Adenosine, 2-fluoro-, 2′,3′,5′-triacetate, with the CAS number 15811-32-2, is a modified nucleoside derivative of adenosine. This compound features a fluorine atom at the 2-position of the ribose sugar, which can influence its biological activity and stability. The presence of three acetyl groups at the 2′, 3′, and 5′ positions enhances its lipophilicity, potentially facilitating cellular uptake and altering its interaction with biological targets. The modification of adenosine in this manner can affect its role in biochemical pathways, particularly in relation to nucleic acid synthesis and signaling. As a chemical entity, it may exhibit unique pharmacological properties, making it of interest in medicinal chemistry and biochemistry research. Its solubility, reactivity, and stability can vary based on environmental conditions, such as pH and temperature. Overall, this compound serves as a valuable tool for studying nucleoside function and for developing therapeutic agents targeting adenosine receptors or related pathways.

Adenosine, 2-fluoro-, 2′,3′,5′-triacetate

15811-32-2: 2-Fluoro-2',3',5'-tri-o-acetyladenosine, 2-Fluoro-2',3',5'-triacetoxyadenosine, 2-Fluoro-2,3,5'-tri-o-acetyladenosine, 2′,3′,5′-Tri-O-acetyl-2-fluoroadenosine, Adenosine, 2-fluoro-, 2′,3′,5′-triacetate, NSC 108853

2'',3'',5''-Tri-O-acetyl-2-fluoroadenosine

2',3',5'-Tri-O-acetyl-2-fluoroadenosine is nucleoside analog of adenosine for use in research. The addition of a fluorine to an adenosine can change adenosine's properties such as its hydrogen bonding ability and how it interacts with water and other biological molecules. It can also increase the stability of adenosine and increase its half-life in biological systems.

CAS 15811-32-2: Adenosine, 2-fluoro-, 2′,3′,5′-triacetate

2'',3'',5''-Tri-O-acetyl-2-fluoroadenosine

Ref: 7W-GN5176

2',3',5'-Tri-O-acetyl-2-fluoroadenosine

Ref: 3D-NT09632

Adenosine, 2-fluoro-, 2',3',5'-triacetate

Ref: IN-DA001PZF