Talk:Brilacidin

Latest comment: 8 years ago by Rod57 in topic arylamide structure

Improvement

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I would suggest to improve the article and to give it more attention as this new drug/class of antibiotics proved to have potent and rapid bactericidal activity against a good number of disease associated bacteria, doesn't develop resistance and it has passed numerous trials. Interestingly, Teixobactin has got an article in Nature and is more famous and hyped, however it is far behind in in-vivo trials. Sources such as http://www.thestreet.com/story/11696242/2/www.thestreet.com/story/12004957/1/cramer-jc-penney-goes-from-bad-to-dire.html might be used and peer-reviewed publications should be available too. Dmatteng (talk) 05:32, 1 April 2015 (UTC)Reply

arylamide structure

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It's described as an arylamide = aryl+amide - Seems to have 3 aromatic rings (2 fluorinated) between 4 amide groups. But what are the two ends called ? - Rod57 (talk) 04:05, 7 January 2016 (UTC)Reply