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Chemical Society Reviews
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February 24, 2015
Dynamic combinatorial chemistry: a tool to facilitate the identification of inhibitors for protein targets
Milon Mondal, Anna K H Hirsch
Journal of Medicinal Chemistry
|
February 27, 2015
Fighting malaria: structure-guided discovery of nonpeptidomimetic plasmepsin inhibitors
Anja P Huizing, Milon Mondal, Anna K H Hirsch
British Journal of Cancer
|
September 9, 2021
UCHL1 as a novel target in breast cancer: emerging insights from cell and chemical biology
Milon Mondal, Daniel Conole, Jaya Nautiyal, et al.
Frontiers in Chemistry
|
January 11, 2020
Recent Developments in Cell Permeable Deubiquitinating Enzyme Activity-Based Probes
Daniel Conole, Milon Mondal, Jaimeen D Majmudar, et al.
The Journal of Organic Chemistry
|
November 8, 2011
Triazole-linked-thiophene conjugate of calix[4]arene: its selective recognition of Zn2+ and as biomimetic model in supporting the events of the metal detoxification and oxidative stress involving metallothionein
Rakesh Kumar Pathak, Vijaya Kumar Hinge, Milon Mondal, et al.
Journal of Biomolecular Structure & Dynamics
|
August 30, 2021
Ebselen suitably interacts with the potential SARS-CoV-2 targets: an <i>in-silico</i> approach
Chandan Sarkar, Mohnad Abdalla, Milon Mondal, et al.
RSC Chemical Biology
|
May 10, 2024
Discovery of potent and selective activity-based probes (ABPs) for the deubiquitinating enzyme USP30
Milon Mondal, Fangyuan Cao, Daniel Conole, et al.
International Journal of Molecular Sciences
|
August 20, 2015
Structure-Based Optimization of Inhibitors of the Aspartic Protease Endothiapepsin
Alwin M Hartman, Milon Mondal, Nedyalka Radeva, et al.
Food & Function
|
June 4, 2021
Therapeutic perspectives of the black cumin component thymoquinone: A review
Chandan Sarkar, Sarmin Jamaddar, Tawhida Islam, et al.
Angewandte Chemie (International Ed. in English)
|
July 13, 2016
Fragment Linking and Optimization of Inhibitors of the Aspartic Protease Endothiapepsin: Fragment-Based Drug Design Facilitated by Dynamic Combinatorial Chemistry
Milon Mondal, Nedyalka Radeva, Hugo Fanlo-Virgós, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 49) with videos related to
Sort By:
Page
of 5
Chemical Society Reviews
|
February 24, 2015
Dynamic combinatorial chemistry: a tool to facilitate the identification of inhibitors for protein targets
Milon Mondal, Anna K H Hirsch
Journal of Medicinal Chemistry
|
February 27, 2015
Fighting malaria: structure-guided discovery of nonpeptidomimetic plasmepsin inhibitors
Anja P Huizing, Milon Mondal, Anna K H Hirsch
British Journal of Cancer
|
September 9, 2021
UCHL1 as a novel target in breast cancer: emerging insights from cell and chemical biology
Milon Mondal, Daniel Conole, Jaya Nautiyal, et al.
Frontiers in Chemistry
|
January 11, 2020
Recent Developments in Cell Permeable Deubiquitinating Enzyme Activity-Based Probes
Daniel Conole, Milon Mondal, Jaimeen D Majmudar, et al.
The Journal of Organic Chemistry
|
November 8, 2011
Triazole-linked-thiophene conjugate of calix[4]arene: its selective recognition of Zn2+ and as biomimetic model in supporting the events of the metal detoxification and oxidative stress involving metallothionein
Rakesh Kumar Pathak, Vijaya Kumar Hinge, Milon Mondal, et al.
Journal of Biomolecular Structure & Dynamics
|
August 30, 2021
Ebselen suitably interacts with the potential SARS-CoV-2 targets: an <i>in-silico</i> approach
Chandan Sarkar, Mohnad Abdalla, Milon Mondal, et al.
RSC Chemical Biology
|
May 10, 2024
Discovery of potent and selective activity-based probes (ABPs) for the deubiquitinating enzyme USP30
Milon Mondal, Fangyuan Cao, Daniel Conole, et al.
International Journal of Molecular Sciences
|
August 20, 2015
Structure-Based Optimization of Inhibitors of the Aspartic Protease Endothiapepsin
Alwin M Hartman, Milon Mondal, Nedyalka Radeva, et al.
Food & Function
|
June 4, 2021
Therapeutic perspectives of the black cumin component thymoquinone: A review
Chandan Sarkar, Sarmin Jamaddar, Tawhida Islam, et al.
Angewandte Chemie (International Ed. in English)
|
July 13, 2016
Fragment Linking and Optimization of Inhibitors of the Aspartic Protease Endothiapepsin: Fragment-Based Drug Design Facilitated by Dynamic Combinatorial Chemistry
Milon Mondal, Nedyalka Radeva, Hugo Fanlo-Virgós, et al.
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