CAS 6165-03-3

6-(benzylsulfanyl)-9-pentofuranosyl-9H-purine

Description:

6-(Benzylsulfanyl)-9-pentofuranosyl-9H-purine, identified by its CAS number 6165-03-3, is a purine derivative characterized by the presence of a benzylsulfanyl group and a pentofuranosyl moiety. This compound features a purine base, which is a fundamental structure in nucleic acids, and its modification with a benzylsulfanyl group can influence its biological activity and solubility. The pentofuranosyl sugar component contributes to its nucleoside-like properties, potentially impacting its interaction with nucleic acid synthesis and metabolism. The presence of sulfur in the benzylsulfanyl group may enhance its reactivity and provide unique chemical properties, such as increased lipophilicity or altered binding affinities to biological targets. Overall, this compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry and drug development. Further studies would be necessary to elucidate its specific biological activities and potential applications.

Formula: C₁₇H₁₈N₄O₄S

InChI: InChI=1/C17H18N4O4S/c22-6-11-13(23)14(24)17(25-11)21-9-20-12-15(21)18-8-19-16(12)26-7-10-4-2-1-3-5-10/h1-5,8-9,11,13-14,17,22-24H,6-7H2/t11-,13-,14-,17-/m1/s1

Synonyms:

• 9H-Purine, 6-((phenylmethyl)thio)-9-beta-D-ribofuranosyl-
• 9H-Purine, 6- (benzylthio)-9-.beta.-D-ribofuranosyl-
• 6-(benzylsulfanyl)-9-(beta-D-ribofuranosyl)-9H-purine
• Purine, 6-benzylthio-9-beta-D-ribofuranosyl-
• 9H-purine, 6-[(phenylmethyl)thio]-9-beta-D-ribofuranosyl-
• 9H-purine, 9-pentofuranosyl-6-[(phenylmethyl)thio]-

6-Benzylthioinosine

CAS: 6165-03-3

6-Benzylthioinosine curbs glucose uptake, glycolysis, and ATP levels with slight ROS and respiration effects.

Formula: C₁₇H₁₈N₄O₄S

Purity: 98%

Color and Shape: Solid

Molecular weight: 374.42

Ref: TM-T26395