CAS 4710-68-3

[(3aS,4R,6R)-4-(6-aminopurin-9-yl)-2-phenyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3,2]dioxaborol-6-yl]methanol

Description:

The chemical substance with the name "[(3aS,4R,6R)-4-(6-aminopurin-9-yl)-2-phenyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3,2]dioxaborol-6-yl]methanol" and CAS number 4710-68-3 is a complex organic compound characterized by its unique structural features, including a fused bicyclic system and a boron-containing dioxaborole moiety. This compound exhibits chirality, with specific stereocenters contributing to its three-dimensional arrangement, which can influence its biological activity and interactions. The presence of an aminopurine group suggests potential applications in medicinal chemistry, particularly in the development of nucleoside analogs or as a scaffold for drug design. Additionally, the phenyl group may enhance lipophilicity, affecting the compound's solubility and permeability. The methanol functional group indicates the potential for hydrogen bonding, which can play a significant role in the compound's reactivity and interactions with biological targets. Overall, this substance's intricate structure and functional groups position it as a candidate for further investigation in pharmaceutical research and development.

Formula: C₁₆H₁₆BN₅O₄

InChI: InChI=1/C16H16BN5O4/c18-14-11-15(20-7-19-14)22(8-21-11)16-13-12(10(6-23)24-16)25-17(26-13)9-4-2-1-3-5-9/h1-5,7-8,10,12-13,16,23H,6H2,(H2,18,19,20)/t10-,12?,13+,16-/m1/s1

Adenosine-2',3'-O-phenylboronate

CAS: 4710-68-3

Formula: C₁₆H₁₆BN₅O₄

Color and Shape: Solid

Molecular weight: 353.1403

Ref: IN-DA00DDEO

Adenosine 2'',3''-O-phenylboronate

CAS: 4710-68-3

Ref: 7W-GN2076

Adenosine 2',3'-O-phenylboronate

CAS: 4710-68-3

Adenosine 2',3'-O-phenylboronate is a nucleoside that is used as an antiviral and anticancer drug. It is used in the treatment of AIDS, leukemia, and lymphoma. Adenosine 2',3'-O-phenylboronate inhibits viral replication by preventing the formation of viral DNA. This nucleoside has also been shown to have antitumor properties and can be used to inhibit cancer cell growth.
br>br>
Adenosine 2',3'-O-phenylboronate can be modified with phosphoramidites, which allow for the synthesis of modified adenosine 2',3'-O-phenylboronates. These modifications include substituting one or more hydrogen atoms with a variety of substituents, including fluorines, chlorine, bromines, nitro groups, alkyl groups, alkoxy groups and others. This modification provides for a novel type of anti

Formula: C₁₆H₁₆BN₅O₄

Purity: Min. 95%

Molecular weight: 353.14 g/mol

Ref: 3D-NA07179