201735-90-2

Upstream product

• 201735-88-8 benzyl N-allyl-N-tert-butoxycarbonyl-5-aminopentanoate 
• 4330-20-5 N-3-benzoylthymine 
• 201735-89-9 benzyl N-tert-butoxycarbonyl-N-(2-hydroxyethyl)-5-aminopentanoate 
• 28737-46-4 1-allyl-2-piperidinone 
• 675-20-7 piperidin-2-one 

Downstream Products

• 201735-92-4 5-{[2-(3-Benzoyl-5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-ethyl]-tert-butoxycarbonyl-amino}-pentanoic acid 
• 201735-93-5 Carbonic acid 2-[[2-(3-benzoyl-5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-ethyl]-(5-{[2-(3-benzoyl-5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-ethyl]-tert-butoxycarbonyl-amino}-pentanoyl)-amino]-ethyl ester benzyl ester 

Relevant academic research and scientific papers

Synthesis and hybridization studies of a 5-aminopentanoic acid nucleobase (APN) dimer

We have prepared a 5-aminopentanoic acid nucleobase (APN) dimer and investigated its hybridization capabilities to complementary DNA using both UV melting and NMR techniques.

Synthesis of oligo(5-aminopentanoic acid)-nucleobases (APN): Potential antisense agents

Oligomers of 5-amino pentanoic acid nucleobases have been prepared for use as antisense agents. The synthesis of the 5'-end starter unit and the 3'-end monomer unit, as well as the coupling procedures used for oligomer formation are described.