31 results on '"Aesculus chinensis"'
Search Results
2. The complete chloroplast genome of Aesculus chinensis var. wilsonii
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Yuxin Zhou, Guohua Zheng, Jingjing Zhang, Zhigang Hu, Zhige Liu, Yifei Liu, and Zhaohua Shi
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0106 biological sciences ,0301 basic medicine ,biology ,Aesculus chinensis ,phylogeny ,biology.organism_classification ,010603 evolutionary biology ,01 natural sciences ,Genome ,Chloroplast ,03 medical and health sciences ,030104 developmental biology ,Phylogenetics ,Botany ,Genetics ,chloroplast genome ,Molecular Biology ,Mitogenome Announcement ,Aesculus chinensis var. wilsonii ,Research Article - Abstract
In this study, we sequenced the complete chloroplast (cp) genome of Aesculus chinensis Bunge var. wilsonii (Rehder) Turland & N. H. Xia and compared it with cp genomes of congeneric species. The cp genome of A. chinensis var. wilsonii is a circular molecule, 156,211 bp in length, with typical quadripartite structure. It has one large single copy (LSC) region of 85,211 bp and one small single copy (SSC) region of 18,124 bp that are separated by two inverted repeat regions (IR) of 26,438 bp. The cp genome encodes 133 genes comprising 85 protein-coding genes, 40 tRNA genes, and eight rRNA ribosomal genes. The overall GC content of the cp genome of A. chinensis var. wilsonii is 37.93%. We conducted amaximum likelihood phylogenetic analysis, which revealed that A. chinensis var. wilsonii is sister to A. wangii and has a close relationship with Acer L. (maples). We expect that the cp genome of A. chinensis var. wilsonii will be useful for DNA barcoding and species delimitation for this species as well as future studies on the conservation, taxonomy, and evolutionary relationships of Aesculus L.
- Published
- 2020
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3. Phenylethanol glycosides from the seeds of Aesculus chinensis var. chekiangensis
- Author
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Di Liu, Feng Qiu, Nan Zhang, Shuxiang Wei, Liqin Ding, Xinchi Feng, Kai Wang, and Shijie Cao
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chemistry.chemical_classification ,biology ,010405 organic chemistry ,Stereochemistry ,Aesculus chinensis ,Glycoside ,Moderate activity ,General Chemistry ,Aesculus chinensis Bge. var. chekiangensis (Hu et Fang) Fang ,010402 general chemistry ,biology.organism_classification ,01 natural sciences ,0104 chemical sciences ,Aesculus ,lcsh:Chemistry ,Phenylethanol glycosides ,Neuroprotective activity ,lcsh:QD1-999 ,chemistry - Abstract
Three new phenylethanol glycosides (1-3) and one known analogue (4) were isolated from the seeds of Aesculus chinensis Bge. var. chekiangensis. To the best of our knowledge, this represents the first isolation of phenylethanol glycosides from the genus of Aesculus, which enriched its chemical composition. Structure elucidations were performed via extensive NMR and HRESIMS data together with comparison with literature data. Thereafter, the isolated compounds were assayed for their neuroprotective activities against CoCl2-induced cytotoxicity in PC12 cells and compound 3 exhibited moderate activity. "Image missing"
- Published
- 2020
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4. Pyrolysis of Aesculus chinensis Bunge Seed with Fe2O3/NiO as nanocatalysts for the production of bio-oil material
- Author
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Yafeng Yang, Nyuk Ling Ma, Wanxi Peng, Yiyang Li, Sabry M. Shaheen, Jörg Rinklebe, Xiangmeng Chen, and Muhammad Aqeel Ashraf
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021110 strategic, defence & security studies ,Environmental Engineering ,biology ,Health, Toxicology and Mutagenesis ,Aesculus chinensis ,0211 other engineering and technologies ,Biomass ,Environmental pollution ,02 engineering and technology ,010501 environmental sciences ,Raw material ,Furfural ,biology.organism_classification ,Fluid catalytic cracking ,Pulp and paper industry ,01 natural sciences ,Pollution ,Nanomaterial-based catalyst ,chemistry.chemical_compound ,chemistry ,Environmental Chemistry ,Waste Management and Disposal ,Pyrolysis ,0105 earth and related environmental sciences - Abstract
The rapid thermal cracking technology of biomass can convert biomass into bio-oil and is beneficial for industrial applications. Agricultural and forestry wastes are important parts of China's energy, and their high-grade utilization is useful to solve the problem of energy shortages and environmental pollution. To the best of our knowledge, the impact of nanocatalysts on converting biowastes for bio-oil has not been studied. Consequently, we examined the production of bio-oil by pyrolysis of Aesculus chinensis Bunge Seed (ACBS) using nanocatalysts (Fe2O3 and NiO catalysts) for the first time. The pyrolysis products of ACBS include 1-hydroxy-2-propanone (3.97%), acetic acid (5.42%), and furfural (0.66%). These chemical components can be recovered for use as chemical feedstock in the form of bio-oil, thus indicating the potential of ACBS as a feedstock to be converted by pyrolysis to produce value-added bio-oil. The Fe2O3 and NiO catalysts enhanced the pyrolysis process, which accelerated the precipitation of gaseous products. The pyrolysis rates of the samples gradually increased at DTGmax, effectively promoting the catalytic cracking of ACBS, which is beneficial to the development and utilization of ACBS to produce high valorization products. Combining ACBS and nanocatalysts can change the development direction of high valorization agricultural and forestry wastes in the future.
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- 2021
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5. Triterpenoid Saponins from the Seeds of Aesculus chinensis and Their Cytotoxicities
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Meng-Jiao Jiao, Jun Zhang, An Liu, Sha Chen, Wen-Jin Cui, Shu-Hui Wang, Chang Chen, Jin-Tang Cheng, Cong Guo, Shi-Tao Chen, and Zhe Deng
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0301 basic medicine ,Aesculus chinensis ,Pharmacology toxicology ,Plant Science ,Toxicology ,Biochemistry ,Anti-tumor activity ,Analytical Chemistry ,Triterpenoid saponins ,03 medical and health sciences ,0302 clinical medicine ,Triterpenoid ,lcsh:Botany ,Ic50 values ,MTT assay ,Pharmacology ,biology ,Traditional medicine ,Chemistry ,Organic Chemistry ,biology.organism_classification ,lcsh:QK1-989 ,Chemical structures ,030104 developmental biology ,030220 oncology & carcinogenesis ,Plant biochemistry ,Original Article ,Food Science - Abstract
Six new triterpenoid saponins, aesculusosides A–F (1–6), together with 19 known ones, were isolated from the seeds of Aesculus chinensis. The new structures were elucidated through extensive spectroscopic analyses and by comparison with previously reported data. Some of the isolates were evaluated for their cytotoxic activities against MCF-7 cell line by an MTT assay, and compounds 15, 16, 19, and 23–25 exhibited inhibitory activities against MCF-7 with IC50 values ranging from 7.1 to 31.3 μM. Graphical Abstract Electronic supplementary material The online version of this article (10.1007/s13659-017-0148-4) contains supplementary material, which is available to authorized users.
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- 2017
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6. Bioactive Triterpenoid Saponins From the Seeds of Aesculus chinensis Bge. var. chekiangensis
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Nan Zhang, Shuxiang Wei, Shijie Cao, Qiang Zhang, Ning Kang, Liqin Ding, and Feng Qiu
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Phytochemistry ,Aesculus chinensis ,Moderate activity ,02 engineering and technology ,010402 general chemistry ,01 natural sciences ,lcsh:Chemistry ,triterpenoid saponins ,Triterpenoid ,Original Research ,cytotoxic activities ,neuroprotective activities ,Traditional medicine ,biology ,Chemistry ,Absolute configuration ,General Chemistry ,Aesculus chinensis Bge. var. chekiangensis (Hu et Fang) Fang ,021001 nanoscience & nanotechnology ,biology.organism_classification ,0104 chemical sciences ,Aesculus ,Hep G2 ,lcsh:QD1-999 ,Phytochemical ,phytochemistry ,0210 nano-technology - Abstract
Phytochemical investigation of Aesculus chinensis Bge. var. chekiangensis (Hu et Fang) Fang obtained 33 triterpenoid saponins, including 14 new ones, aesculiside C–P (1–14). The structure elucidations were performed through comprehensive MS, 1D and 2D-NMR analysis, and their absolute configuration was unambiguously determined by X-ray diffraction analysis as well as Mo2(OAc)4-induced ECD method for the first time. All the substances were examined for their cytotoxic activities against three tumor cell lines, Hep G2, HCT-116, and MGC-803. Of these, compounds 8, 9, 14–16, 18, and 22 exhibited potent cytotoxicities against all cell lines with IC50 of 2–21 μM, while compounds 3, 6, 7, 17–19, 20, 24, and 28 depicted moderate activity (IC50 13 to >40 μM). On these bases, the preliminary structure-activity correlations were also discussed. Meanwhile the neuroprotective properties of triterpenoid saponins from Aesculus genus were evaluated for the first time. Among them, compounds 1, 4, 12, 20, 22, 25, 29, and 31 exhibited moderate activities against COCl2-induced PC12 cell injury.
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- 2020
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7. New Indole Glycosides from Aesculus chinensis var. chekiangensis and Their Neuroprotective Activities
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Nan Zhang, Weixing Huang, Shijie Cao, Feng Qiu, Ning Kang, Liqin Ding, and Pan Li
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Aesculus chinensis ,Pharmaceutical Science ,01 natural sciences ,Neuroprotection ,neuroprotective activity ,Analytical Chemistry ,lcsh:QD241-441 ,03 medical and health sciences ,0302 clinical medicine ,N-glucosylated indoles ,lcsh:Organic chemistry ,Drug Discovery ,Physical and Theoretical Chemistry ,Indole test ,chemistry.chemical_classification ,Aesculus chinensis Bge. var. chekiangensis (Hu et Fang) Fang ,biology ,Traditional medicine ,010405 organic chemistry ,Organic Chemistry ,Glycoside ,biology.organism_classification ,0104 chemical sciences ,Aesculus ,Human tumor ,chemistry ,Chemistry (miscellaneous) ,030220 oncology & carcinogenesis ,Molecular Medicine - Abstract
The dried seeds of Aesculus chinensis Bge. var. chekiangensis (Hu et Fang) Fang, called &ldquo, Suo Luo Zi&rdquo, have been used in traditional Chinese medicine. Nevertheless, most studies have been focused on components of less polarity fractions. In this research, twelve indoles, including six new indole glycosides (1&ndash, 6) as well as six known analogs were isolated from the polar portion which has been seldom studied. This is the first description of N-glucosylated indoles obtained from the genus of Aesculus. Structures of the new compounds (1&ndash, 6) were elucidated based on comprehensive interpretation of HRESIMS, 1D and 2D NMR. Additionally, the neuroprotective activities of the N-glucosylated indoles were evaluated for the first time indicating that compounds 1&ndash, 5 and 9&ndash, 10 exhibited moderate neuroprotective activities. Further cytotoxicity tests of isolates 1&ndash, 10 on three human tumor cell lines suggested that none of these compounds were cytotoxic (IC50 >, 50 &mu, M).
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- 2019
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8. A new leaf-mining moth, Caloptilia aesculi, sp. nov. (Lepidoptera: Gracillariidae: Gracillariinae) feeding on Aesculus chinensis Bunge (Hippocastanaceae) from China
- Author
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Guo-Hua Huang, Issei Ohshima, and Cheng-Qing Liao
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Male ,Microlepidoptera ,China ,biology ,Aesculus chinensis ,Leaf miner ,Aesculus ,Hippocastanaceae ,Moths ,biology.organism_classification ,DNA barcoding ,Pupa ,Lepidoptera genitalia ,Lepidoptera ,Botany ,Animals ,Animal Science and Zoology ,Female ,Gracillariidae ,Ecology, Evolution, Behavior and Systematics ,Phylogeny - Abstract
A new species of the genus Caloptilia associating with the Chinese horse chestnut, Aesculus chinensis Bunge (Hippocastanaceae) from China is described. The photographs of the adults, male and female genitalia, larva and pupa, the leaf mines and leaf shelters (rolls and stacks) are given. This is the first report of host association with Hippocastanaceae in the subfamily Gracillariinae. The sequence of mitochondrial COI barcoding region of this species is provided and its phylogenetic position is analyzed with other Caloptilia species.
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- 2019
9. First Report of Leaf Blotch of Aesculus chinensis Caused by Colletotrichum gloeosporioides and Colletotrichum fructicola in China
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Yuan-Zhi Si, Li-Hua Zhu, Jian-Wei Sun, Guan-Qun Jin, and De-Wei Li
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Horticulture ,Colletotrichum fructicola ,biology ,Colletotrichum gloeosporioides ,New disease ,Aesculus chinensis ,Coelomycetes ,Plant Science ,biology.organism_classification ,Agronomy and Crop Science - Published
- 2020
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10. How dynamic growth of avenue trees affects particulate matter dispersion: CFD simulations in street canyons
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Xue Cui, Hongqiao Qin, Boze Huang, Bo Hong, and Ting Zhang
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Canyon ,geography ,geography.geographical_feature_category ,biology ,Renewable Energy, Sustainability and the Environment ,Geography, Planning and Development ,Aesculus chinensis ,Crown (botany) ,0211 other engineering and technologies ,Transportation ,02 engineering and technology ,010501 environmental sciences ,Particulates ,biology.organism_classification ,Atmospheric sciences ,01 natural sciences ,Cedrus ,Liriodendron chinense ,Acer buergerianum ,Environmental science ,021108 energy ,Leaf area index ,0105 earth and related environmental sciences ,Civil and Structural Engineering - Abstract
This study combined parameterized tree growth model, Reynolds Averaged Navier–Stokes model and revised generalized drift flux model to investigate the effect of dynamic growth of avenue trees on atmospheric particulate pollution dispersion in street canyons. We tested conditions with three street canyon aspect ratios (H/W = 0.45, 0.9 and 1.8) and five common avenue tree species (Gingko biloba, Aesculus chinensis, Acer buergerianum, Liriodendron chinense and Cedrus deodar). Results demonstrated that: 1) Avenue tree age was strongly correlated with their height and crown diameter (R2 ≥ 0.71). 2) PM reduction ratio increased significantly as tree age increased. G. biloba was the most effective at removing the pedestrian-level PM10, while L. chinenses has the greatest capacity to reduce pedestrian-level PM2.5. 3) Pedestrian-level PM on the windward street-side was positively related to H/W ratios. Maximum PM was measured on the leeward street-side at H/W = 0.9. 4) Tree height, crown diameter and crown volume in the street canyons were the primary factors affecting the pedestrian-level PM reduction ratio, while leaf area index and crown base height had less influence. Our results could provide guidelines for selecting avenue trees within street canyons and appropriate biometric characteristics during different plant stages to enhance urban sustainability.
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- 2020
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11. The complete chloroplast genome sequence of Aesculus Chinensis Bunge, a major street tree
- Author
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Xin-Rui Wang, Dong-Xu Zhang, Jiu-Heng Xu, Qing Wang, Qiu-Hong Xiang, Wenbin Guan, and Kuo Sun
- Subjects
0106 biological sciences ,0301 basic medicine ,Whole genome sequencing ,biology ,Aesculus chinensis ,Sapindaceae ,biology.organism_classification ,010603 evolutionary biology ,01 natural sciences ,Genome ,Aesculus ,Chloroplast ,03 medical and health sciences ,030104 developmental biology ,Phylogenetics ,Street tree ,Botany ,Genetics ,Molecular Biology - Abstract
Aesculus chinensis Bunge was widely cultivated as a street tree. The complete chloroplast genome of A. chinensis, a plant species with edible seeds in family Sapindaceae, was generated in this stud...
- Published
- 2019
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12. Leaf traits influencing oviposition preference and larval performance ofCameraria ohridellaon native and novel host plants
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Lilla D’Costa, Julia Koricheva, Monique S. J. Simmonds, Nigel Straw, Bastien Castagneyrol, Royal Holloway [University of London] (RHUL), Royal Botanic Gardens, Forest Research [Great Britain], Biodiversité, Gènes & Communautés (BioGeCo), Institut National de la Recherche Agronomique (INRA)-Université de Bordeaux (UB), and School of Biological Sciences
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0106 biological sciences ,Aesculus hippocastanum ,Host (biology) ,Aesculus turbinata ,fungi ,Aesculus chinensis ,food and beverages ,Leaf miner ,Biology ,biology.organism_classification ,010603 evolutionary biology ,01 natural sciences ,Aesculus ,leaf miner ,plant traits ,preference-performance relationship ,principal component analysis ,Lepidoptera ,Gracillariidae ,Sapindaceae ,010602 entomology ,Aesculus indica ,Insect Science ,Botany ,[SDE.BE]Environmental Sciences/Biodiversity and Ecology ,Ecology, Evolution, Behavior and Systematics - Abstract
International audience; Leaf traits are known to influence the preference and performance of phytophagous insects. Traits that influence oviposition can differ from traits that favour larval development, but in native hosts the association between traits usually leads to positive preference-performance relationships. However, when herbivores interact with novel hosts, traits that influence oviposition and successful larval development can become decoupled, leading to poor preference-performance relationships. We investigated traits associated with preference and performance of the horse-chestnut leaf miner, Cameraria ohridella Deschka & Dimic (Lepidoptera: Gracillariidae), on its native host, Aesculus hippocastanum L. (Sapindaceae), and on other species of Aesculus that are novel hosts for the leaf miner. Cameraria ohridella laid eggs on all species of Aesculus, but showed preferences for A. hippocastanum and the phylogenetically closely related Japanese horse-chestnut, Aesculus turbinata Blume. Successful mine development, however, was observed only on A. hippocastanum and A. turbinata, which indicates a partial mismatch between female oviposition and larval performance. The two susceptible Aesculus species were very similar in their leaf traits, which might explain why larvae performed equally well on these species. In contrast, species resistant to C. ohridella [Aesculus chinensis Bunge, Aesculus indica (Camb) Hook, and Aesculus flava Aiton] showed considerable variation in leaf traits, which suggests that different species of Aesculus might have different mechanisms of resistance to C. ohridella, supporting the idea of different defensive syndromes in different species of plants.
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- 2014
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13. First Report of Powdery Mildew Caused by Sawadaea aesculi on Aesculus chinensis in China
- Author
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G. Cai, A. Jiang, J. Gong, Z. Ke, F. Zhang, and X. Zhou
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Horticulture ,biology ,Aesculus chinensis ,Plant Science ,Sawadaea ,biology.organism_classification ,Agronomy and Crop Science ,Powdery mildew - Published
- 2019
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14. Combining Gas Exchange and Chlorophyll Fluorescence to Assess the Adaptability of Medicinal Plant Aesculus chinensis Compared to Two Imported Aesculus Species
- Author
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Jia Sen Wu, Fu Qiang Song, Xiangshi Kong, Hai Yan Fu, and Dan Dan Qi
- Subjects
Horticulture ,Quenching (fluorescence) ,biology ,Compensation point ,Chemistry ,Aesculus chinensis ,General Engineering ,biology.organism_classification ,Photosynthesis ,Chlorophyll fluorescence ,Photosynthetic capacity ,Tree species ,Aesculus - Abstract
Analysis of gas exchange and determination of chlorophyll fluorescence parameters in leaves of three tree species including Aesculus chinensis, A. octandra and A. hybrida were conducted under field conditions and then comparison was carried out. The results showed that the light compensation point (LCP) was significantly different among the three tree species, of which the LCP of A. chinensis with 12.53 μmol·m-2·s-1 that of the lowest was notable lower than that of the other two species (36.11 and 46.41 μmol·m-2·s-1respectively). On the other hand, the light saturation point (LSP) of the three tree species also showed remarked different and the LSP of A. chinensis was 1475 μmol·m-2·s-1 which was dramatic higher than that of the other two species respective to 1366.67 and 1025 μmol·m-2·s-1. Beside, the maximum net photosynthetic rate (MNPR) was different too, MNPR of A. chinensis was 9.47μmol CO 2·m-2·s-1which was higher than the other two species (5.91 and 2.30 μmol CO 2·m-2·s-1 respectively), indicating A. chinensis had a higher photosynthetic capacity and stronger utilization ability for light energy. Moreover, the electron transport rate (ETR) of A. chinensis was higher than A. octandra and A. hybrida, the ETR of the former was 55.800 that were 1.33 and 1.44 times of the later two respectively. Quantum yield of PSII photochemistry (ФPSII) in A. chinensis was higher than A. octandra and A. hybrida, the ФPSII of the former was 0.470 that were 1.21 and 1.15 times of the later two respectively. Furthermore, the photochemical quenching (qP) of A. chinensis was 0.975 much higher than A. octandra and A. hybrida respective to 1.10 and 1.10 times of the later two respectively. These three photochemical parameters with dramatic different among the three different tree species suggested A. chinensis had a high activity of electron transport and conversion efficiency for light energy.
- Published
- 2013
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15. Morphological and biochemical changes of Aesculus chinensis seeds in the process of maturation
- Author
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Fangyuan Yu and Shufen Chen
- Subjects
Sucrose ,biology ,fungi ,Aesculus chinensis ,food and beverages ,Forestry ,biology.organism_classification ,Trehalose ,Stachyose ,Desiccation tolerance ,Horticulture ,chemistry.chemical_compound ,chemistry ,Botany ,Dormancy ,Raffinose ,Sugar - Abstract
Morphological and biochemical changes of Chinese horse chestnut (Aesculus chinensis Bge.) seeds were studied during the process of maturation. Fruit and seed diameter increased linearly from DPA (Days Post Anthesis) 60 to DPA 150 and were stable thereafter. The weight of fruit and seed increased sigmoidally between DPA 100 and DPA 160. The water contents of whole seeds, axes and cotyledons had a sharp reduction from DPA 110 to DPA 130 but changed little after DPA 130. The water contents of whole seeds, axes and cotyledons were 1.42, 1.93 and 1.30 g g−1DW, respectively at the end of maturation. The starch content of cotyledons from mature seeds was high on a dry weight basis (31.4%) while the total soluble sugar content varied between 12 and 20%. In both axes and cotyledons, the total soluble sugar content decreased during the process of maturation, as did all five soluble sugar components measured (glucose, sucrose, trehalose, raffinose and stachyose). Sucrose and stachyose contents remained relatively high at the time of seed maturation, followed by glucose and a trace level of trehalose. The oligosaccharide/disaccharide (O/D) ratio in the axes was 3.1 at DPA 140. The high level of sucrose and stachyose might contribute to the greater desiccation tolerance of Aesculus chinensis seeds relative to typical recalcitrant tropical seeds. High levels of ABA content in seed coats and a low GA3/ABA ratio in both seed coats and axes might also influence the desiccation tolerance and shallow dormancy of mature Aesculus chinensis seeds.
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- 2011
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16. Molecules and functions of aesculus chinensis bunge bark volatiles
- Author
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Zuming Li
- Subjects
biology ,Vanillin ,Aesculus chinensis ,Maltol ,02 engineering and technology ,010501 environmental sciences ,021001 nanoscience & nanotechnology ,biology.organism_classification ,Furfural ,01 natural sciences ,Applied Microbiology and Biotechnology ,Aesculus ,chemistry.chemical_compound ,chemistry ,visual_art ,Scopoletin ,visual_art.visual_art_medium ,Animal Science and Zoology ,Bark ,Phenols ,Food science ,0210 nano-technology ,Agronomy and Crop Science ,0105 earth and related environmental sciences ,Food Science - Abstract
This paper analyzes the organic solvent extracts of Aesculus chinensis Bunge Bark using TG and Py-GC-MS. The pyrolysis products were analyzed by GC-MS. The results showed that the extracts of Aesculus chinensis Bunge Bark contain a large number of biologically active components, including hydrocarbons, acids, ethers, alcohols, and phenols. The main components in the extract of Aesculus chinensis Bunge Bark are healthy and abundant; the main representatives of the active ingredients are Scopoletin Vanillin, Eugeno, Pyridine, p-Cresol, Indoles, Maltol and Furfural. There are potential applications in bioenergy, biopharmaceuticals, cosmetics, skin care products, and spices.
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- 2018
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17. Starch grain analysis reveals ancient diet at Kuahuqiao site, Zhejiang Province
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Xiaoyan Yang and Leping Jiang
- Subjects
Starch grain ,Multidisciplinary ,biology ,Starch ,Aesculus chinensis ,food and beverages ,biology.organism_classification ,Oryza ,Acorn ,humanities ,Vigna ,chemistry.chemical_compound ,chemistry ,Tracheid ,Botany ,Coix - Abstract
Charred residues adhering to sherds of ceramic cooking vessels, pots (Fu), excavated from the Kuahuqiao site (8000–7000 cal a BP) in Zhejiang Province were examined using the method of starch grain analysis. Ancient starch grains were recovered from charred residues and were classified into 8 genera. Remains from rice (Oryza spp.), job’s-tears (Coix chinesis T.), bean (Vigna spp.), acorn (Quercus spp.) as well as possibly buckeye tree (Aesculus chinensis B.) were identified. Other starch grains from unidentified plants were also recovered. Tracheids with bordered pits from softwood fibers were also found, indicating that some food might have been processed with wooden tools. The range of starch grains in the charred residues adhering to the ceramic pots reveals the diversity of ancient plant foods at the Kuahuqiao site, Zhejiang Province.
- Published
- 2010
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18. Determination of four major saponins in the seeds of Aesculus chinensis Bunge using accelerated solvent extraction followed by high-performance liquid chromatography and electrospray-time of flight mass spectrometry
- Author
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Baijuan Yang, Frank S.C. Lee, Junhui Chen, Xiuchun Guo, Wenlong Li, and Xiaoru Wang
- Subjects
Detection limit ,Spectrometry, Mass, Electrospray Ionization ,Electrospray ,Chromatography ,biology ,Plant Extracts ,Chemistry ,Aesculus chinensis ,Extraction (chemistry) ,Aesculus ,Saponins ,biology.organism_classification ,Mass spectrometry ,Biochemistry ,High-performance liquid chromatography ,Mass Spectrometry ,Analytical Chemistry ,Seeds ,Solvents ,Environmental Chemistry ,Sample preparation ,Time-of-flight mass spectrometry ,Chromatography, High Pressure Liquid ,Spectroscopy - Abstract
A new method based on accelerated solvent extraction (ASE) followed by a reliable high-performance liquid chromatography-diode array detector (HPLC-DAD) and positive ion electrospray-time of flight mass spectrometry (ESI-TOF/MS) analysis has been developed for the characterization and quantification of four major saponins in extracts of the seeds of Aesculus chinensis Bunge (semen aesculi). The saponins escin Ia, escin Ib, isoescin Ia and isoescin Ib were extracted from seeds of A. chinesis Bunge via ASE, and the operational parameters of ASE were optimized, such as extraction solvent, extraction temperature, static extraction time and extraction cycles. The optimized procedure employed 70% MeOH as extraction solvent, 120 degrees C of extraction temperature, 7 min of static extraction time, 60% flush volume and the extraction recoveries of the four compounds were nearly to 100% for two cycles. The HPLC conditions are as follows: SinoChrom ODS BP C18 (4.6 mm x 200 mm, 5 microm) column, acetonitrile and 0.10% phosphoric acid solution as mobile phase, flow rate is 1.0 mL min(-1), detection length of UV is 203 nm, injection volume is 10 microL. The results indicated that the developed HPLC method is simple, sensitive and reliable for the determination of four major saponins in seeds of A. chinesis Bunge with a good linearity (r2 > 0.9994), precision (relative standard deviation (R.S.D.) < 1.5%) and the recovery ranges of 95.2-97.3%. The limits of detection (LOD) of the four compounds were in the range of 0.40-0.75 microg mL(-1). This assay can be readily utilized as a quality control method for semen aesculi and other related medicinal plants.
- Published
- 2007
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19. Preparative HPLC for Purification of Four Isomeric Bioactive Saponins from the Seeds of Aesculus chinensis
- Author
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Rui-Chao Lin, Feng Wei, Jian‐Qiu Lu, Wen-Tao Jin, Xian-Long Cheng, Lin-Yun Ma, and Ikhlas A. Khan
- Subjects
chemistry.chemical_classification ,Solvent system ,Preparative hplc ,Chromatography ,biology ,Clinical Biochemistry ,Aesculus chinensis ,Saponin ,Pharmaceutical Science ,Glycoside ,Pharmacognosy ,biology.organism_classification ,Biochemistry ,High-performance liquid chromatography ,Analytical Chemistry ,Hippocastanaceae ,chemistry - Abstract
Four isomeric bioactive saponin compounds named escin Ia, isoescin Ia, escin Ib, and isoescin Ib were successfully isolated and purified from the crude extract of the seeds of a traditional chinese medicinal plant Aesculus chinensis Bge (Hippocastanaceae) by preparatory high performance liquid chromatography (Pre‐HPLC). The gradient mobile phase solvent system composed of methanol–water–acetic acid was employed. An efficient large scale preparatory method was developed based on the stability investigation of escin Ia for the first time. A total amount of 5.2 g escin Ia, 2.8 g isoescin Ia, 3.8 g escin Ib, and 1.6 g isoescin Ib, separately, over 99% purity was obtained from 50 g of total saponins. The preparatory purification of four isomeric saponins by Pre‐HPLC was completed in 120 min in a one step separation.
- Published
- 2005
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20. Four new triterpene saponins from the seeds ofAesculus Chinensis
- Author
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Xiu-Wei Yang and Jing Zhao
- Subjects
Stereochemistry ,Aesculus chinensis ,Saponin ,Aesculus ,Pharmaceutical Science ,Uronic acid ,Analytical Chemistry ,chemistry.chemical_compound ,Triterpene ,Drug Discovery ,Trisaccharide ,Pharmacology ,chemistry.chemical_classification ,biology ,Spectrum Analysis ,Organic Chemistry ,Glycoside ,General Medicine ,Saponins ,biology.organism_classification ,Triterpenes ,Terpenoid ,Complementary and alternative medicine ,chemistry ,Seeds ,Molecular Medicine - Abstract
Two pairs of new geometrically isomeric triterpenoid saponins were isolated from the seeds of Aesculus chinensis and characterized as 28-acetyl-21-tigloylprotoaescigenin 3-O-[beta-D-xylopyranosyl (1 --2)] [beta-D-glucopyranosyl (1 --4)] [beta-D-glucopyranosiduronic acid (isoescin IIa, 1) and 28-acetyl-21-angeloylprotoaescigenin 3-O-[-beta-D-xylopyranosyl (1 --2)] [beta-D-glucopyranosyl (1 --4)] beta-D-glucopyranosiduronic acid (isoescin IIb, 2); 28-acetyl-21-tigloylbarringtogenol C 3-O-[beta-D-galactopyranosyl (1 --2)] [beta-D-glucopyranosyl (1 --4)] beta-D-glucopyranosiduronic acid (isoescin IIIa, 3) and 28-acetyl-21-angeloylbarringtogenol C 3-O-[beta-D-galactopyranosyl (1 --2)] [beta-D-glucopyranosyl (1 --4)] beta-D-glucopyranosiduronic acid (isoescin IIIb, 4). Their structures were established on the basis of spectroscopic and chemical evidence.
- Published
- 2003
- Full Text
- View/download PDF
21. New Saponins from the Seeds of Aesculus chinensis
- Author
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Dean Guo, Zhizhen Zhang, Junhua Zheng, Tamotsu Nikaido, Zhonghua Jia, and Kazuo Koike
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Folk medicine ,chemistry.chemical_classification ,Plants, Medicinal ,biology ,Stereochemistry ,Spectrum Analysis ,Molecular Sequence Data ,Aesculus chinensis ,General Chemistry ,General Medicine ,Uronic acid ,Saponins ,biology.organism_classification ,chemistry.chemical_compound ,Carbohydrate Sequence ,chemistry ,Triterpene ,Seeds ,Drug Discovery ,Carbohydrate Conformation ,Spectrum analysis - Abstract
Eight new acylated polyhydroxyoleanene triterpenoidal saponins, aesculiosides A-H (1-8), along with four known ones, have been isolated from the seeds of Aesculus chinensis. On the basis of extensive NMR studies, the structures of the new compounds were determined to be 21-O-tigloylprotoaescigenin 3-O-[beta-D-glucopyranosyl-(1-->2)][beta-D-glucopyranosyl-(1-->4)]- beta-D-glucuronopyranosyl acid (1), 21-O-angeloylprotoaescigenin 3-O-[beta-D-glucopyranosyl- (1-->2)][beta-D-glucopyranosyl-(1-->4)]-beta-D-glucuronopyranosyl acid (2), 21,22-O-ditigloylprotoaescigenin 3-O-[beta-D-glucopyranosyl-(1-->2)][beta-d-glucopyranosyl- (1-->4)]-beta-D-glucuronopyranosyl acid (3), 21-O-tigloyl-22-O-angeloylprotoaescigenin 3-O-[beta-D-glucopyranosyl- (1-->2)][beta-D-glucopyranosyl-(1-->4)]-beta-D-glucuronopyranosyl acid (4), 21,22-O-ditigloylprotoaescigenin 3-O-[beta-D-glucopyranosyl- (1-->2)][beta-D-glucopyranosyl-(1-->4)]-methyl beta-d-glucuronopyranosate (5), 21-O-tigloyl-22-O-angeloylprotoaescigenin 3-O-[beta-D-glucopyranosyl-(1-->2)-[beta-D-glucopyranosyl-(1-->4)]-methy l beta-D-glucuronopyranosate (6), 21-O-tigloyl-28-O-acetylprotoaescigenin 3-O-[beta-D-glucopyranosyl-(1-->2)][beta-D-glucopyranosyl-(1-->4)]-methy l beta-D-glucuronopyranosate (7) and 21-O-angeloyl-28-O-acetylprotoaescigenin 3-O-[beta-D-glucopyranosyl-(1-->2)][beta-D-glucopyranosyl-(1-->4)]-methy l beta-D-glucuronopyranosate (8).
- Published
- 1999
- Full Text
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22. Transpiration rates of urban trees, Aesculus chinensis
- Author
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Xiaoke Wang, Zhiyun Ouyang, Ping Zhao, Hua Wang, Hua Zheng, Fuyuan Gao, and Yufen Ren
- Subjects
Hydrology ,China ,Environmental Engineering ,biology ,Vapour Pressure Deficit ,Aesculus chinensis ,Microclimate ,Aesculus ,Plant Transpiration ,General Medicine ,biology.organism_classification ,Trees ,Air temperature ,Principal component analysis ,Environmental Chemistry ,Environmental science ,Seasons ,Leaf area index ,Cities ,Air quality index ,General Environmental Science ,Transpiration - Abstract
Transpiration patterns of Aesculus chinensis in relation to explanatory variables in the microclimatic, air quality, and biological phenomena categories were measured in Beijing, China using the thermal dissipation method. The highest transpiration rate measured as the sap flux density of the trees took place from 10:00 am to 13:00 pm in the summer and the lowest was found during nighttime in the winter. To sort out co-linearity, principal component analysis and variation and hierarchical partitioning methods were employed in data analyses. The evaporative demand index (EDI) consisting of air temperature, soil temperature, total radiation, vapor pressure deficit, and atmospheric ozone (O3), explained 68% and 80% of the hourly and daily variations of the tree transpiration, respectively. The independent and joint effects of EDI variables together with a three-variable joint effect exerted the greatest influences on the variance of transpiration rates. The independent effects of leaf area index and atmospheric O3 and their combined effect exhibited minor yet significant influences on tree transpiration rates.
- Published
- 2013
23. Antiinflammatory Triterpenoid Saponins from the Seeds of Aesculus chinensis
- Author
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Rui-Chao Lin, Ikhlas A. Khan, Feng Wei, Guo-Zhu Han, Shuang-Cheng Ma, Lin-Yun Ma, and Wen-Tao Jin
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Male ,Magnetic Resonance Spectroscopy ,Aesculus chinensis ,Anti-Inflammatory Agents ,Saponin ,Aesculus ,Xylenes ,Terpene ,Mice ,Triterpenoid ,Drug Discovery ,Animals ,Edema ,Spectral data ,Chromatography, High Pressure Liquid ,Triterpenoid saponin ,chemistry.chemical_classification ,Molecular Structure ,Traditional medicine ,biology ,Plant Extracts ,General Chemistry ,General Medicine ,Saponins ,biology.organism_classification ,Triterpenes ,Phytochemical ,chemistry ,Seeds ,Female - Abstract
Phytochemical study of the ethanol extract of the seeds of Aesculus chinensis led to the isolation of a new triterpenoid saponin (6), together with five known triterpenoid saponins (1-5). The structure of the new compound was elucidated on the basis of spectral data to be 21,28-di-O-acetylprotoaescigenin-3-O-[beta-D-glucopyranosyl(1-2)][beta-D-glucopyranosyl(1-4)]-beta-D-glucopyranosiduronic acid (aesculiside A, 6). The antiinflammatory activities of the four main saponins (1-4) were compared with those of total saponin extracts, and single saponins showed more potent activity than total saponin extracts in mice.
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- 2004
- Full Text
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24. Three New Triterpene Saponins from the Seeds of Aesculus chinensis
- Author
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Masao Hattori, Xiu-Wei Yang, and Jing Zhao
- Subjects
China ,Magnetic Resonance Spectroscopy ,Spectrophotometry, Infrared ,Stereochemistry ,Molecular Sequence Data ,Aesculus chinensis ,Saponin ,Uronic acid ,Pharmacognosy ,Hippocastanaceae ,chemistry.chemical_compound ,Triterpene ,Drug Discovery ,chemistry.chemical_classification ,Plants, Medicinal ,biology ,Glycoside ,General Chemistry ,General Medicine ,Saponins ,biology.organism_classification ,Triterpenes ,Aesculus ,Carbohydrate Sequence ,chemistry ,Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ,Seeds - Abstract
Three new triterpenoid saponins were isolated from the seeds of Aesculus chinensis, and characterized as 22-tigloylprotoaescigenin 3-O-[beta-D-glucopyranosyl (1--2)] [beta-D-glucopyranosyl (1--4)]-beta-D-glucopyranosiduronic acid (escin IVg, 1), 22-angeloylprotoaescigenin 3-O-[beta-D-glucopyranosyl (1--2)] [beta-D-glucopyranosyl (1--4)]-beta-D-glucopyranosiduronic acid (escin IVh, 2) and 16-angeloyl-21-acetylprotoaescigenin 3-O-[beta-D-glucopyranosyl (1--2)] [beta-D-glucopyranosyl (1--4)]-beta-D-glucopyranosiduronic acid (escin VIb, 3), together with two known compounds, escin IIIa (4) and desacylescin 1 (5). Their structures were established on the basis of spectroscopic and chemical evidence.
- Published
- 2001
- Full Text
- View/download PDF
25. ChemInform Abstract: New Saponins from the Seeds of Aesculus chinensis
- Author
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Junhua Zheng, Tamotsu Nikaido, Dean Guo, Kazuo Koike, Zhonghua Jia, and Zhizhen Zhang
- Subjects
biology ,Chemistry ,Stereochemistry ,Aesculus chinensis ,General Medicine ,biology.organism_classification - Abstract
Eight new acylated polyhydroxyoleanene triterpenoidal saponins, aesculiosides A-H (1-8), along with four known ones, have been isolated from the seeds of Aesculus chinensis. On the basis of extensive NMR studies, the structures of the new compounds were determined to be 21-O-tigloylprotoaescigenin 3-O-[beta-D-glucopyranosyl-(1-->2)][beta-D-glucopyranosyl-(1-->4)]- beta-D-glucuronopyranosyl acid (1), 21-O-angeloylprotoaescigenin 3-O-[beta-D-glucopyranosyl- (1-->2)][beta-D-glucopyranosyl-(1-->4)]-beta-D-glucuronopyranosyl acid (2), 21,22-O-ditigloylprotoaescigenin 3-O-[beta-D-glucopyranosyl-(1-->2)][beta-d-glucopyranosyl- (1-->4)]-beta-D-glucuronopyranosyl acid (3), 21-O-tigloyl-22-O-angeloylprotoaescigenin 3-O-[beta-D-glucopyranosyl- (1-->2)][beta-D-glucopyranosyl-(1-->4)]-beta-D-glucuronopyranosyl acid (4), 21,22-O-ditigloylprotoaescigenin 3-O-[beta-D-glucopyranosyl- (1-->2)][beta-D-glucopyranosyl-(1-->4)]-methyl beta-d-glucuronopyranosate (5), 21-O-tigloyl-22-O-angeloylprotoaescigenin 3-O-[beta-D-glucopyranosyl-(1-->2)-[beta-D-glucopyranosyl-(1-->4)]-methy l beta-D-glucuronopyranosate (6), 21-O-tigloyl-28-O-acetylprotoaescigenin 3-O-[beta-D-glucopyranosyl-(1-->2)][beta-D-glucopyranosyl-(1-->4)]-methy l beta-D-glucuronopyranosate (7) and 21-O-angeloyl-28-O-acetylprotoaescigenin 3-O-[beta-D-glucopyranosyl-(1-->2)][beta-D-glucopyranosyl-(1-->4)]-methy l beta-D-glucuronopyranosate (8).
- Published
- 2010
- Full Text
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26. In vivo anthelmintic activity of crude extracts of Radix angelicae pubescentis, Fructus bruceae, Caulis spatholobi, Semen aesculi, and Semen pharbitidis against Dactylogyrus intermedius (Monogenea) in goldfish (Carassius auratus)
- Author
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Gao-Xue Wang, Fan Wang, Jing Han, Yong Wang, You-Tao Liu, and Yonghua Wang
- Subjects
Aesculus chinensis ,ved/biology.organism_classification_rank.species ,Ethyl acetate ,Trematode Infections ,Complex Mixtures ,Plant Roots ,chemistry.chemical_compound ,Antiplatyhelmintic Agents ,Fish Diseases ,Goldfish ,Botany ,medicine ,Animals ,Petroleum ether ,Radix ,Anthelmintic ,Medicinal plants ,General Veterinary ,biology ,Traditional medicine ,Plant Stems ,ved/biology ,General Medicine ,biology.organism_classification ,Infectious Diseases ,Brucea javanica ,chemistry ,Platyhelminths ,Insect Science ,Fruit ,Seeds ,Ferns ,Parasitology ,Angelica pubescens ,medicine.drug - Abstract
In search of a natural antiparasitic, in vivo anthelmintic activity of petroleum ether, chloroform, ethyl acetate, methanol, and aqueous extracts of Angelica pubescens roots (Radix angelicae pubescentis), Brucea javanica fruits (Fructus bruceae), Spatholobus suberectus stems (Caulis spatholobi), Aesculus chinensis Bge. seeds (Semen aesculi), and Pharbitis purpurea (L.) Voigt seeds (Semen pharbitidis) were tested against Dactylogyrus intermedius (Monogenea) in goldfish (Carassius auratus). Among the extracts tested, the methanolic and aqueous extracts of S. aesculi were observed to be more efficient than the other plant extracts with EC(50) and EC(90) values of 5.23 and 7.33 mg/L and 6.48 and 12.29 mg/L after 48 h, respectively, followed by methanolic extracts of Fructus bruceae, Radix angelicae pubescentis, Caulis spatholobi, and Semen pharbitidis with EC(50) 49.96, 57.45, 64.92, and 309.47 mg/L. The methanolic and aqueous extracts of S. aesculi exhibited potential results and can be exploited as a preferred natural antiparasitic for the control of D. intermedius.
- Published
- 2010
27. Beta-aescin: a potent natural inhibitor of proliferation and inducer of apoptosis in human chronic myeloid leukemia K562 cells in vitro
- Author
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Yang-Ping Niu, Lian-Da Li, and Li-Mao Wu
- Subjects
Cancer Research ,Aesculus chinensis ,Antineoplastic Agents ,Apoptosis ,Pharmacology ,Leukemia, Myelogenous, Chronic, BCR-ABL Positive ,parasitic diseases ,medicine ,Humans ,Inducer ,Triterpenoid saponin ,Cell Proliferation ,chemistry.chemical_classification ,Escin ,biology ,Dose-Response Relationship, Drug ,G1 Phase ,food and beverages ,Myeloid leukemia ,Hematology ,biology.organism_classification ,medicine.disease ,In vitro ,carbohydrates (lipids) ,Leukemia ,Kinetics ,Oncology ,chemistry ,Immunology ,K562 Cells ,K562 cells - Abstract
Beta-aescin, a natural triterpenoid saponin isolated from the seed of Chinese horse chestnut (Aesculus chinensis), is known to generate a wide variety of biochemical and pharmacological effects. In the present study, the authors investigated the anti-proliferative and apoptotic effects of beta-aescin in human chronic myeloid leukemia K562 cell line in vitro. The anti-proliferative effects were detected by CFU-K562 colony formation and cell viability assay. The apoptotic effects were analysed by morphological analysis, annexin V assay, DNA fragmentation assay and flow cytometry DNA content analysis. The results showed that beta-aescin exhibited potent dose- and time-dependent anti-proliferative effects in K562 cells. Morphological evidence of apoptosis, a significant increase of annexin V+ and PI- cells (early apoptotic) and apoptotic DNA fragmentation, were observed in cells treated with beta-aescin. Flow cytometry analysis revealed that beta-aescin could lead to an accumulation of sub G1 population in K562 cells, and suggesting a potential G1 phase accumulation in cell cycle profile of K562 cells. Our findings revealed that beta-aescin is a potent natural inhibitor of proliferation and inducer of apoptosis in K562 cells, and beta-aescin may be a candidate lead compound to explore potential antileukemia drugs.
- Published
- 2008
28. Synthesis of 3-O-(beta-D-xylopyranosyl-(1--2)-beta-D-glucopyranosyl)-3'-O-(beta-D-glucopyranosyl)tamarixetin, the putative structure of aescuflavoside A from the seeds of Aesculus chinensis
- Author
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Biao Yu, Cunsheng Zhu, Yuwen Li, Wenjie Peng, and Xiuwen Han
- Subjects
chemistry.chemical_classification ,Flavonoids ,Glycosylation ,biology ,Molecular Structure ,Stereochemistry ,Aescuflavoside ,Organic Chemistry ,Aesculus chinensis ,Regioselectivity ,Glycoside ,Aesculus ,General Medicine ,biology.organism_classification ,Biochemistry ,Analytical Chemistry ,carbohydrates (lipids) ,chemistry.chemical_compound ,Tamarixetin ,chemistry ,Carbohydrate Sequence ,Seeds ,Glycosyl ,Nuclear Magnetic Resonance, Biomolecular - Abstract
3-O-(beta-D-xylopyranosyl-(1-->2)-beta-D-glucopyranosyl)-3'-O-(beta-D-glucopyranosyl)tamarixetin, the putative flavonal glycoside named aescuflavoside A, isolated from the seeds of Aesculus chinensis, is synthesized via regioselective glycosylation of 7-O-benzyltamarixetin with glycosyl bromides under phase-transfer-catalyzed conditions.
- Published
- 2006
29. Triterpenoid saponins from the fruits of Aesculus pavia
- Author
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Zhizhen Zhang, Shanmin Zhang, Shiyou Li, and David G. Gorenstein
- Subjects
Aesculus hippocastanum ,Stereochemistry ,Aesculus chinensis ,Molecular Sequence Data ,Saponin ,Aesculus ,Plant Science ,Horticulture ,Biochemistry ,Hippocastanaceae ,chemistry.chemical_compound ,Triterpene ,Molecular Biology ,chemistry.chemical_classification ,biology ,Molecular Structure ,Terpenes ,General Medicine ,Saponins ,biology.organism_classification ,Terpenoid ,carbohydrates (lipids) ,Aglycone ,chemistry ,Carbohydrate Sequence ,Fruit - Abstract
The compounds, named aesculiosides Ia-Ie, IIa-IId, and IVa-IVc, were isolated from an ethanol extract of the fruits of North American Aesculus pavia, along with two known compounds. Their structures were characterized as polyhydroxyoleanene pentacyclic triterpenoid saponins by spectroscopic and chemical analyses. These saponins were divided into three elution zones by chromatography according to the polarity because of the acyl substitution at C-21 and C-22 of the aglycone saponins moiety. These are structurally different from those isolated from Eurasian Aesculus hippocastanum and Aesculus chinensis in their oligosaccharide moieties.
- Published
- 2005
30. Antiviral flavonoids from the seeds of Aesculus chinensis
- Author
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Ikhlas A. Khan, Lin-Yun Ma, Rui-Chao Lin, Paul Pui-Hay But, Feng Wei, and Shuang-Cheng Ma
- Subjects
Flavonoid ,Aesculus chinensis ,Pharmaceutical Science ,Aesculus ,Pharmacognosy ,Antiviral Agents ,Analytical Chemistry ,Hippocastanaceae ,chemistry.chemical_compound ,Inhibitory Concentration 50 ,Glucoside ,Drug Discovery ,Botany ,Medicine, Chinese Traditional ,Pharmacology ,chemistry.chemical_classification ,Flavonoids ,Plants, Medicinal ,biology ,Molecular Structure ,Organic Chemistry ,biology.organism_classification ,Xyloside ,Complementary and alternative medicine ,chemistry ,Polyphenol ,Influenza A virus ,Seeds ,Molecular Medicine - Abstract
A bioassay-guided fractionation of an ethanol extract of the seeds of Aesculus chinensis led to the isolation of two new flavanoids (1 and 2), along with eight known ones (3-10). The structures of the new compounds were elucidated by spectroscopic methods including 2D NMR. All compounds were tested for antiviral activity against respiratory syncytial virus (RSV), parainfluenza virus type 3 (PIV 3), and influenza virus type A (Flu A). Compounds 1, 2, and 6 showed significant antiviral activities against RSV with IC(50) values of 4.5, 6.7, and 4.1 microg/mL and selective index (SI) values of 15.8, 32, and 63.8, respectively. Compound 8 demonstrated significant antiviral activity against Flu A with an IC(50) of 24.5 microg/mL and a SI of 16.0, respectively.
- Published
- 2004
31. Anti-HIV-1 protease triterpenoid saponins from the seeds of Aesculus chinensis
- Author
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Lihe Zhang, Jing Zhao, Yu-Xin Cui, Xue-Hui Liu, Chao-Mei Ma, Masao Hattori, and Xiu-Wei Yang
- Subjects
Anti hiv 1 ,China ,Magnetic Resonance Spectroscopy ,Spectrophotometry, Infrared ,medicine.medical_treatment ,Aesculus chinensis ,Molecular Sequence Data ,Molecular Conformation ,Pharmaceutical Science ,Crystallography, X-Ray ,Analytical Chemistry ,Triterpenoid ,Drug Discovery ,medicine ,Beta (finance) ,Pharmacology ,Protease ,Plants, Medicinal ,Traditional medicine ,biology ,Plant Extracts ,Hydrolysis ,Organic Chemistry ,HIV Protease Inhibitors ,Saponins ,biology.organism_classification ,Triterpenes ,Complementary and alternative medicine ,Biochemistry ,Carbohydrate Sequence ,Molecular Medicine - Abstract
Eight bioactive triterpenoid saponins (1-8) were isolated from the seeds of Aesculus chinensis, four of which are novel compounds. The major saponins were identified as escin Ia (1), Ib (2), isoescin Ia (3) and Ib (4), while the new compounds were identified as 22alpha-tigloyl-28-acetylprotoaescigenin-3beta-O-?beta -D-glucopyranos yl (1-2) ?beta-D-glucopyranosyl (1-4)-beta-D-glucopyranosiduronic acid (escin IVc, 5), 22alpha-angeloyl-28-acetylprotoaescigenin-3beta-O-?bet a-D-glucopyrano syl (1-2) ?beta-D-glucopyranosyl (1-4)-beta-D-glucopyranosiduronic acid (escin IVd, 6), 28-tigloylprotoaescigenin-3beta-O-?beta-D-glucopyranosyl (1-2) ?beta-D-glucopyranosyl (1-4)-beta-D-glucopyranosiduronic acid (escin IVe, 7), and 28-angeloylprotoaescigenin-3beta-O-?beta-D-glucopyranosyl (1-2) ?beta-D-glucopyranosyl (1-4)-beta-D-glucopyranosiduronic acid (escin IVf, 8). The structures were determined by chemical and spectroscopic methods. All the above compounds were evaluated for their inhibitory activity against HIV-1 protease.
- Published
- 1999
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