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Details

Stereochemistry ABSOLUTE
Molecular Formula C15H22N6O5S.C7H8O3S.2H2O4S
Molecular Weight 766.796
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of S-ADENOSYL-L-METHIONINE DISULFATE TOSYLATE, (S)-

SMILES

OS(O)(=O)=O.OS(O)(=O)=O.CC1=CC=C(C=C1)S(O)(=O)=O.C[S@@+](CC[C@H](N)C([O-])=O)C[C@H]2O[C@H]([C@H](O)[C@@H]2O)N3C=NC4=C3N=CN=C4N

InChI

InChIKey=XDCFCHNAIMYBAZ-PFPDJMLESA-N
InChI=1S/C15H22N6O5S.C7H8O3S.2H2O4S/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;1-6-2-4-7(5-3-6)11(8,9)10;2*1-5(2,3)4/h5-8,10-11,14,22-23H,2-4,16H2,1H3,(H2-,17,18,19,24,25);2-5H,1H3,(H,8,9,10);2*(H2,1,2,3,4)/t7-,8+,10+,11+,14+,27-;;;/m0.../s1

HIDE SMILES / InChI

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
Tremor induced by S-adenosyl-L-methionine: possible relation to L-dopa effects.
1978 Dec
Resolution of danazol-induced cholestasis with S-adenosylmethionine.
1993 Mar
Effects of some thiol chelators on enzymatic activities in blood, liver and kidneys of acute arsenic (III) exposed mice.
1998 Mar
Detecting selection using a single genome sequence of M. tuberculosis and P. falciparum.
2004 Apr 29
Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism.
2006 Dec 5
Betaine-homocysteine S-methyltransferase-2 is an S-methylmethionine-homocysteine methyltransferase.
2008 Apr 4
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 Jun
Effects of salvianolic acids on oxidative stress and hepatic fibrosis in rats.
2010 Jan 15
Wilson's disease: changes in methionine metabolism and inflammation affect global DNA methylation in early liver disease.
2013 Feb
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
Name Type Language
S-ADENOSYL-L-METHIONINE DISULFATE TOSYLATE, (S)-
Common Name English
ADENOSINE, 5'-((S)-((3S)-3-AMINO-3-CARBOXYPROPYL)METHYLSULFONIO)-5'-DEOXY-, SULFATE (SALT), 4-METHYLBENZENESULFONATE (SALT) SULFATE (SALT) (1:1:1:1)
Systematic Name English
Code System Code Type Description
FDA UNII
R96GHU97Q3
Created by admin on Sat Dec 16 11:26:51 GMT 2023 , Edited by admin on Sat Dec 16 11:26:51 GMT 2023
PRIMARY
CAS
375798-65-5
Created by admin on Sat Dec 16 11:26:51 GMT 2023 , Edited by admin on Sat Dec 16 11:26:51 GMT 2023
PRIMARY