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Journal of Enzyme Inhibition and Medicinal Chemistry
|
June 7, 2022
Design and biological evaluation of substituted 5,7-dihydro-6<i>H</i>-indolo[2,3-<i>c</i>]quinolin-6-one as novel selective Haspin inhibitors
Sreenivas Avula, Xudan Peng, Xingfen Lang, et al.
Virologie (Montrouge, France)
|
November 3, 2025
[Prozac 2.0 : from antidepressant to antiviral]
Marine O Faucher, Safeh Khemiri, Carole Yaacoub, et al.
Journal of Medicinal Chemistry
|
January 23, 2015
Structural investigation of B-Raf paradox breaker and inducer inhibitors
Rohit Arora, Michela Di Michele, Elisabeth Stes, et al.
Journal of Medicinal Chemistry
|
July 8, 2016
Correction to Structural Investigation of B-Raf Paradox Breaker and Inducer Inhibitors
Rohit Arora, Michela Di Michele, Elisabeth Stes, et al.
European Journal of Medicinal Chemistry
|
May 23, 2026
Identification of novel CLK1 inhibitors by computational fragment-based ligand design, co-crystallization, chemical synthesis and structure activity relationships
Stéphane Bourg, Matthieu Place, Chloé Copin, et al.
European Journal of Medicinal Chemistry
|
May 21, 2018
Structure-based design of novel quinoxaline-2-carboxylic acids and analogues as Pim-1 inhibitors
Bruno Oyallon, Marie Brachet-Botineau, Cédric Logé, et al.
European Journal of Medicinal Chemistry
|
July 6, 2015
Advances in tetrahydropyrido[1,2-a]isoindolone (valmerins) series: Potent glycogen synthase kinase 3 and cyclin dependent kinase 5 inhibitors
Rajâa Boulahjar, Aziz Ouach, Stéphane Bourg, et al.
European Journal of Medicinal Chemistry
|
May 14, 2020
Identification of a new series of flavopiridol-like structures as kinase inhibitors with high cytotoxic potency
Nada Ibrahim, Pascal Bonnet, Jean-Daniel Brion, et al.
European Journal of Medicinal Chemistry
|
February 1, 2026
New fluoxetine analogues as anti-enterovirus agents targeting 2C protein
Safeh Khemiri, Marine O Faucher, Stephane Bourg, et al.
Molecules (Basel, Switzerland)
|
September 10, 2021
Design, Synthesis and SAR in 2,4,7-Trisubstituted Pyrido[3,2-<i>d</i>]Pyrimidine Series as Novel PI3K/mTOR Inhibitors
Frédéric Buron, Nuno Rodrigues, Thibault Saurat, et al.
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Search research articles
Search
Showing results (61-70 of 79) with videos related to
Sort By:
Page
of 8
Journal of Enzyme Inhibition and Medicinal Chemistry
|
June 7, 2022
Design and biological evaluation of substituted 5,7-dihydro-6<i>H</i>-indolo[2,3-<i>c</i>]quinolin-6-one as novel selective Haspin inhibitors
Sreenivas Avula, Xudan Peng, Xingfen Lang, et al.
Virologie (Montrouge, France)
|
November 3, 2025
[Prozac 2.0 : from antidepressant to antiviral]
Marine O Faucher, Safeh Khemiri, Carole Yaacoub, et al.
Journal of Medicinal Chemistry
|
January 23, 2015
Structural investigation of B-Raf paradox breaker and inducer inhibitors
Rohit Arora, Michela Di Michele, Elisabeth Stes, et al.
Journal of Medicinal Chemistry
|
July 8, 2016
Correction to Structural Investigation of B-Raf Paradox Breaker and Inducer Inhibitors
Rohit Arora, Michela Di Michele, Elisabeth Stes, et al.
European Journal of Medicinal Chemistry
|
May 23, 2026
Identification of novel CLK1 inhibitors by computational fragment-based ligand design, co-crystallization, chemical synthesis and structure activity relationships
Stéphane Bourg, Matthieu Place, Chloé Copin, et al.
European Journal of Medicinal Chemistry
|
May 21, 2018
Structure-based design of novel quinoxaline-2-carboxylic acids and analogues as Pim-1 inhibitors
Bruno Oyallon, Marie Brachet-Botineau, Cédric Logé, et al.
European Journal of Medicinal Chemistry
|
July 6, 2015
Advances in tetrahydropyrido[1,2-a]isoindolone (valmerins) series: Potent glycogen synthase kinase 3 and cyclin dependent kinase 5 inhibitors
Rajâa Boulahjar, Aziz Ouach, Stéphane Bourg, et al.
European Journal of Medicinal Chemistry
|
May 14, 2020
Identification of a new series of flavopiridol-like structures as kinase inhibitors with high cytotoxic potency
Nada Ibrahim, Pascal Bonnet, Jean-Daniel Brion, et al.
European Journal of Medicinal Chemistry
|
February 1, 2026
New fluoxetine analogues as anti-enterovirus agents targeting 2C protein
Safeh Khemiri, Marine O Faucher, Stephane Bourg, et al.
Molecules (Basel, Switzerland)
|
September 10, 2021
Design, Synthesis and SAR in 2,4,7-Trisubstituted Pyrido[3,2-<i>d</i>]Pyrimidine Series as Novel PI3K/mTOR Inhibitors
Frédéric Buron, Nuno Rodrigues, Thibault Saurat, et al.
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of 8