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) 0.13%

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 2024-09-08) (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)

2269 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]
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