Neoeriocitrin (BioDeep_00000017388)
Main id: BioDeep_00000400520
human metabolite PANOMIX_OTCML-2023 natural product
代谢物信息卡片
化学式: C27H32O15 (596.1741)
中文名称: 新圣草次苷, 新神经胞苷
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1(O[C@H]2[C@H](O[C@H]3[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O3)[C@@H](O)[C@H](O)[C@@H](CO)O2)C=C2O[C@]([H])(C3C=CC(O)=C(O)C=3)CC(=O)C2=C(O)C=1
InChI: InChI=1S/C27H32O15/c1-9-20(33)22(35)24(37)26(38-9)42-25-23(36)21(34)18(8-28)41-27(25)39-11-5-14(31)19-15(32)7-16(40-17(19)6-11)10-2-3-12(29)13(30)4-10/h2-6,9,16,18,20-31,33-37H,7-8H2,1H3/t9-,16-,18+,20-,21+,22+,23-,24+,25+,26-,27+/m0/s1
描述信息
Neoeriocitrin is a flavanone glycoside that is eriodictyol substituted by a 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl residue at position 7 via a glycosidic linkage. It has a role as a plant metabolite. It is a neohesperidoside, a disaccharide derivative, a trihydroxyflavanone, a flavanone glycoside and a member of 4-hydroxyflavanones. It is functionally related to an eriodictyol.
Neoeriocitrin is a natural product found in Citrus latipes, Citrus hystrix, and other organisms with data available.
A flavanone glycoside that is eriodictyol substituted by a 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl residue at position 7 via a glycosidic linkage.
Neoeriocitrin, isolated from Drynaria Rhizome,?shows activity on proliferation and osteogenic differentiation in MC3T3-E1. Neoeriocitrin is a potent acetylcholinesterase (AChE) inhibitor[1][2].
Neoeriocitrin, isolated from Drynaria Rhizome,?shows activity on proliferation and osteogenic differentiation in MC3T3-E1. Neoeriocitrin is a potent acetylcholinesterase (AChE) inhibitor[1][2].
同义名列表
19 个代谢物同义名
(S)-7-(((2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-2-(3,4-dihydroxyphenyl)-5-hydroxychroman-4-one; (2S)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-tetrahydropyran-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-chroman-4-one; (2S)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-2,3-dihydrochromen-4-one; 7-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-2,3-dihydrochromen-4-one; (2S)-2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-7-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside; (S)-7-((2-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl)oxy)-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5-hydroxy-4H-benzopyran-4-one; (S)-3,4,5,7-Tetrahydroxyflavanone-7-[2-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside]; Neoeriocitrin, analytical reference material; Eriodictyol-7-O-neohesperidoside; Eriodictyol 7-O-neohesperidoside; Eriodictyol 7-neohesperidoside; eriodictyol-7-neohesperidoside; Neoeriocitrin, ~95\\% (HPLC); Isoeriocitrin; MEGxp0_001062; Neoeriocitrin; ACon1_000964; AC1L3FPQ; Neoeriocitrin
数据库引用编号
18 个数据库交叉引用编号
- ChEBI: CHEBI:7502
- KEGG: C09805
- PubChem: 114627
- HMDB: HMDB0302534
- ChEMBL: CHEMBL3609603
- Wikipedia: Neoeriocitrin
- LipidMAPS: LMPK12140359
- MeSH: neoeriocitrin
- ChemIDplus: 0013241322
- CAS: 13241-32-2
- medchemexpress: HY-N4119
- MetaboLights: MTBLC7502
- PubChem: 11993
- KNApSAcK: C00000986
- 3DMET: B03302
- NIKKAJI: J213.772K
- KNApSAcK: 7502
- LOTUS: LTS0274558
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
48 个相关的物种来源信息
- 23809 - Ailanthus: LTS0274558
- 459109 - Ailanthus integrifolia: 10.1248/CPB.42.1669
- 2706 - Citrus: LTS0274558
- 159033 - Citrus aurantiifolia: 10.1021/JF00037A011
- 43166 - Citrus aurantium: 10.1016/0031-9422(93)85237-L
- 43166 - Citrus aurantium: 10.1021/JF00037A011
- 43166 - Citrus aurantium: 10.1104/PP.99.1.67
- 43166 - Citrus aurantium: 10.1111/J.1365-2621.1998.TB15675.X
- 170989 - Citrus hystrix: 10.1016/0305-1978(95)00109-3
- 170989 - Citrus hystrix: LTS0274558
- 135197 - Citrus junos: 10.1016/0305-1978(95)00109-3
- 135197 - Citrus junos: LTS0274558
- 170988 - Citrus latipes: 10.1016/0305-1978(95)00109-3
- 170988 - Citrus latipes: LTS0274558
- 2708 - Citrus limon: 10.1016/0031-9422(93)85237-L
- 2708 - Citrus limon: 10.1021/JF00037A011
- 171249 - Citrus limonia: LTS0274558
- 37334 - Citrus maxima:
- 37334 - Citrus maxima: 10.1016/0021-9673(94)89051-X
- 37334 - Citrus maxima: 10.1016/0031-9422(93)85237-L
- 37334 - Citrus maxima: 10.1111/J.1365-2621.1998.TB15675.X
- 37334 - Citrus maxima: LTS0274558
- 2711 - Citrus sinensis: 10.1016/0031-9422(93)85237-L
- 2711 - Citrus sinensis: 10.1016/S0021-9673(00)00256-9
- 2711 - Citrus sinensis: 10.1021/JF00037A011
- 2711 - Citrus sinensis: LTS0274558
- 37690 - Citrus trifoliata: 10.1016/0031-9422(93)85237-L
- 37690 - Citrus trifoliata: LTS0274558
- 164113 - Citrus × microcarpa: 10.1016/0031-9422(93)85237-L
- 37656 - Citrus × paradisi: 10.1016/0031-9422(93)85237-L
- 37656 - Citrus × paradisi: 10.1021/JF00037A011
- 37656 - Citrus × paradisi: 10.1111/J.1365-2621.1998.TB15675.X
- 35925 - Diospyros kaki: -
- 2759 - Eukaryota: LTS0274558
- 9606 - Homo sapiens: -
- 3398 - Magnoliopsida: LTS0274558
- 33090 - Plants: -
- 3275 - Polypodiaceae: LTS0274558
- 241806 - Polypodiopsida: LTS0274558
- 37881 - Poncirus: LTS0274558
- 156491 - Pyrrosia: LTS0274558
- 347942 - Pyrrosia serpens: 10.1016/0031-9422(90)85359-N
- 347942 - Pyrrosia serpens: LTS0274558
- 23513 - Rutaceae: LTS0274558
- 23808 - Simaroubaceae: LTS0274558
- 35493 - Streptophyta: LTS0274558
- 58023 - Tracheophyta: LTS0274558
- 33090 - Viridiplantae: LTS0274558
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。
文献列表
- Sainan Li, Chunming Liu, Yuchi Zhang, Dongfang Shi, Rong Tsao. Application of accelerated solvent extraction coupled with online two-dimensional countercurrent chromatography for continuous extraction and separation of bioactive compounds from Citrus limon peel.
Journal of separation science.
2020 Oct; 43(19):3793-3805. doi:
10.1002/jssc.202000588. [PMID: 32745365] - Qianqian Zhang, Fang Feng. The Effects of Different Varieties of Aurantii Fructus Immaturus on the Potential Toxicity of Zhi-Zi-Hou-Po Decoction Based on Spectrum-Toxicity Correlation Analysis.
Molecules (Basel, Switzerland).
2019 Nov; 24(23):. doi:
10.3390/molecules24234254. [PMID: 31766682] - Mei-Yu Sun, Jing-Yi Li, Dong Li, Feng-Jie Huang, Di Wang, Hui Li, Quan Xing, Hui-Bin Zhu, Lei Shi. Full-Length Transcriptome Sequencing and Modular Organization Analysis of the Naringin/Neoeriocitrin-Related Gene Expression Pattern in Drynaria roosii.
Plant & cell physiology.
2018 Jul; 59(7):1398-1414. doi:
10.1093/pcp/pcy072. [PMID: 29660070] - Mingliang Zhong, Guibo Sun, Xiaopo Zhang, Guangli Sun, Xudong Xu, Shichun Yu. A new prenylated naphthoquinoid from the aerial parts of Clinopodium chinense (Benth.) O. Kuntze.
Molecules (Basel, Switzerland).
2012 Nov; 17(12):13910-6. doi:
10.3390/molecules171213910. [PMID: 23178306] - Lina Li, Zhen Zeng, Guoping Cai. Comparison of neoeriocitrin and naringin on proliferation and osteogenic differentiation in MC3T3-E1.
Phytomedicine : international journal of phytotherapy and phytopharmacology.
2011 Aug; 18(11):985-9. doi:
10.1016/j.phymed.2011.03.002. [PMID: 21741227] - Chao Li, Chunjuan Yang, Xuling Peng, Zhili Xiong, Famei Li. Simultaneous determination of neoeriocitrin and naringin in rat plasma after oral administration of a Chinese compound formulation by UPLC-MS-MS.
Journal of chromatographic science.
2010 May; 48(5):342-7. doi:
10.1093/chromsci/48.5.342. [PMID: 20515525]
