Nystose (BioDeep_00000230547)

 

Secondary id: BioDeep_00000019381

natural product PANOMIX_OTCML-2023


代谢物信息卡片


(2R,3R,4S,5S,6R)-2-(((2S,3S,4S,5R)-2-((((2R,3S,4S,5R)-2-((((2R,3S,4S,5R)-3,4-Dihydroxy-2,5-bis(hydroxymethyl)tetrahydrofuran-2-yl)oxy)methyl)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)oxy)methyl)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

化学式: C24H42O21 (666.2218)
中文名称: 耐斯糖(蔗果四糖), 蔗果四糖, 耐斯糖
谱图信息: 最多检出来源 Viridiplantae(plant) 83.86%

分子结构信息

SMILES: C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)COC3(C(C(C(O3)CO)O)O)COC4(C(C(C(O4)CO)O)O)CO)O)O)O)O
InChI: InChI=1/C24H42O21/c25-1-8-12(30)16(34)17(35)21(41-8)45-24(20(38)15(33)11(4-28)44-24)7-40-23(19(37)14(32)10(3-27)43-23)6-39-22(5-29)18(36)13(31)9(2-26)42-22/h8-21,25-38H,1-7H2/t8-,9-,10-,11-,12-,13-,14-,15-,16+,17-,18+,19+,20+,21-,22-,23-,24+/m1/s1

描述信息

Nystose is an oligosaccharide.
Nystose is a natural product found in Taraxacum lapponicum, Taraxacum platycarpum, and other organisms with data available.
Nystose is a tetrasaccharide with two fructose molecules linked via beta (1→2) bonds to the fructosyl moiety of sucrose.
Nystose is a tetrasaccharide with two fructose molecules linked via beta (1→2) bonds to the fructosyl moiety of sucrose.

同义名列表

34 个代谢物同义名

(2R,3R,4S,5S,6R)-2-(((2S,3S,4S,5R)-2-((((2R,3S,4S,5R)-2-((((2R,3S,4S,5R)-3,4-Dihydroxy-2,5-bis(hydroxymethyl)tetrahydrofuran-2-yl)oxy)methyl)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)oxy)methyl)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol; (2R,3R,4S,5S,6R)-2-[(2S,3S,4S,5R)-2-[[(2R,3S,4S,5R)-2-[[(2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol; .ALPHA.-D-GLUCOPYRANOSIDE, O-.BETA.-D-FRUCTOFURANOSYL-(2->1)-O-.BETA.-D-FRUCTOFURANOSYL-(2->1)-.BETA.-D-FRUCTOFURANOSYL; alpha-D-Glucopyranoside, O-beta-D-fructofuranosyl-(2-->1)-O-beta-D-fructofuranosyl-(2-->1)-beta-D-fructofuranosyl; 1-O-(1-O-.BETA.-D-FRUCTOFURANOSYL-.BETA.-D-FRUCTOFURANOSYL)-.BETA.-D-FRUCTOFURANOSYL .ALPHA.-D-GLUCOPYRANOSIDE; alpha-D-Glucopyranoside, O-beta-D-fructofuranosyl-(2-1)-O-beta-D-fructofuranosyl-(2-1)-beta-D-fructofuranosyl; beta-D-fructofuranosyl-(2->1)-beta-D-fructofuranosyl-(2->1)-beta-D-fructofuranosyl alpha-D-glucopyranoside; beta-D-Fructofuranosyl-(2->1)beta-D-fructofuranosyl-(2->1)beta-D-fructofuranosyl alpha-D-glucopyranoside; hex-2-ulofuranosyl-(2->1)hex-2-ulofuranosyl-(2->1)hex-2-ulofuranosyl hexopyranoside; O-fructofuranosyl-2-1-O-fructofuranosyl-2-1-fructofuranosyl glucopyranoside; WURCS=2.0/2,4,3/[a2122h-1a_1-5][ha122h-2b_2-5]/1-2-2-2/a1-b2_b1-c2_c1-d2; beta-D-Fruf-(2->1)-beta-D-Fruf-(2->1)-beta-D-Fruf-(2<-->1)-alpha-D-Glup; O-beta-D-Fru(2-1)-O-beta-D-fru-(2-1)-O-beta-D-fru-(2-1)-alpha-D-glc; FRUCTOSYL-(2->1)-FRUCTOSYL-(2->1)-FRUCTOSYL-(2->1)-GLUCOSE; Nystose, analytical standard; nystose trihydrate; 1,1-kestotetraose; UNII-U0MS6Z5RBK; fungitetraose; U0MS6Z5RBK; Nystose; Nistose; GF-3; NYT; (2R,3R,4S,5S,6R)-2-[(2S,3S,4S,5R)-2-[[(2R,3S,4S,5R)-2-[[(2R,3S,4S,5R)-3,4-dihydroxy-2,5-dimethylol-tetrahydrofuran-2-yl]oxymethyl]-3,4-dihydroxy-5-methylol-tetrahydrofuran-2-yl]oxymethyl]-3,4-dihydroxy-5-methylol-tetrahydrofuran-2-yl]oxy-6-methylol-tetrah; (2R,3R,4S,5S,6R)-2-[(2S,3S,4S,5R)-2-[[(2R,3S,4S,5R)-2-[[(2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-(hydroxymethyl)oxane-3,; (2R,3R,4S,5S,6R)-2-[(2S,3S,4S,5R)-2-[[(2R,3S,4S,5R)-2-[[(2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)tetrahydrofuran-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]ox; (2R,3R,4S,5S,6R)-2-[[(2S,3S,4S,5R)-2-[[(2R,3S,4S,5R)-2-[[(2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)-2-tetrahydrofuranyl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)-2-tetrahydrofuranyl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)-2-tetrahydrofuranyl]o; beta-D-Fruf-(2->1)-beta-D-Fruf-(2->1)-beta-D-Fruf-(2-->1)-alpha-D-Glup; STOCK1N-03804; 56218_FLUKA; 13133-07-8; 2-{[2-({[2-({[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol; b-D-Fructofuranosyl-(2->1)-b-D-fructofuranosyl-(2->1)-b-D-fructofuranosyl a-D-glucopyranoside, 9ci



数据库引用编号

14 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(1)

PlantCyc(1)

代谢反应

12 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(2)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(10)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

24 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表


文献列表

  • Zijie Zhang, Wenfei Xiao, Jieren Qiu, Ya Xin, Qinpo Liu, Huizhe Chen, Yaping Fu, Huasheng Ma, Wenyue Chen, Yuqin Huang, Songlin Ruan, Jianli Yan. Nystose regulates the response of rice roots to cold stress via multiple signaling pathways: A comparative proteomics analysis. PloS one. 2020; 15(9):e0238381. doi: 10.1371/journal.pone.0238381. [PMID: 32881942]
  • Zhe Lin, Yan-Fang Liu, Yang Qu, Li-Ying Shi, De-Qiang Dou, Hai-Xue Kuang. Characterisation of oligosaccharides from Baizhu by HILIC-MS. Natural product research. 2015; 29(13):1194-200. doi: 10.1080/14786419.2014.995652. [PMID: 25553654]
  • V F Oliveira, E A Silva, L B P Zaidan, M A M Carvalho. Effects of elevated CO2 concentration and water deficit on fructan metabolism in Viguiera discolor Baker. Plant biology (Stuttgart, Germany). 2013 May; 15(3):471-82. doi: 10.1111/j.1438-8677.2012.00654.x. [PMID: 22882384]
  • Zhen-Yuan Zhu, Hong-Yu Lian, Chuan-Ling Si, Yang Liu, Nian Liu, Jing Chen, Li-Na Ding, Qiang Yao, Yongmin Zhang. The chromatographic analysis of oligosaccharides and preparation of 1-kestose and nystose in yacon. International journal of food sciences and nutrition. 2012 May; 63(3):338-42. doi: 10.3109/09637486.2011.627847. [PMID: 22013906]
  • K H Jung, S H Bang, T K Oh, H J Park. Industrial production of fructooligosaccharides by immobilized cells of Aureobasidium pullulans in a packed bed reactor. Biotechnology letters. 2011 Aug; 33(8):1621-4. doi: 10.1007/s10529-011-0606-8. [PMID: 21479630]
  • Dolores Linde, Isabel Macias, Lucía Fernández-Arrojo, Francisco J Plou, Antonio Jiménez, María Fernández-Lobato. Molecular and biochemical characterization of a beta-fructofuranosidase from Xanthophyllomyces dendrorhous. Applied and environmental microbiology. 2009 Feb; 75(4):1065-73. doi: 10.1128/aem.02061-08. [PMID: 19088319]
  • Denise Altenbach, Eveline Nüesch, Alain D Meyer, Thomas Boller, Andres Wiemken. The large subunit determines catalytic specificity of barley sucrose:fructan 6-fructosyltransferase and fescue sucrose:sucrose 1-fructosyltransferase. FEBS letters. 2004 Jun; 567(2-3):214-8. doi: 10.1016/j.febslet.2004.04.064. [PMID: 15178325]
  • E M Hellwege, D Gritscher, L Willmitzer, A G Heyer. Transgenic potato tubers accumulate high levels of 1-kestose and nystose: functional identification of a sucrose sucrose 1-fructosyltransferase of artichoke (Cynara scolymus) blossom discs. The Plant journal : for cell and molecular biology. 1997 Nov; 12(5):1057-65. doi: 10.1046/j.1365-313x.1997.12051057.x. [PMID: 9418047]
  • A Ohta, S Baba, M Ohtsuki, A Taguchi, T Adachi. Prevention of coprophagy modifies magnesium absorption in rats fed with fructo-oligosaccharides. The British journal of nutrition. 1996 May; 75(5):775-84. doi: 10.1079/bjn19960181. [PMID: 8695604]
  • M Lüscher, C Erdin, N Sprenger, U Hochstrasser, T Boller, A Wiemken. Inulin synthesis by a combination of purified fructosyltransferases from tubers of Helianthus tuberosus. FEBS letters. 1996 Apr; 385(1-2):39-42. doi: 10.1016/0014-5793(96)00343-2. [PMID: 8641462]
  • C Cui, M Yang, Z Yao, B Cao, Z Luo, Y Xu, Y Chen. [Antidepressant active constituents in the roots of Morinda officinalis How]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 1995 Jan; 20(1):36-9, 62. doi: ". [PMID: 7626209]