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  • Deoxyadenosine - Wikipedia
    Deoxyadenosine (symbol dA or dAdo) is a deoxyribonucleoside It is a derivative of the nucleoside adenosine, differing from the latter by the replacement of a hydroxyl group (-OH) by hydrogen (-H) at the 2′ position of its ribose sugar moiety Deoxyadenosine is the DNA nucleoside A, which pairs with deoxythymidine (T) in double-stranded DNA
  • 2-Deoxyadenosine | C10H13N5O3 | CID 13730 - PubChem
    2'-Deoxyadenosine | C10H13N5O3 | CID 13730 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety hazards toxicity information, supplier lists, and more
  • Adenosine vs. Deoxyadenosine - Whats the Difference? | This vs. That
    Adenosine and deoxyadenosine are both nucleosides that play important roles in cellular metabolism Adenosine consists of a purine base (adenine) attached to a ribose sugar molecule, while deoxyadenosine is similar but lacks an oxygen atom in the ribose sugar, making it a deoxyribose sugar
  • Deoxyadenosine - an overview | ScienceDirect Topics
    First, although replicative DNA-synthesis is not important in quiescent lymphocytes, DNA repair synthesis is necessary for survival 2-Chlorodeoxyadenosine is a potent inhibitor of DNA repair in lymphocytes, which progressively accumulate DNA single-strand breaks when exposed to the drug
  • A Comprehensive Overview of 2 Deoxyadenosine - synthorum. com
    2 Deoxyadenosine, often abbreviated as dA, is a derivative of adenosine, lacking an oxygen atom at the 2’ position of the ribose sugar This simple structural alteration gives rise to unique chemical properties that influence its biological roles
  • 5-Deoxyadenosine Metabolism: More than Waste Disposal
    5-Deoxyadenosine (5dAdo) is a by-product of many radical SAM enzyme reactions in all domains of life, and an inhibitor of the radical SAM enzymes themselves Hence, pathways to recycle or dispose of this toxic by-product must exist but remain largely unexplored
  • Deoxyadenosine family: improved synthesis, DNA damage and repair . . .
    Improved synthesis of 2′-deoxyadenosine using Escherichia coli overexpressing some enzymes and gram-scale chemical synthesis of 2′-deoxynucleoside 5′-triphosphates reported recently are described in this review





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