We then show how the resulting retention times, molecular masses, their fragmentation patterns, the Chemnet database and an in-house quinoline database are used in the dereplication process by structural elucidation of some of the compounds when compared with known structures of natural origin. Some molecular masses and the corresponding fragmentations do not correlate with any known compounds, thus revealing potentially novel natural products that could be investigated on a larger scale and could ultimately find application as new drugs against MRSA and other multi-drug-resistant microorganisms.