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  3. N,N-Dimethylglycine hydrochloride

N,N-Dimethylglycine hydrochloride  (Synonyms: Dimethylglycine hydrochloride; DMG hydrochloride; N-Methylsarcosine hydrochloride)

Cat. No.: HY-W001158
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N,N-Dimethylglycine (Dimethylglycine) hydrochloride is a natural N-methylated glycine, is a nutrient supplement and acts as an NMDAR glycine site partial agonist. N,N-Dimethylglycine hydrochloride is a methyl donor, could improve immunity, function as an antioxidant to prevent oxidative stress, and scavenge excess of free radicals. N,N-Dimethylglycine hydrochloride exhibits antidepressant-like and surfactant effects.

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N,N-Dimethylglycine hydrochloride Chemical Structure

N,N-Dimethylglycine hydrochloride Chemical Structure

CAS No. : 2491-06-7

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Based on 1 publication(s) in Google Scholar

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Description

N,N-Dimethylglycine (Dimethylglycine) hydrochloride is a natural N-methylated glycine, is a nutrient supplement and acts as an NMDAR glycine site partial agonist. N,N-Dimethylglycine hydrochloride is a methyl donor, could improve immunity, function as an antioxidant to prevent oxidative stress, and scavenge excess of free radicals. N,N-Dimethylglycine hydrochloride exhibits antidepressant-like and surfactant effects[1][2][3].

IC50 & Target

Human Endogenous Metabolite

 

In Vitro

N,N-Dimethylglycine (40 mg/mL) hydrochloride shows 88.40%, 98.90%, and 87.58% scavenging activities in the DPPH radical scavenging, ABTS+ radical scavenging, and H2O2 scavenging experiments[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

N,N-Dimethylglycine (30-100 mg/kg; intraperitoneal injection; twice a day; 14 days) hydrochloride prevents the behavioral abnormalities and synaptic dysfunction induced by repeated drug exposure in male ICR mice[1].
N,N-Dimethylglycine (12 mg/0.3 mL sterile saline; gavage; single dose; subcutaneous injection 1 hour later) hydrochloride improves the histological morphology of the small intestine, enhances the antioxidant system, reduces oxidative damage, and increases the expression of antioxidant-related genes in male Kunming mice[2].
N,N-Dimethylglycine (12 mg/0.3 mL sterile saline; gavage; twice a day; 28 days) hydrochloride increases the body weight, the organ proportion of the liver and spleen, enhances the antioxidant capacity of serum and liver, and reduces the activities of serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) as well as the malondialdehyde (MDA) content in serum and liver in male Kunming mice[3].
N,N-Dimethylglycine (12 mg/0.3 mL sterile saline; gavage; twice a day; 28 days) hydrochloride reduces the serum ALT and AST contents, the ROS level in hepatic mitochondria, and increases the antioxidant capacity of hepatic mitochondria and the mitochondrial membrane potential (MMP) level in male Kunming mice with Lipopolysaccharides (LPS) (HY-D1056)-induced oxidative stress model[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male ICR mice (body weight 10-12 g, 3-week- old) + Repeated drug exposure (20 mg/kg, i.p., twice daily for 14 days)[1].
Dosage: 30 mg/kg, 100 mg/kg
Administration: Intraperitoneal injection, 20 min prior to each drug injection, twice a day, 14 days.
Result: Prevented the drug-induced memory impairments in novel location recognition test (NLRT) and novel object recognition test (NORT), social withdrawal in reciprocal social interaction test, and enhanced head twitch response induced by serotonergic hallucinogen.
Animal Model: Male Kunming mice (weight 20-25 g, 40 days old) + Indomethacin injection (10 mg/kg BW)[2].
Dosage: 12 mg/0.3 mL sterile saline
Administration: Orally gavage; single dose; and then subcutaneous injection 1 hour later.
Result: Improved the histological morphology of the small intestine. Enhanced the antioxidant system, reduced oxidative damage, and increased the expression of antioxidant-related genes in the small intestine and its mitochondria compared with the indomethacin-treated group2.
Animal Model: Male Kunming mice (weight 20-25 g, 40 days old) + Lipopolysaccharides (LPS) injection (100 μg/kg body weight)[3].
Dosage: 12 mg/0.3 mL sterile saline
Administration: Orally gavage; twice a day; 28 days.
Result: Significantly decreased the serum ALT and AST content, ROS level, and expression of liver antioxidant gene MnSOD, Gpx1, Sirt1.
Significantly increased the hepatic mitochondrial antioxidant capacity (MnSOD, GSH, GPx, GR) and MMP level compared with the LPS-treated group.
Molecular Weight

139.58

Formula

C4H10ClNO2

CAS No.
Appearance

Solid

Color

White to off-white

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Store at room temperature, keep dry and cool

In solvent -80°C 2 years
-20°C 1 year
Purity & Documentation

Purity: ≥98.0%

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N,N-Dimethylglycine hydrochloride
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