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Identification of the Genus Pleione Based on Fingerprinting and Determination of the Content of their Key Components 基于指纹识别及其关键成分含量的 Pleione 属鉴定
IF 1.9 4区 生物学 Q3 CHEMISTRY, APPLIED Pub Date : 2023-12-17 DOI: 10.25135/rnp.422.2308.2878
Lin Ni, Lijun Zheng, Jiarui Fu, Shilin Liu, Lin Chen, Shasha Wu, Xiaoqian Wu, Wenqiang Yan
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引用次数: 0
Chemical Composition, Antibacterial, Synergistic Antibacterial and Cytotoxic Properties of the Essential Oil from Gelsemium elegans (Gardner & Champ.) Benth. Gelsemium elegans (Gardner & Champ.) Benth.精油的化学成分、抗菌、协同抗菌和细胞毒性特性
IF 1.9 4区 生物学 Q3 CHEMISTRY, APPLIED Pub Date : 2023-12-17 DOI: 10.25135/rnp.417.2308.2872
Xiang Xing, Youyi Tang, Xinyu Hu, Fan Xu
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引用次数: 0
Comparative Anti-dengue Activities of Ethanolic and Supercritical Extracts of Lippia origanoides Kunth: in-vitro and in-silico Analyses 牛肝草乙醇提取物和超临界提取物抗登革热活性的体外和计算机分析
IF 1.9 4区 生物学 Q3 CHEMISTRY, APPLIED Pub Date : 2023-08-22 DOI: 10.25135/rnp.401.2303.2720
Elizabeth Quintero-Rueda, S. A. Velandia, R. Ocazionez, E. Stashenko, P. Rondón-Villarreal
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引用次数: 0
Phytochemical and Pharmacological Studies of Natural Saponins from Platycodon grandiflorum 桔梗天然皂苷的植物化学和药理研究
4区 生物学 Q3 CHEMISTRY, APPLIED Pub Date : 2023-08-15 DOI: 10.25135/rnp.409.2201.2328
Kuo Xu, Xinying Du, Runxiang Zhai, Huijiao Li, Xianjun Fu
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引用次数: 0
Callignan A, A New Neolignan from the Leaves of Callicarpa kwangtungensis 广东紫珠叶中新木脂素Callignan A
IF 1.9 4区 生物学 Q3 CHEMISTRY, APPLIED Pub Date : 2023-08-15 DOI: 10.25135/rnp.408.2307.2832
Hancheng Ren, Weiqiang Fei
: In the current study, a new lignan ( 1 ), named callignan, as well as two known ones ( 2 and 3 ), were obtained from the EtOAc extract of the leaves of Callicarpa kwangtungensis . The structure elucidation of 1 was conducted by detailed interpretation of the 1D and 2D NMR spectroscopic data. Optical rotation of compound 1 and ECD data revealed that the compound was a racemic compound. Compounds 1 − 3 showed moderate effects with IC 50 values of 46, 29, and 42  M on NO production in LPS-induced RAW 264.7 cell inflammation model.
本研究从光通珠兰(Callicarpa kwangtungensis)叶的乙酸乙酯提取物中分离得到一种新的木脂素(1)和两种已知的木脂素(2和3)。通过详细解释一维和二维核磁共振波谱数据,对1的结构进行了解析。化合物1的旋光性和ECD数据表明该化合物为外消旋化合物。化合物1−3的IC 50值为46、29和42M时,对lps诱导的RAW 264.7细胞炎症模型的NO生成有中等影响。
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引用次数: 0
Penioctadecatrienoic A: A New Polyketide from Endophytic Fungus Penicillium pinophilum J70 penioctadectrienoic A:来自内生真菌青霉J70的新聚酮
IF 1.9 4区 生物学 Q3 CHEMISTRY, APPLIED Pub Date : 2023-08-03 DOI: 10.25135/rnp.397.2304.2752
Siwen Niu, Juan Wang, Jianlin He, Xin Liu, Bi-hong Hong, Miao-Ling Yu
: Chemical examination of the rice solid fermented cultures of the fungus Penicillium pinophilum J70 isolated from the fresh leaves of Hypericum japonicum Thumb led to the isolation of one new polyketide, namely penioctadecatrienoic A ( 1 ), together with two known compounds ( 2 and 3 ). The structure of the new metabolite 1 was resolved on the basis of extensive spectroscopic analysis (NMR and HRESIMS data), in association with the modified Mosher's method for the absolute configurational assignment. All isolated metabolites were evaluated for their cytotoxic activity against ECA-109, the anti-inflammatory activity against NO production in lipopolysaccharides (LPS) stimulated RAW264.7 cells, and the antibacterial activity on Staphylococcus aureus ATCC 29213. As a result, compounds 1‒3 showed moderately anti-inflammatory effects with the inhibitory rates ranging from 44.5% to 60.7% at the concentration of 20 μ M. In addition, compound 1 exhibited weakly antibacterial effect with an MIC value of 32 µ g/mL.
:对从日本金丝桃鲜叶中分离出的真菌Penicillium pinophilum J70的大米固体发酵培养物进行化学检查,分离出一种新的聚酮,即青霉烯十碳三烯酸A(1),以及两种已知的化合物(2和3)。新代谢物1的结构是在广泛的光谱分析(NMR和HRESIMS数据)的基础上,结合用于绝对构型分配的改良Mosher方法来解析的。评估所有分离的代谢物对ECA-109的细胞毒性活性、对脂多糖(LPS)刺激的RAW264.7细胞中NO产生的抗炎活性以及对金黄色葡萄球菌ATCC 29213的抗菌活性。结果,化合物1-3在20μM浓度下表现出中等的抗炎作用,抑制率在44.5%-60.7%之间。此外,化合物1表现出较弱的抗菌作用,MIC值为32µg/mL。
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引用次数: 0
Essential Oil Constituent, Antimicrobial Activity, and Mosquito Larvicidal Activity of Murraya glabra (Guillaumin) Swingle from Vietnam 越南大叶木纹(Guillaumin)挥发油成分、抗菌活性和杀蚊活性
IF 1.9 4区 生物学 Q3 CHEMISTRY, APPLIED Pub Date : 2023-07-27 DOI: 10.25135/rnp.406.2305.2779
I. Ogunwande, D. Dai, L. T. Huong, N. C. Trường, V. T. Dung, T. Q. Ngan, Nguyen Dinh Tuong
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引用次数: 0
Chemical Composition of Different Parts of the Vitex agnus-castus L. Essential Oils and Their In-Vitro Cytotoxic Activities 牡荆不同部位精油化学成分及体外细胞毒活性研究
IF 1.9 4区 生物学 Q3 CHEMISTRY, APPLIED Pub Date : 2023-07-13 DOI: 10.25135/rnp.404.2304.2761
Ebrar Inal, Ebru ÖZDEMİR NATH, Mahmoud Abudayyak, Şeyma Ulusoy, Hatice Akbal İnan, M. Çiçek, M. Kartal
: The essential oil (EO) compositions and chemotypes of the important ethnomedicinal plant Vitex agnus-castus L. flowers, leaves, and fruits collected from Türkiye (Balıkesir and İstanbul) were identified in the present study. Different parts of the V. agnus-castus EO’s in-vitro cytotoxic effects on the MCF-7 (human breast adenocarcinoma) and A549 (human lung carcinoma) human-origin cell lines were anaylzed in the current study. The composition of hydrodistiled EOs extracted from flowers, leaves, and fruits of V. agnus-castus were analyzed by GC–FID/MS. Monoterpene hydrocarbons and oxygenated monoterpene compounds were detected as the predominant component class of the V. agnus-castus . EOs extracted from Balıkesir region were defined as the “ α - pinene-1,8-cineole” chemotype, while EOs extracted from İstanbul region were defined as the “sabinene-1,8-cineole” chemotype. Sesquiterpene hydrocarbons constituted more than 20% of the compounds in the EOs extracted from the flowers. To the best of our knowledge, this study is the first to analyze the in-vitro cytotoxic effects of flowers. This study is also the first to show the in-vitro cytotoxic effects of fruit, the most commonly used part of the plant, EO on the MCF-7 cell line. Balıkesir region’s EOs were observed as more potent -especially the purple flower’s IC 50 is about 4.68 µg/mL on the MCF7 cell line-than İstanbul regions, which might be attributed to the higher amount of α -pinene, caryophyllene, and limonene content. Our results indicated that the V. agnus-castus EOs, which contain α -pinene, 1,8-cineole, caryophyllene, and limonene as major components, showed relatively high cytotoxic effects compared to the control groups on the MCF7 and A549 cell lines.
本研究对采自 rkiye (Balıkesir和İstanbul)的重要民族药用植物牡荆(Vitex agnus-castus L.)花、叶和果的精油成分和化学型进行了鉴定。本研究分析了V. agnus-castus EO不同部位对MCF-7(人乳腺腺癌)和A549(人肺癌)人源细胞系的体外细胞毒作用。采用气相色谱- fid /MS分析了仙人掌花、叶和果实中乙醇提取物的成分。单萜烃和氧合单萜化合物是蓖麻的主要成分。从Balıkesir区域提取的EOs定义为“α -蒎烯-1,8-桉叶油脑”化学型,从İstanbul区域提取的EOs定义为“sabinene-1,8-桉叶油脑”化学型。倍半萜化合物占从花中提取的EOs化合物的20%以上。据我们所知,这项研究是第一次分析花的体外细胞毒性作用。这项研究也首次证明了果实(植物最常用的部分)EO对MCF-7细胞系的体外细胞毒性作用。在MCF7细胞系上,与İstanbul区域相比,Balıkesir区域的EOs更有效,特别是紫色花的ic50约为4.68µg/mL,这可能是由于α -蒎烯、石竹烯和柠檬烯含量较高。结果表明,与对照组相比,以α -蒎烯、1,8-桉树油脑、石竹烯和柠檬烯为主要成分的银杏叶提取物对MCF7和A549细胞株具有较高的细胞毒作用。
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引用次数: 1
Nocardiopyrone C, a New Antimicrobial Pyran-2-one Derivative from a Marine-derived Actinomycete Strain Nocardiopsis aegyptia ZSN1 Nocardiopyrone C:一种新型埃及诺卡芽孢杆菌ZSN1的抗菌Pyran-2-one衍生物
IF 1.9 4区 生物学 Q3 CHEMISTRY, APPLIED Pub Date : 2023-07-11 DOI: 10.25135/rnp.405.2304.2763
Jiang Yongjun, Zi-jun Chen, Yuhong Tian, Mingzhu Ma
: A new pyran-2-one derivative, Nocardiopyrone C ( 1 ), and three known compounds, Nocardiopyrone B ( 2 ), 1-hydroxy-4-methoxy-2-naphthoic acid ( 3 ), and 2-(aminocarbonyl)-phenylcarbamate ( 4 ) were identified from the marine-derived Nocardiopsis aegyptia ZSN1. The chemical structure of the novel compound ( 1 ) was ascertained as (7 R )-5-(methoxymethyl)-3-methyl-6-(pentan-2-yl)-2 H -pyran-2-one using HRESIMS data, spectroscopic data, and ECD calculations. All four isolated compounds displayed antimicrobial activity, with the new compound 1 having the same MIC value of 50.0 µ M against E. coli , S. aureus , and C. albicans .
从海洋来源的埃及诺卡opsis aegyptia ZSN1中鉴定出新的吡喃-2- 1衍生物Nocardiopyrone C(1)和三个已知化合物Nocardiopyrone B(2)、1-羟基-4-甲氧基-2-萘酸(3)和2-(氨基羰基)-苯氨基甲酸酯(4)。新化合物(1)的化学结构为(7r)-5-(甲氧基甲基)-3-甲基-6-(戊烷-2-基)-2 H -吡喃-2- 1。4个化合物均具有抗菌活性,其中新化合物1对大肠杆菌、金黄色葡萄球菌和白色念珠菌的MIC值相同,均为50.0µM。
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引用次数: 0
Traditional Use, Pharmacology and Toxicology of the Lignans in Genus Kadsura: A Systematic Review 桂皮属木质素的传统用途、药理学和毒理学:系统综述
IF 1.9 4区 生物学 Q3 CHEMISTRY, APPLIED Pub Date : 2023-07-07 DOI: 10.25135/rnp.403.2304.2765
Dongdong Zhang, Haonan Xu, Wei Wang, Xinzhu Li, Yu-ze Li, Yi Jiang, Xiaomei Song, Chong Deng
The genus Kadsura is an important part of traditional Chinese medicine, it has the functions of promoting wind, eliminating dampness, activating blood circulation. Modern pharmacological studies have shown that lignans are one of the main components to possess these medicinal effects. This review aimed to provide a systematic summary on the traditional use, phytochemistry, pharmacology, toxicology and other aspects of lignans in genus Kadsura. In this paper, we collected the relevant literature on Kadsura lignans from 1973 to the present, and isolated more than 337 lignans from this genus, including dibenzocyclooctadienes, aryltetralins, tetrahydrofurans, diarylbutanes, 7,8-secolignans, bisepoxylignans, neolignans, seco-dibenzocyclooctadienes, sesquilignan and coumarin-containing lignan. Previous pharmacological studies have shown that lignans of the genus Kadsura have antitumor, anti-inflammatory, antibacterial, anti-HIV, anti-platelet aggregation, immunomodulatory and antioxidant effects. In clinical practice, it is commonly used to treat Alzheimer's disease, inflammation and insomnia. Kadsura is an important part of the field of Chinese medicine and is widely used in traditional medicine. However, further clarification of its active ingredients and mechanism of action and the establishment of a complete quality standard system are needed in order to provide a scientific basis for in-depth studies of this genus.
桂皮属植物是中药的重要组成部分,具有生风、祛湿、活血的作用。现代药理学研究表明,木脂素是具有这些药理作用的主要成分之一。本综述旨在对桂皮属木脂素的传统用途、植物化学、药理学、毒理学等方面进行系统综述。本文收集了1973年至今关于桂树木脂素的相关文献,从该属植物中分离出337多种木脂素,包括二苯并环辛二烯类、芳基四氢萘类、四氢呋喃类、二芳基丁烷类、7,8-二芳基木脂素类、双环氧木脂素、新木脂素属、仲二苯并环辛二烯类,倍半木脂素和香豆素类木脂素。先前的药理学研究表明,桂皮属木脂素具有抗肿瘤、抗炎、抗菌、抗HIV、抗血小板聚集、免疫调节和抗氧化作用。在临床实践中,它通常用于治疗阿尔茨海默病、炎症和失眠。桂皮是中医领域的重要组成部分,在传统医学中有着广泛的应用。然而,还需要进一步阐明其活性成分和作用机制,建立完整的质量标准体系,为深入研究该属植物提供科学依据。
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Records of Natural Products
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