1,2-Benzoquinone (BioDeep_00000004903)
Secondary id: BioDeep_00001868744
human metabolite Endogenous
代谢物信息卡片
化学式: C6H4O2 (108.0211284)
中文名称:
谱图信息:
最多检出来源 Viridiplantae(plant) 0.85%
分子结构信息
SMILES: C1=CC(=O)C(=O)C=C1
InChI: InChI=1S/C6H4O2/c7-5-3-1-2-4-6(5)8/h1-4H
描述信息
1,2-Benzoquinone is a reactive electrophile that is an intermediate in benzene metabolism. It is substrate for the enzyme Catechol oxidase (EC 1.10.3.1) and can be generated from the oxidation of catechol. 1,2-Benzoquinone is capable of reacting with blood proteins to produce adducts.
1,2-Benzoquinone, also called ortho-benzoquinone or cyclohexa-3,5-diene-1,2-dione, is a ketone, with formula C6H4O2. It is one of the two isomers of quinone, the other being 1,4-benzoquinone. O-Quinone is found in tea.
同义名列表
数据库引用编号
18 个数据库交叉引用编号
- ChEBI: CHEBI:17253
- KEGG: C02351
- PubChem: 11421
- HMDB: HMDB0012133
- Metlin: METLIN62804
- Wikipedia: 1,2-Benzoquinone
- MetaCyc: CPD-385
- foodb: FDB004549
- chemspider: 10941
- CAS: 20526-43-6
- CAS: 583-63-1
- PMhub: MS000017540
- PubChem: 5398
- 3DMET: B00429
- NIKKAJI: J7.445D
- KNApSAcK: 17253
- LOTUS: LTS0219367
- wikidata: Q402601
分类词条
相关代谢途径
Reactome(0)
代谢反应
102 个相关的代谢反应过程信息。
Reactome(0)
Plant Reactome(0)
INOH(0)
PlantCyc(100)
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
- o-diquinones biosynthesis:
O2 + catechol ⟶ 1,2-benzoquinone + H2O
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
2 个相关的物种来源信息
- 9606 - Homo sapiens: -
- 39354 - Salvia abrotanoides: 10.1016/J.BMC.2006.03.047
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
- Hua Liu, Weidan Na, Ziping Liu, Xueqian Chen, Xingguang Su. A novel turn-on fluorescent strategy for sensing ascorbic acid using graphene quantum dots as fluorescent probe.
Biosensors & bioelectronics.
2017 Jun; 92(?):229-233. doi:
10.1016/j.bios.2017.02.005
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British journal of pharmacology.
2012 Nov; 167(6):1271-86. doi:
10.1111/j.1476-5381.2012.02067.x
. [PMID: 22671862] - Katra Kolšek, Janez Mavri, Marija Sollner Dolenc. Reactivity of bisphenol A-3,4-quinone with DNA. A quantum chemical study.
Toxicology in vitro : an international journal published in association with BIBRA.
2012 Feb; 26(1):102-6. doi:
10.1016/j.tiv.2011.11.003
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Cancer prevention research (Philadelphia, Pa.).
2012 Jan; 5(1):73-81. doi:
10.1158/1940-6207.capr-11-0348
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Interdisciplinary toxicology.
2011 Dec; 4(4):173-83. doi:
10.2478/v10102-011-0027-5
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PloS one.
2011 Apr; 6(4):e18127. doi:
10.1371/journal.pone.0018127
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Biosensors & bioelectronics.
2011 Jan; 26(5):2513-9. doi:
10.1016/j.bios.2010.10.047
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PloS one.
2010 Nov; 5(11):e13880. doi:
10.1371/journal.pone.0013880
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IUBMB life.
2010 Oct; 62(10):746-51. doi:
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Medical hypotheses.
2010 Jul; 75(1):1-4. doi:
10.1016/j.mehy.2010.03.002
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PLoS genetics.
2010 Jul; 6(7):e1001008. doi:
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Chemical research in toxicology.
2010 Jun; 23(6):1115-26. doi:
10.1021/tx100137n
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Phytochemical analysis : PCA.
2010 May; 21(3):273-8. doi:
10.1002/pca.1197
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Journal of natural medicines.
2010 Jan; 64(1):85-8. doi:
10.1007/s11418-009-0364-2
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Analytical sciences : the international journal of the Japan Society for Analytical Chemistry.
2009 Oct; 25(10):1231-6. doi:
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Talanta.
2009 Feb; 77(4):1322-7. doi:
10.1016/j.talanta.2008.09.010
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Chemical research in toxicology.
2007 Sep; 20(9):1352-8. doi:
10.1021/tx700205j
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Analytica chimica acta.
2007 Jul; 596(2):210-21. doi:
10.1016/j.aca.2007.06.013
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BMC chemical biology.
2007 Jul; 7(?):2. doi:
10.1186/1472-6769-7-2
. [PMID: 17608946] - Kazuhiko Tamaki, Takeshi Tamaki, Takashi Yamazaki. Studies on the deodorization by mushroom (Agaricus bisporus) extract of garlic extract-induced oral malodor.
Journal of nutritional science and vitaminology.
2007 Jun; 53(3):277-86. doi:
10.3177/jnsv.53.277
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Journal of clinical biochemistry and nutrition.
2007 Mar; 40(2):92-100. doi:
10.3164/jcbn.40.92
. [PMID: 18188410] - Yu-Sheng Lin, Roel Vermeulen, Chin H Tsai, Suramya Waidyanatha, Qing Lan, Nathaniel Rothman, Martyn T Smith, Luoping Zhang, Min Shen, Guilan Li, Songnian Yin, Sungkyoon Kim, Stephen M Rappaport. Albumin adducts of electrophilic benzene metabolites in benzene-exposed and control workers.
Environmental health perspectives.
2007 Jan; 115(1):28-34. doi:
10.1289/ehp.8948
. [PMID: 17366815] - Angel A J Torriero, Eloy Salinas, Eduardo J Marchevsky, Julio Raba, Juana J Silber. Penicillamine determination using a tyrosinase micro-rotating biosensor.
Analytica chimica acta.
2006 Nov; 580(2):136-42. doi:
10.1016/j.aca.2006.07.067
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Biochimica et biophysica acta.
2006 Aug; 1766(1):63-78. doi:
10.1016/j.bbcan.2006.03.001
. [PMID: 16675129] - Monica Sanchez-Gonzalez, John P N Rosazza. Biocatalytic synthesis of butein and sulfuretin by Aspergillus alliaceus.
Journal of agricultural and food chemistry.
2006 Jun; 54(13):4646-50. doi:
10.1021/jf060900k
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Guang pu xue yu guang pu fen xi = Guang pu.
2006 Jun; 26(6):1031-3. doi:
"
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Environmental health perspectives.
2006 Apr; 114 Suppl 1(?):81-9. doi:
10.1289/ehp.8058
. [PMID: 16818251] - Mercedes Jiménez-Atiénzar, Josefa Escribano, Juana Cabanes, Fernando Gandía-Herrero, Francisco García-Carmona. Oxidation of the flavonoid eriodictyol by tyrosinase.
Plant physiology and biochemistry : PPB.
2005 Sep; 43(9):866-73. doi:
10.1016/j.plaphy.2005.07.010
. [PMID: 16289948] - Cristina Gaspar-Marques, M Fátima Simões, Benjamín Rodríguez. A trihomoabietane diterpenoid from Plectranthus grandidentatus and an unusual addition of acetone to the ortho-quinone system of cryptotanshinone.
Journal of natural products.
2005 Sep; 68(9):1408-11. doi:
10.1021/np0580457
. [PMID: 16180825] - Yusuke Sawai, Jae-Hak Moon, Kanzo Sakata, Naoharu Watanabe. Effects of structure on radical-scavenging abilities and antioxidative activities of tea polyphenols: NMR analytical approach using 1,1-diphenyl-2-picrylhydrazyl radicals.
Journal of agricultural and food chemistry.
2005 May; 53(9):3598-604. doi:
10.1021/jf040423a
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Chemical research in toxicology.
2004 Apr; 17(4):564-71. doi:
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The Journal of biological chemistry.
2003 Aug; 278(31):28736-42. doi:
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Bioorganic chemistry.
2003 Jun; 31(3):206-15. doi:
10.1016/s0045-2068(03)00042-7
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Chemico-biological interactions.
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