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.

2-(Methylthio)adenine

1198-83-0: 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

2-(Methylthio)-9H-purin-6-amine is a synthetic purine derivative that has been shown to have bacteriostatic effects on Streptococcus faecalis. This compound inhibits the growth of bacteria by binding to the ribosomes and inhibiting protein synthesis. 2-(Methylthio)-9H-purin-6-amine does not inhibit bacterial DNA synthesis, but does inhibit RNA synthesis in human cells. It binds with high affinity to the receptor for uridine, a component of RNA, and may be useful in the treatment of cancer or viral infections.

2-(Methylthio)-9H-purin-6-amine is a synthetic purine derivative that has been shown to have bacteriostatic effects on Streptococcus faecalis. This compound inhibits the growth of bacteria by binding to the ribosomes and inhibiting protein synthesis. 2-(Methylthio)-9H-purin

CAS 1198-83-0: 2-(Methylthio)adenine

2-(Methylthio)-9H-purin-6-amine

Ref: 3D-BAA19883

2-methylsulfanyl-7H-purin-6-amine

Ref: IN-DA009R3Y

2-(Methylthio)-9H-purin-6-amine

Ref: 10-F540368