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Search for "molecular probes" in Full Text gives 34 result(s) in Beilstein Journal of Organic Chemistry.

Amyloid-β probes: Review of structure–activity and brain-kinetics relationships

  • Todd J. Eckroat,
  • Abdelrahman S. Mayhoub and
  • Sylvie Garneau-Tsodikova

Beilstein J. Org. Chem. 2013, 9, 1012–1044, doi:10.3762/bjoc.9.116

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  • resulted in a variety of radiolabeled molecular probes for in vivo PET/SPECT imaging. The scaffolds from which these newer radiolabeled probes are derived include chalcone (5) and its conformationally restricted analogues flavone (6) and aurone (7); stilbene (8) and its analogues diphenyl-1,2,4-oxadiazole
  • (NIRF) imaging. Review Radiolabels used in PET/SPECT molecular probes Even though they decay rapidly, [11C] (t1/2 = 20 min) and [18F] (t1/2 = 110 min) are the most commonly used radiolabels in PET/SPECT molecular probes for in vivo imaging of Aβ plaques [4]. With a half-life (t1/2) of 6.01 h compatible
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Review
Published 28 May 2013

Use of 3-[18F]fluoropropanesulfonyl chloride as a prosthetic agent for the radiolabelling of amines: Investigation of precursor molecules, labelling conditions and enzymatic stability of the corresponding sulfonamides

  • Reik Löser,
  • Steffen Fischer,
  • Achim Hiller,
  • Martin Köckerling,
  • Uta Funke,
  • Aurélie Maisonial,
  • Peter Brust and
  • Jörg Steinbach

Beilstein J. Org. Chem. 2013, 9, 1002–1011, doi:10.3762/bjoc.9.115

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  • remote imaging detectors, for both research and diagnostic purposes has considerably increased over the recent years. The success of this interdisciplinary field depends substantially on the development of molecular probes equipped with appropriate reporter groups [1]. Among the different imaging
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Published 27 May 2013

Thioester derivatives of the natural product psammaplin A as potent histone deacetylase inhibitors

  • Matthias G. J. Baud,
  • Thomas Leiser,
  • Vanessa Petrucci,
  • Mekala Gunaratnam,
  • Stephen Neidle,
  • Franz-Josef Meyer-Almes and
  • Matthew J. Fuchter

Beilstein J. Org. Chem. 2013, 9, 81–88, doi:10.3762/bjoc.9.11

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  • oncogenesis [3][4] and small molecule inhibitors of these pathways have emerged as highly attractive targets for anticancer therapies [5][6]. Inhibitors of epigenetic pathways should not only be useful as anticancer drugs, but also as molecular probes to study the causative relationships between specific
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Letter
Published 15 Jan 2013

Hydrophobic analogues of rhodamine B and rhodamine 101: potent fluorescent probes of mitochondria in living C. elegans

  • Laurie F. Mottram,
  • Safiyyah Forbes,
  • Brian D. Ackley and
  • Blake R. Peterson

Beilstein J. Org. Chem. 2012, 8, 2156–2165, doi:10.3762/bjoc.8.243

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  • ; fluorescence; fusion; imaging; in vivo; microscopy; mitochondria; model organisms; organelle; rhodamine; spectroscopy; Introduction Fluorescent molecular probes represent critical tools for studies of chemical biology [1]. These compounds allow the creation of sensitive enzyme substrates, sensors of a wide
  • introduce the genetically encoded sensor to each genetic background under investigation. Alternatively, a genetically encoded fluorescent protein may be complemented with these molecular probes to perform experiments such as fluorescence recovery after photobleaching (FRAP), where one of the markers remains
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Published 11 Dec 2012

A Wittig-olefination–Claisen-rearrangement approach to the 3-methylquinoline-4-carbaldehyde synthesis

  • Mukund G. Kulkarni,
  • Mayur P. Desai,
  • Deekshaputra R. Birhade,
  • Yunus B. Shaikh,
  • Ajit N. Dhatrak and
  • Ramesh Gannimani

Beilstein J. Org. Chem. 2012, 8, 1725–1729, doi:10.3762/bjoc.8.197

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  • ] and 5-HT3 receptor antagonists [5]. Quinoline mevalonolactones, prepared from 3-methylquinoline-4-carbaldehyde, act as inhibitors of HMG-CoA reductase [6]. 3-Substituted quinoline-4-carbaldehyde derivatives are used in the development of molecular probes for the identification of extra interaction
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Published 11 Oct 2012

Synthesis of szentiamide, a depsipeptide from entomopathogenic Xenorhabdus szentirmaii with activity against Plasmodium falciparum

  • Friederike I. Nollmann,
  • Andrea Dowling,
  • Marcel Kaiser,
  • Klaus Deckmann,
  • Sabine Grösch,
  • Richard ffrench-Constant and
  • Helge B. Bode

Beilstein J. Org. Chem. 2012, 8, 528–533, doi:10.3762/bjoc.8.60

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  • for 45 min at 28 °C (Molecular Probes, Invitrogen). Hemocyte monolayers were washed with 1× PBS and fixed with 4% paraformaldehyde for 15 min before permeabilizing with 0.2% Triton X-100 in PBS for 10 min. Cells were stained with FITC-conjugated phalloidin and Hoechst 33258 and finally washed with PBS
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Published 11 Apr 2012

Predicting the UV–vis spectra of oxazine dyes

  • Scott Fleming,
  • Andrew Mills and
  • Tell Tuttle

Beilstein J. Org. Chem. 2011, 7, 432–441, doi:10.3762/bjoc.7.56

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  • thiazine dyes are metachromatic [4][5], this investigation is limited to the study of oxazine dyes. Oxazine dyes are useful partly because they exhibit solvatochromism, this makes them sensitive to their surrounding environment, and hence they have been utilized in various applications as molecular probes
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Published 15 Apr 2011

Donor-acceptor substituted phenylethynyltriphenylenes – excited state intramolecular charge transfer, solvatochromic absorption and fluorescence emission

  • Ritesh Nandy and
  • Sethuraman Sankararaman

Beilstein J. Org. Chem. 2010, 6, 992–1001, doi:10.3762/bjoc.6.112

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  • estimated from the electrochemical and spectral data for these derivatives. The HOMO and LUMO surfaces were obtained from DFT calculations. Keywords: charge transfer; fluorescence; solvatochromism; solvent effect; triphenylene; Introduction Fluorescent molecular probes that emit in the visible region and
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Published 18 Oct 2010

Colchitaxel, a coupled compound made from microtubule inhibitors colchicine and paclitaxel

  • Karunananda Bombuwala,
  • Thomas Kinstle,
  • Vladimir Popik,
  • Sonal O. Uppal,
  • James B. Olesen,
  • Jose Viña and
  • Carol A. Heckman

Beilstein J. Org. Chem. 2006, 2, No. 13, doi:10.1186/1860-5397-2-13

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  • Laboratories (San Francisco, CA), was diluted 1:100. As secondary antibodies, FITC-conjugated (U. S. Biochemical Corp., Cleveland, OH) or Alexa 488-conjugated goat anti-mouse immunoglobulin G (Molecular Probes, Eugene, OR) were used as described previously [17]. Wide-field fluorescence images were recorded on
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Published 30 Jun 2006
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