Triazole pyrimidine nucleosides as inhibitors of Ribonuclease A. Synthesis, biochemical, and structural evaluation

V Parmenopoulou, DSM Chatzileontiadou…

文献索引：Bioorganic and Medicinal Chemistry, , vol. 20, # 24 p. 7184 - 7193

被引用次数: 13

摘要

... Bioorganic & Medicinal Chemistry. ... b Institute of Biology, Medicinal Chemistry & Biotechnology, National Hellenic Research Foundation, 48 Vas. ... Therefore, these proteins are pharmaceutical targets for the rational design of specific inhibitors to suppress their activity and hence ...

Mild, versatile, and chemoselective indium (III) triflate-ca...

[Golden, Kathryn C.; Gregg, Brian T.; Quinn, John F. Tetrahedron Letters, 2010 , vol. 51, # 31 p. 4010 - 4013]

Simple method for fast deprotection of nucleosides by trieth...

[Meier, Lidiane; Monteiro, Gustavo C.; Baldissera, Rodrigo A.M.; Sa, Marcus Mandolesi Journal of the Brazilian Chemical Society, 2010 , vol. 21, # 5 p. 859 - 866]

A catalytic method for chemoselective detritylation of 5′-tr...

[Khalafi-Nezhad, Ali; Parhami, Abolfath; Soltani Rad, Mohammad Navid; Zolfigol, Mohammad Ali; Zare, Abdolkarim Tetrahedron Letters, 2007 , vol. 48, # 30 p. 5219 - 5222]

Highly efficient synthesis of 2′, 3′-didehydro-2′, 3′-dideox...

[Robles, Rafael; Rodriguez, Concepcion; Alvarez De Cienfuegos, Luis; Mota, Antonio J. Tetrahedron Asymmetry, 2004 , vol. 15, # 5 p. 831 - 838]

Methoxyethoxymethyl group for the protection of uracil resid...

[Takaku, Hiroshi; Ueda, Souichi; Ito, Tsunehiko Tetrahedron Letters, 1983 , vol. 24, # 48 p. 5363 - 5366]