Literature DB >> 7486948

Minireview: nucleotide prodrugs.

R J Jones1, N Bischofberger.   

Abstract

Nucleotides have shown interesting biological activities in a wide variety of antiviral, antiproliferative, immunomodulatory and other biological assays, and they present promising drug candidates. Because of their negative charge(s) nucleotides suffer from some disadvantages which can be successfully overcome by the utilization of nucleotide prodrugs. Nucleotide prodrugs were successfully used to increase oral absorption of nucleotides in vivo. By taking advantage of intracellular triggers (reducing potential, enzyme activity, pH), nucleotide prodrugs can be used in vitro for the intracellular delivery of the nucleotide resulting in enhanced potency and in some cases enhanced selectivity. Nucleotide prodrugs have also been utilized for tissue specific delivery of the nucleotides in vivo resulting in altered selectivity and reduced toxicity. For nucleotide prodrugs, their ultimate intended use is (in most cases) in vivo for the treatment of a disease. Thus, it is important to incorporate adequate assays and design criteria into any prodrug effort. In vivo systems are complicated because of metabolism, excretion and tissue distribution of the prodrug and the parent. Thus, results of in vitro assays have to be interpreted cautiously because they may be unsuitable predictors of the in vivo situation.

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Year:  1995        PMID: 7486948     DOI: 10.1016/0166-3542(95)00011-a

Source DB:  PubMed          Journal:  Antiviral Res        ISSN: 0166-3542            Impact factor:   5.970


  12 in total

1.  Cross-linked polymeric nanogel formulations of 5'-triphosphates of nucleoside analogues: role of the cellular membrane in drug release.

Authors:  Serguei V Vinogradov; Ekta Kohli; Arin D Zeman
Journal:  Mol Pharm       Date:  2005 Nov-Dec       Impact factor: 4.939

2.  MDL 74,968, a new acyclonucleotide analog: activity against human immunodeficiency virus in vitro and in the hu-PBL-SCID.beige mouse model of infection.

Authors:  C G Bridges; D L Taylor; P S Ahmed; T M Brennan; J M Hornsperger; J F Navé; P Casara; A S Tyms
Journal:  Antimicrob Agents Chemother       Date:  1996-05       Impact factor: 5.191

Review 3.  Current recommendations for the treatment of genital herpes.

Authors:  D T Leung; S L Sacks
Journal:  Drugs       Date:  2000-12       Impact factor: 9.546

4.  Stability of alkoxycarbonylamidine prodrugs.

Authors:  Z Shahrokh; E Lee; A G Olivero; R A Matamoros; K D Robarge; A Lee; K J Weise; B K Blackburn; M F Powell
Journal:  Pharm Res       Date:  1998-03       Impact factor: 4.200

5.  Highly potent oxathiin carboxanilide derivatives with efficacy against nonnucleoside reverse transcriptase inhibitor-resistant human immunodeficiency virus isolates.

Authors:  R W Buckheit; M J Snow; V Fliakas-Boltz; T L Kinjerski; J D Russell; L A Pallansch; W G Brouwer; S S Yang
Journal:  Antimicrob Agents Chemother       Date:  1997-04       Impact factor: 5.191

6.  Differential gene expression in human hepatocyte cell lines exposed to the antiretroviral agent zidovudine.

Authors:  Jia-Long Fang; Tao Han; Qiangen Wu; Frederick A Beland; Ching-Wei Chang; Lei Guo; James C Fuscoe
Journal:  Arch Toxicol       Date:  2013-11-30       Impact factor: 5.153

7.  Interference of cell cycle progression by zidovudine and lamivudine in NIH 3T3 cells.

Authors:  Jia-Long Fang; Lynda J McGarrity; Frederick A Beland
Journal:  Mutagenesis       Date:  2008-10-20       Impact factor: 3.000

8.  Long-term exposure to zidovudine delays cell cycle progression, induces apoptosis, and decreases telomerase activity in human hepatocytes.

Authors:  Jia-Long Fang; Frederick A Beland
Journal:  Toxicol Sci       Date:  2009-06-18       Impact factor: 4.849

9.  Synthesis and biological activity of a gemcitabine phosphoramidate prodrug.

Authors:  Weidong Wu; Jennifer Sigmond; Godefridus J Peters; Richard F Borch
Journal:  J Med Chem       Date:  2007-06-29       Impact factor: 7.446

10.  Aryl phosphoramidates of 5-phospho erythronohydroxamic acid, a new class of potent trypanocidal compounds.

Authors:  Gian Filippo Ruda; Pui Ee Wong; Vincent P Alibu; Suzanne Norval; Kevin D Read; Michael P Barrett; Ian H Gilbert
Journal:  J Med Chem       Date:  2010-08-26       Impact factor: 7.446

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