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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 ...
Juglone is an example of such a molecule inhibiting the growth of other plant species around walnut trees. [ citation needed ] The aquatic vascular plant Myriophyllum spicatum produces ellagic , gallic and pyrogallic acids and (+)- catechin , allelopathic phenolic compounds inhibiting the growth of blue-green alga Microcystis aeruginosa .
For example, aporphine alkaloid liriodenine produced by the tulip tree protects it from parasitic mushrooms. In addition, the presence of alkaloids in the plant prevents insects and chordate animals from eating it. However, some animals are adapted to alkaloids and even use them in their own metabolism. [201]
In positive plant-insect interactions, GLVs are used as a form of defense. They attract predators to plants that are being preyed upon by herbivores. [4] For example, female parasitoid wasps from two different families, Microplitis croceipes and Netelia heroica, can be attracted to plants that are emitting GLVs due to wounding from caterpillars ...
Most fatty alcohols in nature are found as waxes, which are esters of fatty acids and fatty alcohols. [1] They are produced by bacteria, plants and animals for purposes of buoyancy, as source of metabolic water and energy, biosonar lenses (marine mammals) and for thermal insulation in the form of waxes (in plants and insects). [3]
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]
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.
As mentioned above in the History tab, secondary plant metabolites help the plant maintain an intricate balance with the environment, often adapting to match the environmental needs. Plant metabolites that color the plant are a good example of this, as the coloring of a plant can attract pollinators and also defend against attack by animals.