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Milon Mondal
Milon Mondal
Postdoctoral research associate
Verified email at imperial.ac.uk - Homepage
Title
Cited by
Cited by
Year
Chimeric peptidomimetic antibiotics against Gram-negative bacteria
A Luther, M Urfer, M Zahn, M Müller, SY Wang, M Mondal, A Vitale, ...
Nature 576 (7787), 452-458, 2019
2472019
Dynamic combinatorial chemistry: a tool to facilitate the identification of inhibitors for protein targets
M Mondal, AKH Hirsch
Chemical Society Reviews 44 (8), 2455-2488, 2015
2252015
Thanatin targets the intermembrane protein complex required for lipopolysaccharide transport in Escherichia coli
SU Vetterli, K Zerbe, M Müller, M Urfer, M Mondal, SY Wang, K Moehle, ...
Science advances 4 (11), eaau2634, 2018
1092018
Structure‐based design of inhibitors of the aspartic protease endothiapepsin by exploiting dynamic combinatorial chemistry
M Mondal, N Radeva, H Koester, A Park, C Potamitis, M Zervou, G Klebe, ...
Angewandte Chemie International Edition 53 (12), 3259-3263, 2014
942014
Fragment Linking and Optimization of Inhibitors of the Aspartic Protease Endothiapepsin: Fragment‐Based Drug Design Facilitated by Dynamic Combinatorial Chemistry
M Mondal, N Radeva, H Fanlo‐Virgós, S Otto, G Klebe, AKH Hirsch
Angewandte Chemie International Edition 55 (32), 9422-9426, 2016
902016
A Peptidomimetic Antibiotic Interacts with the Periplasmic Domain of LptD from Pseudomonas aeruginosa
G Andolina, LC Bencze, K Zerbe, M Müller, J Steinmann, H Kocherla, ...
ACS chemical biology 13 (3), 666-675, 2018
732018
Discovery of a potent and selective covalent inhibitor and activity-based probe for the deubiquitylating enzyme UCHL1, with antifibrotic activity
N Panyain, A Godinat, T Lanyon-Hogg, S Lachiondo-Ortega, EJ Will, ...
Journal of the American Chemical Society 142 (28), 12020-12026, 2020
592020
Triazole-Linked-Thiophene Conjugate of Calix[4]arene: Its Selective Recognition of Zn2+ and as Biomimetic Model in Supporting the Events of the Metal …
RK Pathak, VK Hinge, M Mondal, CP Rao
The Journal of Organic Chemistry 76 (24), 10039-10049, 2011
482011
Light-mediated discovery of surfaceome nanoscale organization and intercellular receptor interaction networks
M Müller, F Gräbnitz, N Barandun, Y Shen, F Wendt, SN Steiner, ...
Nature Communications 12 (1), 7036, 2021
342021
Fragment‐Based Drug Design Facilitated by Protein‐Templated Click Chemistry: Fragment Linking and Optimization of Inhibitors of the Aspartic Protease Endothiapepsin
M Mondal, MY Unver, A Pal, M Bakker, SP Berrier, AKH Hirsch
Chemistry–A European Journal 22 (42), 14826-14830, 2016
322016
UCHL1 as a novel target in breast cancer: emerging insights from cell and chemical biology
M Mondal, D Conole, J Nautiyal, EW Tate
British Journal of Cancer 126 (1), 24-33, 2022
312022
Fighting Malaria: Structure-Guided Discovery of Nonpeptidomimetic Plasmepsin Inhibitors: Miniperspective
AP Huizing, M Mondal, AKH Hirsch
Journal of Medicinal Chemistry 58 (13), 5151-5163, 2015
282015
Recent developments in cell permeable deubiquitinating enzyme activity-based probes
D Conole, M Mondal, JD Majmudar, EW Tate
Frontiers in Chemistry 7, 876, 2019
262019
Strukturbasiertes Design von Hemmstoffen der Aspartylprotease Endothiapepsin mittels dynamischer kombinatorischer Chemie
M Mondal, N Radeva, H Köster, A Park, C Potamitis, M Zervou, G Klebe, ...
Angewandte Chemie 126 (12), 3324-3328, 2014
252014
Fragment growing exploiting dynamic combinatorial chemistry of inhibitors of the aspartic protease endothiapepsin
M Mondal, DE Groothuis, AKH Hirsch
MedChemComm 6 (7), 1267-1271, 2015
232015
Structure-based optimization of inhibitors of the aspartic protease endothiapepsin
AM Hartman, M Mondal, N Radeva, G Klebe, AKH Hirsch
International Journal of Molecular Sciences 16 (8), 19184-19194, 2015
182015
Photochemical Probe Identification of a Small‐Molecule Inhibitor Binding Site in Hedgehog Acyltransferase (HHAT)
T Lanyon‐Hogg, M Ritzefeld, L Zhang, SA Andrei, B Pogranyi, M Mondal, ...
Angewandte Chemie 133 (24), 13654-13659, 2021
162021
Fragmentverknüpfung und‐optimierung von Hemmstoffen der Aspartylprotease Endothiapepsin: Fragmentbasiertes Wirkstoffdesign beschleunigt durch dynamische kombinatorische Chemie
M Mondal, N Radeva, H Fanlo‐Virgós, S Otto, G Klebe, AKH Hirsch
Angewandte Chemie 128 (32), 9569-9574, 2016
152016
Design and synthesis of bioisosteres of acylhydrazones as stable inhibitors of the aspartic protease endothiapepsin
VR Jumde, M Mondal, RM Gierse, MY Unver, F Magari, RCW van Lier, ...
ChemMedChem 13 (21), 2266-2270, 2018
112018
Light-mediated multi-target protein degradation using arylazopyrazole photoswitchable PROTACs (AP-PROTACs)
Q Zhang, CS Kounde, M Mondal, JL Greenfield, JR Baker, S Kotelnikov, ...
Chemical Communications (Cambridge, England) 58 (78), 10933, 2022
102022
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