V Křen, T Řezanka - FEMS microbiology reviews, 2008 - academic.oup.com
A large number of antibiotics are glycosides. In numerous cases the glycosidic residues are crucial to their activity; sometimes, glycosylation only improves their pharmacokinetic …
DJ Musk Jr, PJ Hergenrother - Current medicinal chemistry, 2006 - ingentaconnect.com
Chemical Countermeasures for the Control of Bacterial Biofilms: Effective Compounds and Promising Targets Page 1 Current Medicinal Chemistry, 2006, 13, 2163-2177 2163 …
Since the characterization of mRNA in 1961, our understanding of the roles of RNA molecules has significantly grown. Beyond serving as a link between DNA and proteins …
The targeting of one mRNA in the transcriptome requires small molecules that bind with substantial affinity and specificity. As such, compounds with specificity for individual RNA …
A key structural feature of the aminoglycoside antibiotics is a 1, 3-diaminocyclohexanetriol termed streptamine or, in cases where the 2-hydroxy function is deoxygenated as in most …
S Kumar, L Xue, DP Arya - Journal of the American Chemical …, 2011 - ACS Publications
A dimeric neomycin− neomycin conjugate 3 with a flexible linker, 2, 2′-(ethylenedioxy) bis (ethylamine), has been synthesized and characterized. Dimer 3 can selectively bind to AT …
A new family of G-quadruplex ligands termed “amido phthalocyanines”(APcs) was synthesized by reacting variable amino acids with tetraamino zinc phthalocyanine. Variation …
M Chittapragada, S Roberts… - … in medicinal chemistry, 2009 - journals.sagepub.com
RNA is increasingly recognized for its significant functions in biological systems and has recently become an important molecular target for therapeutics development …
Potent and selective recognition and modulation of disease-relevant RNAs remain a daunting challenge. We previously examined the utility of the U1A N-terminal RNA …