Themed collection Editor’s Choice Collection

6 items
Open Access Research Article

Antimicrobial triazinedione inhibitors of the translocase MraY–protein E interaction site: synergistic effects with bacitracin imply a new mechanism of action

A set of triazinedione peptidomimetics of an Arg-Trp-x-x-Trp motif found in MraY were found to show antimicrobial activity against antibiotic-resistant clinical isolates, via a novel mechanism of action.

Graphical abstract: Antimicrobial triazinedione inhibitors of the translocase MraY–protein E interaction site: synergistic effects with bacitracin imply a new mechanism of action
From the themed collection: Highlights from Industry
Open Access Research Article

Design and synthesis of cyclic lipidated peptides derived from the C-terminus of Cx43 for hemichannel inhibition and cardiac endothelium targeting

Potent and stable cyclic peptide inhibitors of Cx43 were identified. Their therapeutic potential was enhanced by the addition of a lipid motif (preserving water solubility), and a targeting peptide, for delivery to cardiac endothelial cells.

Graphical abstract: Design and synthesis of cyclic lipidated peptides derived from the C-terminus of Cx43 for hemichannel inhibition and cardiac endothelium targeting
From the themed collection: Editor’s Choice Collection
Open Access Research Article

Novel PROTAC probes targeting KDM3 degradation to eliminate colorectal cancer stem cells through inhibition of Wnt/β-catenin signaling

We designed and synthesized novel IOX1-based PROTACs, which can selectively degrade KDM3A and KDM3B to eliminate colorectal cancer stem cells through inhibition of Wnt signaling.

Graphical abstract: Novel PROTAC probes targeting KDM3 degradation to eliminate colorectal cancer stem cells through inhibition of Wnt/β-catenin signaling
From the themed collection: Induced-Proximity Pharmacology
Open Access Research Article

Identification of lysosomotropism using explainable machine learning and morphological profiling cell painting data

Explainable ML was used to identify important chemical structural properties that contribute to lysosomotropism.

Graphical abstract: Identification of lysosomotropism using explainable machine learning and morphological profiling cell painting data
From the themed collection: AI in Medicinal Chemistry
Open Access Research Article

Live cell screening to identify RNA-binding small molecule inhibitors of the pre-let-7–Lin28 RNA–protein interaction

Dysregulation of the networking of RNA-binding proteins (RBPs) and RNAs drives many human diseases, including cancers, and the targeting of RNA–protein interactions (RPIs) has emerged as an exciting area of RNA-targeted drug discovery.

Graphical abstract: Live cell screening to identify RNA-binding small molecule inhibitors of the pre-let-7–Lin28 RNA–protein interaction
From the themed collection: Highlights from Industry
Open Access Research Article

1,5-Disubstituted tetrazoles as PD-1/PD-L1 antagonists

Utilizing a combination of structure-based design, MCR synthesis, biophysics, and protein crystallography to innovate a novel tetrazole scaffold targeting the PD-1/PD-L1 immune checkpoint protein complex.

Graphical abstract: 1,5-Disubstituted tetrazoles as PD-1/PD-L1 antagonists
From the themed collection: Editor’s Choice Collection
6 items

About this collection

Handpicked by our Editorial Board, the RSC Medicinal Chemistry Editor’s Choice Collection showcases some of the most exciting recent articles published in the journal. 
For extra details on the articles, including comments from the Editorial Board, please visit the RSC Medicinal Chemistry blog at https://blogs.rsc.org/md/.
This collection will be updated regularly with the new articles highlighted, so please keep revisiting this page to see the latest updates.

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