Cas no 4229-50-9 (N6-Methyladenosine-5'-monophosphate Sodium Salt)

N6-Methyladenosine-5'-monophosphate Sodium Salt (m6A-5'-MP Na Salt) is a modified nucleotide derivative featuring methylation at the N6 position of adenosine. This compound serves as a critical tool in RNA research, particularly in studies involving epitranscriptomics, RNA metabolism, and methylation dynamics. Its sodium salt form enhances solubility in aqueous solutions, facilitating experimental applications. The product is characterized by high purity and stability, ensuring reliable performance in enzymatic assays, structural studies, and synthetic biology. As a key intermediate or standard, it supports investigations into RNA modification pathways and their regulatory roles in cellular processes. Suitable for use in molecular biology and biochemistry research.
N6-Methyladenosine-5'-monophosphate Sodium Salt structure
4229-50-9 structure
Product Name:N6-Methyladenosine-5'-monophosphate Sodium Salt
CAS No:4229-50-9
MF:C11H16N5O7P
MW:361.247802734375
CID:1516854
PubChem ID:16760025
Update Time:2025-06-08

N6-Methyladenosine-5'-monophosphate Sodium Salt Chemical and Physical Properties

Names and Identifiers

    • 5'-Adenylic acid, N-methyl-
    • [(2R,3S,4R,5R)-3,4-dihydroxy-5-[6-(methylamino)purin-9-yl]oxolan-2-yl]methyl dihydrogen phosphate
    • CHEMBL1230507
    • N(6)-methyladenosine 5'-monophosphate
    • Q27120391
    • N-Methyl-5'-adenylic acid
    • NCGC00163320-01
    • DTXSID60587882
    • N(6)-methyl-AMP
    • 4229-50-9
    • SCHEMBL4307198
    • n6-methyl-adenosine monophosphate
    • N6-METHYLADENOSINE-5'-MONOPHOSPHATE
    • CHEMBL609083
    • N-methyladenosine 5'-(dihydrogen phosphate)
    • ((2R,3S,4R,5R)-3,4-Dihydroxy-5-(6-(methylamino)-9H-purin-9-yl)tetrahydrofuran-2-yl)methyl dihydrogen phosphate
    • {[(2R,3S,4R,5R)-3,4-dihydroxy-5-[6-(methylamino)-9H-purin-9-yl]oxolan-2-yl]methoxy}phosphonic acid
    • PD045691
    • N(6)-methyl-5'-phosphoadenosine
    • BDBM50367106
    • N(6)-methyl-[5']adenylic acid
    • N(6)-methyl-5'-adenylic acid
    • CHEBI:40196
    • N6-Methyladenosine-5'-monophosphate Sodium Salt
    • Inchi: 1S/C11H16N5O7P/c1-12-9-6-10(14-3-13-9)16(4-15-6)11-8(18)7(17)5(23-11)2-22-24(19,20)21/h3-5,7-8,11,17-18H,2H2,1H3,(H,12,13,14)(H2,19,20,21)/t5-,7-,8-,11-/m1/s1
    • InChI Key: WETVNPRPZIYMAC-IOSLPCCCSA-N
    • SMILES: P(=O)(O)(O)OC[C@@H]1[C@H]([C@H]([C@H](N2C=NC3C(NC)=NC=NC2=3)O1)O)O

Computed Properties

  • Exact Mass: 361.07888
  • Monoisotopic Mass: 361.07873486g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 5
  • Hydrogen Bond Acceptor Count: 11
  • Heavy Atom Count: 24
  • Rotatable Bond Count: 5
  • Complexity: 495
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 4
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -2.9
  • Topological Polar Surface Area: 172?2

Experimental Properties

  • PSA: 172.08
  • LogP: -1.33050

N6-Methyladenosine-5'-monophosphate Sodium Salt Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
M275898-1mg
N6-Methyladenosine-5'-monophosphate Sodium Salt
4229-50-9
1mg
$ 63.00 2023-09-07
TRC
M275898-5mg
N6-Methyladenosine-5'-monophosphate Sodium Salt
4229-50-9
5mg
$ 178.00 2023-09-07
TRC
M275898-10mg
N6-Methyladenosine-5'-monophosphate Sodium Salt
4229-50-9
10mg
$ 311.00 2023-09-07

N6-Methyladenosine-5'-monophosphate Sodium Salt Related Literature

Additional information on N6-Methyladenosine-5'-monophosphate Sodium Salt

Comprehensive Overview of N6-Methyladenosine-5'-monophosphate Sodium Salt (CAS No. 4229-50-9): Structure, Applications, and Research Insights

N6-Methyladenosine-5'-monophosphate Sodium Salt (CAS 4229-50-9), often abbreviated as m6A-5'-MP Na Salt, is a chemically modified nucleotide derivative that has garnered significant attention in biochemical and pharmaceutical research. This compound features a methyl group at the N6 position of adenosine, combined with a 5'-monophosphate moiety, and is stabilized by sodium ions. Its unique structure makes it a critical tool for studying RNA epigenetics, post-transcriptional modifications, and cellular signaling pathways.

Recent advancements in epitranscriptomics have highlighted the pivotal role of N6-methyladenosine (m6A) in regulating gene expression. As a synthetic analog of endogenous m6A, N6-Methyladenosine-5'-monophosphate Sodium Salt serves as a valuable standard in LC-MS and HPLC analyses, enabling precise quantification of m6A levels in RNA samples. Researchers also utilize it to investigate the enzymatic mechanisms of methyltransferases (e.g., METTL3/METTL14 complex) and demethylases (e.g., FTO, ALKBH5), which are linked to diseases like cancer and metabolic disorders.

The compound’s solubility in aqueous solutions (due to its sodium salt form) enhances its utility in in vitro assays, such as kinase activity studies and nucleotide-protein interaction experiments. Its stability under physiological pH conditions further supports applications in cell culture and drug discovery pipelines. Notably, the rise of mRNA-based therapeutics and vaccine development has spurred demand for high-purity modified nucleotides like this compound to optimize mRNA stability and translational efficiency.

From a commercial perspective, CAS 4229-50-9 is supplied by leading biochemical vendors with ≥95% purity, often verified by NMR and mass spectrometry. Storage recommendations typically include -20°C desiccated conditions to prevent hydrolysis. FAQs from researchers often focus on its compatibility with PCR systems, enzymatic incorporation rates, and alternatives for radiolabeled probes, reflecting its diverse utility.

Emerging trends connect m6A modifications to neurodegenerative diseases (e.g., Alzheimer’s) and immune response modulation, aligning with Google Scholar’s top-searched terms like "m6A and cancer immunotherapy" or "RNA methylation inhibitors." This positions N6-Methyladenosine-5'-monophosphate Sodium Salt as a cornerstone reagent for cutting-edge studies, bridging gaps between basic research and therapeutic innovation.

In summary, the multifaceted applications of CAS 4229-50-9 underscore its importance in modern molecular biology. Its integration into high-throughput screening platforms and diagnostic kit development further cements its relevance. As epitranscriptomics evolves, this compound will remain indispensable for decoding the biological functions of RNA modifications and their clinical implications.

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