9-[(2S,3S,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one - Names and Identifiers
Name | L-Inosine
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Synonyms | L-Inosine Hypoxanthine, 9-β-L-ribofuranosyl- (7CI, 8CI) 6H-Purin-6-one, 1,9-dihydro-9-β-L-ribofuranosyl- 1,9-Dihydro-9-beta-L-ribofuranosyl-6H-purin-6-one 9-[(2S,3S,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 9-((2S,3S,4R,5S)-3,4-Dihydroxy-5-(hydroxyMethyl)tetrahydrofuran-2-yl)-1H-purin-6(9H)-one
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CAS | 21138-24-9
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EINECS | 500-100-4 |
9-[(2S,3S,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one - Physico-chemical Properties
Molecular Formula | C10H12N4O5
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Molar Mass | 268.23 |
Density | 2.08 |
Melting Point | 218 ºC |
Boling Point | 797.9±60.0 °C(Predicted) |
pKa | 8.92±0.70(Predicted) |
Storage Condition | Room Temprature |
9-[(2S,3S,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one - Introduction
L-Inosine(L-Inosine) is an organic compound, belonging to the nucleoside class of substances. Its chemical formula is C10H12N4O5. L-Inosine is composed of adenine (adenine) and β-D-ribose (D-ribose) linked by N-glycosidic bond, similar in structure to adenosine.
L-Inosine is widely present in organisms, especially in RNA nucleotides. It is mainly converted into nucleotide sarcosine (inosinic acid) by adenosine deaminase (adenosine deaminase), which is involved in the metabolism and synthesis of purine nucleotides. In addition, L-Inosine is also considered to be a biologically active substance, which plays an important role in cell signaling, protein synthesis and immune regulation.
L-Inosine also have some applications in the field of medicine. It is often used as an intermediate for the synthesis of antiviral drugs. In addition, L-Inosine are used as chemical compounds in laboratories for research and analytical experiments.
There are many methods for preparing L-Inosine, and the commonly used methods are enzymatic reactions or chemical synthesis. In enzymatic reactions, nucleoside deaminase is often used to catalyze the conversion of adenosine to inosine. In terms of chemical synthesis, a method of synthesizing an organic compound can be used to prepare the L-Inosine.
There is no clear toxicity report and no documented side effects regarding the safety of the L-Inosine. However, as with any chemical substance, use should follow safe practices and be careful to avoid skin contact, inhalation or ingestion. At the same time, the use and handling of L-Inosine should also follow relevant regulations and guidelines to ensure safety and reliability. When using the L-Inosine, it is recommended to follow the laboratory safety operation guidelines and use it under the guidance of professionals.
Last Update:2024-04-09 21:11:58