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Aldehyde structure. In organic chemistry, an aldehyde (/ ˈ æ l d ɪ h aɪ d /) is an organic compound containing a functional group with the structure R−CH=O. [1] The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group. Aldehydes are a common motif in many ...
Alkaloid production in plants appeared to have evolved in response to feeding by herbivorous animals; however, some animals have evolved the ability to detoxify alkaloids. [169] Some alkaloids can produce developmental defects in the offspring of animals that consume but cannot detoxify the alkaloids.
Larvae of the model animal Galleria mellonella, also called waxworms, can be used to test the antioxidant effect of individual molecules using boric acid in food to induce an oxidative stress. [39] The content of malondialdehyde , an oxidative stress indicator, and activities of the antioxidant enzymes superoxide dismutase , catalase ...
It is a colorless liquid or gas, boiling near room temperature. It is one of the most important aldehydes, occurring widely in nature and being produced on a large scale in industry. Acetaldehyde occurs naturally in coffee, bread, and ripe fruit, [11] and is produced by plants.
Fatty aldehydes are a natural component of many natural ingredients such as the essential oils of various citrus fruits. Decanal, for example, is a component of orange peel. [1] The pheromone cocktails of various insect pheromones contain fatty aldehydes. [2] Fat aldehydes were also detected in the heart muscle of mammals. [3]
Retinal was originally called retinene, [3] and was renamed [4] after it was discovered to be vitamin A aldehyde. [5] [6] Vertebrate animals ingest retinal directly from meat, or they produce retinal from carotenoids – either from α-carotene or β-carotene – both of which are carotenes. They also produce it from β-cryptoxanthin, a type of ...
Xylose (cf. Ancient Greek: ξύλον, xylon, "wood") is a sugar first isolated from wood, and named for it.Xylose is classified as a monosaccharide of the aldopentose type, which means that it contains five carbon atoms and includes an aldehyde functional group.
Although their assignment to the alkaloid is not universally accepted, [12] they are both found in plants and animals. [13] The tryptamine skeleton is part of the vast majority of indole alkaloids. [14] For example, N,N-dimethyltryptamine (DMT), psilocin and its phosphorylated psilocybin are the simplest derivatives of tryptamine. [13]