trans-Piceid (BioDeep_00000230980)

 

Secondary id: BioDeep_00000003245, BioDeep_00000406166

human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite Chemicals and Drugs


代谢物信息卡片


(2S,3R,4S,5S,6R)-2-[3-hydroxy-5-[(E)-2-(4-hydroxyphenyl)vinyl]phenoxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol

化学式: C20H22O8 (390.1314612)
中文名称: (E/Z)-虎杖苷, 白藜芦醇苷, 云杉新甙, 虎杖甙, 虎杖苷
谱图信息: 最多检出来源 Viridiplantae(plant) 26.93%

分子结构信息

SMILES: C1=C(O)C=C(/C=C/C2=CC=C(O)C=C2)C=C1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1
InChI: InChI=1S/C20H22O8/c21-10-16-17(24)18(25)19(26)20(28-16)27-15-8-12(7-14(23)9-15)2-1-11-3-5-13(22)6-4-11/h1-9,16-26H,10H2/b2-1+/t16-,17+,18+,19-,20-/m1/s1

描述信息

Trans-piceid is a stilbenoid that is trans-resveratrol substituted at position 3 by a beta-D-glucosyl residue. It has a role as a metabolite, a potassium channel modulator, an anti-arrhythmia drug, a hepatoprotective agent, an antioxidant, a nephroprotective agent and a geroprotector. It is a stilbenoid, a polyphenol, a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a trans-resveratrol.
Polydatin, or Piceid, is a natural precursor and glycoside form of resveratrol with a monocrystalline structure. While it is isolated from the bark of *Picea sitchensis* or *Polygonum cuspidatum*, polydatin may be detected in grape, peanut, hop cones, red wines, hop pellets, cocoa-containing products, chocolate products and many daily diets. Polydatin possesses anti-inflammatory, immunoregulatory, anti-oxidative and anti-tumor activities. It is shown to mediate a cytotoxic action on colorectal cancer cells by inducing cell arrest and apoptosis.
Polydatin is a natural product found in Vitis rupestris, Vitis labrusca, and other organisms with data available.
trans-Piceid is found in alcoholic beverages. trans-Piceid is present in grapeskins and red wine. It is isolated from Polygonum cuspidatum (Japanese knotweed).Piceid is a stilbenoid glucoside and is a major resveratrol derivative in grape juices
A stilbenoid that is trans-resveratrol substituted at position 3 by a beta-D-glucosyl residue.
(E/Z)-Polydatin ((E/Z)-Piceid) is a monocrystalline compound originally isolated from the root and rhizome of Polygonum cuspidatum. (E/Z)-Polydatin has anti-platelet aggregation, anti-oxidative action of low-density lipoprotein (LDL), cardioprotective activity, anti-inflammatory and immune-regulating functions[1].
(E/Z)-Polydatin ((E/Z)-Piceid) is a monocrystalline compound originally isolated from the root and rhizome of Polygonum cuspidatum. (E/Z)-Polydatin has anti-platelet aggregation, anti-oxidative action of low-density lipoprotein (LDL), cardioprotective activity, anti-inflammatory and immune-regulating functions[1].
(E/Z)-Polydatin ((E/Z)-Piceid) is a monocrystalline compound originally isolated from the root and rhizome of Polygonum cuspidatum. (E/Z)-Polydatin has anti-platelet aggregation, anti-oxidative action of low-density lipoprotein (LDL), cardioprotective activity, anti-inflammatory and immune-regulating functions[1].
Polydatin (Piceid), extracted from the roots of Reynoutria japonica, a widely used traditional Chinese remedies, possesses anti-inflammatory activity in several experimental models. Polydatin (Piceid) inhibits G6PD and induces oxidative and ER stresses.
Polydatin (Piceid), extracted from the roots of Reynoutria japonica, a widely used traditional Chinese remedies, possesses anti-inflammatory activity in several experimental models. Polydatin (Piceid) inhibits G6PD and induces oxidative and ER stresses.
Polydatin (Standard) is the analytical standard of Polydatin. This product is intended for research and analytical applications. Polydatin (Piceid), extracted from the roots of Reynoutria japonica, a widely used traditional Chinese remedies, possesses anti-inflammatory activity in several experimental models. Polydatin (Piceid) inhibits G6PD and induces oxidative and ER stresses.

同义名列表

121 个代谢物同义名

(2S,3R,4S,5S,6R)-2-[3-hydroxy-5-[(E)-2-(4-hydroxyphenyl)vinyl]phenoxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol; .beta.-D-Glucopyranoside, 3-hydroxy-5-[(1E)-2-(4-hydroxyphenyl)ethenyl]phenyl3,5,4-Trihydroxystilbene 3-glucoside; (2S,3R,4S,5S,6R)-2-(3-hydroxy-5-((E)-4-hydroxystyryl)phenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol; (2S,3R,4S,5S,6R)-2-[3-hydroxy-5-[(E)-2-(4-hydroxyphenyl)vinyl]phenoxy]-6-methylol-tetrahydropyran-3,4,5-triol; (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[3-[(E)-2-(4-hydroxyphenyl)ethenyl]-5-oxidanyl-phenoxy]oxane-3,4,5-triol; (2S,3R,4S,5S,6R)-2-{3-hydroxy-5-[(1E)-2-(4-hydroxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol; (2S,3R,4S,5S,6R)-2-[3-hydroxy-5-[(E)-2-(4-hydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol; (2S,3R,4S,5S,6R)-2-{3-hydroxy-5-[(E)-2-(4-hydroxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol; (2S,3R,4S,5S,6R)-2-(3-Hydroxy-5-(4-hydroxystyryl)phenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol; 5-((1E)-2-(4-HYDROXYPHENYL)ETHENYL)-1,3-BENZENEDIOL-3-.BETA.-MONO-D-GLUCOSIDE; beta-D-Glucopyranoside, 3-hydroxy-5-(2-(4-hydroxyphenyl)ethenyl)phenyl-, (E)-; .BETA.-D-GLUCOPYRANOSIDE, 3-HYDROXY-5-((1E)-2-(4-HYDROXYPHENYL)ETHENYL)PHENYL; beta-D-GLUCOPYRANOSIDE, 3-HYDROXY-5-((1E)-2-(4-HYDROXYPHENYL)ETHENYL)PHENYL; 5-((1E)-2-(4-HYDROXYPHENYL)ETHENYL)-1,3-BENZENEDIOL-3-beta-MONO-D-GLUCOSIDE; 3-Hydroxy-5-[(1E)-2-(4-hydroxyphenyl)ethenyl]phenyl-beta-D-glucopyranoside; 3-Hydroxy-5-[(1E)-2-(4-hydroxyphenyl)ethenyl]phenyl beta-D-glucopyranoside; 3-hydroxy-5-((E)-2-(4-hydroxyphenyl)ethenyl)phenyl beta-D-glucopyranoside; 3-hydroxy-5-[(E)-2-(4-hydroxyphenyl)ethenyl]phenyl beta-D-glucopyranoside; .BETA.-D-GLUCOPYRANOSIDE, 3-HYDROXY-5-(2-(4-HYDROXYPHENYL)ETHENYL)PHENYL; 3-Hydroxy-5-[(1E)-2-(4-hydroxyphenyl)ethenyl]phenyl β-D-glucopyranoside; b-D-Glucopyranoside,3-hydroxy-5-[(1E)-2-(4-hydroxyphenyl)ethenyl]phenyl; beta-D-Glucopyranoside, 3-hydroxy-5-(2-(4-hydroxyphenyl)ethenyl)phenyl; 3-Hydroxy-5-[2-(4-hydroxyphenyl)ethenyl]phenyl beta-D-glucopyranoside; b-D-Glucopyranoside, 3-hydroxy-5-[2-(4-hydroxyphenyl)ethenyl]phenyl; GLUCOPYRANOSIDE, 3-HYDROXY-5-(P-HYDROXYSTYRYL)PHENYL, .BETA.-D-; 3-hydroxy-5-(2-(4-hydroxyphenyl)ethenyl)phenyl-beta-D-glucoside; GLUCOPYRANOSIDE, 3-HYDROXY-5-(P-HYDROXYSTYRYL)PHENYL, beta-D-; 3,4-5-Trihydroxystilbene-3-beta-D-glucopyranoside, 97\\%; 3,3,4,5-Tetrahydroxystilbene 3-O-beta-D-glucopyranoside; trans-3,5,4-Trihydroxystilbene 3-O-beta-glucopyranoside; trans-3,5,4’-Trihydroxystilbene 3-O-β-glucopyranoside; trans-3,5,4-Trihydroxystilbene 3-O-β-glucopyranoside; 3-Hydroxy-5-(p-hydroxystyryl)phenyl beta-D-glucoside; 3,4-5-TRIHYDROXYSTILBENE-3-.BETA.-D-GLUCOPYRANOSIDE; trans-3,5,4-Trihydroxystilbene 3-O-beta-glucoside; 3,4-5-Trihydroxystilbene-3-beta-D-glucopyranoside; (-)-trans-Resveratrol 13-O-beta-D-glucopyranoside; 3-Hydroxy-5-(p-hydroxystyryl)phenyl β-D-glucoside; 3,5,4-Trihydroxystilbene 3-O-beta-glucopyranoside; 5,4-dihydroxystilbene-3-O-beta-D-glucopyranoside; 3,5,4’-Trihydroxystilbene 3-O-β-glucopyranoside; trans-3,5,4’-Trihydroxystilbene 3-O-β-glucoside; 3,4,5-Trihydroxystilbene-3-b-D-glucopyranoside; 3,5,4-Trihydroxystilbene 3-O-β-glucopyranoside; (-)-trans-Resveratrol 13-O-β-D-glucopyranoside; trans-3,5,4-Trihydroxystilbene 3-O-β-glucoside; trans-3,5,4’-Trihydroxystilbene 3-O-glucoside; 3,4,5-TRIHYDROXYSTILBENE-3-BETA-MONOGLUCOSIDE; 3,4,5-trihydroxystilbene-3-beta-monoglucoside; trans-3,5,4-Trihydroxystilbene 3-O-glucoside; trans-3,5,4’-Trihydroxystilbene 3-glucoside; 3,4,5-trihydroxystilbene-3-beta-D-glucoside; 3,5,4-Trihydroxystilbene 3-O-beta-glucoside; 3,4,5-Trihydroxystilbene-3-β-monoglucoside; trans-3,5,4-Trihydroxystilbene 3-glucoside; trans-resveratrol 3-beta-d-glucopyranoside; RESVERATROL 3-.BETA.-MONO-D-GLUCOSIDE [MI]; (E)-Resveratrol 3-O-beta-D-glucopyranoside; 3,4,5-Trihydroxystilbene-3-b-monoglucoside; 3,5,4’-Trihydroxystilbene 3-O-β-glucoside; 5-Trihydroxystilbene-3-beta-monoglucoside; 3,5,4-Trihydroxystilbene 3-O-β-glucoside; 3,4,5-Trihydroxystilbene-3-b-D-glucoside; 3,4,5-Trihydroxystilbene-3-β-D-glucoside; (E)-Resveratrol 3-O-β-D-glucopyranoside; Sooryehan Pure Whitening Spot Treatment; 3,5,4’-Trihydroxystilbene 3-O-glucoside; 3,5,4-Trihydroxystilbene 3-O-glucoside; trans-resveratrol 3-O-beta-D-glucoside; Resveratrol 3-.beta.-mono-d-glucoside; 5,4-dihydroxystilbene-3-O-beta-D-Glcp; 3,5,4’-Trihydroxystilbene 3-glucoside; Resveratrol 3-O-beta-glucopyranoside; 3,5,4-Trihydroxystilbene 3-glucoside; trans-resveratrol 3-beta-D-glucoside; trans-Resveratrol 3-O-β-D-glucoside; Resveratrol 3-beta-mono-D-glucoside; trans-Resveratrol 3-O-b-D-glucoside; resveratrol-3-O-b-mono-D-glucoside; trans-resveratrol 3-beta-glucoside; trans-Resveratrol 3-β-D-glucoside; Resveratrol 3-O-β-glucopyranoside; trans-Resveratrol 3-b-D-glucoside; Sooryehan Pure-Whitening Essence; resveratrol 3-O-beta-D-glucoside; trans-Resveratrol 3-b-glucoside; trans-Resveratrol 3-β-glucoside; trans-Resveratrol 3-O-glucoside; Resveratrol 3-beta-D-glucoside; Resveratrol 3-O-β-D-glucoside; trans-Resveratrol 3-glucoside; Resveratrol beta-D-glucoside; HSTZMXCBWJGKHG-CUYWLFDKSA-N; Resveratrol beta-glucoside; Resveratrol β-D-glucoside; resveratrol-3-O-glucoside; Resveratrol 3-O-glucoside; Resveratrol 5-O-glucoside; 3-O-Glucosyl-resveratrol; Sooryehan Pure-Whitening; Resveratrol 3-Glucoside; Resveratrol β-glucoside; polydatin, (E)-isomer; Resveratrol glucoside; Polydotin peceid; trans-Polydatin; (E/Z)-Polydatin; (E)-Polydatin; E/Z-Polydatin; (E/Z)-Piceid; Trans-Piceid; (E)-Piceid; E/Z-Piceid; 3,4,5-Tsg; Polydatin; Pieceid; piceid; 5-Tsg; Piceid (Standard); Polydatin (Standard); Piceid



数据库引用编号

25 个数据库交叉引用编号

分类词条

相关代谢途径

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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)

53 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

  • Ke Liu, Jiaxi Liu, Anjian Xu, Junying Ding. The role of polydatin in inhibiting oxidative stress through SIRT1 activation: A comprehensive review of molecular targets. Journal of ethnopharmacology. 2024 Sep; 331(?):118322. doi: 10.1016/j.jep.2024.118322. [PMID: 38729537]
  • Thanh Dat Mai, Hyun Min Kim, Seo Young Park, Sang Hoon Ma, Ju Hui Do, Won Choi, Hye Min Jang, Hyeon Bae Hwang, Eun Gyeong Song, Jae Sung Shim, Young Hee Joung. Metabolism of phenolic compounds catalyzed by Tomato CYP736A61. Enzyme and microbial technology. 2024 May; 176(?):110425. doi: 10.1016/j.enzmictec.2024.110425. [PMID: 38479200]
  • Tao Liu, Rui Han, Yiqi Yan. Preliminary study on molecular mechanism of COVID-19 intervention by Polygonum cuspidatum through computer bioinformatics. Medicine. 2024 Jan; 103(2):e36918. doi: 10.1097/md.0000000000036918. [PMID: 38215091]
  • Soykan Agar, Barbaros Akkurt, Engin Ulukaya. The Inhibition Mechanism of Pancreatic Ductal Adenocarcinoma via LXR Receptors: A Multifaceted Approach Integrating Molecular Docking, Molecular Dynamics and Post-MD Inter-Molecular Contact Analysis. Asian Pacific journal of cancer prevention : APJCP. 2023 Dec; 24(12):4103-4109. doi: 10.31557/apjcp.2023.24.12.4103. [PMID: 38156844]
  • Jie Tang, Lixiang Wang, Mengge Shi, Shuaixia Feng, Tong Zhang, Han Han. Study on the mechanism of Shuganzhi Tablet against nonalcoholic fatty liver disease and lipid regulation effects of its main substances in vitro. Journal of ethnopharmacology. 2023 Nov; 316(?):116780. doi: 10.1016/j.jep.2023.116780. [PMID: 37311504]
  • Jiannan Liu, Jianlin Huang, Bo Gong, Songtao Cheng, Yadong Liu, Yaodong Chen, Qiang Feng, Jun Li, Mingxing Qiu, Gui Yu, Yong Liao. Polydatin protects against calcium oxalate crystal-induced renal injury through the cytoplasmic/mitochondrial reactive oxygen species-NLRP3 inflammasome pathway. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2023 Nov; 167(?):115621. doi: 10.1016/j.biopha.2023.115621. [PMID: 37793278]
  • Yongli Liu, Fang Xie, Changhuai Lu, Zongbo Zhou, Shudong Li, Jia Zhong, Qian Li, Xianfang Shao. Polydatin inhibited TNF-α-induced apoptosis of skeletal muscle cells through AKT-mediated p38 MAPK and NF-κB pathways. General physiology and biophysics. 2023 Nov; 42(6):521-529. doi: 10.4149/gpb_2023027. [PMID: 37994428]
  • Xiaodan Guan, Liang Jin, Huifen Zhou, Jing Chen, Haofang Wan, Yida Bao, Jiehong Yang, Daojun Yu, Haitong Wan. Polydatin prevent lung epithelial cell from Carbapenem-resistant Klebsiella pneumoniae injury by inhibiting biofilm formation and oxidative stress. Scientific reports. 2023 10; 13(1):17736. doi: 10.1038/s41598-023-44836-7. [PMID: 37853059]
  • Ruimin Wang, Ruyan Fan, Tingyu Meng, Lu Wang. Exploration of the inhibitory mechanisms of trans-polydatin/resveratrol on α-glucosidase by multi-spectroscopic analysis, in silico docking and molecular dynamics simulation. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 2023 Oct; 299(?):122866. doi: 10.1016/j.saa.2023.122866. [PMID: 37201332]
  • Yiliu Chen, Yonghong Jiang, Xiuxiu Liu, Xiufeng Chen, Qiuyue Fan, Zhen Xiao. Polydatin alleviates mycoplasma pneumoniae-induced injury via inhibition of Caspase-1/GSDMD-dependent pyroptosis. International journal of medical microbiology : IJMM. 2023 Sep; 313(5):151586. doi: 10.1016/j.ijmm.2023.151586. [PMID: 37776814]
  • Jingxiao Yang, Yuanqing Wang, Xiong Cai, Binqing Qu, Ye Zhang, Zhicheng Sun, Jianye Yan. Comparative pharmacokinetics and tissue distribution of polydatin, resveratrol, and emodin after oral administration of Huzhang and Huzhang-Guizhi herb-pair extracts to rats. Journal of ethnopharmacology. 2023 Aug; ?(?):117010. doi: 10.1016/j.jep.2023.117010. [PMID: 37557937]
  • Zhengju Zhang, Xinqi Deng, Wen Gu, Yang Jiao, Canyu Su, Hui Liu, Weiguo Ma, Honghong Zhang, Ruiyang Xiang, Dali Wang, Yanan Wang, Wang Chunguo, Fengxian Meng. Jianghu decoction and its active component polydatin inhibit inflammation and fibrotic lesions in the lungs of ILD mice via the AMPK signaling pathway. Journal of ethnopharmacology. 2023 Aug; 318(Pt B):117003. doi: 10.1016/j.jep.2023.117003. [PMID: 37543150]
  • Zhengming Xu, Shuang Liu, Huining Lai, Lijun You, Zhengang Zhao. Green-Efficient Enzymatic Synthesis and Characterization of Liposoluble 6'/6″-O-Lauryl Phenolic Glycosides with Enhanced Intestinal Permeability. Journal of agricultural and food chemistry. 2023 May; 71(20):7689-7702. doi: 10.1021/acs.jafc.3c00527. [PMID: 37167604]
  • Liqing Wang, Menghan Chen, Qihui Sun, Yong Yang, Rong Rong. Discovery of the potential neuraminidase inhibitors from Polygonum cuspidatum by ultrafiltration combined with mass spectrometry guided by molecular docking. Journal of separation science. 2023 May; 46(10):e2200937. doi: 10.1002/jssc.202200937. [PMID: 36905353]
  • Xiaonan Zhang, Zeping Wang, Xiaoya Li, Jiye Che, Zongliang Yu, Xin Li, Changxin Sun, Lanqing Hu, Min Wu, Longtao Liu. Polydatin protects against atherosclerosis by activating autophagy and inhibiting pyroptosis mediated by the NLRP3 inflammasome. Journal of ethnopharmacology. 2023 Mar; ?(?):116304. doi: 10.1016/j.jep.2023.116304. [PMID: 36870461]
  • Y P Hai, A C H Lee, K Chen, G J Kahaly. Traditional Chinese medicine in thyroid-associated orbitopathy. Journal of endocrinological investigation. 2023 Feb; ?(?):. doi: 10.1007/s40618-023-02024-4. [PMID: 36781592]
  • Huajie Tian, Yi Fang, Wei Liu, Jun Wang, Jianan Zhao, Hao Tang, Yixiao Yin, Yiyang Hu, Jinghua Peng. Inhibition on XBP1s-driven lipogenesis by Qushi Huayu Decoction contributes to amelioration of hepatic steatosis induced by fructose. Journal of ethnopharmacology. 2023 Jan; 301(?):115806. doi: 10.1016/j.jep.2022.115806. [PMID: 36216198]
  • Qin Li, Peng Zhao, Yu Wen, Zhimin Zou, Xihe Qin, Hongping Tan, Jian Gong, Qihua Wu, Chen Zheng, Kun Zhang, Qiaobing Huang, Marc Maegele, Zhengtao Gu, Li Li. Polydatin ameliorates TBI induced secondary brain injury by inhibiting NLRP3-induced neuroinflammation associated with SOD2 acetylation. Shock (Augusta, Ga.). 2022 Dec; ?(?):. doi: 10.1097/shk.0000000000002066. [PMID: 36477654]
  • Wenqi Jin, Meiling Fan, Yuxin Zhang, Qi Zhang, Chenxu Jing, Rui Jiang, Chunli Piao, Liwei Sun. Polydatin prevents lipotoxicity-induced dysfunction in pancreatic β-cells by inhibiting endoplasmic reticulum stress and excessive autophagy. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2022 Nov; 106(?):154410. doi: 10.1016/j.phymed.2022.154410. [PMID: 36030747]
  • Muhammad Ajmal Shah, Ayesha Hamid, Hafiza Ishmal Faheem, Azhar Rasul, Tourki A S Baokbah, Muhammad Haris, Rimsha Yousaf, Uzma Saleem, Shabnoor Iqbal, Maria Silvana Alves, Zahid Khan, Ghulam Hussain, Ifat Alsharfi, Haroon Khan, Philippe Jeandet. Uncovering the Anticancer Potential of Polydatin: A Mechanistic Insight. Molecules (Basel, Switzerland). 2022 Oct; 27(21):. doi: 10.3390/molecules27217175. [PMID: 36364001]
  • Dajie Wang, Zhaofeng Zhou, Liang Yuan. Polydatin reverses oxidation low lipoprotein (oxLDL)-induced apoptosis of human umbilical vein endothelial cells via regulating the miR-26a-5p/BID axis. European journal of histochemistry : EJH. 2022 Sep; 66(4):. doi: 10.4081/ejh.2022.3505. [PMID: 36128773]
  • Yao-Jun Liu, Wei-Heng Xu, Li-Ming Fan, Yu-Qin Zhang, Wen Xu, Ya-Ping Chen, Lin-Lin Chen, Li Chen, Wei Xu, Yan Wang, Ke-Dan Chu, Jun-Ping Zhang. Polydatin alleviates DSS- and TNBS-induced colitis by suppressing Th17 cell differentiation via directly inhibiting STAT3. Phytotherapy research : PTR. 2022 Sep; 36(9):3662-3671. doi: 10.1002/ptr.7533. [PMID: 35766233]
  • Rong-Hong Zhang, Dan Yang, Xiang-Ming Liao, Hong Zhang, Guo-Qi Chen, Wen-Li Zhang, Yu-Chan Wang, Cong Wang, Shang-Gao Liao, Meng Zhou, Yong-Lin Wang, Yong-Jun Li. Design, synthesis, and in vitro protective effect evaluation of α-carboline derivatives against H2O2-induced cardiomyocyte injury. European journal of medicinal chemistry. 2022 Aug; 238(?):114469. doi: 10.1016/j.ejmech.2022.114469. [PMID: 35605360]
  • Lin Huang, Jiawei Chen, Xiaojie Li, Mingxin Huang, Jilou Liu, Na Qin, Zhenhua Zeng, Xingmin Wang, Fen Li, Hong Yang. Polydatin Improves Sepsis-Associated Encephalopathy by Activating Sirt1 and Reducing p38 Phosphorylation. The Journal of surgical research. 2022 08; 276(?):379-393. doi: 10.1016/j.jss.2022.03.008. [PMID: 35447391]
  • Jinli Luo, Shuo Chen, Li Wang, Xiaohua Zhao, Chunli Piao. Pharmacological effects of polydatin in the treatment of metabolic diseases: A review. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2022 Jul; 102(?):154161. doi: 10.1016/j.phymed.2022.154161. [PMID: 35636169]
  • Y Yuan, G Feng, J Yang, C Yang, Y-H Tu. Polydatin alleviates osteoporosis by enhancing the osteogenic differentiation of osteoblasts. European review for medical and pharmacological sciences. 2022 Jun; 26(12):4392-4402. doi: 10.26355/eurrev_202206_29078. [PMID: 35776040]
  • Xuemei Xue, Fei Deng, Zhenkai Ge, Jingwen Meng, Xiya Liu, Yongheng Zhao, Yanggen Hu, Xu Ling. Conductive polymer sorbent for extraction and determination of resveratrol and polydatin in Polygonum cuspidatum root samples. Phytochemical analysis : PCA. 2022 Jun; 33(4):590-598. doi: 10.1002/pca.3112. [PMID: 35098595]
  • Can Liu, Wenyi Wang, Kaixin Zhang, Qiudi Liu, Tongyao Ma, Li Tan, Lanqing Ma. Protective Effects of Polydatin from Grapes and Reynoutria japonica Houtt. on Damaged Macrophages Treated with Acetaminophen. Nutrients. 2022 May; 14(10):. doi: 10.3390/nu14102077. [PMID: 35631218]
  • Jie Zhou, Meng Liang, Yu Lin, Hao Pang, Yutuo Wei, Ribo Huang, Liqin Du. Application of β-Glucosidase in a Biphasic System for the Efficient Conversion of Polydatin to Resveratrol. Molecules (Basel, Switzerland). 2022 Feb; 27(5):. doi: 10.3390/molecules27051514. [PMID: 35268615]
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