In vitro and in vivo evaluation of 6-azido-2',3'-dideoxy-2'-fluoro-beta-D-arabinofuranosylpurine and N6-methyl-2',3'-dideoxy-2'-fluoro-beta-D-arabinofuranosyladenine as prodrugs of the anti-HIV nucleosides 2'-F-ara-ddA and 2'-F-ara-ddI. 1996

T Koudriakova, and K K Manouilov, and K Shanmuganathan, and L P Kotra, and F D Boudinot, and E Cretton-Scott, and J P Sommadossi, and R F Schinazi, and C K Chu
Department of Medicinal Chemistry and Pharmaceutics, College of Pharmacy, University of Georgia, Athens 30602-2352, USA.

In an effort to improve the pharmacokinetic properties and tissue distribution of 2'-F-ara-ddI, two lipophilic prodrugs, 6-azido-2'-3'-dideoxy-2'-fluoro-beta-D- arabinofuranosylpurine (FAAddP, 4) and N6-methyl-2'-3'-dideoxy-2'-fluoro-beta-D-arabinofuranosyladenine (FMAddA, 5), were synthesized and their biotransformation was investigated in vitro and in vivo, in mice. Compounds 4 and 5 were synthesized via the intermediate 2. For the in vitro studies, FAAddP and FMAddA were incubated in mouse serum, liver homogenate, and brain homogenate. FAAddP was metabolized in liver homogenate by the reduction of the azido to the amino moiety followed by deamination, yielding 2'-F-ara-ddI. The conversion of FAAddP to 2'-F-ara-ddA was mediated by microsomal P-450 NADPH reductase system, as shown by the liver microsomal assay. FAAddP was also converted to 2'-F-ara-ddI at a slower rate in the brain than in the liver. FMAddA, however, was stable in brain homogenate and was slowly metabolized in the liver homogenate. Metabolic conversion of FMAddA in vitro was stimulated by the addition of adenosine deaminase. In the in vivo metabolism study, FAAddP underwent reduction to 2'-F-ara-ddA followed by deamination to 2'-F-ara-ddI. FMAddA did not result in increased brain delivery of 2'-F-ara-ddI in vivo, probably due to the slow conversion as observed in the in vitro studies. However, there was an increase in the half-life of 2'-F-ara-ddI produced from FMAddA. This report is the first example in the design of prodrugs using the azido group for adenine- and hypoxanthine-containing nucleosides. This interesting and novel approach can be extended to other antiviral and anticancer nucleosides.

UI MeSH Term Description Entries
D008862 Microsomes, Liver Closed vesicles of fragmented endoplasmic reticulum created when liver cells or tissue are disrupted by homogenization. They may be smooth or rough. Liver Microsomes,Liver Microsome,Microsome, Liver
D009682 Magnetic Resonance Spectroscopy Spectroscopic method of measuring the magnetic moment of elementary particles such as atomic nuclei, protons or electrons. It is employed in clinical applications such as NMR Tomography (MAGNETIC RESONANCE IMAGING). In Vivo NMR Spectroscopy,MR Spectroscopy,Magnetic Resonance,NMR Spectroscopy,NMR Spectroscopy, In Vivo,Nuclear Magnetic Resonance,Spectroscopy, Magnetic Resonance,Spectroscopy, NMR,Spectroscopy, Nuclear Magnetic Resonance,Magnetic Resonance Spectroscopies,Magnetic Resonance, Nuclear,NMR Spectroscopies,Resonance Spectroscopy, Magnetic,Resonance, Magnetic,Resonance, Nuclear Magnetic,Spectroscopies, NMR,Spectroscopy, MR
D011355 Prodrugs A compound that, on administration, must undergo chemical conversion by metabolic processes before becoming the pharmacologically active drug for which it is a prodrug. Drug Precursor,Drug Precursors,Pro-Drug,Prodrug,Pro-Drugs,Precursor, Drug,Precursors, Drug,Pro Drug,Pro Drugs
D005260 Female Females
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001386 Azides Organic or inorganic compounds that contain the -N3 group. Azide
D001711 Biotransformation The chemical alteration of an exogenous substance by or in a biological system. The alteration may inactivate the compound or it may result in the production of an active metabolite of an inactive parent compound. The alterations may be divided into METABOLIC DETOXICATION, PHASE I and METABOLIC DETOXICATION, PHASE II.
D013056 Spectrophotometry, Ultraviolet Determination of the spectra of ultraviolet absorption by specific molecules in gases or liquids, for example Cl2, SO2, NO2, CS2, ozone, mercury vapor, and various unsaturated compounds. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed) Ultraviolet Spectrophotometry
D014740 Vidarabine A nucleoside antibiotic isolated from Streptomyces antibioticus. It has some antineoplastic properties and has broad spectrum activity against DNA viruses in cell cultures and significant antiviral activity against infections caused by a variety of viruses such as the herpes viruses, the VACCINIA VIRUS and varicella zoster virus. Adenine Arabinoside,Ara-A,Arabinofuranosyladenine,Arabinosyladenine,9-beta-Arabinofuranosyladenine,9-beta-D-Arabinofuranosyladenine,Ara A,Vira-A,alpha-Ara A,alpha-D-Arabinofuranosyladenine,beta-Ara A,9 beta Arabinofuranosyladenine,9 beta D Arabinofuranosyladenine,Arabinoside, Adenine,Vira A,ViraA,alpha Ara A,alpha D Arabinofuranosyladenine,beta Ara A
D016048 Dideoxyadenosine A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by a hydrogen. This modification prevents the formation of phosphodiester linkages which are needed for the completion of nucleic acid chains. The compound is an inhibitor of HIV replication, acting as a chain-terminator of viral DNA by binding to reverse transcriptase. Its principal side effect is nephrotoxicity. In vivo, dideoxyadenosine is rapidly metabolized to DIDANOSINE (ddI) by enzymatic deamination; ddI is then converted to dideoxyinosine monophosphate and ultimately to dideoxyadenosine triphosphate, the putative active metabolite. 2',3'-Dideoxyadenosine,ddA (Antiviral),2',3' Dideoxyadenosine

Related Publications

T Koudriakova, and K K Manouilov, and K Shanmuganathan, and L P Kotra, and F D Boudinot, and E Cretton-Scott, and J P Sommadossi, and R F Schinazi, and C K Chu
July 1990, Journal of medicinal chemistry,
T Koudriakova, and K K Manouilov, and K Shanmuganathan, and L P Kotra, and F D Boudinot, and E Cretton-Scott, and J P Sommadossi, and R F Schinazi, and C K Chu
January 2005, Nucleosides, nucleotides & nucleic acids,
T Koudriakova, and K K Manouilov, and K Shanmuganathan, and L P Kotra, and F D Boudinot, and E Cretton-Scott, and J P Sommadossi, and R F Schinazi, and C K Chu
January 2003, Nucleosides, nucleotides & nucleic acids,
T Koudriakova, and K K Manouilov, and K Shanmuganathan, and L P Kotra, and F D Boudinot, and E Cretton-Scott, and J P Sommadossi, and R F Schinazi, and C K Chu
April 2007, Journal of medicinal chemistry,
T Koudriakova, and K K Manouilov, and K Shanmuganathan, and L P Kotra, and F D Boudinot, and E Cretton-Scott, and J P Sommadossi, and R F Schinazi, and C K Chu
July 2000, Nucleosides, nucleotides & nucleic acids,
T Koudriakova, and K K Manouilov, and K Shanmuganathan, and L P Kotra, and F D Boudinot, and E Cretton-Scott, and J P Sommadossi, and R F Schinazi, and C K Chu
April 1995, Bioorganic & medicinal chemistry,
T Koudriakova, and K K Manouilov, and K Shanmuganathan, and L P Kotra, and F D Boudinot, and E Cretton-Scott, and J P Sommadossi, and R F Schinazi, and C K Chu
January 2001, Nucleosides, nucleotides & nucleic acids,
T Koudriakova, and K K Manouilov, and K Shanmuganathan, and L P Kotra, and F D Boudinot, and E Cretton-Scott, and J P Sommadossi, and R F Schinazi, and C K Chu
June 2004, Journal of medicinal chemistry,
T Koudriakova, and K K Manouilov, and K Shanmuganathan, and L P Kotra, and F D Boudinot, and E Cretton-Scott, and J P Sommadossi, and R F Schinazi, and C K Chu
November 1999, Bioorganic & medicinal chemistry,
T Koudriakova, and K K Manouilov, and K Shanmuganathan, and L P Kotra, and F D Boudinot, and E Cretton-Scott, and J P Sommadossi, and R F Schinazi, and C K Chu
January 2014, Nucleosides, nucleotides & nucleic acids,
Copied contents to your clipboard!