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. 2021 Jun 17;7(6):e07329. doi: 10.1016/j.heliyon.2021.e07329

Figure 2.

Figure 2

(a) Concentration-effect relationships for l-menthol–mediated inhibition of the binding of [3H]-WIN35,428 to the human recombinant dopamine transporter and for GBR12909. Tests were duplicated at each concentration, and data are expressed as the mean values of duplicate samples. (b) Linearized concentration-effect relationships for l-menthol–mediated inhibition of the [3H]-WIN35,428 binding and for GBR12909, prepared using logit transformation. Y = logit y = ln (y/1 – y); y = (B–N)/(B0–N); B = the amount of radioactivity bound in the presence of the test compound, B0 = the amount of radioactivity bound in the absence of the test compound, N = the amount of radioactivity nonspecifically bound: X = log x; x = the concentration of l-menthol or positive control substance.