A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Safety of 5-Methoxy-3-piperidin-4-yl-1H-indole, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 52157-82-1, Name is 5-Methoxy-3-piperidin-4-yl-1H-indole, molecular formula is C14H18N2O. In a Article, authors is Wei, Jianmei，once mentioned of 52157-82-1
High potency pyrazole-based noncovalent inhibitors of human cathepsin S (CatS) were developed by modification of the benzo-fused 5-membered ring heterocycles found in earlier series of CatS inhibitors. Although substitutions on this heterocyclic framework had a moderate impact on enzymatic potency, dramatic effects on cellular activity were observed. Optimization afforded indole- and benzothiophene-derived analogues that were high affinity CatS inhibitors (IC50 = 20-40 nM) with good cellular potency (IC50 = 30-340 nM).
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Reference：
Piperidine – Wikipedia,
Piperidine | C5H18669N – PubChem