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Details

Stereochemistry EPIMERIC
Molecular Formula C15H22N6O5S
Molecular Weight 398.437
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ADEMETIONINE

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-AIRLBKTGSA-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 EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 5 / 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
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
Reversal of extrahepatic membrane cholesterol deposition in patients with chronic liver diseases by S-adenosyl-L-methionine.
1992 Sep
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
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
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
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
S-adenosylmethionine blocks collagen I production by preventing transforming growth factor-beta induction of the COL1A2 promoter.
2005 Sep 2
Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism.
2006 Dec 5
Tolcapone decreases plasma levels of S-adenosyl-L-homocysteine and homocysteine in treated Parkinson's disease patients.
2006 Jun
DLPC and SAMe prevent alpha1(I) collagen mRNA up-regulation in human hepatic stellate cells, whether caused by leptin or menadione.
2006 Nov 10
Protein interactions in the human methionine synthase-methionine synthase reductase complex and implications for the mechanism of enzyme reactivation.
2007 Jun 12
Efficacy of methylcobalamin and folinic acid treatment on glutathione redox status in children with autism.
2009 Jan
Mthfd1 is an essential gene in mice and alters biomarkers of impaired one-carbon metabolism.
2009 Jan 16
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 Apr
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 Aug 15
Effects of salvianolic acids on oxidative stress and hepatic fibrosis in rats.
2010 Jan 15
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
Wilson's disease: changes in methionine metabolism and inflammation affect global DNA methylation in early liver disease.
2013 Feb
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 Fri Dec 15 18:56:58 UTC 2023
Edited
by admin
on Fri Dec 15 18:56:58 UTC 2023
Record UNII
7LP2MPO46S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ADEMETIONINE
INN   MART.   WHO-DD  
INN  
Official Name English
MSI-195
Code English
SAME
Code English
5'-((3S)-(3-AMINO-3-CARBOXYPROPYL)METHYLSULFONIO)-5'-DEOXYADENOSINE INNER SALT
Common Name English
TRANSMETIL
Brand Name English
ademetionine [INN]
Common Name English
S-(5'-DESOXYADENOSIN-5'-YL)-L-METHIONINE
Systematic Name English
ADOMET
Brand Name English
Ademetionine [WHO-DD]
Common Name English
ADENOSYLMETHIONINE
Common Name English
S-ADENOSYLMETHIONINE
MI   VANDF  
Systematic Name English
S-ADENOSYL-L-METHIONINE
Common Name English
S-ADENOSYLMETHIONINE [MI]
Common Name English
SAM-E
Code English
SAM
Common Name English
ADEMETIONINE [MART.]
Common Name English
S-ADENOSYLMETHIONINE [VANDF]
Common Name English
Classification Tree Code System Code
LOINC 78966-9
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
NCI_THESAURUS C275
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
FDA ORPHAN DRUG 111498
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
WHO-ATC A16AA02
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
DSLD 591 (Number of products:14)
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
LOINC 80182-9
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
LIVERTOX 867
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
LOINC 80177-9
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
DSLD 1257 (Number of products:115)
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
Code System Code Type Description
FDA UNII
7LP2MPO46S
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
CAS
29908-03-0
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
DRUG BANK
DB00118
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
CHEBI
33442
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
SMS_ID
100000092113
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
EVMPD
SUB05266MIG
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
EPA CompTox
DTXSID6032019
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
CHEBI
67040
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
ECHA (EC/EINECS)
249-946-8
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
ChEMBL
CHEMBL1088977
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
PUBCHEM
34755
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
LACTMED
SAM-e
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
DRUG CENTRAL
2414
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
RXCUI
9504
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY RxNorm
CAS
78548-84-2
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
ALTERNATIVE
CHEBI
15414
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
MERCK INDEX
m1414
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY Merck Index
MESH
D012436
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
WIKIPEDIA
S-Adenosyl methionine
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
NCI_THESAURUS
C100098
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
DAILYMED
7LP2MPO46S
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
INN
5479
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
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METABOLITE -> PARENT
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ACTIVE MOIETY