Organic & Biomolecular Chemistry 2012-04-07

2-Aminopyrimidine as a novel scaffold for biofilm modulation.

Erick A Lindsey, Roberta J Worthington, Cristina Alcaraz, Christian Melander

Index: Org. Biomol. Chem. 10(13) , 2552-61, (2012)

Full Text: HTML

Abstract

An efficient synthetic route to a series of substituted 2-aminopyrimidine (2-AP) derivatives has been developed. Subsequent biofilm screening has allowed comparison between the biological activity of these new derivatives and that of the 2-aminoimidazole class of anti-biofilm compounds. Several derivatives displayed the ability to modulate bacterial biofilm formation, exhibiting greater activity against Gram-positive strains than Gram-negative strains. Additionally some 2-aminopyrmidines were able to suppress MRSA resistance to conventional antibiotics.


Related Compounds

Related Articles:

Cocrystals of 5-fluorocytosine. I. Coformers with fixed hydrogen-bonding sites.

2012-08-01

[Acta Crystallogr. B 68(Pt 4) , 431-43, (2012)]

Synthesis and Structural Study of Some Pyrimidinium Hexafluoridosilicates.

2015-01-01

[Acta Chim. Slov. 62 , 297-303, (2015)]

Synthesis and cytotoxic activity of 2-methylimidazo[1,2-a]pyridine- and quinoline-substituted 2-aminopyrimidine derivatives.

2010-01-01

[Eur. J. Med. Chem. 45 , 379-86, (2010)]

Assessment of antiplatelet activity of 2-aminopyrimidines.

2012-04-01

[Eur. J. Med. Chem. 50 , 428-32, (2012)]

Spectroscopic, electronic structure and natural bond analysis of 2-aminopyrimidine and 4-aminopyrazolo[3,4-d]pyrimidine: a comparative study.

2012-10-01

[Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 96 , 226-41, (2012)]

More Articles...