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Romain M Wolf

Showing results (11-20 of 18) with videos related to

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Bioorganic & Medicinal Chemistry Letters|November 7, 2016
Discovery of novel pyrrolidineoxy-substituted heteroaromatics as potent and selective PI3K delta inhibitors with improved physicochemical propertiesKlemens Hoegenauer, Nicolas Soldermann, Christina Hebach, et al.
ACS Medicinal Chemistry Letters|September 27, 2017
Discovery of CDZ173 (Leniolisib), Representing a Structurally Novel Class of PI3K Delta-Selective InhibitorsKlemens Hoegenauer, Nicolas Soldermann, Frédéric Zécri, et al.
Journal of Medicinal Chemistry|November 28, 2023
Discovery of Amino Alcohols as Highly Potent, Selective, and Orally Efficacious Inhibitors of Leukotriene A4 HydrolaseGebhard Thoma, Christian Markert, Rainer Lueoend, et al.
ACS Medicinal Chemistry Letters|August 27, 2016
Discovery and Pharmacological Characterization of Novel Quinazoline-Based PI3K Delta-Selective InhibitorsKlemens Hoegenauer, Nicolas Soldermann, Frédéric Stauffer, et al.
Journal of Medicinal Chemistry|July 11, 2018
Optimizing a Weakly Binding Fragment into a Potent RORγt Inverse Agonist with Efficacy in an in Vivo Inflammation ModelDavid A Carcache, Anna Vulpetti, Joerg Kallen, et al.
Journal of Medicinal Chemistry|February 18, 2010
1-Alkyl-4-phenyl-6-alkoxy-1H-quinazolin-2-ones: a novel series of potent calcium-sensing receptor antagonistsLeo Widler, Eva Altmann, René Beerli, et al.
Scientific Reports|October 21, 2017
Feasibility and physiological relevance of designing highly potent aminopeptidase-sparing leukotriene A4 hydrolase inhibitorsShin Numao, Franziska Hasler, Claire Laguerre, et al.
Journal of Medicinal Chemistry|February 17, 2025
Discovery of GJG057, a Potent and Highly Selective Inhibitor of Leukotriene C4 SynthaseGebhard Thoma, Wolfgang Miltz, Rudolf Waelchli, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Bioorganic & Medicinal Chemistry Letters|November 7, 2016
Discovery of novel pyrrolidineoxy-substituted heteroaromatics as potent and selective PI3K delta inhibitors with improved physicochemical propertiesKlemens Hoegenauer, Nicolas Soldermann, Christina Hebach, et al.
ACS Medicinal Chemistry Letters|September 27, 2017
Discovery of CDZ173 (Leniolisib), Representing a Structurally Novel Class of PI3K Delta-Selective InhibitorsKlemens Hoegenauer, Nicolas Soldermann, Frédéric Zécri, et al.
Journal of Medicinal Chemistry|November 28, 2023
Discovery of Amino Alcohols as Highly Potent, Selective, and Orally Efficacious Inhibitors of Leukotriene A4 HydrolaseGebhard Thoma, Christian Markert, Rainer Lueoend, et al.
ACS Medicinal Chemistry Letters|August 27, 2016
Discovery and Pharmacological Characterization of Novel Quinazoline-Based PI3K Delta-Selective InhibitorsKlemens Hoegenauer, Nicolas Soldermann, Frédéric Stauffer, et al.
Journal of Medicinal Chemistry|July 11, 2018
Optimizing a Weakly Binding Fragment into a Potent RORγt Inverse Agonist with Efficacy in an in Vivo Inflammation ModelDavid A Carcache, Anna Vulpetti, Joerg Kallen, et al.
Journal of Medicinal Chemistry|February 18, 2010
1-Alkyl-4-phenyl-6-alkoxy-1H-quinazolin-2-ones: a novel series of potent calcium-sensing receptor antagonistsLeo Widler, Eva Altmann, René Beerli, et al.
Scientific Reports|October 21, 2017
Feasibility and physiological relevance of designing highly potent aminopeptidase-sparing leukotriene A4 hydrolase inhibitorsShin Numao, Franziska Hasler, Claire Laguerre, et al.
Journal of Medicinal Chemistry|February 17, 2025
Discovery of GJG057, a Potent and Highly Selective Inhibitor of Leukotriene C4 SynthaseGebhard Thoma, Wolfgang Miltz, Rudolf Waelchli, et al.
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