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首页> 外文期刊>Medicinal chemistry >Synthesis and biological activities of 2,6-dihydroxy-4- isopentenyloxychalcone as an antimicrobial and anti-inflammatory compound
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Synthesis and biological activities of 2,6-dihydroxy-4- isopentenyloxychalcone as an antimicrobial and anti-inflammatory compound

机译:2,6-二羟基-4-异戊烯氧基查尔酮作为抗菌消炎化合物的合成及生物活性

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摘要

Chalcones are a group of plant-derived polyphenolic compounds possessing a wide variety of biological activities. The aim of this study was to synthesize 2,6-dihydroxy-4-isopentenyloxychalcone (1), a chalcone found in plants belonging to the genera Helichrysum, Pleiotaxix and Metalasia, and evaluate its antimicrobial effects against major oral pathogens as well as its anti-inflammatory properties. Compound 1 was synthesized using a simple two-step procedure. Among the seven pathogens tested, Porphyromonas gingivalis and Prevotella intermedia were the most susceptible to inhibition by 1. This chalcone also attenuated the secretion of interleukin-8 and chemokine (C-C motif) ligand 5 (CCL5) by lipopolysaccharide (LPS)-stimulated oral epithelial cells as well as the secretion of matrix metalloproteinase 2 (MMP-2) by LPS-stimulated gingival fibroblasts. In conclusion, our study showed that 1 exerts a dual effect by acting on both oral pathogens and the host inflammatory response and thus represents a molecule of interest for periodontal infections.
机译:查尔酮是一组具有多种生物活性的植物来源的多酚化合物。这项研究的目的是合成2,6-二羟基-4-异戊烯基氧基查尔酮(1),一种在蜡菊属,Pleiotaxix和Metalasia属植物中发现的查尔酮,并评估其对主要口腔病原体的抗菌作用及其抗-炎症特性。使用简单的两步法合成化合物1。在所测试的7种病原体中,牙龈卟啉单胞菌和中间致病菌最易被1抑制。这种查尔酮还通过脂多糖(LPS)刺激的口腔上皮细胞减弱了白介素8和趋化因子(CC基序)配体5(CCL5)的分泌。 LPS刺激的牙龈成纤维细胞分泌基质金属蛋白酶2(MMP-2)。总之,我们的研究表明1通过同时作用于口腔病原体和宿主炎症反应发挥双重作用,因此代表了牙周感染的重要分子。

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