Some background, based on quick research, not personal knowledge, so please correct if anything's wrong:<p>This class of antibiotics, ADEP, was discovered as a naturally produced substance isolated from the bacteria <i>Streptomyces hawaiiensis</i> in 1985 (<i>Streptomyces</i> has been a fertile source of naturally occurring antibiotics). After some promising results, there was work on synthetically synthesizing it and producing "optimized" synthetic variants. ADEP4 is one of those, and was reported in a paper published in 2005. There's a short 1-page summary of that work in <i>Nature Reviews Drug Discovery</i> 4: 957. See page 19 of this PDF, article "Peptide power": <a href="http://journals2005.pasteur.ac.ir/NR/4%2812%29.pdf" rel="nofollow">http://journals2005.pasteur.ac.ir/NR/4%2812%29.pdf</a><p>There's a lot of work trying to understand its mechanism, e.g. here's one open-access paper that also has some background: <a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955292/" rel="nofollow">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955292/</a><p>Here's the paper discussed in the linked article, unfortunately paywalled, but with an abstract available that's actually a good summary: <a href="http://www.nature.com/nature/journal/vaop/ncurrent/full/nature12790.html" rel="nofollow">http://www.nature.com/nature/journal/vaop/ncurrent/full/natu...</a>