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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

Molecular Formula H2O4S
Molecular Weight 98.078
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C7H8O3S
Molecular Weight 172.202
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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
Tremor induced by S-adenosyl-L-methionine: possible relation to L-dopa effects.
1978 Dec
Ethynylestradiol-induced impairment of bile secretion in the rat: protective effects of S-adenosyl-L-methionine and its implication in estrogen metabolism.
1981 Jan
Modulation by S-adenosyl-L-methionine of hepatic Na+,K+-ATPase, membrane fluidity, and bile flow in rats with ethinyl estradiol-induced cholestasis.
1983 Jan-Feb
Open trial of S-adenosylmethionine for treatment of depression.
1984 Mar
S-adenosylmethionine: studies on chemical and enzymatic synthesis.
1987 Feb
Parkinson's disease-like effects of S-adenosyl-L-methionine: effects of L-dopa.
1992 Oct
Reversal of extrahepatic membrane cholesterol deposition in patients with chronic liver diseases by S-adenosyl-L-methionine.
1992 Sep
Resolution of danazol-induced cholestasis with S-adenosylmethionine.
1993 Mar
S-adenosyl-L-methionine decreases motor activity in the rat: similarity to Parkinson's disease-like symptoms.
1993 May
Differential kinetic properties of L-2-amino-4-methylthio-cis-but-3-enoic acid, a methionine analog inhibitor of S-adenosylmethionine synthetase.
1993 Sep 3
The clinical potential of ademetionine (S-adenosylmethionine) in neurological disorders.
1994 Aug
Enzymatic methylation of arsenic compounds: assay, partial purification, and properties of arsenite methyltransferase and monomethylarsonic acid methyltransferase of rabbit liver.
1995 Dec
Effects of S-adenosylmethionine on lipid peroxidation and liver fibrogenesis in carbon tetrachloride-induced cirrhosis.
1996 Aug
Effects of some thiol chelators on enzymatic activities in blood, liver and kidneys of acute arsenic (III) exposed mice.
1998 Mar
Farnesyl-L-cysteine analogs block SAM-induced Parkinson's disease-like symptoms in rats.
2000 Aug
Effect of different doses of S-adenosyl-L-methionine on paracetamol hepatotoxicity in a mouse model.
2000 Dec
Effect of tauroursodeoxycholate and S-adenosyl-L-methionine on 17beta-estradiol glucuronide-induced cholestasis.
2001 Feb
Decrease of methionine and S-adenosylmethionine and increase of homocysteine in treated patients with Parkinson's disease.
2001 Jul 27
Spontaneous oxidative stress and liver tumors in mice lacking methionine adenosyltransferase 1A.
2002 Aug
Identification of protein arginine methyltransferase 2 as a coactivator for estrogen receptor alpha.
2002 Aug 9
Chemoprevention of hepatocarcinogenesis: S-adenosyl-L-methionine.
2002 Jul
Inhibition mechanism of S-adenosylmethionine-induced movement deficits by prenylcysteine analogs.
2003 Dec
Detecting selection using a single genome sequence of M. tuberculosis and P. falciparum.
2004 Apr 29
Heterodimeric interactions among the 1-amino-cyclopropane-1-carboxylate synthase polypeptides encoded by the Arabidopsis gene family.
2004 Feb 24
Characterization of glycine N-methyltransferase from rabbit liver.
2004 Jun
Inhibition of CYP2E1 catalytic activity in vitro by S-adenosyl-L-methionine.
2005 Apr 1
Folate transport gene inactivation in mice increases sensitivity to colon carcinogenesis.
2005 Feb 1
S-adenosylmethionine/homocysteine cycle alterations modify DNA methylation status with consequent deregulation of PS1 and BACE and beta-amyloid production.
2005 Jan
Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism.
2006 Dec 5
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 Jul 30
Improvement of aggressive behavior and quality of life impairment following S-adenosyl-methionine (SAM-e) augmentation in schizophrenia.
2009 Jan
Methotrexate-induced myelopathy responsive to substitution of multiple folate metabolites.
2010 May
S-adenosylmethionine decreases lipopolysaccharide-induced phosphodiesterase 4B2 and attenuates tumor necrosis factor expression via cAMP/protein kinase A pathway.
2011 May
Arsenic induces functional re-expression of estrogen receptor α by demethylation of DNA in estrogen receptor-negative human breast cancer.
2012
Novel protective mechanisms for S-adenosyl-L-methionine against acetaminophen hepatotoxicity: improvement of key antioxidant enzymatic function.
2012 Aug 3
The role of catechol-O-methyltransferase in catechol-enhanced erythroid differentiation of K562 cells.
2013 Dec 15
Alterations in hepatic metabolism of sulfur amino acids in non-obese type-2 diabetic Goto-Kakizaki rats.
2013 Jul 5
Arsenic trioxide attenuates the invasion potential of human liver cancer cells through the demethylation-activated microRNA-491.
2014 Jun 5
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 Sat Dec 16 11:26:51 GMT 2023
Edited
by admin
on Sat Dec 16 11:26:51 GMT 2023
Record UNII
R96GHU97Q3
Record Status Validated (UNII)
Record Version
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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
Related Record Type Details
RACEMATE -> ENANTIOMER