Discovery of 36768-62-4

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Reference of 36768-62-4, you can also check out more blogs about36768-62-4

Reference of 36768-62-4, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 36768-62-4, Name is 4-Amino-2,2,6,6-tetramethylpiperidine, molecular formula is C9H20N2. In a Article,once mentioned of 36768-62-4

Various 2-thiopyrimidine derivatives have been synthesized by an efficient, one-pot reaction of functionalized amines with either 4-isothiocyanato-4- methyl-2-pentanone or 3-isothiocyanatobutanal. All the synthesized compounds were fully characterized by elemental analysis (CHN), FT-IR, 1H NMR, and mass spectral data. One of the compounds, 7,7,8a-trimethyl-hexahydro- thiazolo[3,2-c]pyrimidine-5-thione (17) showed good anti-inflammatory (37.4% at 100 mg/kg p.o.) and analgesic activity (75% at 100 mg/kg p.o.). 7-(1-Mercapto-3,3,4a-trimethyl-4,4a,5,9b-tetrahydro-3H-pyrido[4,3-b]indol-7-yl) -3,3,4a-trimethyl-3,4,4a,5-tetrahydro-benzo[4,5]imidazo[1,2-c] pyrimidine-1-thiol (3) showed moderate activity against CDK-1 (IC50 = 5 muM). The other compounds showed moderate anti-inflammatory (5-20%), analgesic (25-75%) and protein kinase (CDK-5, GSK-3) inhibitory activities (IC50 > 10 muM).

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Reference of 36768-62-4, you can also check out more blogs about36768-62-4

Reference:
Piperidine – Wikipedia,
Piperidine | C5H8569N – PubChem