Modified Nucleoside Phosphoramidites | LGC, Biosearch Technologies

A C-nucleoside phosphoramidite that is isosteric with deoxycytidine and has additional hydrogen-bonding ability.

Photochromic nucleoside (PCN) phosphoramidite that provides reversible duplex regulation via a light induced trans-cis isomerization.

Universal base phosphoramidite.

Useful amino-modified deoxyadenosine phosphoramidite.

Useful addtion to the nebularine family for hydrogen bonding studies.

Useful phosphoramidite for oxidative studies of thymidine.

Phosphoramidite enables incorporation of a nitrogen atom in place of the methine group at position 6 of the thymine ring in oligonucleotides.

Phosphoramidite enables incorporation of an N3-o-anisoyl protected 6-aza-dU residue into oligonucleotides.

Useful for incorporating 7-Deaza-modified guanosine into oligonucleotides to disrupt unwanted hydrogen bonding.

Convertible nucleoside phosphoramidite that allows the formation of N4-alkyl-C residues in RNA for structural studies.

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