939772-16-4

Upstream product

• 136869-50-6 6-allylamino-2-amino-4-chloro-5-formylpyrimidine 
• 100-51-6 benzyl alcohol 
• 5604-46-6 2-amino-4,6-dichloropyrimidine-5-carboxaldehyde 
• 343332-56-9 4-allylamino-2,6-dichloro-pyrimidine-5-carbaldehyde 

Downstream Products

• 939772-21-1 C₂₅H₃₂N₄O₆ 
• 939772-18-6 C₂₆H₃₂N₆O₆ 
• 939772-24-4 C₃₆H₄₈N₆O₁₀ 
• 939772-19-7 C₃₅H₄₆N₆O₁₁ 
• 939772-17-5 C₂₅H₃₁N₅O₅ 
• 939772-23-3 C₂₆H₃₂N₆O₆ 

Relevant academic research and scientific papers

Molecular basis for water-promoted supramolecular chirality inversion in helical rosette nanotubes

Helical rosette nanotubes (RNTs) are obtained through the self-assembly of the G∧C motif, a self-complementary DNA base analogue featuring the complementary hydrogen bonding arrays of both guanine and cytosine. The first step of this process is the format

DIVALENT NUCLEOBASE COMPOUNDS AND USES THEREFOR

Described herein are divalent nucleobases that each binds two nucleic acid strands, matched or mismatched when incorporated into a nucleic acid or nucleic acid analog backbone, such as in a γ-peptide nucleic acid (γPNA). Also provided are genetic recognition reagents comprising one or more of the divalent nucleobases and a nucleic acid or nucleic acid analog backbone, such as a γPNA backbone. Uses for the divalent nucleobases and monomers and genetic recognition reagents containing the divalent nucleobases also are provided.