CAS 103913-16-2
:Oxetanocin
Description:
Oxetanocin, with the CAS number 103913-16-2, is a synthetic nucleoside analog that exhibits unique structural characteristics, including a four-membered oxetane ring fused to a purine base. This compound is notable for its potential antiviral properties, particularly against certain viruses by interfering with their replication processes. Oxetanocin's structure allows it to mimic natural nucleosides, which can lead to its incorporation into viral RNA or DNA, ultimately disrupting viral replication. The compound has been studied for its pharmacological effects, including its ability to inhibit specific enzymes involved in viral life cycles. Additionally, its stability and solubility in biological systems are important factors that influence its efficacy as a therapeutic agent. Research continues to explore its full potential and mechanisms of action, as well as its safety profile and possible applications in treating viral infections. Overall, Oxetanocin represents a significant area of interest in medicinal chemistry and virology.
Formula:C10H13N5O3
InChI:InChI=1S/C10H13N5O3/c11-8-7-9(13-3-12-8)15(4-14-7)10-5(1-16)6(2-17)18-10/h3-6,10,16-17H,1-2H2,(H2,11,12,13)/t5-,6-,10-/m1/s1
InChI key:InChIKey=LMJVXGOFWKVXAW-OXOINMOOSA-N
SMILES:C(O)[C@H]1[C@H](N2C=3C(N=C2)=C(N)N=CN3)O[C@@H]1CO
Synonyms:- (2S,3R,4R)-4-(6-Amino-9H-purin-9-yl)-2,3-oxetanedimethanol
- 2,3-Oxetanedimethanol, 4-(6-amino-9H-purin-9-yl)-, (2S,3R,4R)-
- 2,3-Oxetanedimethanol, 4-(6-amino-9H-purin-9-yl)-, (2S-(2-alpha,3-beta,4-alpha))-
- 2,3-Oxetanedimethanol, 4-(6-amino-9H-purin-9-yl)-, [2S-(2α,3β,4α)]-
- 9-((2R,3R,4S)-3,4-Bis(hydroxymethyl)-2-oxetanyl)adenine
- Nk 84-0218
- Oxetanocin A
- [(2S,3R,4R)-4-(6-amino-9H-purin-9-yl)oxetane-2,3-diyl]dimethanol
- Oxetanocin
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Found 2 products.
Oxetanocin
CAS:<p>Oxetanocin is an antiviral compound, functioning as a nucleoside analog, which is derived from natural sources, specifically bacterial strains. Its mode of action involves the inhibition of viral replication through the interference with nucleic acid synthesis. By incorporating into viral DNA or RNA, Oxetanocin disrupts the normal replication process, thereby preventing the proliferation of the virus.</p>Formula:C10H13N5O3Purity:Min. 95%Molecular weight:251.24 g/mol
