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Cyclic and non-cyclic glutamate analogues, such as L-α-aminopimelate and (S)-4-carboxyphenylglycine, show cross-activity with glutamatergic receptors due to the structure similarity with glutamate (Yu et al., 2019) were demonstrated

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In future experiments, I would like to perform a transient overexpression of genes early in the brassinosteroid pathway to determine whether this would also increase cardiac glycosides, implying that these two phytosterols share pathway intermediates