S-ADENOSYL-L-METHIONINE IODIDE SALT Chemical Properties

storage temp. 

-20°C

solubility 

H₂O: 100 mg/mL

BRN 

4120787

Safety Information

Hazard Codes 

Xi

Risk Statements 

36/37/38

Safety Statements 

22-24/25-36-26

WGK Germany 

3

F 

8-10-23

MSDS

• Language:English Provider:SigmaAldrich

S-ADENOSYL-L-METHIONINE IODIDE SALT Usage And Synthesis

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.

S-ADENOSYL-L-METHIONINE IODIDE SALT(3493-13-8)Related Product Information

• S-ADENOSYL-L-METHIONINE P-TOLUENESULFONATE SALT
• S-ADENOSYL-L-METHIONINE
• S-ADENOSYL-L-METHIONINE CHLORIDE SALT
• S-Adenosyl-L-methionine
• S-ADENOSYL-L-METHIONINE DISULFATE TOSYLATE USP/EP/BP
• S-ADENOSYL-L-METHIONINE IODIDE SALT
• Adenosine
• L-Methionine
• DL-ETHIONINE
• D,L-BUTHIONINE
• 5'-DEOXY-5'-METHYLTHIOADENOSINE
• 3-Mercapto-1,2-propanediol
• L-ETHIONINE
• Trimethylsulfonium iodide
• 5'-DEOXY-S-ADENOSYL-L-HOMOCYSTEINE
• 3-METHYLTHIO-1,2-PROPANEDIOL
• L-BUTHIONINE
• 2-(BUTYLTHIO)ETHANOL