(2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4 - Names and Identifiers
Name | (2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
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Synonyms | NSC 54251 6-Hydroxyethyladenosine N-(2-Hydroxyethyl)adenosine N6-(2-Hydroxyethyl)adenosine Adenosine, N-(2-hydroxyethyl)- (2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4 (2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-di (2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)aMino)-9H-purin-9-yl)-5-(hydroxyMethyl)tetrahydrofuran-3,4-diol (2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
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CAS | 4338-48-1
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EINECS | 200-001-2 |
(2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4 - Physico-chemical Properties
Molecular Formula | C12H17N5O5
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Molar Mass | 311.29 |
Density | 1.88 |
Melting Point | 194-195℃ |
Boling Point | 725.8°C at 760 mmHg |
Solubility | Soluble in water, methanol, ethanol, soluble in hot water, insoluble in chloroform and benzene. |
Appearance | White to white-like crystalline powder |
Color | White to Off-White |
Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
MDL | MFCD00056977 |
(2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4 - Reference
Reference Show more | 1. Zhang Meng Li Chai one autumn Fang Ming Zhang Si Han Baoyu. Antihypertensive activity of N ~ 6-(2-hydroxyethyl) adenosine extracted from Cordyceps cicadae and its interaction with human serum albumin [J]. Journal of Mycology 2019 38(06):907-916. |
(2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4 - Introduction
(2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol is a compound, the chemical formula is C14H19N5O6. It is a compound prepared by the reaction of adenosine and 2-hydroxyethylamine. In this compound, the adenosine moiety is linked to the Hydroxyethyl group via a bond at the N6 position.
(2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol is a biologically active compound that has a variety of physiological effects in the body. It is often used as a substrate or mediator for biological reactions. The compounds have the ability to promote cell proliferation and enhance immune function. It also acts as a precursor for antiviral and antitumor drugs. In addition,(2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol is also used as a standard substance in biochemical experiments and research.
Preparation of (2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3, the method of 4-diol is generally by reacting adenosine with 2-hydroxyethylamine under appropriate conditions to produce the target compound. The specific synthesis method can be adjusted according to needs and experimental conditions.
For safety information,(2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol is a relatively safe compound. However, appropriate laboratory practices still need to be followed when using the compounds. When handling and storing the compound, care should be taken to avoid contact with skin and eyes, and to maintain good ventilation conditions. In addition, the use of the compound, should follow the relevant laboratory safety instructions, take the necessary protective measures.
Last Update:2024-04-09 20:52:54