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    beta-Nicotinamide adenine dinucleotide phosphate sodium salt hydrate

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      beta-Nicotinamide adenine dinucleotide phosphate sodium salt hydrate

      SKU
      N0151

      Category: Metabolites

      Synonyms
      Coenzyme II , β-NADP , NADP+ , TPN , Triphosphopyridine nucleotide sodium salt hydrate
      698999-85-8
      CAS-Number
      C21H27N7NaO17P3 . xH2O
      Molecular Formula
      765.39 (anhydrous)
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥98% (HPLC)
      Appearance
      White to off-white powder
      Identity
      1H-NMR

      Properties

      Solvents
      water (30 mg/ml)
      Shipping
      AMBIENT
      Short Term Storage
      +4°C
      Long Term Storage
      -20°C
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at -20°C.
      Hazard statements
      H319
      Precautionary statements
      P280-P305 + P351 + P338-P337 + P313
      GHS Symbol
      GHS07
      Signal word
      Warning
      Transportation
      Not dangerous goods
      Description
      NADP+ is the oxidized form of the electron donor nicotinamide adenine dinucleotide phosphate. It is a cofactor used in anabolic reactions, such as the Calvin cycle, lipid syntheses and nucleic acid syntheses, which require NADPH as a reducing agent. It serves as a cofactor in various biological reactions. In addition, the balance between these reduced and oxidized forms plays key roles in diverse cellular functions, including cell survival, the maintenance of redox status and intracellular signaling. For example, binding of NADP+ to β-subunits of Kv channels activates ion transport, whereas NADPH stabilizes channel inactivation. NADP+ is biosynthesized from NAD+ by NAD kinase, with ATP as the phosphoryl donor. NADP+ might be useful for immunometabolism research.
      Smiles
      O[C@H]1[C@@H](OP(O)(O)=O)[C@H](N2C=NC3=C2N=CN=C3N)O[C@@H]1COP([O-])(OP(OC[C@@H]4[C@@H](O)[C@@H](O)[C@H]([N+]5=CC(C(N)=O)=CC=C5)O4)([O-])=O)=O.[Na+]
      InChi Key
      JNUMDLCHLVUHFS-QYZPTAICSA-M
      References
      (1) F. Shi, et al., Acta Biochim. Biophys. Sin. 41, 352 (2009) , (2) J.B. Jackson, BBA 1817, 1839 (2012) , (3) M. Nakamura, et al., Circ. Res. 111, 604 (2012) , (4) P.J. Kilfoil, et al., Circ. Res. 112, 721 (2013) , (5) M. Ziegler, FEBS J. 272, 4561 (2014) , (6) R. Ramalho, et al., Sem. Immunopathol. 42, 279 (2020)
      InChi
      InChI=1S/C21H28N7O17P3.Na/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32,/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39),/q,+1/p-1/t10-,11-,13-,14-,15-,16-,20-,21-,/m1./s1

      NADP+ is the oxidized form of the electron donor nicotinamide adenine dinucleotide phosphate. It is a cofactor used in anabolic reactions, such as the Calvin cycle, lipid syntheses and nucleic acid syntheses, which require NADPH as a reducing agent. It serves as a cofactor in various biological reactions. In addition, the balance between these reduced and oxidized forms plays key roles in diverse cellular functions, including cell survival, the maintenance of redox status and intracellular signaling. For example, binding of NADP+ to β-subunits of Kv channels activates ion transport, whereas NADPH stabilizes channel inactivation. NADP+ is biosynthesized from NAD+ by NAD kinase, with ATP as the phosphoryl donor. NADP+ might be useful for immunometabolism research.

      SKU: N0151 Category: Metabolites
      • Additional information

      Additional information

      Synonyms

      Coenzyme II, β-NADP, NADP+, TPN, Triphosphopyridine nucleotide sodium salt hydrate

      Purity

      ≥98% (HPLC)

      Appearance

      White to off-white powder

      CAS-Number

      698999-85-8

      Molecular Formula

      C21H27N7NaO17P3 . xH2O

      Molecular Weight

      765.39 (anhydrous)

      Identity

      1H-NMR

      Solvents

      water (30 mg/ml)

      Smiles

      O[C@H]1[C@@H](OP(O)(O)=O)[C@H](N2C=NC3=C2N=CN=C3N)O[C@@H]1COP([O-])(OP(OC[C@@H]4[C@@H](O)[C@@H](O)[C@H]([N+]5=CC(C(N)=O)=CC=C5)O4)([O-])=O)=O.[Na+]

      InChi Key

      JNUMDLCHLVUHFS-QYZPTAICSA-M

      Shipping

      AMBIENT

      Short Term Storage

      +4°C

      Long Term Storage

      -20°C

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at -20°C.

      Hazard statements

      H319

      Precautionary statements

      P280-P305 + P351 + P338-P337 + P313

      GHS Symbol

      GHS07

      Signal word

      Warning

      Transportation

      Not dangerous goods

      References

      (1) F. Shi, et al., Acta Biochim. Biophys. Sin. 41, 352 (2009), (2) J.B. Jackson, BBA 1817, 1839 (2012), (3) M. Nakamura, et al., Circ. Res. 111, 604 (2012), (4) P.J. Kilfoil, et al., Circ. Res. 112, 721 (2013), (5) M. Ziegler, FEBS J. 272, 4561 (2014), (6) R. Ramalho, et al., Sem. Immunopathol. 42, 279 (2020)

      InChi

      InChI=1S/C21H28N7O17P3.Na/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32,/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39),/q,+1/p-1/t10-,11-,13-,14-,15-,16-,20-,21-,/m1./s1

      Quantity

      500 mg, 1 g, Bulk

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