1. PI3K/Akt/mTOR NF-κB Stem Cell/Wnt JAK/STAT Signaling Metabolic Enzyme/Protease
  2. mTOR NF-κB STAT HIF/HIF Prolyl-Hydroxylase
  3. L-Glutamine

L-Glutamine GMP is L-Glutamine (HY-N0390) produced by using GMP guidelines. GMP small molecules works appropriately as an auxiliary reagent for cell therapy manufacture. L-Glutamine is an orally active nutritional agent and cellular metabolism regulator. L-Glutamine is taken up in a Na+-dependent manner and targets multiple key molecules including glutaminase, mTORC1, NF-κB, STAT-3 and HIF-1α. L-Glutamine enhances glutaminolytic catabolism, drives the conversion of glutamate to α-ketoglutarate, thereby regulating gene expression, integrating metabolic signals, mediating glutamine flux and maintaining redox homeostasis. L-Glutamine also promotes cell proliferation, osteogenic differentiation and fracture healing, exerts neuroprotective and cardioprotective effects, and inhibits osteoarthritis. L-Glutamine can be applied to research related to osteoporosis, osteoarthritis, ischemic stroke and acute cantharidin-induced cardiotoxicity.

For research use only. We do not sell to patients.

L-Glutamine

L-Glutamine Chemical Structure

CAS No. : 56-85-9

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Description

L-Glutamine GMP is L-Glutamine (HY-N0390) produced by using GMP guidelines. GMP small molecules works appropriately as an auxiliary reagent for cell therapy manufacture. L-Glutamine is an orally active nutritional agent and cellular metabolism regulator. L-Glutamine is taken up in a Na+-dependent manner and targets multiple key molecules including glutaminase, mTORC1, NF-κB, STAT-3 and HIF-1α. L-Glutamine enhances glutaminolytic catabolism, drives the conversion of glutamate to α-ketoglutarate, thereby regulating gene expression, integrating metabolic signals, mediating glutamine flux and maintaining redox homeostasis. L-Glutamine also promotes cell proliferation, osteogenic differentiation and fracture healing, exerts neuroprotective and cardioprotective effects, and inhibits osteoarthritis. L-Glutamine can be applied to research related to osteoporosis, osteoarthritis, ischemic stroke and acute cantharidin-induced cardiotoxicity[1][2][3][4].

IC50 & Target

mTORC1

 

STAT3

 

HIF-1α

 

In Vitro

L-Glutamine (GMP) is essential for osteoclast differentiation, maturation, and bone-resorbing activity via SLC1A5-mediated uptake and conversion to α-KG for anaplerosis, with hypoxia-stimulated uptake supporting biosynthetic needs[1].
L-Glutamine (GMP) promotes BMSC proliferation via upregulation of cell cycle regulators, activation of GLS and GDH through mTOR/S6 and MAPK pathways, and amino acid transaminase-dependent α-KG production[1].
L-Glutamine (GMP) promotes BMSC osteogenic differentiation via GLS-dependent TCA cycle anaplerosis, regulation by ERRα and mTOR signaling pathways, and glutathione-mediated ROS neutralization, but does not contribute to adipocytic differentiation of BMSCs[1].
L-Glutamine (GMP) (High-dose) enhances the immunosuppressive properties of BMSCs by modulating cytokine production via reduced NF-κB and increased STAT-3 activity, and inhibits lymphocyte and macrophage proliferation in coculture[1].
L-Glutamine (GMP) improves osteoblast viability, enhances glucose utilization, and promotes matrix mineralization in human osteoblast-like cell lines and mouse calvarial osteoblasts[1].
L-Glutamine (GMP) supports chondrocyte extracellular matrix synthesis, enhances hypoxia tolerance via HIF-1α/GLS1-mediated α-KG production, and protects chondrocytes from injury and apoptosis through glutathione and HSP70 upregulation[1].

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

In Vivo

L-Glutamine GMP (0.75 g/kg; i.p.; daily; initiated immediately after MCAO and continued for 3 days) reduces the ischemic cerebral infarction volume by approximately 60% in male ICR mice, improves neurobehavioral recovery, upregulates HSP70 expression, enhances antioxidant capacity, reduces neuronal apoptosis, and promotes astrocyte proliferation via an HSP70-dependent mechanism[3].
Pretreatment with L-Glutamine GMP (1-2 g/kg; p.o.; once every 2 days; for 5 days) significantly attenuates Cantharidin (HY-N0209)-induced body weight loss in female BALB/c mice[4].
Pretreatment with L-Glutamine GMP (1-2 g/kg; p.o.; once every 2 days; for a total of 5 days) reduces the mortality rate of female BALB/c mice exposed to 3 mg/kg Cantharidin[4].
Pretreatment with L-Glutamine GMP (1-2 g/kg; p.o.; single dose) significantly normalizes cardiac mass index, cardiac biomarkers, oxidative stress markers, and succinate dehydrogenase activity, and alleviates histopathological damage in female BALB/c mice with acute cardiotoxicity induced by Cantharidin[4].
Pretreatment with L-Glutamine GMP (1-2 g/kg; p.o.; single dose) reduces Cantharidin-induced ST-segment elevation and alleviates myocardial injury in female BALB/c mice[4].

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

Animal Model: BALB/c (female, 6 weeks old, 18 g)[4]
Dosage: 1 g/kg; 2 g/kg
Administration: p.o.; once every 2 days; 5 days
Result: Reduced cantharidin-induced weight loss.
Showed a statistically significant protective effect at 2 g/kg dose compared to the cantharidin-only group.\nDelayed cantharidin-induced mortality.
Resulted in slower death rates compared to the cantharidin-only group over the 5-day observation period.
Molecular Weight

146.14

Formula

C5H10N2O3

CAS No.
SMILES

N[C@@H](CCC(N)=O)C(O)=O

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Room temperature in continental US; may vary elsewhere.

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Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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