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Saponine

Saponins dismpt red blood cells and may produce diarrhea and vomiting. They may also have a beneficial effect by complexing with cholesterol [57-88-5] and thus lowering semm cholesterol levels (24,25). In humans, intestinal microflora seem to either destroy saponins or inactivate them in small concentrations. [Pg.476]

Alginates, alkaloids, glycerides, gutta, phenols, rosins, rubber, saponins sterols, tall oils, tannins, terpenes, waxes... [Pg.27]

Soybeans and peanuts also contain saponins, which are glucoside derivatives of triterpenoid alcohols (37). Saponins range from 0.09 to 0.32% in 457 soybean varieties (38). [Pg.296]

Sapogenins and Saponins. Steroids isolated from a variety of plant sources that contain a spiroketal between hydroxyl moieties at C16 and C26 and a carbonyl at C22 are called sapogenins (33). [Pg.419]

Saponins. Although the hypocholesterolemic activity of saponins has been known since the 1950s, thek low potency and difficult purification sparked Htde interest in natural saponins as hypolipidemic agents. Synthetic steroids (292, 293) that are structurally related to saponins have been shown to lower plasma cholesterol in a variety of different species (252). Steroid (292) is designated CP-88,818 [99759-19-0]. The hypocholesterolemic agent CP-148,623 [150332-35-7] (293) is not absorbed into the systemic ckculation and does not inhibit enzymes involved in cholesterol synthesis, release, or uptake. Rather, (293) specifically inhibits cholesterol absorption into the intestinal mucosa (253). As of late 1996, CP-148,623 is in clinical trials as an agent that lowers blood concentrations of cholesterol (254). [Pg.447]

Glycosides, particularly of phenoHc compounds, are widely distributed in plant tissues (2,10). Glycosides of anthocyanidins, flavones, flavanols, flavanones, flavanonols, stilbenes and saponins, gaUic acid derivatives, and condensed tannins are all common. [Pg.475]

Berkman and Egloff explain that some additives increase the flexi-bihty or toughness of bubble walls, rather than their viscosity, to render them more durable. They cite as illustrations the addition of small quantities of soap to saponin solutions or of glycerin to soap solution to yield much more stable foam. The increased stability with ionic additives is probably due to elec trostatic repulsion between charged, nearly parallel surfaces of the hquid film, which acts to retard draining and hence rupture. [Pg.1418]

The effective surface viscosity is best found by experiment with the system in question, followed by back calculation through Eq. (22-55). From the precursors to Eq. (22-55), such experiments have yielded values of [L, on the order of (dyn-s)/cm for common surfactants in water at room temperature, which agrees with independent measurements [Lemhch, Chem. Eng. ScL, 23, 932 (1968) and Shih and Lem-lich. Am. Inst. Chem. Eng. J., 13, 751 (1967)]. However, the expected high [L, for aqueous solutions of such sldn-forming substances as saponin and albumin was not attained, perhaps because of their non-newtonian surface behavior [Shih and Lemhch, Ind. Eng. Chem. Fun-dam., 10, 254 (1971) andjashnani and Lemlich, y. Colloid Inteiface ScL, 46, 13(1974)]. [Pg.2021]

Alkaloid- and saponin-containing drugs, as well as bearberry leaves, as a moderately fine powder (particle size ca. 0.5 mm). [Pg.25]

These methods are employed for the detection and determination of antibiotics and substances with similar effects, like alkaloids, insecticides, fungicides, mycotoxins, vitamins, bitter principles and saponins [14]. [Pg.7]

A skinned fiber is a muscle fiber, the sarcolemma of which has been mechanically removed or which is made freely permeable to small molecules, such as Ca2+, Mg2+, EGTA, ATP, soluble enzymes and others by a chemical agent (saponin, (3-escin or Staphylococcus a-toxin). The organization of the sarcoplasmic reticulum (SR) and myofibrils is kqrt as they are in the living muscle. [Pg.1133]

The first soaps were probably the saps of plants such as Chloro-galum pomeridianum, the roots of which can be crushed in water to form a lather. Other plants, such as soapbark (Quillaja saponaria), soapberry (Sapindus mukorossi), and soapwort (Saponaria officinalis) also contain the same main ingredient, a compound called saponin, which forms the foamy lather. [Pg.207]

Saponin can also be used in fishing a toxin, it is introduced into streams to stupefy fish and make them easy to catch.)... [Pg.207]

Saponins la 7,411,430 -, bioautographic determination la 109 Sarcosine Ia435 lbl24 Scandium cations, detection la 144 Scanner, optical trains la 30,39 S-Chamber (small chamber) la 126,127 SCHiFF s bases lb 52 Scintillators la 12 Scopolamine lb 231,252,255,323 Scopoletin lb 216-218,365 Screening process lb 45 Sebacic acid la 178,233,249,308 Sebuthylazine lb 418 Selectivity, enhancement by derivatiza-tion la 55... [Pg.494]

Sandwich chamber 126,127 Sapogenins 43,195, 206, 411 -, steroid 69, 206 -, trifluoroacetates 69 Saponins 7,109, 411, 430 Sarcosine 435 Scandium cations 144 Scanners, optical trains 30, 39 S-chamber see Sandwich chamber Scintillators 12 Sebacic acid 178,233,249, 308 Selectivity... [Pg.733]

E. C. (1988b). Incorporation of the major outer membrane protein of Neisseria gonorrhoeae in saponin-Upid complexes (Iscoms) Chemical analysis, some structural features, and comparison of their immunogenicity with three other antigen delivery systems, Inf. Immun., 56, 432-438. [Pg.324]

MTX exceeds any other marine toxins known in the mouse lethality (0.13 ig/kg) and is 80 times more potent than commercial saponin (Merck) in hemolytic activity. According to Terao (72), MTX induced severe pathomorphological change in the stomach, heart and lymphoid tissues in mice and rats by i.p. injection of 200... [Pg.121]


See other pages where Saponine is mentioned: [Pg.189]    [Pg.345]    [Pg.352]    [Pg.230]    [Pg.311]    [Pg.273]    [Pg.278]    [Pg.308]    [Pg.413]    [Pg.419]    [Pg.420]    [Pg.420]    [Pg.27]    [Pg.113]    [Pg.20]    [Pg.109]    [Pg.411]    [Pg.430]    [Pg.671]    [Pg.406]    [Pg.1114]    [Pg.300]    [Pg.94]    [Pg.125]    [Pg.436]    [Pg.439]    [Pg.439]    [Pg.262]    [Pg.224]    [Pg.557]    [Pg.708]   
See also in sourсe #XX -- [ Pg.35 ]

See also in sourсe #XX -- [ Pg.216 ]

See also in sourсe #XX -- [ Pg.248 , Pg.576 ]




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Absolute configuration of sugars saponins

Absorption enhancers saponins

Acacia auriculiformis triterpenoid saponin from

Aesculus saponins

Aglycone skeletons saponins

Alkaloids triterpene saponins

Analysis of Ginseng Saponins

Anti-inflammatories saponins

Anti-obesity action of saponin

Antifungal effects Steroidal saponins

Antigen saponins

Antinociception action of dispsacus saponin

Application of Saponins as Surfactants and Emulsifiers

Aster saponin

Astragalus saponin

Bidesmosidic saponin sandrosaponin

Bidesmosidic saponins

Bidesmosidic triterpene saponin

Bioactive saponins

Bioactive saponins bioactivity

Bioactive saponins developments

Bioactive saponins from plants

Biological activities saponin

Cancer saponins

Caryophyllaceae saponins

Chestnuts, saponin

Chikusetsa saponin

Cholestane saponins

Cholesterol saponins

Chromatography Ginseng saponins

Chromatography Saponins

Cucurbitaceae saponins from

Cycloartane saponins

Cytotoxic effects Steroidal saponins

Dammaran-type saponins

Dammarane saponins

Dammarane type saponins

Dammarane-type triterpene saponins

Dianthus saponin

Dispsacus saponin

Dispsacus saponin antinociceptive effects

Dodonaea saponins

Dodonea saponins

Entada saponins

Ester saponins

Food components saponins

Food saponin content

Fungicidal saponins

Furostane-type saponin

Furostanol saponins

Genus Astragalus saponins from

Ginseng saponins

Ginseng saponins action

Ginseng total saponin

Gleditsia japonica saponin C from

Gleditsia saponins

Glucuronide saponins

Glycoalkaloid saponins

Glycosidic saponins

Glycyrrhizin (triterpene saponin

Gymaemasaponin III saponin

Gymnemic saponins

Gymnocladus chinensis saponin D from

Gypsophila saponins

Hederagenin saponins

Hepatoprotective effects saponins

Hepatoprotective saponin

Herniaria saponins

Immunoadjuvant saponins

Immunoadjuvants saponins

Immunostimulant saponins

Immunostimulants saponins

Kalopanax saponin

Leguminosae saponins from

Licorice-saponin

Liliaceae saponin from

Maidong saponin

Monodesmosidic saponins

Ocotillol-type saponins

Of saponin

Oleanane saponins

Oleanane-type saponins

Oleanane-type triterpene saponins

Oleanolic acid-type glucuronides saponins

Oleanolic saponins

Oligosaccharidic moiety of saponins

Panax ginseng saponins

Panax notoginseng saponins

Panax plant saponins from

Panax saponins

Panax saponins from

Panax saponins structures

Panaxadiol saponins

Panaxatriol saponins

Peanuts saponins

Permeabilization Saponin

Permeabilization with Saponin

Permeabilized smooth muscle saponin

Phytochemicals saponins

Plant saponin

Polygalaceae saponins

Polypodium glycyrrhiza steroidal saponin from

Potato-saponin

Primula saponin

Production of Saponins by Tissue Culture

Protopanaxadiol saponin

Quillaja saponin

Quillaja saponin mixture

Quinoa saponins

S saponins

Saponaria officinalis Saponins

Saponin Glycyrrhiza glabra from

Saponin Glycyrrhiza uralensis from

Saponin INDEX

Saponin Lysis Concentration for Filariae

Saponin OSW

Saponin Subject

Saponin akebin

Saponin avenacin

Saponin drugs

Saponin fraction

Saponin from Hovenia dulcis Thunb. var

Saponin glycosides

Saponin hemolysis

Saponin hydrolases

Saponin legume

Saponin mixture

Saponin sulphate

Saponin tomentella Makino

Saponin, protective action

Saponin, smooth muscle permeabilization

Saponin-Based Surfactants

Saponin-III

Saponines

Saponins

Saponins Scale

Saponins absorption

Saponins alfalfa

Saponins analysis

Saponins and Cardenolides

Saponins and Glycosides

Saponins and sapogenins

Saponins antitumor activity

Saponins antiviral activity

Saponins applications

Saponins as immunoadjuvants

Saponins as immunostimulants

Saponins basic structures

Saponins biological effects

Saponins biosynthesis

Saponins calendula

Saponins carboxylic acids

Saponins chemical structures

Saponins common structure, examples

Saponins detection

Saponins digitalis

Saponins disruption

Saponins fenugreek

Saponins from Gleditsia japonica

Saponins from Sea Cucumbers

Saponins from Starfish

Saponins from Triterpenes

Saponins fungitoxicity

Saponins glucose

Saponins glucosyltransferases

Saponins group

Saponins immunostimulant activity

Saponins in Ginseng Roots

Saponins in food

Saponins in plants

Saponins isolation

Saponins macrophage activation

Saponins marine invertebrates

Saponins micelles with bile acids

Saponins molecular properties

Saponins molluscicidal activity

Saponins neutral

Saponins of Chinese Sanchi-Ginseng

Saponins of Ginseng and related plants

Saponins of Other Panax spp

Saponins of P. ginseng Leaves and Flower Buds

Saponins of P. zingiberensis Rhizomes

Saponins of Red Ginseng

Saponins of cycloartane series

Saponins oligosaccharidic moiety

Saponins onion

Saponins pathway

Saponins physical

Saponins physiological

Saponins properties

Saponins purification

Saponins quillaia

Saponins release

Saponins rhamnose

Saponins saponification

Saponins sarsaparilla

Saponins sources

Saponins structural elucidation

Saponins structure

Saponins structure determination

Saponins structure elucidation

Saponins synthetic

Saponins toxic properties

Saponins toxicity

Saponins yucca

Saponins, acid-catalyzed

Saponins, acid-catalyzed hydrolysis

Saponins, antitumour

Saponins, chemical nature

Saponins, health benefits

Schidegera saponin

Smilax saponin

Solidago saponins

Sources of Saponins

Soy saponins

Soyabean saponins

Soyabean saponins hypocholesterdemic effects

Soybean saponin

Spiroketals (Saponins)

Spirostane saponin

Spirostane-type saponin

Spirostanol saponins

Steroid saponin

Steroidal saponin from Yucca

Steroidal saponin from Yucca schidigera

Steroidal saponins

Steroidal saponins, hydrolysis

Structural elucidation of saponins

Structure elucidation of saponins

Structure of saponins

Structures of Ginseng Saponins

Structures of Minor Saponins

Sweetness inhibitors Zizyphus saponin

Sweetness inhibitors saponin

Tea saponin

Tea saponin effect on parametrial adipose

Tea saponin effect on triacylglycerol content

Tea saponin weight

Terpenoids saponins

Toxic saponins

Triterpene saponins

Triterpene saponins cytotoxic activity

Triterpenoid saponins

Triterpenoid saponins acetylastragaloside

Triterpenoid saponins agroastragaloside

Triterpenoid saponins agroastragaloside III

Triterpenoid saponins alexandroside

Triterpenoid saponins asemestioside

Triterpenoid saponins askendoside

Triterpenoid saponins askenodoside

Triterpenoid saponins astrachrysoside

Triterpenoid saponins astragaloside

Triterpenoid saponins astragaloside III

Triterpenoid saponins astragaloside VII

Triterpenoid saponins astragaloside VIII

Triterpenoid saponins astramembrannin

Triterpenoid saponins astrasieversianin

Triterpenoid saponins astrasieversianin III

Triterpenoid saponins astrasieversianin VII

Triterpenoid saponins astrasieversianin VIII

Triterpenoid saponins astrasieversianin XII

Triterpenoid saponins astrasieversianin XIII

Triterpenoid saponins astraverrucin

Triterpenoid saponins brachyoside

Triterpenoid saponins cycloalpioside

Triterpenoid saponins cyclocanthoside

Triterpenoid saponins cyclosieversioside

Triterpenoid saponins from Astragalus spp

Triterpenoid saponins of saikosaponin

Triterpenoids and saponins

Triterpenoids triterpenoid saponins

Zahna africana oleanane saponins from

Ziziphus jujuba P. Miller zizyphus saponin I-III from

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