6-Hydroxyethyladenosine

6-Hydroxyethyladenosine - Names and Identifiers

Name	(2R,3R,4S,5R)-2-(6-((2-Hydroxyethyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
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
CAS	4338-48-1
EINECS	200-001-2

6-Hydroxyethyladenosine - Physico-chemical Properties

Molecular Formula	C12H17N5O5
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

6-Hydroxyethyladenosine - Reference

Reference

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.

6-Hydroxyethyladenosine - 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