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S-(5′-Adenosyl)-L-methionine iodide_Molecular_structure_CAS_3493-13-8)
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S-(5′-Adenosyl)-L-methionine iodide

Catalog No. A4377 Name Sigma Aldrich
CAS Number 3493-13-8 Website http://www.sigmaaldrich.com
M. F. C15H23IN6O5S Telephone 1-800-521-8956
M. W. 526.34979 Fax
Purity ≥80% (HPLC) Email
Storage Chembase ID: 132357

SYNONYMS

IUPAC name
[(3S)-3-amino-3-carboxypropyl]({[(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl})methylsulfanium iodide
IUPAC Traditional name
SAMe iodide
Synonyms
AdoMet
SAM

DATABASE IDS

MDL Number MFCD00043192
PubChem SID 24890852
Beilstein Number 4120787
EC Number 222-486-5
CAS Number 3493-13-8

PROPERTIES

Biological Source from yeast
Purity ≥80% (HPLC)
Purity ≥80% (spectrophotometric assay)
Shipped in dry ice
Solubility H2O: soluble100 mg/mL
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H317
Personal Protective Equipment Eyeshields, Faceshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
GHS Precautionary statements P280
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Analysis Note
Purity based on UV and HPLC.
Biochem/physiol Actions
Methyl donor; cofactor for enzyme-catalyzed methylations, including catechol O-methyltransferase (COMT) and DNA methyltransferases (DNMT). Although present in all cells, it is concentrated in liver where 85% of all methylation reactions occur. It is also involved in regulating liver function, growth, and response to injury.
Caution
This material is very unstable at room temperature.

REFERENCES