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Chemmedchem
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June 18, 2026
Structure-Based Design, Synthesis, and Evaluation of Novel Ponatinib Derivatives With a Significantly Altered Selectivity Profile
Tobias 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 Biosynthesis
Silvia 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 inhibitors
Christian 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 inhibitors
Mona 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 metabolism
Nermin 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 substituents
Habiba 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 agents
Salma 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 TRPV4
Frank 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 analogs
Najim 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 modification
Sarah S Darwish, Mohammad Abdel-Halim, Ahmed K ElHady, et al.
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Search research articles
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Showing results (21-30 of 79) with videos related to
Sort By:
Page
of 8
Chemmedchem
|
June 18, 2026
Structure-Based Design, Synthesis, and Evaluation of Novel Ponatinib Derivatives With a Significantly Altered Selectivity Profile
Tobias 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 Biosynthesis
Silvia 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 inhibitors
Christian 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 inhibitors
Mona 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 metabolism
Nermin 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 substituents
Habiba 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 agents
Salma 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 TRPV4
Frank 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 analogs
Najim 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 modification
Sarah S Darwish, Mohammad Abdel-Halim, Ahmed K ElHady, et al.
Page
of 8