Design of a nonnatural deoxyribonucleoside for recognition of GC base pairs by oligonucleotide-directed triple helix formation

DOI: 10.1021/ja00030a050

Source and publish data:

Journal of the American Chemical Society p. 1470 - 1478 (1992)

Update date:2022-08-03

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Authors:

Koh, Jong Sung

Dervan, Peter B.

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Article abstract of DOI:10.1021/ja00030a050

The deoxyribonucleoside 1-(2-deoxy-β-D-ribofuranosyl)-3-methyl-5-amino-1H-pyrazolo[4,3-d]pyrimidin- 7-one (P1) was designed such that two specific hydrogen bonds would form with guanine (G) of a Watson-Crick guanine-cytosine (GC) base pair in the major gr

Full text of DOI:10.1021/ja00030a050

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Product name:ethyl 1-<2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-ribofuranosyl>-5-methyl-4-nitro-1H-pyrazole-3-carboxylate

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