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Search for "peptide-based" in Full Text gives 35 result(s) in Beilstein Journal of Organic Chemistry.

Come-back of phenanthridine and phenanthridinium derivatives in the 21st century

  • Lidija-Marija Tumir,
  • Marijana Radić Stojković and
  • Ivo Piantanida

Beilstein J. Org. Chem. 2014, 10, 2930–2954, doi:10.3762/bjoc.10.312

Graphical Abstract
  • , characterised by the specific fluorescence band sensitive to the pH as well as on the interactions with ds-DNA. Interestingly, all peptide-based phenanthridines revealed excellent water solubility combined with low in vitro toxicity, thus being good candidates for development of new safe fluorimetric DNA and
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Published 10 Dec 2014

Automated solid-phase peptide synthesis to obtain therapeutic peptides

  • Veronika Mäde,
  • Sylvia Els-Heindl and
  • Annette G. Beck-Sickinger

Beilstein J. Org. Chem. 2014, 10, 1197–1212, doi:10.3762/bjoc.10.118

Graphical Abstract
  • osteoporosis, cardiovascular diseases and inflammation can be treated by peptide-based drugs [4][5]. Within the last decades, the fast development of omics technologies such as genomics, proteomics and transcriptomics led to the identification of a great number of target peptides or proteins [6]. This trend
  • revolutionized by new methods and strategies for automated approaches, which simplifies peptide manufacturing. Combined with the mentioned advantages of peptide-based drugs, their application as novel biopharmaceuticals is pushed forward. Within the last years, the global market for peptide therapeutics expanded
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Published 22 May 2014

New tridecapeptides of the theonellapeptolide family from the Indonesian sponge Theonella swinhoei

  • Annamaria Sinisi,
  • Barbara Calcinai,
  • Carlo Cerrano,
  • Henny A. Dien,
  • Angela Zampella,
  • Claudio D’Amore,
  • Barbara Renga,
  • Stefano Fiorucci and
  • Orazio Taglialatela-Scafati

Beilstein J. Org. Chem. 2013, 9, 1643–1651, doi:10.3762/bjoc.9.188

Graphical Abstract
  • , Indonesia), which proved to be rich in aurantosides [6] and 4-methylene steroids [18], while polyketide macrolides and peptide-based derivatives were extremely rare if not absent. Remarkably, the chemical analysis of a different specimen of T. swinhoei, collected in the same area as the previous one
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Published 13 Aug 2013

Efficient regio- and stereoselective access to novel fluorinated β-aminocyclohexanecarboxylates

  • Loránd Kiss,
  • Melinda Nonn,
  • Reijo Sillanpää,
  • Santos Fustero and
  • Ferenc Fülöp

Beilstein J. Org. Chem. 2013, 9, 1164–1169, doi:10.3762/bjoc.9.130

Graphical Abstract
  • protein–ligand or protein–protein interactions, thereby determining thermal or metabolic stabilities, which is of great importance in peptide-based drug research [11][12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28][29][30][31][32][33][34][35]. These changes in properties may be more
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Published 17 Jun 2013

Modulating the activity of short arginine-tryptophan containing antibacterial peptides with N-terminal metallocenoyl groups

  • H. Bauke Albada,
  • Alina-Iulia Chiriac,
  • Michaela Wenzel,
  • Maya Penkova,
  • Julia E. Bandow,
  • Hans-Georg Sahl and
  • Nils Metzler-Nolte

Beilstein J. Org. Chem. 2012, 8, 1753–1764, doi:10.3762/bjoc.8.200

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  • innate immune system, the name “antimicrobial peptides” (abbreviated as AMPs) defines a larger group of peptides that also encompasses synthetic peptides, and peptidomimetics, for example. Among these, synthetic peptide-based antimicrobial agents are especially interesting because isolation and/or
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Published 15 Oct 2012

Synthetic studies towards bottromycin

  • Stefanie Ackermann,
  • Hans-Georg Lerchen,
  • Dieter Häbich,
  • Angelika Ullrich and
  • Uli Kazmaier

Beilstein J. Org. Chem. 2012, 8, 1652–1656, doi:10.3762/bjoc.8.189

Graphical Abstract
  • endothiopeptide and ring closure between proline and glycine. The same group also undertook some modifications on the natural product [26]. Results and Discussion Our group is also involved in the synthesis of peptide-based natural products [27][28][29][30][31][32], and of course the structure of bottromycin is
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Published 01 Oct 2012

Parallel solid-phase synthesis of diaryltriazoles

  • Matthias Wrobel,
  • Jeffrey Aubé and
  • Burkhard König

Beilstein J. Org. Chem. 2012, 8, 1027–1036, doi:10.3762/bjoc.8.115

Graphical Abstract
  • peptide-based compounds [8], can be overcome by compounds stabilized by non-natural amino acids [9] or cross-linked between side chains and the backbone [10]. Replacement of the complete backbone by a nonpeptidic scaffold, which positions side chains in the typical i, i+3 and i+7 arrangement of an α-helix
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Published 06 Jul 2012

Exceptionally small supramolecular hydrogelators based on aromatic–aromatic interactions

  • Junfeng Shi,
  • Yuan Gao,
  • Zhimou Yang and
  • Bing Xu

Beilstein J. Org. Chem. 2011, 7, 167–172, doi:10.3762/bjoc.7.23

Graphical Abstract
  • represents the lowest molecular weight (MW = 295.33 g/mol) peptide-based hydrogelator prepared to date. The supramolecular hydrogels were characterized by transmission electron micrograph (TEM) and fluorescence spectroscopy, and the results obtained by both techniques correlate well with their rheological
  • possibility of peptide-based hydrogelators that are smaller than the aroyl L-cystine noted above. Here, we reported the systematic synthesis and examination of a series of phenylalanine derivatives and the identification of the lowest molecular weight peptide-based hydrogelator (MW = 295.33 g/mol) produced to
  • phenyl groups. Conclusion In summary, we have demonstrated that an aromatic group (fluorenyl, naphthyl, naphthalenoxyl, or cinnamoyl) covalently attached to phenylalanine gives rise to a series of new low molecular weight hydrogelators and the identification of the lowest molecular weight peptide-based
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Published 07 Feb 2011

Differences between β-Ala and Gly-Gly in the design of amino acids-based hydrogels

  • Andreea Pasc,
  • Firmin Obounou Akong,
  • Sedat Cosgun and
  • Christine Gérardin

Beilstein J. Org. Chem. 2010, 6, 973–977, doi:10.3762/bjoc.6.109

Graphical Abstract
  • networks as a result of intimate interactions between gelator molecules. Keywords: amino acid; histidine; hydrogel; peptide-based surfactant; soft matter; supramolecular; Introduction Hydrogels continue to attract much interest due to their versatile applications in tissue engineering, biosensing, drug
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Published 11 Oct 2010

An enantiomerically pure siderophore type ligand for the diastereoselective 1 : 1 complexation of lanthanide(III) ions

  • Markus Albrecht,
  • Olga Osetska,
  • Thomas Abel,
  • Gebhard Haberhauer and
  • Eva Ziegler

Beilstein J. Org. Chem. 2009, 5, No. 78, doi:10.3762/bjoc.5.78

Graphical Abstract
  • C81H99N15O9 [M + Na]+: m/z = 1448.7642; found 1448.7639. HRMS (ESI): calcd. for C81H99N15O9 [M + H]+: m/z = 1426.7823; found 1426.7808. HRMS (ESI): [M + 2Na]++: m/z = 735.8739; found 735.8767. Synthesis and characterization of macrocyclic imidazole peptide based tris(N,N-diethyl-8-hydroxyquinoline-2
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Published 11 Dec 2009
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