Chlorimuron ethyl (BioDeep_00000008409)

   


代谢物信息卡片


CHLORIMURON-ETHYL

化学式: C15H15ClN4O6S (414.0401)
中文名称: 氯嘧磺隆
谱图信息: 最多检出来源 Mentha canadensis(plant) 84.21%

分子结构信息

SMILES: CCOC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC2=NC(=CC(=N2)Cl)OC
InChI: InChI=1S/C15H15ClN4O6S/c1-3-26-13(21)9-6-4-5-7-10(9)27(23,24)20-15(22)19-14-17-11(16)8-12(18-14)25-2/h4-8H,3H2,1-2H3,(H2,17,18,19,20,22)

描述信息

同义名列表

3 个代谢物同义名

CHLORIMURON-ETHYL; Chlorimuron ethyl; Chlorimuron-ethyl



数据库引用编号

11 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)

0 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。

亚细胞结构定位 关联基因列表
Cytoplasm 5 ARHGAP45, CHL1, GLUL, HPGDS, SLC9A1
Peripheral membrane protein 2 COQ10A, PPOX
Endoplasmic reticulum membrane 1 HSP90B1
Nucleus 3 CHL1, GLUL, HSP90B1
cytosol 5 ARHGAP45, GLUL, HAO2, HPGDS, HSP90B1
dendrite 1 CHL1
mitochondrial membrane 1 PPOX
centrosome 1 CHL1
nucleoplasm 4 CD2, CHL1, HPGDS, SLC9A1
Cell membrane 4 CD2, CHL1, GLUL, SLC9A1
Lipid-anchor 1 GLUL
lamellipodium 1 SLC9A1
ruffle membrane 1 ARHGAP45
Multi-pass membrane protein 1 SLC9A1
Synapse 2 C1QA, PPOX
cell surface 3 ART1, CD2, SLC9A1
glutamatergic synapse 1 C1QA
Golgi apparatus 1 CD2
mitochondrial inner membrane 2 COQ10A, PPOX
postsynapse 2 C1QA, PPOX
smooth endoplasmic reticulum 1 HSP90B1
synaptic vesicle 1 PPOX
Cytoplasm, cytosol 1 GLUL
plasma membrane 6 ARHGAP45, ART1, CD2, CHL1, GLUL, SLC9A1
Membrane 4 ARHGAP45, CHL1, HSP90B1, SLC9A1
apical plasma membrane 1 SLC9A1
basolateral plasma membrane 1 SLC9A1
extracellular exosome 4 CHL1, GLUL, HSP90B1, SLC9A1
endoplasmic reticulum 2 GLUL, HSP90B1
perinuclear region of cytoplasm 3 HSP90B1, PPOX, SLC9A1
intercalated disc 1 SLC9A1
mitochondrion 4 COQ10A, GLUL, PPOX, SLC9A1
protein-containing complex 2 CD2, HSP90B1
intracellular membrane-bounded organelle 1 HPGDS
Single-pass type I membrane protein 2 CD2, CHL1
Secreted 1 C1QA
extracellular region 5 ARHGAP45, C1QA, CD2, HSP90B1, PPOX
cytoplasmic side of plasma membrane 1 CD2
Single-pass membrane protein 1 CHL1
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 1 CHL1
external side of plasma membrane 1 CD2
T-tubule 1 SLC9A1
neuronal dense core vesicle lumen 1 PPOX
cytoplasmic vesicle 1 PPOX
nucleolus 1 CHL1
midbody 2 CHL1, HSP90B1
apical part of cell 1 CHL1
cell-cell junction 1 CD2
Cell projection, ruffle membrane 1 ARHGAP45
Mitochondrion inner membrane 2 COQ10A, PPOX
Matrix side 1 COQ10A
Membrane raft 1 SLC9A1
focal adhesion 2 HSP90B1, SLC9A1
Peroxisome 1 HAO2
collagen trimer 1 C1QA
peroxisomal matrix 1 HAO2
mitochondrial intermembrane space 1 PPOX
collagen-containing extracellular matrix 2 C1QA, HSP90B1
chromatin 1 CHL1
Chromosome 1 CHL1
Nucleus, nucleolus 1 CHL1
spindle pole 1 CHL1
Basolateral cell membrane 1 SLC9A1
Cytoplasm, cytoskeleton, spindle pole 1 CHL1
Melanosome 1 HSP90B1
cell body 1 GLUL
side of membrane 1 ART1
sperm plasma membrane 1 HSP90B1
Microsome 1 GLUL
secretory granule lumen 1 ARHGAP45
endoplasmic reticulum lumen 1 HSP90B1
[Processed neural cell adhesion molecule L1-like protein]: Secreted, extracellular space, extracellular matrix 1 CHL1
azurophil granule lumen 1 ARHGAP45
Sarcoplasmic reticulum membrane 1 ART1
Sarcoplasmic reticulum lumen 1 HSP90B1
Rough endoplasmic reticulum 1 PPOX
Intermembrane side 1 PPOX
glial cell projection 1 GLUL
endocytic vesicle lumen 1 HSP90B1
complement component C1 complex 1 C1QA
complement component C1q complex 1 C1QA
extrinsic component of postsynaptic membrane 1 C1QA
extrinsic component of presynaptic membrane 1 C1QA
endoplasmic reticulum chaperone complex 1 HSP90B1
cation-transporting ATPase complex 1 SLC9A1


文献列表

  • Qianhang Zhai, Shuanglan Zheng, Cheng Zhang, Zhou Lu, Shuang Liang, Ranhong Li, Xianghui Zhang, Hongyu Pan, Hao Zhang. Kj-mhpC Enzyme in Klebsiella jilinsis 2N3 Is Involved in the Degradation of Chlorimuron-Ethyl via De-Esterification. Journal of agricultural and food chemistry. 2024 Mar; 72(10):5176-5184. doi: 10.1021/acs.jafc.3c08918. [PMID: 38417018]
  • Xiao-Yue Hu, Zi-Wei Hua, Lun-Guang Yao, Li Du, Qiu-Hong Niu, Yu-Ying Li, Lu Yan, Zhao-Jin Chen, Hao Zhang. [Effects of Combined Stress of High Density Polyethylene Microplastics and Chlorimuron-ethyl on Soybean Growth and Rhizosphere Bacterial Community]. Huan jing ke xue= Huanjing kexue. 2024 Feb; 45(2):1161-1172. doi: 10.13227/j.hjkx.202304023. [PMID: 38471953]
  • Sisheng Zhang, Cheng Zhang, Fengjie Sun, Zhengyi Zhang, Xianghui Zhang, Hongyu Pan, Peng Sun, Hao Zhang. Glutathione-S-transferase (GST) catalyzes the degradation of Chlorimuron-ethyl by Klebsiella jilinsis 2N3. The Science of the total environment. 2020 Aug; 729(?):139075. doi: 10.1016/j.scitotenv.2020.139075. [PMID: 32388135]
  • Cheng Zhang, Qingkai Hao, Sisheng Zhang, Zhengyi Zhang, Xianghui Zhang, Peng Sun, Hongyu Pan, Hao Zhang, Fengjie Sun. Transcriptomic analysis of Chlorimuron-ethyl degrading bacterial strain Klebsiella jilinsis 2N3. Ecotoxicology and environmental safety. 2019 Nov; 183(?):109581. doi: 10.1016/j.ecoenv.2019.109581. [PMID: 31446172]
  • Cheng Zhang, Qingkai Hao, Zhengyi Zhang, Xianghui Zhang, Hongyu Pan, Jiahuan Zhang, Hao Zhang, Fengjie Sun. Whole Genome Sequencing and Analysis of Chlorimuron-Ethyl Degrading Bacteria Klebsiella pneumoniae 2N3. International journal of molecular sciences. 2019 Jun; 20(12):. doi: 10.3390/ijms20123053. [PMID: 31234527]
  • Douglas J Spaunhorst, Haozhen Nie, James R Todd, Julie M Young, Bryan G Young, William G Johnson. Confirmation of herbicide resistance mutations Trp574Leu, ΔG210, and EPSPS gene amplification and control of multiple herbicide-resistant Palmer amaranth (Amaranthus palmeri) with chlorimuron-ethyl, fomesafen, and glyphosate. PloS one. 2019; 14(3):e0214458. doi: 10.1371/journal.pone.0214458. [PMID: 30913269]
  • Hao Zhang, Feng Chen, Hua-Zhu Zhao, Jia-Sen Lu, Meng-Jun Zhao, Qing Hong, Xing Huang. Colonization on Cucumber Root and Enhancement of Chlorimuron-ethyl Degradation in the Rhizosphere by Hansschlegelia zhihuaiae S113 and Root Exudates. Journal of agricultural and food chemistry. 2018 May; 66(18):4584-4591. doi: 10.1021/acs.jafc.8b00041. [PMID: 29672047]
  • Xiong Pan, Saige Wang, Nan Shi, Hua Fang, Yunlong Yu. Biodegradation and detoxification of chlorimuron-ethyl by Enterobacter ludwigii sp. CE-1. Ecotoxicology and environmental safety. 2018 Apr; 150(?):34-39. doi: 10.1016/j.ecoenv.2017.12.023. [PMID: 29268112]
  • Alvaro S Larran, Valeria E Palmieri, Valeria E Perotti, Lucas Lieber, Daniel Tuesca, Hugo R Permingeat. Target-site resistance to acetolactate synthase (ALS)-inhibiting herbicides in Amaranthus palmeri from Argentina. Pest management science. 2017 Dec; 73(12):2578-2584. doi: 10.1002/ps.4662. [PMID: 28703943]
  • Palas Samanta, Namita Bandyopadhyay, Sandipan Pal, Aloke Kumar Mukherjee, Apurba Ratan Ghosh. Histopathological and ultramicroscopical changes in gill, liver and kidney of Anabas testudineus (Bloch) after chronic intoxication of almix (metsulfuron methyl 10.1\%+chlorimuron ethyl 10.1\%) herbicide. Ecotoxicology and environmental safety. 2015 Dec; 122(?):360-7. doi: 10.1016/j.ecoenv.2015.08.022. [PMID: 26318971]
  • Jun Xu, Ying Zhang, Fengshou Dong, Xingang Liu, Xiaohu Wu, Yongquan Zheng. Effects of repeated applications of chlorimuron-ethyl on the soil microbial biomass, activity and microbial community in the greenhouse. Bulletin of environmental contamination and toxicology. 2014 Feb; 92(2):175-82. doi: 10.1007/s00128-013-1156-7. [PMID: 24264144]
  • Jane E Allison, Céline Boutin, David Carpenter. Influence of soil organic matter on the sensitivity of selected wild and crop species to common herbicides. Ecotoxicology (London, England). 2013 Oct; 22(8):1289-302. doi: 10.1007/s10646-013-1116-3. [PMID: 23996626]
  • Daryl L Richie, Katherine V Thompson, Christian Studer, Vivian C Prindle, Thomas Aust, Ralph Riedl, David Estoppey, Jianshi Tao, Jessica A Sexton, Thomas Zabawa, Joseph Drumm, Simona Cotesta, Jürg Eichenberger, Sven Schuierer, Nicole Hartmann, N Rao Movva, John A Tallarico, Neil S Ryder, Dominic Hoepfner. Identification and evaluation of novel acetolactate synthase inhibitors as antifungal agents. Antimicrobial agents and chemotherapy. 2013 May; 57(5):2272-80. doi: 10.1128/aac.01809-12. [PMID: 23478965]
  • Yu-Ting Lee, Chang-Jun Cui, Eve W L Chow, Nason Pue, Thierry Lonhienne, Jian-Guo Wang, James A Fraser, Luke W Guddat. Sulfonylureas have antifungal activity and are potent inhibitors of Candida albicans acetohydroxyacid synthase. Journal of medicinal chemistry. 2013 Jan; 56(1):210-9. doi: 10.1021/jm301501k. [PMID: 23237384]
  • Hua Wu, Jun-Tao Feng, Kai-Chun Lin, Xing Zhang. Synthesis and herbicidal activity of substituted pyrazole isothiocyanates. Molecules (Basel, Switzerland). 2012 Oct; 17(10):12187-12196. doi: 10.3390/molecules171012187. [PMID: 23075815]
  • David M G Anderson, Vikki A Carolan, Susan Crosland, Kate R Sharples, Malcolm R Clench. Examination of the translocation of sulfonylurea herbicides in sunflower plants by matrix-assisted laser desorption/ionisation mass spectrometry imaging. Rapid communications in mass spectrometry : RCM. 2010 Nov; 24(22):3309-19. doi: 10.1002/rcm.4767. [PMID: 20973006]
  • Caixia Jin, Qixing Zhou, Qingxiang Zhou, Jing Fan. Effects of chlorimuron-ethyl and cadimum on biomass growth and cadimum accumulation of wheat in the phaiozem area, Northeast China. Bulletin of environmental contamination and toxicology. 2010 Apr; 84(4):395-400. doi: 10.1007/s00128-009-9635-6. [PMID: 20237912]
  • Meie Wang, Qixing Zhou, Liping Ren. Toxicological responses in wheat Triticum aestivum under joint stress of chlorimuron-ethyl and copper. Ecotoxicology and environmental safety. 2009 Nov; 72(8):2121-9. doi: 10.1016/j.ecoenv.2007.09.009. [PMID: 19748121]
  • Cai-Xi Jin, Qi-Xing Zhou, Jing Fan, Jian-Ling Wang. [Changes of Cd forms on wheat root-soil interface under stress of combined Cd and chlorimuron-ethyl]. Ying yong sheng tai xue bao = The journal of applied ecology. 2007 Jul; 18(7):1498-504. doi: ". [PMID: 17886641]
  • Mei-E Wang, Qi-Xing Zhou. Joint stress of chlorimuron-ethyl and cadmium on wheat Triticum aestivum at biochemical levels. Environmental pollution (Barking, Essex : 1987). 2006 Nov; 144(2):572-80. doi: 10.1016/j.envpol.2006.01.024. [PMID: 16530309]
  • Meie Wang, Qixing Zhou. Effects of herbicide chlorimuron-ethyl on physiological mechanisms in wheat (Triticum aestivum). Ecotoxicology and environmental safety. 2006 Jun; 64(2):190-7. doi: 10.1016/j.ecoenv.2005.03.032. [PMID: 15925408]
  • Jennifer A McCourt, Siew Siew Pang, Jack King-Scott, Luke W Guddat, Ronald G Duggleby. Herbicide-binding sites revealed in the structure of plant acetohydroxyacid synthase. Proceedings of the National Academy of Sciences of the United States of America. 2006 Jan; 103(3):569-73. doi: 10.1073/pnas.0508701103. [PMID: 16407096]
  • Myriam S Zawoznik, María L Tomaro. Effect of chlorimuron-ethyl on Bradyrhizobium japonicum and its symbiosis with soybean. Pest management science. 2005 Oct; 61(10):1003-8. doi: 10.1002/ps.1077. [PMID: 15920784]
  • Hamed K Abbas, Bobbie J Johnson, Dan J Pantone, Loyd M Wax, Ron Hine, W Thomas Shier. Response of multiple seeded cocklebur and other cocklebur types to herbicide treatment. Pest management science. 2005 Jul; 61(7):643-8. doi: 10.1002/ps.1033. [PMID: 15712354]
  • Jennifer A McCourt, Siew Siew Pang, Luke W Guddat, Ronald G Duggleby. Elucidating the specificity of binding of sulfonylurea herbicides to acetohydroxyacid synthase. Biochemistry. 2005 Feb; 44(7):2330-8. doi: 10.1021/bi047980a. [PMID: 15709745]
  • Meie Wang, Qixing Zhou. Single and joint toxicity of chlorimuron-ethyl, cadmium, and copper acting on wheat Triticum aestivum. Ecotoxicology and environmental safety. 2005 Feb; 60(2):169-75. doi: 10.1016/j.ecoenv.2003.12.012. [PMID: 15546632]
  • S S Pang, L W Guddat, R G Duggleby. Crystallization of Arabidopsis thaliana acetohydroxyacid synthase in complex with the sulfonylurea herbicide chlorimuron ethyl. Acta crystallographica. Section D, Biological crystallography. 2004 Jan; 60(Pt 1):153-5. doi: 10.1107/s0907444903025423. [PMID: 14684914]
  • Ryan P Miller, Krishona B Martinson, Robert B Sothern, Beverly R Durgan, Jeffrey L Gunsolus. Circadian response of annual weeds in a natural setting to high and low application rates of four herbicides with different modes of actions. Chronobiology international. 2003 Mar; 20(2):299-324. doi: 10.1081/cbi-120019344. [PMID: 12723887]
  • Dolores M Bartholomew, Drew E Van Dyk, Sze-Mei Cindy Lau, Daniel P O'Keefe, Philip A Rea, Paul V Viitanen. Alternate energy-dependent pathways for the vacuolar uptake of glucose and glutathione conjugates. Plant physiology. 2002 Nov; 130(3):1562-72. doi: 10.1104/pp.008334. [PMID: 12428021]