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Details

Stereochemistry ABSOLUTE
Molecular Formula C15H22N6O5S
Molecular Weight 398.437
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ADEMETIONINE, (R)-

SMILES

C[S@+](CC[C@H](N)C([O-])=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)N2C=NC3=C2N=CN=C3N

InChI

InChIKey=MEFKEPWMEQBLKI-TYYLHDHTSA-N
InChI=1S/C15H22N6O5S/c1-27(3-2-7(16)15(24)25)4-8-10(22)11(23)14(26-8)21-6-20-9-12(17)18-5-19-13(9)21/h5-8,10-11,14,22-23H,2-4,16H2,1H3,(H2-,17,18,19,24,25)/t7-,8+,10+,11+,14+,27+/m0/s1

HIDE SMILES / InChI

Molecular Formula C15H22N6O5S
Molecular Weight 398.437
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including http://depressionet.com.au/articles/same.pdf http://umm.edu/health/medical/altmed/supplement/sadenosylmethionine https://www.ncbi.nlm.nih.gov/pubmed/?term=22659519

S-Adenosylmethionine (often referred to as SAMe) is a methyl donor and a 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. SAM is anti-apoptotic in normal hepatocytes and normal colon epithelial cells but pro-apoptotic in liver human hepatocellular carcinoma (HCC), HepG2 cells and colon cancer cells. Because of structural instability, stable salt forms of SAM are required for its use as an oral drug. The commonly used salts: tosylate, butanedisulfonate, disulfate tosylate, disulfate ditosylate, and disulfate monotosylate. SAMe has been marketed in some European countries since the mid-1980s for the treatment of depression and for other medical conditions such as osteoarthritis (joint disease that causes joint pain and stiffness), fibromyalgia (widespread pain and stiffness). In addition, it is used to treat liver disease and migraine headaches. However, it is not formally approved in the UK for the treatment of depression, and in the USA, it is classified only as a dietary supplement. Some research suggests that it is more effective than placebo in treating mild-to-moderate depression and is just as effective as antidepressant medications without the side effects (headaches, sleeplessness, and sexual dysfunction). In addition, antidepressants tend to take 6 to 8 weeks to begin working, while It seems to begin more quickly. Researchers are not sure how SAMe works to relieve depression. But they speculate it might increase the amount of serotonin in the brain just as some antidepressants do. Many studies have examined injectable forms of SAMe, not oral supplements.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Palliative
Unknown

Approved Use

Unknown
Palliative
Unknown

Approved Use

Unknown
Palliative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Arsenic trioxide attenuates the invasion potential of human liver cancer cells through the demethylation-activated microRNA-491.
2014-06-05
The role of catechol-O-methyltransferase in catechol-enhanced erythroid differentiation of K562 cells.
2013-12-15
Alterations in hepatic metabolism of sulfur amino acids in non-obese type-2 diabetic Goto-Kakizaki rats.
2013-07-05
Wilson's disease: changes in methionine metabolism and inflammation affect global DNA methylation in early liver disease.
2013-02
Novel protective mechanisms for S-adenosyl-L-methionine against acetaminophen hepatotoxicity: improvement of key antioxidant enzymatic function.
2012-08-03
Arsenic induces functional re-expression of estrogen receptor α by demethylation of DNA in estrogen receptor-negative human breast cancer.
2012
S-adenosylmethionine decreases lipopolysaccharide-induced phosphodiesterase 4B2 and attenuates tumor necrosis factor expression via cAMP/protein kinase A pathway.
2011-05
Temporal study of acetaminophen (APAP) and S-adenosyl-L-methionine (SAMe) effects on subcellular hepatic SAMe levels and methionine adenosyltransferase (MAT) expression and activity.
2010-08-15
Methotrexate-induced myelopathy responsive to substitution of multiple folate metabolites.
2010-05
Induction of avian musculoaponeurotic fibrosarcoma proteins by toxic bile acid inhibits expression of glutathione synthetic enzymes and contributes to cholestatic liver injury in mice.
2010-04
Effects of salvianolic acids on oxidative stress and hepatic fibrosis in rats.
2010-01-15
Mthfd1 is an essential gene in mice and alters biomarkers of impaired one-carbon metabolism.
2009-01-16
Efficacy of methylcobalamin and folinic acid treatment on glutathione redox status in children with autism.
2009-01
Improvement of aggressive behavior and quality of life impairment following S-adenosyl-methionine (SAM-e) augmentation in schizophrenia.
2009-01
Melatonin exerts a more potent effect than S-adenosyl-l-methionine against iron metabolism disturbances, oxidative stress and tissue injury induced by obstructive jaundice in rats.
2008-07-30
Nonsurgical resolution of gallbladder mucocele in two dogs.
2008-06-01
Ethanol inhibits methionine adenosyltransferase II activity and S-adenosylmethionine biosynthesis and enhances caspase-3-dependent cell death in T lymphocytes: relevance to alcohol-induced immunosuppression.
2008-06
Betaine-homocysteine S-methyltransferase-2 is an S-methylmethionine-homocysteine methyltransferase.
2008-04-04
Comparison of S-adenosyl-L-methionine (SAMe) and N-acetylcysteine (NAC) protective effects on hepatic damage when administered after acetaminophen overdose.
2008-02-03
S-adenosylmethionine prevents Mallory Denk body formation in drug-primed mice by inhibiting the epigenetic memory.
2008-02
Protein interactions in the human methionine synthase-methionine synthase reductase complex and implications for the mechanism of enzyme reactivation.
2007-06-12
Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism.
2006-12-05
DLPC and SAMe prevent alpha1(I) collagen mRNA up-regulation in human hepatic stellate cells, whether caused by leptin or menadione.
2006-11-10
Tolcapone decreases plasma levels of S-adenosyl-L-homocysteine and homocysteine in treated Parkinson's disease patients.
2006-06
S-adenosylmethionine blocks collagen I production by preventing transforming growth factor-beta induction of the COL1A2 promoter.
2005-09-02
Inhibition of CYP2E1 catalytic activity in vitro by S-adenosyl-L-methionine.
2005-04-01
Folate transport gene inactivation in mice increases sensitivity to colon carcinogenesis.
2005-02-01
S-adenosylmethionine/homocysteine cycle alterations modify DNA methylation status with consequent deregulation of PS1 and BACE and beta-amyloid production.
2005-01
Characterization of glycine N-methyltransferase from rabbit liver.
2004-06
Detecting selection using a single genome sequence of M. tuberculosis and P. falciparum.
2004-04-29
Heterodimeric interactions among the 1-amino-cyclopropane-1-carboxylate synthase polypeptides encoded by the Arabidopsis gene family.
2004-02-24
Inhibition mechanism of S-adenosylmethionine-induced movement deficits by prenylcysteine analogs.
2003-12
Identification of protein arginine methyltransferase 2 as a coactivator for estrogen receptor alpha.
2002-08-09
Spontaneous oxidative stress and liver tumors in mice lacking methionine adenosyltransferase 1A.
2002-08
Chemoprevention of hepatocarcinogenesis: S-adenosyl-L-methionine.
2002-07
Decrease of methionine and S-adenosylmethionine and increase of homocysteine in treated patients with Parkinson's disease.
2001-07-27
Effects of some thiol chelators on enzymatic activities in blood, liver and kidneys of acute arsenic (III) exposed mice.
1998-03
Effects of S-adenosylmethionine on lipid peroxidation and liver fibrogenesis in carbon tetrachloride-induced cirrhosis.
1996-08
Enzymatic methylation of arsenic compounds: assay, partial purification, and properties of arsenite methyltransferase and monomethylarsonic acid methyltransferase of rabbit liver.
1995-12
The clinical potential of ademetionine (S-adenosylmethionine) in neurological disorders.
1994-08
Differential kinetic properties of L-2-amino-4-methylthio-cis-but-3-enoic acid, a methionine analog inhibitor of S-adenosylmethionine synthetase.
1993-09-03
S-adenosyl-L-methionine decreases motor activity in the rat: similarity to Parkinson's disease-like symptoms.
1993-05
Resolution of danazol-induced cholestasis with S-adenosylmethionine.
1993-03
Parkinson's disease-like effects of S-adenosyl-L-methionine: effects of L-dopa.
1992-10
Reversal of extrahepatic membrane cholesterol deposition in patients with chronic liver diseases by S-adenosyl-L-methionine.
1992-09
S-adenosylmethionine: studies on chemical and enzymatic synthesis.
1987-02
Open trial of S-adenosylmethionine for treatment of depression.
1984-03
Modulation by S-adenosyl-L-methionine of hepatic Na+,K+-ATPase, membrane fluidity, and bile flow in rats with ethinyl estradiol-induced cholestasis.
1983-01-01
Ethynylestradiol-induced impairment of bile secretion in the rat: protective effects of S-adenosyl-L-methionine and its implication in estrogen metabolism.
1981-01
Tremor induced by S-adenosyl-L-methionine: possible relation to L-dopa effects.
1978-12
Patents

Sample Use Guides

SAMe tosylate disulfate (STD) 1000 mg for 5 days, either in enteric-coated tablet formulation or as a 250-mL IV infusion
Route of Administration: Other
In Vitro Use Guide
Curator's Comment: Effect of S-adenosyl-L-methionine disulfate tosylate salt (SAMe-ST) and L-methionine (L-Met) on primary cultured rat hepatocytes were studied. In cultured hepatocytes treated with CCl4, SAMe-ST and L-Met suppressed the decrease in urea-nitrogen secretion as well as the leakages of GOT and GPT. The membrane-protective action of these two compounds was verified by the histological data. Failure of SAMe-ST to counteract CCl4-induced reduction of radioactive leucine incorporation into the trichloroacetic acid-insoluble materials in hepatocytes indicates that the observed effects of SAMe-ST or L-Met do not involve acceleration of protein synthesis. The present results indicate that SAMe-ST remarkably protects hepatocytes from CCl4-induced hepatotoxicity, probably by either changing the structure or compositions of membrane phospholipids or by modifying the interaction of CCl4 with the intracellular drug-metabolizing enzyme systems.
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:35:34 GMT 2025
Edited
by admin
on Mon Mar 31 23:35:34 GMT 2025
Record UNII
K093C397UL
Record Status Validated (UNII)
Record Version
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Name Type Language
R,S-ADENOSYLMETHIONINE
Preferred Name English
ADEMETIONINE, (R)-
Common Name English
ADENOSINE, 5'-((R)-((3S)-3-AMINO-3-CARBOXYPROPYL)METHYLSULFONIO)-5'-DEOXY-, INNER SALT
Systematic Name English
Code System Code Type Description
FDA UNII
K093C397UL
Created by admin on Mon Mar 31 23:35:34 GMT 2025 , Edited by admin on Mon Mar 31 23:35:34 GMT 2025
PRIMARY
CAS
91279-78-6
Created by admin on Mon Mar 31 23:35:34 GMT 2025 , Edited by admin on Mon Mar 31 23:35:34 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> ENANTIOMER
RACEMATE -> ENANTIOMER