AI3-26293 (BioDeep_00000860957)

   


代谢物信息卡片


InChI=1\C14H22O\c1-13(2,3)10-8-7-9-11(12(10)15)14(4,5)6\h7-9,15H,1-6H

化学式: C14H22O (206.1670562)
中文名称: 2,6-二叔丁基酚
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC(C)(C)C1=C(C(=CC=C1)C(C)(C)C)O
InChI: InChI=1S/C14H22O/c1-13(2,3)10-8-7-9-11(12(10)15)14(4,5)6/h7-9,15H,1-6H3

描述信息

同义名列表

30 个代谢物同义名

InChI=1\C14H22O\c1-13(2,3)10-8-7-9-11(12(10)15)14(4,5)6\h7-9,15H,1-6H; Phenol, 2,6-bis(1,1-dimethylethyl)-; 1,3-DITERT.BUTYL,2-HYDROXY-BENZENE; 2,6-Bis(1,1-dimethylethyl)phenol; Phenol, 2,6-di-tert-butyl-; 2,6-Bis(tert-butyl)phenol; 2,6-DI-TERT-BUTYLPHENOL; 2,6 Di-tert-butylphenol; 2,6-ditert-butylphenol; 2,6-Di-t-butylphenol; Di-tert-butylphenol; EINECS 204-884-0; NCGC00164272-01; D48400_ALDRICH; Dibutylphenol; ZINC01681254; Ethyl AN 701; Ethanox 701; 50356-17-7; CCRIS 5828; Hitec 4701; Isonox 103; HSDB 5616; AI3-26293; Ethyl 701; NSC 49175; ST5214492; 128-39-2; NSC49175; AN 701



数据库引用编号

6 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)

1 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

  • Mauricio Tavares Jacques, Viviane de Souza, Flávio Augusto Rocha Barbosa, Rômulo Faria Santos Canto, Samantha Cristiane Lopes, Rui Daniel Prediger, Antônio Luiz Braga, Michael Aschner, Marcelo Farina. Novel Probucol Analogue, 4,4'-Diselanediylbis (2,6-Di-tert-Butylphenol), Prevents Oxidative Glutamate Neurotoxicity In Vitro and Confers Neuroprotection in a Rodent Model of Ischemic Stroke. ACS chemical neuroscience. 2023 Jul; ?(?):. doi: 10.1021/acschemneuro.3c00138. [PMID: 37499207]
  • Ons Ousji, Lekha Sleno. Identification of In Vitro Metabolites of Synthetic Phenolic Antioxidants BHT, BHA, and TBHQ by LC-HRMS/MS. International journal of molecular sciences. 2020 Dec; 21(24):. doi: 10.3390/ijms21249525. [PMID: 33333739]
  • D B Shpakovsky, A A Shtil, E V Kharitonashvili, V Yu Tyurin, T A Antonenko, A A Nazarov, V P Osipova, N T Berberova, L S Foteeva, C Schmidt, I Ott, E R Milaeva. The antioxidant 2,6-di-tert-butylphenol moiety attenuates the pro-oxidant properties of the auranofin analogue. Metallomics : integrated biometal science. 2018 03; 10(3):406-413. doi: 10.1039/c7mt00286f. [PMID: 29399682]
  • Peter Kusch, Susanne Deininger, Sabine Specht, Rudeka Maniako, Stefanie Haubrich, Tanja Pommerening, Paul Kong Thoo Lin, Achim Hoerauf, Annette Kaiser. In Vitro and In Vivo Antimalarial Activity Assays of Seeds from Balanites aegyptiaca: Compounds of the Extract Show Growth Inhibition and Activity against Plasmodial Aminopeptidase. Journal of parasitology research. 2011; 2011(?):368692. doi: 10.1155/2011/368692. [PMID: 21687598]
  • E R Milaeva, S I Filimonova, N N Meleshonkova, L G Dubova, E F Shevtsova, S O Bachurin, N S Zefirov. Antioxidative activity of ferrocenes bearing 2,6-di-tert-butylphenol moieties. Bioinorganic chemistry and applications. 2010; ?(?):165482. doi: 10.1155/2010/165482. [PMID: 20631836]
  • E R Milaeva, O A Gerasimova, Zhang Jingwei, D B Shpakovsky, S A Syrbu, A S Semeykin, O I Koifman, E G Kireeva, E F Shevtsova, S O Bachurin, N S Zefirov. Synthesis and antioxidative activity of metalloporphyrins bearing 2,6-di-tert-butylphenol pendants. Journal of inorganic biochemistry. 2008 May; 102(5-6):1348-58. doi: 10.1016/j.jinorgbio.2008.01.022. [PMID: 18321586]
  • Masahiro Ogata, Kazuo Shin-Ya, Shiro Urano, Toyoshige Endo. Antioxidant activity of propofol and related monomeric and dimeric compounds. Chemical & pharmaceutical bulletin. 2005 Mar; 53(3):344-6. doi: 10.1248/cpb.53.344. [PMID: 15744114]
  • Jörg Ahrens, Gertrud Haeseler, Martin Leuwer, Bahram Mohammadi, Klaus Krampfl, Reinhard Dengler, Johannes Bufler. 2,6 di-tert-butylphenol, a nonanesthetic propofol analog, modulates alpha1beta glycine receptor function in a manner distinct from propofol. Anesthesia and analgesia. 2004 Jul; 99(1):91-96. doi: 10.1213/01.ane.0000120083.10269.54. [PMID: 15281510]
  • Maria Pia Rigobello, Roberto Stevanato, Federico Momo, Sabrina Fabris, Guido Scutari, Rita Boscolo, Alessandra Folda, Alberto Bindoli. Evaluation of the antioxidant properties of propofol and its nitrosoderivative. comparison with homologue substituted phenols. Free radical research. 2004 Mar; 38(3):315-21. doi: 10.1080/03079450310001652031. [PMID: 15129739]
  • M D Krasowski, A Jenkins, P Flood, A Y Kung, A J Hopfinger, N L Harrison. General anesthetic potencies of a series of propofol analogs correlate with potency for potentiation of gamma-aminobutyric acid (GABA) current at the GABA(A) receptor but not with lipid solubility. The Journal of pharmacology and experimental therapeutics. 2001 Apr; 297(1):338-51. doi: ". [PMID: 11259561]
  • O A Reshetnik, E G Kanevskaia, L Kh Gordon, A V Lygin, G O Ezhkova. [The effect of antioxidant on the growth and lipid composition of Saccharomyces cerevisiae yeasts at different phases of the development of a culture]. Izvestiia Akademii nauk. Seriia biologicheskaia. 1997 Mar; ?(2):172-6. doi: ". [PMID: 9190219]
  • O A Reshetnik, G O Ezhkova, E G Kanevskaia, P A Kirpichnikov. [Regulation by an antioxidant of growth, composition, and physico-chemical features of lipids from Saccharomyces cerevisiae]. Doklady Akademii nauk. 1996 Feb; 346(5):705-7. doi: ". [PMID: 8664837]
  • A W Girotti, G J Bachowski, J E Jordan. Lipid peroxidation in erythrocyte membranes: cholesterol product analysis in photosensitized and xanthine oxidase-catalyzed reactions. Lipids. 1987 Jun; 22(6):401-8. doi: 10.1007/bf02537268. [PMID: 3112484]
  • Y Fujimoto, H Tanioka, E Toibana, T Yamamoto, T Fujita. Inhibition of prostaglandin synthesis in rabbit kidney medulla slices by antioxidants. The Journal of pharmacy and pharmacology. 1984 Mar; 36(3):195-7. doi: 10.1111/j.2042-7158.1984.tb06939.x. [PMID: 6144757]
  • F Z Meerson. Pathogenesis and prophylaxis of cardiac lesions in stress. Advances in myocardiology. 1983; 4(?):3-21. doi: 10.1007/978-1-4757-4441-5_1. [PMID: 6190205]