3,3-Dimethylquercetin (BioDeep_00000397263)

 

Secondary id: BioDeep_00000266235, BioDeep_00000369801, BioDeep_00000863589

PANOMIX_OTCML-2023


代谢物信息卡片


4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-methoxy-

化学式: C17H14O7 (330.0739)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1(O)=CC2OC(C3C=C(OC)C(O)=CC=3)=C(OC)C(=O)C=2C(O)=C1
InChI: InChI=1S/C17H14O7/c1-22-12-5-8(3-4-10(12)19)16-17(23-2)15(21)14-11(20)6-9(18)7-13(14)24-16/h3-7,18-20H,1-2H3

描述信息

3,3-dimethylquercetin is a dimethoxyflavone that is quercetin in which the hydroxy groups at position 3 and 3 have been replaced by methoxy groups. It has been isolated from several plant species and exhibits anti-bacterial and anti-cancer properties. It has a role as a plant metabolite, an antibacterial agent, an antineoplastic agent and an apoptosis inducer. It is a trihydroxyflavone, a dimethoxyflavone and a member of 3-methoxyflavones. It is functionally related to a quercetin.
Quercetin 3,3-dimethyl ether is a natural product found in Psiadia viscosa, Cleome amblyocarpa, and other organisms with data available.
A dimethoxyflavone that is quercetin in which the hydroxy groups at position 3 and 3 have been replaced by methoxy groups. It has been isolated from several plant species and exhibits anti-bacterial and anti-cancer properties.

同义名列表

24 个代谢物同义名

4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-methoxy-; 4H-1-Benzoyran-4-one, 5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-methoxy-; 5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-methoxy-4H-1-benzopyran-4-one; 4H-1-Benzopyran-4-one,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-methoxy-; 5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-methoxy-4H-chromen-4-one #; 5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-methoxy-4H-chromen-4-one; 5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-methoxychromen-4-one; Flavone, 4,5,7-trihydroxy-3,3-dimethoxy-; Flavone,5,7-trihydroxy-3,3-dimethoxy-; 5,7,4-Trihydroxy-3,3-dimethoxyflavone; 4,5,7-trihydroxy-3,3-dimethoxyflavone; Quercetin 3,3-dimethyl ether; Quercetin-3,3-dimethyl ether; FMEHGPQTMOPUGM-UHFFFAOYSA-N; Quercetin-3,3-dimethylether; 3,3-O-dimethyl quercetin; 3,3-di-O-methylquercetin; 3,3-O-DIMETHYLQUERCETIN; 3-O-methylisorhamnetin; 3,3-dimethoxyquercetin; 3,3-Dimethylquercetin; 3,3-Dimethylquercetol; UNII-J03N0KJ42I; J03N0KJ42I



数据库引用编号

9 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(1)

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。

亚细胞结构定位 关联基因列表


文献列表

  • Wamidh H Talib, Musa H Abu Zarga, Adel M Mahasneh. Antiproliferative, antimicrobial and apoptosis inducing effects of compounds isolated from Inula viscosa. Molecules (Basel, Switzerland). 2012 Mar; 17(3):3291-303. doi: 10.3390/molecules17033291. [PMID: 22418930]
  • Jihua Wang, Jingfeng Lou, Chao Luo, Ligang Zhou, Mingan Wang, Lan Wang. Phenolic compounds from Halimodendron halodendron (Pall.) voss and their antimicrobial and antioxidant activities. International journal of molecular sciences. 2012; 13(9):11349-11364. doi: 10.3390/ijms130911349. [PMID: 23109858]
  • Jihua Wang, Haifeng Gao, Jianglin Zhao, Qi Wang, Ligang Zhou, Jianguo Han, Zhu Yu, Fuyu Yang. Preparative separation of phenolic compounds from Halimodendron halodendron by high-speed counter-current chromatography. Molecules (Basel, Switzerland). 2010 Aug; 15(9):5998-6007. doi: 10.3390/molecules15095998. [PMID: 20877205]
  • Maher M Al-Dabbas, Kanefumi Kitahara, Toshihiko Suganuma, Fumio Hashimoto, Kenjiro Tadera. Antioxidant and alpha-amylase inhibitory compounds from aerial parts of Varthemia iphionoides Boiss. Bioscience, biotechnology, and biochemistry. 2006 Sep; 70(9):2178-84. doi: 10.1271/bbb.60132. [PMID: 16960381]
  • Xin Zhao, Rui-Liang Zhu, Biao Jiang, Hao Huang. [Studies on chemical constituents of cytotoxic fraction from leaves of Elaeagnus pungens]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2006 Mar; 31(6):472-4. doi: . [PMID: 16722375]
  • Tyng-Shyan Huang, Dominique Anzellotti, Fabienne Dedaldechamp, Ragai K Ibrahim. Partial purification, kinetic analysis, and amino acid sequence information of a flavonol 3-O-methyltransferase from Serratula tinctoria. Plant physiology. 2004 Apr; 134(4):1366-76. doi: 10.1104/pp.103.036442. [PMID: 15084728]
  • Jiao Shi, Bo Chen, Zhi-hua Sun, Chang-qi Hu. [Studies on flavonoid constituents of Caragana intermediia]. Yao xue xue bao = Acta pharmaceutica Sinica. 2003 Aug; 38(8):599-602. doi: ". [PMID: 14628451]
  • J C Meng, Y F Hu, J H Chen, R X Tan. Antifungal highly oxygenated guaianolides and other constituents from Ajania fruticulosa. Phytochemistry. 2001 Dec; 58(7):1141-5. doi: 10.1016/s0031-9422(01)00389-2. [PMID: 11730880]
  • X P Dong, C T Che, N R Farnsworth. Cytotoxic flavonols from Gutierrezia microcephala. Journal of natural products. 1987 Mar; 50(2):337-8. doi: 10.1021/np50050a065. [PMID: 3655803]
  • . . . . doi: . [PMID: 21343428]