Extracurricular laboratory: Synthetic route of 10466-61-2

This compound(H-Leu-NH2.HCl)Related Products of 10466-61-2 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Related Products of 10466-61-2. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: H-Leu-NH2.HCl, is researched, Molecular C6H15ClN2O, CAS is 10466-61-2, about Structural requirement of leucine for activation of p70 S6 kinase. Author is Shigemitsu, Kaori; Tsujishita, Yosuke; Miyake, Hiroshi; Hidayat, Sujuti; Tanaka, Noriaki; Hara, Kenta; Yonezawa, Kazuyoshi.

The addition of leucine induced activation of p70S6k in amino acid-depleted H4IIE cells. Whereas the activation of p70S6k by leucine was transient, the complete amino acid stimulated p70S6k more persistently. The effect of leucine on p70S6k was sensitive to rapamycin, but less sensitive to wortmannin. Using various amino acids and derivatives of leucine, we found that the chirality, the structure of the four branched hydrocarbons, and the primary amine are required for the ability of leucine to stimulate p70S6k, indicating that the structural requirement of leucine to induce p70S6k activation is very strict and precise. In addition, some leucine derivatives exhibited the ability to stimulate p70S6k and the other derivatives acted as inhibitors against the leucine-induced activation of p70S6k.

This compound(H-Leu-NH2.HCl)Related Products of 10466-61-2 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare