Luteolin-4Glucoside (BioDeep_00000397187)

Main id: BioDeep_00000398269

 

PANOMIX_OTCML-2023


代谢物信息卡片


5,7-dihydroxy-2-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-phenyl]chromen-4-one

化学式: C21H20O11 (448.1006)
中文名称: 藤黄菌素-4 -O-葡糖苷
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O
InChI: InChI=1S/C21H20O11/c22-7-16-18(27)19(28)20(29)21(32-16)31-13-2-1-8(3-10(13)24)14-6-12(26)17-11(25)4-9(23)5-15(17)30-14/h1-6,16,18-25,27-29H,7H2/t16-,18-,19+,20-,21-/m1/s1

描述信息

Luteolin-4-O-beta-D-glucopyranoside is a glycosyloxyflavone that is luteolin substituted by a beta-D-glucopyranosyl residue at position 4 via a glycosidic linkage. It has been isolated from Olea europaea. It has a role as a plant metabolite. It is a glycosyloxyflavone, a monosaccharide derivative, a beta-D-glucoside and a trihydroxyflavone. It is functionally related to a luteolin.
Luteolin-4-o-glucoside is a natural product found in Leontodon saxatilis, Urospermum dalechampii, and other organisms with data available.
A glycosyloxyflavone that is luteolin substituted by a beta-D-glucopyranosyl residue at position 4 via a glycosidic linkage. It has been isolated from Olea europaea.

同义名列表

11 个代谢物同义名

5,7-dihydroxy-2-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-phenyl]chromen-4-one; 5,7-dihydroxy-2-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one; 4H-1-Benzopyran-4-one, 2-[4-(.beta.-D-glucopyranosyloxy)-3-hydroxyphenyl]-5,7-dihydroxy-; 4-(5,7-dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2-hydroxyphenyl beta-D-glucopyranoside; 5,7,3-trihydroxyflavone 4-O-beta-D-glucopyranoside; 3,4,5,7-Tetrahydroxyflavone 4-.beta.-D-glucoside; luteolin-4-o-beta-d-glucopyranoside; UHNXUSWGOJMEFO-QNDFHXLGSA-N; luteolin 4-O-glucoside; Luteolin-4-O-glucoside; Luteolin-4Glucoside



数据库引用编号

7 个数据库交叉引用编号

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)

0 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

  • Elbert van der Klift, Alexandre Villela, Goverdina C H Derksen, Peter P Lankhorst, Teris A van Beek. Microextraction of Reseda luteola-Dyed Wool and Qualitative Analysis of Its Flavones by UHPLC-UV, NMR and MS. Molecules (Basel, Switzerland). 2021 Jun; 26(13):. doi: 10.3390/molecules26133787. [PMID: 34206334]
  • Chen Zeng, Siyuan Luo, Shiling Feng, Tao Chen, Lijun Zhou, Ming Yuan, Yan Huang, Jinqiu Liao, Chunbang Ding. Phenolic Composition, Antioxidant and Anticancer Potentials of Extracts from Rosa banksiae Ait. Flowers. Molecules (Basel, Switzerland). 2020 Jul; 25(13):. doi: 10.3390/molecules25133068. [PMID: 32640514]
  • Yan Lin, Pei-Gang Liu, Wei-Qing Liang, Yi-Juan Hu, Pan Xu, Jie Zhou, Jin-Bao Pu, Hong-Jian Zhang. Luteolin-4'-O-glucoside and its aglycone, two major flavones of Gnaphalium affine D. Don, resist hyperuricemia and acute gouty arthritis activity in animal models. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2018 Mar; 41(?):54-61. doi: 10.1016/j.phymed.2018.02.002. [PMID: 29519319]
  • Souichi Nakashima, Yoshimi Oda, Seikou Nakamura, Jiang Liu, Koko Onishi, Miki Kawabata, Hisako Miki, Yugo Himuro, Masayuki Yoshikawa, Hisashi Matsuda. Inhibitors of melanogenesis in B16 melanoma 4A5 cells from flower buds of Lawsonia inermis (Henna). Bioorganic & medicinal chemistry letters. 2015 Jul; 25(13):2702-6. doi: 10.1016/j.bmcl.2015.04.052. [PMID: 25987378]
  • Chi-Chih Chang, Sheau Ling Ho, Shoei-Sheng Lee. Acylated glucosylflavones as α-glucosidase inhibitors from Tinospora crispa leaf. Bioorganic & medicinal chemistry. 2015 Jul; 23(13):3388-96. doi: 10.1016/j.bmc.2015.04.053. [PMID: 25999202]
  • Filipa Marcelo, Catarina Dias, Alice Martins, Paulo J Madeira, Tiago Jorge, M Helena Florêncio, F Javier Cañada, Eurico J Cabrita, Jesús Jiménez-Barbero, Amélia P Rauter. Molecular recognition of rosmarinic acid from Salvia sclareoides extracts by acetylcholinesterase: a new binding site detected by NMR spectroscopy. Chemistry (Weinheim an der Bergstrasse, Germany). 2013 May; 19(21):6641-9. doi: 10.1002/chem.201203966. [PMID: 23536497]
  • Qun Sun, Ye Lu, Shuang-Qing Wu, Shi Yao, Jian Zhang. [Study on the chemical constituents from Gnaphalium hypoleucum]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2012 Apr; 35(4):566-8. doi: ". [PMID: 23019902]
  • Yihui Yang, Xianmei Piao, Mingyu Zhang, Xiaodan Wang, Bing Xu, Jiuxin Zhu, Zhiwei Fang, Yunlong Hou, Yanjie Lu, Baofeng Yang. Bioactivity-guided fractionation of the triglyceride-lowering component and in vivo and in vitro evaluation of hypolipidemic effects of Calyx seu Fructus Physalis. Lipids in health and disease. 2012 Mar; 11(?):38. doi: 10.1186/1476-511x-11-38. [PMID: 22413998]
  • Sara Vitalini, Giangiacomo Beretta, Marcello Iriti, Simone Orsenigo, Nicoletta Basilico, Stefano Dall'Acqua, Maria Iorizzi, Gelsomina Fico. Phenolic compounds from Achillea millefolium L. and their bioactivity. Acta biochimica Polonica. 2011; 58(2):203-9. doi: 10.18388/abp.2011_2266. [PMID: 21503279]
  • Yuanhu Zhang, Li He, Huanyu Guan, Jiming Zhang, Xiaosheng Yang. [Flavonoids of Lysimachia paridiformis var. stenophylla]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2010 Jul; 35(14):1824-6. doi: 10.4268/cjcmm20101412. [PMID: 20939277]
  • Giovanni Agati, Giovanni Stefano, Stefano Biricolti, Massimiliano Tattini. Mesophyll distribution of 'antioxidant' flavonoid glycosides in Ligustrum vulgare leaves under contrasting sunlight irradiance. Annals of botany. 2009 Oct; 104(5):853-61. doi: 10.1093/aob/mcp177. [PMID: 19633310]
  • Cristina Moiteiro, Helena Gaspar, Ana I Rodrigues, João F Lopes, Valdemar Carnide. HPLC quantification of dye flavonoids in Reseda luteola L. from Portugal. Journal of separation science. 2008 Dec; 31(21):3683-7. doi: 10.1002/jssc.200800383. [PMID: 19003809]
  • G Innocenti, E Vegeto, S Dall'Acqua, P Ciana, M Giorgetti, E Agradi, A Sozzi, G Fico, F Tomè. In vitro estrogenic activity of Achillea millefolium L. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2007 Feb; 14(2-3):147-52. doi: 10.1016/j.phymed.2006.05.005. [PMID: 16860978]
  • Stefan Schwaiger, Christoph Seger, Bettina Wiesbauer, Peter Schneider, Ernst P Ellmerer, Sonja Sturm, Hermann Stuppner. Development of an HPLC-PAD-MS assay for the identification and quantification of major phenolic edelweiss (Leontopodium alpium Cass.) constituents. Phytochemical analysis : PCA. 2006 Sep; 17(5):291-8. doi: 10.1002/pca.917. [PMID: 17019930]
  • Yashodharan Kumarasamy, Lutfun Nahar, Maureen Byres, Abbas Delazar, Satyajit D Sarker. The assessment of biological activities associated with the major constituents of the methanol extract of 'wild carrot' (Daucus carota L) seeds. Journal of herbal pharmacotherapy. 2005; 5(1):61-72. doi: ". [PMID: 16093236]
  • Liselotte Krenn, Anca Miron, Enne Pemp, Ursula Petr, Brigitte Kopp. Flavonoids from Achillea nobilis L. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2003 Jan; 58(1-2):11-6. doi: 10.1515/znc-2003-1-202. [PMID: 12622219]
  • Ming Hong Lee, Yeon Kyoung Son, Yong Nam Han. Tissue factor inhibitory flavonoids from the fruits of Chaenomeles sinensis. Archives of pharmacal research. 2002 Dec; 25(6):842-50. doi: 10.1007/bf02977002. [PMID: 12510836]
  • F Z Ren, X H Luan, Y M Zhao, H H Qu. [Studies on flavonoids from leaves of Callicarpa bodinieri Levl]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2001 Dec; 26(12):841-4. doi: ". [PMID: 12776333]
  • A Braca, N De Tommasi, L Di Bari, C Pizza, M Politi, I Morelli. Antioxidant principles from Bauhinia tarapotensis. Journal of natural products. 2001 Jul; 64(7):892-5. doi: 10.1021/np0100845. [PMID: 11473417]
  • K Y Park, S H Lee, B K Min, K S Lee, J S Choi, S R Chung, K R Min, Y Kim. Inhibitory effect of luteolin 4'-O-glucoside from Kummerowia striata and other flavonoids on interleukin-5 bioactivity. Planta medica. 1999 Jun; 65(5):457-9. doi: 10.1055/s-2006-960812. [PMID: 10418337]