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TargetMol | Compound Library

Glutamine Metabolism Compound Library

Catalog No. L2550

L-glutamine is a non-essential amino acid that is often simply called glutamine. It is produced by the body. Glutamine is synthesized from NH4+ and glutamate. The conversion of glutamate to glutamine is regulated by glutamine synthetase (GS) and is a key step in nitrogen metabolism. Although normally synthesized in adequate amounts, endogenous glutamine production may be inadequate during periods of metabolic stress or under the condition of disease.

Glutamine is crucial for many metabolic functions, including protein and glutathione synthesis, energy production, maintenance of optimal antioxidant status, and immune function. Glutamine is the main metabolic substrate of macrophages and important for the function of macrophages; Glutamine is an important biosynthetic precursor for amino acid, protein and nucleic acid synthesis; Glutamine serves as a source of fuel for the cells lining the intestines, and without it, these cells may waste away; Glutamine is significantly involved in the synthesis of glutathione, a very important intracellular antioxidant and detoxication factor.

Cancer cells undergo a reprogramming of metabolism in order to maintain bioenergetics, redox status, cell signaling and biosynthesis, in what is often a poorly vascularized, nutrient-deprived microenvironment. A metabolic characteristic of many cancer cells is a dependence on an exogenous supply of glutamine, exhibiting "glutamine addiction". Glutamine enters the cell through the amino acid transporter, ASCT2/SLC1A5, and is converted to glutamate in the mitochondria through a deamination reaction catalyzed by glutaminase (GLS). Glutamate is converted to the TCA cycle intermediate α-ketoglutarate (α-KG) by either glutamate dehydrogenase (GDH) or by the alanine or aspartate transaminases (TAs), which produce their corresponding amino acid in addition to α-KG, a process termed glutaminolysis. Humans express 4 isoforms of glutaminase which is the restriction and initiation enzyme in the glutaminolytic pathway. GLS encodes 2 types of kidney-type glutaminase with a high activity and low Km. GLS2 encodes 2 forms of liver-type glutaminase with a low activity and allosteric regulation.

Glutamine coordinates intracellular signaling to promote cancer growth in addition to acting as an important substrate for carbon and nitrogen production. For example, MYC transcriptionally represses miR-23a/b, leading to higher expression of mitochondrial glutaminase. Glutamine stimulates mTORC1 activity and in turn, impairs autophagy initiation through the negative regulation of ULK1 by several mechanisms. Thus, intervention in glutamine metabolic processes could provide novel approaches to improve cancer treatment.

TargetMol owns a unique collection of 941 compounds targeting the mainly proteins and enzymes involved in glutamine metabolism pathway. Glutamine Metabolism compound library is a useful tool for research in glutamine metabolic processes and drug discovery.

All products from TargetMol are for Research Use Only. Not for Human or Veterinary or Therapeutic Use.

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Catalog No. L2550

Glutamine Metabolism Compound Library

sizeIn stock

  • 1 mg
  • 10 μL x 10 mM (in DMSO)
  • 20 μL x 10 mM (in DMSO)
  • 30 μL x 10 mM (in DMSO)
  • 50 μL x 10 mM (in DMSO)
  • 100 μL x 10 mM (in DMSO)
  • 250 μL x 10 mM (in DMSO)
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Product Description Product Description

  • A unique collection of 941 glutamine metabolism related compounds can be used for high throughput screening (HTS) and high content screening (HCS), and also is an effective tool for research in glutamine metabolism and cancer;
  • Targets include glutaminase(GLS)、ASCT2、glutamate dehydrogenase、c-Myc, etc.
  • Some compounds have been approved by the FDA;
  • Structurally diverse, medicinally active, and cell permeable;
  • Detailed compound information with structure, target, IC50 value, and bioactivity information;
  • NMR and HPLC/LCMS validated to ensure high purity

Packaging And Storage Packaging And Storage

  • Powder or pre-dissolved DMSO solutions in 96/384 well plate with optional 2D barcode
  • Shipped with blue ice
  • This compound library is provided at a concentration of 10 mM in DMSO. A small number of compounds may be provided in different solvents or concentrations due to solubility or stability requirements. Please refer to the specific product information for details.

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Apoptosis
Autophagy
GluR
mTOR
iGluR
Akt
AMPK
PI3K
HIF/HIF Prolyl-Hydroxylase
Endogenous Metabolite
Glucocorticoid Receptor
Sirtuin
Ras
ERK
NMDAR
HIF
Antibacterial
NF-κB
Raf
Dehydrogenase
ROS
MDM-2/p53
Reactive Oxygen Species
Ferroptosis
p53
SGLT
c-Myc
Glutathione Peroxidase
COX
S6 Kinase
DNA-PK
Antibiotic
Caspase
VEGFR
MEK
p38 MAPK
TNF
Mitophagy
PPAR
Parasite
Glutaminase
Calcium Channel
Cytochromes P450
transporter
STAT
Isocitrate Dehydrogenase (IDH)
Influenza Virus
Src
HIV Protease
JNK
Potassium Channel
Nrf2
HMG-CoA Reductase
CDK
Interleukin
PKC
Estrogen/progestogen Receptor
NADPH
DNA/RNA Synthesis
Rho
Bcl-2 Family
PKM
E1/E2/E3 Enzyme
PDGFR
AChR
Mitochondrial Metabolism
Mdm2
GABA Receptor
Sodium Channel
NO Synthase
Virus Protease
Wnt/beta-catenin
Amino Acids and Derivatives
Adrenergic Receptor
FLT
c-Kit
Lipoxygenase
Phosphatase
PKA
ATM/ATR
Antifungal
IL Receptor
MMP
PARP
Tyrosinase
FGFR
Microtubule Associated
SARS-CoV
c-RET
ADC Cytotoxin
TRP/TRPV Channel
ROCK
Annexin A
CaMK
Beta Amyloid
PDK
Progesterone Receptor
GST
Aryl Hydrocarbon Receptor
LRRK2
NADPH-oxidase
Bcr-Abl
Aurora Kinase
Antioxidant
HSV
HDAC
Histamine Receptor
GSK-3
Epigenetic Reader Domain
Kras
Gamma-secretase
MAPK
Anti-infection
EGFR
NOS
HCV Protease
CXCR
Pyroptosis
FKBP
GPX
Cannabinoid Receptor
GlyT
Androgen Receptor
FAK
Cholinesterase (ChE)
ATP Citrate Lyase
Tie-2
JAK
TGF-beta/Smad
HSP
Serine Protease
Glucagon Receptor
Trk receptor
c-Fms
PLK
Complement System
Antiviral
5-HT Receptor
c-Met/HGFR
Adenosine Receptor
GTPase
CaSR
ASCT
Reverse Transcriptase
ROS Kinase
PD-1/PD-L1
Chloride channel
DNA Alkylator/Crosslinker
FXR
Topoisomerase
PTEN
Cadherin
OXPHOS
P-gp
Histone Methyltransferase
RIP kinase
Drug Metabolite
Fatty Acid Synthase
Carbonic Anhydrase
HBV
IGF-1R
Casein Kinase
Hydroxylase
Integrin
Reductase
Glutathione reductase
Decarboxylase
IκB/IKK
Phospholipase
PGK1
ROR
Glucokinase
Angiotensin-converting Enzyme (ACE)
Chk
KLF
PI4K
YAP
IFNAR
BACE
Necroptosis
Hck
IDO
MT Receptor
ACK1
Lipid
TMV
SGK
BMI-1
DNA Methyltransferase
AhR
NOD-like Receptor (NLR)
Monoamine Oxidase
GPCR
Y Box Binding Protein 1
Arginase
Liver X Receptor
MAO
PAK
Histone Acetyltransferase
AIM2
PAI-1
ALK
NOD
Proton pump
Monocarboxylate transporter
Melatonin Receptor
Cysteine Protease
Amylase
Prolyl Endopeptidase (PREP)
LDL
Guanylate cyclase
Norepinephrine
Huntingtin
Prostaglandin Receptor
STING
TLR
Retinoid Receptor
MLK
Dopamine Receptor
MRP
PYK2
Adenylate cyclase
UGT
Indoleamine 2,3-Dioxygenase (IDO)
Survivin
Urea Transporter
ASK
Methionine Adenosyltransferase (MAT)
Cuproptosis
Kinesin
ATPase
Histone Demethylase
PERK
NR4A
Monoamine Transporter
glycosidase
p62
CFTR
NPC1L1
RAAS
Estrogen Receptor/ERR
SIK
Myosin
Glucosidase
Smo
Beta-Secretase
Acyltransferase
Liposome

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