85426-74-0

Usage

Uses

Used in Pharmaceutical Industry:
6-aminoallopurinol riboside is used as an immunotherapeutic agent for its potential to modulate immune responses and treat various diseases. It has been studied in the context of guanosine analogs, which are being researched for their potential applications in immunotherapy.
Used in Research and Development:
6-aminoallopurinol riboside is used as a research compound for the development of new drugs and therapies. Its unique structure and properties make it a valuable tool for studying the mechanisms of action and potential applications in various fields, including immunology and oncology.

InChI:InChI=1/C10H13N5O5/c11-10-13-7-3(8(19)14-10)1-12-15(7)9-6(18)5(17)4(2-16)20-9/h1,4-6,9,12,16-18H,2H2,(H2,11,14,19)/t4-,5-,6-,9-/m1/s1

Upstream product

• 76690-46-5 6-Methylthio-4(5H)-oxo-1-β-D-ribofuranosylpyrazolo<3,4-d>pyrimidine 
• 70421-30-6 1-(β-D-Ribofuranosyl)-4,6-diaminopyrazolo<3,4-d>pyrimidine 
• 53762-14-4 5-amino-1-(2',3'O-isopropylidene-β-D-ribofuranosyl)pyrazole-4-carboxamide 
• 129797-24-6 1-(2,3-O-isopropylidene-β-D-ribofuranosyl)-5-<(N'-benzoylthiocarbamoyl)amino>pyrazole-4-carboxamide 
• 74525-92-1 1-(β-D-Ribofuranosyl)-4,6-dimethylmercaptopyrazolo<3,4-d>pyrimidine 
• 96555-41-8 C₃₁H₂₄BrN₅O₈ 
• 96555-39-4 3-bromo-4(5H)-oxopyrazolo[3,4-d]pyrimidin-6-yl methyl sulfoxide 
• 96555-36-1 3,6-dibromo-1H-pyrazolo[3,4-d]pyrimidin-4(5H)-one 
• 96575-35-8 6-amino-3-bromopyrazolo[3,4-d]pyrimidin-4(5H)-one 
• 96555-35-0 6-bromoallopurinol 
• 5334-26-9 6-(methylthio)pyrazolo<3,4-d>pyrimidin-4(5H)-one 
• 24521-76-4 6-thioxo-1,5,6,7-tetrahydropyrazolo<3,4-d>pyrimidin-4-one 
• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 96555-37-2 6-amino-3-bromo-1-β-D-ribofuranosylpyrazolo<3,4-d>pyrimidin-4(5H)-one 

Relevant academic research and scientific papers

Investigation of 8-aza-7-deaza purine nucleoside derivatives

Glycosylation of 6-amino-4-methoxy-1H-pyrazolo[3,4-d]pyrimidine and its iodo- and bromo- analogues with the protected ribofuranose and 20-deoxyribofuranose under different conditions resulted in the synthesis of N9- and N8

Pyrazolo[3,4-d]pyrimidine ribonucleosides related to 2-aminoadenosine and isoguanosine: Synthesis, deamination and tautomerism

The syntheses and properties of 8-aza-7-deazapurine (pyrazolo[3,4-d] pyrimidine) ribonucleosides related to 2-aminoadenosine and isoguanosine are described. Glycosylation of 8-aza-7-deazapurine-2,6-diamine 5 with 1-O-acetyl-2,3,5-tri-O-benzoyl-β-d-ribofur

Synthesis and biological activity of 6-azacadeguomycin and certain 3,4,6-trisubstituted pyrazolo[3,4-d]pyrimidine ribonucleosides

Several 3,4,6-trisubstituted pyrazolo[3,4-d]pyrimidine ribonucleosides were prepared and tested for their biological activity. High-temperature glycosylation of 3,6-dibromoallopurinol with 1-O-acetyl-2,3,5-tri-O-benzoyl-D-ribofuranose in the presence of B