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Small molecules comprising two mononucleotides, adenosine monophosphate (AMP) and nicotinamide mononucleotide (NMN); oxidized and reduced nicotinamide adenine dinucleotides in their unphosphorylated (NAD+ or NADH) and phosphorylated (NADP+ or NADPH) forms.
Nicotinamide mononucleotide ( -NM NMN) one of the key precursors of NAD and products of the NAMPT reaction is converted to NAD by nicotinamide mononucleotide adenylyltransferase
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Nicotinic acid mononucleotide (NaMN) is a nucleotide intermediate in the biosynthesis of NAD+. It is produced from nicotinic acid via phosphoribosyltransferase and serves as a substrate for adenylyltransferases involved in NAD+ metabolism. Supplied as a research-grade reagent for biochemical and enzymatic studies.
Intermediate in NAD+ biosynthesis and metabolism.
Substrate for adenylyltransferase and enzymatic assays.
High purity, typically ~98%.
Molecular weight 335.2 g·mol⁻1; formula C11H14NO9P.
Intended for research use only; not for human consumption.
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A derivative of 6-mercaptopurine; active against S. faecalis when used at 0.05 to 15 mg/ml; inhibits autophagy and cholesterol synthesis in isolated and washed rat hepatocytes at 0.5, 1, or 1.5 mM; decreases tumor growth in mice bearing 6-mercaptopurine susceptible adenocarcinoma 755 tumors at 17, 35, or 70 mg/kg per day
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Nicotinamide (CAS 98-92-0) is a small-molecule inhibitor of poly(ADP-ribose) polymerase-1 (PARP-1) an enzyme critical in DNA repair pathways Under pathological conditions such as ischemia or trauma PARP-1 hyperactivation depletes cellular NAD triggering neuronal cell death In vitro studies indicate that transporter-mediated uptake of nicotinamide confers protection against PARP-1-induced astrocyte injury In vivo studies in diabetic rat models demonstrate that nicotinamide administration normalizes hepatic antioxidant enzymes reducing oxidative stress Clinical trials have shown dose-dependent upregulation of frataxin expression following sustained nicotinamide treatment suggesting therapeutic potential in disorders like Friedreich s ataxia
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Nicotinamide (CAS 98-92-0) is a small-molecule inhibitor of poly(ADP-ribose) polymerase-1 (PARP-1) an enzyme critical in DNA repair pathways Under pathological conditions such as ischemia or trauma PARP-1 hyperactivation depletes cellular NAD triggering neuronal cell death In vitro studies indicate that transporter-mediated uptake of nicotinamide confers protection against PARP-1-induced astrocyte injury In vivo studies in diabetic rat models demonstrate that nicotinamide administration normalizes hepatic antioxidant enzymes reducing oxidative stress Clinical trials have shown dose-dependent upregulation of frataxin expression following sustained nicotinamide treatment suggesting therapeutic potential in disorders like Friedreich s ataxia
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Nicotinamide adenine dinucleotide (NAD CAS number 53-84-9) is a coenzyme involved in oxidation-reduction reactions accepting electrons to form NADH Additionally NAD functions as a substrate in enzymatic processes mediated by poly(ADP-ribose) polymerases sirtuins and cyclic ADP-ribose synthases NAD analogs demonstrate inhibitory activity against CD38-associated NAD glycohydrolase (NADase) with reported IC50 values ranging from 2 mM to 10 mM In biomedical research NAD supplementation is investigated for addressing fatigue and fatigue-associated disorders
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Nicotinamide riboside malate is the malate salt form of nicotinamide riboside, a bioavailable precursor of nicotinamide adenine dinucleotide (NAD+) used in research to elevate intracellular NAD+ levels and probe sirtuin-mediated pathways. It is commonly employed in studies of metabolism, aging, and mitochondrial function and is provided as a solid reagent for laboratory research (CAS 2415659-01-5).
Orally bioavailable NAD+ precursor.
Supports increased intracellular NAD+ levels.
Enables sirtuin activation and metabolic pathway studies.
Suitable for research on aging and mitochondrial function.
Supplied as a solid powder for laboratory use.
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Kinetin riboside (Adenosine, N-(2-furanylmethyl)-) is a ribosylated cytokinin analog used in biochemical and cell biology research. It induces apoptosis in cancer cells and inhibits proliferation of HCT-15 cells (IC50 = 2.5 μM). The reagent is supplied as a high-purity solid and is intended for cell-based assays investigating apoptosis, proliferation, and cytotoxicity.
High purity: 99.88%.
Molecular weight: 347.33 g/mol.
Chemical formula: C15H17N5O5.
Appearance: solid, white to off-white.
Storage: powder -20°C for long term; in solvent -80°C recommended.