欢迎光临~北京凯森莱科技有限公司
语言选择: 中文版 ∷  英文版
  • 80394-72-5 , Oxanosine, 5-氨基-3-beta-D-呋喃核糖基咪唑并(4,5-d)(1,3)恶嗪-7(3H)-酮, CAS:80394-72-5
  • 80394-72-5 , Oxanosine, 5-氨基-3-beta-D-呋喃核糖基咪唑并(4,5-d)(1,3)恶嗪-7(3H)-酮, CAS:80394-72-5
80394-72-5 , Oxanosine, 5-氨基-3-beta-D-呋喃核糖基咪唑并(4,5-d)(1,3)恶嗪-7(3H)-酮, CAS:80394-72-580394-72-5 , Oxanosine, 5-氨基-3-beta-D-呋喃核糖基咪唑并(4,5-d)(1,3)恶嗪-7(3H)-酮, CAS:80394-72-5

80394-72-5 , Oxanosine, 5-氨基-3-beta-D-呋喃核糖基咪唑并(4,5-d)(1,3)恶嗪-7(3H)-酮, CAS:80394-72-5

80394-72-5 , Oxanosine ,
5-氨基-3-beta-D-呋喃核糖基咪唑并(4,5-d)(1,3)恶嗪-7(3H)-酮,
CAS:80394-72-5
C10H12N4O6 / 284.225
MFCD01720542

Oxanosine

5-氨基-3-beta-D-呋喃核糖基咪唑并(4,5-d)(1,3)恶嗪-7(3H)-酮

Oxanosine is a modified nucleoside that has recently gained attention in scientific research due to its potential biological applications. In this paper, we will discuss the background, physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, limitations, and future directions of Oxanosine.

Definition and Background

Oxanosine is a modified nucleoside that was first discovered in 1975 by K. Maeda and Y. Miyazawa in a culture of Streptomyces iizukae. It contains a hydroxy group on the 3'-position of the ribofuranose ring and a methoxy group on the 4'-position. Oxanosine is usually found in transfer RNA (tRNA) and is thought to play a role in translational fidelity. It has also been found to exhibit antitumor activity and may be used in cancer drug research.

Synthesis and Characterization

Oxanosine can be synthesized from uridine, which is readily available commercially. The synthesis involves a series of chemical reactions that modify the sugar moiety of uridine. The purification and characterization of oxanosine can be achieved through a combination of techniques such as high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) spectroscopy.

Analytical Methods

Several analytical methods have been developed to detect and quantify oxanosine in biological samples. These methods include HPLC coupled with UV detection, fluorescence detection, and mass spectrometry. NMR spectroscopy can also be used for analysis of oxanosine.

Biological Properties

Oxanosine has been shown to exhibit antitumor activity in vitro and in vivo. It also plays a role in translational fidelity by preventing ribosomal frameshifting. Oxanosine has been found to inhibit viral replication and has been proposed as a potential antiviral agent. However, more research is needed to fully understand its biological properties.

Toxicity and Safety in Scientific Experiments

There is limited information about the toxicity and safety of oxanosine in scientific experiments. However, it has been reported to exhibit low toxicity in animal studies.

Applications in Scientific Experiments

Oxanosine has potential applications in cancer research as it exhibits antitumor activity. It may also be used as an antiviral agent due to its ability to inhibit viral replication. Additionally, oxanosine could be used in the development of new antibiotics and other pharmaceutical drugs.

Current State of Research

There have been relatively few studies on oxanosine, and its potential applications are still being explored. It has been found to exhibit antitumor activity, but more research is needed to fully understand its biological properties and potential applications.

Potential Implications in Various Fields of Research and Industry

Oxanosine has potential implications in various fields of research and industry, including cancer research, antiviral research, and pharmaceutical drug development. It may also be used in the development of new antibiotics.

Limitations and Future Directions

One limitation of the current research on oxanosine is the lack of information on its toxicity and safety. Further research is needed to fully understand its biological properties and potential applications. Future directions for research on oxanosine include studying its mechanisms of action, investigating its potential as an antiviral agent, and optimizing its synthesis.

In addition, there is a need for more research on the safety and pharmacokinetics of oxanosine in humans. Further elucidation of the mechanisms underlying its biological properties would also pave the way for more targeted drug development efforts. Finally, optimizing methods for its synthesis and purification would enable increased access to this compound for research purposes.

Conclusion

In conclusion, oxanosine is a modified nucleoside with potential applications in cancer research, antiviral research, and drug development. It exhibits antitumor activity and has been found to inhibit viral replication. However, more research is needed to fully understand its biological properties and potential applications. Further investigation into its safety and toxicity in humans and optimization of its synthesis and purification methods are also needed.

CAS Number80394-72-5
Product NameOxanosine
IUPAC Name5-amino-3-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]imidazo[4,5-d][1,3]oxazin-7-one
Molecular FormulaC10H12N4O6
Molecular Weight284.225 g/mol
InChIInChI=1S/C10H12N4O6/c11-10-13-7-4(9(18)20-10)12-2-14(7)8-6(17)5(16)3(1-15)19-8/h2-3,5-6,8,15-17H,1H2,(H2,11,13)/t3-,5-,6-,8-/m1/s1
InChI KeyPWVUOVPUCZNICU-MMRIIKACSA-N
SMILESC1=NC2=C(N1C3C(C(C(O3)CO)O)O)N=C(OC2=O)N
Synonyms5-amino-3-beta-D-ribofuranosyl-3H-imidazo(4,5-d)(1,3)oxazin-7-one, oxanosine
Canonical SMILESC1=NC2=C(N1C3C(C(C(O3)CO)O)O)N=C(OC2=O)N
Isomeric SMILESC1=NC2=C(N1[C@H]3C(C([C@H](O3)CO)O)O)N=C(OC2=O)N


在线询价

用手机扫描二维码关闭
二维码