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Home - Products - Membrane Transporter/Ion Channel - Chloride Channel - S-(5'-Adenosyl)-L-methionine tosylate

S-(5'-Adenosyl)-L-methionine tosylate

CAS No. 52248-03-0

S-(5'-Adenosyl)-L-methionine tosylate( —— )

Catalog No. M18717 CAS No. 52248-03-0

S-(5'-Adenosyl)-L-methionine (SAM) is a ubiquitous methyl donor involved in a wide variety of biological reactions, including those mediated by DNA and protein methyltransferases.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    S-(5'-Adenosyl)-L-methionine tosylate
  • Note
    Research use only, not for human use.
  • Brief Description
    S-(5'-Adenosyl)-L-methionine (SAM) is a ubiquitous methyl donor involved in a wide variety of biological reactions, including those mediated by DNA and protein methyltransferases.
  • Description
    S-(5'-Adenosyl)-L-methionine (SAM) is a ubiquitous methyl donor involved in a wide variety of biological reactions, including those mediated by DNA and protein methyltransferases. SAM (tosylate) (SAMe) is a stable salt of SAM that is included in nutritional supplements for oral use. SAMe reportedly ameliorates depression, pain associated with osteoarthritis and fibromyalgia, and liver toxicity.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    Chloride Channel
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    52248-03-0
  • Formula Weight
    570.64
  • Molecular Formula
    C22H30N6O8S2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?H2O : 150 mg/mL (262.86 mM)
  • SMILES
    Cc1ccc(cc1)S([O-])(=O)=O.C[S+](CC[C@H](N)C(O)=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Chiang P. Biological Effects of Inhibitors of S-Adenosylhomocysteine Hydrolase[J]. Pharmacology & Therapeutics, 1998, 77(2):115.
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