Adenosine, 5′-[[(3S)-3-amino-3-carboxypropyl]methylsulfonio]-5′-deoxy-, sulfate, 4-methylbenzenesulfonate sulfate (1:1:1:1)
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![Adenosine, 5′-[[(3S)-3-amino-3-carboxypropyl]methylsulfonio]-5′-deoxy-, sulfate, 4-methylbenzenesulfonate sulfate (1:1:1:1) structure](https://file.echemi.com/fileManage/upload/canonicalSmiles/20220812/e48ae818c0f64593aeb26d29290e8db6.png "Adenosine, 5′-[[(3S)-3-amino-3-carboxypropyl]methylsulfonio]-5′-deoxy-, sulfate, 4-methylbenzenesulfonate sulfate (1:1:1:1)")
Adenosine, 5′-[[(3S)-3-amino-3-carboxypropyl]methylsulfonio]-5′-deoxy-, sulfate, 4-methylbenzenesulfonate sulfate (1:1:1:1)
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CAS No:
97540-22-2
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Formula:
C15H23N6O5S.C7H8O3S.H2O4S.HO4S
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Chemical Name:
Adenosine, 5′-[[(3S)-3-amino-3-carboxypropyl]methylsulfonio]-5′-deoxy-, sulfate, 4-methylbenzenesulfonate sulfate (1:1:1:1)
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Synonyms:
Adenosine,5′-[[(3S)-3-amino-3-carboxypropyl]methylsulfonio]-5′-deoxy-,sulfate,4-methylbenzenesulfonate sulfate (1:1:1:1);Adenosine,5′-[(3-amino-3-carboxypropyl)methylsulfonio]-5′-deoxy-,(3S)-,sulfate (salt),4-methylbenzenesulfonate (salt) sulfate (salt) (1:1:1:1);Adenosine,5′-[[(3S)-3-amino-3-carboxypropyl]methylsulfonio]-5′-deoxy-,sulfate (salt),4-methylbenzenesulfonate (salt) sulfate (salt) (1:1:1:1);FO 1561;S-Adenosyl-L-methionine disulfate tosylate;110899-33-7;113883-52-6;137088-54-1;89365-51-5
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CAS No:
Description
S-Adenosyl-L-methionine disulfate tosylate is the principal biological methyl donor synthesized in all mammalian cells but most abundantly in the liver.
S-Adenosyl-L-Methionine Disulfate P-Toluene-Sulfonate is the disulfate salt of the stable p-toluene-sulfonate complex of s-adenosyl-L-methionine (SAMe) with chemopreventive activity. SAMe disulfate p-toluene-sulfonate undergoes hydrolytic conversion to its active compound SAMe within cells. Although the mechanism of action is largely unknown, SAMe attenuates experimental liver damage and prevents experimental hepatocarcinogenesis. In addition, SAMe may reduce mitochondrial cytochrome C release, caspase 3 activation, and poly(ADP-ribose) polymerase cleavage, and attenuate okadaic acid-mediated hepatocyte apoptosis in a dose-dependent manner. SAMe is an essential compound in cellular transmethylation reactions and a precursor of polyamine and glutathione synthesis in the liver; SAMe deficiency is associated with chronic liver disease-associated decreases in the activity of methionine adenosyltransferase 1A (MAT1A), the enzyme that catalyzes the production of SAMe as the first step in methionine catabolism.|Physiologic methyl radical donor involved in enzymatic transmethylation reactions and present in all living organisms. It possesses anti-inflammatory activity and has been used in treatment of chronic liver disease. (From Merck, 11th ed)
Adenosine, 5′-[[(3S)-3-amino-3-carboxypropyl]methylsulfonio]-5′-deoxy-, sulfate, 4-methylbenzenesulfonate sulfate (1:1:1:1) Basic Attributes
766.8
766.091431
R96GHU97Q3|4G5PYL0DR1|564ROC9U09
C71745
2934999090
Adenosine, 5′-[[(3S)-3-amino-3-carboxypropyl]methylsulfonio]-5′-deoxy-, sulfate, 4-methylbenzenesulfonate sulfate (1:1:1:1) Use and Manufacturing
Ademetionine Disulfate Tosylate is used to study the survival time in various damage brain models.
Computed Properties
Molecular Weight:766.8
Hydrogen Bond Donor Count:9
Hydrogen Bond Acceptor Count:21
Rotatable Bond Count:7
Exact Mass:766.09141371
Monoisotopic Mass:766.09141371
Topological Polar Surface Area:415
Heavy Atom Count:48
Complexity:815
Defined Atom Stereocenter Count:5
Covalently-Bonded Unit Count:4
Compound Is Canonicalized:Yes
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Adenosine, 5′-[[(3S)-3-amino-3-carboxypropyl]methylsulfonio]-5′-deoxy-, sulfate, 4-methylbenzenesulfonate sulfate (1:1:1:1)
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