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ro 24-5098 and dideoxyadenosine

ro 24-5098 has been researched along with dideoxyadenosine in 6 studies

*Dideoxyadenosine: A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by a hydrogen.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. [MeSH]

*Dideoxyadenosine: A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by a hydrogen.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. [MeSH]

Compound Research Comparison

Studies
(ro 24-5098)
Trials
(ro 24-5098)
Recent Studies (post-2010)
(ro 24-5098)
Studies
(dideoxyadenosine)
Trials
(dideoxyadenosine)
Recent Studies (post-2010) (dideoxyadenosine)
800422138

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's5 (83.33)18.2507
2000's1 (16.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Anderson, BD; Broder, S; Huryn, DM; Mitsuya, H; Sim, I; Sluboski, BC; Tam, SY; Weigele, M1
Connell, EV; Frank, KB; Holman, MJ; Huryn, DM; Mitsuya, H; Richman, DD; Sluboski, BC; Tam, SY; Todaro, LJ; Weigele, M1
abu Sheikha, G; Cappellacci, L; de Montis, A; Franchetti, P; Grifantini, M; La Colla, P; Loi, AG; Messini, L; Spiga, MG; Tramontano, E1
Boone, LR; Dornsife, RE; Hazen, RJ; Krasny, HC; Nair, V; Najera, I; Paff, MT; Reardon, JE; St Clair, MH; Tisdale, M1
Cappellacci, L; Franchetti, P; Girardet, JL; Gosselin, G; Grifantini, M; Imbach, JL; La Colla, P; Loi, AG; PĂ©rigaud, C; Pompon, A; Valette, G1
Nair, V; Pal, S1

Reviews

1 review(s) available for ro 24-5098 and dideoxyadenosine

ArticleYear
Anabolism and mechanism of action of Ro24-5098, an isomer of 2',3'-dideoxyadenosine (ddA) with anti-HIV activity.
    Annals of the New York Academy of Sciences, 1990, Volume: 616

    Topics: Antiviral Agents; Dideoxyadenosine; HIV; Humans; Isomerism; Reverse Transcriptase Inhibitors

1990

Other Studies

5 other study(ies) available for ro 24-5098 and dideoxyadenosine

ArticleYear
Synthesis and anti-HIV activity of isonucleosides.
    Journal of medicinal chemistry, 1992, Jun-26, Volume: 35, Issue:13

    Topics: Antiviral Agents; Cells, Cultured; Chromatography, Liquid; Dideoxynucleosides; Drug Stability; Gene Products, gag; HIV-1; Humans; Isomerism; Monocytes; Spectrum Analysis; Virus Replication

1992
Synthesis and evaluation of the anti-HIV activity of aza and deaza analogues of isoddA and their phosphates as prodrugs.
    Journal of medicinal chemistry, 1994, Oct-14, Volume: 37, Issue:21

    Topics: Adenosine Triphosphate; Antiviral Agents; Aza Compounds; Dideoxyadenosine; Dideoxynucleotides; HIV Reverse Transcriptase; HIV-1; HIV-2; Molecular Structure; Phosphates; Recombinant Proteins; Reverse Transcriptase Inhibitors

1994
Antiviral, metabolic, and pharmacokinetic properties of the isomeric dideoxynucleoside 4(S)-(6-amino-9H-purin-9-yl)tetrahydro-2(S)-furanmethanol.
    Antimicrobial agents and chemotherapy, 1995, Volume: 39, Issue:9

    Topics: Adenosine Deaminase; Animals; Antibody-Dependent Cell Cytotoxicity; Antiviral Agents; Cells, Cultured; Dideoxyadenosine; DNA, Viral; Drug Resistance, Microbial; Erythroid Precursor Cells; Hepatitis B virus; HIV-1; HIV-2; Humans; Nucleic Acid Synthesis Inhibitors; Phosphorylation; Polymerase Chain Reaction; Rats; Viral Plaque Assay

1995
Decomposition pathways and in vitro HIV inhibitory effects of isoddA pronucleotides: toward a rational approach for intracellular delivery of nucleoside 5'-monophosphates.
    Journal of medicinal chemistry, 1996, May-10, Volume: 39, Issue:10

    Topics: Cell Line; Dideoxyadenosine; HIV-1; HIV-2; Humans; Kinetics; Magnetic Resonance Spectroscopy; Nucleotides; Spectrometry, Mass, Fast Atom Bombardment

1996
Phosphorylation of the anti-HIV compound (S,S)-isodideoxyadenosine by human recombinant deoxycytidine kinase.
    Biochemical pharmacology, 2000, Nov-15, Volume: 60, Issue:10

    Topics: Animals; Anti-HIV Agents; Cattle; Deoxycytidine Kinase; Dideoxyadenosine; Humans; Liver; Phosphorylation; Recombinant Proteins

2000