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Synthesis of 7-azoniabicyclo[2.2.1]heptane-based dicationic liquids
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- Conference Paper
- C3
- open access
In vitro celecoxib supplementation impacts the functional capacities of the gut microbiota
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Anticancer chalcones : selective or multitarget ligands?
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Discovery of anti-invasive tools and leads for the study and treatment of metastatic cancer : two case studies
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Chalcones as anti-invasive agents : challenges and opportunities
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- Journal Article
- A1
- open access
Improved synthesis and comparative analysis of the tool properties of new and existing D-ring modified (S)-blebbistatin analogs
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- Journal Article
- A1
- open access
Insights into the myosin II inhibitory potency of A-ring-modified (S)-blebbistatin analogs
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A new class of bicyclic dicationic salts based on the 7-azoniabicyclo[2.2.1]heptane scaffold
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- Journal Article
- A1
- open access
Discovery of (S)-3′-hydroxyblebbistatin and (S)-3′-aminoblebbistatin : polar myosin II inhibitors with superior research tool properties
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Discovery of anti-invasive tools and leads for the study and treatment of metastatic cancer : two case studies
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Discovery and development of new anti-invasive agents, an unmet clinical need
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Discovery of novel nonmuscle myosin II inhibitors as chemical tools and antimetastatic therapeutics leads
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Discovery of novel nonmuscle myosin II inhibitors as antimetastatic therapeutics leads and chemical tools
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4-Fluoro-3',4',5'-trimethoxychalcone as a new anti-invasive agent: from discovery to initial validation in an in vivo metastasis model
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4-Fluoro-3',4',5'-trimethoxychalcone as a new anti-invasive agent : from discovery to initial validation in an in vivo metastasis model
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Pharmacological evaluation of the anti-invasive agent 4-fluoro-3',4',5'-trimethoxychalcone
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4-Fluoro-3',4',5'-trimethoxychalcone as a new anti-invasive agent: from discovery to initial validation in an in vivo metastasis model
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Chick heart invasion assay for testing the invasiveness of cancer cells and the activity of potentially anti-invasive compounds
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- Journal Article
- A1
- open access
Microbial inhibition of oral epithelial wound recovery: potential role for quorum sensing molecules?
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4-Fluoro-3',4',5'-trimethoxychalcone as a new anti-invasive agent: from discovery to initial validation in an in vivo metastasis model
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A new class of antimicrobial biosurfactants: quaternary ammonium sophorolipids
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Further studies on anti-invasive chemotypes: an excursion from chalcones to curcuminoids
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Homogeneous gold-catalyzed cyclization reactions of alkynes with N- and S-nucleophiles
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Beyond the Diketopiperazine Family with Alternatively Bridged Brevianamide F Analogues
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Feruloylbenzotriazole and Weinreb amide as bioinspired building blocks: a reactivity study towards O-, N-, S-, and C- nucleophiles
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Feruloyl benzotriazole and Weinreb amide as bioinspired building blocks: a reactivity study
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On the quest for new anti-invasive agents: from the discovery of 4-fluoro-3',4','5'-trimethoxychalcone to its initial validation in an in vivo metastasis model
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Functions incorporating a halogen and another group other than a halogen or a chalcogen
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Assessment of the antineoplastic potential of chalcones in animal models
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The quest for antimetastatic agents: from natural chalcones to anti-invasive lead candidates
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Feruloyl benzotriazole and Weinreb amide as bioinspired building blocks: a reactivity study
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Design, synthesis and structure-activity relationships of some novel, highly potent anti-invasive (E)- and (Z)-stilbenes
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Synthesis of isoindoles and related iso-condensed heteroaromatic pyrroles
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Synthesis and reactivity of novel 1H-isochromeno[3,4-d]imidazol-1-onium salts
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Continuous synthesis of peralkylated imidazoles and their transformation into ionic liquids with improved (electro)chemical stabilities
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Exploration of the SAR of anti-invasive chalcones: synthesis and biological evaluation of conformationally restricted analogues
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- Conference Paper
- C3
- open access
(Q)SAR directed design, synthesis and evaluation of anti-invasive chalcones and analogues
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QSAR-directed design, synthesis and evaluation of anti-invasive chalcones and analogues
(2012) -
QSAR directed design, synthesis and evaluation of anti-invasive chalcones and analogues
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Exploration of the SAR of anti-invasive chalcones: synthesis and biological evaluation of conformationally restricted analogues
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- Conference Paper
- C3
- open access
Application of microreactor technology for cyanohydrin production : extending the scope towards renewable resources
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- Conference Paper
- C3
- open access
Study on the synthesis, reactivity and melting points of novel 1H-isochromeno[3,4-d]imidazol-1-onium salts
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A safe production method for acetone cyanohydrin
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Synthesis of β-, γ-, δ-, ..., ω-halogenated ketones and aldehydes
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Experimental and computational study of the ring opening of tricyclic oxanorbornenes to polyhydro isoindole phosphonates
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- Conference Paper
- C3
- open access
Exploring multicomponent and heterocyclic coupling reactions using microreactor technology
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- Conference Paper
- C3
- open access
Synthesis, biological evaluation and 2D-QSAR analysis of chalcones as anti-invasive cancer agents
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- Conference Paper
- C3
- open access
Cleavage of the Oxanorbornene Oxygen Bridge with Lewis Acids: Computation and Experiment
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- Conference Paper
- C3
- open access
Synthesis, biological evaluation and 2D-QSAR analysis of chalcones as anti-invasive cancer agents
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Microreactor technology : continuous synthesis of 1H-isochromeno[3,4-d]imidazol-5-ones