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  • 1. Barlind, Jonas G.
    et al.
    Buckett, Linda K.
    Crosby, Sharon G.
    Davidsson, Ojvind
    Emtenas, Hans
    Ertan, Anne
    Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).
    Jurva, Ulrik
    Lemurell, Malin
    Gutierrez, Pablo Morentin
    Nilsson, Karolina
    O'Mahony, Gavin
    Petersson, Annika U.
    Redzic, Alma
    Wagberg, Fredrik
    Yuan, Zhong-Qing
    Identification and design of a novel series of MGAT2 inhibitors2013In: Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, E-ISSN 1090-2120, Vol. 23, no 9, p. 2721-2726Article in journal (Refereed)
    Abstract [en]

    [Acyl CoA]monoacylglycerol acyltransferase 2 (MGAT2) is of interest as a target for therapeutic treatment of diabetes, obesity and other diseases which together constitute the metabolic syndrome. In this Letter we report our discovery and optimisation of a novel series of MGAT2 inhibitors. The development of the SAR of the series and a detailed discussion around some key parameters monitored and addressed during the lead generation phase will be given. The in vivo results from an oral lipid tolerance test (OLTT) using the MGAT2 inhibitor (S)-10, shows a significant reduction (68% inhibition relative to naive, p < 0.01) in plasma triacylglycerol (TAG) concentration.

  • 2.
    Bielawski, Marcin
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Olofsson, Berit
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Efficient one-pot synthesis of bis(4-tert-butylphenyl)iodonium triflate2009In: Organic Syntheses, ISSN 0078-6209, Vol. 86, p. 308-314Article in journal (Refereed)
  • 3. Hammarström, Lars G. J.
    et al.
    Harmel, Robert K.
    Granath, Mikael
    Ringom, Rune
    Gravenfors, Ylva
    Stockholm University, Faculty of Science, Department of Organic Chemistry. Stockholm University, Science for Life Laboratory (SciLifeLab).
    Färnegårdh, Katarina
    Stockholm University, Faculty of Science, Department of Organic Chemistry. Stockholm University, Science for Life Laboratory (SciLifeLab).
    Svensson, Per H.
    Wennman, David
    Lundin, Göran
    Roddis, Ylva
    Kitambi, Satish S.
    Bernlind, Alexandra
    Lehmann, Fredrik
    Ernfors, Patrik
    The Oncolytic Efficacy and in Vivo Pharmacokinetics of [2-(4-Chlorophenyl)quinolin-4-yl](piperidine-2-yl)methanol (Vacquinol-1) Are Governed by Distinct Stereochemical Features2016In: Journal of Medicinal Chemistry, ISSN 0022-2623, E-ISSN 1520-4804, Vol. 59, no 18, p. 8577-8592Article in journal (Refereed)
    Abstract [en]

    Glioblastoma remains an incurable brain cancer. Drugs developed in the past 20 years have not improved the prognosis for patients, necessitating the development of new treatments. We have previously reported the therapeutic potential of the quinoline methanol Vacquinol-1 (1) that targets glioblastoma cells and induces cell death by catastrophic vacuolization. Compound 1 is a mixture of four stereoisomers due to the two adjacent stereogenic centers in the molecule, complicating further development in the preclinical setting. This work describes the isolation and characterization of the individual isomers of 1 and shows that these display stereospecific pharmacokinetic and pharmacodynamic features. In addition, we present a stereoselective synthesis of the active isomers, providing a basis for further development of this compound series into a novel experimental therapeutic for glioblastoma.

  • 4.
    Jönsson, Daniel
    Stockholm University, Faculty of Science, Department of Neurochemistry and Neurotoxicology.
    Applications of multi-component condensations and development of polyamine synthesis on solid-phase2002Doctoral thesis, comprehensive summary (Other academic)
    Abstract [en]

    Solid-phase synthesis of small non-polymeric molecules has become increasingly important as a tool in the development of pharmacologically active compounds. Of particular interest are the syntheses of compounds with low molecular weight, low polarity and a reduced flexibility of the functional groups, i.e. physiochemical properties typical for the majority of drugs currently in use.

    The first part of this thesis describes the synthesis of polycyclic structures with constrained conformation, by the application of multi-component condensations on solid-phase. The 8-azabicyclo[3.2.1]octan-3-one structure of the tropane alkaloids was synthesized on solid-phase by a modification of the well known Robinson tropinone synthesis. The 3-component reaction was performed with the amino component anchored to a solid support, consisting of polyethyleneglycol-grafted polystyrene. Treatment of the primary amine with 1,3-acetonedicarboxylic acid and excess of succinaldehyde, resulted in high purity of the corresponding tropane derivative. Further derivatization of the resin-bound tropane derivative was performed by reduction of the keto-group and acylation of the hydroxyl-group.

    The oxygen-bridged tetrahydropyridones are relatively complex polycyclic structures, which previously have been synthesized in solution by condensation of primary amines, coumarin-3-carboxylic acid and ketones. In the evaluation of a solid-phase approach of this 3-component condensation, several members of this class of compounds were synthesized with the amine anchored to a solid support. The yield and purity of the products were dependent on the ketones used in the reaction, but the expected products were obtained using both acyclic and cyclic ketones and substituted acetophenones.

    The second part of this thesis describes the development of a solid-phase polyamine synthesis. The polyamines are a class of compounds with a wide range of pharmacological and physiological effects, which are constituents in many types of venoms of wasps and spiders. Synthesis of polyamines in homogenous solution is accompanied with several problems concerning selectivity, work-up and yield. By employing a solid-phase approach, a rapid and convenient method for synthesis of polyamines is achieved. In the developed protocol, acid labile benzhydryls are used as amino-protecting groups. The polyamine backbone is assembled sequentially by reductive alkylation of the protected secondary amine with Fmoc-amino aldehydes. The protecting groups allow the use of excess of aldehyde, to avoid underivatized amines, without the risking dialkaylation of the amines, which occurs during reductive alkylations of primary amines with unhindered aliphatic aldehydes. The versatility of the method is displayed by a convenient synthesis of four analogues of a wasp toxin, philanthotoxin.

  • 5. Kiss, Anita
    et al.
    Herman, Bianka Edina
    Görbe, Tamás
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Mernyak, Erzsebet
    Molnar, Barnabas
    Wolfling, Janos
    Szecsi, Mihaly
    Schneider, Gyula
    Synthesis of novel 17-triazolyl-androst-5-en-3-ol epimers via Cu(I)-catalyzed azide-alkyne cycloaddition and their inhibitory effect on 17 alpha-hydroxylase/ C-17,C-20-lyase2018In: Steroids, ISSN 0039-128X, E-ISSN 1878-5867, Vol. 135, p. 79-91Article in journal (Refereed)
    Abstract [en]

    The regioselective Cu(I)-catalyzed 1,3-dipolar cycloaddition of 17 alpha- and 17 beta-azidoandrost-5-en-3 beta-ol epimers (3b and 5b) with different terminal alkynes afforded novel 1,4-substituted triazolyl derivatives (8a-k and 9a-k). For the preparation of 5'-iodo-l',2',3'-triazoles (8m-n and 9m-n), an improved method was developed, directly from steroidal azides and terminal alkynes, in reaction mediated by Cul and IC1 as iodinating agents. Acetolysis and subsequent hydrolysis of 8n and 9n yielded 5'-hydroxy-l',2',3'-triazoles 8o and 9o. The inhibitory effect of 8a-o, 9a-o, 3, and 5 on rat testicular C-17,C-20-lyase was investigated by means of an in vitro radioincubation technique. The results revealed that the C-17 epimers of steroidal triazoles influence the C-17,C-20-lyase effect. Inhibitors were found only in the 17 alpha-triazolyl series (8a-o), whereas in the C-17 azide pair the 17 beta compound (5b) was more potent.

  • 6.
    Merritt, Eleanor A.
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Malmgren, Joel
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Klinke, Felix J.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Olofsson, Berit
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Synthesis of diaryliodonium triflates using environmentally benign oxidizing agents2009In: Synlett: Accounts and Rapid Communications in Synthetic Organic Chemistry, ISSN 0936-5214, E-ISSN 1437-2096, no 14, p. 2277-2280Article in journal (Refereed)
  • 7.
    Oscarsson, Karin
    Stockholm University.
    Rational design and synthesis of protease inhibitors: targeting HIV-1, Malaria Plm I and II and Hepatitis C virus NS3 proteases2002Doctoral thesis, comprehensive summary (Other academic)
  • 8. Wangsell, Fredrik
    et al.
    Nordeman, Patrik
    Savmarker, Jonas
    Emanuelsson, Rikard
    Jansson, Katarina
    Lindberg, Jimmy
    Rosenquist, Asa
    Samuelsson, Bertil
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Larhed, Mats
    Investigation of alpha-phenylnorstatine and alpha-benzylnorstatine as transition state isostere motifs in the search for new BACE-1 inhibitors2011In: Bioorganic & Medicinal Chemistry, ISSN 0968-0896, E-ISSN 1464-3391, Vol. 19, no 1, p. 145-155Article in journal (Refereed)
    Abstract [en]

    Inhibition of the BACE-1 protease enzyme has over the recent decade developed into a promising drug strategy for Alzheimer therapy. In this report, more than 20 new BACE-1 protease inhibitors based on alpha-phenylnorstatine, alpha-benzylnorstatine, iso-serine, and beta-alanine moieties have been prepared. The inhibitors were synthesized by applying Fmoc solid phase methodology and evaluated for their inhibitory properties. The most potent inhibitor, tert-alcohol containing (R)-12 (IC(50) = 0.19 mu M) was co-crystallized in the active site of the BACE-1 protease, furnishing a novel binding mode in which the N-terminal amine makes a hydrogen bond to one of the catalytic aspartic acids.

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