Abstract: A new nonglycosidic iridoid, sambulin B (1), was isolated from the methanol extract of Sambucus ebulus L. leaves along with a recently reported new nonglycosidic iridoid, 10-O-acetylpatrinoside aglycone (sambulin A) (2); 2 flavonoids, isorhamnetin-3-O-eta-D-glucopyranoside (3) and isorhamnetin-3-O-rutinoside (4); and a mixture of 2 flavonoids (5), quercetin-3-O-eta-D-glucopyranoside and quercetin-3-O-eta-D-galactopyranoside. Their structures were elucidated by 1-D and 2-D nuclear magnetic resonance spectroscopy (NMR) and mass spectrometry (MS) experiments.
The synthesis of a novel series of Mannich bases of 5-methyl-3-substituted piperazinomethyl-2-benzoxazolinones is described. The structures attributed to compounds 3c, 3d and 3f-3n were elucidated using IR and 1H NMR spectroscopic techniques as well as elemental analysis. The compounds were examined for their in vivo anti-inflammatory and analgesic activities in 2 different bioassays, namely, carrageenan-induced hind paw edema and p-benzoquinone-induced abdominal constriction tests in mice, respectively. In addition, the ulcerogenic effects of the compounds were determined. Among the derivatives tested the most promising results wer . . .e obtained for the compounds bearing electron-withdrawing substituents (F, Cl, COCH_3) in the para position of the phenyl nucleus on the piperazine ring at the 3 position of benzoxazolinone moiety (3a, 3c, 3i). The analgesic activities of all compounds are higher than their anti-inflammatory activities and therefore these high analgesic activities indicated that the compounds could a show central effect
Daha fazlası
Daha az
...
6698 sayılı Kişisel Verilerin Korunması Kanunu kapsamında yükümlülüklerimiz ve çerez politikamız hakkında bilgi sahibi olmak için alttaki bağlantıyı kullanabilirsiniz.
