Zobrazeno 1 - 10
of 13
pro vyhledávání: '"MESH: Ketones"'
Autor:
Schell, Ursula, Simon, Sylvia, Sahr, Tobias, Hager, Dominik, Albers, Michael F., Kessler, Aline, Fahrnbauer, Felix, Trauner, Dirk, Hedberg, Christian, Buchrieser, Carmen, Hilbi, Hubert
Publikováno v:
Molecular Microbiology
Molecular Microbiology, Wiley, 2016, 99 (4), pp.778-793. ⟨10.1111/mmi.13265⟩
Molecular Microbiology, 2016, 99 (4), pp.778-793. ⟨10.1111/mmi.13265⟩
Molecular Microbiology, Wiley, 2016, 99 (4), pp.778-793. ⟨10.1111/mmi.13265⟩
Molecular Microbiology, 2016, 99 (4), pp.778-793. ⟨10.1111/mmi.13265⟩
International audience; The causative agent of Legionnaires' disease, Legionella pneumophila, employs the autoinducer compound LAI-1 (3-hydroxypentadecane-4-one) for cell-cell communication. LAI-1 is produced and detected by the Lqs (Legionella quoru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7385ba9180638110188fe68ab1497ffc
https://hal-pasteur.archives-ouvertes.fr/pasteur-01423073
https://hal-pasteur.archives-ouvertes.fr/pasteur-01423073
Publikováno v:
Organic Letters
Organic Letters, 2012, 14 (1), pp.58-61. ⟨10.1021/ol202829u⟩
Organic Letters, American Chemical Society, 2012, 14 (1), pp.58-61. ⟨10.1021/ol202829u⟩
Organic Letters, 2012, 14 (1), pp.58-61. ⟨10.1021/ol202829u⟩
Organic Letters, American Chemical Society, 2012, 14 (1), pp.58-61. ⟨10.1021/ol202829u⟩
International audience; We report a TMSI-promoted Prins cyclization reaction with ketones as carbonyl partners to prepare polysubstituted chiral spirotetrahydropyrans. In the presence of racemic 2-methylcyclohexanone a dynamic kinetic resolution occu
Autor:
Jean-Yves Winum, Jean-Louis Montero, Stephan Köhler, Pascale Joseph, Marie-Rose Abdo, Rose-Anne Boigegrain
Publikováno v:
Antimicrobial Agents and Chemotherapy
Antimicrobial Agents and Chemotherapy, American Society for Microbiology, 2007, 51 (10), pp.3752-5. ⟨10.1128/AAC.00572-07⟩
Antimicrobial Agents and Chemotherapy, American Society for Microbiology, 2007, 51 (10), pp.3752-5. ⟨10.1128/AAC.00572-07⟩
Brucella suis histidinol dehydrogenase (HDH) can be efficiently targeted by substrate analogues. The growth of this pathogen in minimal medium was inhibited and the multiplication in human macrophages was totally abolished in the presence of the drug
Autor:
van den Heuvel, R.H.H., Tahallah, N., Kamerbeek, N.M, Fraaije, M.W., Berkel, W.J.H., Janssen, D.B., Heck, A.J.R., van Berkel, WJH
Publikováno v:
The Journal of Biological Chemistry, 280(37), 32115-32121. AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2005, 280 (37), pp.32115-21. ⟨10.1074/jbc.M503758200⟩
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2005, 280 (37), pp.32115-21. ⟨10.1074/jbc.M503758200⟩
International audience; The NADPH-dependent dimeric flavoenzyme 4-hydroxyacetophenone monooxygenase (HAPMO) catalyzes Baeyer-Villiger oxidations of a wide range of ketones, thereby generating esters or lactones. In the current work, we probed HAPMO-c
Autor:
Hui-Kuo G. Shu, Nabendu Pore, Gilles Pagès, Donald M. O'Rourke, Amit Maity, Bin Li, Eric J. Bernhard, Julie Milanini-Mongiat, Shuang Liu, David Stokoe, Daphne A. Haas-Kogan
Publikováno v:
Molecular Biology of the Cell
Molecular Biology of the Cell, American Society for Cell Biology, 2004, 15 (11), pp.4841-53. ⟨10.1091/mbc.E04-05-0374⟩
Molecular Biology of the Cell, American Society for Cell Biology, 2004, 15 (11), pp.4841-53. ⟨10.1091/mbc.E04-05-0374⟩
International audience; Increased expression of vascular endothelial growth factor (VEGF) contributes to the growth of many tumors by increasing angiogenesis. Although hypoxia is a potent inducer of VEGF, we previously showed that epidermal growth fa
Publikováno v:
Biochemistry
Biochemistry, American Chemical Society, 2007, pp.10237-10247
Biochemistry, American Chemical Society, 2007, 46 (36), pp.10237-47. ⟨10.1021/bi700876a⟩
Biochemistry, American Chemical Society, 2007, 46 (36), pp.10237-47. 〈10.1021/bi700876a〉
Biochemistry, 2007, pp.10237-10247
Biochemistry, 2007, 46 (36), pp.10237-47. ⟨10.1021/bi700876a⟩
Biochemistry, American Chemical Society, 2007, pp.10237-10247
Biochemistry, American Chemical Society, 2007, 46 (36), pp.10237-47. ⟨10.1021/bi700876a⟩
Biochemistry, American Chemical Society, 2007, 46 (36), pp.10237-47. 〈10.1021/bi700876a〉
Biochemistry, 2007, pp.10237-10247
Biochemistry, 2007, 46 (36), pp.10237-47. ⟨10.1021/bi700876a⟩
The oxidation of six derivatives of terfenadone by recombinant human CYP2J2 (CYP = cytochrome P450) was studied by high-performance liquid chromatography coupled to mass spectrometry (MS) using tandem MS techniques and by 1H NMR spectroscopy. CYP2J2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62f5295373619791c2e567d42d8697a8
https://hal.archives-ouvertes.fr/hal-00259028
https://hal.archives-ouvertes.fr/hal-00259028
Autor:
Sylvie Buffet-Bataillon, Vincent Bessonneau, Adèle Berrubé, Olivier Thomas, Luc Mosqueron, Gaël Mukensturm, Jean-Pierre Gangneux
Publikováno v:
PLoS ONE
PLoS ONE, Public Library of Science, 2013, 8 (2), pp.e55535. ⟨10.1371/journal.pone.0055535⟩
PLoS ONE, Vol 8, Iss 2, p e55535 (2013)
PLoS ONE, 2013, 8 (2), pp.e55535. ⟨10.1371/journal.pone.0055535⟩
PLoS ONE, Public Library of Science, 2013, 8 (2), pp.e55535. ⟨10.1371/journal.pone.0055535⟩
PLoS ONE, Vol 8, Iss 2, p e55535 (2013)
PLoS ONE, 2013, 8 (2), pp.e55535. ⟨10.1371/journal.pone.0055535⟩
International audience; BACKGROUND: We aimed to assess, for the first time, the nature of the indoor air contamination of hospitals. METHODS AND FINDINGS: More than 40 volatile organic compounds (VOCs) including aliphatic, aromatic and halogenated hy
Publikováno v:
Journal of Peptide Science
Journal of Peptide Science, Wiley, 2012, 18 (3), pp.147-54. ⟨10.1002/psc.1429⟩
Journal of Peptide Science, Wiley, 2012, 18 (3), pp.147-54. ⟨10.1002/psc.1429⟩
International audience; C-terminally modified peptides aldehyde (glycinal and alpha-oxo aldehyde peptides) and ketone (pyruvic acid-containing peptide) were synthesised to get new insights into the mechanism of acido-catalysed oxime ligation. Their t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::111f263768a91c913d72208eca13be6f
https://hal.archives-ouvertes.fr/hal-00721799
https://hal.archives-ouvertes.fr/hal-00721799
Autor:
Carmen Gil, Pablo D. Dans, Ana Martínez, F. Javier Luque, Santiago Conde, Concepción Pérez, Valle Palomo, Daniel I. Perez
Publikováno v:
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry, American Chemical Society, 2011, 54 (12), pp.4042-56. ⟨10.1021/jm1016279⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname
Journal of Medicinal Chemistry, American Chemical Society, 2011, 54 (12), pp.4042-56. ⟨10.1021/jm1016279⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname
Development of kinase-targeted therapies for central nervous system (CNS) diseases is a great challenge. Glycogen synthase kinase 3 (GSK-3) offers a great potential for severe CNS unmet diseases, being one of the inhibitors on clinical trials for dif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92abbaadba245808bf2575ecb396976a
https://hal-riip.archives-ouvertes.fr/pasteur-00686303
https://hal-riip.archives-ouvertes.fr/pasteur-00686303
Autor:
Mat Ropi Mukhtar, Khalijah Awang, Marc Litaudon, Noel F. Thomas, A Hamind A Hadi, Zunoliza Abdullah, Faridahanim Mohd Jaafar
Publikováno v:
Natural Product Research
Natural Product Research, Taylor & Francis, 2009, 23 (7), pp.652-8. ⟨10.1080/14786410802323743⟩
Natural Product Research, Taylor & Francis, 2009, 23 (7), pp.652-8. ⟨10.1080/14786410802323743⟩
International audience; Dunaliine A (1), a new amino diketone, has been isolated from the leaves of Desmos dunalii together with four known dihydrochalcones: 2',4-dihydroxy-4',6'-dimethoxy-3',5'-dimethyldihydrochalcone (2), 2',4-dihydroxy-4',6'-dimet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46c167b064354acfb9353d5894748683
https://hal.archives-ouvertes.fr/hal-00433292
https://hal.archives-ouvertes.fr/hal-00433292