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I. indica

Arabinogalactans (AGs) are widely spread throughout the plant kingdom. Many edible and inedible plants are rich sources of these polysaccharides. AGs occur in two structurally different forms described as type I and type II, associated with the pectin cell-wall component by physical bonds and some of them are covalently linked to the complex pectin molecule as neutral side chains. Commercial pectins always contain AG 10-15%). AG of type I has a linear (1 4)-y0-o-Galp backbone, bearing 20-40% of of-L-Ara/ residues (1 5)-linked in short chains, in general at position 3. It is commonly found in pectins from citrus, apple and potato [6]. Recently, this AG type has been isolated from the skin of Opuntia ficus indica pear fruits [372]. [Pg.45]

Shanker et al. [120] prepared bimetallic Au-core/ Ag-shell nanoparticles by the simultaneous reduction of Au(III) and Ag(I) ions in the presence of neem (Azadirachta indica) leaf broth as an extracting agent. [Pg.54]

Pott, I., M. Marx, S. Neidhart et al. 2003. Quantitative determination of (3-carotene stereoisomers in fresh, dried, and solar-dried mangoes (Mangifera indica L.). J. Agric. Food Chem. 51 4527—4531. [Pg.252]

Arcoleo A, Ruccia M and Cusmano S. 1961. Sui pigmenti llavonici delle Opuntiae. Nota I. Isoranmetina dai fiori di O. ficus indica Mill. Ann Chim 51 751—758. [Pg.37]

Galati EM, Tripodo, MM, Trovato A, Miceli N and Monforte MT. 2002. Biological effect of Opuntia ficus-indica (L) Mill (Cactacea) waste matter. Note I diuretic activity. J Ethnopharmacol 79(1) 17—21. [Pg.41]

Pott I, Breithaupt DE and Carle R. 2003b. Detection of unusual carotenoid esters in fresh mango (Mangifera indica L. Cv. Kent). Phytochemistry 64 825-829. [Pg.218]

Robles-Sanchez RM, Rojas-Graii MA, Odriozola-Serrano I, Gonzalez-Aguilar GA and Martin-Belloso O. 2009. Effect of minimal processing on bioactive compounds and antioxidant activity of fresh-cut Kent mango (Mangifera indica L.). Postharvest Biol Technol 51(3) 384-390. [Pg.338]

Plant. Trifluralin was absorbed by carrot roots in greenhouse soils pretreated with the herbicide (0.75 Ib/acre). The major metabolite formed was a,a,a-trifluoro-2,6-dinitro-7V-(/i-propyl-toluene)-p-toluidine (Golab et al., 1967). Two metabolites of trifluralin that were reported in goosegrass Eleucine indica) were 3-methoxy-2,6-dinitro-A7A-dipropyl-4-(trifluoromethyl)benz-enamine and A-(2,6-dinitro-4-(trifluoromethyl)phenyl)-jV-propylpropanamide (Duke et al., 1991). [Pg.1116]

Idris, M. and Prakash, I. (1987). Scent marking activity in the Indian gerbil, Tatera indica, in relation to population density. AnimalBehaviourSS, 920-941. [Pg.472]

Aristolactam (13) (in some papers, aristololactam) was first prepared by catalytic hydrogenation or zinc reduction in acetic acid from aristolochic acid I (25). It has been isolated from seveizl Aristolochic plants, including A. debilis and A. fangchi (24). Kupchan and Merianos isolated the first aristolactam iV-glucoside (19) from A. indica (37). [Pg.32]

Kupchan and Doskotsch (9) found that an alcoholic extract of A. indica possessed reproducible activity against the adenocarcinoma 755 test system. The active principle, aristolochic acid I, was isolated and characterized. Kamatsh and co-workers (97) reported that growth of mouse sarcoma-37 cells incubated with aristolochic acid at concentration of 100-200 p-g/ml for 3 hr was completely inhibited. Treatment of mice with aristolochic acid (1.25-5 mg/kg ip per day) for 3 days after subcutaneous implantation of sarcoma-37 cells inhibited tumor growth in 40-50%. A dose of 2.5-5 mg/kg ip per day for 5 days remarkably prolonged survival. The cytotoxic effect on HeLa cells in culture was observed at a concentration of 25 p-g/ml. [Pg.54]

Yadava, R.N. and Reddy, K.I.S., A novel prenylated flavone glycoside from the seeds of Erythrina indica, Fitoterapia, 70, 357, 1999. [Pg.796]

Mustapha A, Yakasai I A, Aguye lA. Effect of Tamarindus indica L. on the bioavailability of aspirin in healthy human volunteers. Eur J Drug Metab Pharmacokinet 1996 21 223-226. [Pg.43]

I. noli-tangere, I. textori, Melilotus alba, M. suaveolens, M. indica, Nerum indicum, Physochlaina infundibularis, Viburnum sargenti Erycibe henryi, E. aenea, Nerum indicum Hyoscyamus bohemicus Corydalis incisa, C. bungeana... [Pg.480]

Piattelli, M. and Minale, L. 1964. Pigments of cen-trospermae-I. Betacyanins from Phyllocactus hybridus Hort. and Opuntia ficus-indica mill. Phytochemistry 3 307-311. [Pg.896]

In 1898, King s American Dispensatory called Cannabis indica one of the most important of our remedies, particularly for marked nervous depression.. .. [I]t has been efficient in delirium tremens, wakefulness in fevers, neuralgia, gout, rheumatism, infantile... [Pg.295]


See other pages where I. indica is mentioned: [Pg.62]    [Pg.94]    [Pg.169]    [Pg.539]    [Pg.556]    [Pg.562]    [Pg.568]    [Pg.62]    [Pg.94]    [Pg.169]    [Pg.539]    [Pg.556]    [Pg.562]    [Pg.568]    [Pg.529]    [Pg.530]    [Pg.181]    [Pg.406]    [Pg.310]    [Pg.724]    [Pg.112]    [Pg.332]    [Pg.46]    [Pg.157]    [Pg.312]    [Pg.391]    [Pg.399]    [Pg.542]    [Pg.494]    [Pg.20]    [Pg.861]    [Pg.39]    [Pg.52]    [Pg.101]    [Pg.117]    [Pg.118]    [Pg.141]    [Pg.194]    [Pg.16]   
See also in sourсe #XX -- [ Pg.62 , Pg.169 , Pg.234 , Pg.539 ]




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