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Antineoplastic Agents. 585. Isolation of Bridelia ferruginea Anticancer Podophyllotoxins and Synthesis of 4-Aza-podophyllotoxin Structural Modifications.抗肿瘤药物。585. 锈毛算盘子抗癌鬼臼毒素的分离及4-氮杂鬼臼毒素结构修饰的合成。
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Purification and characterization of flavonoids from the leaves of Zanthoxylum bungeanum and correlation between their structure and antioxidant activity.花椒叶中黄酮类化合物的纯化与表征及其结构与抗氧化活性的相关性
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Molecules. 2013 Oct 11;18(10):12633-44. doi: 10.3390/molecules181012633.
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Anti-hyperalgesic activity of corilagin, a tannin isolated from Phyllanthus niruri L. (Euphorbiaceae).鞣花酸(Phyllanthus niruri L.(大戟科)中分离得到的一种单宁)的抗痛觉过敏活性。
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Bridelia ferruginea Produces Antineuroinflammatory Activity through Inhibition of Nuclear Factor-kappa B and p38 MAPK Signalling.密蒙花通过抑制核因子-κB 和 p38 MAPK 信号通路发挥抗神经炎症活性。
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Isolation and structure elucidation of a flavanone, a flavanone glycoside and vomifoliol from Echiochilon fruticosum growing in Tunisia.从突尼斯生长的多枝糙草中分离并鉴定一种黄烷酮、一种黄烷酮糖苷和vomifoliol的结构。
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Complement-Inhibiting Constituents of Bridelia ferruginea Stem Bark.铁锈叶算盘子茎皮的补体抑制成分。
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对生长于尼日利亚的铁锈叶巴豆进行的化学与生物学研究。

Chemical and biological studies on Bridelia ferruginea grown in Nigeria.

作者信息

Afolayan Michael, Srivedavyasasri Radhakrishnan, Asekun Olayinka T, Familoni Oluwole B, Ross Samir A

机构信息

a National Center for Natural Product Research , University of Mississippi , University , MS , USA.

b Department of Chemistry , University of Lagos , Lagos , Nigeria.

出版信息

Nat Prod Res. 2019 Jan;33(2):287-291. doi: 10.1080/14786419.2018.1440225. Epub 2018 Feb 19.

DOI:10.1080/14786419.2018.1440225
PMID:29457749
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6098982/
Abstract

Phytochemical investigation of the methanolic extract of dried leaves of Bridelia ferruginea led to the isolation and identification of fourteen compounds (1-14): compound 1 [mixture of palmitic, stearic and oleic acids], stearyl monoester of 2-O-β-ᴅ-glucosylglycerol (2), 6β-hydroxy-(20R)-24-ethylcholest-4-en-3-one (3a), 6β-hydroxy-(20R)-24-ethylcholest-4,22-dien-3-one (3b), lutein (4), vomifoliol (5), corilagin (6), kaempferide-3-O-β-ᴅ-glucoside (7), myricetin (8), isomericitrin (9), isoquercetin (10), myricitrin (11), quercitrin (12), rutin (13), and β-sitosterol glucoside (14). The total extract exhibited moderate activity towards CB2 receptor and 90% inhibition against leishmanial pathogen Trypanosoma brucei. Compound 4 exhibited 73% displacement in CB2 receptor with IC 56.47 μM, and 93% inhibition towards T. brucei with IC 4.16 μM. Compound 11 showed 99% inhibition towards Escherichia coli with IC 1.123 μM.

摘要

对锈毛算盘子干燥叶的甲醇提取物进行植物化学研究,分离并鉴定出14种化合物(1 - 14):化合物1 [棕榈酸、硬脂酸和油酸的混合物]、2 - O-β -ᴅ-葡萄糖基甘油硬脂单酯(2)、6β - 羟基 - (20R)-24 - 乙基胆甾 - 4 - 烯 - 3 - 酮(3a)、6β - 羟基 - (20R)-24 - 乙基胆甾 - 4,22 - 二烯 - 3 - 酮(3b)、叶黄素(4)、vomifoliol(5)、柯里拉京(6)、山柰酚 - 3 - O-β -ᴅ-葡萄糖苷(7)、杨梅素(8)、异鼠李素(9)、异槲皮苷(10)、杨梅苷(11)、槲皮苷(12)、芦丁(13)和β - 谷甾醇葡萄糖苷(14)。总提取物对CB2受体表现出中等活性,对利什曼原虫病原体布氏锥虫有90%的抑制作用。化合物4在CB2受体中的取代率为73%,IC56.47 μM,对布氏锥虫的抑制率为93%,IC4.16 μM。化合物11对大肠杆菌的抑制率为99%,IC1.123 μM。