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ChemicalBook--->CAS DataBase List--->3493-13-8

3493-13-8

3493-13-8 Structure

3493-13-8 Structure
IdentificationBack Directory
[Name]

S-ADENOSYL-L-METHIONINE IODIDE SALT
[CAS]

3493-13-8
[Synonyms]

SAM-I
adomet
AdoMet, SAM
SAM iodide salt
SAM-E IODIDE SALT
S-adenosylmethione
S-ADENOSYLMETHIONINE IODIDE
S-ADENOSYL-L-METHIONINE IODIDE
S-ADENOSYL METHIONINE IODIDE SALT
S-(5'-ADENOSYL)-L-METHIONINE IODIDE
S-ADENOSYL-L-METHIONINE IODIDE SALT
ADENOSYL-L-METHIONINE, S-IODIDE SALT
ADENOSYL-L-METHIONINE IODIDE, S-(RG)
S-(5'-deoxy-5'-adenosyl)methionine iodide
S-ADENOSYL-L-METHIONINE IODIDE SALT USP/EP/BP
S-(5′-Adenosyl)-L-Methionine iodide froM yeast
S-(5'-Adenosyl)-L-methionine iodide;SAM iodide salt
5'-[[(3S)-3-Amino-3-carboxypropyl]methylsulfonio]-5'-deoxy-Adenosine iodide
(3S)-5'-((3-amino-3-carboxypropyl)methylsulphonio)-5'-deoxyadenosine iodide
S-(5'-Adenosyl)-L-methionine iodide >=80% (HPLC), >=80% (spectrophotometric assay)
(3-amino-4-hydroxy-4-oxobutyl)-[[5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl]-methylsulfanium iodide
[5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methyl-(3-azanyl-4-hydroxy-4-oxo-butyl)-methyl-sulfanium iodide
(5-adenin-9-yl-3,4-dihydroxy-tetrahydrofuran-2-yl)methyl-(3-amino-4-hydroxy-4-keto-butyl)-methyl-sulfonium iodide
[EINECS(EC#)]

222-486-5
[Molecular Formula]

C15H23IN6O5S
[MDL Number]

MFCD00043192
[MOL File]

3493-13-8.mol
[Molecular Weight]

526.35
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
[solubility ]

H2O: 100 mg/mL
[form ]

powder
[color ]

white to off-white
[Water Solubility ]

H2O: 100mg/mL
[BRN ]

4120787
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H317
[Precautionary statements ]

P261-P272-P280-P302+P352-P333+P313-P362+P364
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

22-24/25-36-26
[WGK Germany ]

3
[F ]

8-10-23
Hazard InformationBack Directory
[Uses]

S-(5′-Adenosyl)-L-methionine (SAM, AdoMet) is used as a primary methyl donor molecule in mammalian cell culture and the first step metabolite in methionine biosynthesis.
[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.
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