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Cells
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April 23, 2022
Target Hopping from Protein Kinases to PXR: Identification of Small-Molecule Protein Kinase Inhibitors as Selective Modulators of Pregnane X Receptor from TüKIC Library
Enni-Kaisa Mustonen, Tatu Pantsar, Azam Rashidian, et al.
Computational and Structural Biotechnology Journal
|
July 5, 2022
Discrepancy in interactions and conformational dynamics of pregnane X receptor (PXR) bound to an agonist and a novel competitive antagonist
Azam Rashidian, Enni-Kaisa Mustonen, Thales Kronenberger, et al.
Molecules (Basel, Switzerland)
|
June 28, 2019
Design, Synthesis and Biological Evaluation of 7-Chloro-9<i>H</i>-pyrimido[4,5-<i>b</i>]indole-based Glycogen Synthase Kinase-3β Inhibitors
Stanislav Andreev, Tatu Pantsar, Francesco Ansideri, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences
|
April 13, 2018
The use of molecular descriptors in the development of co-amorphous formulations
Helena Meng-Lund, Georgia Kasten, Katrine Tarp Jensen, et al.
European Journal of Medicinal Chemistry
|
October 23, 2020
Design and synthesis of novel fluorescently labeled analogs of vemurafenib targeting MKK4
Theresa Kircher, Tatu Pantsar, Andreas Oder, et al.
Journal of Medicinal Chemistry
|
May 29, 2020
Bioisosteric Replacement of Arylamide-Linked Spine Residues with <i>N</i>-Acylhydrazones and Selenophenes as a Design Strategy to Novel Dibenzosuberone Derivatives as Type I 1/2 p38α MAP Kinase Inhibitors
Júlia G B Pedreira, Philipp Nahidino, Mark Kudolo, et al.
Bioorganic Chemistry
|
June 5, 2024
Bromo-substituted indirubins for inhibition of protein kinase-mediated signalling involved in inflammatory mediator release in human monocytes
Vivien Bachmann, Patrick Schädel, Jan Westhoff, et al.
European Journal of Medicinal Chemistry
|
May 17, 2019
Pyridinylimidazoles as dual glycogen synthase kinase 3β/p38α mitogen-activated protein kinase inhibitors
Fabian Heider, Francesco Ansideri, Roberta Tesch, et al.
Molecular Pharmacology
|
December 26, 2013
Mutation of Cys242 of human monoacylglycerol lipase disrupts balanced hydrolysis of 1- and 2-monoacylglycerols and selectively impairs inhibitor potency
Tuomo Laitinen, Dina Navia-Paldanius, Roosa Rytilahti, et al.
Molecular Pharmacology
|
August 21, 2014
Robust hydrolysis of prostaglandin glycerol esters by human monoacylglycerol lipase (MAGL)
Juha R Savinainen, Emilia Kansanen, Tatu Pantsar, et al.
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Search research articles
Search
Showing results (11-20 of 31) with videos related to
Sort By:
Page
of 4
Cells
|
April 23, 2022
Target Hopping from Protein Kinases to PXR: Identification of Small-Molecule Protein Kinase Inhibitors as Selective Modulators of Pregnane X Receptor from TüKIC Library
Enni-Kaisa Mustonen, Tatu Pantsar, Azam Rashidian, et al.
Computational and Structural Biotechnology Journal
|
July 5, 2022
Discrepancy in interactions and conformational dynamics of pregnane X receptor (PXR) bound to an agonist and a novel competitive antagonist
Azam Rashidian, Enni-Kaisa Mustonen, Thales Kronenberger, et al.
Molecules (Basel, Switzerland)
|
June 28, 2019
Design, Synthesis and Biological Evaluation of 7-Chloro-9<i>H</i>-pyrimido[4,5-<i>b</i>]indole-based Glycogen Synthase Kinase-3β Inhibitors
Stanislav Andreev, Tatu Pantsar, Francesco Ansideri, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences
|
April 13, 2018
The use of molecular descriptors in the development of co-amorphous formulations
Helena Meng-Lund, Georgia Kasten, Katrine Tarp Jensen, et al.
European Journal of Medicinal Chemistry
|
October 23, 2020
Design and synthesis of novel fluorescently labeled analogs of vemurafenib targeting MKK4
Theresa Kircher, Tatu Pantsar, Andreas Oder, et al.
Journal of Medicinal Chemistry
|
May 29, 2020
Bioisosteric Replacement of Arylamide-Linked Spine Residues with <i>N</i>-Acylhydrazones and Selenophenes as a Design Strategy to Novel Dibenzosuberone Derivatives as Type I 1/2 p38α MAP Kinase Inhibitors
Júlia G B Pedreira, Philipp Nahidino, Mark Kudolo, et al.
Bioorganic Chemistry
|
June 5, 2024
Bromo-substituted indirubins for inhibition of protein kinase-mediated signalling involved in inflammatory mediator release in human monocytes
Vivien Bachmann, Patrick Schädel, Jan Westhoff, et al.
European Journal of Medicinal Chemistry
|
May 17, 2019
Pyridinylimidazoles as dual glycogen synthase kinase 3β/p38α mitogen-activated protein kinase inhibitors
Fabian Heider, Francesco Ansideri, Roberta Tesch, et al.
Molecular Pharmacology
|
December 26, 2013
Mutation of Cys242 of human monoacylglycerol lipase disrupts balanced hydrolysis of 1- and 2-monoacylglycerols and selectively impairs inhibitor potency
Tuomo Laitinen, Dina Navia-Paldanius, Roosa Rytilahti, et al.
Molecular Pharmacology
|
August 21, 2014
Robust hydrolysis of prostaglandin glycerol esters by human monoacylglycerol lipase (MAGL)
Juha R Savinainen, Emilia Kansanen, Tatu Pantsar, et al.
Page
of 4