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Justin Dietrich

Showing results (11-20 of 19) with videos related to

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Bioorganic & Medicinal Chemistry|December 8, 2009
Application of a novel [3+2] cycloaddition reaction to prepare substituted imidazoles and their use in the design of potent DFG-out allosteric B-Raf inhibitorsJustin Dietrich, Vijay Gokhale, Xiadong Wang, et al.
Molecular Diversity|January 13, 2012
Facile, novel two-step syntheses of benzimidazoles, bis-benzimidazoles, and bis-benzimidazole-dihydroquinoxalinesZhigang Xu, Arthur Y Shaw, Justin Dietrich, et al.
Bioorganic & Medicinal Chemistry Letters|April 21, 2012
Synthesis and biological activity of 2-aminothiazoles as novel inhibitors of PGE2 production in cellsBreland Smith, Hui-Hua Chang, Federico Medda, et al.
Bioorganic & Medicinal Chemistry Letters|December 15, 2012
Synthesis and biological activity of aminophthalazines and aminopyridazines as novel inhibitors of PGE2 production in cellsFederico Medda, Earlphia Sells, Hui-Hua Chang, et al.
Organic Letters|December 3, 2019
A Strategy for the Synthesis of Sulfonamides on DNAWei Liu, Wei Deng, Saisai Sun, et al.
Journal of Medicinal Chemistry|July 4, 2018
De Novo Design, Synthesis, and Biological Evaluation of 3,4-Disubstituted Pyrrolidine Sulfonamides as Potent and Selective Glycine Transporter 1 Competitive InhibitorsYing Wang, Hongyu Zhao, Jason T Brewer, et al.
Journal of Medicinal Chemistry|August 7, 2018
Discovery of Novel Aminotetralines and Aminochromanes as Selective and Competitive Glycine Transporter 1 (GlyT1) InhibitorsWilli Amberg, Udo E W Lange, Michael Ochse, et al.
Nature Chemical Biology|August 31, 2017
Erratum: The EED protein-protein interaction inhibitor A-395 inactivates the PRC2 complexYupeng He, Sujatha Selvaraju, Michael L Curtin, et al.
Nature Chemical Biology|January 31, 2017
The EED protein-protein interaction inhibitor A-395 inactivates the PRC2 complexYupeng He, Sujatha Selvaraju, Michael L Curtin, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Bioorganic & Medicinal Chemistry|December 8, 2009
Application of a novel [3+2] cycloaddition reaction to prepare substituted imidazoles and their use in the design of potent DFG-out allosteric B-Raf inhibitorsJustin Dietrich, Vijay Gokhale, Xiadong Wang, et al.
Molecular Diversity|January 13, 2012
Facile, novel two-step syntheses of benzimidazoles, bis-benzimidazoles, and bis-benzimidazole-dihydroquinoxalinesZhigang Xu, Arthur Y Shaw, Justin Dietrich, et al.
Bioorganic & Medicinal Chemistry Letters|April 21, 2012
Synthesis and biological activity of 2-aminothiazoles as novel inhibitors of PGE2 production in cellsBreland Smith, Hui-Hua Chang, Federico Medda, et al.
Bioorganic & Medicinal Chemistry Letters|December 15, 2012
Synthesis and biological activity of aminophthalazines and aminopyridazines as novel inhibitors of PGE2 production in cellsFederico Medda, Earlphia Sells, Hui-Hua Chang, et al.
Organic Letters|December 3, 2019
A Strategy for the Synthesis of Sulfonamides on DNAWei Liu, Wei Deng, Saisai Sun, et al.
Journal of Medicinal Chemistry|July 4, 2018
De Novo Design, Synthesis, and Biological Evaluation of 3,4-Disubstituted Pyrrolidine Sulfonamides as Potent and Selective Glycine Transporter 1 Competitive InhibitorsYing Wang, Hongyu Zhao, Jason T Brewer, et al.
Journal of Medicinal Chemistry|August 7, 2018
Discovery of Novel Aminotetralines and Aminochromanes as Selective and Competitive Glycine Transporter 1 (GlyT1) InhibitorsWilli Amberg, Udo E W Lange, Michael Ochse, et al.
Nature Chemical Biology|August 31, 2017
Erratum: The EED protein-protein interaction inhibitor A-395 inactivates the PRC2 complexYupeng He, Sujatha Selvaraju, Michael L Curtin, et al.
Nature Chemical Biology|January 31, 2017
The EED protein-protein interaction inhibitor A-395 inactivates the PRC2 complexYupeng He, Sujatha Selvaraju, Michael L Curtin, et al.
Pageof 2