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斑马鱼作为毒理学新方法 (NAM) 的不可或缺作用

Robyn L Tanguay1

  • 1Sinnhuber Aquatic Research Laboratory, Department of Environmental and Molecular Toxicology, Oregon State University, 28645 East Highway 34, Corvallis, OR, 97333, USA.

Toxicological sciences : an official journal of the Society of Toxicology
|September 1, 2025
PubMed
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No abstract available in PubMed .

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2° Amines to N-Nitrosamines: Reaction with NaNO201:20

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Secondary amines react with nitrous acid to form N-nitrosamines, as depicted in Figure 1. Nitrous acid, a weak and unstable acid, is formed in situ from an aqueous solution of sodium nitrite and strong acids, such as hydrochloric acid or sulfuric acid, in cold conditions. In the presence of an acid, the nitrous acid gets protonated. The subsequent loss of water results in the formation of the electrophile known as nitrosonium ion.
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Amines with low molecular weight are usually gaseous at room temperature, while those with high molecular weight are liquid or solids in nature. Usually, low molecular weight amines have a rotten fish-like smell. Diamines typically have a pungent smell. For instance, cadaverine and putrescine, depicted in Figure 1, are two molecules responsible for decaying tissue.
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