The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.499-40-1, Name is (2R,3S,4R,5R)-2,3,4,5-Tetrahydroxy-6-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)hexanal, molecular formula is C12H22O11. In a Article£¬once mentioned of 499-40-1, COA of Formula: C12H22O11
Novel Cu(II), Co(II) and Zn(II) metal complexes containing 6?methylpyridine?2?carboxylic acid and 2,2?-dipyridylamine {[Cu(6-mpa)(dipya)(OAc)]¡¤3H2O (1), [Co(6-mpa)(dipya)Cl2]¡¤2H2O (2), [Zn(6-mpa)2(dipya)] (3)} were synthesized for the first time. Their structural and spectroscopic analyses were performed by XRD, LC-MS/MS, FT-IR and UV?Vis spectroscopic techniques. The DFT/HSEh1PBE/6?311G(d,p)/LanL2DZ level was also used to obtain optimal molecular geometry, vibrational wavenumbers, electronic spectral behaviors and major contributions to the electronic transitions for the complexes 1?3. Their effects on alpha-glucosidase activity were evaluated. All complexes inhibited alpha-glucosidase with the IC50 values ranging from 513.10 to >600 muM. Finally, in order to display interactions between the synthesized complexes (1?3) and target protein (the template structure S. cerevisiae isomaltase), the molecular docking study was fulfilled.
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.COA of Formula: C12H22O11, you can also check out more blogs about499-40-1
Reference£º
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics