
CAS 110522-82-2
:2'-Deoxy-5'-O-DMT-N6-phenoxyacetyl-D-adenosine
Description:
2'-Deoxy-5'-O-DMT-N6-phenoxyacetyl-D-adenosine, with the CAS number 110522-82-2, is a modified nucleoside derivative of adenosine. This compound features a deoxyribose sugar, which distinguishes it from ribonucleosides, and is characterized by the presence of a dimethoxytrityl (DMT) protecting group at the 5' position, enhancing its stability and solubility. The N6-phenoxyacetyl modification at the adenine base contributes to its unique chemical properties, potentially influencing its biological activity and interaction with nucleic acid structures. Such modifications are often employed in the synthesis of oligonucleotides and can affect the compound's pharmacokinetics and binding affinity. The presence of these functional groups suggests potential applications in molecular biology, particularly in the development of therapeutic agents or as tools in genetic research. Overall, this compound exemplifies the intricate design of nucleoside analogs for specific biochemical applications.
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Found 4 products.
5'-O-DMT-PAC-dA
CAS:<p>5’-O-DMT-PAC-dA can be used in the synthesis of oligoribonucleotides[1].</p>Formula:C39H37N5O7Color and Shape:SolidMolecular weight:687.742'-Deoxy-5'-O-DMT-N6-phenoxyacetyladenosine
CAS:<p>2'-Deoxy-5'-O-DMT-N6-phenoxyacetyladenosine is a novel phosphoramidite nucleoside that is an antiviral and anticancer agent. It can be used as a monophosphate or diphosphate. 2'-Deoxy-5'-O-DMT-N6-phenoxyacetyladenosine has been shown to inhibit the replication of DNA, RNA, and protein synthesis. This compound also has an activating effect on the immune system by inducing lymphocyte proliferation and increasing NK activity. It inhibits the growth of viruses such as HIV and influenza A virus. The purity of 2'-Deoxy-5'-O-DMT-N6-phenoxyacetyladenosine is high, with a CAS number of 11052282-2.</p>Formula:C39H37N5O7Purity:Min. 95%Color and Shape:PowderMolecular weight:687.76 g/mol




