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, SDS of cas: 499-40-1
Structurally diverse manganese(II)-diclofenac complexes showing enhanced antioxidant activity and affinity to serum albumins in comparison to sodium diclofenac
The interactions of MnII ions with the nonsteroidal anti-inflammatory drug sodium diclofenac in the presence of 1,10-phenanthroline and 2,2′-dipyridylamine lead to the formation of the trinuclear [Mn3(diclofenac)6(1,10-phenanthroline)2(MeOH)] (1) and the mononuclear [Mn(diclofenac)2(2,2′-dipyridylamine)] (2), respectively, which have been characterized by X-ray crystallography. Three different coordination modes of the diclofenac ligands exist in 1, whereas the bidentate chelating mode is observed in 2. In the initial evaluation of their biological properties and potential applications, the complexes exhibited good binding propensity to human or bovine serum albumin proteins and have relatively high binding constants. The ability of the compounds to scavenge 1,1-diphenylpicrylhydrazyl, 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid), and hydroxyl radicals was evaluated, and 1 was the most-effective scavenger among 1, 2, and sodium diclofenac.
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.SDS of cas: 499-40-1, you can also check out more blogs about499-40-1
Reference£º
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics