Synthesis of novel chlorophyll a derivatives bearing glucose moieties and estimation of their photocytotoxic activity

被引:0
|
作者
Mal'shakova, M. V. [1 ]
Rasova, E. E. [2 ]
Velegzhaninov, I. O. [2 ]
Belykh, D. V. [1 ]
机构
[1] Russian Acad Sci, Inst Chem, Fed Res Ctr Komi Sci Ctr, Ural Branch, 48 Pervomayskaya, Syktyvkar 167000, Russia
[2] Ural Branch Russian Acad Sci, Inst Biol, Fed Res Ctr Komi Sci Ctr, 28 Kommunisticheskaya, Syktyvkar 167982, Russia
关键词
chlorophyll a; methyl pheophorbide a; pheophorbide a; pyropheophorbide a; D-glucose; 1,2:5,6-di-O-isopropylidene-D-glucofuranose; photocytotoxic activity; Mukaiyama reagent; PHOTODYNAMIC THERAPY; CHLORIN DERIVATIVES; NATURAL CHLORINS; D-GALACTOSE; PHOTOSENSITIZERS; PORPHYRINS; CYTOTOXICITY; DIAGNOSTICS; PERIPHERY; FRAGMENT;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of chlorophyll a derivatives bearing glucose moieties linked to the porphyrin macrocycle via ester bonds were synthesized. The dark cytotoxicity and photocytotoxicity of new chlorin-glucose conjugates were competitively evaluated in comparison with those of structurally similar chlorin-galactose derivatives synthesized previously. It was revealed that the introduction of the glucose moiety into the molecule of chlorophyll a derivative facilitates a decrease in the dark cytotoxicity relative to chlorin-galactose conjugates.
引用
收藏
页码:531 / 537
页数:7
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