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Raw Materials for the Synthesis of PI Polyamide to Recognize DNA Sequences

The amino group sides and the carbonyl group sides in PIPs (pyrrole-imidazole (Py-Im) polyamides) face each other in antiparallel to form Py/Py or Py/Im pairs. They recognize specific DNA base pairs via hydrogen bonds, enter the minor-groove of the DNA double helix to bind sequence-selectively. By changing the sequence of Py and Im, it is possible to design and bind to any DNA base sequences.1-4) Both 1-methyl-pyrrole (1, 2) and 1-methyl-imidazole (3, 4) monomers with Boc- or Fmoc-protected amino groups have been used as raw materials for the synthesis of PIPs. In addition, the PyIm block (5), which is difficult to lengthen by solid-phase synthesis, is also available.5-7)

Raw Materials for the Synthesis of PI Polyamide to Recognize DNA Sequences

Related Products

B6351
4-(Boc-amino)-1-methyl-1H-pyrrole-2-carboxylic Acid (= Boc-Py-OH)
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4-(Fmoc-amino)-1-methyl-1H-pyrrole-2-carboxylic Acid (= Fmoc-Py-OH)
B6350
4-(Boc-amino)-1-methyl-1H-imidazole-2-carboxylic Acid (= Boc-Im-OH)
F1313
4-(Fmoc-amino)-1-methyl-1H-imidazole-2-carboxylic Acid (= Fmoc-Im-OH)
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Fmoc-PyIm-COOH
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N-Boc-4-aminobutyric Acid
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N-Fmoc-4-aminobutyric Acid

References

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