scholarly journals Design, Synthesis, and Analysis of Minor Groove Binder Pyrrolepolyamide-2′-Deoxyguanosine Hybrids

2010 ◽  
Vol 2010 ◽  
pp. 1-13
Author(s):  
Etsuko Kawashima ◽  
Yusuke Ohba ◽  
Yusuke Terui ◽  
Kazuo Kamaike

Pyrrolepolyamide-2′-deoxyguanosine hybrids (Hybrid2and Hybrid3) incorporating the 3-aminopropionyl or 3-aminopropyl linker were designed and synthesized on the basis of previously reported results of a pyrrolepolyamide-adenosine hybrid (Hybrid1). Evaluation of the DNA binding sequence selectivity of pyrrolepolyamide-2′-deoxyguanosine hybrids was performed by CD spectral andTmanalyses. It was shown that Hybrid3possessed greater binding specificity than distamycin A, Hybrid1and Hybrid2.

2002 ◽  
Vol 45 (17) ◽  
pp. 3630-3638 ◽  
Author(s):  
Pier Giovanni Baraldi ◽  
Romeo Romagnoli ◽  
Antonio Entrena Guadix ◽  
Maria Josè Pineda de las Infantas ◽  
Miguel Angel Gallo ◽  
...  

2011 ◽  
Vol 53 (02) ◽  
pp. 107-113
Author(s):  
Pier Baraldi ◽  
Mojgan Tabrizi ◽  
Maria Pavani ◽  
Maria Nuñez ◽  
Rimma Makaeva ◽  
...  

2005 ◽  
Vol 48 (5) ◽  
pp. 1344-1358 ◽  
Author(s):  
Scott C. Jeffrey ◽  
Michael Y. Torgov ◽  
Jamie B. Andreyka ◽  
Laura Boddington ◽  
Charles G. Cerveny ◽  
...  

1999 ◽  
Vol 52 (4) ◽  
pp. 291 ◽  
Author(s):  
Stuart A. Bateman ◽  
David P. Kelly ◽  
Jonathan M. White ◽  
Roger F. Martin

A series of bibenzimidazole derivatives based on the known DNA minor groove binder Hoechst 33258 have been prepared to include a 1,2-dicarba-closo-dodecaborane cage for potential use in boron neutron capture therapy (BNCT). The carborane derivatives (5){(7) were chosen to reduce the steric inhibition of minor groove DNA binding displayed by the previously prepared carborane ligand (4). The synthesis and preliminary DNA binding studies of these bibenzimidazole derivatives are presented herein.


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