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Glutamine Metabolism Compound Library
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Glutamine Metabolism Compound Library
MCE 站:Glutamine Metabolism Compound Library
Glutamine is an important metabolic fuel that helps rapidly proliferating cells meet the increased demand for ATP, biosynthetic precursors, and reducing agents. Glutamine Metabolism pathway involves the initial deamination of glutamine by glutaminase(GLS), yielding glutamate and ammonia. 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), to produce both ATP and anabolic carbons for the synthesis of amino acids, nucleotides and lipids. During periods of hypoxia or mitochondrial dysfunction, α-KG can be converted to citrate in a reductive carboxylation reaction catalyzed by IDH2. The newly formed citrate exits the mitochondria where it is used to synthesize fatty acids and amino acids and produce the reducing agent, NADPH.Cancer cells display an altered metabolic circuitry that is directly regulated by oncogenic mutations and loss of tumor suppressors. Mounting evidence indicates that altered glutamine metabolism in cancer cells has critical roles in supporting macromolecule biosynthesis, regulating signaling pathways, and maintaining redox homeostasis, all of which contribute to cancer cell proliferation and survival. Thus, intervention in glutamine metabolic processes could provide novel approaches to improve cancer treatment.MCE owns a unique collection of 537 compounds targeting the mainly proteins and enzymes involved in glutamine metabolism pathway. Glutamine Metabolism compound library is a useful tool for intervention in glutamine metabolic processes.
Description & Advantages:
? A unique collection of 537 glutamine metabolism -related small molecules for high throughput screening (HTS) and high content screening (HCS).
? Targets such as glucose transporter, glutamate dehydrogenase , glutaminase, c-Myc ,etc.
? A useful tool for glutamine metabolism research and anti-cancer drug discovery.
? Bioactivity and safety confirmed by preclinical research and clinical trials. Some inhibitors have been approved by FDA.
? Structurally diverse, medicinally active, and cell permeable.
? More detailed compound information with structure, IC50, and brief introduction.
? NMR and HPLC validated to ensure high purity and quality.
? All compounds are in stock and continuously updated.
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