CAS 20535-04-0

9-(5-deoxypent-4-enofuranosyl)-9H-purin-6-amine

Description:

9-(5-Deoxypent-4-enofuranosyl)-9H-purin-6-amine, also known by its CAS number 20535-04-0, is a nucleoside analog that features a purine base linked to a modified sugar moiety. This compound is characterized by the presence of a 9H-purine structure, which is a bicyclic aromatic compound consisting of fused imidazole and pyrimidine rings. The sugar component is a deoxyribose derivative, specifically a 5-deoxypent-4-enofuranosyl group, which indicates that it has a double bond and lacks an oxygen atom at the 5-position of the sugar ring. This structural modification can influence the compound's biological activity, potentially affecting its role in nucleic acid metabolism or as an antiviral agent. The compound may exhibit unique solubility and stability properties due to its specific functional groups, and its interactions with enzymes or receptors could be of interest in medicinal chemistry and drug development. Overall, this substance represents a fascinating area of study in the field of biochemistry and pharmacology.

Formula: C₁₀H₁₁N₅O₃

InChI: InChI=1/C10H11N5O3/c1-4-6(16)7(17)10(18-4)15-3-14-5-8(11)12-2-13-9(5)15/h2-3,6-7,10,16-17H,1H2,(H2,11,12,13)

SMILES: C=C1C(C(C(n2cnc3c(N)ncnc23)O1)O)O

Synonyms:

• 4’,5’-Didehydro-5’-deoxyadenosine, 1-(5-Deoxy-beta-D-erythro-pent-4-enofuranosyl)adenine
• Adenosine, 4',5'-didehydro-5'-deoxy-
• CALCIUM BIS(CYCLOHEXYLSULFAMATE)
• 4',5'-Didehydro-5'-deoxyadenosine

4',5'-Didehydro-5'-deoxyadenosine

CAS: 20535-04-0

4',5'-Didehydro-5'-deoxyadenosine is a Nucleoside Derivative - 5'-Modified nucleoside.

Formula: C₁₀H₁₁N₅O₃

Color and Shape: Solid

Molecular weight: 249.23

Ref: TM-TNU0881