Synthesis of an Original Oxygenated Taxuspine X Analogue: a Versatile "Non-Natural" Natural Product with Remarkable P-gp Modulating Activity (English)
- New search for: Avramova, Stanislava I
- New search for: Avramova, Stanislava I
- New search for: Galletti, Elena
- New search for: Renzulli, Michela L
- New search for: Giorgi, Gianluca
- New search for: Sgaragli, Gianpietro
- New search for: Alderighi, Daniela
- New search for: Ghiron, Chiara
- New search for: Corelli, Federico
- New search for: Radi, Marco
- New search for: Botta, Maurizio
In:
ChemMedChem
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3
, 5
; 745-748
;
2008
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ISSN:
- Article (Journal) / Print
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Title:Synthesis of an Original Oxygenated Taxuspine X Analogue: a Versatile "Non-Natural" Natural Product with Remarkable P-gp Modulating Activity
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Contributors:
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Published in:ChemMedChem ; 3, 5 ; 745-748
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Publisher:
- New search for: Wiley-VCH
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Place of publication:Weinheim
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Publication date:2008
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ISSN:
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ZDBID:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
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Keywords:
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Classification:
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Source:
Table of contents – Volume 3, Issue 5
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 677
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Cover Picture: Rapid Identification of a Putative Interaction between β2‐Adrenoreceptor Agonists and ATF4 using a Chemical Genomics Approach (ChemMedChem 5/2008)Ladwa, Sweta R. / Dilly, Suzanne J. / Clark, Andrew J. / Marsh, Andrew / Taylor, Paul C. et al. | 2008
- 677
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Cover Picture: Rapid Identification of a Putative Interaction between b2-Adrenoreceptor Agonists and ATF4 using a Chemical Genomics Approach (ChemMedChem 5/2008)Ladwa, S. R. / Dilly, S. J. / Clark, A. J. / Marsh, A. / Taylor, P. C. et al. | 2008
- 679
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Graphical Abstract: ChemMedChem 5/2008| 2008
- 686
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Spotlights on our sister journals: ChemMedChem 5/2008| 2008
- 690
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G‐Quadruplexes: Targets in Anticancer Drug DesignOu, Tian‐miao / Lu, Yu‐jing / Tan, Jia‐heng / Huang, Zhi‐shu / Wong, Kwok‐Yin / Gu, Lian‐quan et al. | 2008
- 715
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Click Chemistry and Medicinal Chemistry: A Case of “Cyclo‐Addiction”Moorhouse, A. D. / Moses, J. E. et al. | 2008
- 725
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A Dual Selective Antitumor Agent and Fluorescence Probe: the Binary BMVC–Porphyrin PhotosensitizerKang, Chi‐Chih / Chen, Chin‐Tin / Cho, Chih‐Chien / Lin, Yu‐Chen / Chang, Cheng‐Chung / Chang, Ta‐Chau et al. | 2008
- 729
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Oxali‐Titanocene Y: A Potent Anticancer DrugClaffey, James / Hogan, Megan / Müller‐Bunz, Helge / Pampillón, Clara / Tacke, Matthias et al. | 2008
- 732
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Carba‐nucleosides as Potent Antagonists of the Adenosine 5′‐Diphosphate (ADP) Purinergic Receptor (P2Y12) on Human PlateletsYe, Hong / Chen, Cailin / Zhang, Han‐Cheng / Haertlein, Barbara / Parry, Tom J. / Damiano, Bruce P. / Maryanoff, Bruce E. et al. | 2008
- 732
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Carba-nucleosides as Potent Antagonists of the Adenosine 5prime-Diphosphate (ADP) Purinergic Receptor (P2Y12) on Human PlateletsYe, H. / Chen, C. / Zhang, H. C. / Haertlein, B. / Parry, T. J. / Damiano, B. P. / Maryanoff, B. E. et al. | 2008
- 737
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Towards a Self‐Adjuvanting Multivalent B and T cell Epitope Containing Synthetic Glycolipopeptide Cancer VaccineRenaudet, Olivier / BenMohamed, Lbachir / Dasgupta, Gargi / Bettahi, Ilham / Dumy, Pascal et al. | 2008
- 742
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Rapid Identification of a Putative Interaction between b2-Adrenoreceptor Agonists and ATF4 using a Chemical Genomics ApproachLadwa, S. R. / Dilly, S. J. / Clark, A. J. / Marsh, A. / Taylor, P. C. et al. | 2008
- 742
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Rapid Identification of a Putative Interaction between β2‐Adrenoreceptor Agonists and ATF4 using a Chemical Genomics ApproachLadwa, Sweta R. / Dilly, Suzanne J. / Clark, Andrew J. / Marsh, Andrew / Taylor, Paul C. et al. | 2008
- 745
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Synthesis of an Original Oxygenated Taxuspine X Analogue: a Versatile “Non‐Natural” Natural Product with Remarkable P‐gp Modulating ActivityAvramova, Stanislava I. / Galletti, Elena / Renzulli, Michela L. / Giorgi, Gianluca / Sgaragli, Gianpietro / Alderighi, Daniela / Ghiron, Chiara / Corelli, Federico / Radi, Marco / Botta, Maurizio et al. | 2008
- 749
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Inhibition of HIV‐1 by a Peptide Ligand of the Genomic RNA Packaging Signal ΨDietz, Julia / Koch, Joachim / Kaur, Ajit / Raja, Chinnappan / Stein, Stefan / Grez, Manuel / Pustowka, Anette / Mensch, Sarah / Ferner, Jan / Möller, Lars et al. | 2008
- 756
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Competitive Inhibitors of Helicobacter pylori Type II Dehydroquinase: Synthesis, Biological Evaluation, and NMR StudiesSánchez‐Sixto, Cristina / Prazeres, Verónica F. V. / Castedo, Luis / Suh, Se Won / Lamb, Heather / Hawkins, Alastair R. / Cañada, Francisco Javier / Jiménez‐Barbero, Jesús / González‐Bello, Concepción et al. | 2008
- 771
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Synthesis and Biological Evaluation of Isosteric Analogues of FK866, an Inhibitor of NAD SalvageGalli, Ubaldina / Ercolano, Emanuela / Carraro, Lorenzo / Blasi Roman, Cintia R. / Sorba, Giovanni / Canonico, Pier Luigi / Genazzani, Armando A. / Tron, Gian Cesare / Billington, Richard A. et al. | 2008
- 780
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The First Potent Subtype‐Selective Retinoid X Receptor (RXR) Agonist Possessing a 3‐Isopropoxy‐4‐isopropylphenylamino Moiety, NEt‐3IP (RXRα/β‐dual agonist)Takamatsu, Kayo / Takano, Atsushi / Yakushiji, Nobumasa / Morohashi, Kazunori / Morishita, Ken‐ichi / Matsuura, Nobuyasu / Makishima, Makoto / Tai, Akihiro / Sasaki, Kenji / Kakuta, Hiroki et al. | 2008
- 780
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The First Potent Subtype-Selective Retinoid X Receptor (RXR) Agonist Possessing a 3-Isopropoxy-4-isopropylphenylamino Moiety, NEt-3IP (RXRa/b-dual agonist)Takamatsu, K. / Takano, A. / Yakushiji, N. / Morohashi, K. / Morishita, K. i. / Matsuura, N. / Makishima, M. / Tai, A. / Sasaki, K. / Kakuta, H. et al. | 2008
- 788
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18F‐Labeled FAUC 346 and BP 897 Derivatives as Subtype‐Selective Potential PET Radioligands for the Dopamine D3 ReceptorHocke, Carsten / Prante, Olaf / Salama, Ismael / Hübner, Harald / Löber, Stefan / Kuwert, Torsten / Gmeiner, Peter et al. | 2008
- 794
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Development of Pyrrolo[2,1‐c][1,4]benzodiazepine β‐Galactoside Prodrugs for Selective Therapy of Cancer by ADEPT and PMTKamal, Ahmed / Tekumalla, Venkatesh / Krishnan, Anita / Pal‐Bhadra, Manika / Bhadra, Utpal et al. | 2008
- 794
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Development of Pyrrolo[2,1-c][1,4]benzodiazepine b-Galactoside Prodrugs for Selective Therapy of Cancer by ADEPT and PMTKamal, A. / Tekumalla, V. / Krishnan, A. / Pal-Bhadra, M. / Bhadra, U. et al. | 2008
- 803
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A Study of the Binding Energies of Efavirenz to Wild‐Type and K103N/Y181C HIV‐1 Reverse Transcriptase Based on the ONIOM MethodSrivab, Pensri / Hannongbua, Supa et al. | 2008
- 812
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Zinc‐Binding Groups Modulate Selective Inhibition of MMPsAgrawal, Arpita / Romero‐Perez, Diego / Jacobsen, Jennifer A. / Villarreal, Francisco J. / Cohen, Seth M. et al. | 2008
- 821
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SyGMa: Combining Expert Knowledge and Empirical Scoring in the Prediction of MetabolitesRidder, Lars / Wagener, Markus et al. | 2008
- 833
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pH Effects on the Conformational Preferences of Amyloid β‐Peptide (1–40) in HFIP Aqueous Solution by NMR SpectroscopyValerio, Mariacristina / Porcelli, Fernando / Zbilut, Joseph P. / Giuliani, Alessandro / Manetti, Cesare / Conti, Filippo et al. | 2008
- 833
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pH Effects on the Conformational Preferences of Amyloid b-Peptide (1-40) in HFIP Aqueous Solution by NMR SpectroscopyValerio, M. / Porcelli, F. / Zbilut, J. P. / Giuliani, A. / Manetti, C. / Conti, F. et al. | 2008
- 846
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Preview: ChemMedChem 6/2008| 2008