The assay measures AmpC beta lactamase inhibition using an aggregation profiling approach that involves measuring inhibition in the presence and absence of 0.01% Triton X-100. Compounds that inhibited only in the absence of detergent were considered likely promiscuous aggregators. The assay was performed using a 96-well format and a set of 1,030 compounds, and AmpC activity was measured by monitoring the absorbance at 480 nm using nitrocefin as a chromogenic substrate. The assay was conducted in Brian Shoichet's lab using AmpC beta lactamase provided by Shoichet Lab at UCSF. Is the molecule effective to this assay?