CAS 90947-51-6

6,6'-sulfanediylbis(5H-purine)

Description:

6,6'-Sulfanediylbis(5H-purine), with the CAS number 90947-51-6, is a chemical compound that features a purine structure linked by a sulfanediyl (–S–S–) group. This compound is characterized by its dual purine moieties, which are heterocyclic aromatic compounds containing nitrogen atoms in their rings. The presence of the sulfanediyl group suggests that it may exhibit properties related to redox chemistry, potentially acting as a reducing agent or participating in electron transfer processes. The purine rings contribute to its biological relevance, as purines are fundamental components of nucleic acids (DNA and RNA) and play critical roles in cellular metabolism and energy transfer, particularly in the form of ATP. The compound may also exhibit solubility in polar solvents, depending on its specific substituents and structural features. Its unique structure could make it of interest in medicinal chemistry, particularly in the development of pharmaceuticals targeting purine metabolism or related pathways. However, detailed studies on its biological activity and potential applications would be necessary to fully understand its characteristics and uses.

Formula: C₁₀H₆N₈S

InChI: InChI=1/C10H6N8S/c1-11-5-7(13-1)15-3-17-9(5)19-10-6-8(14-2-12-6)16-4-18-10/h1-6H

SMILES: C1=NC2C(=N1)N=CN=C2SC1=NC=NC2=NC=NC12

6,6'-Thiobis-9H-purine

Controlled Product

CAS: 90947-51-6

Applications 6,6'-Thiobis-9H-purine is used in the study of the activity of topoisomerase IIα.
References Jensen, L.H., et al.: Molecular Pharmacology, 70, 1503 (2006);

Formula: C₁₀H₆N₈S

Color and Shape: Neat

Molecular weight: 270.27

Ref: TR-T348060

Mercaptopurine Impurity 1

CAS: 90947-51-6

Formula: C₁₀H₆N₈S

Molecular weight: 270.27

Ref: ST-EA-CP-M81005