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关键词:'C102202'
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N G Palmen et al.
Archives of toxicology, 72(5), 270-276 (1998-06-18)
Both oximes and hydroxylamine (HYAM) are compounds with known oxidative capacity. We tested in vitro whether acetaldoxime (AAO), cyclohexanone oxime (CHO), methyl ethyl ketoxime (MEKO) or HYAM affect haemoglobin oxidation (into HbFe3+), formation of thiobarbituric acid reactive substances (TBARS), and
Moa Andresen Bergström et al.
Journal of medicinal chemistry, 51(8), 2541-2550 (2008-03-29)
Metabolic activation of chemicals (prohaptens) in the skin can cause allergic contact dermatitis. We have explored structure-allergenic activity relationships for seven potential oxime prohaptens using the local lymph node assay and a GSH trapping screen with liver microsomes. The general
S Ramalingam et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 96, 207-220 (2012-06-12)
In the present analysis, FT-IR/FT-Raman spectra of the cyclohexanone oxime (CHO, C(6)H(11)NO) are recorded. The observed vibrational frequencies are assigned and the computational calculations are carried out by HF and DFT (B3LYP and B3PW91) methods with 6-311++G(d,p) basis set and
M J Derelanko et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 5(1), 117-127 (1985-02-01)
Cyclohexanone oxime (CHO) was given po to male and female Fischer 344 rats at dose levels of 10, 25, 75, 150, and 300 mg/kg, five times a week for a period of 2 weeks. Control animals received distilled water. All
R E Glover et al.
Chemical research in toxicology, 12(10), 952-957 (1999-10-20)
Cyclohexanone oxime (CHOX), an intermediate used in the synthesis of polycaprolactam (Nylon-6), has been reported to be hematotoxic in Fischer rats. The in vivo metabolism of CHOX was found to release nitric oxide, which was detected in venous blood by
Raphaël Turgis et al.
ChemSusChem, 3(12), 1403-1408 (2010-12-01)
Brønsted-acidic ionic liquids that bear a sulfonic acid group, known as Forbes acids, show a good catalytic activity for the Beckmann rearrangement, used to prepare ε-caprolactam, which is a precursor of Nylon 6. The activity essentially stems from the acidity of
S C Gad et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 5(1), 128-136 (1985-02-01)
Dermal exposure of rabbits to cyclohexanone oxime (CHO) for 24 hr at 0, 0.8, 2, and 5 g/kg caused dose-related reticulocytosis on the day after dosing as well as a decrease in hemoglobin in the 5-g/kg females 7 days postdosing.
Wen-Cui Li et al.
Journal of the American Chemical Society, 127(36), 12595-12600 (2005-09-08)
In this study, we present a synthetic pathway for the fabrication of self-supporting zeolite monoliths consisting of crystallized nanoparticles. A resorcinol-formaldehyde-based organic aerogel is used as a template, and silicalite-1 is used as the zeolite example. The silicalite-1 monoliths obtained
Shelli J Schomaker et al.
Toxicology and applied pharmacology, 185(1), 48-54 (2002-12-04)
The purpose of these studies was to evaluate bone marrow from male CD rats following exposure to known hematotoxins using flow cytometry (FC) and a monoclonal antibody to the cell surface antigen CD71. Rats were treated with either CHO (300
D Parmar et al.
Drug metabolism and disposition: the biological fate of chemicals, 19(6), 1101-1107 (1991-11-01)
Cyclohexanone oxime (CHOX), an intermediate used in the synthesis of Polycaprolactam/Nylon, was found to be rapidly absorbed and cleared from the body within 24 hours after a single oral administration of 1, 10 and 30 mg/kg of [14C]-CHOX to the
M J Prival
Mutation research, 497(1-2), 1-9 (2001-08-30)
The basis for the observed mutagenicity of cyclohexanone oxime in the presence of hamster liver S9 in Salmonella typhimurium strain TA1535, but not in TA100, was explored. While the chemical had no effect on the appearance of the background lawn
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