The present invention provides a method for exploiting changes in the stereoelectronic nature of differentially charged resonance forms of 9 aminoacridine , {TAIL ~ their differential stacking} due to {HEAD ~ their π cloud interactions} and the use of multiplexed combinatorial matrix analyte interactions to provide high throughput coverage for the identification and quantitative analysis of the metabolome 
The present invention provides a method for exploiting changes in the stereoelectronic nature of differentially charged resonance forms of 9 aminoacridine , { TAIL ~ their differential stacking } due to { HEAD ~ their π cloud interactions } and the use of multiplexed combinatorial matrix analyte interactions to provide high throughput coverage for the identification and quantitative analysis of the metabolome
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