enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    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 ...

  3. Naturally occurring phenols - Wikipedia

    en.wikipedia.org/wiki/Naturally_occurring_phenols

    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 .

  4. Alkaloid - Wikipedia

    en.wikipedia.org/wiki/Alkaloid

    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]

  5. Green leaf volatiles - Wikipedia

    en.wikipedia.org/wiki/Green_leaf_volatiles

    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 ...

  6. List of naturally occurring phenethylamines - Wikipedia

    en.wikipedia.org/wiki/List_of_naturally...

    Tyramine is a phenethylamine that occurs widely in plants [1] and animals, and is metabolized by various enzymes, including monoamine oxidases. Substituted phenethylamines like mescaline and lophophine are found in psychoactive cactus.

  7. Indole alkaloid - Wikipedia

    en.wikipedia.org/wiki/Indole_alkaloid

    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]

  8. Acetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde

    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.

  9. Plant secondary metabolism - Wikipedia

    en.wikipedia.org/wiki/Plant_secondary_metabolism

    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.