Rutin (BioDeep_00000000225)

 

Secondary id: BioDeep_00000242252, BioDeep_00000332518, BioDeep_00000896012

natural product human metabolite PANOMIX_OTCML-2023 blood metabolite PANOMIX-Anthocyanidin BioNovoGene_Lab2019 Volatile Flavor Compounds


代谢物信息卡片


2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one;Rutin

化学式: C27H30O16 (610.153378)
中文名称: 维生素 P, 紫槲皮甙, 路丁粉, 紫皮甙, 芸香甙, 路丁, 芦丁, 络通, 槲皮素 3-O-洋槐糖苷, 槲皮素3-O-芸香糖苷, 芸香苷水合物
谱图信息: 最多检出来源 Homo sapiens(blood) 1.52%

分子结构信息

SMILES: c(c5)(O)cc(c(c52)C(C(O[C@H](O3)[C@@H]([C@H]([C@@H]([C@H]3CO[C@@H]([C@@H]4O)O[C@H]([C@@H]([C@H]4O)O)C)O)O)O)=C(O2)c(c1)ccc(O)c1O)=O)O
InChI: InChI=1/C27H30O16/c1-8-17(32)20(35)22(37)26(40-8)39-7-15-18(33)21(36)23(38)27(42-15)43-25-19(34)16-13(31)5-10(28)6-14(16)41-24(25)9-2-3-11(29)12(30)4-9/h2-6,8,15,17-18,20-23,26-33,35-38H,7H2,1H3/t8-,15+,17-,18+,20+,21-,22+,23+,26+,27-/m0/s1

描述信息

Rutin is a flavonoid known to have a variety of biological activities including antiallergic, anti-inflammatory, antiproliferative, and anticarcinogenic properties. A large number of flavonoids, mostly O-glycosides, are polyphenolic compounds of natural origin that are present in most fruits and vegetables. The average intake of the compounds by humans on a normal diet is more than 1 g per day. Although flavonoids are devoid of classical nutritional value, they are increasingly viewed as beneficial dietary components that act as potential protectors against human diseases such as coronary heart disease, cancers, and inflammatory bowel disease. Rutin acts as a quercetin deliverer to the large intestine; moreover, quercetin is extensively metabolized in the large intestine, which suggests that quercetin liberated from rutin and/or its colonic metabolites may play a role. Rutins anti-inflammatory actions are mediated through a molecular mechanism that underlies the quercetin-mediated therapeutic effects: quercetin-mediated inhibition of tumor necrosis factor-alpha (TNF-alpha)-induced nuclear factor kappa B (NFkB) activation. TNF-alpha-induced NFkB activity plays a central role in the production of pro-inflammatory mediators involved in progression of gut inflammation. (PMID:16132362).
Rutin is a rutinoside that is quercetin with the hydroxy group at position C-3 substituted with glucose and rhamnose sugar groups. It has a role as a metabolite and an antioxidant. It is a disaccharide derivative, a quercetin O-glucoside, a tetrahydroxyflavone and a rutinoside.
A flavonol glycoside found in many plants, including buckwheat; tobacco; forsythia; hydrangea; viola, etc. It has been used therapeutically to decrease capillary fragility.
Rutin is a natural product found in Ficus virens, Visnea mocanera, and other organisms with data available.
A flavonol glycoside found in many plants, including BUCKWHEAT; TOBACCO; FORSYTHIA; HYDRANGEA; VIOLA, etc. It has been used therapeutically to decrease capillary fragility.
See also: Quercetin (related); Ginkgo (part of); Chamomile (part of) ... View More ...
First isolated from Ruta graveolens (rue). Bioflavanoid. Quercetin 3-rutinoside is found in many foods, some of which are tea, bilberry, common oregano, and lemon grass.
A rutinoside that is quercetin with the hydroxy group at position C-3 substituted with glucose and rhamnose sugar groups.
C - Cardiovascular system > C05 - Vasoprotectives > C05C - Capillary stabilizing agents > C05CA - Bioflavonoids
IPB_RECORD: 541; CONFIDENCE confident structure
[Raw Data] CBA04_Rutin_neg_50eV.txt
[Raw Data] CBA04_Rutin_pos_50eV.txt
[Raw Data] CBA04_Rutin_neg_40eV.txt
[Raw Data] CBA04_Rutin_pos_10eV.txt
[Raw Data] CBA04_Rutin_neg_20eV.txt
[Raw Data] CBA04_Rutin_neg_10eV.txt
[Raw Data] CBA04_Rutin_neg_30eV.txt
[Raw Data] CBA04_Rutin_pos_40eV.txt
[Raw Data] CBA04_Rutin_pos_30eV.txt
[Raw Data] CBA04_Rutin_pos_20eV.txt
Rutin (Rutoside) is a flavonoid found in many plants and shows a wide range of biological activities including anti-inflammatory, antidiabetic, antioxidant, neuroprotective, nephroprotective, hepatoprotective and reducing Aβ oligomer activities. Rutin can cross the blood brain barrier. Rutin attenuates vancomycin-induced renal tubular cell apoptosis via suppression of apoptosis, mitochondrial dysfunction, and oxidative stress[1][2][3].
Rutin (Rutoside) is a flavonoid found in many plants and shows a wide range of biological activities including anti-inflammatory, antidiabetic, antioxidant, neuroprotective, nephroprotective, hepatoprotective and reducing Aβ oligomer activities. Rutin can cross the blood brain barrier. Rutin attenuates vancomycin-induced renal tubular cell apoptosis via suppression of apoptosis, mitochondrial dysfunction, and oxidative stress[1][2][3].

同义名列表

187 个代谢物同义名

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one;Rutin; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yloxy)methyl)tetrahydro-2H-pyran-2-yloxy)-4H-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-4H-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one; 2-(3,4-dihydroxyphenyl)-4,5-dihydroxy-3-(3,4,5-trihydroxy-6-((3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl)oxymethyl)tetrahydropyran-2-yl)oxy-chromen-7-one; 4H-1-Benzopyran-4-one, 3-[[6-O-(6-deoxy-.alpha.-L-mannopyranosyl)-.beta.-D-glucopyranosyl]-oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-; 4H-1-Benzopyran-4-one, 3-[[6-O-(6-deoxy-.alpha.-L-mannopyranosyl)-.beta.-D-glucopyranosyl]oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-; 4H-1-Benzopyran-4-one, 3-((6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl)oxy)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-; 3-((6-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl)oxy)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one; 3-[[6-O-(6-Deoxy-alpha-l-mannopyranosyl)-beta-d-glucopyranosyl]oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one; 4H-1-Benzopyran-4-one,3-[[6-O-(6-deoxy-a-L-mannopyranosyl)-b-D-glucopyranosyl]oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-; 3-[[6-O-(6-Deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one; 3-[[6-O-(6-Deoxy-a-L-mannopyranosyl)-b-D-glucopyranosyl]oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one; 2-(3,4-DIHYDROXYPHENYL)-5,7-DIHYDROXY-4-OXO-4H-CHROMEN-3-YL 6-O-(6-DEOXY-ALPHA-L-MANNOPYRANOSYL)-BETA-D-GLUCOPYRANOSIDE; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl 6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-mannopyranoside; 2-(3,4-DIHYDROXYPHENYL)-5,7-DIHYDROXY-4H-CHROMEN-4-ONE-3-YL 6-O-.ALPHA.-L-RHAMNOPYRANOSYL-.BETA.-D-GLUCOSIDE; Rutinoside, 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl; Glucopyranoside, quercetin-3 6-O-(6-deoxy-alpha-L-mannopyranosyl)-, beta-D-; Quercetin, 3-(6-0-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside); 3,3,4,5,5,7-Hexahydroxyflavone (6-O-alpha-L-rhamnosyl-beta-D-glucoside); Quercetin-3-O-[alpha-L-rhamnopyranosyl-(1->6)-beta-D-glucopyranoside]; Quercetin-3-O-[alpha-L-rhamnopyranosyl-(1→6)-beta-D-glucopyranoside]; Quercetin 3-O-alpha-L-rhamnopyranosyl-(1->6)-beta-D-glucopyranoside; Quercetin 3-O-alpha-L-rhamnopyranosyl-(1→6)-beta-D-glucopyranoside; Quercetin, 3-(6-O-alpha-L-rhamnopyranosyl-beta-D-glucopyranoside); Quercetin 3-O-beta-D-(6-O-alpha-L-rhamnopyranosyl)glucopyranoside; Glucopyranoside, quercetin-3 6-O-alpha-L-rhamnopyranosyl-, beta-D; QUERCETIN 3-O-.ALPHA.-L-RHAMNOPYRANOSYL-.BETA.-D-GLUCOPYRANOSIDE; Quercetin 3-O-alpha-rhamnopyranosyl(1->6)-beta-D-glucopyranoside; Quercetin 3-(6-O-alpha-L-rhamnopyranosyl-beta-D-glucopyranoside); Quercetin 3-O-alpha-rhamnopyranosyl-(1->6)-beta-glucopyranoside; Quercetin 3-O-alpha-rhamnopyranosyl(1→6)-beta-D-glucopyranoside; RUTIN (QUERCETIN-3-O-RUTINOSIDE) (CONSTITUENT OF GINKGO) [DSC]; Quercetin 3-O-alpha-rhamnopyranosyl-(1→6)-beta-glucopyranoside; Quercetin 3-O-alpha-rhamnopyranosyl(1->6)-beta-glucopyranoside; Quercetin 3-O-alpha-rhamnopyranosyl(1→6)-beta-glucopyranoside; Quercetin-3-O-[α-L-rhamnopyranosyl-(1→6)-β-D-glucopyranoside]; Quercetin 3-O-β-D-(6’’-O-α-L-rhamnopyranosyl)glucopyranoside; Quercetin 3-O-alpha-L-rhamnopyranosyl-beta-D-glucopyranoside; Quercetin 3-O-α-rhamnopyranosyl-(1’’’→6’’)-β-glucopyranoside; Quercetin 3-O-α-rhamnopyranosyl(1’’→6’)-β-D-glucopyranoside; Quercetin 3-O-α-L-rhamnopyranosyl-(1→6)-β-D-glucopyranoside; Quercetin 3-O-β-D-(6-O-α-L-rhamnopyranosyl)glucopyranoside; Flavone, 3,3,4,5,7-pentahydroxy-, 3-(O-rhamnosylglucoside); Quercetin 3-(6-O-α-L-rhamnopyranosyl-β-D-glucopyranoside); quercetin 3-O-[alpha-L-rhamnosyl-(1->6)-beta-D-glucoside]; Quercetin 3-O-α-rhamnopyranosyl(1→6)-β-D-glucopyranoside; Quercetin 3-O-α-rhamnopyranosyl-(1→6)-β-glucopyranoside; Quercetin 3-O-α-rhamnopyranosyl(1→6)-β-glucopyranoside; Quercetin 3-O-α-L-rhamnopyranosyl-β-D-glucopyranoside; 3-Rhamnoglucoside of 3,3,4,5,7-pentahydroxyflavone; 3-RHAMNOGLUCOSIDE OF 5,7,3,4-TETRAHYDROXYFLAVONOL; Quercetin 6-O-alpha-L-rhamnosyl-beta-D-glucoside; 3,3,4,5,7-PENTAHYDROXYFLAVONE-3-RHAMNOGLUCOSIDE; 3,3’,4’,5,7-Pentahydroxyflavone 3-O-rutinoside; 5,7,3’,4’-Tetrahydroxyflavonol-3-O-rutinoside; tetrahydro-2H-pyran-2-yloxy)-4H-chromen-4-one; 3,3,4,5,7-Pentahydroxyflavone 3-O-rutinoside; 5-18-05-00519 (Beilstein Handbook Reference); 3,3’,4’,5,7-Pentahydroxyflavone 3-rutinoside; 5,7,3,4-Tetrahydroxyflavonol-3-O-rutinoside; 3,3,4,5,7-Pentahydroxyflavone-3-rutinoside; 3,3,4,5,7-Pentahydroxyflavone 3-rutinoside; Quercetin 6-O-α-L-rhamnosyl-β-D-glucoside; methyltetrahydro-2H-pyran-2-yloxy)methyl); Quercetin 3-O-alpha-L-rhamnopyranosyl-(1-; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3; -((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-; Quercetin 3-O-beta-delta-rutinoside; (+)-Quercetin 3-O-beta-rutinoside; Quercetin, 3-Rhamnosyl-Glucosyl; Quercetin 3-O-beta-D-rutinoside; Rutin from Sophora japonica L.; 3-Rhamnosyl-Glucosyl Quercetin; Rutinoside, quercetin-3, beta-; Quercetin 3-O-beta-rutinoside; Quercetin 3-O-β-D-rutinoside; (+)-Quercetin 3-O-rutinoside; Quercetin 3-beta-rutinoside; Quercetin 3-rhamnoglucoside; Quercetol 3-rhamnoglucoside; beta-Quercetin-3-rutinoside; Quercetin-3beta-rutinoside; Quercetin 3-O-β-rutinoside; 3-Rhamnoglucosylquercetin; 6)-beta-D-glucopyranoside; Quercetin rhamnoglucosine; 345,7-tetOH-Flavone-3-rut; quercetin-3-O-rutinoside; Quercetin 3-β-rutinoside; Quercetin 3-O-rutinoside; 3-O-Rutinosylquercetin; Quercetin-3-rutinoside; Rutosido (INN-Spanish); Quercetin 3-rutinoside; Rutosido [INN-Spanish]; Quercetin 3 Rutinoside; Quercitin 3-rutinoside; 3-Rutinosyl quercetin; Rutoside [INN:JAN:NF]; Rutosidum (INN-Latin); Rutosidum [INN-Latin]; 3-Rutinosylquercetin; hydroxyethylrutoside; Quercetin rutinoside; RUTOSIDE [WHO-DD]; Rutin (Rutoside); Rutoside (rutin); Globulariacitrin; Rutin trihydrate; Violaquercetrin; Globularicitrin; Violaquercitrin; UNII-5G06TVY3R7; Rutin [JAN:NF]; Tox21_111945_1; Rutoside (INN); Not Applicable; RUTIN (USP-RS); Venoruton (TN); RUTIN [USP-RS]; Rutoside [INN]; Rutin, Powder; DivK1c_000644; MEGxp0_000068; RUTIN [VANDF]; Rutinion acid; Birutan Forte; Rutinic acid; ACon1_000075; KBio1_000644; Bioflavonoid; RUTIN [INCI]; Tox21_111945; Myrticolorin; Myrticalorin; Tox21_202602; Neoisorutin; Novarrutina; Paliuroside; Myticolorin; IDI1_000644; RUTIN [DSC]; Yunxianggan; Phytomelin; RUTIN [MI]; Ilixanthin; Troxerutin; 5G06TVY3R7; Rutin,(S); AI3-19098; Rutosidum; Osyritrin; Ilixathin; Venoruton; USAF CF-5; Vitamin P; Tanrutin; Rutabion; Sophorin; Oxyritin; Rutosido; rutoside; Rutinum; Birutin; Rutosid; Rutozid; C05CA01; Rutozyd; Birutan; Rutine; Eldrin; Melin; Rutin; RUT; Quercetin 3-O-β-δ-rutinoside; Quercetin 3-O-β-D-rutinoside; β-quercetin-3Rutinoside; Quercetin 3-O-rhamnosyl-(1-; Quercetin 3-O-robinobioside; Quercetin 3-O-robibioside; Quercetin 3-O-robinoside; Quercetin 3-robinoside; 6)-galactoside; Rutin



数据库引用编号

67 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(5)

PlantCyc(5)

代谢反应

15 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(4)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(11)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

1980 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。



文献列表

  • Libo Wang, Yilin Huang, Yanjuan Ren, Haoran Wang, Yue Ding, Guangyue Ren, Tongtong Wang, Zaigui Li, Ju Qiu. Effect of ethanol addition on the physicochemical, structural and in vitro digestive properties of Tartary buckwheat starch-quercetin/rutin complexes. Food chemistry. 2024 Sep; 451(?):139350. doi: 10.1016/j.foodchem.2024.139350. [PMID: 38663246]
  • Yinsheng Wu, Yong Wang, Fengyan Chen, Bingzhang Wang. Loading rutin on surfaces by the layer-by-layer assembly technique to improve the oxidation resistance and osteogenesis of titanium implants in osteoporotic rats. Biomedical materials (Bristol, England). 2024 May; 19(4):. doi: 10.1088/1748-605x/ad4aa8. [PMID: 38740037]
  • Kseniya Bushmeleva, Alexandra Vyshtakalyuk, Dmitriy Terenzhev, Timur Belov, Evgeniy Nikitin, Vladimir Zobov. Effect of Flavonols of Aronia melanocarpa Fruits on Morphofunctional State of Immunocompetent Organs of Rats under Cyclophosphamide-Induced Immunosuppression. Biomolecules. 2024 May; 14(5):. doi: 10.3390/biom14050578. [PMID: 38785985]
  • Dili Lai, Kaixuan Zhang, Yuqi He, Yu Fan, Wei Li, Yaliang Shi, Yuanfen Gao, Xu Huang, Jiayue He, Hui Zhao, Xiang Lu, Yawen Xiao, Jianping Cheng, Jingjun Ruan, Milen I Georgiev, Alisdair R Fernie, Meiliang Zhou. Multi-omics identification of a key glycosyl hydrolase gene FtGH1 involved in rutin hydrolysis in Tartary buckwheat (Fagopyrum tataricum). Plant biotechnology journal. 2024 May; 22(5):1206-1223. doi: 10.1111/pbi.14259. [PMID: 38062934]
  • Tongtong Yi, Wei Zhang, Ying Hua, Xingpan Xin, Zhenyu Wu, Ying Li, Chengping Wen, Yongsheng Fan, Jinjun Ji, Li Xu. Rutin alleviates lupus nephritis by inhibiting T cell oxidative stress through PPARγ. Chemico-biological interactions. 2024 May; 394(?):110972. doi: 10.1016/j.cbi.2024.110972. [PMID: 38555047]
  • Yanmei Shi, Kai Hu, Lin Mei, Liqin Chao, Mingxia Wu, Zhihong Chen, Xiangxiang Wu, Jingyi Qiao, Pingsheng Zhu, Mingsan Miao, Sisen Zhang. Platforms of graphene/MXene heterostructure for electrochemical monitoring of rutin in drug and Tartary buckwheat tea. Talanta. 2024 Apr; 270(?):125548. doi: 10.1016/j.talanta.2023.125548. [PMID: 38104427]
  • Yadi Liu, Zhongyan Sun, Ruixue Dong, Peiyu Liu, Xi Zhang, Yiran Li, Xiaoshan Lai, Hio-Fai Cheong, Yuwei Wu, Yilin Wang, Hua Zhou, Dingkun Gui, Youhua Xu. Rutin ameliorated lipid metabolism dysfunction of diabetic NAFLD via AMPK/SREBP1 pathway. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2024 Apr; 126(?):155437. doi: 10.1016/j.phymed.2024.155437. [PMID: 38394735]
  • Youwei Du, Huiya Ma, Yuanyuan Liu, Rui Gong, Yu Lan, Jianhua Zhao, Guangli Liu, Yiming Lu, Shuanghong Wang, Hongchen Jia, Na Li, Rong Zhang, Junru Wang, Guangyu Sun. Major quality regulation network of flavonoid synthesis governing the bioactivity of black wolfberry. The New phytologist. 2024 Apr; 242(2):558-575. doi: 10.1111/nph.19602. [PMID: 38396374]
  • M Mesud Hurkul, Seyda Yayla, Ahmet Cetinkaya, S Irem Kaya, Lokman Uzun, Sibel A Ozkan. A novel electrochemical sensor based on a molecularly imprinted polymer for highly selective and sensitive determination of rutin from herbal supplements and plant extracts. Analytical methods : advancing methods and applications. 2024 Mar; 16(10):1480-1488. doi: 10.1039/d3ay02318d. [PMID: 38372557]
  • Magdalena Lasota, Paulina Lechwar, Wirginia Kukula-Koch, Marcin Czop, Karolina Czech, Katarzyna Gaweł-Bęben. Pulp or Peel? Comparative Analysis of the Phytochemical Content and Selected Cosmetic-Related Properties of Annona cherimola L., Diospyros kaki Thumb., Cydonia oblonga Mill. and Fortunella margarita Swingle Pulp and Peel Extracts. Molecules (Basel, Switzerland). 2024 Mar; 29(5):. doi: 10.3390/molecules29051133. [PMID: 38474645]
  • Lei Wang, Jiali Zhao, Yuanbin Mao, Linling Liu, Chenglei Li, Huala Wu, Haixia Zhao, Qi Wu. Tartary buckwheat rutin: Accumulation, metabolic pathways, regulation mechanisms, and biofortification strategies. Plant physiology and biochemistry : PPB. 2024 Mar; 208(?):108503. doi: 10.1016/j.plaphy.2024.108503. [PMID: 38484679]
  • N D H Cheong, E Mohamed, N Haron, S N Camalxaman, A Abdullah, M I Mohamad Yusof, A R Ishak, S Ab-Rahim, Z Eshak, A R Tualeka. Phytochemical quantification and HPLC analysis of Parkia speciosa pod extract. The Medical journal of Malaysia. 2024 Mar; 79(Suppl 1):34-39. doi: ". [PMID: 38555883]
  • Jayshree V Changade, Harsha Thanvi, Chandrashekhar Raut, Manasi Chavan, Prachi Prasad, Vaibhav S Ladke. In vitro Evaluation of Anti-Cancer Potential of Different Solvent Extracts Derived from Clerodendrum Infortunatum Linn against Cervical Cancer. Asian Pacific journal of cancer prevention : APJCP. 2024 Mar; 25(3):1065-1075. doi: 10.31557/apjcp.2024.25.3.1065. [PMID: 38546089]
  • Nattira On-Nom, Sirinapa Thangsiri, Woorawee Inthachat, Piya Temviriyanukul, Yuraporn Sahasakul, Amornrat Aursalung, Chaowanee Chupeerach, Uthaiwan Suttisansanee. Optimized Conditions for the Extraction of Phenolic Compounds from Aeginetia indica L. and Its Potential Biological Applications. Molecules (Basel, Switzerland). 2024 Feb; 29(5):. doi: 10.3390/molecules29051050. [PMID: 38474563]
  • Dennis Soosai, Ravindhran Ramalingam, Elumalai Perumal, Kaviarasan Veeramani, Charles Pancras, Mikhlid H Almutairi, Leo Arockia Raj Savarimuthu, Duraipandiyan Veeramuthu, Stalin Antony. Anticancer effects of rutin from Fagopyrum tataricum (tartary buckwheat) against osteosarcoma cell line. Molecular biology reports. 2024 Feb; 51(1):312. doi: 10.1007/s11033-024-09218-w. [PMID: 38374412]
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