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Matthias Engel

Showing results (21-30 of 79) with videos related to

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Chemmedchem|June 18, 2026
Structure-Based Design, Synthesis, and Evaluation of Novel Ponatinib Derivatives With a Significantly Altered Selectivity ProfileTobias Betzholz, Ting Liu, Andreas Krämer, et al.
Journal of Medicinal Chemistry|March 4, 2016
Exploiting the Chromone Scaffold for the Development of Inhibitors of Corticosteroid BiosynthesisSilvia Gobbi, Qingzhong Hu, Christina Zimmer, et al.
Plos One|March 29, 2014
Design and synthesis of a library of lead-like 2,4-bisheterocyclic substituted thiophenes as selective Dyrk/Clk inhibitorsChristian Schmitt, Dagmar Kail, Marica Mariano, et al.
Bioorganic Chemistry|March 6, 2024
Synthesis and evaluation of novel N1-acylated 5-(4-pyridinyl)indazole derivatives as potent and selective haspin inhibitorsMona M Shawky, Mennatallah Abdallah, Hend Khalifa, et al.
European Journal of Medicinal Chemistry|February 21, 2016
Design and synthesis of novel tamoxifen analogues that avoid CYP2D6 metabolismNermin S Ahmed, Nehal H Elghazawy, Ahmed K ElHady, et al.
Archiv Der Pharmazie|March 13, 2024
N<sub>1</sub>-Benzoylated 5-(4-pyridinyl)indazole-based kinase inhibitors: Attaining haspin and Clk4 selectivity via modulation of the benzoyl substituentsHabiba G Aboelfotouh, Mennatallah Abdallah, Hend Khalifa, et al.
Bioorganic Chemistry|March 30, 2020
Synthesis of novel 1,2-diarylpyrazolidin-3-one-based compounds and their evaluation as broad spectrum antibacterial agentsSalma A Mokbel, Reem K Fathalla, Lina Y El-Sharkawy, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 18, 2019
Acetaminophen-induced liver injury is mediated by the ion channel TRPV4Frank Echtermeyer, Mirjam Eberhardt, Linus Risser, et al.
Archiv Der Pharmazie|September 25, 2014
New CYP17 hydroxylase inhibitors: synthesis, biological evaluation, QSAR, and molecular docking study of new pregnenolone analogsNajim A Al-Masoudi, Dawood S Ali, Bahjat Saeed, et al.
European Journal of Medicinal Chemistry|September 18, 2018
Development of novel amide-derivatized 2,4-bispyridyl thiophenes as highly potent and selective Dyrk1A inhibitors. Part II: Identification of the cyclopropylamide moiety as a key modificationSarah S Darwish, Mohammad Abdel-Halim, Ahmed K ElHady, et al.
Pageof 8

Showing results (21-30 of 79) with videos related to

Sort By:
Pageof 8
Chemmedchem|June 18, 2026
Structure-Based Design, Synthesis, and Evaluation of Novel Ponatinib Derivatives With a Significantly Altered Selectivity ProfileTobias Betzholz, Ting Liu, Andreas Krämer, et al.
Journal of Medicinal Chemistry|March 4, 2016
Exploiting the Chromone Scaffold for the Development of Inhibitors of Corticosteroid BiosynthesisSilvia Gobbi, Qingzhong Hu, Christina Zimmer, et al.
Plos One|March 29, 2014
Design and synthesis of a library of lead-like 2,4-bisheterocyclic substituted thiophenes as selective Dyrk/Clk inhibitorsChristian Schmitt, Dagmar Kail, Marica Mariano, et al.
Bioorganic Chemistry|March 6, 2024
Synthesis and evaluation of novel N1-acylated 5-(4-pyridinyl)indazole derivatives as potent and selective haspin inhibitorsMona M Shawky, Mennatallah Abdallah, Hend Khalifa, et al.
European Journal of Medicinal Chemistry|February 21, 2016
Design and synthesis of novel tamoxifen analogues that avoid CYP2D6 metabolismNermin S Ahmed, Nehal H Elghazawy, Ahmed K ElHady, et al.
Archiv Der Pharmazie|March 13, 2024
N<sub>1</sub>-Benzoylated 5-(4-pyridinyl)indazole-based kinase inhibitors: Attaining haspin and Clk4 selectivity via modulation of the benzoyl substituentsHabiba G Aboelfotouh, Mennatallah Abdallah, Hend Khalifa, et al.
Bioorganic Chemistry|March 30, 2020
Synthesis of novel 1,2-diarylpyrazolidin-3-one-based compounds and their evaluation as broad spectrum antibacterial agentsSalma A Mokbel, Reem K Fathalla, Lina Y El-Sharkawy, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 18, 2019
Acetaminophen-induced liver injury is mediated by the ion channel TRPV4Frank Echtermeyer, Mirjam Eberhardt, Linus Risser, et al.
Archiv Der Pharmazie|September 25, 2014
New CYP17 hydroxylase inhibitors: synthesis, biological evaluation, QSAR, and molecular docking study of new pregnenolone analogsNajim A Al-Masoudi, Dawood S Ali, Bahjat Saeed, et al.
European Journal of Medicinal Chemistry|September 18, 2018
Development of novel amide-derivatized 2,4-bispyridyl thiophenes as highly potent and selective Dyrk1A inhibitors. Part II: Identification of the cyclopropylamide moiety as a key modificationSarah S Darwish, Mohammad Abdel-Halim, Ahmed K ElHady, et al.
Pageof 8