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See also: meta-oxy-para-methoxycinnamic acid or isoferulic acid, C,oHioO4
.
We may here include various See also: coumarin and benzo-y-pyrone derivatives
.
Aesculin, C16H16O9, occurring in See also: horse-See also: chestnut, and daphnin, occurring in See also: Daphne alpine, are isomeric; the former hydrolyses to See also: glucose and aesculetin (4.5-dioxycoumarin), the latter to glucose and daphnetin (3.4-dioxycoumarin)
.
Fraxin, C,EH,80,o, occurring in Fraxinus excelsior, and with aesculin in horse-chestnut, hydrolyses to glucose and fraxetin, the mono-methyl ester of a trioxycoumarin
.
Flavone or benzo-7-pyrone derivatives are very numerous; in many cases they (or the non-See also: sugar See also: part of the molecule) are See also: vegetable dyestuffs
.
Quercitrin, C21H22O12, is a yellow dyestuff found in Quercus tinctoria; it hydrolyses to rhamnose and quercetin, a dioxy-/3-phenyl-trioxybenzoy-pyrone
.
Rhamnetin, a splitting product of the glucosides of Rhamnus, is monomethyl quercetin; fisetin, from Rhus cotinus, is monoxyquercetin; chrysin is phenyl-dioxybenzo-y-pyrone
.
Saponarin, a See also: glucoside found.in Saponaria officinalis, is a related compound
.
Strophanthin is the name given to three different compounds, two obtained from See also: Strophanthus Kombe and one from S. hispidus
.
4
.
Anthracene Derivatives.—These are generally substituted anthraquinones; many have medicinal applications, being used as purgatives, while one, ruberythric acid, yields the valuable dye-stuff See also: madder, the See also: base of which is See also: alizarin (q.v.)
.
Chrysophanic acid, a dioxymethylanthraquinone, occurs in See also: rhubarb, which also contains emodin, a trioxymethylanthraquinone; this substance occurs in combination with rhamnose in frangula bark
.
The most important cyanogenetic glucoside is amygdalin, which occurs in bitter almonds . The enzyme maltase decomposes it into glucose and mandelic nitrile glucoside; the latter is broken down by emulsin into glucose, benzaldehyde and prussic acid . Emulsin also decomposes amygdalin directly into these compounds without the intermediate formation of mandelic nitrile glucoside . Several other glucosides of this nature have been isolated . The saponins are aSee also: group of substances characterized by forming a lather with See also: water; they occur in See also: soap-bark (q.v.)
.
Mention may also be made of indican, the glucoside of the indigo plant; this is hydrolysed by the indigo ferment, indimulsin, to indoxyl and indiglucin
.
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