Название продукции:8-Fluoroadenosine

IUPAC Name:(2R,3R,4S,5R)-2-(6-amino-8-fluoro-9H-purin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol

CAS:23205-67-6
Молекулярная формула:C10H12FN5O4
Чистота:97%
Номер в каталоге:CM261477
Молекулярная масса:285.24

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Информация о продукции

Номер CAS:23205-67-6
Молекулярная формула:C10H12FN5O4
Точка плавления:-
Smiles-код:OC[C@@H]1[C@H]([C@H]([C@H](N2C(F)=NC3=C2N=CN=C3N)O1)O)O
Плотность:
Номер в каталоге:CM261477
Молекулярная масса:285.24
Точка кипения:
Номер Mdl:
Хранение:

Category Infos

Nucleosides and Nucleotides
Nucleosides consist of a nucleotide and a five-carbon sugar, and a nucleotide consists of a nucleotide, a five-carbon sugar, and one or more phosphate groups.
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Product Other Information

Product Overview 8-Fluoroadenosine (8-F-Ado) is a synthetic nucleoside analogue of adenosine, an endogenous purine nucleoside found in all living organisms. 8-F-Ado is a versatile compound with a wide range of applications in biochemical and physiological research, including its use as an imaging agent for positron emission tomography (PET) and as a therapeutic agent for the treatment of cancer. 8-F-Ado has also been used as a probe for studying the enzymatic activities of adenosine-metabolizing enzymes, as a tool for studying the role of adenosine in signal transduction pathways, and as an inhibitor of adenosine-metabolizing enzymes.
Synthesis and Application The synthesis of 8-Fluoroadenosine is achieved through a two-step procedure involving the preparation of a 5-F-Ado intermediate, followed by a nucleophilic substitution reaction to form 8-Fluoroadenosine. The first step involves the preparation of 5-F-Ado from a 5-fluorouracil (5-FU) derivative and an adenosine-5'-phosphoramidite. The second step involves the reaction of 5-F-Ado with a nucleophile, such as sodium azide or sodium ethoxide, to form 8-Fluoroadenosine. The resulting 8-Fluoroadenosine is then isolated and purified by high-performance liquid chromatography (HPLC). 8-Fluoroadenosine is a useful tool for studying the enzymatic activities of adenosine-metabolizing enzymes. It has been used to study the roles of adenosine-metabolizing enzymes in signal transduction pathways, and as an inhibitor of adenosine-metabolizing enzymes. 8-Fluoroadenosine has also been used to study the physiological effects of adenosine in the central nervous system. Additionally, 8-Fluoroadenosine has been used as an imaging agent for positron emission tomography (PET), and as a therapeutic agent for the treatment of cancer.
Future Directions The potential future directions for 8-Fluoroadenosine are numerous. 8-Fluoroadenosine could be used to study the role of adenosine in the regulation of various physiological processes, such as inflammation, cell proliferation and apoptosis. 8-Fluoroadenosine could also be used to study the role of adenosine in the development of neurological and cardiovascular diseases, as well as cancer. Additionally, 8-Fluoroadenosine could be used as a therapeutic agent for the treatment of various diseases, such as cancer and neurological disorders. Finally, 8-Fluoroadenosine could be used as an imaging agent for positron emission tomography (PET).