Aids-002850
2',3'-Dideoxyxanthosine
CAS: 132194-28-6
Molecular Formula: C10H12N4O4
Aids-002850 - Names and Identifiers
| Name | 2',3'-Dideoxyxanthosine |
| Synonyms | Aids002850 Aids-002850 2',3'-Dideoxyxanthosine Xanthosine, 2',3'-dideoxy- Xanthosine, 2',3'-dideoxy- (9CI) 9-[(2R,5S)-5-(Hydroxymethyl)oxolan-2-yl]-3H-purine-2,6-dione 9-(2,3-Dideoxy-.beta.-D-glycero-pentofuranosyl)-9H-xanthosine 9-[(2R,5S)-5-(hydroxymethyl)tetrahydrofuran-2-yl]-3,9-dihydro-1H-purine-2,6-dione |
| CAS | 132194-28-6 |
| InChI | InChI=1/C10H12N4O4/c15-3-5-1-2-6(18-5)14-4-11-7-8(14)12-10(17)13-9(7)16/h4-6,15H,1-3H2,(H2,12,13,16,17)/t5-,6+/m0/s1 |
Aids-002850 - Physico-chemical Properties
| Molecular Formula | C10H12N4O4 |
| Molar Mass | 252.23 |
| Density | 1.91g/cm3 |
| Refractive Index | 1.837 |
Aids-002850 - Introduction
The 2 ',3'-dideoxyxanthine nucleoside is a xanthine nucleoside compound. Its molecular formula is C10H13N5O3 and its molecular weight is 251.24. It is a deoxynucleoside compound, meaning that its deoxy groups are located at the 2 'and 3' positions.
2 ',3'-dideoxyxanthine nucleosides have important physiological functions in organisms, especially play a key role in nucleic acid synthesis and metabolism. It can be one of the constituent units of DNA and RNA, involved in the transmission and maintenance of genetic information. In addition, it is involved in biological processes such as energy metabolism, signal transduction and cell regulation.
Regarding the preparation of 2 ',3'-dideoxyxanthine nucleosides, a common method is to use chemical synthesis. This compound can be synthesized by the steps of protection and deprotection of xanthine and deoxygenation.
When using 2 ',3'-dideoxyxanthine nucleosides or related compounds, it is necessary to pay attention to their safety. It may be toxic and irritant, so it is necessary to take appropriate safety measures when handling. At the same time, relevant laboratory practices should be followed, and this compound should be stored and handled properly to prevent accidents and environmental pollution. During use, avoid contact with skin and eyes, and maintain proper ventilation conditions. If necessary, consult a professional for more detailed safety information.
2 ',3'-dideoxyxanthine nucleosides have important physiological functions in organisms, especially play a key role in nucleic acid synthesis and metabolism. It can be one of the constituent units of DNA and RNA, involved in the transmission and maintenance of genetic information. In addition, it is involved in biological processes such as energy metabolism, signal transduction and cell regulation.
Regarding the preparation of 2 ',3'-dideoxyxanthine nucleosides, a common method is to use chemical synthesis. This compound can be synthesized by the steps of protection and deprotection of xanthine and deoxygenation.
When using 2 ',3'-dideoxyxanthine nucleosides or related compounds, it is necessary to pay attention to their safety. It may be toxic and irritant, so it is necessary to take appropriate safety measures when handling. At the same time, relevant laboratory practices should be followed, and this compound should be stored and handled properly to prevent accidents and environmental pollution. During use, avoid contact with skin and eyes, and maintain proper ventilation conditions. If necessary, consult a professional for more detailed safety information.
Last Update：2024-04-10 22:29:15
