5'-Deoxy-5'-(methylthio)adenosine-d3

CAT:
804-HY-W654139
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For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
5'-Deoxy-5'-(methylthio)adenosine-d3 - image 1

5'-Deoxy-5'-(methylthio)adenosine-d3

  • UNSPSC Description:

    5'-Deoxy-5'-(methylthio)adenosine-d3 is deuterium labeled 5'-Methylthioadenosine. 5'-Methylthioadenosine (5'-(Methylthio)-5'-deoxyadenosine) is a nucleoside generated from S-adenosylmethionine (SAM) during polyamine synthesis[1][2][3]. 5'-Methylthioadenosine suppresses tumors by inhibiting tumor cell proliferation, invasion, and the induction of apoptosis while controlling the inflammatory micro-environments of tumor tissue. 5'-Methylthioadenosine and its associated materials have striking regulatory effects on tumorigenesis.
  • Target Antigen:

    Apoptosis; Endogenous Metabolite; Isotope-Labeled Compounds; Parasite
  • Type:

    Reference compound
  • Related Pathways:

    Anti-infection;Apoptosis;Metabolic Enzyme/Protease;Others
  • Field of Research:

    Metabolic Disease
  • Smiles:

    O[C@H]1[C@H]([C@@H](O[C@@H]1N2C3=C(N=C2)C(N)=NC=N3)CSC([2H])([2H])[2H])O
  • Molecular Weight:

    300.35
  • References & Citations:

    [1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216.|[2]Tang Y, et al. 5'-Methylthioadenosine attenuates ischemia reperfusion injury after liver transplantation in rats. Inflammation. 2014;37(5):1366-1373.|[3]Li Y, et al. 5'-Methylthioadenosine and Cancer: old molecules, new understanding. J Cancer. 2019;10(4):927-936.|[4]Tang B, et al. Specific Targeting of MTAP-Deleted Tumors with a Combination of 2'-Fluoroadenine and 5'-Methylthioadenosine. Cancer Res. 2018;78(15):4386-4395.|[5]Yaofeng Li, et al. 5'-Methylthioadenosine and Cancer: old molecules, new understanding. J Cancer. 2019;10(4):927-936.
  • Shipping Conditions:

    Room temperature
  • Clinical Information:

    No Development Reported
  • CAS Number:

    2699607-01-5