Interesting scientific research on 151266-23-8

Interested yet? Read on for other articles about 151266-23-8, you can contact me at any time and look forward to more communication. Application In Synthesis of 3-Iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine.

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 151266-23-8, Name is 3-Iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine, SMILES is NC1=C2C(NN=C2I)=NC=N1, in an article , author is Araie, Yuki, once mentioned of 151266-23-8, Application In Synthesis of 3-Iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine.

Combined use of chemically modified nucleobases and nanostructured DNA for enhanced immunostimulatory activity of CpG oligodeoxynucleotide

Oligodeoxynucleotide (ODN) containing a cytosine-phosphate-guanine (CpG) motif, or CpG ODN, is considered suitable for treating immune diseases, including allergies. Although the phosphorothioate modification is used to enhance the stability and immunostimulatory activity of CpG ODNs, it is associated with the risk of adverse effects. Construction of nanostructured DNA assemblies, such as tripod- and hexapod-like structured DNAs, tripodna and hexapodna, respectively, were also found to increase this activity. The chemical modification of nucleobases could be another approach for enhancing CpG ODN activity. Here, we examined whether chemically modified nucleobase substitutions can enhance CpG ODN activity by measuring tumor necrosis factor alpha (TNF-alpha) release after addition to murine macrophage-like RAW264.7 cells. First, the guanine at the 18th position of phosphodiester CpG 1668 was substituted with several chemically modified guanines, and then the various guanines were substituted. Among all tested substitutions, 15,18-(th)dG, in which two guanines outside the CpG motif were substituted with the 2-aminothieno[3,4-d]pyrimidine guanine mimic ((th)dG), was the most effective. Compared to P-32-CpG 1668, P-32-15,18-(th)dG was taken up more efficiently by the RAW264.7 cells. Then, 15,18-(th)dG was incorporated into tripodna and hexapodna. 15,18-(th)dG/tri-or hexapodna induced higher TNF-alpha release from the RAW264.7 cells than PO CpG 1668/tri-or hexapodna, respectively. These results indicate that the( th)dG substitution is a useful effective strategy for enhancing the immunostimulatory activity of CpG DNAs in both single stranded and DNA nanostructure forms.

Interested yet? Read on for other articles about 151266-23-8, you can contact me at any time and look forward to more communication. Application In Synthesis of 3-Iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine.

Reference:
Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia