Pyrrolepolyamide-2′-deoxyguanosine hybrids (Hybrid 2 and Hybrid 3) incorporatng the 3-aminopropionyl or 3-aminopropyl linker were designed and synthesized on the basis of previously reported results of a pyrrolepolyamide-adenosine hybrid (Hybrid 1). Evaluation of the DNA binding sequence selectivity of pyrrolepolyamide- 2′-deoxyguanosine hybrids was performed by CD spectral and Tm analyses. It was shown that Hybrid 3 possessed greater binding specificity than distamycin A, Hybrid 1 and Hybrid 2. Copyright © 2010 Etsuko Kawashima et al.
CITATION STYLE
Kawashima, E., Ohba, Y., Terui, Y., & Kamaike, K. (2010). Design, synthesis, and analysis of minor groove binder pyrrolepolyamide- ′-deoxyguanosine hybrids. Journal of Nucleic Acids, 2010. https://doi.org/10.4061/2010/235240
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