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Hydroxyanthracene
Hydroxyanthracenes are a class of natural phenolic compounds. They can be found in ''Cassia alata'' and ''Cassia senna ''Senna alexandrina'' (Alexandrian senna, in Arabic عشرج or عشرق or سنامكي and see below) is an ornamental plant in the genus '' Senna''. It is used in herbalism. It grows natively in upper Egypt, especially in the Nubian regio ...'' ( sennosides A, B, C and D). References Natural phenols {{aromatic-stub ...
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Sennoside A
Senna glycoside, also known as sennoside or senna, is a medication used to treat constipation and empty the large intestine before surgery. The medication is taken by mouth or via the rectum. It typically begins working in around 30 minutes when given by rectum and within twelve hours when given by mouth. It is a weaker laxative than bisacodyl or castor oil. Common side effects of senna glycoside include abdominal cramps. It is not recommended for long-term use, as it may result in poor bowel function or electrolyte problems. While no harm has been found to result from use while breastfeeding, such use is not typically recommended. It is not typically recommended in children. Senna may change urine to a somewhat reddish color. Senna derivatives are a type of stimulant laxative and are of the anthraquinone type. While its mechanism of action is not entirely clear, senna is thought to act by increasing fluid secretion within and contraction of the large intestine. It is on ...
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Phenols
In organic chemistry, phenols, sometimes called phenolics, are a class of chemical compounds consisting of one or more hydroxyl groups (— O H) bonded directly to an aromatic hydrocarbon group. The simplest is phenol, . Phenolic compounds are classified as simple phenols or polyphenols based on the number of phenol units in the molecule. Phenols are both synthesized industrially and produced by plants and microorganisms. Properties Acidity Phenols are more acidic than typical alcohols. The acidity of the hydroxyl group in phenols is commonly intermediate between that of aliphatic alcohols and carboxylic acids (their pKa is usually between 10 and 12). Deprotonation of a phenol forms a corresponding negative phenolate ion or phenoxide ion, and the corresponding salts are called phenolates or phenoxides (aryloxides according to the IUPAC Gold Book). Condensation with aldehydes and ketones Phenols are susceptible to Electrophilic aromatic substitutions. Condensation with ...
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Cassia Alata
''Senna alata'' is an important medicinal tree, as well as an ornamental flowering plant in the subfamily Caesalpinioideae. It also known as emperor's candlesticks, candle bush, candelabra bush, Christmas candles, empress candle plant, ringworm shrub, or candletree. A remarkable species of '' Senna'', it was sometimes separated in its own genus, ''Herpetica''. Geographic range ''Senna alata'' is native to most of the Neotropics (from Mexico and the West Indies to Paraguay), and can be found in diverse habitats. In the tropics, it grows up to an altitude of . It is an invasive species in Austronesia distributed in ranges from India to America. These plants have a greater ornamental and medicinal value in the southeast Asia, North Australia and African ranges. Description The shrub stands tall, with leaves long. The leaves close in the dark. The inflorescence looks like a yellow candle. The fruit, shaped like a straight pod, is up to 25 cm long. Its seeds are distribut ...
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Cassia Senna
''Senna alexandrina'' (Alexandrian senna, in Arabic عشرج or عشرق or سنامكي and see below) is an ornamental plant in the genus '' Senna''. It is used in herbalism. It grows natively in upper Egypt, especially in the Nubian region, and near Khartoum (Sudan), where it is cultivated commercially. It is also grown elsewhere, notably in India and Somalia. Description Alexandrian Senna is a shrubby plant that reaches 0.5–1 metres (20" to 40"), rarely two metres (6') in height with a branched, pale-green erect stem and long spreading branches bearing four or five pairs of leaves. These leaves form complex, feathery, mutual pairs. The leaflets vary from 4 to 6 pairs, fully edged, with a sharp top. The midribs are equally divided at the base of the leaflets. The flowers are in a raceme interior blossoms, big in size, coloured yellow that tends to brown. Its legume fruit are horned, broadly oblong, compressed and flat and contain about six seeds. Uses When culti ...
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Sennoside A
Senna glycoside, also known as sennoside or senna, is a medication used to treat constipation and empty the large intestine before surgery. The medication is taken by mouth or via the rectum. It typically begins working in around 30 minutes when given by rectum and within twelve hours when given by mouth. It is a weaker laxative than bisacodyl or castor oil. Common side effects of senna glycoside include abdominal cramps. It is not recommended for long-term use, as it may result in poor bowel function or electrolyte problems. While no harm has been found to result from use while breastfeeding, such use is not typically recommended. It is not typically recommended in children. Senna may change urine to a somewhat reddish color. Senna derivatives are a type of stimulant laxative and are of the anthraquinone type. While its mechanism of action is not entirely clear, senna is thought to act by increasing fluid secretion within and contraction of the large intestine. It is on ...
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Quinizarin
1,4-Dihydroxyanthraquinone, also called quinizarin or Solvent Orange 86, is an organic compound derived from anthroquinone. Quinizarin is an orange or red-brown crystalline powder. It is formally derived from anthraquinone by replacement of two hydrogen atoms by hydroxyl (OH) groups. It is one of ten dihydroxyanthraquinone isomers and occurs in small amounts (as a glycoside) in the root of the madder plant, ''Rubia tinctorum''. Production Quinizarin is produced by the reaction of phthalic anhydride and 4-chlorophenol followed by hydrolysis of the chloride: It can also be prepared less efficiently from phthalic anhydride and hydroquinone. Uses Quinizarin is an inexpensive dye that is used to colour gasoline and some heating oils. It is used as an intermediate for the synthesis of indanthrene- and alizarin-derived dyes. The OH groups can be replaced by chloride. Chlorination and bromination afford other dyes. Amination (replacement of one OH by ArNH) with aniline derivatives ...
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