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S-Adenosyl-L-methionine (Ademetionine) Methyl Donor

Cat.No.S5109

Ademetionine (AdoMet, S-Adenosylmethionine, SAMe), also known as SAMe, is a specific form of the amino acid methionine known as S-adenosyl-methionine. It is essential for the formation of glutathione, a water-soluble peptide that helps the body fight free radicals.
S-Adenosyl-L-methionine (Ademetionine) Endogenous Metabolite inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 398.44

Quality Control

Chemical Information, Storage & Stability

Molecular Weight 398.44 Formula

C15H22N6O5S

Storage (From the date of receipt) 3 years -20°C powder (seal)
CAS No. 29908-03-0 Download SDF Storage of Stock Solutions

Synonyms AdoMet, S-Adenosylmethionine, SAMe Smiles C[S+](CCC(C(=O)[O-])N)CC1C(C(C(O1)N2C=NC3=C(N=CN=C32)N)O)O

Solubility

In vitro
Batch:

DMSO : 80 mg/mL (200.78 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : 80 mg/mL

Ethanol : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
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Mechanism of Action

In vitro
Ademetionine (S-adenosylmethionine; SAMe) is a ubiquitous metabolite present in all cells and biological fluids, and serves as a methyl donor in a multitude of different methylation reactions involving proteins, phospholipids, catecholamines and DNA[1].
In vivo
SAMe is able to cross the intestinal wall and increase plasma levels. Studies in rats reveal that absorption of the drug is much better after intraduodenal administration compared to oral administration. The systemic bioavailability after oral SAMe administration appears to be low. SAMe dose-dependently (12.5, 25, 50, 100 and 200 mg/kg sc.) decreases immobility time in the forced swimming test in mice and rats. Chronic treatment with SAMe is associated with an increase in density of b-receptors, and a decrease in the affinity of a1 adrenoceptors for phenylephrine in rat cerebral membranes[1].
References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2024-05-22)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT05312372 Withdrawn
Esophageal Squamous Cell Carcinoma
Institut de Recherches Internationales Servier|ADIR a Servier Group company|Servier
May 2025 Phase 1|Phase 2
NCT05775718 Recruiting
Bone Marrow Transplant|Stem Cell Transplant
University of Colorado Denver|GlaxoSmithKline
December 1 2024 Phase 2
NCT05279196 Not yet recruiting
Muscle Injury
University Hospital Montpellier
September 2024 Not Applicable
NCT06309173 Not yet recruiting
Multiple Sclerosis
University Hospital Basel Switzerland
September 2024 --
NCT06251999 Not yet recruiting
Elderly Patients
Shanghai 6th People''s Hospital
August 1 2024 Phase 4
NCT06280742 Not yet recruiting
Multiple Sclerosis
Assistance Publique - Hôpitaux de Paris
July 1 2024 Not Applicable

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