Design, synthesis, and analysis of minor groove binder pyrrolepolyamide- ′-deoxyguanosine hybrids

3Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free