65370-90-3Relevant academic research and scientific papers
The first silicon(iv) phthalocyanine-nucleoside conjugates with high photodynamic activity
Shen, Xiao-Min,Zheng, Bi-Yuan,Huang, Xiu-Rong,Wang, Lei,Huang, Jian-Dong
supporting information, p. 10398 - 10403 (2013/07/26)
A series of novel silicon(iv) phthalocyanines conjugated axially with different nucleoside moieties (uridine, 5-methyluridine, cytidine, and 5-N-cytidine derivatives) have been synthesized and evaluated for their photodynamic activities. The uridine-containing compound 1 exhibits the highest photocytotoxicity against HepG2 human hepatocarcinoma cells with an IC 50 value as low as 6 nM, which can be attributed to its high cellular uptake and non-aggregated nature in the biological media. This compound shows high affinity toward the mitochondria of HepG2 cells and causes cell death mainly through apoptosis upon illumination. The result indicates that 1 is a highly promising photosensitizer for photodynamic therapy.
Preparation of Some Derivatives of 5-Azacytidine and 2'-Deoxy-5-azacytidine
Piskala, Alois,Masojidkova, Milena,Saman, David
, p. S23 - S25 (2007/10/03)
Acetylation of 2',3',5'-tri-O-benzoyl-5-azacytidine (3) gave N4-acetyl derivative 4 which was hydrolyzed to the formylamidinourea 5.The same compound was obtained by ribosylation of the silylated triazine 6 and subsequent hydrolysis of the prod
