Synthesis and in vitro photodynamic activities of pegylated distyryl boron dipyrromethene derivatives
Research output: Journal Publications and Reviews (RGC: 21, 22, 62) › 21_Publication in refereed journal › peer-review
Author(s)
Detail(s)
Original language | English |
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Pages (from-to) | 3097-3102 |
Journal / Publication | Journal of Medicinal Chemistry |
Volume | 54 |
Issue number | 8 |
Publication status | Published - 28 Apr 2011 |
Externally published | Yes |
Link(s)
Abstract
A series of pegylated distyryl boron dipyrromethenes have been prepared and characterized. Their in vitro photodynamic activities in Tween 80 emulsions have also been investigated against HT29 human colorectal carcinoma cells. The derivative having five triethylene glycol chains (compound 8) exhibits the highest photocytotoxicity with an IC50 as low as 7 nM. It is also localized preferentially in the endoplasmic reticulum of the cells and can induce predominately apoptosis upon illumination. © 2011 American Chemical Society.
Citation Format(s)
Synthesis and in vitro photodynamic activities of pegylated distyryl boron dipyrromethene derivatives. / He, Hui; Lo, Pui-Chi; Yeung, Sin-Lui et al.
In: Journal of Medicinal Chemistry, Vol. 54, No. 8, 28.04.2011, p. 3097-3102.
In: Journal of Medicinal Chemistry, Vol. 54, No. 8, 28.04.2011, p. 3097-3102.
Research output: Journal Publications and Reviews (RGC: 21, 22, 62) › 21_Publication in refereed journal › peer-review