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1.
J Environ Biol ; 2008 Jul; 29(4): 475-8
Article de Anglais | IMSEAR | ID: sea-113629

RÉSUMÉ

Two inhibitors of Taq DNA polymerase were isolated from the marine red alga Symphyocladia latiuscula. The inhibitors were purified by methanol extraction, molecular fractionation below 3000 MW and reverse-phase HPLC. The purified compound SL-1 containing three bromines was identified as 2,3,6-tribromo-4,5-dihydroxybenzyl alcohol (C7H5Br3O3: MW374) by NMR and MS analyses. The purified compound SL-2 was identified as 2,3, 6-tribromo-4,5-dihydroxybenzyl methyl ether(C8H7Br3O3: MW388). In a 25-microl reaction mixture containing 1.5 units of Taq DNA polymerase, the enzyme was completely inhibited by 0.5 microg SL-1 or 5 microg SL-2.


Sujet(s)
Rhodophyta/composition chimique , Séquence nucléotidique , Chromatographie en phase liquide à haute performance , Électrophorèse sur gel d'agar , Antienzymes/composition chimique , Éthers , Hydrocarbures bromés/composition chimique , Méthanol/composition chimique , Masse moléculaire , Réaction de polymérisation en chaîne , Analyse spectrale , TAQ polymerase/antagonistes et inhibiteurs
2.
J Environ Biol ; 2008 Jul; 29(4): 479-84
Article de Anglais | IMSEAR | ID: sea-113610

RÉSUMÉ

Silica gel chromatography HPLC, El-Mass, and NMR analyses were performed in order to determine the structure obtained from the separation and refinement of the main components of an ethanol extraction of Sargassum siliquastrum, which indicated its antioxidant activity An ethanol extraction of Sargassum siliquastrum demonstrated the strongest antioxidant activities of ethyl acetate when isolated by silica gel chromatography This amounts to 84.9 +/- 1.2% of its 0.5 mg ml(-1) concentration. The thiobarbituric acid reactive substances (TBARS) measurements from 3 isolations of an HPLC separation of ethyl acetate showed that the antioxidant activity of peak 2 was the most dominant at 84.08% in a 0.5 mg ml(-1) concentration. Peak 2 was verified as a type of chromene through El-Mass and NMR analysis. Its metal sealing characteristic was low while its characteristic of TBARS and DPPH erasure indicated similar or higher levels of metal sealing characteristic. The NMR spectroscopic data was used to elucidate the structure of this new compound, which showed strong antioxidant activity in the assay.


Sujet(s)
Acétates/isolement et purification , Antioxydants/isolement et purification , Benzopyranes/isolement et purification , Chélateurs/pharmacologie , Chromatographie en phase liquide à haute performance , Éthanol/composition chimique , Piégeurs de radicaux libres/pharmacologie , Sargassum/composition chimique , Analyse spectrale , Substances réactives à l'acide thiobarbiturique/isolement et purification
3.
J Environ Biol ; 2008 Jul; 29(4): 465-9
Article de Anglais | IMSEAR | ID: sea-113478

RÉSUMÉ

Thirty-seven species of common seaweeds from the coast of Korea were screened for anti-inflammatory activity Methanol extracts of the seaweeds were tested against mouse ear edema and erythema induced by phorbol myristate acetate. At 40 mg ml(-1) of extract, edema was strongly suppressed by the seaweeds Undaria pinnatifida and Ulva linza, with relative inhibition of 85 and 84%, respectively These two seaweeds also showed the greatest suppression of erythema, with inhibition of 78 and 70%, respectively IC50 values of U. pinnatifida were 10, 15, and 18 mg ml(-1) when inflammation symptoms of edema, erythema, and blood flow, respectively were measured. The IC50 of U. linza was 20, 26, and 31 mg ml(-1) when edema, erythema, and blood flow, respectively, were measured. A linear correlation among inhibition rates of edema, erythema, and blood flow was observed with high confidence.


Sujet(s)
Animaux , Anti-inflammatoires/pharmacologie , Vitesse du flux sanguin , Relation dose-effet des médicaments , Oreille/anatomopathologie , Oedème/induit chimiquement , Érythème/induit chimiquement , Inflammation/induit chimiquement , Concentration inhibitrice 50 , Corée , Méthanol/composition chimique , Souris , Souris de lignée BALB C , Extraits de plantes/pharmacologie , Algue marine/composition chimique , 12-Myristate-13-acétate de phorbol
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