vitexin-2 inverted exclamation marka-o-rhamnoside (BioDeep_00000184982)
Main id: BioDeep_00000003344
human metabolite PANOMIX_OTCML-2023 blood metabolite natural product
代谢物信息卡片
化学式: C27H30O14 (578.163548)
中文名称: 牡荆素鼠李糖苷
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC=C(C=C5)O)O)O)CO)O)O)O)O)O
InChI: InChI=1S/C27H30O14/c1-9-19(33)21(35)23(37)27(38-9)41-26-22(36)20(34)16(8-28)40-25(26)18-13(31)6-12(30)17-14(32)7-15(39-24(17)18)10-2-4-11(29)5-3-10/h2-7,9,16,19-23,25-31,33-37H,8H2,1H3
描述信息
Vitexin 2-rhamnoside is a member of the class of compounds known as flavonoid 8-c-glycosides. Flavonoid 8-c-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone. Vitexin 2-rhamnoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Vitexin 2-rhamnoside can be found in oat and soy bean, which makes vitexin 2-rhamnoside a potential biomarker for the consumption of these food products.
Vitexin-2"-O-rhamnoside, a main flavonoid glycoside of the leaves of Cratagus pinnatifida Bge, contributes to the protection against H2O2-mediated oxidative stress damage and has potential to treat cardiovascular system diseases[1].
Vitexin-2"-O-rhamnoside, a main flavonoid glycoside of the leaves of Cratagus pinnatifida Bge, contributes to the protection against H2O2-mediated oxidative stress damage and has potential to treat cardiovascular system diseases[1].
同义名列表
10 个代谢物同义名
8-[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one; 8-[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one; vitexin-2 inverted exclamation marka-o-rhamnoside; 8-Glycosyl-apigenin-rhamnoside; Vitexin-2-O-rhamnoside; vitexin-2-O-rhamnoside; Vitexin 2-rhamnoside; Vitexin rhamnoside; Vitexin-2"-O-rhamnoside; Vitexin 2''-O-beta-L-rhamnoside
数据库引用编号
10 个数据库交叉引用编号
- PubChem: 5874704
- HMDB: HMDB0259860
- foodb: FDB021638
- chemspider: 4730614
- CAS: 64820-99-1
- medchemexpress: HY-N0534
- KEGG: C12628
- PubChem: 583018
- KNApSAcK: 32298
- LOTUS: LTS0104007
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)
42 个相关的物种来源信息
- 3481 - Cannabaceae: LTS0104007
- 13408 - Celtis: LTS0104007
- 236733 - Celtis australis: 10.2298/JSC090817049K
- 236733 - Celtis australis: LTS0104007
- 2706 - Citrus: LTS0104007
- 76966 - Citrus japonica: 10.1080/00021369.1985.10858531
- 76966 - Citrus japonica: 10.1080/00021369.1985.10866832
- 76966 - Citrus japonica: LTS0104007
- 36607 - Cotoneaster: LTS0104007
- 1851000 - Cotoneaster orbicularis: 10.1016/S0031-9422(99)00598-1
- 1851000 - Cotoneaster orbicularis: LTS0104007
- 510735 - Crataegus pinnatifida: 10.1080/1028602021000054982
- 50180 - Dacrycarpus: LTS0104007
- 56888 - Dacrycarpus dacrydioides: 10.1016/S0031-9422(00)84944-4
- 56888 - Dacrycarpus dacrydioides: LTS0104007
- 2759 - Eukaryota: LTS0104007
- 3803 - Fabaceae: LTS0104007
- 3846 - Glycine: LTS0104007
- 3847 - Glycine max: 10.1016/S0031-9422(00)82629-1
- 3847 - Glycine max: LTS0104007
- 9606 - Homo sapiens: -
- 3433 - Lauraceae: LTS0104007
- 251260 - Machilus: LTS0104007
- 325535 - Machilus japonica: 10.1021/NP9000653
- 325535 - Machilus japonica: LTS0104007
- 3398 - Magnoliopsida: LTS0104007
- 3683 - Passifloraceae: LTS0104007
- 58019 - Pinopsida: LTS0104007
- 33090 - Plants: -
- 3362 - Podocarpaceae: LTS0104007
- 3363 - Podocarpus: LTS0104007
- 56901 - Podocarpus totara: LTS0104007
- 56901 - Podocarpus totara: NA
- 3745 - Rosaceae: LTS0104007
- 23513 - Rutaceae: LTS0104007
- 35493 - Streptophyta: LTS0104007
- 58023 - Tracheophyta: LTS0104007
- 45183 - Turnera: LTS0104007
- 329212 - Turnera diffusa: 10.1021/NP060253R
- 329212 - Turnera diffusa: LTS0104007
- 45182 - Turneraceae: LTS0104007
- 33090 - Viridiplantae: LTS0104007
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
- Isabela M Lorizola, Cibele P B Furlan, Mariana Portovedo, Marciane Milanski, Patrícia B Botelho, Rosângela M N Bezerra, Beatriz R Sumere, Maurício A Rostagno, Caroline D Capitani. Beet Stalks and Leaves (Beta vulgaris L.) Protect Against High-Fat Diet-Induced Oxidative Damage in the Liver in Mice.
Nutrients.
2018 Jul; 10(7):. doi:
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Phytotherapy research : PTR.
2017 Jun; 31(6):871-884. doi:
10.1002/ptr.5819
. [PMID: 28464411] - Feng Han, Yupin Guo, Huiyan Gu, Fenglan Li, Baozhong Hu, Lei Yang. Application of alkyl polyglycoside surfactant in ultrasonic-assisted extraction followed by macroporous resin enrichment for the separation of vitexin-2″-O-rhamnoside and vitexin from Crataegus pinnatifida leaves.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
2016 Feb; 1012-1013(?):69-78. doi:
10.1016/j.jchromb.2016.01.017
. [PMID: 26807707] - Yucong Gao, Yang Du, Zheming Ying, Aijing Leng, Wenjie Zhang, Yihan Meng, Cuiyu Li, Liang Xu, Xixiang Ying, Tingguo Kang. Hepatic, gastric and intestinal first-pass effects of vitexin-2''-O-rhamnoside in rats by ultra-high-performance liquid chromatography.
Biomedical chromatography : BMC.
2016 Feb; 30(2):111-6. doi:
10.1002/bmc.3522
. [PMID: 26031900] - Kexin Hou, Fengli Chen, Yuangang Zu, Lei Yang. Ionic liquids-lithium salts pretreatment followed by ultrasound-assisted extraction of vitexin-4″-O-glucoside, vitexin-2″-O-rhamnoside and vitexin from Phyllostachys edulis leaves.
Journal of chromatography. A.
2016 Jan; 1431(?):17-26. doi:
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. [PMID: 26763300] - Hongjuan Li, Ying Liu, Haizhu Jin, Sujing Liu, Shengtao Fang, Chunhua Wang, Chuanhai Xia. Separation of vitexin-4″-O-glucoside and vitexin-2″-O-rhamnoside from hawthorn leaves extracts using macroporous resins.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
2015 Dec; 1007(?):23-9. doi:
10.1016/j.jchromb.2015.10.043
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Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
2015 Feb; 69(?):139-44. doi:
10.1016/j.biopha.2014.11.010
. [PMID: 25661350] - Wenjuan Wei, Xixiang Ying, Wenjie Zhang, Yinghui Chen, Aijing Leng, Chen Jiang, Jing Liu. Effects of vitexin-2"-O-rhamnoside and vitexin-4"-O-glucoside on growth and oxidative stress-induced cell apoptosis of human adipose-derived stem cells.
The Journal of pharmacy and pharmacology.
2014 Jul; 66(7):988-97. doi:
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Natural product research.
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10.1080/14786419.2013.832675
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Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2012 Mar; 37(6):829-31. doi:
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Natural product research.
2012; 26(23):2247-50. doi:
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. [PMID: 22250700] - Wenjun Zhang, Ming Xu, Chaoqun Yu, Guofeng Zhang, Xing Tang. Simultaneous determination of vitexin-4''-O-glucoside, vitexin-2''-O-rhamnoside, rutin and vitexin from hawthorn leaves flavonoids in rat plasma by UPLC-ESI-MS/MS.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
2010 Jul; 878(21):1837-44. doi:
10.1016/j.jchromb.2010.05.023
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Phytochemical analysis : PCA.
2008 Nov; 19(6):534-40. doi:
10.1002/pca.1081
. [PMID: 18618435] - Lu Qu, Hang-Sheng Zheng, Nian-Ping Feng, Song-Ming Li. [Determination of vitexin-rhamnoside in Beagle dog plasma and preliminary pharmacokinetics of Yixintong sustained release tablets].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2008 May; 33(10):1168-70. doi:
NULL
. [PMID: 18720869] - Ying-ai Xu, Guorong Fan, Shen Gao, Zhanying Hong. Assessment of intestinal absorption of vitexin-2''-o-rhamnoside in hawthorn leaves flavonoids in rat using in situ and in vitro absorption models.
Drug development and industrial pharmacy.
2008 Feb; 34(2):164-70. doi:
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. [PMID: 18302035] - Xixiang Ying, Shuo Gao, Wenliang Zhu, Yujin Bi, Feng Qin, Xiaoqin Li, Famei Li. High-performance liquid chromatographic determination and pharmacokinetic study of vitexin-2''-O-rhamnoside in rat plasma after intravenous administration.
Journal of pharmaceutical and biomedical analysis.
2007 Jul; 44(3):802-6. doi:
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Journal of pharmaceutical and biomedical analysis.
2007 May; 44(1):243-9. doi:
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. [PMID: 17329058] - Shan Cheng, Feng Qiu, Jia Huang, Junqi He. Simultaneous determination of vitexin-2"-O-glucoside, vitexin-2"-O-rhamnoside, rutin, and hyperoside in the extract of hawthorn (Crataegus pinnatifida Bge.) leaves by RP-HPLC with ultraviolet photodiode array detection.
Journal of separation science.
2007 Mar; 30(5):717-21. doi:
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Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials.
2006 Nov; 29(11):1169-73. doi:
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Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2006 Apr; 31(7):566-9. doi:
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. [PMID: 16780160] - Juan Su, Wei-dong Zhang, Yun Zhou, Jing Zhou, Zheng-bing Gu. [Determination of flavoniod-glycosides in Yixintong pills by HPLC].
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2004 Jun; 29(6):525-7. doi:
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General pharmacology.
1995 Nov; 26(7):1565-70. doi:
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