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CAS 1198-83-0

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2-(Methylthio)adenine

Description:
2-(Methylthio)adenine is a purine derivative characterized by the presence of a methylthio group at the 2-position of the adenine structure. This compound is known for its role as a nucleobase analog and is often studied in the context of biochemical research, particularly in relation to its effects on nucleic acid metabolism and cellular processes. It exhibits properties typical of purines, including the ability to participate in hydrogen bonding and base pairing, which can influence its interactions with nucleic acids. The methylthio group contributes to its unique chemical reactivity and solubility characteristics. Additionally, 2-(Methylthio)adenine may exhibit biological activity, potentially acting as a substrate or inhibitor in various enzymatic reactions. Its structural modifications compared to adenine can lead to altered pharmacological properties, making it of interest in medicinal chemistry and drug development. Overall, this compound serves as a valuable tool in understanding the biochemical pathways involving purines and their derivatives.
Formula:C6H7N5S
InChI:InChI=1S/C6H7N5S/c1-12-6-10-4(7)3-5(11-6)9-2-8-3/h2H,1H3,(H3,7,8,9,10,11)
InChI key:InChIKey=FXGXEFXCWDTSQK-UHFFFAOYSA-N
SMILES:NC1=C2C(=NC(SC)=N1)N=CN2
Synonyms:
  • 1H-Purin-6-amine, 2-(methylthio)-
  • 2-(Methylsulfanyl)-9H-purin-6-amine
  • 2-(Methylthio)-9H-purin-6-amine
  • 2-(Methylthio)adenine
  • 2-(methylsulfanyl)-5H-purin-6-amine
  • 2-Methylthio-6-aminopurine
  • 6-Amino-2-(methylthio)purine
  • 9H-Purin-6-amine, 2-(methylthio)-
  • Adenine, 2-(methylthio)-
  • NSC 7235
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