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NADP+ (sodium salt hydrate)

 
Catalog No.
C4639
 
组合的产品项目
规格价格库存 数量
100mg
¥ 650.00
现货
250mg
¥ 1,300.00
现货

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背景

NADP+ (sodium salt hydrate) is the oxidized form of the electron donor, reduced nicotinamide adenine dinucleotide phosphate (NADPH) [1].

NADP+ and NADPH are two fundamental common mediators involved in many biological processes, such as energy metabolism, mitochondrial functions, calcium homeostasis, antioxidation/generation of oxidative stress, gene expression, immunological functions, aging, and cell death. NADP+ and NADPH are mainly used by the enzymes that catalyze substrate reduction [1].

In cell extracts of human heteroploid cell lines HeLa and T-9, addition of NADP+ at 10-3 M stabilized glucose-6-phosphate dehydrogenase [2]. In air-dried and intact cells of Gluconobacter suboxydans, increasing concentrations of NADP+, up to 10 μmol/ml, led to increased NADPH production. However, NADP+ at concentrations more than 50 μmol/ml did not increase or markedly decrease the production of NADPH, which was considered to be due to acidification of the reaction mixture on the addition of a high concentration of free NADP+ and also on the formation of a large amount of gluconic acid via gluconolactone [3].

References:

[1]. Ying W. NAD+/NADH and NADP+/NADPH in cellular functions and cell death: regulation and biological consequences. Antioxidants & Redox Signaling, 2008, 10(2): 179-206.

[2]. Alekseev S B, Mamaev V B, Zgurskii A A, et al. Stability of glucose-6-phosphate dehydrogenase in human cells cultivated in vitro. Biokhimiia, 1979, 44(6): 1093-1100.

[3]. Izumi Y , Nath P K , Yamamoto H , et al. NADPH production from NADP+ with a glucose dehydrogenase system involving whole cells and immobilized cells of Gluconobacter suboxydans. Applied Microbiology and Biotechnology, 1989, 30(4): 337-342.

化学属性

Physical AppearanceA crystalline solid
StorageStore at -20°C
M.Wt783.4
Cas No.698999-85-8
FormulaC21H29N7NaO18P3
Solubilityinsoluble in DMSO; insoluble in EtOH; ≥51.1 mg/mL in H2O
SDFDownload SDF
Canonical SMILESO[C@H]1[C@H]([C@@H](O[C@@H]1COP(OP(OC[C@@H]2[C@H]([C@H]([C@@H](O2)[N+]3=CC(C(N)=O)=CC=C3)O)O)([O-])=O)([O-])=O)N4C=NC5=C4N=CN=C5N)OP(O)(O)=O.[Na+].O
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