171855-77-9

Upstream product

• 149376-67-0 [6-N-(benzyloxycarbonyl)-adenin-9-yl]-acetic acid 
• 161713-31-1 N-(carbamoylmethyl)-β-alanine ethylester 
• 4244-84-2 ethyl β-alaninate hydrochloride 

Downstream Products

• 171855-78-0 N-(N-tert-butyloxycarbonylaminomethyl)-N-(N⁹-benzyloxycarbonyladenin-9-ylacetyl)-β-alanine ethyl ester 
• 171855-80-4 N-(N-tert-butyloxycarbonylaminomethyl)-N-(N⁹-benzyloxycarbonyladenin-9-ylacetyl)-β-alanine 

Relevant academic research and scientific papers

A 'Retro-Inverso' PNA: Structural implications for DNA and RNA binding

'Retro-inverso' peptide nucleic acid (PNA) monomers of thymine (T*: N-(amidomethyl)-N-(N1-thyminylacetyl)-β-alanyl) (and adenine) have been prepared and introduced in PNA oligomers. A homo 'retro-inverso' T*8 PNA was found not to hybridize to a complementary DNA or RNA oligonucleotide, whereas introduction of one retro-inverso thymine unit into the middle of a normal PNA 15-mer resulted in a ca. 8°C destabilization of the complex of this oligomer with a complementary DNA or RNA oligomer. In an effort to compensate for the structural nucleobase 'phase-shift' caused by the T*monomer by also introducing a β-alanine monomer it is concluded that the effect of the T* backbone is -7°C when hybridizing to DNA and -4.5°C when hybridizing to RNA. Nonetheless, the T*unit shows good sequence discrimination comparable to that of normal PNA. Molecular dynamics simulations indicate an unfavourable conformation of the backbone amide carbonyl group resulting in reduced interaction with the aqueous medium and an 'electrostatic clash' with the carbonyl of the nucleobase linker. These results show that a simple inversion of an amide bond in the PNA backbone has a dramatic, and hardly predictable, effect on the DNA mimicking properties of the oligomer. Copyright (C) 1998 Elsevier Science Ltd.

Synthetic procedures for peptide nucleic acids

A novel class of compounds, known as peptide nucleic acids, bind complementary ssDNA and RNA strands more strongly than a corresponding DNA. The peptide nucleic acids generally comprise ligands such as naturally occurring DNA bases attached to a peptide backbone through a suitable linker.

Synthesis of 'retro-inverso' peptide nucleic acids: 1. Characterization of the monomers

Novel monomeric building blocks 4a and 4b of peptide nucleic acids with an N-(aminomethyl)β-alanine backbone ('retro-inverso' PNA) are conveniently synthesized via Hofmann rearrangement. In the major rotamer the side chain carbonyl points toward the C terminus.