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Wohldefinierte polymere Paclitaxel-Prodrugs über eine Grafting-From-Methode ausgehend vom Arzneistoff.
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- Angewandte Chemie, 2016, v. 128, n. 39, p. 11967, doi. 10.1002/ange.201605892
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- Article
Hamamelitannin Analogues that Modulate Quorum Sensing as Potentiators of Antibiotics against Staphylococcus aureus.
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- Angewandte Chemie, 2016, v. 128, n. 22, p. 6661, doi. 10.1002/ange.201601973
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- Article
Radiosynthesis, in vitro and preliminary biological evaluation of [<sup>18</sup>F]2‐amino‐4‐((2‐((3‐fluorobenzyl)oxy)benzyl)(2‐((3‐(fluoromethyl)benzyl)oxy)benzyl)amino)butanoic acid, a novel alanine serine cysteine transporter 2 inhibitor‐based positron emission tomography tracer
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2020, v. 63, n. 10, p. 442, doi. 10.1002/jlcr.3863
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- Article
Cytotoxic Activity of Laserpitium latifolium L. Extract and Its Daucane and Phenylpropanoid Constituents.
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- Records of Natural Products, 2013, v. 7, n. 3, p. 245
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Practical and Divergent Synthesis of Carbocyclic Pyrazolo[3,4‐d]pyrimidine Nucleoside Analogues.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 19, p. 1, doi. 10.1002/ejoc.202400181
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- Article
Well-Defined Polymer-Paclitaxel Prodrugs by a Grafting-from-Drug Approach.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 39, p. 11791, doi. 10.1002/anie.201605892
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- Article
Hamamelitannin Analogues that Modulate Quorum Sensing as Potentiators of Antibiotics against Staphylococcus aureus.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 22, p. 6551, doi. 10.1002/anie.201601973
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- Article
Cloning and Characterization of Trypanosoma congolense and T. vivax Nucleoside Transporters Reveal the Potential of P1-Type Carriers for the Discovery of Broad-Spectrum Nucleoside-Based Therapeutics against Animal African Trypanosomiasis.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 4, p. 3144, doi. 10.3390/ijms24043144
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- Article
Ex Vivo Feedback Control of Neurotransmission Using a Photocaged Adenosine A1 Receptor Agonist.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 16, p. 8887, doi. 10.3390/ijms23168887
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A Toxoplasma gondii Oxopurine Transporter Binds Nucleobases and Nucleosides Using Different Binding Modes.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 2, p. 710, doi. 10.3390/ijms23020710
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- Article
The bovine CD1D gene has an unusual gene structure and is expressed but cannot present α-galactosylceramide with a C26 fatty acid.
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- International Immunology, 2013, v. 25, n. 2, p. 91, doi. 10.1093/intimm/dxs092
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- Article
Towards New Antimalarial Drugs: Synthesis of Non-Hydrolyzable Phosphate Mimics as Feed for a Predictive QSAR Study on 1-Deoxy- D-xylulose-5-phosphate Reductoisomerase Inhibitors.
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- Chemistry & Biodiversity, 2008, v. 5, n. 4, p. 643, doi. 10.1002/cbdv.200890060
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- Article
6‐Methyl‐7‐Aryl‐7‐Deazapurine Nucleosides as Anti‐Trypanosoma cruzi Agents: Structure‐Activity Relationship and in vivo Efficacy.
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- ChemMedChem, 2021, v. 16, n. 14, p. 2231, doi. 10.1002/cmdc.202100144
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- Article
4"‐O‐Alkylated α‐Galactosylceramide Analogues as iNKT‐Cell Antigens: Synthetic, Biological, and Structural Studies.
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- ChemMedChem, 2019, v. 14, n. 1, p. 147, doi. 10.1002/cmdc.201800649
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Design, Synthesis, and Biological Evaluation of Bivalent Ligands Targeting Dopamine D<sub>2</sub>‐Like Receptors and the μ‐Opioid Receptor.
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- ChemMedChem, 2018, v. 13, n. 9, p. 944, doi. 10.1002/cmdc.201700787
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- Article
The Quorum Sensing Inhibitor Hamamelitannin Increases Antibiotic Susceptibility of Staphylococcus aureus Biofilms by Affecting Peptidoglycan Biosynthesis and eDNA Release.
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- Scientific Reports, 2016, p. 20321, doi. 10.1038/srep20321
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- Article
An <i>In Silico</i> Approach for Modelling T-Helper Polarizing iNKT Cell Agonists.
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- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0087000
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- Article
Crystal Structures of Bovine CD1d Reveal Altered αGalCer Presentation and a Restricted A' Pocket Unable to Bind Long-Chain Glycolipids.
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- PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0047989
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- Article
Structure-Activity Relationship of Cinnamaldehyde Analogs as Inhibitors of AI-2 Based Quorum Sensing and Their Effect on Virulence of Vibrio spp.
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- PLoS ONE, 2011, v. 6, n. 1, p. 1, doi. 10.1371/journal.pone.0016084
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- Article
Ceramide‐Templated Macrolactams: Total Synthesis and Biological Evaluation of Macrocyclic α‐Galactosylceramide Analogues and their Aglycons.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 12, p. 2253, doi. 10.1002/ejoc.201801839
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- Article
Regioselective Ring Opening of 1,3‐Dioxane‐Type Acetals in Carbohydrates.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 46, p. 6405, doi. 10.1002/ejoc.201801245
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- Article
Synthesis and Conformational Analysis of 2′-Deoxy-2′-(3-methoxybenzamido)adenosine, a rational-designed inhibitor of trypanosomal glyceraldehyde phosphate dehydrogenase (GAPDH).
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- Helvetica Chimica Acta, 1994, v. 77, n. 3, p. 631, doi. 10.1002/hlca.19940770306
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- Article
Phenethyl-4-ANPP: A Marginally Active Byproduct Suggesting a Switch in Illicit Fentanyl Synthesis Routes.
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- Journal of Analytical Toxicology, 2022, v. 46, n. 4, p. 350, doi. 10.1093/jat/bkab032
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- Article
Report on a New Opioid NPS: Chemical and In Vitro Functional Characterization of a Structural Isomer of the MT-45 Derivative Diphenpipenol.
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- Journal of Analytical Toxicology, 2021, v. 45, n. 2, p. 134, doi. 10.1093/jat/bkaa066
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- Article
First Report on Brorphine: The Next Opioid on the Deadly New Psychoactive Substance Horizon?
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- Journal of Analytical Toxicology, 2020, v. 44, n. 9, p. 937, doi. 10.1093/jat/bkaa094
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- Article
Combining tubercidin and cordycepin scaffolds results in highly active candidates to treat late-stage sleeping sickness.
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- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-13522-6
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- Article
Mycobacterium tuberculosis Thymidine Monophosphate Kinase Inhibitors: Biological Evaluation and Conformational Analysis of 2'- and 3'-Modified Thymidine Analogues.
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- European Journal of Organic Chemistry, 2003, v. 2003, n. 15, p. 2911, doi. 10.1002/ejoc.200300177
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- Article
Galactose-modified iNKT cell agonists stabilized by an induced fit of CD1d prevent tumour metastasis.
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- EMBO Journal, 2011, v. 30, n. 11, p. 2294, doi. 10.1038/emboj.2011.145
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- Article
Host metabolites stimulate the bacterial proton motive force to enhance the activity of aminoglycoside antibiotics.
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- PLoS Pathogens, 2019, v. 15, n. 4, p. 1, doi. 10.1371/journal.ppat.1007697
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- Article
Alternative Reagents for Methotrexate as Immobilizing Anchor Moieties in the Optimization of MASPIT: Synthesis and Biological Evaluation.
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- ChemBioChem, 2015, v. 16, n. 5, p. 834, doi. 10.1002/cbic.201402702
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- Article
Unbreakable Codes in Electrospun Fibers: Digitally Encoded Polymers to Stop Medicine Counterfeiting.
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- Advanced Materials, 2010, v. 22, n. 24, p. 2657, doi. 10.1002/adma.201000130
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- Article
Phenotypic Evaluation of Nucleoside Analogues against Trypanosoma cruzi Infection: In Vitro and In Vivo Approaches.
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- Molecules, 2022, v. 27, n. 22, p. 8087, doi. 10.3390/molecules27228087
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- Article
The Trypanosoma cruzi TcrNT2 Nucleoside Transporter Is a Conduit for the Uptake of 5-F-2′-Deoxyuridine and Tubercidin Analogues.
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- Molecules, 2022, v. 27, n. 22, p. 0, doi. 10.3390/molecules27228045
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4E Interacting Protein as a Potential Novel Drug Target for Nucleoside Analogues in Trypanosoma brucei.
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- Microorganisms, 2021, v. 9, n. 4, p. 826, doi. 10.3390/microorganisms9040826
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Trapping mammalian protein complexes in viral particles.
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- Nature Communications, 2016, v. 7, n. 4, p. 11416, doi. 10.1038/ncomms11416
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- Article
Determination of paramethoxyamphetamine and other amphetamine-related designer drugs by liquid chromatography/sonic spray ionization mass spectrometry.
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- Rapid Communications in Mass Spectrometry: RCM, 2002, v. 16, n. 9, p. 865, doi. 10.1002/rcm.657
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- Article
Synthesis of α-Aryl-Substituted and Conformationally Restricted Fosmidomycin Analogues as Promising Antimalarials.
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- European Journal of Organic Chemistry, 2006, v. 2006, n. 17, p. 3856, doi. 10.1002/ejoc.200600202
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- Article
Analytical characterization of "etonitazepyne," a new pyrrolidinyl‐containing 2‐benzylbenzimidazole opioid sold online.
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- Drug Testing & Analysis, 2021, v. 13, n. 9, p. 1627, doi. 10.1002/dta.3113
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- Article
Report on a novel emerging class of highly potent benzimidazole NPS opioids: Chemical and in vitro functional characterization of isotonitazene.
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- Drug Testing & Analysis, 2020, v. 12, n. 4, p. 422, doi. 10.1002/dta.2738
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- Article
1-(1-Arylethylpiperidin-4-yl)thymine Analogs as Antimycobacterial TMPK Inhibitors.
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- Molecules, 2020, v. 25, n. 12, p. 2805, doi. 10.3390/molecules25122805
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- Article
Design, Synthesis and Characterization of a New Series of Fluorescent Metabotropic Glutamate Receptor Type 5 Negative Allosteric Modulators.
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- Molecules, 2020, v. 25, n. 7, p. 1532, doi. 10.3390/molecules25071532
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- Article
Synthesis of Extended Uridine Phosphonates Derived from an Allosteric P2Y<sub>2</sub> Receptor Ligand.
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- Molecules, 2014, v. 19, n. 4, p. 4313, doi. 10.3390/molecules19044313
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- Article
Synthetic Fosmidomycin Analogues with Altered Chelating Moieties Do Not Inhibit 1-Deoxy-D-xylulose 5-phosphate Reductoisomerase or Plasmodium falciparum Growth In Vitro.
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- Molecules, 2014, v. 19, n. 2, p. 2571, doi. 10.3390/molecules19022571
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- Article
New fluoroethyl phenylalanine analogues as potential LAT1-targeting PET tracers for glioblastoma.
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- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-40013-x
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- Article
Nanobody-mediated SPECT/CT imaging reveals the spatiotemporal expression of programmed death-ligand 1 in response to a CD8<sup>+</sup> T cell and iNKT cell activating mRNA vaccine.
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- Theranostics, 2023, v. 13, n. 15, p. 5483, doi. 10.7150/thno.85106
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- Article
Targeting an Aromatic Hotspot in Plasmodium falciparum 1-Deoxy- d-xylulose-5-phosphate Reductoisomerase with β-Arylpropyl Analogues of Fosmidomycin.
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- ChemMedChem, 2016, v. 11, n. 18, p. 2024, doi. 10.1002/cmdc.201600249
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- Article
A 'Clickable' MTX Reagent as a Practical Tool for Profiling Small-Molecule-Intracellular Target Interactions via MASPIT.
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- ChemMedChem, 2013, v. 8, n. 3, p. 521, doi. 10.1002/cmdc.201200493
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The Synthesis and in vivo Evaluation of 2′,2′-Difluoro KRN7000.
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- ChemMedChem, 2009, v. 4, n. 3, p. 329, doi. 10.1002/cmdc.200800348
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- Article
Synthesis and in vitro Evaluation of α-GalCer Epimers.
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- ChemMedChem, 2008, v. 3, n. 7, p. 1061, doi. 10.1002/cmdc.200800021
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Synthesis and Biological Evaluation of Bicyclic Nucleosides as Inhibitors of M. tuberculosis Thymidylate Kinase.
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- ChemMedChem, 2006, v. 1, n. 10, p. 1081, doi. 10.1002/cmdc.200600028
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- Article