015, 21, 15, 5898-5908.

  ǂ equal contribution

onlinelibrary.wiley.com/doi/10.1002/chem.201405413/full

 

Synthesis of aromatic 13C/2H-α-ketoacid precursors to be used in selective phenylalanine and tyrosine protein labeling. Lichtenecker RJ* Org. Biomol. Chem. 2014, 12, 7551-7560.

pubs.rsc.org/en/content/articlehtml/2014/ob/c4ob01129e

 

α-Ketoacids as precursors for phenylalanine and tyrosine labelling in cell-based protein overexpression. Lichtenecker RJ*, Weinhaeupl K, Schmid W, Konrat R J. Biomol. NMR 2013 57(4): 327-331.

link.springer.com/article/10.1007/s10858-013-9796-9

 

Independent valine and leucine isotope labeling in Escherichia coli protein overexpression systems. Lichtenecker RJ*, Weinhaeupl K, Reuther L, Schoerghuber J, Schmid W, Konrat R J. Biomol. NMR 2013 57(3): 205-209.

link.springer.com/article/10.1007/s10858-013-9786-y/fulltext.html

 

Iterative Antimicrobial Candidate Selection from Informed D-/L-Peptide Dimer Libraries. Lichtenecker RJ, Ellinger B, Han H-M, Jadhav KB, Baumann S, Makarewicz O, Grabenbauer M, Arndt H-D* ChemBioChem. 2013 14(18): 2492-2499.

onlinelibrary.wiley.com/doi/10.1002/cbic.201300243/full

 

Selective Isotope Labelling of Leucine Residues by Using α-Ketoacid Precursor Compounds. Lichtenecker RJ*, Coudevylle N, Konrat R, Schmid W ChemBioChem. 2013 14:818-21.

onlinelibrary.wiley.com/doi/10.1002/cbic.201200737/full

 

Biomimetic synthesis of azole- and aryl-peptide alkaloids. Arndt H-D*, Lichtenecker R, Loos P, Milroy L-G Biomimetic Organic Synthesis (Edited by E. Poupon, B. Nay), Wiley 2011 1: 317-355.

 

Application of various ionic liquids as cosolvents for chloroperoxidase-catalysed biotransformations. Lichtenecker RJ, Schmid W* Monatsh. Chem. 2009 140(5): 509-512.

 

Synthetic tools for addressing biological and medicinal chemical questions. Braitsch M, Fischer M, Hollaus R, Lentsch C, Lichtenecker R, Nagl M, Nowikow C, Schmoelzer C, Schmid W* Joint Meeting on Medicinal Chemistry: Hungarian-Austrian-Czech-German-Greek-Italian-Polish-Slovak-Slovenian 2009, 21-26.

 

Direct methods and residue type specific isotope labeling in NMR structure determination and model-driven sequential assignment. Schedlbauer A, Auer R, Ledolter K, Tollinger M, Kloiber K, Lichtenecker R, Ruedisser S, Hommel U, Schmid W, Konrat R, Kontaxis G* J. Biomol. NMR 2008 42(2): 111-127.

 

An Isolated Helix Persists in a Sparsely Populated Form of KIX under Native Conditions. Tollinger M*, Kloiber K, Agoston B, Dorigoni C, Lichtenecker R, Schmid W, Konrat R Biochemistry 2006 45(29): 8885-8893.

 

Simplification of protein NOESY spectra using bioorganic precursor synthesis and NMR spectral editing. Lichtenecker R, Ludwiczek ML, Schmid W, Konrat R* J. Am. Chem. Soc. 2004 126(17): 5348-5349.

 

Tuning of Redox Potentials for the Design of Ruthenium Anticancer Drugs – an Electrochemical Study of [trans-RuCl4L(DMSO)]- and [trans-RuCl4L2]- Complexes, where L = Imidazole, 1,2,4-Triazole, Indazole. Reisner E, Arion VB*, Guedes da Silva MFC, Lichtenecker R, Eichinger A, Keppler BK*, Vadim Y, Pombeiro AJL* Inorganic Chemistry 2004 43(22): 7083-7093.

 

Two novel trans-tetrachloro(dimethyl sulfoxide)azoleruthenate(III) complexes, their antiproliferative activity and the coordination mode of triazole in H2trz[RuCl4(dmso)(Htrz)] Unfried P*, Reisner E, Fremuth M, Jakupec MA, Lichtenecker R, Arion VB, Keppler BK J. Inorg. Biochem. 2003, 96, 1, 243.