Chinizarin (BioDeep_00000864936)

Main id: BioDeep_00000017483

 

PANOMIX_OTCML-2023 Volatile Flavor Compounds


代谢物信息卡片


InChI=1\C14H8O4\c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18\h1-6,15-16

化学式: C14H8O4 (240.0422568)
中文名称: 1,4-二羟基蒽醌
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC=C2C(=C1)C(=O)C3=C(C=CC(=C3C2=O)O)O
InChI: InChI=1S/C14H8O4/c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18/h1-6,15-16H

描述信息

同义名列表

49 个代谢物同义名

InChI=1\C14H8O4\c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18\h1-6,15-16; 9,10-Anthracenedione, 1,4-dihydroxy-; 1,4-Dihydroxy-9,10-anthracene-dione; 1,4-dihydroxyanthracene-9,10-dione; 1,4-DIHYDROXY-9,10-ANTHRACENEDIONE; 1,4-Dihydroxyanthrachinon [Czech]; 1,4-Dioxyanthraquinone [Russian]; 1,4-Dihydroxyanthra-9,10-quinone; 1,4-dihydroxy-9,10-anthraquinone; Anthraquinone, 1,4-dihydroxy-; 1,4-dihydroxyanthraquinone; 1,4-Dihydroxyanthrachinon; WLN: L C666 BV IVJ DQ GQ; 1,4-Dioxyanthraquinone; Macrolex Orange GG; Solvent Orange 86; 1,4-Doa [Russian]; EINECS 201-368-7; SR-01000637713-1; Smoke Orange R; MEGxp0_001867; Q906_ALDRICH; ZINC03847495; NCI60_001089; ACon1_000101; ZINC00135828; 103220-12-8; CHEBI:37487; Quinizarine; 37480_FLUKA; AIDS-001374; CCRIS 3524; C.I. 58050; AIDS001374; Chinizarin; NSC 646569; Quinizarin; NSC229036; HSDB 5242; ST5330576; NSC 15367; NSC646569; AI3-17616; NSC40899; NSC15367; CI 58050; 81-64-1; 1,4-Doa; 1,4-Dihydroxyanthraquinone



数据库引用编号

5 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)

2 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

  • V Sachithanandam, P Lalitha, A Parthiban, Jayaraman Muthukumaran, Monika Jain, Ranjita Misra, T Mageswaran, R Sridhar, R Purvaja, R Ramesh. A comprehensive in silico and in vitro studies on quinizarin: a promising phytochemical derived from Rhizophora mucronata Lam. Journal of biomolecular structure & dynamics. 2022 10; 40(16):7218-7229. doi: 10.1080/07391102.2021.1894983. [PMID: 33682626]
  • Jin Ree, Jun Il Kim, Chang Won Lee, Jisun Lee, Hyeon Jeong Kim, Seong Cheol Kim, Jae Kyung Sohng, Yong Il Park. Quinizarin suppresses the differentiation of adipocytes and lipogenesis in vitro and in vivo via downregulation of C/EBP-beta/SREBP pathway. Life sciences. 2021 Dec; 287(?):120131. doi: 10.1016/j.lfs.2021.120131. [PMID: 34767806]
  • Mark J Henderson, Kathleen A Trychta, Shyh-Ming Yang, Susanne Bäck, Adam Yasgar, Emily S Wires, Carina Danchik, Xiaokang Yan, Hideaki Yano, Lei Shi, Kuo-Jen Wu, Amy Q Wang, Dingyin Tao, Gergely Zahoránszky-Kőhalmi, Xin Hu, Xin Xu, David Maloney, Alexey V Zakharov, Ganesha Rai, Fumihiko Urano, Mikko Airavaara, Oksana Gavrilova, Ajit Jadhav, Yun Wang, Anton Simeonov, Brandon K Harvey. A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome. Cell reports. 2021 04; 35(4):109040. doi: 10.1016/j.celrep.2021.109040. [PMID: 33910017]
  • Máté Kozsup, Orsolya Dömötör, Sándor Nagy, Etelka Farkas, Éva A Enyedy, Péter Buglyó. Synthesis, characterization and albumin binding capabilities of quinizarin containing ternary cobalt(III) complexes. Journal of inorganic biochemistry. 2020 03; 204(?):110963. doi: 10.1016/j.jinorgbio.2019.110963. [PMID: 31874363]
  • Xiufang Hu, Yanqin Cao, Xu Yin, Li Zhu, Yingyu Chen, Wenfeng Wang, Jianda Hu. Design and synthesis of various quinizarin derivatives as potential anticancer agents in acute T lymphoblastic leukemia. Bioorganic & medicinal chemistry. 2019 04; 27(7):1362-1369. doi: 10.1016/j.bmc.2019.02.041. [PMID: 30827866]
  • Sameer Shakeel Ansari, Rizwan Hasan Khan, Saeeda Naqvi. Probing the intermolecular interactions into serum albumin and anthraquinone systems: a spectroscopic and docking approach. Journal of biomolecular structure & dynamics. 2018 Oct; 36(13):3362-3375. doi: 10.1080/07391102.2017.1388284. [PMID: 28974158]
  • Farid A Badria, Ahmed S Ibrahim. Evaluation of natural anthracene-derived compounds as antimitotic agents. Drug discoveries & therapeutics. 2013 Apr; 7(2):84-9. doi: . [PMID: 23715507]
  • Arne Schwelm, Rosie E Bradshaw. Genetics of dothistromin biosynthesis of Dothistroma septosporum: an update. Toxins. 2010 11; 2(11):2680-98. doi: 10.3390/toxins2112680. [PMID: 22069571]
  • Anna Frackowiak, Przemysław Skibiński, Wiesław Gaweł, Ewa Zaczyńska, Anna Czarny, Roman Gancarz. Synthesis of glycoside derivatives of hydroxyanthraquinone with ability to dissolve and inhibit formation of crystals of calcium oxalate. Potential compounds in kidney stone therapy. European journal of medicinal chemistry. 2010 Mar; 45(3):1001-7. doi: 10.1016/j.ejmech.2009.11.042. [PMID: 20005021]
  • Itsuko Fukuda, Atsushi Kaneko, Shin Nishiumi, Masaya Kawase, Rika Nishikiori, Nobuhide Fujitake, Hitoshi Ashida. Structure-activity relationships of anthraquinones on the suppression of DNA-binding activity of the aryl hydrocarbon receptor induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin. Journal of bioscience and bioengineering. 2009 Mar; 107(3):296-300. doi: 10.1016/j.jbiosc.2008.10.008. [PMID: 19269596]
  • M I Maguregui, R M Alonso, M Barandiaran, R M Jimenez, N García. Micellar electrokinetic chromatography method for the determination of several natural red dyestuff and lake pigments used in art work. Journal of chromatography. A. 2007 Jun; 1154(1-2):429-36. doi: 10.1016/j.chroma.2007.03.089. [PMID: 17452040]
  • Katarzyna Skupińska, Monika Zylm, Irena Misiewicz, Teresa Kasprzycka-Guttman. Interaction of anthracene and its oxidative derivatives with human serum albumin. Acta biochimica Polonica. 2006; 53(1):101-12. doi: . [PMID: 16404478]
  • Sung-Woo Kim, Byoung-Kee Jo, Ji-Hean Jeong, Sun-Uk Choi, Yong-Il Hwang. Induction of extracellular matrix synthesis in normal human fibroblasts by anthraquinone isolated from Morinda citrifolia (Noni) fruit. Journal of medicinal food. 2005; 8(4):552-5. doi: 10.1089/jmf.2005.8.552. [PMID: 16379572]
  • Bo-Kyung Sung, Moo-Key Kim, Wang-Hyu Lee, Dong-Heon Lee, Hoi-Seon Lee. Growth responses of Cassia obtusifolia toward human intestinal bacteria. Fitoterapia. 2004 Jul; 75(5):505-9. doi: 10.1016/j.fitote.2004.03.012. [PMID: 15261390]
  • H Matsuda, H Shimoda, T Morikawa, M Yoshikawa. Phytoestrogens from the roots of Polygonum cuspidatum (Polygonaceae): structure-requirement of hydroxyanthraquinones for estrogenic activity. Bioorganic & medicinal chemistry letters. 2001 Jul; 11(14):1839-42. doi: 10.1016/s0960-894x(01)00318-3. [PMID: 11459643]
  • H S Yun-Choi, J H Kim, M Takido. Potential inhibitors of platelet aggregation from plant sources, V. Anthraquinones from seeds of Cassia obtusifolia and related compounds. Journal of natural products. 1990 May; 53(3):630-3. doi: 10.1021/np50069a014. [PMID: 2213033]