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40 Years of Duocarmycins: A Graphical Structure/Function Review of Their Chemical Evolution, from SAR to Prodrugs and ADCs

[Image: see text] Synthetic analogues of the DNA-alkylating cytotoxins of the duocarmycin class have been extensively investigated in the past 40 years, driven by their high potency, their unusual mechanism of bioactivity, and the beautiful modularity of their structure–activity relationship (SAR)....

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Detalles Bibliográficos
Autores principales: Felber, Jan G., Thorn-Seshold, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795467/
https://www.ncbi.nlm.nih.gov/pubmed/36590260
http://dx.doi.org/10.1021/jacsau.2c00448

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