2,3,5-Triiodobenzoic acid (BioDeep_00000173537)

   

human metabolite blood metabolite


代谢物信息卡片


2,3,5-Triiodobenzoic acid, potassium salt

化学式: C7H3I3O2 (499.72673480000003)
中文名称: 2,3,5-三碘苯甲酸
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=C(C=C(C(=C1C(=O)O)I)I)I
InChI: InChI=1S/C7H3I3O2/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2H,(H,11,12)

描述信息

D006133 - Growth Substances > D010937 - Plant Growth Regulators > D014283 - Triiodobenzoic Acids

同义名列表

17 个代谢物同义名

2,3,5-Triiodobenzoic acid, potassium salt; 2,3,5-Triiodobenzoic acid, ammonia salt; 2,3,5-Triiodobenzoic acid, 14C-labeled; 2,3,5-Triiodobenzoic acid, sodium salt; Acide 2,3,5-triiodobenzoique; 2,3,5-Tri-iodobenzoic acid; 2,3,5-Triiodobenzoic acid; 2,3,5-Tri-iodobenzoate; 2,3,5-Iodobenzoic acid; 2,3,5-Triiodobenzoate; Triiodobenzoic acid; Triiodobenzoate; Floraltone; 2,3,5-TIBA; NSC 2582; Regim-8; TIBA



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

  • Nidhi Kandhol, Aakriti Srivastava, Padmaja Rai, Shivesh Sharma, Sangeeta Pandey, Vijay Pratap Singh, Durgesh Kumar Tripathi. Cytokinin and indole-3-acetic acid crosstalk is indispensable for silicon mediated chromium stress tolerance in roots of wheat seedlings. Journal of hazardous materials. 2024 Apr; 468(?):133134. doi: 10.1016/j.jhazmat.2023.133134. [PMID: 38387171]
  • Pooja Singh, Saumya Jaiswal, Durgesh Kumar Tripathi, Vijay Pratap Singh. Nitric oxide acts upstream of indole-3-acetic acid in ameliorating arsenate stress in tomato seedlings. Plant physiology and biochemistry : PPB. 2024 Mar; 208(?):108461. doi: 10.1016/j.plaphy.2024.108461. [PMID: 38461754]
  • Ricardo I Castro, Ana González-Feliu, Marcelo Muñoz-Vera, Felipe Valenzuela-Riffo, Carolina Parra-Palma, Luis Morales-Quintana. Effect of Exogenous Auxin Treatment on Cell Wall Polymers of Strawberry Fruit. International journal of molecular sciences. 2021 Jun; 22(12):. doi: 10.3390/ijms22126294. [PMID: 34208198]
  • Agata Kućko, Emilia Wilmowicz, Wojciech Pokora, Juan De Dios Alché. Disruption of the Auxin Gradient in the Abscission Zone Area Evokes Asymmetrical Changes Leading to Flower Separation in Yellow Lupine. International journal of molecular sciences. 2020 May; 21(11):. doi: 10.3390/ijms21113815. [PMID: 32471291]
  • Yu-Sian Wu, Chin-Ying Yang. Comprehensive Transcriptomic Analysis of Auxin Responses in Submerged Rice Coleoptile Growth. International journal of molecular sciences. 2020 Feb; 21(4):. doi: 10.3390/ijms21041292. [PMID: 32075118]
  • Christopher R Johnston, Anish Malladi, William K Vencill, Timothy L Grey, A Stanley Culpepper, Gerald Henry, Mark A Czarnota, Taylor M Randell. Investigation of physiological and molecular mechanisms conferring diurnal variation in auxinic herbicide efficacy. PloS one. 2020; 15(8):e0238144. doi: 10.1371/journal.pone.0238144. [PMID: 32857790]
  • Ruth E Márquez-López, Cleyre Pérez-Hernández, Ángela Ku-González, Rosa María Galaz-Ávalos, Víctor Manuel Loyola-Vargas. Localization and transport of indole-3-acetic acid during somatic embryogenesis in Coffea canephora. Protoplasma. 2018 Mar; 255(2):695-708. doi: 10.1007/s00709-017-1181-1. [PMID: 29119309]
  • Kinuka Ohtaka, Koichi Hori, Yuri Kanno, Mitsunori Seo, Hiroyuki Ohta. Primitive Auxin Response without TIR1 and Aux/IAA in the Charophyte Alga Klebsormidium nitens. Plant physiology. 2017 Jul; 174(3):1621-1632. doi: 10.1104/pp.17.00274. [PMID: 28533212]
  • Jin Woo Choi, Ju-Hwan Park, Hye Rim Cho, Jin Wook Chung, Dae-Duk Kim, Hyo-Cheol Kim, Hyun-Jong Cho. Sorafenib and 2,3,5-triiodobenzoic acid-loaded imageable microspheres for transarterial embolization of a liver tumor. Scientific reports. 2017 04; 7(1):554. doi: 10.1038/s41598-017-00709-4. [PMID: 28373713]
  • Li-Wei Gao, Shan-Wu Lyu, Jun Tang, Dao-Yun Zhou, Guusje Bonnema, Dong Xiao, Xi-Lin Hou, Chang-Wei Zhang. Genome-wide analysis of auxin transport genes identifies the hormone responsive patterns associated with leafy head formation in Chinese cabbage. Scientific reports. 2017 02; 7(?):42229. doi: 10.1038/srep42229. [PMID: 28169368]
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  • Yun-He Li, Ming-Hong Zou, Bi-Hong Feng, Xia Huang, Zhi Zhang, Guang-Ming Sun. Molecular cloning and characterization of the genes encoding an auxin efflux carrier and the auxin influx carriers associated with the adventitious root formation in mango (Mangifera indica L.) cotyledon segments. Plant physiology and biochemistry : PPB. 2012 Jun; 55(?):33-42. doi: 10.1016/j.plaphy.2012.03.012. [PMID: 22522578]
  • Julia Köster, Corinna Thurow, Kerstin Kruse, Alexander Meier, Tim Iven, Ivo Feussner, Christiane Gatz. Xenobiotic- and jasmonic acid-inducible signal transduction pathways have become interdependent at the Arabidopsis CYP81D11 promoter. Plant physiology. 2012 May; 159(1):391-402. doi: 10.1104/pp.112.194274. [PMID: 22452854]
  • Gregory Heller, Karl Lundén, Roger D Finlay, Frederick O Asiegbu, Malin Elfstrand. Expression analysis of Clavata1-like and Nodulin21-like genes from Pinus sylvestris during ectomycorrhiza formation. Mycorrhiza. 2012 May; 22(4):271-7. doi: 10.1007/s00572-011-0402-2. [PMID: 21751039]
  • Thomas Péron, Christophe Véronési, Eric Mortreau, Jean-Bernard Pouvreau, Séverine Thoiron, Nathalie Leduc, Philippe Delavault, Philippe Simier. Role of the sucrose synthase encoding PrSus1 gene in the development of the parasitic plant Phelipanche ramosa L. (Pomel). Molecular plant-microbe interactions : MPMI. 2012 Mar; 25(3):402-11. doi: 10.1094/mpmi-10-11-0260. [PMID: 22088196]
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  • Christine Böttcher, Paul K Boss, Christopher Davies. Acyl substrate preferences of an IAA-amido synthetase account for variations in grape (Vitis vinifera L.) berry ripening caused by different auxinic compounds indicating the importance of auxin conjugation in plant development. Journal of experimental botany. 2011 Aug; 62(12):4267-80. doi: 10.1093/jxb/err134. [PMID: 21543520]
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  • Chong Wei Jin, Shao Ting Du, Imran Haider Shamsi, Bing Fang Luo, Xian Yong Lin. NO synthase-generated NO acts downstream of auxin in regulating Fe-deficiency-induced root branching that enhances Fe-deficiency tolerance in tomato plants. Journal of experimental botany. 2011 Jul; 62(11):3875-84. doi: 10.1093/jxb/err078. [PMID: 21511908]
  • Parankusam Santisree, Sapana Nongmaithem, Himabindu Vasuki, Yellamaraju Sreelakshmi, Maria G Ivanchenko, Rameshwar Sharma. Tomato root penetration in soil requires a coaction between ethylene and auxin signaling. Plant physiology. 2011 Jul; 156(3):1424-38. doi: 10.1104/pp.111.177014. [PMID: 21571667]
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