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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
  • 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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Autophagy
GluR
Apoptosis
mTOR
Akt
iGluR
AMPK
Glucocorticoid Receptor
PI3K
Endogenous Metabolite
Sirtuin
HIF/HIF Prolyl-Hydroxylase
HIF
NMDAR
ERK
NF-κB
Raf
Dehydrogenase
Antibacterial
p53
Ferroptosis
SGLT
Glutathione Peroxidase
Ras
Reactive Oxygen Species
c-Myc
DNA-PK
S6 Kinase
COX
Antibiotic
Mitophagy
MEK
Glutaminase
PPAR
VEGFR
p38 MAPK
transporter
Isocitrate Dehydrogenase (IDH)
HMG-CoA Reductase
HIV Protease
STAT
Src
Estrogen/progestogen Receptor
TNF
Parasite
NADPH
Influenza Virus
PKM
Calcium Channel
Rho
PKC
CDK
Potassium Channel
Caspase
JNK
Cytochromes P450
E1/E2/E3 Enzyme
Mdm2
PDGFR
Sodium Channel
AChR
c-Kit
DNA/RNA Synthesis
Lipoxygenase
ATM/ATR
Virus Protease
PKA
FLT
Amino Acids and Derivatives
IL Receptor
GABA Receptor
c-RET
Mitochondrial Metabolism
Adrenergic Receptor
Epigenetic Reader Domain
ROS
MMP
NADPH-oxidase
Histamine Receptor
HDAC
PDK
Annexin A
PARP
Bcl-2 Family
Aurora Kinase
Tyrosinase
Microtubule Associated
Nrf2
ROCK
Antifungal
Progesterone Receptor
Antioxidant
LRRK2
ADC Cytotoxin
FGFR
NOS
Cannabinoid Receptor
TRP/TRPV Channel
MAPK
HSP
GlyT
GPX
Phosphatase
Cholinesterase (ChE)
HSV
EGFR
GSK-3
HCV Protease
GST
Androgen Receptor
Aryl Hydrocarbon Receptor
Wnt/beta-catenin
Casein Kinase
c-Fms
Interleukin
JAK
Serine Protease
Glutathione reductase
Bcr-Abl
Decarboxylase
DNA Alkylator/Crosslinker
SARS-CoV
Carbonic Anhydrase
CaMK
Phospholipase
CXCR
Antiviral
Topoisomerase
Hydroxylase
P-gp
FAK
Glucagon Receptor
Chloride channel
HBV
Reverse Transcriptase
ATP Citrate Lyase
5-HT Receptor
Integrin
GTPase
IGF-1R
PERK
NO Synthase
IκB/IKK
Beta Amyloid
PLK
Prostaglandin Receptor
Adenosine Receptor
ALK
Histone Demethylase
YAP
Monoamine Transporter
Drug Metabolite
LDL
MT Receptor
Pyroptosis
Tie-2
Gamma-secretase
PYK2
RAAS
NPC1L1
Norepinephrine
c-Met/HGFR
Glucokinase
Retinoid Receptor
MRP
ROR
ROS Kinase
Amylase
DNA Methyltransferase
BMI-1
Melatonin Receptor
OXPHOS
GPCR
PAI-1
Histone Methyltransferase
UGT
TLR
SGK
BACE
SIK
Smo
Lipid
KLF
AhR
Proton pump
Guanylate cyclase
CRISPR/Cas9
Pim
CFTR
ACK1
PTEN
Dopamine Receptor
CaSR
PI4K
Complement System
FXR
Liver X Receptor
Arginase
Beta-Secretase
MAO
ATPase
Trk receptor
IFNAR
Acyltransferase
Fatty Acid Synthase
Estrogen Receptor/ERR
Myosin
PD-1/PD-L1
Chk
PAK
TGF-beta/Smad
Kras