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Organic & Biomolecular Chemistry|February 28, 2015
Crispene E, a cis-clerodane diterpene inhibits STAT3 dimerization in breast cancer cellsJulia Mantaj, S M Abdur Rahman, Bishwajit Bokshi, et al.Communications Biology|July 29, 2022
DNA sequence-selective G-A cross-linking ADC payloads for use in solid tumour therapiesGeorge Procopiou, Paul J M Jackson, Daniella di Mascio, et al.RSC Medicinal Chemistry|May 12, 2025
A novel DNA sequence-selective, guanine mono-alkylating ADC payload suitable for solid tumour treatmentPaolo Andriollo, Daniella di Mascio, Paul J M Jackson, et al.European Journal of Medicinal Chemistry|October 9, 2025
Synthesis, SAR, and biophysical mechanism of action of cyclopropabenzindole-pyridinobenzodiazepine (CBI-PDD) guanine-adenine DNA cross-linking agentsGeorge Procopiou, Paul J M Jackson, Daniella di Mascio, et al.Bioorganic & Medicinal Chemistry Letters|July 2, 2013
Investigation of the protein alkylation sites of the STAT3:STAT3 inhibitor Stattic by mass spectrometrySibylle Heidelberger, Giovanna Zinzalla, Dyeison Antonow, et al.Journal of Medicinal Chemistry|July 30, 2013
An extended pyrrolobenzodiazepine-polyamide conjugate with selectivity for a DNA sequence containing the ICB2 transcription factor binding siteFederico Brucoli, Rachel M Hawkins, Colin H James, et al.Cancers|April 26, 2020
A Novel Antibody-Drug Conjugate (ADC) Delivering a DNA Mono-Alkylating Payload to Chondroitin Sulfate Proteoglycan (CSPG4)-Expressing MelanomaRicarda M Hoffmann, Silvia Crescioli, Silvia Mele, et al.Journal of Medicinal Chemistry|March 22, 2013
GC-targeted C8-linked pyrrolobenzodiazepine-biaryl conjugates with femtomolar in vitro cytotoxicity and in vivo antitumor activity in mouse modelsKhondaker M Rahman, Paul J M Jackson, Colin H James, et al.Pageof 2