Diarylethene moiety as an enthalpy-entropy switch: Photoisomerizable stapled peptides for modulating p53/MDM2 interaction
Organic & Biomolecular Chemistry
(2020)
18
5359
(doi: 10.1039/d0ob00831a)
C(sp 3 )–H arylation to construct all- syn cyclobutane-based heterobicyclic systems: a novel fragment collection
Chem Commun (Camb)
(2020)
56
7423
(doi: 10.1039/d0cc03237a)
Efficient and selective antibody modification with functionalised divinyltriazines.
Org Biomol Chem
(2020)
18
4739
(doi: 10.1039/d0ob01002b)
General dual functionalisation of biomacromolecules via a cysteine bridging strategy
Organic & Biomolecular Chemistry
(2020)
18
4224
(doi: 10.1039/d0ob00907e)
Fsp3-rich and diverse fragments inspired by natural products as a collection to enhance fragment-based drug discovery.
Chemical Communications
(2020)
56
2280
(doi: 10.1039/c9cc09796a)
Development of a Novel Cell-Permeable Protein-Protein Interaction Inhibitor for the Polo-box Domain of Polo-like Kinase 1
ACS omega
(2019)
5
822
(doi: 10.1021/acsomega.9b03626)
A cryptic hydrophobic pocket in the polo-box domain of the polo-like kinase PLK1 regulates substrate recognition and mitotic chromosome segregation.
Sci Rep
(2019)
9
15930
(doi: 10.1038/s41598-019-50702-2)
A cryptic hydrophobic pocket in the polo-box domain of the polo-like kinase PLK1 regulates substrate recognition and mitotic chromosome segregation
Scientific Reports
(2019)
9
(doi: 10.1038/s41598-019-50702-2)
Direct Synthesis of N-Functionalized Dipropargylamine Linkers as Models for Use in Peptide Stapling
Synlett
(2019)
30
2153
(doi: 10.1055/s-0039-1690217)
Cycloaddition Strategies for the Synthesis of Diverse Heterocyclic Spirocycles for Fragment-Based Drug Discovery.
European J Org Chem
(2019)
2019
5219
(doi: 10.1002/ejoc.201900847)
Hotspots API: A toolkit for the application of Fragment Hotspot Mapping to Structure Based Drug Discovery
Acta Crystallographica Section A Foundations and Advances
(2019)
75
A227
(doi: 10.1107/S0108767319097782)
Macrocyclisation and functionalisation of unprotected peptides via divinyltriazine cysteine stapling
Chem Commun (Camb)
(2019)
55
9499
(doi: 10.1039/c9cc05042f)
Targeted covalent inhibitors of MDM2 using electrophile-bearing stapled peptides.
Chemical communications (Cambridge, England)
(2019)
55
7914
(doi: 10.1039/C9CC04022F)
Strategies for the Diversity-Oriented Synthesis of Macrocycles.
Chemical Reviews
(2019)
119
10288
(doi: 10.1021/acs.chemrev.9b00084)
Cleavable linkers in antibody–drug conjugates
Chemical Society Reviews
(2019)
48
4361
(doi: 10.1039/c8cs00676h)
Spirocycles as Rigidified sp3-Rich Scaffolds for a Fragment Collection.
Org Lett
(2019)
21
4600
(doi: 10.1021/acs.orglett.9b01499)
Efficient development of stable and highly functionalised peptides targeting the CK2α/CK2β protein–protein interaction
Chemical Science
(2019)
10
5056
(doi: 10.1039/c9sc00798a)
Toolbox of Diverse Linkers for Navigating the Cellular Efficacy Landscape of Stapled Peptides
ACS chemical biology
(2019)
14
526
(doi: 10.1021/acschembio.9b00063)
Synthesis and Reactivity of a Bis-Strained Alkyne Derived from 1,1'-Biphenyl-2,2',6,6'-tetrol.
ACS Omega
(2019)
4
2160
(doi: 10.1021/acsomega.8b03634)
A general approach for the site-selective modification of native proteins, enabling the generation of stable and functional antibody-drug conjugates (vol 10, 2019)
Chem Sci
(2019)
10
633
(doi: 10.1039/c8sc90248h)