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Nupharamine
Nupharamine is an alkaloid found in ''Nuphar japonica'' and in castoreum. ''Nuphar japonica'' contains nupharamine, and methyl and ethyl esters of nupharamine. References 3-Furyl compounds Piperidine alkaloids Tertiary alcohols {{alkaloid-stub ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Nuphar Japonica
''Nuphar japonica'', known as East Asian yellow water-lily, is an aquatic plant species in the genus ''Nuphar'' found in Japan and the Korean Peninsula. It is endangered in Russia. The species was not accepted by The Plant List , which regarded it as an "unresolved name". ''Nuphar'' × ''saijoensis'' (Shimoda) Padgett is a hybrid between ''N. japonica'' and ''Nuphar pumila, N. pumila''. ''N. japonica'' contains the alkaloids nupharidin, 1-desoxynupharidin, nupharamine, methyl and ethyl esters of nupharamine. The fruits also contains the alkaloids (0.06%) nupharine, beta-nupharidin, desoxynupharidin. In the rhizomes are found the steroid sitosterol, alkaloids acids, higher fatty acids (palmitic, oleic acid) and the ellagitanins nupharin A, nupharin B, B, nupharin C, C, nupharin D, D, nupharin E, E and nupharin F, F.Tannins and Related Compounds. LXXIX. Isolation and Characterization of Novel Dimeric and Trimeric Hydrolyzable Tannins, Nuphrins C, D, E and F, from Nuphar japonicum D ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Castoreum
Castoreum is a yellowish exudate from the castor sacs of mature beavers. Beavers use castoreum in combination with urine to scent mark their territory. Both beaver sexes have a pair of castor sacs and a pair of anal glands, located in two cavities under the skin between the pelvis and the base of the tail. The castor sacs are not true glands ( endocrine or exocrine) on a cellular level, hence references to these structures as preputial glands, castor glands, or scent glands are misnomers. It is used as a tincture in some perfumesInternational Perfume Museum, Grasse, France, Website: and was sometimes used as a food additive in the early 1900s. The sacs brought per ounce when auctioned at the May–June 2016 North American Fur Auction. Chemical composition At least 24 compounds are known constituents of beaver castoreum. Several of these have pheromonal activity, of which the phenols 4-ethylphenol and catechol and the ketones acetophenone and 3-hydroxyacetophenone were s ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Piperidine Alkaloids
Piperidine alkaloids are naturally occurring chemical compounds from the group of alkaloids, which are chemically derived from piperidine. Alkaloids with a piperidine building block are widespread and are usually further subdivided according to their occurrence and biogenetic origin. The most important representative of piperidine alkaloids is piperine, which is responsible for the pungent taste of pepper. The piperidine alkaloids also include the sedum alkaloids (e.g. sedamine), pelletierine, the lobelia alkaloids (e.g. lobeline), the conium alkaloids (such as coniine) and the pinus alkaloids. Piperin.svg, Piperine Lobeline Structural Formula V2.svg, Lobeline (S)-Coniine Structural Formula V.1.svg, (''S'')-Coniine (2R,8R)-Sedamine Structural Formula V4.svg, Sedamin Solenopsin Structural Formula V.1.svg, Solenopsin Solenopsin is a lipophilic alkaloid with the molecular formula C17H35N found in the venom of fire ants (''Solenopsis''). It is considered the primary toxin in th ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
