1567408-63-2

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 176446-62-1 5-(4-methoxyphenyl)dipyrromethane 
• 1350764-72-5 C₁₆H₁₁BBr₂F₂N₂O 
• 171364-79-7 2-(4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 104-92-7 1-bromo-4-methoxy-benzene 

Relevant academic research and scientific papers

Photostable BODIPY-based molecule with simultaneous type i and type II photosensitization for selective photodynamic cancer therapy

We introduce a new class of photostable, efficient photosensitizers based on boron-dipyrromethene (BODIPY) derivatives that can generate singlet oxygen and superoxide simultaneously under irradiation. First, we report the synthesis and design of how to control the generation of a specifically substituted position of BODIPY. Second, after biologically evaluating the uptake, localization and phototoxicity in cell lines, we conclude that 2,6-di-anisole substituted BODIPY is a potentially selective photodynamic therapy candidate because its photodamage is more efficient in cancer cells than in normal cells without significant dark toxicity.