| Weight | 399.453 g/mol |
|---|---|
| Formula | C15H23N6O5S+ |
| Hydrogen Acceptors | 10 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 7 |
S-adenosylmethionine (29908-03-0)
AdoMet · Ademetionine · SAM-e
Score:
#817 in Biochemistry
,
#2204 in Biology
,
#2709 in Chemistry
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- Sigma-Aldrich - Search for S-adenosylmethionine
- Fisher Scientific - Search for S-adenosylmethionine
- TCI - Search for S-adenosylmethionine
- AdoMet-dependent methylation, DNA methyltransferases and base flipping (Nucleic Acids Research, 2001)
- Universal catalytic domain structure of AdoMet-dependent methyltransferases (Journal of Molecular Biology, 1995)
- Purification and cDNA cloning of the AdoMet-binding subunit of the human mRNA (N6-adenosine)-methyltransferase. (RNA, 1997)
- The Clinical Potential of Ademetionine (S-Adenosylmethionine) in Neurological Disorders (Drugs, 1994)
- Structure and evolution of AdoMet-dependent methyltransferase. (1999)
- Mechanism of histone lysine methyl transfer revealed by the structure of SET7/9-AdoMet (The EMBO Journal, 2003)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - AdoMet
- Ademetionine
- SAM-e
- S Amet
- S-Adenosyl-L-Methionine
- FO-1561
- S Adenosyl L Methionine
- FO 1561
- S Adenosylmethionine
- Samyr
- S-Adenosylmethionine Sulfate Tosylate
- S Adenosylmethionine Sulfate Tosylate
- FO1561
- Gumbaral
-
SMILESC[S+](CCC(C(=O)O)N)CC1C(C(C(O1)N2C=NC3=C2N=CN=C3N)O)O
-
InChIKeyMEFKEPWMEQBLKI-UHFFFAOYSA-O
- Pubchem - S-adenosylmethionine
- Wikipedia - S-Adenosylmethionine
S-Adenosyl methionine is a common cosubstrate involved in methyl group transfers, transsulfuration, and aminopropylation. Although these anabolic reactions occur throughout the body, most SAM-e is produced and consumed in the liver. More than 40 methyl transfers from SAM-e are known, to various substrates such as nucleic acids, proteins, lipids and secondary metabolites.
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