Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Jay R. Carreon"'
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 17:5182-5185
A series of fluorescent compounds suitable for live cell imaging is described. Functionalized forms of four different asymmetric cyanine dyes are reported that are amenable to peptide conjugation. The photophysical properties of the modified dyes and
Autor:
Marc D. Roy, Jessica L. Rouge, Erin G. Prestwich, Shana O. Kelley, Kerry P. Mahon, Jay R. Carreon, Stephanie Shin
Publikováno v:
ChemBioChem. 7:766-773
The properties of a novel family of peptide-based DNA-cleavage agents are described. Examination of the DNA-cleavage activities of a systematic series of peptide-intercalator conjugates revealed trends that show a strong dependence on peptide sequenc
Publikováno v:
Organic Letters. 7:99-102
Peptide conjugates of the xanthene dye rose bengal (RB) are described featuring sequences that promote DNA binding. The complexation of these conjugates with DNA causes efficient quenching of the fluorophore singlet state and suppresses singlet oxyge
Publikováno v:
The FASEB Journal. 27
Publikováno v:
Organic Letters. 6:517-519
[structure: see text] Derivatives of the highly fluorescent and DNA-binding dye thiazole orange (TO) are described that feature appended peptides. Functionalization of TO can be achieved at either of the endocyclic nitrogens, and the photophysical pr
Publikováno v:
The FASEB Journal. 24
Publikováno v:
Angewandte Chemie (International ed. in English). 44(17)
Publikováno v:
Organic letters. 7(1)
Peptide conjugates of the xanthene dye rose bengal (RB) are described featuring sequences that promote DNA binding. The complexation of these conjugates with DNA causes efficient quenching of the fluorophore singlet state and suppresses singlet oxyge
Autor:
Gerard F. Graminski, Solveig LaTurner, Maralee Mcvean, Josh R. Ziemer, Scott M. Vanderwerf, Mark R. Burns, Jay R. Carreon, Bruce H. Devens, Reitha S. Weeks, C. Lance Carlson
Publikováno v:
Bioorganicmedicinal chemistry letters. 12(9)
A series of aromatic substituted diamines was synthesized and characterized for their cytotoxic profiles against human breast and prostate tumor cell lines. Following a structure function analysis of the effects of changes of the benzyl substituents
Autor:
Kerry P. Mahon, Marc D. Roy, Jay R. Carreon, Erin G. Prestwich, Jessica L. Rouge, Stephanie Shin, Shana O. Kelley
Publikováno v:
ChemBioChem; May2006, Vol. 7 Issue 5, p766-773, 8p