| Literature DB >> 16722624 |
Petr Vachal1, Jeffrey J Hale, Zhe Lu, Eric C Streckfuss, Sander G Mills, Malcolm MacCoss, Daniel H Yin, Kimberly Algayer, Kimberly Manser, Filippos Kesisoglou, Soumojeet Ghosh, Laman L Alani.
Abstract
Alendronate derivatives were evaluated as potential prodrugs for the osteoporosis drug alendronate sodium in an attempt to enhance the systemic exposure after oral administration. An investigation of the chemical behavior of alendronate derivatives led to development of practical synthetic strategies and prediction of each structural class's prodrug potential. Pharmacokinetic studies of N-myristoylalendronic acid revealed that 25% have been converted in vivo after i.v. administration in rat, providing an important proof-of-concept for this strategy.Entities:
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Year: 2006 PMID: 16722624 DOI: 10.1021/jm060398v
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446