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. Author manuscript; available in PMC: 2022 May 19.
Published in final edited form as: Eur J Med Chem. 2021 Oct 9;227:113903. doi: 10.1016/j.ejmech.2021.113903

Fig. 8.

Fig. 8.

Result summary of human plasma stability assay. Experiments were performed in triplicate. % remaining = 100 × (PAR at appointed incubation time/PAR at time T0). PAR is the peak area ratio of a test compound to the internal standard. Accuracy should be within 80–120% of the indicated value.