Definition of Germacranolide. Meaning of Germacranolide. Synonyms of Germacranolide

Here you will find one or more explanations in English for the word Germacranolide. Also in the bottom left of the page several parts of wikipedia pages related to the word Germacranolide and, of course, Germacranolide synonyms and on the right images related to the word Germacranolide.

Definition of Germacranolide

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Meaning of Germacranolide from wikipedia

- Germacranolides are a group of natural chemical compounds classified as sesquiterpene lactones. They are found in a variety of plant species and are known...
- coumarin, glycoside, herniarin, flavonoid, farnesol, nerolidol and germacranolide. Despite the presence of coumarin, as chamomile's effect on the coagulation...
- inulin (8) Cyanogenic glycosides Prunasin Sesquiterpene lactones (of the germacranolide type) 11β, 13-dihydrolactucin Ixerin D Ainslioside taraxinic acid β-glucopyranosyl...
- Parthenolide is a sesquiterpene lactone of the germacranolide class which occurs naturally in the plant feverfew (Tanacetum parthenium), after which it...
- 2-hydroxyisodavanone, farnesol, geranyl acetate, sesquiterpene lactones, and germacranolides are also found. The amount of davanone and linalool decreased while...
- Sesquiterpene lactones can be divided into several main classes including germacranolides, heliangolides, guaianolides, pseudoguaianolides, hypocretenolides...
- found in the aerial parts of A. herba-alba. Mainly, eudesmanolides and germacranolides types were reported in most cases. A variety of flavonoids were also...
- include flavones such as acacetin and sesquiterpene lactones such as germacranolides. The compound that is thought to cause the effects of Calea ternifolia...
- TNFα and IL-1β. Elephantopus scaber contains elephantopin which is a germacranolide sesquiterpene lactone containing two lactone rings and an epoxide functional...
- Murata, Gilbert Revial, Kazuo Yoshihara: "Synthesis of the cytotoxic germacranolide eucannabinolide", in: J. Am. Chem. Soc., 1983, 105, pp. 625–627; doi:10...