α-Phenyl-n-tert-butyl-nitrone attenuates lipopolysaccharide-induced neuronal injury in the neonatal rat brain
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منابع مشابه
Reactivities of Substituted α-Phenyl-N-tert-butyl Nitrones
In this work, a series of α-phenyl-N-tert-butyl nitrones bearing one, two, or three substituents on the tert-butyl group was synthesized. Cyclic voltammetry (CV) was used to investigate their electrochemical properties and showed a more pronounced substituent effect for oxidation than for reduction. Rate constants of superoxide radical (O2(•-)) reactions with nitrones were determined using a UV...
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Antioxidant treatment has previously been shown to be neuroprotective in experimental bacterial meningitis. To obtain quantitative evidence for oxidative stress in this disease, we measured the major brain antioxidants ascorbate and reduced glutathione, and the lipid peroxidation endproduct malondialdehyde in the cortex of infant rats infected with Streptococcus pneumoniae. Cortical levels of t...
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Di-n-butyl phthalate (DBP) is a well-known plasticizer and cause a wide range of reproductive or endocrine disruptive disorders. Exposure to DBP during gestation shown to disrupt testosterone synthesis and male sexual development in the fetal rat, however, the underlying mechanisms and its impact on the cortical and cerebellar neuronal development remain poorly understood. Here, we examine the ...
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The title mol-ecule, C(21)H(26)O(3), has a six-membered planar carbon ring as the central core, substituted at position 1 with phen-oxy-carbonyl, at position 2 with hy-droxy and at positions 3 and 5 with tert-butyl groups. The structure shows two independent but very similar mol-ecules within the asymmetric unit. For both independent mol-ecules, the ester carboxyl-ate group is coplanar with the...
متن کاملN-Phenyl-tert-butanesulfinamide
In the racemic title compound, C(10)H(15)NOS, the packing exhibits centrosymmetric pairs of mol-ecules linked by N-H⋯O=S hydrogen bonds in a head-to-tail fashion. The N-C(ar-yl) bond [1.4083 (12) Å] is considerably shorter than the N-C(alk-yl) bonds typically found in N-alkyl-alkanesulfinamides (1.470-1.530 Å).
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ژورنال
عنوان ژورنال: Neuroscience
سال: 2008
ISSN: 0306-4522
DOI: 10.1016/j.neuroscience.2007.09.087