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Alkane-induced edema formation and cutaneous barrier dysfunction.
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Certain mineral oils and hydrocarbons require repeated topical application to cause irritation. A structure activity relationship of pure n-alkanes was undertaken in a mouse ear edema model to investigate the mechanism of cumulative irritancy. Alkanes were applied twice daily over a 4-day period.
Acute lung injury induced by a commercial leather conditioner.
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Following a formulation change, a leather conditioner was involved in a 1992 nationwide outbreak of respiratory illness. We investigated the composition and toxicity of the conditioner produced before (previous product) and after (new product) the disease outbreak. The new product induced tachypnea,
Comparative toxicology of ozone and t-butyl hydroperoxide on isolated rat lung.
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Comparative studies were undertaken on the effects of ozone and t-butyl hydroperoxide (t-BuOOH) on alkane production, glutathione and lactate dehydrogenase (LDH) release from isolated rat lungs. Specifically, ethane and pentane production, as well as glutathione and LDH release were simultaneously
[Non-bullous erythroderma (congenital) ichthyosiforme with perinuclear shells].
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A congenital dermatosis with an unusual course is described in a 5-year-old girl. During the first months of life she was found to have erythrokeratodermatic plaques, which developed into a non-bullous (congenital) ichthyosiform erythroderma (CIE) within 1 year. Since then, the clinical picture has
Phytochemical investigation and anti-inflammatory activity of aerial parts of Stachys byzanthina C. Koch.
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From the aerial parts of Stachys byzanthina C. Koch., an acyclic diterpene ester, phytyl nonadecanoate, was isolated for the first time. In addition, two normal alkanes, one fatty acid and two sterols were also identified. Stuctures were established by conventional methods of analysis and confirmed
Synthesis and biological screening of 5-(alkyl(1H-indol-3-yl))-2-(substituted)-1,3,4-oxadiazoles as antiproliferative and anti-inflammatory agents.
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A series of 5-(alkyl(1H-indol-3-yl))-2-(substituted)-1,3,4-oxadiazoles were efficiently synthesized by oxidative cyclisation of N'-benzylidene-(1H-indol-3-yl)alkane hydrazides using di(acetoxy)iodobenzene. N'-Benzylidene-(1H-indol-3-yl)alkane hydrazides themselves were derived from simple
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