B Gil, M J Sanz, M C Terencio, M L Ferrándiz, G Bustos, M Payá, R Gunasegaran, M J Alcaraz
Index: Life Sci. 54(20) , PL333-8, (1994)
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Six flavonoid derivatives were tested for their influence on Naja naja and human recombinant synovial phospholipase A2. They showed a selectivity for the last enzyme with IC50 = 14.3, 17.6, 12.2 and 28.2 microM for quercetagetin, kaempferol-3-O-galactoside, scutellarein and scutellarein-7-O-glucuronide, respectively, while reduced effects were observed for hispidulin and hibifolin. After topical application all the flavonoids inhibited 12-O-tetradecanoylphorbol-13-acetate-induced ear oedema in mice with a potency comparable to that of indomethacin and they were also able to inhibit carrageenan-induced mouse paw oedema at a dose of 150 mg/kg p.o. The blockade of the free hydroxyl at C-7 or C-6 reduced the anti-inflammatory activity and also the inhibitory effect on human recombinant synovial phospholipase A2. These results are in accordance with the notion that group II phospholipases A2 may play a role in experimental inflammation, although several mechanisms seems to be involved in the anti-inflammatory effect of this group of flavonoids.
Structure | Name/CAS No. | Molecular Formula | Articles |
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Hispidulin
CAS:1447-88-7 |
C16H12O6 |
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Inhibition of [methyl-3H]diazepam binding to rat brain membr...
1994-09-01 [Zhongguo Yao Li Xue Bao 15(5) , 385-8, (1994)] |
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Hispidulin protection against hepatotoxicity induced by brom...
1994-01-01 [Life Sci. 55(8) , PL145-50, (1994)] |
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2013-09-05 [Eur. J. Pharmacol. 715(1-3) , 96-104, (2013)] |
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