Towards a glutathione-cleavable azobenzene linker for antibody–drug conjugates
Chemical communications (Cambridge, England)
(2025)
(doi: 10.1039/d5cc05824d)
Recent progress towards catalytic asymmetric construction of inherently chiral scaffolds.
Chemical Society Reviews
(2025)
54
10856
(doi: 10.1039/d5cs00235d)
Exploiting the Cryptic αD Pocket of Casein Kinase 2α (CK2α) to Deliver Highly Potent and Selective Type 1 Inhibitors.
Journal of medicinal chemistry
(2025)
68
21587
(doi: 10.1021/acs.jmedchem.5c01807)
β-Lactamase cleavable antimicrobial peptide-drug conjugates
Chem Sci
(2025)
16
19288
(doi: 10.1039/d5sc06369h)
Development of D-box peptides to inhibit the anaphase-promoting complex/cyclosome
eLife
(2025)
14
RP104238
(doi: 10.7554/elife.104238)
A Dynamic Silver(I) Nanocluster Holds Together a 3 x 3 Self-Assembled Grid
Journal of the American Chemical Society
(2025)
147
30842
(doi: 10.1021/jacs.5c07271)
A Platform for SpyCatcher Conjugation to Native Antibodies
Chem Sci
(2025)
16
10602
(doi: 10.1039/d5sc02286j)
Development of D-box peptides to inhibit the Anaphase Promoting Complex/Cyclosome
(2025)
(doi: 10.7554/elife.104238.2)
Methods for the Generation of Single‐Payload Antibody‐Drug Conjugates
Chemmedchem
(2025)
20
e202500132
(doi: 10.1002/cmdc.202500132)
Pseudomonas aeruginosa acyl-CoA dehydrogenases and structure-guided inversion of their substrate specificity
Nature Communications
(2025)
16
2334
(doi: 10.1038/s41467-025-57532-z)
Pseudomonas aeruginosa PfpI is a methylglyoxalase.
Journal of Biological Chemistry
(2025)
301
108374
(doi: 10.1016/j.jbc.2025.108374)
The 2-methylcitrate cycle and the glyoxylate shunt in Pseudomonas aeruginosa are linked through enzymatic redundancy.
J Biol Chem
(2025)
301
108355
(doi: 10.1016/j.jbc.2025.108355)
Advances in the Release of Amide-Containing Molecules
Chemistry (Weinheim an der Bergstrasse, Germany)
(2025)
31
e202404413
(doi: 10.1002/chem.202404413)
Development of D-box peptides to inhibit the Anaphase Promoting Complex/Cyclosome
(2025)
(doi: 10.7554/elife.104238.1)
MMP-Cleavable Linker Platform for Tumour-Responsive Homo- and Heterobivalent Antibody-Drug Conjugates
Chemical Science
(2025)
(doi: 10.1039/d5sc06664f)
Publisher Correction: Novel immunotherapeutics against LGR5 to target multiple cancer types.
EMBO Molecular Medicine
(2024)
16
3026
(doi: 10.1038/s44321-024-00139-6)
Selective Aurora A‑TPX2 Interaction Inhibitors Have In Vivo Efficacy as Targeted Antimitotic Agents
J Med Chem
(2024)
67
15521
(doi: 10.1021/acs.jmedchem.4c01165)
Novel immunotherapeutics against LGR5 to target multiple cancer types
EMBO molecular medicine
(2024)
16
2583
(doi: 10.1038/s44321-024-00121-2)
Tuneable thiol exchange linkers for traceless drug release applications in prodrugs and ADCs
Chemical communications (Cambridge, England)
(2024)
60
7025
(doi: 10.1039/d4cc01558d)
Towards the Targeted Protein Degradation of PRMT1.
Chemmedchem
(2024)
19
e202400269
(doi: 10.1002/cmdc.202400269)