Molecular structure of Adenosine 5′-Monophosphate, Disodium Salt, CAS Number: 4578-31-8
Adenosine 5′-Monophosphate, Disodium Salt (CAS 4578-31-8)
Alternate Names:
5′-AMP⋅2Na
Application:
Adenosine 5′-Monophosphate, Disodium Salt is a nucleotide involved in the reactions of cellular energy transfers
CAS Number:
4578-31-8
Purity:
≥98%
Molecular Weight:
391.19
Molecular Formula:
C10H12N5Na2O7P
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Adenosine 5′-Monophosphate, Disodium Salt, or AMP disodium salt, is a compound derived from adenosine. It plays a role in cellular energy metabolism as a precursor for adenosine triphosphate (ATP) synthesis. Additionally, it functions in cellular signaling pathways and regulates enzyme activity. Adenosine 5′-Monophosphate, Disodium Salt is widely used in research and pharmaceutical applications for studying cellular processes and conducting biochemical assays. Adenosine 5′-Monophosphate, Disodium Salt is an activator of AMPK.
Adenosine 5′-Monophosphate, Disodium Salt (CAS 4578-31-8) References
- Coordination properties of adenosine-5'-monophosphate and related ligands towards Me2Sn(IV)2+ in aqueous solution. | Jankovics, H., et al. 2002. J Inorg Biochem. 92: 55-64. PMID: 12230988
- The pH-dependence of preferential solvation as studied by intermolecular homo- and heteronuclear NOE measurements of adenosine in water-trifluoroethanol mixtures. | Angulo, M. and Berger, S. 2004. Anal Bioanal Chem. 378: 1555-60. PMID: 15214416
- Charge transfer complexes of adenosine-5'-monophosphate and cytidine-5'-monophosphate with water-soluble cobalt(II) Schiff base complexes in aqueous solution. | Boghaei, DM. and Gharagozlou, M. 2006. Spectrochim Acta A Mol Biomol Spectrosc. 63: 139-48. PMID: 15950536
- Effects of adenosine 5'-monophosphate on epidermal turnover. | Furukawa, F., et al. 2008. Arch Dermatol Res. 300: 485-93. PMID: 18758798
- Nucleotide recognition and phosphate linkage hydrolysis at a lipid cubic interface. | Murgia, S., et al. 2010. J Am Chem Soc. 132: 16176-84. PMID: 20977215
- Preparation and biological effect of nucleotide-capped CdSe/ZnS quantum dots on Tetrahymena thermophila. | Xiao, Q., et al. 2012. Biol Trace Elem Res. 147: 346-53. PMID: 22161288
- Bitter taste inhibiting agents for whey protein hydrolysate and whey protein hydrolysate beverages. | Leksrisompong, P., et al. 2012. J Food Sci. 77: S282-7. PMID: 22809256
- Dielectric spectra broadening as a signature for dipole-matrix interaction. III. Water in adenosine monophosphate/adenosine-5'-triphosphate solutions. | Puzenko, A., et al. 2012. J Chem Phys. 137: 194502. PMID: 23181321
- The effect of adenosine 5'-monophosphate (AMP) on tenderness, microstructure and chemical-physical index of duck breast meat. | Wang, D., et al. 2016. J Sci Food Agric. 96: 1467-73. PMID: 25953510
- Application and optimization of the tenderization of pig Longissimus dorsi muscle by adenosine 5'-monophosphate (AMP) using the response surface methodology. | Deng, S., et al. 2016. Anim Sci J. 87: 439-48. PMID: 26212625
- Surface grafting of rare-earth ions doped hydroxyapatite nanorods (HAp:Ln(Eu/Tb)) with hydrophilic copolymers based on ligand exchange reaction: Biological imaging and cancer treatment. | Heng, C., et al. 2018. Mater Sci Eng C Mater Biol Appl. 91: 556-563. PMID: 30033287
- Optimization of the Tenderization of Duck Breast Meat by Adenosine 5'-Monophosphate (AMP) using Response Surface Methodology. | Wang, D., et al. 2016. J Poult Sci. 53: 93-101. PMID: 32908370
- Microwave-Assisted Hydrothermal Rapid Synthesis of Ultralong Hydroxyapatite Nanowires Using Adenosine 5'-Triphosphate. | Zhang, Y., et al. 2022. Molecules. 27: PMID: 35956970
- Sorption and distribution performance of organophosphorus compound (Adenosine 5'-monophosphate)on marine sediments. | Cao, XY., et al. 2022. Environ Pollut. 311: 119993. PMID: 35995290
- Atropine resistant excitation of the urinary bladder: the possibility of transmission via nerves releasing a purine nucleotide. | Burnstock, G., et al. 1972. Br J Pharmacol. 44: 451-61. PMID: 4339250
Activator of:
AMPK, and PYGB.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Adenosine 5′-Monophosphate, Disodium Salt, 5 g | sc-202444 | 5 g | $59.00 | |||
Adenosine 5′-Monophosphate, Disodium Salt, 25 g | sc-202444A | 25 g | $158.00 | |||
Adenosine 5′-Monophosphate, Disodium Salt, 100 g | sc-202444B | 100 g | $260.00 | |||
Adenosine 5′-Monophosphate, Disodium Salt, 1 kg | sc-202444C | 1 kg | $908.00 |