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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

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  • Powder or pre-dissolved DMSO solutions in 96/384 well plate with optional 2D barcode
  • Shipped with blue ice

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