Camphorquinone (BioDeep_00000009949)

Main id: BioDeep_00000012238

 

human metabolite blood metabolite


代谢物信息卡片


1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione bornane-2,3-dione

化学式: C10H14O2 (166.09937440000002)
中文名称: 1,7,7-三甲基-二环[2.2.1]庚烷-2,3-二酮, (±)-樟脑醌
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C12C(C(=O)C(CC1)(C)C2(C)C)=O
InChI: InChI=1S/C10H14O2/c1-9(2)6-4-5-10(9,3)8(12)7(6)11/h6H,4-5H2,1-3H3

描述信息

同义名列表

10 个代谢物同义名

1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione bornane-2,3-dione; Bicyclo[2.2.1]heptane-2,3-dione, 1,7,7-trimethyl-; 1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione; bornane-2,3-dione; 2,3-bornanedione; camphoroquinone; camphor quinone; Camphorquinone; camphoquinone; Oxocamphor



数据库引用编号

13 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)

3 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

  • Renke Perduns, Joachim Volk, Melanie Plum, André Jochums, Frank Gutzki, Volkhard Kaever, Werner Geurtsen. Camphorquinone alters the expression of extracellular proteases in a 3D co-culture model of the oral mucosa. Dental materials : official publication of the Academy of Dental Materials. 2021 02; 37(2):236-248. doi: 10.1016/j.dental.2020.11.005. [PMID: 33257085]
  • Satoshi Endo, Namiki Miyagi, Toshiyuki Matsunaga, Akira Ikari. Rabbit dehydrogenase/reductase SDR family member 11 (DHRS11): Its identity with acetohexamide reductase with broad substrate specificity and inhibitor sensitivity, different from human DHRS11. Chemico-biological interactions. 2019 May; 305(?):12-20. doi: 10.1016/j.cbi.2019.03.026. [PMID: 30926317]
  • Mingsheng Chen, Ying Zhang, Vladimir Dusevich, Yi Liu, Qingsong Yu, Yong Wang. Non-thermal atmospheric plasma brush induces HEMA grafting onto dentin collagen. Dental materials : official publication of the Academy of Dental Materials. 2014 Dec; 30(12):1369-77. doi: 10.1016/j.dental.2014.10.004. [PMID: 25458523]
  • Ying Zhang, Qingsong Yu, Yong Wang. Non-thermal atmospheric plasmas in dental restoration: improved resin adhesive penetration. Journal of dentistry. 2014 Aug; 42(8):1033-42. doi: 10.1016/j.jdent.2014.05.005. [PMID: 24859333]
  • Joachim Volk, Gabriele Leyhausen, Miriam Wessels, Werner Geurtsen. Reduced glutathione prevents camphorquinone-induced apoptosis in human oral keratinocytes. Dental materials : official publication of the Academy of Dental Materials. 2014 Feb; 30(2):215-26. doi: 10.1016/j.dental.2013.11.008. [PMID: 24355435]
  • Mingsheng Chen, Ying Zhang, Xiaomei Yao, Hao Li, Qingsong Yu, Yong Wang. Effect of a non-thermal, atmospheric-pressure, plasma brush on conversion of model self-etch adhesive formulations compared to conventional photo-polymerization. Dental materials : official publication of the Academy of Dental Materials. 2012 Dec; 28(12):1232-9. doi: 10.1016/j.dental.2012.09.005. [PMID: 23018084]
  • F H F Loureiro, S Consani, R D Guiraldo, R L X Consani, S B Berger, R V Carvalho, L Correr-Sobrinho, M A C Sinhoreti. Comparison between two methods to evaluate temperature changes produced by composite light curing units and polymerization techniques. Minerva stomatologica. 2011 Oct; 60(10):501-8. doi: NULL. [PMID: 22082855]
  • Richard B T Price, Daniel Labrie, Frederick A Rueggeberg, Christopher M Felix. Irradiance differences in the violet (405 nm) and blue (460 nm) spectral ranges among dental light-curing units. Journal of esthetic and restorative dentistry : official publication of the American Academy of Esthetic Dentistry ... [et al.]. 2010 Dec; 22(6):363-77. doi: 10.1111/j.1708-8240.2010.00368.x. [PMID: 21126292]
  • Hiroyuki Arikawa, Hideo Takahashi, Takahito Kanie, Seiji Ban. Effect of various visible light photoinitiators on the polymerization and color of light-activated resins. Dental materials journal. 2009 Jul; 28(4):454-60. doi: 10.4012/dmj.28.454. [PMID: 19721283]
  • Rahul A Datar, Fredrick A Rueggeberg, Gretchen B Caughman, John C Wataha, Jill B Lewis, George S Schuster. Effects of sub-toxic concentrations of camphorquinone on cell lipid metabolism. Journal of biomaterials science. Polymer edition. 2005; 16(10):1293-302. doi: 10.1163/156856205774269557. [PMID: 16268254]
  • Ralf Janda, Jean-François Roulet, Martin Kaminsky, Glenn Steffin, Mark Latta. Color stability of resin matrix restorative materials as a function of the method of light activation. European journal of oral sciences. 2004 Jun; 112(3):280-5. doi: 10.1111/j.1600-0722.2004.00125.x. [PMID: 15154928]
  • Maria Cattani-Lorente, Serge Bouillaguet, Chantal Godin, Jean-Marc Meyer, Pierre Payot, Jacques Forchelet. [Characterization of three light sources. Study of their efficiency]. Schweizer Monatsschrift fur Zahnmedizin = Revue mensuelle suisse d'odonto-stomatologie = Rivista mensile svizzera di odontologia e stomatologia. 2003; 113(11):1165-70. doi: NULL. [PMID: 14699950]
  • Tomoko Magoshi, Takehisa Matsuda. Formation of polymerized mixed heparin/albumin surface layer and cellular adhesional responses. Biomacromolecules. 2002 Sep; 3(5):976-83. doi: 10.1021/bm0200377. [PMID: 12217043]
  • Toru Kawada, Yasuhide Nakayama, Can Zheng, Shoji Ohya, Kannna Okuda, Kenji Sunagawa. A novel photocurable insulator material for autonomic nerve activity recording. Biomaterials. 2002 Aug; 23(15):3169-74. doi: 10.1016/s0142-9612(02)00063-7. [PMID: 12102188]
  • Z Tarle, A Meniga, A Knezević, J Sutalo, M Ristić, G Pichler. Composite conversion and temperature rise using a conventional, plasma arc, and an experimental blue LED curing unit. Journal of oral rehabilitation. 2002 Jul; 29(7):662-7. doi: 10.1046/j.1365-2842.2002.00866.x. [PMID: 12153456]
  • W Chai, H Hamada, J Suhara, C A Horiuchi. Biotransformation of (+)- and (-)-camphorquinones by plant cultured cells. Phytochemistry. 2001 Jul; 57(5):669-73. doi: 10.1016/s0031-9422(01)00133-9. [PMID: 11397432]
  • H V Thulasiram, V B Bhat, M K Madyastha. Effect of ring size in R-(+)-pulegone-mediated hepatotoxicity: studies on the metabolism of R-(+)-4-methyl-2-(1-methylethylidene)-cyclopentanone and DL-camphorone in rats. Drug metabolism and disposition: the biological fate of chemicals. 2001 Jun; 29(6):821-9. doi: NULL. [PMID: 11353750]
  • D J Minick, J H Frenz, M A Patrick, D A Brent. A comprehensive method for determining hydrophobicity constants by reversed-phase high-performance liquid chromatography. Journal of medicinal chemistry. 1988 Oct; 31(10):1923-33. doi: 10.1021/jm00118a010. [PMID: 3172126]