Issue 15, 2022

Photoinduced cytotoxicity of photochromic symmetric diarylethene derivatives: the relation of structure and cytotoxicity

Abstract

Photopharmacology has been attracting attention for the development of drugs with fewer side effects and lower toxicity by introducing a photoswitch structure in the drug and controlling its spatiotemporal effects by light irradiation. Ideally, to achieve precise spatiotemporal control, it is desirable to use photoresponsive molecules that act as anticancer agents based on molecular switch mechanisms at the molecular level. However, very few reports on photoinduced cytotoxicity have used photoresponsive molecules with simple structures. Here, we investigate the photoinduced cytotoxicity of twelve diarylethene derivatives having thiazole or pyridine rings in their molecules and evaluate them in terms of molecular structure and size. Our results provide insight into molecular design principles for diarylethene with a simple structure toward achieving precise control based on molecular-level switch mechanisms.

Graphical abstract: Photoinduced cytotoxicity of photochromic symmetric diarylethene derivatives: the relation of structure and cytotoxicity

Supplementary files

Article information

Article type
Paper
Submitted
02 Feb 2022
Accepted
23 Mar 2022
First published
25 Mar 2022

Org. Biomol. Chem., 2022,20, 3211-3217

Photoinduced cytotoxicity of photochromic symmetric diarylethene derivatives: the relation of structure and cytotoxicity

Y. Nakagawa, T. Hishida, E. Hatano, K. Sumaru, K. Morishita, M. Morimoto, S. Yokojima, S. Nakamura and K. Uchida, Org. Biomol. Chem., 2022, 20, 3211 DOI: 10.1039/D2OB00224H

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