RNA mimetics: oligoribonucleotide N3′→P5′ phosphoramidates
Allosteric inhibitors of telomerase: oligonucleotide N3′→P5′ phosphoramidates
Oligonucleotide N3′→P5′ Phosphoramidates as Antisense Agents
Zwitterionic oligodeoxyribonucleotide N3′→P5′ phosphoramidates: Synthesis and properties
Synthesis of nucleotide antibiotics having N-acyl phosphoramidate linkages
Insect Infection Model for Campylobacter jejuni Reveals That O-methyl Phosphoramidate Has Insecticidal Activity
Re-examination of the intrinsic, dynamic and hydration properties of phosphoramidate DNA
Polymerase-catalyzed synthesis of DNA from phosphoramidate conjugates of deoxynucleotides and amino acids
An Oligodeoxyribonucleotide N3′→P5′ Phosphoramidate Duplex Forms an A-type Helix in Solution
RNase H-independent antisense activity of oligonucleotide N3′→P5′ phosphoramidates
Hydration effects on the duplex stability of phosphoramidate DNA—RNA oligomers
Oligo-2′-Fluoro-2′-Deoxynucleotide N3′→P5′ Phosphoramidates: Synthesis and Properties
Synthesis and properties of RNA analogs—oligoribonucleotide N3′→P5′ phosphoramidates
α-Oligodeoxyribonucleotide N3′→P5′ phosphoramidates: synthesis and duplex formation
Promotion of triplex formation by N3′→P5′ phosphoramidate modification: Thermodynamic and kinetic studies
Matrix-induced fragmentation of P3′-N5′ phosphoramidate-containing DNA: high-throughput MALDI-TOF analysis of genomic sequence polymorphisms
Cationic phosphoramidate α‐oligonucleotides efficiently target single‐stranded DNA and RNA and inhibit hepatitis C virus IRES‐mediated translation
Oligodeoxynucleoside Phosphoramidates (P-NH2): Synthesis and Thermal Stability of Duplexes With DNA and RNA Targets
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1 any ion, salt, or ester of phosphoramidic acid; amidophosphoric acid; (OH)2PO−NH2.
2 any compound containing the group (OH)2PO−NH− or (OH)2PO−N<.
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