172945-44-7Relevant academic research and scientific papers
Selective Inhibition of Trypanosomal Glyceraldehyde-3-phosphate Dehydrogenase by Protein Structure-Based Design: Toward New Drugs for the Treatment of Sleeping Sickness
Verlinde, Christophe L. M. J.,Callens, Mia,Calenbergh, Serge Van,Aerschot, Arthur Van,Herdewijn, Piet,et al.
, p. 3605 - 3613 (1994)
Within the framework of a project aimed at rational design of drugs against diseases caused by trypanosomes and related hemoflagellate parasites, selective inhibitors of trypanosomal glycolysis were designed, synthesized, and tested.The design was based u
PURINE NUCLEOTIDE DERIVATIVES
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Page/Page column 21; 43, (2010/02/15)
This invention provides novel 8-carbyl substituted cAMPS and a novel procedures for the preparation of 8-Br-cAMP, a key starting material.
Synthesis of novel 2-aryl AICAR derivatives
Kohyama, Naoki,Katashima, Tomoyuki,Yamamoto, Yukio
, p. 2799 - 2804 (2007/10/03)
Novel 2-aryl AICAR (5-Amino-1-β-D-ribofuranosylimidazole-4- carboxamide) derivatives 8 were synthesized via the Suzuki-Miyaura cross-coupling reactions of 8-bromoadenosine. Following conversion of the adenine moiety of 4 to hypoxanthine (5) and the introduction of a MEM group, hydrolysis of 7 gave desired 2-aryl AICAR derivatives 8.
Palladium catalysis in the synthesis of 8-position modified adenosine, 2'- deoxyadenosine and guanosine
Tu,Keane,Eaton
, p. 1631 - 1638 (2007/10/02)
Adenosine and guanosine analogs with 8-position vinyl and aryl groups were prepared by palladium catalyzed cross-coupling of organostannanes with 8- bromopurine nucleosides. The reaction conditions and catalyst composition were improved so that both vinyl
