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The network pharmacology approach remained exploratory, with no experimental verification of the predicted targets and pathways
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In this study, we reassigned the initiator fMet to ClAc L Y ( N -chloroacetyl-L-Tyr) or ClAc D Y ( N -chloroacetyl-D-Tyr) in the FIT system and used an mRNA library with a complexity of 10 14 that was designed to have random sequences designated by (NNK) n , ( n =415) flanked by the initiator AUG (ClAc L/D Y) and UGC (Cys) codons, followed by a short linker peptide
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