Photoredox C(2)-Arylation of Indole- and Tryptophan-Containing Biomolecules
Organic letters
(2024)
26
4065
(doi: 10.1021/acs.orglett.4c01019)
Development of D-box peptides to inhibit the Anaphase Promoting Complex/Cyclosome
(2024)
(doi: 10.1101/2024.04.30.590460)
Unlocking Amides: A General Method for the Self‐Immolative Release of Amide‐Containing Molecules
Angewandte Chemie
(2024)
136
e202402267
(doi: 10.1002/ange.202402267)
Unlocking Amides: A General Method for the Self‐Immolative Release of Amide‐Containing Molecules
Angewandte Chemie (International ed. in English)
(2024)
63
e202402267
(doi: 10.1002/anie.202402267)
CK2 Inhibitors Targeting Inside and Outside the Catalytic Box
Kinases and Phosphatases
(2024)
2
110
Site-selective peptide functionalisation mediated via vinyl-triazine linchpins
Chem Commun (Camb)
(2024)
60
706
(doi: 10.1039/d3cc05213c)
Red-light modulated
ortho
-chloro azobenzene photoswitch for peptide stapling
via
aromatic substitution
RSC Chemical Biology
(2024)
5
49
(doi: 10.1039/d3cb00176h)
A recombinant approach for stapled peptide discovery yields inhibitors of the RAD51 recombinase
Chem Sci
(2023)
14
13915
(doi: 10.1039/d3sc03331g)
Red-light modulated ortho-chloro azobenzene photoswitch for peptide stapling via aromatic substitution.
RSC Chem Biol
(2023)
5
49
(doi: 10.1039/d3cb00176h)
A cell-active cyclic peptide targeting the Nrf2/Keap1 protein-protein interaction
CHEMICAL SCIENCE
(2023)
14
10800
(doi: 10.1039/d3sc04083f)
A cell-active cyclic peptide targeting the Nrf2/Keap1 protein-protein interaction
Chemical Science
(2023)
14
10800
(doi: 10.1039/d3sc04083f)
Disulfide re-bridging reagents for single-payload antibody-drug conjugates.
Chem Commun (Camb)
(2023)
59
9868
(doi: 10.1039/d3cc02980h)
Tryptophan in Multicomponent Petasis Reactions for Peptide Stapling and Late‐Stage Functionalisation
Angewandte Chemie
(2023)
135
e202307782
(doi: 10.1002/ange.202307782)
Tryptophan in Multicomponent Petasis Reactions for Peptide Stapling and Late-Stage Functionalisation
Angewandte Chemie International Edition
(2023)
62
e202307782
(doi: 10.1002/anie.202307782)
Synthesis of sp3-rich heterocyclic frameworks by a divergent synthesis strategy
Organic & Biomolecular Chemistry
(2023)
21
4591
(doi: 10.1039/d3ob00351e)
Identification of macrocyclic peptides which activate bacterial cylindrical proteases.
RSC Medicinal Chemistry
(2023)
14
1186
(doi: 10.1039/d3md00136a)
Development of constrained peptide inhibitors targeting an oncogenic E3 ubiquitin ligase
(2023)
(doi: 10.1101/2023.04.27.535981)
Selective Aurora A-TPX2 interaction inhibitors have in vivo efficacy as targeted anti-mitotic agents
(2023)
(doi: 10.1101/2023.03.22.533679)
A Recombinant Approach For Stapled Peptide Discovery Yields Inhibitors of the RAD51 Recombinase
(2023)
(doi: 10.1101/2023.02.24.529929)
The human proton pump inhibitors inhibit <i>Mycobacterium tuberculosis</i> rifampicin efflux and macrophage-induced rifampicin tolerance.
Proc Natl Acad Sci U S A
(2023)
120
e2215512120
(doi: 10.1073/pnas.2215512120)