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Search for "peptides" in Full Text gives 373 result(s) in Beilstein Journal of Organic Chemistry. Showing first 200.

Synthesis and application of trifluoroethoxy-substituted phthalocyanines and subphthalocyanines

  • Satoru Mori and
  • Norio Shibata

Beilstein J. Org. Chem. 2017, 13, 2273–2296, doi:10.3762/bjoc.13.224

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  • ][91] or a peptide [92]. For example, TFEO-Pcs conjugated with peptides (15) have been reported [93]. A3B type TFEO-Pc was successfully condensed with peptides by palladium-catalyzed cross-coupling reactions in good yield (Scheme 5). These TFEO-Pc-peptide conjugates, which show a sharp Q band in the UV
  • -substituted phthalocyanines conjugated with peptides. Synthesis of trifluoroethoxy-substituted phthalocyanines conjugated with deoxyribonucleosides. Synthesis of trifluoroethoxy-substituted phthalocyanines conjugated with cyclodextrin. Synthesis of fluoropolymer-bearing phthalocyanine side groups. Synthesis
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Published 27 Oct 2017

Phosphonic acid: preparation and applications

  • Charlotte M. Sevrain,
  • Mathieu Berchel,
  • Hélène Couthon and
  • Paul-Alain Jaffrès

Beilstein J. Org. Chem. 2017, 13, 2186–2213, doi:10.3762/bjoc.13.219

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  • -butyl phosphonate was used for the synthesis of phosphonic acid analogues of peptides like protein-tyrosine kynases (PTKs) [134] or to prepare gadolinium complexes used as magnetic resonance imaging (MRI) contrast agents [135][136]. The introduction of the di-tert-butyl phosphonate was achieved by the
  • function was used. 3.5. Other conditions for dealkylation of phosphonate The dealkylation of diethyl phosphonate groups present in amino acids or peptides requires mild conditions to avoid the reactivity with the other functional groups. If Me3SiBr can be used to dealkylate peptides functionalized with
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Published 20 Oct 2017

A mechanochemical approach to access the proline–proline diketopiperazine framework

  • Nicolas Pétry,
  • Hafid Benakki,
  • Eric Clot,
  • Pascal Retailleau,
  • Farhate Guenoun,
  • Fatima Asserar,
  • Chakib Sekkat,
  • Thomas-Xavier Métro,
  • Jean Martinez and
  • Frédéric Lamaty

Beilstein J. Org. Chem. 2017, 13, 2169–2178, doi:10.3762/bjoc.13.217

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  • feature, used for the preparation of biologically active peptides and peptidomimetics [7], for applications in organocatalysis [8][9][10], and for the preparation of novel materials [11][12]. An interesting sub-family of these compounds are DKPs derived from the amino acid proline and its analogues, which
  • it would avoid a potential pressure build-up (release of CO2) which could occur with NaHCO3. Noteworthy, no epimerization could be detected by NMR or HPLC analyses. Both peptides 7 and 8 were then deprotected and cyclized into the corresponding diketopiperazine 9. Palladium-catalyzed hydrogenolysis
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Published 19 Oct 2017

Synthesis of 2-aminosuberic acid derivatives as components of some histone deacetylase inhibiting cyclic tetrapeptides

  • Shital Kumar Chattopadhyay,
  • Suman Sil and
  • Jyoti Prasad Mukherjee

Beilstein J. Org. Chem. 2017, 13, 2153–2156, doi:10.3762/bjoc.13.214

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  • and the synthesis of peptides of biological relevance. Keywords: α-amino acid; catalysis; chiral pool; cross metathesis; cyclic peptides; Introduction α-Aminosuberic acid (Asu) is a component of apicidin F (1, Figure 1) belonging to an interesting class of cyclic tetrapeptides displaying
  • applications remains important. During the course of our work on the synthesis of amino acids and peptides relevant to HDAC inhibition [12], we required orthogonally protected Asu derivatives. Herein we describe an alternate synthesis of the important building block 2-aminoheptenoic acid and its application to
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Published 17 Oct 2017

Peptide synthesis: ball-milling, in solution, or on solid support, what is the best strategy?

  • Ophélie Maurin,
  • Pascal Verdié,
  • Gilles Subra,
  • Frédéric Lamaty,
  • Jean Martinez and
  • Thomas-Xavier Métro

Beilstein J. Org. Chem. 2017, 13, 2087–2093, doi:10.3762/bjoc.13.206

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  • build more efficient and sustainable peptide syntheses in the near future. Keywords: ball-mill; green chemistry; mechanochemistry; peptide synthesis; SPPS; Introduction Peptides play a central role both in biological mechanisms and in therapeutic solutions of the future [1][2]. Pharmaceutical
  • companies are showing a renewed interest for this type of therapeutics. A recent study showed that 140 peptides are currently evaluated in clinical trials and more than 500 are in preclinical development [3]. In the recent years, much progress has been made in the administration modes and in the strategies
  • to improve their in vivo bioavailability and stability. This progresses empowered the potential of therapeutic peptides, suggesting a production surge in the future. Besides this high potential, actual peptide production techniques suffer from major environmental issues [4][5][6]. Indeed, large
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Published 06 Oct 2017

Mechanochemical synthesis of small organic molecules

  • Tapas Kumar Achar,
  • Anima Bose and
  • Prasenjit Mal

Beilstein J. Org. Chem. 2017, 13, 1907–1931, doi:10.3762/bjoc.13.186

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  • amines were safely controlled at maximum contacts (solvent-free) by the acid salt NaHSO4. Using 2.0 equiv of both NaHSO4 and PIDA, 72–92% of amides were isolated within 2 h (Scheme 17) [81]. Amino acids are one of the important biomolecules for example as building block of peptides and proteins [75][82
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Published 11 Sep 2017

Enzymatic synthesis of glycosides: from natural O- and N-glycosides to rare C- and S-glycosides

  • Jihen Ati,
  • Pierre Lafite and
  • Richard Daniellou

Beilstein J. Org. Chem. 2017, 13, 1857–1865, doi:10.3762/bjoc.13.180

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  • sugar donor scope, and our group has shown the potency of this enzyme as a biocatalyst for the chemoenzymatic synthesis of non-natural desulfoglycosinolates [22]. More recently, S-glycosylated peptides have been identified, and characterized. In bacteria the structures of sublancin [23], glycocin F [24
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Published 05 Sep 2017

Selective enzymatic esterification of lignin model compounds in the ball mill

  • Ulla Weißbach,
  • Saumya Dabral,
  • Laure Konnert,
  • Carsten Bolm and
  • José G. Hernández

Beilstein J. Org. Chem. 2017, 13, 1788–1795, doi:10.3762/bjoc.13.173

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  • products or materials [2][3]. In organic chemistry, amino acids and short peptides are not only known for being stable under automated ball milling conditions during their preparation [4], but also when applied as catalysts to perform stereoselective transformations [5][6][7]. Encouraged by these facts, we
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Published 25 Aug 2017

Mechanochemical enzymatic resolution of N-benzylated-β3-amino esters

  • Mario Pérez-Venegas,
  • Gloria Reyes-Rangel,
  • Adrián Neri,
  • Jaime Escalante and
  • Eusebio Juaristi

Beilstein J. Org. Chem. 2017, 13, 1728–1734, doi:10.3762/bjoc.13.167

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  • resolution; mechanochemistry; Introduction β-Amino acids are rather interesting molecules that frequently exhibit exceptional biological properties [1][2][3]; for instance, some of them are efficient inhibitors of several enzymes [4][5]. Furthermore, β-amino acid residues can be used to protect peptides and
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Published 18 Aug 2017

Chemical systems, chemical contiguity and the emergence of life

  • Terrence P. Kee and
  • Pierre-Alain Monnard

Beilstein J. Org. Chem. 2017, 13, 1551–1563, doi:10.3762/bjoc.13.155

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  • eutectic phase in water/ice [35][36][37], but computer modelling [38] and preliminary wet-chemistry experiments, which show a selective accumulation of long oligomers [39], already hint at the possibility of similar processes taking place in mineral formations. In the same environments, short peptides
  • /association with the chemical system structure or to the encapsulation of a reaction “machinery” within it. Interface-linked catalysis: The oligomerization of peptides from amino acids with condensing agents has been demonstrated to occur in the presence of phospholipid vesicles [65][66][67]. In these studies
  • ], the complexity of de novo RNA synthesis and its functional interconnection with other biopolymers in the cellular context question its early, single-handed role. The polymerization of short RNA chains and peptides has been investigated within aqueous vesicle lumens as well as water/oil emulsions, and
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Published 07 Aug 2017

A new member of the fusaricidin family – structure elucidation and synthesis of fusaricidin E

  • Marcel Reimann,
  • Louis P. Sandjo,
  • Luis Antelo,
  • Eckhard Thines,
  • Isabella Siepe and
  • Till Opatz

Beilstein J. Org. Chem. 2017, 13, 1430–1438, doi:10.3762/bjoc.13.140

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  • 2,2-dimethylated pseudoproline (ΨMe,Me'Pro). This method has been reported to improve yields of macrolactamizations through stabilizing the cis-configuration of the amide bond and working as a turn inducer in peptides [17][18][19][20]. The ΨMe,Me'Pro unit turned out not to be completely stable during
  • correct (see pages S38 and S39 of Supporting Information File 1). Conclusion In summary, two new members of the fusaricidin family, fusaricidins E and F, were isolated from fermentation broths of Paenibacillus sp. strain Lu16774 as an inseparable mixture of homologs. Structure elucidation of both peptides
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Published 20 Jul 2017

An improved preparation of phorbol from croton oil

  • Alberto Pagani,
  • Simone Gaeta,
  • Andrei I. Savchenko,
  • Craig M. Williams and
  • Giovanni Appendino

Beilstein J. Org. Chem. 2017, 13, 1361–1367, doi:10.3762/bjoc.13.133

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  • unclear. The use of THF was inspired by the work of Seebach on the solubility of peptides in ether-type organic solvents in the presence of certain alkaline cations [20], and it is not unconceivable that the interaction with sodium ions substantially diversifies the relative polarity of glycerol and
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Published 11 Jul 2017

BODIPY-based fluorescent liposomes with sesquiterpene lactone trilobolide

  • Ludmila Škorpilová,
  • Silvie Rimpelová,
  • Michal Jurášek,
  • Miloš Buděšínský,
  • Jana Lokajová,
  • Roman Effenberg,
  • Petr Slepička,
  • Tomáš Ruml,
  • Eva Kmoníčková,
  • Pavel B. Drašar and
  • Zdeněk Wimmer

Beilstein J. Org. Chem. 2017, 13, 1316–1324, doi:10.3762/bjoc.13.128

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  • . Specific drug targeting can be achieved by using, for example, antibodies, peptides, polyethylene glycol polymers, and last but not least, liposomes, which have been nowadays extensively investigated [1][2]. In general, liposomes are employed in order to enhance the therapeutic index of an applied drug by
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Published 04 Jul 2017

Biomimetic molecular design tools that learn, evolve, and adapt

  • David A Winkler

Beilstein J. Org. Chem. 2017, 13, 1288–1302, doi:10.3762/bjoc.13.125

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  • , and peptides and oligonucleotides can also be synthesized efficiently using automated methods, it is not yet possible to carry out chemical syntheses in a general sense using these technologies. However, several groups are making significant breakthroughs in generalizing and expanding the automated
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Published 29 Jun 2017

Towards open-ended evolution in self-replicating molecular systems

  • Herman Duim and
  • Sijbren Otto

Beilstein J. Org. Chem. 2017, 13, 1189–1203, doi:10.3762/bjoc.13.118

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  • peptides and oligopeptides under prebiotic conditions. However, initially only very short peptides were produced in experiments under such conditions, raising doubts over their potential role as a precursor of life. When forming α-helices however, longer polypeptides can be stabilized by the formation of
  • enhanced by electrostatic interactions between amino acids residing on the c and g positions of the α-helices. Ghadiri et al. showed that such coiled-coil peptides are capable of self-replication [35]. As depicted in Figure 7, helical polypeptides can act as a template for shorter peptide fragments by
  • -replicating system involving peptides capable of diversification using a systems chemistry approach [52]. Following the discovery of an exponentially growing self-replicating system [53], we used two building blocks, 1 and 2, to form a dynamic combinational library (DCL) of self-replicating molecules. These
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Published 21 Jun 2017

From chemical metabolism to life: the origin of the genetic coding process

  • Antoine Danchin

Beilstein J. Org. Chem. 2017, 13, 1119–1135, doi:10.3762/bjoc.13.111

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  • summary, the most likely compounds that make the very first metabolic pathways are charged compounds with one to three carbon atoms, amino acids and a variety of peptides or related compounds, certainly not RNA [25]. Phosphates, with their remarkable metastable state in water were selected as surface
  • (Figure 1). This created a collection of charged metabolites that would stick to surfaces and come in contact with each other, promoting a variety of reactions. The first stages of reproductive surface metabolism were prone to produce charged variants of peptides. Among the minerals that would carry over
  • the first (iso)peptide-based metabolic pathways one finds iron–sulfur clusters (pyrite) [20] and polyphosphates [27]. Obviously, selected peptides would be part of the first prebiotic building blocks and compounds, exhibiting a range of promiscuous catalytic activities. This includes hydrolytic self
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Published 12 Jun 2017

An eco-compatible strategy for the diversity-oriented synthesis of macrocycles exploiting carbohydrate-derived building blocks

  • Sushil K. Maurya and
  • Rohit Rana

Beilstein J. Org. Chem. 2017, 13, 1106–1118, doi:10.3762/bjoc.13.110

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  • ] glycosides and macrocyclic glycolipids [11]. Similarly, the copper-catalyzed azide–alkyne cycloaddition (CuAAC) reaction has found wide application in medicinal chemistry [33], biology [34][35], polymer chemistry [36], carbohydrates [37][38][39][40], peptides [41][42][43][44] and in materials science [45][46
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Published 09 Jun 2017

G-Protein coupled receptors: answers from simulations

  • Timothy Clark

Beilstein J. Org. Chem. 2017, 13, 1071–1078, doi:10.3762/bjoc.13.106

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  • , that the opsin/rhodopsin structures [15][16] used so-called high-affinity peptides to mimic the G-protein. It is likely that these proteins behave more like the native G-protein than the protein nanobodies. Review General GPCR structure Figure 2 shows a schematic diagram of the general structure of
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Published 02 Jun 2017

Glyco-gold nanoparticles: synthesis and applications

  • Federica Compostella,
  • Olimpia Pitirollo,
  • Alessandro Silvestri and
  • Laura Polito

Beilstein J. Org. Chem. 2017, 13, 1008–1021, doi:10.3762/bjoc.13.100

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  • diameter range can be obtained [4]. Moreover, this synthetic procedure allows to introduce different types of carbohydrates and other ligands (i.e., polyethylene chains, lipids, peptides, DNA, RNA or fluorescent dyes) in controlled ratios [4]. A modification of this technique consists in the application of
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Published 24 May 2017

Conformational study of L-methionine and L-cysteine derivatives through quantum chemical calculations and 3JHH coupling constant analyses

  • Weslley G. D. P. Silva,
  • Carolyne B. Braga and
  • Roberto Rittner

Beilstein J. Org. Chem. 2017, 13, 925–937, doi:10.3762/bjoc.13.94

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  • analysis; cysteine; methionine; NMR spectroscopy; quantum chemical calculations; Introduction Amino acids constitute the building blocks of proteins and peptides, which play an important role in numerous biological processes [1][2]. However, their studies in both isolated and condensed phases have been
  • disulfide bonds formed by the oxidized thiol groups of cysteine confer exceptional stability for the peptides and proteins where they are present [10]. Thus, a systematic study on the conformational behavior of L-Met and L-Cys can reveal unique properties about the formation of proteins and peptides that
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Published 17 May 2017

Chemoselective synthesis of diaryl disulfides via a visible light-mediated coupling of arenediazonium tetrafluoroborates and CS2

  • Jing Leng,
  • Shi-Meng Wang and
  • Hua-Li Qin

Beilstein J. Org. Chem. 2017, 13, 903–909, doi:10.3762/bjoc.13.91

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  • tetrafluoroborates; carbon disulfide; chemoselectivity; diaryl disulfides; photocatalyst; Findings The development of methods for the functionalization of peptides and proteins under mild conditions is a current frontier in the fields of chemistry, biology and drug discovery [1][2][3][4]. Most of the
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Published 15 May 2017

Expression, purification and structural analysis of functional GABA transporter 1 using the baculovirus expression system

  • Jing Hu,
  • Chris Weise,
  • Christoph Böttcher,
  • Hua Fan and
  • Jian Yin

Beilstein J. Org. Chem. 2017, 13, 874–882, doi:10.3762/bjoc.13.88

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  • , and tryptic peptides were analyzed either directly by matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry (MALDI–TOF MS) or guanidinated and then analyzed by MALDI. The labeled peptide peaks (Figure 2B) in the mass spectrum were identified as either GAT or GFP by matching the
  • peptides from primary sequence databases with Mascot (http://www.matrixscience.com/). The biological function of recombinant proteins of mammalian origin expressed in insect cells may be altered by different N-glycan status. We observed that the terminal sialic acid residues are essential for the GABA
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Published 11 May 2017

DMAP-assisted sulfonylation as an efficient step for the methylation of primary amine motifs on solid support

  • Johnny N. Naoum,
  • Koushik Chandra,
  • Dorit Shemesh,
  • R. Benny Gerber,
  • Chaim Gilon and
  • Mattan Hurevich

Beilstein J. Org. Chem. 2017, 13, 806–816, doi:10.3762/bjoc.13.81

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  • Methylated amines and amides are common motifs found in natural and synthetic compounds, e.g., small molecules, peptides, and oligonucleotides [1][2][3][4][5][6][7][8]. Methylation of amines and amides has found many applications in the fields of pharmacological research, materials science, and in synthetic
  • peptides, proteins, and small molecules on solid support, in addition to other organic compounds in solution phase [22][24][25][27]. We found that the introduction of a single methyl group to an amine adjacent to a hindered moiety using the state-of-the-art strategies is extremely challenging (Figure 1A
  • Supporting Information File 1). After completing the new procedure the methylated amine can be coupled with an amino acid to form a methylated amide. This procedure was, hence, suitable for the synthesis of peptides with multiple sites methylated amides. To further evaluate the efficiency of the new
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Published 03 May 2017

Sulfamide chemistry applied to the functionalization of self-assembled monolayers on gold surfaces

  • Loïc Pantaine,
  • Vincent Humblot,
  • Vincent Coeffard and
  • Anne Vallée

Beilstein J. Org. Chem. 2017, 13, 648–658, doi:10.3762/bjoc.13.64

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  • applications in medicinal chemistry, sulfamide groups have been incorporated in self-assembling molecules [22][23][24][25][26][27], peptides [28], polymers [29], ligands [30], chiral auxiliaries [31][32][33] and in organocatalysts [34][35][36][37]. In light of the importance of the sulfamide functionality, our
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Published 04 Apr 2017

Synthesis of 1-indanones with a broad range of biological activity

  • Marika Turek,
  • Dorota Szczęsna,
  • Marek Koprowski and
  • Piotr Bałczewski

Beilstein J. Org. Chem. 2017, 13, 451–494, doi:10.3762/bjoc.13.48

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  • -amino acid peptides with vasoconstrictor properties, produced primarily in the endothelium. They play a key role in vascular homeostasis and are responsible for proper vascular tone and vascular perfusion maintaining. In 2006, Miyaura et al. have synthesized selective endothelin A receptor antagonists
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Published 09 Mar 2017
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