Synthesis of Hsp90 inhibitor dimers as potential antitumor agents
K Muranaka, A Sano, S Ichikawa, A Matsuda
Index: Muranaka, Kazuhiro; Sano, Akiko; Ichikawa, Satoshi; Matsuda, Akira Bioorganic and Medicinal Chemistry, 2008 , vol. 16, # 11 p. 5862 - 5870
Full Text: HTML
Citation Number: 15
Abstract
Structure-based drug design was used to systematically synthesize PU3-dimers. The cytotoxicity of PU3 dimers 6 against breast cancer cell lines was evaluated, and their potency increased as the length of the bridging linker increased. Among the compounds tested, 6e with a C-20 linker was the most potent and exhibited a 20-to 30-fold increase in activity compared with that of the parent compound 5. Western blot analyses of the cell ...
Related Articles:
[Marino, Joseph P.; Nguyen, Hanh Nho Journal of Organic Chemistry, 2002 , vol. 67, # 18 p. 6291 - 6296]
[Pflieger, D.; Muckensturm, B. Tetrahedron, 1989 , vol. 45, # 7 p. 2031 - 2040]
[Kita, Yasuyuki; Okunaka, Ryuichi; Honda, Takao; Shindo, Miki; Taniguchi, Miyako; et al. Journal of Organic Chemistry, 1991 , vol. 56, # 1 p. 119 - 125]
[Tsujiyama; Ono; Yoshino; Okamoto; Sato Tetrahedron Letters, 1990 , vol. 31, # 31 p. 4481 - 4484]
[Tsujiyama; Ono; Yoshino; Okamoto; Sato Tetrahedron Letters, 1990 , vol. 31, # 31 p. 4481 - 4484]