Apiole
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Apiole
Apiole is a phenylpropene, also known as apiol, parsley apiol, or parsley camphor. Its chemical name is 1-allyl-2,5-dimethoxy-3,4-methylenedioxybenzene. It is found in the essential oils of celery leaf and all parts of parsley. Heinrich Christoph Link, an apothecary in Leipzig, discovered the substance in 1715 as greenish crystals reduced by steam from oil of parsley. In 1855 Joret and Homolle discovered that ''apiol'' was an effective treatment of amenorrea or lack of menstruation. In medicine it has been used, as essential oil or in purified form, for the treatment of menstrual disorders and as an abortifacient. It is an irritant and, in high doses, it can cause liver and kidney damage. Cases of death due to attempted abortion using apiole have been reported. Hippocrates wrote about parsley as an herb to cause an abortion. Plants containing apiole were used by women in the Middle Ages to terminate pregnancies. Now that safer methods of abortion are available, apiol is almost fo ...
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Dillapiole
Dillapiole is an organic chemical compound and essential oil commonly extracted from dill weed, though it can be found in a variety of other plants such as fennel root. This compound is closely related to apiole, having a methoxy group positioned differently on the benzene ring. Dillapiole works synergically with certain insecticides like pyrethrins similarly to piperonyl butoxide, which likely results from inhibition of the Mixed-function_oxidase, MFO enzyme of insects. No carcinogenicity was detected with parsley apiol or dill apiol in mice. References See also

* Apiole * Phenylpropene Phenylpropenes O-methylated phenylpropanoids Benzodioxoles Allyl compounds Pyrogallol ethers Hydroxyquinol ethers {{aromatic-stub ...
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Dillapiole
Dillapiole is an organic chemical compound and essential oil commonly extracted from dill weed, though it can be found in a variety of other plants such as fennel root. This compound is closely related to apiole, having a methoxy group positioned differently on the benzene ring. Dillapiole works synergically with certain insecticides like pyrethrins similarly to piperonyl butoxide, which likely results from inhibition of the Mixed-function_oxidase, MFO enzyme of insects. No carcinogenicity was detected with parsley apiol or dill apiol in mice. References See also

* Apiole * Phenylpropene Phenylpropenes O-methylated phenylpropanoids Benzodioxoles Allyl compounds Pyrogallol ethers Hydroxyquinol ethers {{aromatic-stub ...
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DMMDA
2,5-Dimethoxy-3,4-methylenedioxyamphetamine (DMMDA) is a psychedelic drug of the phenethylamine and amphetamine chemical classes. It was first synthesized by Alexander Shulgin and was described in his book '' PiHKAL''. Shulgin listed the dosage as 30–75 mg and the duration as 6–8 hours. He reported DMMDA as producing LSD-like images, mydriasis, ataxia, and time dilation. Pharmacology The mechanism behind DMMDA's hallucinogenic effects has not been specifically established, however Shulgin describes that a 75 milligram dose of DMMDA is equivalent to a 75–100 microgram dose of LSD. LSD is a known 5-HT2A partial agonist. DMMDA also has an affinity for the 5-HT2A receptor in the human brain. Because similiar chemicals, such as MDA and MMDA, are act as agonists on the 5-HT2A, it is likely that DMMDA also acts as an agonist of the 5-HT2A receptor. This may suggest that the hallucinogenic effects of DMMDA result from its agonism of the 5-HT2A receptor in the human ...
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Dill
Dill (''Anethum graveolens'') is an annual herb in the celery family Apiaceae. It is the only species in the genus ''Anethum''. Dill is grown widely in Eurasia, where its leaves and seeds are used as a herb or spice for flavouring food. Growth Dill grows up to , with slender hollow stems and alternate, finely divided, softly delicate leaves long. The ultimate leaf divisions are broad, slightly broader than the similar leaves of fennel, which are threadlike, less than broad, but harder in texture. The flowers are white to yellow, in small umbels diameter. The seeds are long and thick, and straight to slightly curved with a longitudinally ridged surface. Etymology The word ''dill'' and its close relatives are found in most of the Germanic languages; its ultimate origin is unknown. The generic name ''Anethum'' is the Latin form of Greek ἄνῑσον / ἄνησον / ἄνηθον / ἄνητον, which meant both 'dill' and 'anise'. The form ''anīsum'' came to be used fo ...
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Phenylpropene
Phenylpropene is the organic compound with the formula C6H5CH2CH=CH2. It is a colorless liquid. The compound consists of a phenyl group attached to allyl. Phenylpropene isomerizes to trans-propenylbenzene. In plant biochemistry, the phenylpropene skeleton is the parent (simplest representation) of the phenylpropanoids. Prominent derivatives include eugenol, safrole Safrole is an organic compound with the formula CH2O2C6H3CH2CH=CH2. It is a colorless oily liquid, although impure samples can appear yellow. A member of the phenylpropanoid family of natural products, it is found in sassafras plants, among oth ..., and many others. References External links * {{Phenylpropene ...
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Jamaican Ginger
Jamaica ginger extract, known in the United States by the slang name Jake, was a late 19th-century patent medicine that provided a convenient way to obtain alcohol during the era of Prohibition in the United States, Prohibition, since it contained approximately 70% to 80% ethanol by weight. In the 1930s, a large number of users of Jamaica ginger were afflicted with a paralysis of the hands and feet that quickly became known as Jamaica ginger paralysis or jake paralysis. Early use and Prohibition Since the 1860s, Jamaica ginger had been widely sold at drug stores and roadside stands in bottles. In small doses, mixed with water, it was used as a remedy for headaches, upper respiratory infections, menstrual disorders, and intestinal gas. Despite its strong ginger flavour, it was popular as an alcoholic beverage in Dry county, dry counties in the United States, where it was a convenient and legal method of obtaining alcohol. It was often mixed with a soft drink to improve the taste ...
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Abortifacients
An abortifacient ("that which will cause a miscarriage" from Latin: ''abortus'' "miscarriage" and '' faciens'' "making") is a substance that induces abortion. This is a nonspecific term which may refer to any number of substances or medications, ranging from herbs to prescription medications. Common abortifacients used in performing medical abortions include mifepristone, which is typically used in conjunction with misoprostol in a two-step approach. Synthetic oxytocin, which is routinely used safely during term labor, is also commonly used to induce abortion in the second or third trimester. For thousands of years writers in many parts of the world have described and recommended herbal abortifacients to women who seek to terminate a pregnancy, although their use may carry risks to the health of the woman. Medications Because "abortifacient" is a broad term used to describe a substance's effects on pregnancy, there is a wide range of drugs that can be described as abortifa ...
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Phenylpropenes
Phenylpropene is the organic compound with the formula C6H5CH2CH=CH2. It is a colorless liquid. The compound consists of a phenyl group attached to allyl. Phenylpropene isomerizes to trans-propenylbenzene. In plant biochemistry, the phenylpropene skeleton is the parent (simplest representation) of the phenylpropanoids. Prominent derivatives include eugenol, safrole Safrole is an organic compound with the formula CH2O2C6H3CH2CH=CH2. It is a colorless oily liquid, although impure samples can appear yellow. A member of the phenylpropanoid family of natural products, it is found in sassafras plants, among oth ..., and many others. References External links * {{Phenylpropene ...
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Myristicin
Myristicin is a naturally occurring compound found in common herbs and spices, the most well known being nutmeg. It is an insecticide, and has been shown to enhance the effectiveness of other insecticides in combination. Myristicin is also a precursor for substituted amphetamine derivative compounds structurally related to MMDA and MDMA; it was believed to be metabolized in the liver into MMDA, but unlikely since no MMDA was found in urine, in the body it produces hallucinogenic effects, and can be converted to MMDMA in controlled chemical synthesis. It interacts with many enzymes and signaling pathways in the body, is cytotoxic to living cells, and may also have chemoprotective properties. Uses Isolated myristicin has proven an effective insecticide against many agricultural pests, including ''Aedes aegypti'' mosquito larvae, '' Spilosoma obliqua'' (hairy caterpillars), ''Epilachna varivestis'' (Mexican bean beetles), ''Acyrthosiphon pisum'' (pea aphids), mites, and ''Dr ...
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Crowea Angustifolia
''Crowea angustifolia'' is a flowering plant in the family Rutaceae, and is endemic to the south-west of Western Australia. It is an erect shrub growing to high by in diameter with white or pink flowers in spring. Description Crowea angustifolia is a variable shrub growing to a height of high, either erect or spreading and diffuse. The leaves are thin, glabrous, linear to broad elliptic, or egg-shaped with the narrower end towards the base. They are long and less than wide. The flowers usually appear singly in the axils of the leaves on a pedicel long. There are between two and four bracteoles at the base of the flower and five separate sepals which are papery, more or less round and about long. There are five white or pink petals which are egg-shaped, thin and about long. The ten stamens and style are about long. Flowering occurs from September to December. Taxonomy ''Crowea angustifolia'' was first formally described by James Edward Smith in 1808 from a specimen coll ...
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Crowea Exalata
''Crowea exalata'', commonly known as small crowea or waxflower, is a flowering plant in the family Rutaceae and is endemic to the states of Queensland, New South Wales and Victoria in Australia. It is an attractive small shrub and is a popular garden plant. It flowers mainly from late summer to mid-winter when few others are flowering but usually has some flowers at other times of the year. Description ''Crowea exalata'' is a small shrub, growing to a height of about with thin branches, often spreading to more than . Its leaves are narrow oblong to narrow egg-shaped with the narrower end towards the base and are long and wide. They have many oil glands and have a characteristic scent when crushed. The star-like flowers appear on the ends of the branches or in the axils of the leaves on a stalk long. The five petals are egg-shaped, about and usually pink, sometimes white and a range of colours in the cultivars. The stamens in the centre of the flower almost overlap. Flowerin ...
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