436-32-8 (BioDeep_00000859468)

Main id: BioDeep_00000276810

 

PANOMIX_OTCML-2023 Volatile Flavor Compounds


代谢物信息卡片


Benzoic acid, 2,4-dimethoxy-3,6-dimethyl-, 4-carboxy-3-hydroxy-2,5-dimethylphenyl ester

化学式: C20H22O7 (374.1365462)
中文名称: 地弗地衣酸
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1=CC(=C(C(=C1C(=O)O)O)C)OC(=O)C2=C(C(=C(C=C2C)OC)C)OC
InChI: InChI=1S/C20H22O7/c1-9-8-14(11(3)17(21)15(9)19(22)23)27-20(24)16-10(2)7-13(25-5)12(4)18(16)26-6/h7-8,21H,1-6H3,(H,22,23)

描述信息

Diffractaic acid, a major constituent of U. longissimi, acts as an effective proapoptotic agent in various disorders research[1]. Diffractaic acid is the analgesic and antipyretic component of Usnea diffracta[2].
Diffractaic acid, a major constituent of U. longissimi, acts as an effective proapoptotic agent in various disorders research[1]. Diffractaic acid is the analgesic and antipyretic component of Usnea diffracta[2].

同义名列表

43 个代谢物同义名

Benzoic acid, 2,4-dimethoxy-3,6-dimethyl-, 4-carboxy-3-hydroxy-2,5-dimethylphenyl ester; 4-(2,4-dimethoxy-3,6-dimethyl-phenyl)carbonyloxy-2-hydroxy-3,6-dimethyl-benzoic acid; 4-[(2,4-dimethoxy-3,6-dimethylphenyl)-oxomethoxy]-2-hydroxy-3,6-dimethylbenzoic acid; 4-(2,4-Dimethoxy-3,6-dimethylphenylcarbonyloxy)-2-hydroxy-3,6-dimethylbenzoic acid; 4-(2,4-dimethoxy-3,6-dimethyl-benzoyl)oxy-2-hydroxy-3,6-dimethyl-benzoic acid; 4-(2,4-dimethoxy-3,6-dimethylbenzoyl)oxy-2-hydroxy-3,6-dimethylbenzoic acid; beta-Resorcylic acid, 3,6-dimethyl-, 4-(2,4-dimethoxy-3,6-dimethylbenzoate); 3-10-00-01544 (Beilstein Handbook Reference); DIFFRACTANIC ACID; Spectrum3_001103; DIFFRACTOIC ACID; Diffractaic acid; Spectrum2_000730; Spectrum5_000723; Spectrum4_001934; Dirhizomic acid; Dirbizomic acid; NCGC00095683-01; SpecPlus_000832; Spectrum_000043; SPECTRUM1504118; BSPBio_002806; KBioGR_002309; KBioSS_000423; STOCK1N-26012; DivK1c_006928; KBio2_002991; SPBio_000660; SMR000386936; KBio3_002026; MLS001049104; KBio2_005559; KBio2_000423; KBio1_001872; AIDS-092382; BRN 2915070; NSC 685595; AIDS092382; NSC685595; NSC 5901; 436-32-8; NSC5901; Diffractaic acid



数据库引用编号

5 个数据库交叉引用编号

分类词条

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代谢反应

0 个相关的代谢反应过程信息。

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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

  • Hanxue Wang, Tao Yang, Xuemei Cheng, Sukfan Kwong, Chenghai Liu, Rui An, Guowen Li, Xinhong Wang, Changhong Wang. Simultaneous determination of usnic, diffractaic, evernic and barbatic acids in rat plasma by ultra-high-performance liquid chromatography-quadrupole exactive Orbitrap mass spectrometry and its application to pharmacokinetic studies. Biomedical chromatography : BMC. 2018 Mar; 32(3):. doi: 10.1002/bmc.4123. [PMID: 29055065]
  • Changlei Sun, Feng Liu, Jie Sun, Jia Li, Xiao Wang. Optimisation and establishment of separation conditions of organic acids from Usnea longissima Ach. by pH-zone-refining counter-current chromatography: Discussion of the eluotropic sequence. Journal of chromatography. A. 2016 Jan; 1427(?):96-101. doi: 10.1016/j.chroma.2015.12.016. [PMID: 26686561]
  • Fehmi Odabasoglu, Omer S Yildirim, Hayati Aygun, Zekai Halici, Mesut Halici, Fazli Erdogan, Elif Cadirci, Ahmet Cakir, Zafer Okumus, Bunyamin Aksakal, Ali Aslan, Deniz Unal, Yasin Bayir. Diffractaic acid, a novel proapoptotic agent, induces with olive oil both apoptosis and antioxidative systems in Ti-implanted rabbits. European journal of pharmacology. 2012 Jan; 674(2-3):171-8. doi: 10.1016/j.ejphar.2011.11.019. [PMID: 22119377]
  • Y Bayir, F Odabasoglu, A Cakir, A Aslan, H Suleyman, M Halici, C Kazaz. The inhibition of gastric mucosal lesion, oxidative stress and neutrophil-infiltration in rats by the lichen constituent diffractaic acid. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2006 Sep; 13(8):584-90. doi: 10.1016/j.phymed.2005.07.002. [PMID: 16920514]
  • K C Kumar, K Müller. Lichen metabolites. 2. Antiproliferative and cytotoxic activity of gyrophoric, usnic, and diffractaic acid on human keratinocyte growth. Journal of natural products. 1999 Jun; 62(6):821-3. doi: 10.1021/np980378z. [PMID: 10395495]
  • K C Kumar, K Müller. Lichen metabolites. 1. Inhibitory action against leukotriene B4 biosynthesis by a non-redox mechanism. Journal of natural products. 1999 Jun; 62(6):817-20. doi: 10.1021/np9803777. [PMID: 10395494]