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首页> 外文期刊>Химия природных соединений >ACYLATED TRITERPENOIDS,FLAVONOIDS,AND LIGNANS ISOLATED FROM THE STEMS OF Tetracera loureiri
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ACYLATED TRITERPENOIDS,FLAVONOIDS,AND LIGNANS ISOLATED FROM THE STEMS OF Tetracera loureiri

机译:酰化的三萜类化合物,黄酮类化合物和从曲酮叶茎中分离的木质素

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摘要

The genus Tetracera(family Dilleniaceae)contains about 50 species with a pantropical distribution,of which 20 occur in the Neotropical area.In traditional folk medicine,some species have been used as febrifuge,diuretic agent,and antijaundice [1].Tetracera species has been reported to exhibit a broad range of pharmacological activities such as antidiabetic,analgesic,anti-inflammatory,antipyrexic,anti-HIV and anti-reverse transcriptase,antihyperglycemic,anti-mycobacterial,antioxidant,anti-ulcerogenic,hepatoprotective,DNA polymerase(3 inhibitory,glucose-uptake modulating,and xanthine oxidase inhibition activity [2-12].Previous phytochemical investigations of members of this genus have resulted in the isolation of several classes of compounds,including flavonoids and terpenoids [9-13].Among them,flavonoids from T.indica induced significant adipogenesis like insulin and enhanced adipogenesis like rosiglitazone [4].Tetraceranoate from stem bark of T.potatoria showed potent anti-mycobacterial activities[11].T loureiri(Finet & Gagnep.)Pierre ex Craib is a woody vine inhabiting evergreen forests in South east Asia,including many parts of Cambodia,Laos,Thailand,and Vietnam.A decoction of its stems with other herbal plants is the traditional Thai medicine used for the alleviation of fatigue and improvement of jaundice [8].There is only one previous report on the pharmacological activity of this plant [12].To our knowledge,there has been no report of a phytochemical investigation of T.loureiri so far.In continuation of our studies on chemical constituents from the stems of T.loureiri,12 compounds were isolated and elucidated as betulinic acid(1),erjthro-carolignan E(2),thгео-carolignan E(3),eucalyptolic acid(4),Зβ-o-trans-feruloyl-2α-hydroxyurs-12-en-28-oic acid(5),3β-O-(trans-p-coumaroyl)maslinic acid(6),jacoumaric acid(7),quercetin(8),europetin(9),kaempferol(10),rhamnetin(11),and rhamnocitrin(12).To the best our knowledge,compounds 2,3,5,7,and 9 were obtained from the genus Tetracera for the first time.Moreover,compounds 4 and 6 has not been reported in the species of T.loureiri.
机译:Tetracera(家族Dilleniaceae)含有大约50种具有腹腔分布的物种,其中20种发生在探访中。在传统的民间医学中,一些物种被用作FeBrifuge,利尿剂和抗磨练[1] .tetracera物种据报道,表现出广泛的药理学活动,如抗糖尿病,镇痛,抗炎,防脂,抗艾滋病毒和抗逆转录酶,抗血糖,抗分枝杆菌,抗氧化剂,抗溃疡性,肝保护剂,DNA聚合酶(3个抑制性,葡萄糖摄取调节和黄嘌呤氧化酶抑制活性[2-12]。该属成员的prvoychemical研究导致分离几种类化合物,包括黄酮类化合物和萜类化合物[9-13] .among它们,黄酮类化合物来自T.indica诱导显着的脂肪发生,如胰岛素和增强的脂肪发生,如罗格列酮[4]。来自T.potatoria的茎树皮的二甲酸酯显示出有效的抗分枝杆菌活动[11。是用于减轻疲劳和改善黄疸的传统泰国医学[8]。此前只有一个关于该植物的药理活性的报告[12]。据我们所知,迄今为止,迄今为止没有报告T.loureii的植物化学调查。继续我们对来自T.Lourei的茎的化学成分的研究,将12种化合物分离并阐明作为桦木酸(1),Erjthro -Carolignan E(2),Thгео-carolignane(3),桉醇酸(4),Зβ-O-反式 - Feruloyl-2α-羟基毒剂-12-烯-28-OIC酸(5),3β-O-( Trans-p-coumaroyl)唾液酸(6),jacoumaric acid酸(7),槲皮素(8),eUropetin(9),kaempferol(10),rhamnetin(11),和rhamnocitrin(12)。至于我们的知识,第一时间从四氧化物属中获得化合物2,3,5,7和9.尚未在T.Lourei的种类中报道化合物4和6。

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    Bio-Center Gyeonggido Business &

    Science Accelerator(GBSA) 16229 Suwon Republic of Korea;

    Bio-Center Gyeonggido Business &

    Science Accelerator(GBSA) 16229 Suwon Republic of Korea;

    Bio-Center Gyeonggido Business &

    Science Accelerator(GBSA) 16229 Suwon Republic of Korea;

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