Acyclic Nucleoside Phosphonates as Potential Antineoplastic Agents
Authors:
I. Votruba 1; B. Otová 2; A. Holý 1
Authors place of work:
Ústav organické chemie a biochemie, v. v. i., AV ČR, Praha
1; Ústav biologie a lékařské genetiky 1. LF UK a VFN, Praha
2
Published in the journal:
Čas. Lék. čes. 2008; 147: 471-477
Category:
Review Article
Summary
Recently, Gilead Sciences (Foster City, CA, USA) presented a potential cytostatic drug GS-9219. It is a novel lipophilic prodrug of cyprPMEDAP, in vivo releasing the active compound PMEG in a two-step process. GS-9219 has shown a substantial therapeutic potential in treatment of spontaneous non-Hodgkin’s lymphoma in dogs and its utilization in the human medicine is prospective. Hence, cyprPMEDAP represents a key intermediate in the intracellular activation of GS-9219. Both acyclic nucleoside phosphonates PMEG and cyprPMEDAP, serving as the basis for development of GS-9219, were discovered and their mechanism of action was investigated in detail at the Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic. The biological studies using the rat lymphoma were carried out at the First Faculty of Medicine, Charles University.
Key words:
PMEG, GS-9219, non-Hodgkin lymphoma.
Zdroje
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