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Abstract Book - 3rd International Symposium on Medicinal Plants ...

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evaluati<strong>on</strong> were included 4 species of D. kaki L.f., D. virginiana L. (male - m and female - f<br />

genotypes), D. lotus L. (male – m and female - f genotypes), and an interspecies hybrid D.<br />

virginiana L. x D. kaki L.f. All tested plants were grown in the Botanical Garden of M. M. Grishko of<br />

the Nati<strong>on</strong>al Academy of Sciences in Kiev, Ukraine. In the withdrawn leaves and defoliated <strong>on</strong>eyear<br />

old offshoots were determined the ascorbic acid c<strong>on</strong>tent and their dry-weight in <strong>on</strong>e-m<strong>on</strong>th<br />

intervals. With leaves were c<strong>on</strong>trolled their length and width as well. Medium length of the leaf<br />

blade ranged from 120.19 (D. virginiana L.- m) up to 190.94 mm (D. virginiana L.) and the width<br />

from 50.17 mm (D. virginiana L.- m) to 100.12 mm (D. virginiana L. x D. kaki L.f). Using the method<br />

of time-interval the ascorbic acid medium increment coefficient in the leaves has been detected in<br />

ranges from -0.19 (D. virginiana L.) up to -0.41 (D. kaki L.f.) and in the case of offshoots from -0.34<br />

(D. virginiana L.) to -0.54 (D. virginiana L.-m). Leaves medium growth rate varried between 58.87<br />

(D. kaki L.f.) and 80.07 % (D. virginiana L.) and for offshoots 45.44 (D. virginiana L.) and 65.19 %<br />

(D. virginiana L.). Am<strong>on</strong>g the tested species, significant differences were found in the antioxidati<strong>on</strong><br />

activity as well Leaves and ofshoots are important products, which could be utilized as resources<br />

of biologically active substances for pharmaceutical products.<br />

Key words: Ascorbic acid, diospyros, virginiana L, lotus L, leaves.<br />

3.21 Sec<strong>on</strong>dary Metabolites from Algerian Plant Atractylis flava<br />

Haba Hamada 1 , Chabani S 1 ., Lavaud C 2 ., Harakat D 2 ., and Benkhaled M. 1<br />

1 Department of Chemistry, Faculty of Science, Batna University, 05000, Batna, Algeria. 2 Institut de<br />

Chimie Moléculaire de Reims, CNRS UMR 6229, BP 1039, 51097 Reims Cedex 2, France<br />

<str<strong>on</strong>g>Abstract</str<strong>on</strong>g>: The plant Atractylis flava Desf. bel<strong>on</strong>gs to the family Asteraceae. This family is <strong>on</strong>e of<br />

the most important botanical families of plants kingdom. It c<strong>on</strong>tains a large number of species so<br />

different by their vegetative appearance, approximately 25000 species, distributed in temperate<br />

z<strong>on</strong>es of the globe, Northern Africa (Algeria, Morocco and Tunisia) and in Southern Europe (Italy,<br />

Greece, Spain and Portugal). The genus Atractylis is chemically little investigated. As such the<br />

studies have been realized <strong>on</strong> the toxic species Atractylis gummifera, its toxicity was attributed to<br />

atractyloside and carboxyatractyloside, two diterpenoid glucosides capable of inhibiting<br />

mitoch<strong>on</strong>drial oxidative phosphorylati<strong>on</strong>. Triterpenoids and flav<strong>on</strong>oids were isolated previously<br />

from this genus. Atractylis flava Desf. (syn. Atractylis carduus (Forsk.) Christ.) known as yellow<br />

thistle, is a perennial plant growing in the Saharan regi<strong>on</strong>. Atractylis plants have been used in folk<br />

medicine to treat circulatory disorders, intestinal parasites, ulcers, and snake-bite pois<strong>on</strong>ing.The<br />

present work describes the isolati<strong>on</strong> by chromatographic methods of eight sec<strong>on</strong>dary metabolites<br />

from ethyl acetate extract of A. flava; three flav<strong>on</strong>oids: chrysin, quercetin 5,7,4‟-trihydroxy-3‟-<br />

methoxy-3-O-α-L-rhamnopyranosyl-(1-6)-β-D-galactopyranosylflav<strong>on</strong>ol, three triterpenes: oleanolic<br />

acid, hedragenin acid and 3β,22β-dihydroxyolean-12-en-28-oic acid and two steroids: β-sitosterol<br />

glucoside and stigmasterol glucoside. Their structures were determined by spectroscopic analysis<br />

including 1D and 2D NMR ( 1 H, 13 C, COSY, TOCSY, HSQC, HMBC, NOESY) and mass<br />

spectrometry (ESI-MS) and comparis<strong>on</strong> with literature data. In the biological part, crude extracts<br />

(dichloromethane, ethyl acetate and n-butanol) of A. flava exhibit antibacterial activity against<br />

Gram positive and negative strains: Staphylococcus aureus ATCC23, Staphylococcus aureus<br />

ATCC582, Pseudom<strong>on</strong>as aeruginosa ATCC 374 and Pseudom<strong>on</strong>as aeruginosa ATCC 53. The<br />

anti-oxidant activity was estimated <strong>on</strong> the extracts by the DPPH test.<br />

Key words: Algerian plant, Atractylis flava, flav<strong>on</strong>oids, sec<strong>on</strong>dary metabolites, species.<br />

3.22 A flav<strong>on</strong>e glucoside from the roots of Salvadora persica (Rutaceae)<br />

Hassan Abdalla Almahy<br />

Chemistry Department, Faculty of Science and Educati<strong>on</strong>, Taif University, Kingdom of Saudi<br />

Arabia<br />

<str<strong>on</strong>g>Abstract</str<strong>on</strong>g>: A flav<strong>on</strong>e glucoside, luteolin 8-C-ı-d-glucopyranoside was isolated from the ethyl<br />

acetate extract of the roots of Salvadora persica and separated using column chromatography<br />

techniques. The structure of the compound was established by UV, IR, 1 H-NMR, 13 C-NMR, COSY,<br />

76

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