Date published: 2026-2-2

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6-Methoxypurine (CAS 1074-89-1)

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Application:
6-Methoxypurine is a Phosphoribosyltransferase inhibitor
CAS Number:
1074-89-1
Molecular Weight:
150.1
Molecular Formula:
C6H6N4O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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6-Methoxypurine is a Phosphoribosyltransferase inhibitor. 6-Methoxypurine, a extensively studied purine base in biochemistry exhibits a unique heterocyclic structure, comprising a fused pyrimidine ring and an imidazole ring. Its versatility has led to its widespread utilization in various scientific research applications. One of its primary roles lies in serving as a valuable probe for investigating protein structure and function, facilitating a deeper understanding of these essential biomolecules. Moreover, researchers have harnessed its potential as a substrate for enzymatic reactions, amplifying its significance in biochemical studies. This multifaceted compound contributes to the exploration of protein folding and stability, examination of catalytic enzyme properties, and probing the effects of mutations on protein behavior. While the precise mechanism of action of 6-methoxypurine remains not entirely elucidated, it is hypothesized to interact with proteins through various means, including hydrogen bonding, electrostatic interactions, and covalent bonds. In addition, hydrophobic interactions, van der Waals forces, and pi-pi stacking interactions are believed to play a role in its interaction with proteins. 6-Methoxypurine emerges as a pivotal player in the realms of biochemistry offering researchers a potent tool to unravel the mysteries of protein function and structure.


6-Methoxypurine (CAS 1074-89-1) References

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  2. Reaction of O6-alkylguanine-DNA alkyltransferase with O6-methylguanine analogues: evidence that the oxygen of O6-methylguanine is protonated by the protein to effect methyl transfer.  |  Spratt, TE. and de los Santos, H. 1992. Biochemistry. 31: 3688-94. PMID: 1314648
  3. Synthesis and biological studies of unsaturated acyclonucleoside analogues of S-adenosyl-L-homocysteine hydrolase inhibitors.  |  Hasan, A. and Srivastava, PC. 1992. J Med Chem. 35: 1435-9. PMID: 1573637
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  7. Stacking interaction between different species: purine and 6-methoxypurine.  |  Danner, J. and Helmkamp, GK. 1971. Biochim Biophys Acta. 232: 227-33. PMID: 5553679
  8. Purine N-oxides. XXV. 3-N-oxides of adenine and hypoxanthine.  |  Scheinfeld, I., et al. 1969. J Phys Chem. 34: 2153-6. PMID: 5788208
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

6-Methoxypurine, 250 mg

sc-291383
250 mg
$40.00

6-Methoxypurine, 1 g

sc-291383A
1 g
$66.00