Quercitrin (BioDeep_00000000015)

 

Secondary id: BioDeep_00000270677

natural product human metabolite PANOMIX_OTCML-2023


代谢物信息卡片


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

化学式: C21H20O11 (448.100557)
中文名称: 榭黄甙, 槲皮甙, 槲皮苷, 橡皮甙, 栎素
谱图信息: 最多检出来源 Viridiplantae(plant) 0.09%

Reviewed

Last reviewed on 2024-07-09.

Cite this Page

Quercitrin. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/quercitrin (retrieved 2024-11-03) (BioDeep RN: BioDeep_00000000015). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: c1(cc(c2c(c1)oc(c(c2=O)O[C@@H]1O[C@H]([C@@H]([C@H]([C@@H]1O)O)O)C)c1ccc(c(c1)O)O)O)O
InChI: InChI=1/C21H20O11/c1-7-15(26)17(28)18(29)21(30-7)32-20-16(27)14-12(25)5-9(22)6-13(14)31-19(20)8-2-3-10(23)11(24)4-8/h2-7,15,17-18,21-26,28-29H,1H3/t7-,15-,17+,18+,21-/m0/s1

描述信息

Quercitrin, also known as quercimelin or quercitronic acid, belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position. A quercetin O-glycoside that is quercetin substituted by a alpha-L-rhamnosyl moiety at position 3 via a glycosidic linkage. Quercitrin exists in all living organisms, ranging from bacteria to humans. Quercitrin is found, on average, in the highest concentration within a few different foods, such as lingonberries, american cranberries, and olives and in a lower concentration in common beans, tea, and welsh onions. Quercitrin has also been detected, but not quantified, in several different foods, such as guava, bilberries, common pea, apricots, and spearmints.
Quercitrin is a quercetin O-glycoside that is quercetin substituted by a alpha-L-rhamnosyl moiety at position 3 via a glycosidic linkage. It has a role as an antioxidant, an antileishmanial agent, an EC 1.1.1.184 [carbonyl reductase (NADPH)] inhibitor, an EC 1.1.1.21 (aldehyde reductase) inhibitor, an EC 1.14.18.1 (tyrosinase) inhibitor and a plant metabolite. It is a monosaccharide derivative, a tetrahydroxyflavone, an alpha-L-rhamnoside and a quercetin O-glycoside. It is a conjugate acid of a quercitrin-7-olate.
Quercitrin is a natural product found in Xylopia emarginata, Lotus ucrainicus, and other organisms with data available.
Quercitrin is a glycoside formed from the flavonoid quercetin and the deoxy sugar rhamnose. It is a constituent of the dye quercitron. Quercitrin is found in many foods, some of which are garden tomato (variety), kiwi, italian sweet red pepper, and guava.
A quercetin O-glycoside that is quercetin substituted by a alpha-L-rhamnosyl moiety at position 3 via a glycosidic linkage.

[Raw Data] CBA03_Quercitrin_pos_10eV.txt
[Raw Data] CBA03_Quercitrin_pos_20eV.txt
[Raw Data] CBA03_Quercitrin_neg_50eV.txt
[Raw Data] CBA03_Quercitrin_neg_30eV.txt
[Raw Data] CBA03_Quercitrin_neg_10eV.txt
[Raw Data] CBA03_Quercitrin_neg_40eV.txt
[Raw Data] CBA03_Quercitrin_neg_20eV.txt
[Raw Data] CBA03_Quercitrin_pos_50eV.txt
[Raw Data] CBA03_Quercitrin_pos_30eV.txt
[Raw Data] CBA03_Quercitrin_pos_40eV.txt

Quercitrin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=522-12-3 (retrieved 2024-07-09) (CAS RN: 522-12-3). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Quercitrin (Quercetin 3-rhamnoside) is a bioflavonoid compound with potential anti-inflammation, antioxidative and neuroprotective effect. Quercitrin induces apoptosis of colon cancer cells. Quercitrin can be used for the research of cardiovascular and neurological disease research[1][2].
Quercitrin (Quercetin 3-rhamnoside) is a bioflavonoid compound with potential anti-inflammation, antioxidative and neuroprotective effect. Quercitrin induces apoptosis of colon cancer cells. Quercitrin can be used for the research of cardiovascular and neurological disease research[1][2].
Quercitrin (Quercetin 3-rhamnoside) is a bioflavonoid compound with potential anti-inflammation, antioxidative and neuroprotective effect. Quercitrin induces apoptosis of colon cancer cells. Quercitrin can be used for the research of cardiovascular and neurological disease research[1][2].

同义名列表

105 个代谢物同义名

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yloxy)-4H-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-4H-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one; 4H-1-Benzopyran-4-one, 3-((6-deoxy-.alpha.-L-mannopyranosyl)oxy)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-; 4H-1-Benzopyran-4-one, 3-[(6-deoxy-.alpha.-L-mannopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-; 4H-1-Benzopyran-4-one, 3-((6-deoxy-alpha-L-mannopyranosyl)oxy)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-; 3-((6-Deoxy-alpha-L-mannopyranosyl)-oxy)-2-(3,4-dihydr oxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one; 3-((6-DEOXY-.ALPHA.-L-MANNOPYRANOSYL)OXY)-2-(3,4-DIHYDROXYPHENYL)-5,7-DIHYDROXY-4H-1-BENZOPYRAN-4-ONE; 3-((6-Deoxy-alpha-L-mannopyranosyl)-oxy)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one; 3-((6-DEOXY-alpha-L-MANNOPYRANOSYL)OXY)-2-(3,4-DIHYDROXYPHENYL)-5,7-DIHYDROXY-4H-1-BENZOPYRAN-4-ONE; 3-((6-Deoxy-alpha-L-mannopyranosyl)oxy)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-benzopyran-4-one; 3-((6-Deoxy-α-L-mannopyranosyl)-oxy)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one; 3-((6-Deoxy-a-L-mannopyranosyl)-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-deoxy-.alpha.-L-mannopyranoside; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl 6-deoxy-alpha-L-mannopyranoside; Flavone, 3,3,4,5,7-pentahydroxy-, 3-(6-deoxy-alpha-L-mannopyranoside); QUERCITRIN (QUERCETIN-3-O- RHAMNOSIDE) (CONSTITUENT OF GINKGO) [DSC]; QUERCITRIN (QUERCETIN-3-O-RHAMNOSIDE) (CONSTITUENT OF GINKGO); 3-O-a-L-Rhamnopyranosyloxy-3,4,5,7-tetrahydroxyflavone; Quercitrin, primary pharmaceutical reference standard; 5,7,3,4-Tetrahydroxyflavone 3-O-alpha-L-rhamnoside; 3,3,4,5,7-Pentahydroxyflavone 3-alpha-L-rhamnoside; 3,3’,4’,5,7-Pentahydroxyflavone 3-α-L-rhamnoside; 5,7,3’,4’-Tetrahydroxyflavone 3-O-α-L-rhamnoside; Mannopyranoside, quercetin-3 6-deoxy-, alpha-L-; Flavone, 3,3,4,5, 7-pentahydroxy-, 3-rhamnoside; Quercetin, 3-(6-deoxy-alpha-L-mannopyranoside); 5,7,3,4-Tetrahydroxyflavone 3-O-α-L-rhamnoside; Flavone, 3,3,4,5,7-pentahydroxy-, 3-rhamnoside; 3,3,4,5,7-Pentahydroxyflavone 3-α-L-rhamnoside; 3,3,4,5,7-PENTAHYDROXYFLAVONE 3-L-RHAMNOSIDE; 5-18-05-00514 (Beilstein Handbook Reference); 3,3,4,5,7-Pentahydroxyflavone-3-L-rhamnoside; 5,7,3,4-TETRAHYDROXYFLAVONOL 3-O-RHAMNOSIDE; luteolin 6-deoxy-alpha-L-mannopyranoside; QUERCETIN 3-O-.ALPHA.-L-RHAMNOPYRANOSIDE; QUERCETIN 3-O-.ALPHA.-RHAMNOPYRANOSIDE; quercetin 3-O-alpha-L-rhamnopyranoside; 3-O-.ALPHA.-L-RHAMNOPYRANOSYLQUERCETIN; 3-O-alpha-L-RHAMNOPYRANOSYLQUERCETIN; Luteolin 6-deoxy-α-L-mannopyranoside; quercetin 3-O-alpha-rhamnopyranoside; Luteolin 6-deoxy-a-L-mannopyranoside; Quercetin3-O-alpha-rhamnopyranoside; Quercetin 3-O-α-L-rhamnopyranoside; Quercetin 3-O-a-L-rhamnopyranoside; Quercetin 3-O-.alpha.-L-rhamnoside; quercetin 3-O-alpha-L-rhamnoside; 5-trihydroxy-6-methyltetrahydro-; QUERCETIN-3-O-.ALPHA.-RHAMNOSIDE; 3-O-α-L-Rhamnopyranosylquercetin; Quercetin 3-O-α-rhamnopyranoside; quercetin 3-O-rhamnopyranoside; quercetin-3-O-alpha-rhamnoside; Quercetin 3-O-alpha-rhamnoside; Quercetin 3-alpha-L-rhamnoside; quercetin-3-O-alpha-rhamnosid; Quercetin 3-O-α-L-rhamnoside; Quercetin 3-alpha-rhamnoside; quercetin 3-rhamnopyranoside; OXGUCUVFOIWWQJ-HQBVPOQASA-N; quercetin 3-O-L-rhamnoside; Quercetin 3-O-α-rhamnoside; Quercetin 3-α-L-rhamnoside; quercetin 3-O-rhamnoside; Quercetin-3-O-rhamnoside; quercetin-3-L-rhamnoside; Quercetin 3-L-rhamnoside; 2-(3,4-dihydroxyphenyl)-; Quercetin 3-α-rhamnoside; Rhamnoside, quercetin-3; ((2S,3R,4R,5R,6S)-3,4,; quercetin 3-rhamnoside; 3-O-RHAMNOSYLQUERCETIN; Quercetin-3-rhamnoside; Quercitin-3-rhamnoside; Rhamnosyl-3-quercitin; 3-rhamnosyl quercetin; Quercetin rhamnoside; Quercetrin-3-O-rham; Quercitronic acid; Quercitroside,(S); QUERCITRIN [HSDB]; 5,7-dihydroxy-3-; UNII-2Y8906LC5P; QUERCITRIN [MI]; MEGxp0_000185; quercitroside; Quercitronate; ACon1_000189; SMP1_000253; quercimelin; 2Y8906LC5P; Quercitrin; quercetrin; AI3-36095; Usaf cf-2; thujin; 4gue; QCT; Quercetin 3-O-α-L-rhamnopyranoside; Quercetin-3-O-alpha-L-rhamnopyranoside; Quer_3_Rha



数据库引用编号

79 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

1 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(1)

PharmGKB(0)

671 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

  • Meihe Li, Shan Gao, Minchao Kang, Xuan Zhang, Ping Lan, Xiaoling Wu, Xiaofei Yan, Huimin Dang, Jin Zheng. Quercitrin alleviates lipid metabolism disorder in polycystic ovary syndrome-insulin resistance by upregulating PM20D1 in the PI3K/Akt pathway. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2023 Aug; 117(?):154908. doi: 10.1016/j.phymed.2023.154908. [PMID: 37321077]
  • Qingjie Li, Lianping Wang, Jingwen Xu, Shuang Liu, Zeyu Song, Tingting Chen, Xuming Deng, Jianfeng Wang, Qianghua Lv. Quercitrin Is a Novel Inhibitor of Salmonella enterica Serovar Typhimurium Type III Secretion System. Molecules (Basel, Switzerland). 2023 Jul; 28(14):. doi: 10.3390/molecules28145455. [PMID: 37513327]
  • Lixin Wang, Jinxia Sun, Zhulei Miao, Xin Jiang, Yuejuan Zheng, Guizhen Yang. Quercitrin improved cognitive impairment through inhibiting inflammation induced by microglia in Alzheimer's disease mice. Neuroreport. 2022 05; 33(8):327-335. doi: 10.1097/wnr.0000000000001783. [PMID: 35594435]
  • Junren Chen, Gangmin Li, Chen Sun, Fu Peng, Lei Yu, Yan Chen, Yuzhu Tan, Xiaoyu Cao, Yunli Tang, Xiaofang Xie, Cheng Peng. Chemistry, pharmacokinetics, pharmacological activities, and toxicity of Quercitrin. Phytotherapy research : PTR. 2022 Apr; 36(4):1545-1575. doi: 10.1002/ptr.7397. [PMID: 35253930]
  • Yi Zhou, Zhanqiang Li, Dejun Zhang, Benyin Zhang. Screening of bioactive ingredients of Tsantan Sumtang in ameliorating H9c2 cells injury. Journal of ethnopharmacology. 2022 Mar; 285(?):114854. doi: 10.1016/j.jep.2021.114854. [PMID: 34808301]
  • Wiem Elloumi, Asma Mahmoudi, Sergio Ortiz, Sabrina Boutefnouchet, Mohamed Chamkha, Sami Sayadi. Wound healing potential of quercetin-3-O-rhamnoside and myricetin-3-O-rhamnoside isolated from Pistacia lentiscus distilled leaves in rats model. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2022 Feb; 146(?):112574. doi: 10.1016/j.biopha.2021.112574. [PMID: 35062055]
  • Shi-Tang Ma, Xin-Yuan Zhang, Ning Zhang, Xiao-Lin Bi, Cheng-Tao Feng. Quantitative Determination of Quercitrin Levels in Rat Plasma Using UHPLC-MS/MS and its Application in a Pharmacokinetic Study after the Oral Administration of Polygoni cuspidati Folium Capsules. Current pharmaceutical biotechnology. 2022; 23(3):457-465. doi: 10.2174/1389201022666210519114647. [PMID: 34011255]
  • Norliza Abdul Latiff, Pei Ying Ong, Siti Nor Azlina Abd Rashid, Luqman Chuah Abdullah, Nor Amaiza Mohd Amin, Noor Akhmazillah Mohd Fauzi. Enhancing recovery of bioactive compounds from Cosmos caudatus leaves via ultrasonic extraction. Scientific reports. 2021 08; 11(1):17297. doi: 10.1038/s41598-021-96623-x. [PMID: 34453075]
  • Saulo Duarte Ozelin, Juliana Marques Senedese, Jacqueline Morais Alves, Carla Carolina Munari, Juliana De Carvalho Da Costa, Flávia Aparecida Resende, Débora Leite Campos, Ildercílio Mota De Souza Lima, Augusto Faria Andrade, Eliana Aparecida Varanda, Jairo Kenupp Bastos, Denise Crispim Tavares. Preventive activity of Copaifera langsdorffii Desf. leaves extract and its major compounds, afzelin and quercitrin, on DNA damage in in vitro and in vivo models. Journal of toxicology and environmental health. Part A. 2021 07; 84(14):569-581. doi: 10.1080/15287394.2021.1898505. [PMID: 33730993]
  • Mark J Henderson, Kathleen A Trychta, Shyh-Ming Yang, Susanne Bäck, Adam Yasgar, Emily S Wires, Carina Danchik, Xiaokang Yan, Hideaki Yano, Lei Shi, Kuo-Jen Wu, Amy Q Wang, Dingyin Tao, Gergely Zahoránszky-Kőhalmi, Xin Hu, Xin Xu, David Maloney, Alexey V Zakharov, Ganesha Rai, Fumihiko Urano, Mikko Airavaara, Oksana Gavrilova, Ajit Jadhav, Yun Wang, Anton Simeonov, Brandon K Harvey. A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome. Cell reports. 2021 04; 35(4):109040. doi: 10.1016/j.celrep.2021.109040. [PMID: 33910017]
  • Dimas Rahadian Aji Muhammad, Emmy Tuenter, Graha Darma Patria, Kenn Foubert, Luc Pieters, Koen Dewettinck. Phytochemical composition and antioxidant activity of Cinnamomum burmannii Blume extracts and their potential application in white chocolate. Food chemistry. 2021 Mar; 340(?):127983. doi: 10.1016/j.foodchem.2020.127983. [PMID: 32919354]
  • Hafssa El Cadi, Hajar El Bouzidi, Ginane Selama, Asmae El Cadi, Btissam Ramdan, Yassine Oulad El Majdoub, Filippo Alibrando, Paola Dugo, Luigi Mondello, Asmae Fakih Lanjri, Jamal Brigui, Francesco Cacciola. Physico-Chemical and Phytochemical Characterization of Moroccan Wild Jujube "Zizyphus lotus (L.)" Fruit Crude Extract and Fractions. Molecules (Basel, Switzerland). 2020 Nov; 25(22):. doi: 10.3390/molecules25225237. [PMID: 33182717]
  • Jennyfer Andrea Aldana, Rone Aparecido De Grandis, Heloiza Nicolella, Ana Paula Prado Guissoni, Iara Squarisi, Caroline Arruda, Victor Pena Ribeiro, Denise Crispim Tavares, Gustavo Rafael Mazzaron Barcelos, Lusânia Maria Greggi Antunes, Jairo Kenupp Bastos. Evaluation of cytoprotective effects of compounds isolated from Copaifera langsdorffii Desf. against induced cytotoxicity by exposure to methylmercury and lead. Natural product research. 2020 Sep; 34(17):2528-2532. doi: 10.1080/14786419.2018.1543673. [PMID: 30623721]
  • Chung Shil Kwak, Jiwon Yang, Chang-Yup Shin, Jin Ho Chung. Rosa multiflora Thunb Flower Extract Attenuates Ultraviolet-Induced Photoaging in Skin Cells and Hairless Mice. Journal of medicinal food. 2020 Sep; 23(9):988-997. doi: 10.1089/jmf.2019.4610. [PMID: 32721259]
  • Erna Karalija, Adisa Parić, Sabina Dahija, Renata Bešta-Gajević, Sanja Ćavar Zeljković. Phenolic compounds and bioactive properties of Verbascum glabratum subsp. bosnense (K. Malý) Murb., an endemic plant species. Natural product research. 2020 Aug; 34(16):2407-2411. doi: 10.1080/14786419.2018.1538221. [PMID: 30580595]
  • Lin Zheng, Yueting Li, Zuying Zhou, Wenying Xiang, Zipeng Gong, Siying Chen, Yonglin Wang, Aimin Wang, Yanyu Lan, Yongjun Li, Yong Huang. Comparative pharmacokinetics of quercitrin, astragalin, afzelin and taxifolin in plasma after oral administration of Polygonum orientale inflorescence in sham-operated and myocardial ischemia-reperfusion injury rats. Xenobiotica; the fate of foreign compounds in biological systems. 2020 Jul; 50(7):822-830. doi: 10.1080/00498254.2019.1700319. [PMID: 31791186]
  • Cezara Zagrean-Tuza, Augustin C Mot, Tomasz Chmiel, Attila Bende, Ioan Turcu. Sugar matters: sugar moieties as reactivity-tuning factors in quercetin O-glycosides. Food & function. 2020 Jun; 11(6):5293-5307. doi: 10.1039/d0fo00319k. [PMID: 32458896]
  • Stefania Cicolari, Marco Dacrema, Arold Jorel Tsetegho Sokeng, Jianbo Xiao, Achille Parfait Atchan Nwakiban, Carmen Di Giovanni, Cristina Santarcangelo, Paolo Magni, Maria Daglia. Hydromethanolic Extracts from Adansonia digitata L. Edible Parts Positively Modulate Pathophysiological Mechanisms Related to the Metabolic Syndrome. Molecules (Basel, Switzerland). 2020 Jun; 25(12):. doi: 10.3390/molecules25122858. [PMID: 32575811]
  • Wei Zhang, Zhi-Tian Fu, Yao Xie, Zhi-Wen Duan, Yu Wang, Rong-Hua Fan. High resolution UPLC-MS/MS method for simultaneous separation and determination of six flavonoids from semen cuscutae extract in rat plasma: application to comparative pharmacokinetic studies in normal and kidney-deficient rats. Natural product research. 2020 May; 34(10):1446-1451. doi: 10.1080/14786419.2018.1511556. [PMID: 30375249]
  • Youjiao Wu, Zhifeng Zhang, Tingbo Chen, Chunsong Cheng, Ziling Zhang, Hua Zhou, Pei Luo. Comparison of two Polygonum chinense varieties used in Chinese cool tea in terms of chemical profiles and antioxidant/anti-inflammatory activities. Food chemistry. 2020 Apr; 310(?):125840. doi: 10.1016/j.foodchem.2019.125840. [PMID: 31806390]
  • Fatma Tuğçe Gürağaç Dereli, Mert Ilhan, Esra Küpeli Akkol. Identification of the main active antidepressant constituents in a traditional Turkish medicinal plant, Centaurea kurdica Reichardt. Journal of ethnopharmacology. 2020 Mar; 249(?):112373. doi: 10.1016/j.jep.2019.112373. [PMID: 31689479]
  • Luciana Arantes Dantas, Márcio Rosa, Erika Crispim Resende, Fabiano Guimarães Silva, Paulo Sérgio Pereira, Ana Cristina Lourenço Souza, Fernando Higino de Lima E Silva, Aurélio Rubio Neto. Spectral quality as an elicitor of bioactive compound production in Solanum aculeatissimum JACQ cell suspension. Journal of photochemistry and photobiology. B, Biology. 2020 Mar; 204(?):111819. doi: 10.1016/j.jphotobiol.2020.111819. [PMID: 32062388]
  • Tobie D Lee, Olivia W Lee, Kyle R Brimacombe, Lu Chen, Rajarshi Guha, Sabrina Lusvarghi, Bethilehem G Tebase, Carleen Klumpp-Thomas, Robert W Robey, Suresh V Ambudkar, Min Shen, Michael M Gottesman, Matthew D Hall. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Molecular pharmacology. 2019 11; 96(5):629-640. doi: 10.1124/mol.119.115964. [PMID: 31515284]
  • Yong Huang, Zuying Zhou, Wu Yang, Zipeng Gong, Yueting Li, Siying Chen, Yonglin Wang, Aimin Wang, Yanyu Lan, Ting Liu, Lin Zheng. Comparative Pharmacokinetics of Gallic Acid, Protocatechuic Acid, and Quercitrin in Normal and Pyelonephritis Rats after Oral Administration of a Polygonum capitatum Extract. Molecules (Basel, Switzerland). 2019 Oct; 24(21):. doi: 10.3390/molecules24213873. [PMID: 31717895]
  • Andrezza S Ramos, Josiana M Mar, Laiane S da Silva, Leonard D R Acho, Bárbara Janaína P Silva, Emerson S Lima, Pedro H Campelo, Edgar A Sanches, Jaqueline A Bezerra, Francisco Célio M Chaves, Francinete R Campos, Marcos B Machado. Pedra-ume caá fruit: An Amazon cherry rich in phenolic compounds with antiglycant and antioxidant properties. Food research international (Ottawa, Ont.). 2019 09; 123(?):674-683. doi: 10.1016/j.foodres.2019.05.042. [PMID: 31285017]
  • Marina Santos, Renée H Fortunato, Viviana G Spotorno. Analysis of flavonoid glycosides with potential medicinal properties on Bauhinia uruguayensis and Bauhinia forficata subspecies pruinosa. Natural product research. 2019 Sep; 33(17):2574-2578. doi: 10.1080/14786419.2018.1460826. [PMID: 29620448]
  • Anca Toiu, Laurian Vlase, Dan Cristian Vodnar, Ana-Maria Gheldiu, Ilioara Oniga. Solidago graminifolia L. Salisb. (Asteraceae) as a Valuable Source of Bioactive Polyphenols: HPLC Profile, In Vitro Antioxidant and Antimicrobial Potential. Molecules (Basel, Switzerland). 2019 Jul; 24(14):. doi: 10.3390/molecules24142666. [PMID: 31340530]
  • Yumi Kitahiro, Hiroshi Ikeda, Hyoung-Tak Im, Eiichi Kodaira, Makio Shibano. Phytochemical characterization of Rosa multiflora Thunb. (Rosaceae) in Japan and South Korea, with a focus on the bioactive flavonol glycoside 'multiflorin A'. Journal of natural medicines. 2019 Jun; 73(3):555-565. doi: 10.1007/s11418-019-01302-x. [PMID: 30949951]
  • Satoshi Endo, Namiki Miyagi, Toshiyuki Matsunaga, Akira Ikari. Rabbit dehydrogenase/reductase SDR family member 11 (DHRS11): Its identity with acetohexamide reductase with broad substrate specificity and inhibitor sensitivity, different from human DHRS11. Chemico-biological interactions. 2019 May; 305(?):12-20. doi: 10.1016/j.cbi.2019.03.026. [PMID: 30926317]
  • Yunus Dönder, Türkmen B Arikan, Mehmet Baykan, Muhammet Akyüz, A Bahadır Öz. Effects of quercitrin on bacterial translocation in a rat model of experimental colitis. Asian journal of surgery. 2018 Nov; 41(6):543-550. doi: 10.1016/j.asjsur.2017.12.002. [PMID: 29371051]
  • Pietro G Signorile, Rosa Viceconte, Alfonso Baldi. Novel dietary supplement association reduces symptoms in endometriosis patients. Journal of cellular physiology. 2018 08; 233(8):5920-5925. doi: 10.1002/jcp.26401. [PMID: 29243819]
  • Zhaochen Wu, Wei Wang, Fengyuan He, Dengwu Li, Dongmei Wang. Simultaneous Enrichment and Separation of Four Flavonoids from Zanthoxylum bungeanum Leaves by Ultrasound-Assisted Extraction and Macroporous Resins with Evaluation of Antioxidant Activities. Journal of food science. 2018 Aug; 83(8):2109-2118. doi: 10.1111/1750-3841.14282. [PMID: 30080245]
  • Pham Thi Nhat Trinh, Nguyen Huu An, Pham Ngoc An, Mai Dinh Tri, Cao Van Du, Phan Nhat Minh, Nguyen Thi Le Thuy, Nguyen Trong Tuan, Vang Thi Kim Thoa, Nguyen Ngoc Tuan, Le Tien Dung. A new benzofuran derivative from the leaves of Ficus pumila L. Natural product research. 2018 Jul; 32(14):1648-1652. doi: 10.1080/14786419.2017.1395427. [PMID: 29072969]
  • Robert Lotha, Niranjana Sri Sundaramoorthy, Bhanuvalli R Shamprasad, Saisubramanian Nagarajan, Aravind Sivasubramanian. Plant nutraceuticals (Quercetrin and Afzelin) capped silver nanoparticles exert potent antibiofilm effect against food borne pathogen Salmonella enterica serovar Typhi and curtail planktonic growth in zebrafish infection model. Microbial pathogenesis. 2018 Jul; 120(?):109-118. doi: 10.1016/j.micpath.2018.04.044. [PMID: 29715535]
  • Sławomir Dresler, Jozef Kováčik, Maciej Strzemski, Ireneusz Sowa, Magdalena Wójciak-Kosior. Methodological aspects of biologically active compounds quantification in the genus Hypericum. Journal of pharmaceutical and biomedical analysis. 2018 Jun; 155(?):82-90. doi: 10.1016/j.jpba.2018.03.048. [PMID: 29621655]
  • Desirée Magalhães Dos Santos, Camila Valesca Jardim Rocha, Elita Ferreira da Silveira, Marcelo Augusto Germani Marinho, Marisa Raquel Rodrigues, Nichole Osti Silva, Ailton da Silva Ferreira, Neusa Fernandes de Moura, Gabriel Jorge Sagrera Darelli, Elizandra Braganhol, Ana Paula Horn, Vânia Rodrigues de Lima. In Vitro Anti/Pro-oxidant Activities of R. ferruginea Extract and Its Effect on Glioma Cell Viability: Correlation with Phenolic Compound Content and Effects on Membrane Dynamics. The Journal of membrane biology. 2018 04; 251(2):247-261. doi: 10.1007/s00232-018-0017-z. [PMID: 29417170]
  • Ana Paula Beber, Priscila de Souza, Thaise Boeing, Lincon Bordignon Somensi, Luísa Nathália Bolda Mariano, Benhur Judah Cury, Ligia Moura Burci, Cristiane Bezerra da Silva, Euclésio Simionatto, Sérgio Faloni de Andrade, Luísa Mota da Silva. Constituents of leaves from Bauhinia curvula Benth. exert gastroprotective activity in rodents: role of quercitrin and kaempferol. Inflammopharmacology. 2018 Apr; 26(2):539-550. doi: 10.1007/s10787-017-0313-8. [PMID: 28176198]
  • Oluwafemi Adeleke Ojo, Adebola Busola Ojo, Basiru Olaitan Ajiboye, Babatunji Emmanuel Oyinloye, Ayodele Jacob Akinyemi, Mary Abiola Okesola, Aline Augusti Boligon, Marli Matiko Anraku de Campos. Chromatographic fingerprint analysis, antioxidant properties, and inhibition of cholinergic enzymes (acetylcholinesterase and butyrylcholinesterase) of phenolic extracts from Irvingia gabonensis (Aubry-Lecomte ex O'Rorke) Baill bark. Journal of basic and clinical physiology and pharmacology. 2018 Mar; 29(2):217-224. doi: 10.1515/jbcpp-2017-0063. [PMID: 29381472]
  • Jacob K Akintunde, Michael O Aina, Aline A Boligon. Launaea taraxacifolia (Willd.) Amin ex C. Jeffrey inhibits oxidative damage and econucleotidase followed by increased cellular ATP in testicular cells of rats exposed to metropolitan polluted river water. Journal of basic and clinical physiology and pharmacology. 2018 Mar; 29(2):141-153. doi: 10.1515/jbcpp-2016-0187. [PMID: 29360627]
  • Mihai Babotă, Andrei Mocan, Laurian Vlase, Ovidiu Crișan, Irina Ielciu, Ana-Maria Gheldiu, Dan Cristian Vodnar, Gianina Crișan, Ramona Păltinean. Phytochemical Analysis, Antioxidant and Antimicrobial Activities of Helichrysum arenarium (L.) Moench. and Antennaria dioica (L.) Gaertn. Flowers. Molecules (Basel, Switzerland). 2018 Feb; 23(2):. doi: 10.3390/molecules23020409. [PMID: 29438342]
  • Agnieszka Szopa, Anna Starzec, Halina Ekiert. The importance of monochromatic lights in the production of phenolic acids and flavonoids in shoot cultures of Aronia melanocarpa, Aronia arbutifolia and Aronia × prunifolia. Journal of photochemistry and photobiology. B, Biology. 2018 Feb; 179(?):91-97. doi: 10.1016/j.jphotobiol.2018.01.005. [PMID: 29351879]
  • Navneet Kishore, Danielle Twilley, Analike Blom van Staden, Praveen Verma, Bikram Singh, Giorgia Cardinali, Daniela Kovacs, Mauro Picardo, Vivek Kumar, Namrita Lall. Isolation of Flavonoids and Flavonoid Glycosides from Myrsine africana and Their Inhibitory Activities against Mushroom Tyrosinase. Journal of natural products. 2018 01; 81(1):49-56. doi: 10.1021/acs.jnatprod.7b00564. [PMID: 29300477]
  • Luke P Robertson, Sandra Duffy, Yun Wang, Dongdong Wang, Vicky M Avery, Anthony R Carroll. Pimentelamines A-C, Indole Alkaloids Isolated from the Leaves of the Australian Tree Flindersia pimenteliana. Journal of natural products. 2017 12; 80(12):3211-3217. doi: 10.1021/acs.jnatprod.7b00587. [PMID: 29236492]
  • Ju-Heon Kim, Jong-Suep Baek, Jin-Kyu Park, Bong-Joo Lee, Min-Soo Kim, Sung-Joo Hwang, Jae-Young Lee, Cheong-Weon Cho. Development of Houttuynia cordata Extract-Loaded Solid Lipid Nanoparticles for Oral Delivery: High Drug Loading Efficiency and Controlled Release. Molecules (Basel, Switzerland). 2017 Dec; 22(12):. doi: 10.3390/molecules22122215. [PMID: 29236057]
  • Yali Zhang, Yucheng Guo, Mimi Wang, Huanhuan Dong, Jingfang Zhang, Liyu Zhang. Quercetrin from Toona sinensis leaves induces cell cycle arrest and apoptosis via enhancement of oxidative stress in human colorectal cancer SW620 cells. Oncology reports. 2017 Dec; 38(6):3319-3326. doi: 10.3892/or.2017.6042. [PMID: 29039609]
  • Yongjiao Sun, Lingyun Jia, Zhanbo Huang, Jing Wang, Jincai Lu, Jing Li. Hepatoprotective effect against CCl4-induced acute liver damage in mice and High-performance liquid chromatography mass spectrometric method for analysis of the constituents of extract of Rubus crataegifolius. Natural product research. 2017 Nov; 31(22):2695-2699. doi: 10.1080/14786419.2017.1292264. [PMID: 28322066]
  • Meta Kokalj Ladan, Janka Straus, Eva Tavčar Benković, Samo Kreft. FT-IR-based method for rutin, quercetin and quercitrin quantification in different buckwheat (Fagopyrum) species. Scientific reports. 2017 08; 7(1):7226. doi: 10.1038/s41598-017-07665-z. [PMID: 28775318]
  • Pham Thi Nhat Trinh, Ngoc Quoc Luan, Mai Dinh Tri, Vu Duy Khanh, Nguyen Huu An, Phan Nhat Minh, Pham Ngoc An, Nguyen Thi Le Thuy, Nguyen Kim Phi Phung, Le Tien Dung. New naphthalene derivative from the leaves of Cassia grandis L. Natural product research. 2017 Aug; 31(15):1733-1738. doi: 10.1080/14786419.2017.1290615. [PMID: 28278658]
  • Manuela Mandrone, Monica Scognamiglio, Antonio Fiorentino, Cinzia Sanna, Luca Cornioli, Fabiana Antognoni, Francesca Bonvicini, Ferruccio Poli. Phytochemical profile and α-glucosidase inhibitory activity of Sardinian Hypericum scruglii and Hypericum hircinum. Fitoterapia. 2017 Jul; 120(?):184-193. doi: 10.1016/j.fitote.2017.06.020. [PMID: 28647480]
  • Ioannis Erkekoglou, Nikolaos Nenadis, Efrosini Samara, Fani Th Mantzouridou. Functional Teas from the Leaves of Arbutus unedo: Phenolic Content, Antioxidant Activity, and Detection of Efficient Radical Scavengers. Plant foods for human nutrition (Dordrecht, Netherlands). 2017 Jun; 72(2):176-183. doi: 10.1007/s11130-017-0607-4. [PMID: 28421300]
  • Cristina Sgherri, Usue Pérez-López, Francesco Micaelli, Jon Miranda-Apodaca, Amaia Mena-Petite, Alberto Muñoz-Rueda, Mike Frank Quartacci. Elevated CO2 and salinity are responsible for phenolics-enrichment in two differently pigmented lettuces. Plant physiology and biochemistry : PPB. 2017 Jun; 115(?):269-278. doi: 10.1016/j.plaphy.2017.04.006. [PMID: 28411511]
  • Yunliang Wei, Changsheng Guo, Jingsheng Zhao, Jun Yang, Weiguo Yi, Hong Liu, Xinwei Lin, Zhengchen Zhang. X indening oral liquid improves cardiac function of rats with chronic cardiac failure via TGF-ß1/Smad3 and p38 MAPK pathway. Anatolian journal of cardiology. 2017 May; 17(5):367-373. doi: 10.14744/anatoljcardiol.2016.7438. [PMID: 28100897]
  • Liancai Zhu, Jinqiu Chen, Jun Tan, Xi Liu, Bochu Wang. Flavonoids from Agrimonia pilosa Ledeb: Free Radical Scavenging and DNA Oxidative Damage Protection Activities and Analysis of Bioactivity-Structure Relationship Based on Molecular and Electronic Structures. Molecules (Basel, Switzerland). 2017 Feb; 22(3):. doi: 10.3390/molecules22030195. [PMID: 28245624]
  • Yong Huang, Hui-Yuan Sun, Xiao-Li Qin, Yong-Jun Li, Shang-Gao Liao, Zi-Peng Gong, Yuan Lu, Yong-Lin Wang, Ai-Min Wang, Yan-Yu Lan, Lin Zheng. A UPLC-MS/MS Method for Simultaneous Determination of Free and Total Forms of a Phenolic Acid and Two Flavonoids in Rat Plasma and Its Application to Comparative Pharmacokinetic Studies of Polygonum capitatum Extract in Rats. Molecules (Basel, Switzerland). 2017 Feb; 22(3):. doi: 10.3390/molecules22030353. [PMID: 28245598]
  • Nicolas Baert, Jorma Kim, Maarit Karonen, Juha-Pekka Salminen. Inter-population and inter-organ distribution of the main polyphenolic compounds of Epilobium angustifolium. Phytochemistry. 2017 Feb; 134(?):54-63. doi: 10.1016/j.phytochem.2016.11.003. [PMID: 27866749]
  • Xiao-Li Qin, Hui-Yuan Sun, Wu Yang, Yong-Jun Li, Lin Zheng, Ting Liu, Yong Huang. [Analysis of metabolites of quercitrin in rat intestinal flora by using UPLC-ESI-Q-TOF-MS/MS]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2017 Jan; 42(2):357-362. doi: 10.19540/j.cnki.cjcmm.20161222.018. [PMID: 28948744]
  • Myrto Maria Fouseki, Harilaos Damianakos, George Albert Karikas, Christos Roussakis, Mahabir P Gupta, Ioanna Chinou. Chemical constituents from Cordia alliodora and C. colloccoca (Boraginaceae) and their biological activities. Fitoterapia. 2016 Dec; 115(?):9-14. doi: 10.1016/j.fitote.2016.09.004. [PMID: 27659390]
  • Ning Li, Ying Wang, Xuezheng Li, Hong Zhang, Di Zhou, Wenli Wang, Wei Li, Xiangrong Zhang, Xinyu Li, Yue Hou, Dali Meng. Bioactive phenols as potential neuroinflammation inhibitors from the leaves of Xanthoceras sorbifolia Bunge. Bioorganic & medicinal chemistry letters. 2016 10; 26(20):5018-5023. doi: 10.1016/j.bmcl.2016.08.094. [PMID: 27623545]
  • Nguyen Phuong Thao, Bui Thi Thuy Luyen, Jang Hoon Kim, Ah Reum Jo, Nguyen Tien Dat, Phan Van Kiem, Chau Van Minh, Young Ho Kim. Identification, characterization, kinetics, and molecular docking of flavonoid constituents from Archidendron clypearia (Jack.) Nielsen leaves and twigs. Bioorganic & medicinal chemistry. 2016 07; 24(14):3125-32. doi: 10.1016/j.bmc.2016.05.034. [PMID: 27246857]
  • Van-Long Truong, Se-Yeon Ko, Mira Jun, Woo-Sik Jeong. Quercitrin from Toona sinensis (Juss.) M.Roem. Attenuates Acetaminophen-Induced Acute Liver Toxicity in HepG2 Cells and Mice through Induction of Antioxidant Machinery and Inhibition of Inflammation. Nutrients. 2016 Jul; 8(7):. doi: 10.3390/nu8070431. [PMID: 27428996]
  • Lin Zheng, Wu Yang, Wen-ying Xiang, Jia Sun, Si-ying Chen, Yong-jun Li. [Simultaneous Determination of Protocatechuic Acid,Kaempferol Biotin Glucoside and Quercitrin in Rat Plasma and Pharmacokinetics By UPLC-MS/MS]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2016 Jul; 39(7):1574-7. doi: . [PMID: 30204361]
  • Kangkang Zhi, Maoquan Li, Jun Bai, Yongfa Wu, Sili Zhou, Xiaoping Zhang, Lefeng Qu. Quercitrin treatment protects endothelial progenitor cells from oxidative damage via inducing autophagy through extracellular signal-regulated kinase. Angiogenesis. 2016 07; 19(3):311-24. doi: 10.1007/s10456-016-9504-y. [PMID: 27017346]
  • Kadiyala Gopi, K Anbarasu, Kadali Renu, S Jayanthi, B S Vishwanath, Gurunathan Jayaraman. Quercetin-3-O-rhamnoside from Euphorbia hirta protects against snake Venom induced toxicity. Biochimica et biophysica acta. 2016 Jul; 1860(7):1528-40. doi: 10.1016/j.bbagen.2016.03.031. [PMID: 27033089]
  • Wei Li, Hu Li, Mu Zhang, Mengqi Wang, Youxiu Zhong, Hezhen Wu, Yanfang Yang, Laurence Morel, Qun Wei. Quercitrin ameliorates the development of systemic lupus erythematosus-like disease in a chronic graft-versus-host murine model. American journal of physiology. Renal physiology. 2016 07; 311(1):F217-26. doi: 10.1152/ajprenal.00249.2015. [PMID: 26911849]
  • Fengyuan He, Dengwu Li, Dongmei Wang, Ming Deng. Extraction and Purification of Quercitrin, Hyperoside, Rutin, and Afzelin from Zanthoxylum Bungeanum Maxim Leaves Using an Aqueous Two-Phase System. Journal of food science. 2016 Jul; 81(7):C1593-602. doi: 10.1111/1750-3841.13331. [PMID: 27240023]
  • Cheng-Can Lu, Lin Zhao, Yong-Xin Huang, Xin Shao, Wen-Yi Kang. [Simultaneous determination of quercitrin, phloridzin and 3-hydroxyl phloridzin in leaves of Malus halliana by ultrasound-assisted ionic liquid-reversed phase liquid chromatography]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2016 Jun; 41(11):2131-2136. doi: 10.4268/cjcmm20161125. [PMID: 28901112]
  • Seol Hwa Seo, Soung-Hoon Lee, Pu-Hyeon Cha, Mi-Yeon Kim, Do Sik Min, Kang-Yell Choi. Polygonum aviculare L. and its active compounds, quercitrin hydrate, caffeic acid, and rutin, activate the Wnt/β-catenin pathway and induce cutaneous wound healing. Phytotherapy research : PTR. 2016 May; 30(5):848-54. doi: 10.1002/ptr.5593. [PMID: 26929003]
  • Mariel de Barros, Luisa Mota da Silva, Thaise Boeing, Lincon Bordignon Somensi, Benhur Judah Cury, Ligia de Moura Burci, José Roberto Santin, Sérgio Faloni de Andrade, Franco Delle Monache, Valdir Cechinel-Filho. Pharmacological reports about gastroprotective effects of methanolic extract from leaves of Solidago chilensis (Brazilian arnica) and its components quercitrin and afzelin in rodents. Naunyn-Schmiedeberg's archives of pharmacology. 2016 Apr; 389(4):403-17. doi: 10.1007/s00210-015-1208-0. [PMID: 26758066]
  • Fang-hui Xu, Yu-xiang Ding, Qiang Wang. [Chemical Constituents of Ethyl Acetate Fraction from Hypericum ascyron]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2016 Feb; 39(2):322-5. doi: . [PMID: 30080367]
  • Ji-Hye Seo, Jung-Eun Kim, Jung-Hyun Shim, Goo Yoon, Mi-Ae Bang, Chun-Sik Bae, Kyung-Jin Lee, Dae-Hun Park, Seung-Sik Cho. HPLC Analysis, Optimization of Extraction Conditions and Biological Evaluation of Corylopsis coreana Uyeki Flos. Molecules (Basel, Switzerland). 2016 Jan; 21(1):94. doi: 10.3390/molecules21010094. [PMID: 26784157]
  • Nikolaos Nenadis, Laura Llorens, Agathi Koufogianni, Laura Díaz, Joan Font, Josep Abel Gonzalez, Dolors Verdaguer. Interactive effects of UV radiation and reduced precipitation on the seasonal leaf phenolic content/composition and the antioxidant activity of naturally growing Arbutus unedo plants. Journal of photochemistry and photobiology. B, Biology. 2015 Dec; 153(?):435-44. doi: 10.1016/j.jphotobiol.2015.10.016. [PMID: 26562808]
  • Camila Carla Guimarães, Denise Dias Oliveira, Mayara Valdevite, Ana Lúcia Fachin Saltoratto, Sarazete Izidia Vaz Pereira, Suzelei de Castro França, Ana Maria Soares Pereira, Paulo Sérgio Pereira. The glycosylated flavonoids vitexin, isovitexin, and quercetrin isolated from Serjania erecta Radlk (Sapindaceae) leaves protect PC12 cells against amyloid-β25-35 peptide-induced toxicity. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2015 Dec; 86(?):88-94. doi: 10.1016/j.fct.2015.09.002. [PMID: 26385725]
  • Lucie Zemanova, Jakub Hofman, Eva Novotna, Kamil Musilek, Tereza Lundova, Jana Havrankova, Anna Hostalkova, Jakub Chlebek, Lucie Cahlikova, Vladimír Wsol. Flavones Inhibit the Activity of AKR1B10, a Promising Therapeutic Target for Cancer Treatment. Journal of natural products. 2015 Nov; 78(11):2666-74. doi: 10.1021/acs.jnatprod.5b00616. [PMID: 26529431]
  • Frederik De Bruyn, Maarten Van Brempt, Jo Maertens, Wouter Van Bellegem, Dries Duchi, Marjan De Mey. Metabolic engineering of Escherichia coli into a versatile glycosylation platform: production of bio-active quercetin glycosides. Microbial cell factories. 2015 Sep; 14(?):138. doi: 10.1186/s12934-015-0326-1. [PMID: 26377568]
  • Yingzhan Tang, Junhong Ling, Peng Zhang, Xiangrong Zhang, Na Zhang, Wenli Wang, Jiayuan Li, Ning Li. Potential therapeutic agents for circulatory diseases from Bauhinia glauca Benth.subsp. pernervosa. (Da Ye Guan Men). Bioorganic & medicinal chemistry letters. 2015 Aug; 25(16):3217-20. doi: 10.1016/j.bmcl.2015.05.089. [PMID: 26096681]
  • Alba Córdoba, Marta Monjo, Margarita Hierro-Oliva, María Luisa González-Martín, Joana Maria Ramis. Bioinspired Quercitrin Nanocoatings: A Fluorescence-Based Method for Their Surface Quantification, and Their Effect on Stem Cell Adhesion and Differentiation to the Osteoblastic Lineage. ACS applied materials & interfaces. 2015 Aug; 7(30):16857-64. doi: 10.1021/acsami.5b05044. [PMID: 26167954]
  • Sheela Verjee, Daniela Brügger, Heba Abdel-Aziz, Veronika Butterweck. Permeation Characteristics of Hypericin across Caco-2 Monolayers in the Absence or Presence of Quercitrin - A Mass Balance Study. Planta medica. 2015 Aug; 81(12-13):1111-20. doi: 10.1055/s-0035-1546034. [PMID: 26018919]
  • Ju Hee Lee, Jongmin Ahn, Jin Woong Kim, Sang Gook Lee, Hyun Pyo Kim. Flavonoids from the aerial parts of Houttuynia cordata attenuate lung inflammation in mice. Archives of pharmacal research. 2015 Jul; 38(7):1304-11. doi: 10.1007/s12272-015-0585-8. [PMID: 25743630]
  • Zeynep Birsu Cincin, Miray Unlu, Bayram Kiran, Elif Sinem Bireller, Yusuf Baran, Bedia Cakmakoglu. Apoptotic Effects of Quercitrin on DLD-1 Colon Cancer Cell Line. Pathology oncology research : POR. 2015 Apr; 21(2):333-8. doi: 10.1007/s12253-014-9825-3. [PMID: 25096395]
  • Eszter Riethmüller, Gergő Tóth, Ágnes Alberti, Krisztina Végh, Ilaria Burlini, Árpád Könczöl, György Tibor Balogh, Ágnes Kéry. First characterisation of flavonoid- and diarylheptanoid-type antioxidant phenolics in Corylus maxima by HPLC-DAD-ESI-MS. Journal of pharmaceutical and biomedical analysis. 2015 Mar; 107(?):159-67. doi: 10.1016/j.jpba.2014.12.016. [PMID: 25594894]
  • João Victor Narducci Ferrreira, Simone Dos S Grecco, João Henrique G Lago, Luciano Caseli. Ultrathin films of lipids to investigate the action of a flavonoid with cell membrane models. Materials science & engineering. C, Materials for biological applications. 2015 Mar; 48(?):112-7. doi: 10.1016/j.msec.2014.11.061. [PMID: 25579903]
  • Ricardo Andrade Furtado, Cristiane Teixeira Vilhena Bernardes, Mauro Nogueira da Silva, Karina Furlani Zoccal, Lúcia Helena Faccioli, Jairo Kenupp Bastos. Antiedematogenic Evaluation of Copaifera langsdorffii Leaves Hydroethanolic Extract and Its Major Compounds. BioMed research international. 2015; 2015(?):913152. doi: 10.1155/2015/913152. [PMID: 26078969]
  • Walter A Roman Junior, Angelo L Piato, Greicy M M Conterato, Silvana M Wildner, Matheus Marcon, Ricieri Mocelin, Mauren P Emanuelli, Tatiana Emanuelli, Angelita Nepel, Andersson Barison, Cid A M Santos. Hypolipidemic effects of Solidago chilensis hydroalcoholic extract and its major isolated constituent quercetrin in cholesterol-fed rats. Pharmaceutical biology. 2015; 53(10):1488-95. doi: 10.3109/13880209.2014.989622. [PMID: 25898223]
  • Yujuan Zhang, Ziwen Luo, Dongmei Wang. Efficient quantification of the phenolic profiles of Zanthoxylum bungeanum leaves and correlation between chromatographic fingerprint and antioxidant activity. Natural product research. 2015; 29(21):2024-9. doi: 10.1080/14786419.2015.1015018. [PMID: 25707294]
  • Jin-Long Li, Li-Xin Gao, Fan-Wang Meng, Chun-Lan Tang, Ru-Jun Zhang, Jing-Ya Li, Cheng Luo, Jia Li, Wei-Min Zhao. PTP1B inhibitors from stems of Angelica keiskei (Ashitaba). Bioorganic & medicinal chemistry letters. 2015; 25(10):2028-32. doi: 10.1016/j.bmcl.2015.04.003. [PMID: 25891102]
  • Marcos Salazar, Lilia Chérigo, Hildaura Acosta, Rafael Otero, Sergio Martínez-Luis. Evaluation of anti-Bothrops asper venom activity of ethanolic extract of Brownea rosademonte leaves. Acta pharmaceutica (Zagreb, Croatia). 2014 Dec; 64(4):475-83. doi: 10.2478/acph-2014-0033. [PMID: 25531787]
  • Si-Hwan Park, Hyun Jung Kim, Soon-Ho Yim, Ah-Ra Kim, Nisha Tyagi, Haihong Shen, Kyung Keun Kim, Boo Ahn Shin, Da-Woon Jung, Darren R Williams. Delineation of the role of glycosylation in the cytotoxic properties of quercetin using novel assays in living vertebrates. Journal of natural products. 2014 Nov; 77(11):2389-96. doi: 10.1021/np500231g. [PMID: 25397870]
  • Soumendranath Bhakat, Wilson Karubiu, Venkatesan Jayaprakash, Mahmoud E S Soliman. A perspective on targeting non-structural proteins to combat neglected tropical diseases: Dengue, West Nile and Chikungunya viruses. European journal of medicinal chemistry. 2014 Nov; 87(?):677-702. doi: 10.1016/j.ejmech.2014.10.010. [PMID: 25305334]
  • Joaquim T Marquês, Ana S Viana, Rodrigo F M de Almeida. A biomimetic platform to study the interactions of bioelectroactive molecules with lipid nanodomains. Langmuir : the ACS journal of surfaces and colloids. 2014 Oct; 30(42):12627-37. doi: 10.1021/la503086a. [PMID: 25267380]
  • Akinori Kakumu, Masayuki Ninomiya, Mai Efdi, Morina Adfa, Masahiro Hayashi, Kaori Tanaka, Mamoru Koketsu. Phytochemical analysis and antileukemic activity of polyphenolic constituents of Toona sinensis. Bioorganic & medicinal chemistry letters. 2014 Sep; 24(17):4286-90. doi: 10.1016/j.bmcl.2014.07.022. [PMID: 25074815]
  • Zeynep Birsu Cincin, Miray Unlu, Bayram Kiran, Elif Sinem Bireller, Yusuf Baran, Bedia Cakmakoglu. Molecular mechanisms of quercitrin-induced apoptosis in non-small cell lung cancer. Archives of medical research. 2014 Aug; 45(6):445-54. doi: 10.1016/j.arcmed.2014.08.002. [PMID: 25193878]
  • Chi-Yu He, Jie Fu, Jing-Yi Ma, Ru Feng, Xiang-Shan Tan, Min Huang, Jia-Wen Shou, Zhen-Xiong Zhao, Xiao-Yang Li, Xian-Feng Zhang, Yangchao Chen, Yan Wang. Biotransformation and in vitro metabolic profile of bioactive extracts from a traditional Miao-nationality herbal medicine, Polygonum capitatum. Molecules (Basel, Switzerland). 2014 Jul; 19(7):10291-308. doi: 10.3390/molecules190710291. [PMID: 25033057]
  • Daniel Plano, Shantu Amin, Arun K Sharma. Importance of sphingosine kinase (SphK) as a target in developing cancer therapeutics and recent developments in the synthesis of novel SphK inhibitors. Journal of medicinal chemistry. 2014 Jul; 57(13):5509-24. doi: 10.1021/jm4011687. [PMID: 24471412]
  • Le-Yue Du, Min Zhao, Jun Xu, Da-Wei Qian, Shu Jiang, Er-Xin Shang, Jian-Ming Guo, Pei Liu, Shu-Lan Su, Jin-Ao Duan, Xue-Jiao Leng. Identification of the metabolites of myricitrin produced by human intestinal bacteria in vitro using ultra-performance liquid chromatography/quadrupole time-of-flight mass spectrometry. Expert opinion on drug metabolism & toxicology. 2014 Jul; 10(7):921-31. doi: 10.1517/17425255.2014.918954. [PMID: 24882500]
  • Yong Zhao, Chang-An Geng, Chang-Li Sun, Yun-Bao Ma, Xiao-Yan Huang, Tuan-Wu Cao, Kang He, Hao Wang, Xue-Mei Zhang, Ji-Jun Chen. Polyacetylenes and anti-hepatitis B virus active constituents from Artemisia capillaris. Fitoterapia. 2014 Jun; 95(?):187-93. doi: 10.1016/j.fitote.2014.03.017. [PMID: 24685503]
  • Shu Wang, Rui Su, Shufang Nie, Ming Sun, Jia Zhang, Dayong Wu, Naima Moustaid-Moussa. Application of nanotechnology in improving bioavailability and bioactivity of diet-derived phytochemicals. The Journal of nutritional biochemistry. 2014 Apr; 25(4):363-76. doi: 10.1016/j.jnutbio.2013.10.002. [PMID: 24406273]
  • Lorena Ramos Freitas de Sousa, Suelem Demuner Ramalho, Marcela Carmen de Melo Burger, Liliane Nebo, João Batista Fernandes, Maria Fátima das Graças Fernandes da Silva, Mônica Rosas da Costa Iemma, Caroindes Julia Corrêa, Dulce Helena Ferreira de Souza, Maria Inês Salgueiro Lima, Paulo Cezar Vieira. Isolation of arginase inhibitors from the bioactivity-guided fractionation of Byrsonima coccolobifolia leaves and stems. Journal of natural products. 2014 Feb; 77(2):392-6. doi: 10.1021/np400717m. [PMID: 24521209]
  • Shu Jiang, Jing Yang, Dawei Qian, Jianming Guo, Er-xin Shang, Jin-ao Duan, Jun Xu. Rapid screening and identification of metabolites of quercitrin produced by the human intestinal bacteria using ultra performance liquid chromatography/quadrupole-time-of-flight mass spectrometry. Archives of pharmacal research. 2014 Feb; 37(2):204-13. doi: 10.1007/s12272-013-0172-9. [PMID: 23754166]
  • Wei-Jern Tsai, Chien-Chang Shen, Tung-Hu Tsai, Lie-Chwen Lin. Lignans from the aerial parts of Saururus chinensis: isolation, structural characterization, and their effects on platelet aggregation. Journal of natural products. 2014 Jan; 77(1):125-31. doi: 10.1021/np400772h. [PMID: 24387347]