A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Safety of 3-Carbethoxy-2-piperidone, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 3731-16-6, Name is 3-Carbethoxy-2-piperidone, molecular formula is C8H13NO3. In a Article, authors is Guengoer, Timur，once mentioned of 3731-16-6
Novel N6-(indol-3-yl)alkyl derivatives of adenosine were synthesized.The adenosine receptor affinity and the antinociceptive activity of these compounds were assessed in binding studies and the phenylbenzoquinone-induced writhing test.Most of these analogues exhibited a potent analgesic activity without side effects.Among them, compound 3c (UP 202-32) bound to A1 (Ki = 110 nM) and A2 (Ki = 350 nM) adenosine receptors in a specific manner since it did not interact with many other receptors, especially opioid binding sites.The antinociceptive activity in the phenylbenzoquinone assay (ED50 = 3.3 mg/kg po) was antagonized by 8-cyclopentyltheophylline, suggesting that an adenosinergic mechanism underlies the analgesic activity observed with this compound.The data obtained with these new N6-substituted adenosine receptor agonists emphasize the interest of such compounds in the treatment of pain.
Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about is helpful to your research. Safety of 3-Carbethoxy-2-piperidone
Reference：
Piperidine – Wikipedia,
Piperidine | C5H9846N – PubChem