The chemical substance known as "6H-Purin-6-one, 2-amino-9-[2,5-anhydro-4-C-(3,5,7,7-tetrahydroxy-3,5,7-trioxido-2,4,6-trioxa-3,5,7-triphosphahept-1-yl)-α-L-lyxofuranosyl]-1,9-dihydro-" with CAS number 1233876-29-3 is a complex organic compound that features a purine base structure, which is characteristic of nucleobases found in nucleic acids. This compound includes multiple functional groups, such as amino and hydroxyl groups, contributing to its potential biological activity. The presence of a furanosyl sugar moiety indicates that it may play a role in nucleoside or nucleotide chemistry. Additionally, the incorporation of phosphorus-containing groups suggests potential applications in biochemistry, particularly in the context of nucleic acid analogs or as a therapeutic agent. The intricate structure implies that it may exhibit unique solubility and reactivity profiles, which could be of interest in medicinal chemistry and drug development. Overall, this compound represents a significant area of study due to its structural complexity and potential biological implications.

6H-Purin-6-one, 2-amino-9-[2,5-anhydro-4-C-(3,5,7,7-tetrahydroxy-3,5,7-trioxido-2,4,6-trioxa-3,5,7-triphosphahept-1-yl)-α-L-lyxofuranosyl]-1,9-dihydro- (ACI)

1233876-29-3: The chemical substance known as "6H-Purin-6-one, 2-amino-9-[2,5-anhydro-4-C-(3,5,7,7-tetrahydroxy-3,5,7-trioxido-2,4,6-trioxa-3,5,7-triphosphahept-1-yl)-α-L-lyxofuranosyl]-1,9-dihydro-" with CAS number 1233876-29-3 is a complex organic compound that features a purine base structure, which is characteristic of nucleobases found in nucleic acids. This compound includes multiple functional groups, such as amino and hydroxyl groups, contributing to its potential biological activity. The presence of a furanosyl sugar moiety indicates that it may play a role in nucleoside or nucleotide chemistry. Additionally, the incorporation of phosphorus-containing groups suggests potential applications in biochemistry, particularly in the context of nucleic acid analogs or as a therapeutic agent. The intricate structure implies that it may exhibit unique solubility and reactivity profiles, which could be of interest in medicinal chemistry and drug development. Overall, this compound represents a significant area of study due to its structural complexity and potential biological implications.

<p>LNA-GTP is a nucleotide analog used in the synthesis of oligonucleotides.</p>

CAS 1233876-29-3

6H-Purin-6-one, 2-amino-9-[2,5-anhydro-4-C-(3,5,7,7-tetrahydroxy-3,5,7-trioxido-2,4,6-trioxa-3,5,7-triphosphahept-1-yl)-α-L-lyxofuranosyl]-1,9-dihydro- (ACI)

LNA-GTP

Ref: TM-TSW-00969