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5'-DEOXY-5'-METHYLTHIOADENOSINE

Product Name
5'-DEOXY-5'-METHYLTHIOADENOSINE
CAS No.
2457-80-9
Chemical Name
5'-DEOXY-5'-METHYLTHIOADENOSINE
Synonyms
MTA;Methylthioadenosine;Adenylthiomethylpentose;MESADO;Adenosyl Methionine Impurity 1;beta-D-Ribofuranose, 1-(6-amino-9H-purin-9-yl)-1-deoxy-5-S-methyl-5-thio-;(2R,3R,4S,5S)-2-(6-Amino-9H-purin-9-yl)-5-((methylthio)methyl)tetrahydrofuran-3,4-diol;SKL060;NSC 335422;vitaminl(sub2)
CBNumber
CB9392566
Molecular Formula
C11H15N5O3S
Formula Weight
297.33
MOL File
2457-80-9.mol
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5'-DEOXY-5'-METHYLTHIOADENOSINE Property

Melting point:
210-213 °C (dec.)
Boiling point:
642.7±65.0 °C(Predicted)
Density 
1.85±0.1 g/cm3(Predicted)
storage temp. 
-20°C
solubility 
DMF (Sparingly), DMSO (Slightly), Methanol (Slightly)
pka
13.10±0.70(Predicted)
form 
White solid
color 
White to Off-White
BRN 
42420
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Safety

Safety Statements 
22-24/25
WGK Germany 
3
RTECS 
AU7410000
10-21
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
D5011
Product name
5?-Deoxy-5?-methylthioadenosine
Packaging
1g
Price
$1150
Updated
2024/03/01
Sigma-Aldrich
Product number
260585
Product name
5?-Deoxy-5?-methylthioadenosine
Packaging
50mg
Price
$144
Updated
2024/03/01
Cayman Chemical
Product number
15593
Product name
5?-Deoxy-5?-methylthioadenosine
Purity
≥99%
Packaging
25mg
Price
$41
Updated
2024/03/01
Cayman Chemical
Product number
15593
Product name
5?-Deoxy-5?-methylthioadenosine
Purity
≥99%
Packaging
50mg
Price
$78
Updated
2024/03/01
Sigma-Aldrich
Product number
D5011
Product name
5?-Deoxy-5?-methylthioadenosine
Packaging
25mg
Price
$74.2
Updated
2024/03/01
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5'-DEOXY-5'-METHYLTHIOADENOSINE Chemical Properties,Usage,Production

Uses

5′-Deoxy-5′-(methylthio)adenosine has been used as a protein methylation inhibitor to reduce E2F transcription factor 1 (E2F1) protein abundance in hepatocellular carcinoma (HCC) cells. It has also been used to inhibit histone methylation modification and study its role in hypoxia inducible factor-1 (Hif-1) nuclear transport.

Definition

ChEBI: Adenosine with the hydroxy group at C-5' substituted with a methylthio (methylsulfanyl) group.

Biological Activity

ki = 62 μm for s49-derived high-affinity camp phosphodiesterasemethylthioadenosine (mta) is a naturally occurring sulfur-containing nucleoside in all mammalian tissues. mta is mainly produced from s-adenosylmethionine via the polyamine biosynthetic pathway, behaving as a powerful inhibitory product.

Biochem/physiol Actions

5′-Deoxy-5′-(methylthio)adenosine (Methylthioadenosine) may be used as a substrate to study the specificity and kinetics of 5′-methylthioadenosinephosphorylase (MTAP) (EC2.4.2.28), a tumor suppressor gene expressed enzyme that supports the S-adenosylmethionine (AdoMet) and methionine salvage pathways.

in vitro

mta was found to be solely metabolized by mta-phosphorylase, to yield 5-methylthioribose-1-phosphate and adenine, which was a key step in methionine and purine salvage pathways, respectively. previous studies suggested that mta coud affect various cellular processes. mta had been shown to be albe to influence plenty of critical cell responses, such as proliferation, gene expression regulation, differentiation as well as apoptosis. though most of such responses had been only observed at the pharmacological level, their specificity made it tempting to speculate that endogenous mta might play a regulatory role in the cell [1].

in vivo

the hepatoprotective effects of mta had been evaluated in a model of ccl4-induced chronic liver damage in rats. in this study, mta could reproduce the human lesions induced by alcohol and viral infections of the liver. in addition, replenishment of the hepatic pool of mta showed strong anti-oxidant effects and also reduced liver cell damage and fibrosis [2].

Purification Methods

Recrystallise it from H2O and sublime it at 200o/0.004mm. [v.Euler & Myrb.ck Hoppe Seyler's Z physiol Chem 177 237 1928, Weygand & Trauth Chem Ber 84 633 1951, Baddiley et al. J Chem Soc 2662 1953.] The hydrochloride has m 161-162o [Kuhn & Henkel Hoppe Seyler's Z Physiol Chem 269 41 1941]. The picrate has m 183o(dec) (from H2O). [Beilstein 26 III/IV 3675.]

References

[1] avila ma,garcía-trevijano er,lu sc,corrales fj,mato jm. methylthioadenosine. int j biochem cell biol.2004 nov;36(11):2125-30.
[2] pascale rm,simile mm,de miglio mr,feo f. chemoprevention of hepatocarcinogenesis: s-adenosyl-l-methionine. alcohol.2002 jul;27(3):193-8.

5'-DEOXY-5'-METHYLTHIOADENOSINE Preparation Products And Raw materials

Raw materials

Preparation Products

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5'-DEOXY-5'-METHYLTHIOADENOSINE Suppliers

TopScience Biochemical
Tel
00852-68527855
Fax
00852-26406298
Email
info@itopbiochem.com
Country
China Hong Kong
ProdList
902
Advantage
58
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View Lastest Price from 5'-DEOXY-5'-METHYLTHIOADENOSINE manufacturers

Shanghai UCHEM Inc.
Product
5'-S-Methyl-5'-thioadenosine 2457-80-9
Price
US $376.00-1719.00/g
Min. Order
1g
Purity
0.98
Supply Ability
10kh
Release date
2023-12-18
ShenZhen H&D Pharmaceutical Technology Co., LTD
Product
Methyl-thioadenosine 2457-80-9
Price
US $0.00-0.00/mg
Min. Order
10mg
Purity
0.98
Supply Ability
10g
Release date
2024-04-26
R&D Scientific Inc.
Product
5'-Deoxy-5'-(methylthio)adenosine 2457-80-9
Price
US $1500.00/g
Min. Order
1g
Purity
98
Supply Ability
500 Kg
Release date
2024-05-28

2457-80-9, 5'-DEOXY-5'-METHYLTHIOADENOSINERelated Search:


  • 2-(6-aminopurin-9-yl)-5-(methylsulfanylmethyl)oxolane-3,4-diol
  • 7-(5-Methylthio-5-deoxy-D-ribofuranosyl)-7H-purine-6-amine
  • 7-[Tetrahydro-3α,4α-dihydroxy-5β-(methylthiomethyl)furan-2-yl]-7H-purin-6-amine
  • 5'-S-Methyl-5'-thioadesine
  • 5'-Deoxy-5'-(methylthio)adenosine ,98%
  • 1-(6-AMino-9H-purin
  • 5'-Deoxy(Methylthio)adenosine
  • NSC 335422
  • Adenosine, 5'-S-Methyl-5'-thio-
  • 2,3-Dihydro-2-thioxo-9H-purin-6(1H)-one
  • Adenylthiomethylpentose
  • 5-Deoxy-5-methylthioadenosine - CAS 2457-80-9 - Calbiochem
  • ′-S-Methyl-5′-thioadenosine
  • Ademetionine 1,4-Butanedisulfonate Impurity 3
  • MTA
  • Methylthioadenosine reference substance
  • 5'-Methylthioadenosine (VitaMin L2)
  • (2R,3R,4S,5S)-2-(6-Amino-9H-purin-9-yl)-5-((methylthio)methyl)tetrahydrofuran-3,4-diol
  • 5'-(Methylthio)-5'-deoxyadenosine
  • 5’-(methylthio)adenosine
  • 5’-methylthioadenosine
  • 5’-s-methyl-5’-thio-adenosin
  • 5’-s-methylthioadenosine
  • 5'-S-Methyl-5'-thioadenosine
  • beta-D-Ribofuranose, 1-(6-amino-9H-purin-9-yl)-1-deoxy-5-S-methyl-5-thio-
  • Methylthioadenosine
  • vitaminl(sub2)
  • 5'-DEOXY-5'-METHYLTHIOADENOSINE
  • MESADO
  • Adenosyl Methionine Impurity 1
  • 5'-DEOXY-5'-METHYLTHIOADENOSINE USP/EP/BP
  • SKL060
  • 13C5]-5'-deoxy-5'-methylthioadenosine
  • 5'-DEOXY-5'-METHYLTHIOADENOSINE
  • 5'-Methylthioadenosine
  • 13C5]-5'-Deoxy-5'-methylthioadenosine([13C5]-MTA)
  • 5'-S-Methyl-5'-Thioadenosine
  • 2457-80-9
  • C11H15N5O3S
  • C11H15N5O3S1
  • Nucleoside Analogs
  • Nucleosides, Nucleotides, Oligonucleotides
  • Biochemicals and Reagents
  • BioChemical
  • Biochemicals and Reagents
  • Nucleoside Analogs
  • Nucleosides, Nucleotides, Oligonucleotides