Stilben-4-ol (BioDeep_00000010134)

 

Secondary id: BioDeep_00001874748


代谢物信息卡片


trans-4-hydroxystilbene;

化学式: C14H12O (196.08881019999998)
中文名称: 反式-4-羟基二苯乙烯
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1(O)=CC=C(/C=C/C2=CC=CC=C2)C=C1
InChI: InChI=1S/C14H12O/c15-14-10-8-13(9-11-14)7-6-12-4-2-1-3-5-12/h1-11,15H/b7-6+

描述信息

同义名列表

5 个代谢物同义名

trans-4-hydroxystilbene;; Trans-4-hydroxystilbene; 4-Hydroxystilbene; (E)-4-stilbenol; Stilben-4-ol



数据库引用编号

14 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

0 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。



文献列表

  • Antonio González-Sarrías, Juan Carlos Espín-Aguilar, Salvador Romero-Reyes, Julio Puigcerver, Mateo Alajarín, José Berná, María Victoria Selma, Juan Carlos Espín. Main Determinants Affecting the Antiproliferative Activity of Stilbenes and Their Gut Microbiota Metabolites in Colon Cancer Cells: A Structure-Activity Relationship Study. International journal of molecular sciences. 2022 Dec; 23(23):. doi: 10.3390/ijms232315102. [PMID: 36499424]
  • Fatma M Abdel Bar, Ghada M Abbas, Ahmed A Gohar, Mohamed-Farid I Lahloub. Antiproliferative activity of stilbene derivatives and other constituents from the stem bark of Morus nigra L. Natural product research. 2020 Dec; 34(24):3506-3513. doi: 10.1080/14786419.2019.1573236. [PMID: 30822142]
  • Syuhei Nakao, Miyuki Mabuchi, Shenglan Wang, Yoko Kogure, Tadashi Shimizu, Koichi Noguchi, Akito Tanaka, Yi Dai. Synthesis of resveratrol derivatives as new analgesic drugs through desensitization of the TRPA1 receptor. Bioorganic & medicinal chemistry letters. 2017 07; 27(14):3167-3172. doi: 10.1016/j.bmcl.2017.05.025. [PMID: 28576617]
  • Hsing-Chun Lin, Ming-Ju Hsieh, Chiung-Huei Peng, Shun-Fa Yang, Chien-Ning Huang. Pterostilbene Inhibits Vascular Smooth Muscle Cells Migration and Matrix Metalloproteinase-2 through Modulation of MAPK Pathway. Journal of food science. 2015 Oct; 80(10):H2331-5. doi: 10.1111/1750-3841.13002. [PMID: 26409033]
  • Yun-Wei Shi, Cai-Ping Wang, Lei Liu, Yang-Liu Liu, Xing Wang, Ye Hong, Zhen Li, Ling-Dong Kong. Antihyperuricemic and nephroprotective effects of resveratrol and its analogues in hyperuricemic mice. Molecular nutrition & food research. 2012 Sep; 56(9):1433-44. doi: 10.1002/mnfr.201100828. [PMID: 22865646]
  • Xiaoli Chang, Ernst Heene, Fei Qiao, Peter Nick. The phytoalexin resveratrol regulates the initiation of hypersensitive cell death in Vitis cell. PloS one. 2011; 6(10):e26405. doi: 10.1371/journal.pone.0026405. [PMID: 22053190]
  • Hong Fang, Weida Tong, William S Branham, Carrie L Moland, Stacy L Dial, Huixiao Hong, Qian Xie, Roger Perkins, William Owens, Daniel M Sheehan. Study of 202 natural, synthetic, and environmental chemicals for binding to the androgen receptor. Chemical research in toxicology. 2003 Oct; 16(10):1338-58. doi: 10.1021/tx030011g. [PMID: 14565775]
  • Peter Lorenz, Sanjoy Roychowdhury, Mario Engelmann, Gerald Wolf, Thomas F W Horn. Oxyresveratrol and resveratrol are potent antioxidants and free radical scavengers: effect on nitrosative and oxidative stress derived from microglial cells. Nitric oxide : biology and chemistry. 2003 Sep; 9(2):64-76. doi: 10.1016/j.niox.2003.09.005. [PMID: 14623172]
  • Mar Larrosa, Francisco A Tomás-Barberán, Juan Carlos Espín. Grape polyphenol resveratrol and the related molecule 4-hydroxystilbene induce growth inhibition, apoptosis, S-phase arrest, and upregulation of cyclins A, E, and B1 in human SK-Mel-28 melanoma cells. Journal of agricultural and food chemistry. 2003 Jul; 51(16):4576-84. doi: 10.1021/jf030073c. [PMID: 14705880]
  • Yu Jun Cai, Jian Guo Fang, Lan Ping Ma, Li Yang, Zhong Li Liu. Inhibition of free radical-induced peroxidation of rat liver microsomes by resveratrol and its analogues. Biochimica et biophysica acta. 2003 Jan; 1637(1):31-8. doi: 10.1016/s0925-4439(02)00174-6. [PMID: 12527404]
  • Jian-Guo Fang, Man Lu, Zhi-Hua Chen, Hui-He Zhu, Yan Li, Li Yang, Long-Min Wu, Zhong-Li Liu. Antioxidant effects of resveratrol and its analogues against the free-radical-induced peroxidation of linoleic acid in micelles. Chemistry (Weinheim an der Bergstrasse, Germany). 2002 Sep; 8(18):4191-8. doi: 10.1002/1521-3765(20020916)8:18<4191::aid-chem4191>3.0.co;2-s. [PMID: 12298009]
  • Christelle Privat, João Paulo Telo, Vania Bernardes-Genisson, Abel Vieira, Jean-Pierre Souchard, Françoise Nepveu. Antioxidant properties of trans-epsilon-viniferin as compared to stilbene derivatives in aqueous and nonaqueous media. Journal of agricultural and food chemistry. 2002 Feb; 50(5):1213-7. doi: 10.1021/jf010676t. [PMID: 11853506]
  • S Stojanović, H Sprinz, O Brede. Efficiency and mechanism of the antioxidant action of trans-resveratrol and its analogues in the radical liposome oxidation. Archives of biochemistry and biophysics. 2001 Jul; 391(1):79-89. doi: 10.1006/abbi.2001.2388. [PMID: 11414688]
  • A A Calderón, M A Pedreño, A Ros-Barceló, R Muñoz. Zymographic screening of plant peroxidase isoenzymes oxidizing 4-hydroxystilbenes. Electrophoresis. 1990 Jun; 11(6):507-8. doi: 10.1002/elps.1150110614. [PMID: 1697538]
  • A A Calderón, M A Pedreño, A Ros Barceló, R Muñoz. A spectrophotometric assay for quantitative analysis of the oxidation of 4-hydroxystilbene by peroxidase-H2O2 systems. Journal of biochemical and biophysical methods. 1990 Mar; 20(3):171-80. doi: 10.1016/0165-022x(90)90075-n. [PMID: 2161027]
  • I M Nilsson, S E Bergentz, U Hedner, K Kullenberg. Gastric fibrinolysis. Thrombosis et diathesis haemorrhagica. 1975 Nov; 34(2):409-18. doi: 10.1055/s-0038-1651400. [PMID: 807]