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Sku CI29902_100_G
Chem Impex
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Product Information

Product Name
S-Adenosyl-L-methionine disulfate tosylate
Brand Name
Chem Impex
Product Number
29902
CAS
97540-22-2
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
45072193
IUPAC Name
(2S)-2-amino-4-(2S,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-ylmethyl-methylsulfoniobutanoate;4-methylbenzenesulfonic acid;sulfuric acid
InChI Key
XDCFCHNAIMYBAZ-XQVUROGGSA-N
SMILES
CC1=CC=C(C=C1)S(=O)(=O)O.CS+(CCC@@H(C(=O)O-)N)CC@@H1C@H(C@H(C@@H(O1)N2C=NC3=C(N=CN=C32)N)O)O.OS(=O)(=O)O.OS(=O)(=O)O

Application

S-Adenosyl-L-methionine disulfate tosylate is widely utilized in research focused on:

Biochemical Research: This compound serves as a key methyl donor in various biochemical reactions, making it essential for studies involving methylation processes in DNA and proteins.

Pharmaceutical Development: It plays a crucial role in the synthesis of drugs, particularly in the development of antidepressants and anti-inflammatory medications, due to its ability to influence neurotransmitter levels.

Plant Biology: Researchers use it to study plant metabolism and growth, as it is involved in the biosynthesis of important plant hormones, aiding in agricultural advancements.

Clinical Applications: It is explored in clinical settings for its potential benefits in treating liver diseases and promoting liver health, providing a therapeutic avenue for patients.

Genetic Studies: The compound is utilized in genetic engineering and molecular biology to enhance gene expression and regulation, offering insights into genetic functions and disorders.

References Data Source From Pubchem

Antireactive properties of 'chondroprotective' drugs

Publication Name: International journal of tissue reactions
Publication Date: 1992

Yakuri to Chiryo. Pharmacology and Therapeutics., 15(4471), 1987