Quinclorac (BioDeep_00000002038)

 

Secondary id: BioDeep_00001868043

human metabolite blood metabolite


代谢物信息卡片


3,7-Dichloro-8-quinolinecarboxylic acid

化学式: C10H5Cl2NO2 (240.9697)
中文名称: 二氯喹啉酸
谱图信息: 最多检出来源 Viridiplantae(plant) 38.46%

分子结构信息

SMILES: C1=CC(=C(C2=NC=C(C=C21)Cl)C(=O)O)Cl
InChI: InChI=1S/C10H5Cl2NO2/c11-6-3-5-1-2-7(12)8(10(14)15)9(5)13-4-6/h1-4H,(H,14,15)

描述信息

CONFIDENCE standard compound; INTERNAL_ID 647; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7880; ORIGINAL_PRECURSOR_SCAN_NO 7877
CONFIDENCE standard compound; INTERNAL_ID 647; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7876; ORIGINAL_PRECURSOR_SCAN_NO 7873
CONFIDENCE standard compound; INTERNAL_ID 647; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7833; ORIGINAL_PRECURSOR_SCAN_NO 7831
CONFIDENCE standard compound; INTERNAL_ID 647; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7836; ORIGINAL_PRECURSOR_SCAN_NO 7833
CONFIDENCE standard compound; INTERNAL_ID 647; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7792; ORIGINAL_PRECURSOR_SCAN_NO 7790
CONFIDENCE standard compound; INTERNAL_ID 647; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7882; ORIGINAL_PRECURSOR_SCAN_NO 7879
D010575 - Pesticides > D006540 - Herbicides
D016573 - Agrochemicals

同义名列表

6 个代谢物同义名

3,7-Dichloro-8-quinolinecarboxylic acid; 3,7-Dichloroquinoline-8-carboxylic acid; 3,7-Dichloroquinoline carboxylic acid; 3,7-Dichloro-8-quinolinecarboxylate; Quinclorac; Quinclorac



数据库引用编号

19 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。

亚细胞结构定位 关联基因列表
Cytoplasm 8 ALB, ALS2, ARHGAP45, CAT, DNA2, HPGDS, NQO1, POP1
Peripheral membrane protein 3 CYP1B1, MGLL, PPOX
Endoplasmic reticulum membrane 2 CYP1B1, MGLL
Nucleus 6 ALB, ALS2, DNA2, GLRX, NQO1, POP1
cytosol 12 ALB, ALS2, ARHGAP45, CAT, GLRX, HPGDS, LIPE, MGLL, NQO1, NQO2, PHYH, POP1
dendrite 2 ALS2, NQO1
mitochondrial membrane 1 PPOX
centrosome 2 ALB, ALS2
nucleoplasm 5 ATP2B1, DNA2, HPGDS, NQO2, POP1
Cell membrane 3 ATP2B1, GLRA2, LIPE
lamellipodium 1 ALS2
ruffle membrane 1 ARHGAP45
Multi-pass membrane protein 3 ATP2B1, GLRA2, POP1
Synapse 4 ATP2B1, GLRA2, NQO1, PPOX
cell junction 1 POP1
glutamatergic synapse 2 ALS2, ATP2B1
Golgi apparatus 2 ALB, ATRN
Golgi membrane 1 INS
growth cone 1 ALS2
mitochondrial inner membrane 1 PPOX
neuronal cell body 1 NQO1
postsynapse 1 PPOX
presynaptic membrane 1 ATP2B1
sarcolemma 1 POP1
synaptic vesicle 1 PPOX
Cytoplasm, cytosol 3 LIPE, MGLL, NQO1
plasma membrane 6 ARHGAP45, ATP2B1, ATRN, GLRA2, MGLL, POP1
synaptic vesicle membrane 1 ATP2B1
Membrane 9 ARHGAP45, ATP2B1, CAT, CYP1B1, GLRA2, LIPE, MGLL, NQO1, POP1
basolateral plasma membrane 1 ATP2B1
caveola 2 LIPE, POP1
extracellular exosome 7 ALB, ATP2B1, ATRN, CAT, GLRX, NQO2, SOD2
endoplasmic reticulum 1 ALB
extracellular space 4 ALB, ATRN, INS, POP1
perinuclear region of cytoplasm 1 PPOX
Cell junction, tight junction 1 POP1
bicellular tight junction 1 POP1
mitochondrion 5 CAT, CYP1B1, DNA2, PPOX, SOD2
protein-containing complex 3 ALB, ALS2, CAT
intracellular membrane-bounded organelle 6 ALS2, ATP2B1, CAT, CYP1B1, GLRA2, HPGDS
Microsome membrane 1 CYP1B1
postsynaptic density 1 ALS2
Single-pass type I membrane protein 1 ATRN
Secreted 2 ALB, INS
extracellular region 5 ALB, ARHGAP45, CAT, INS, PPOX
[Isoform 2]: Secreted 1 ATRN
Mitochondrion matrix 1 SOD2
mitochondrial matrix 2 CAT, SOD2
anchoring junction 1 ALB
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 1 ATP2B1
dendritic spine 1 ALS2
neuronal dense core vesicle lumen 1 PPOX
cytoplasmic vesicle 1 PPOX
nucleolus 1 POP1
Early endosome 1 ALS2
vesicle 1 ALS2
Cell membrane, sarcolemma 1 POP1
Cell projection, ruffle membrane 1 ARHGAP45
Mitochondrion inner membrane 1 PPOX
focal adhesion 1 CAT
GABA-ergic synapse 1 GLRA2
mitochondrial nucleoid 2 DNA2, SOD2
Peroxisome 2 CAT, PHYH
Peroxisome matrix 1 CAT
peroxisomal matrix 2 CAT, PHYH
peroxisomal membrane 1 CAT
mitochondrial intermembrane space 1 PPOX
lateral plasma membrane 2 ATP2B1, POP1
Postsynaptic cell membrane 1 GLRA2
ruffle 1 ALS2
neuron projection 1 GLRA2
ciliary basal body 1 ALB
cell projection 2 ATP2B1, GLRA2
centriole 1 ALB
Nucleus, nucleolus 1 POP1
spindle pole 1 ALB
chromosome, telomeric region 1 DNA2
blood microparticle 1 ALB
transmembrane transporter complex 1 GLRA2
Basolateral cell membrane 1 ATP2B1
[Isoform 3]: Secreted 1 ATRN
endosome lumen 1 INS
Lipid droplet 1 LIPE
Membrane, caveola 2 LIPE, POP1
chloride channel complex 1 GLRA2
Presynaptic cell membrane 1 ATP2B1
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 3 ARHGAP45, CAT, INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 ALB, INS
platelet alpha granule lumen 1 ALB
transport vesicle 1 INS
azurophil granule lumen 1 ARHGAP45
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
immunological synapse 1 ATP2B1
9+0 non-motile cilium 1 PHYH
IkappaB kinase complex 1 POP1
Lateral cell membrane 1 POP1
postsynaptic specialization membrane 1 GLRA2
[Isoform 1]: Cell membrane 1 ATRN
Rough endoplasmic reticulum 1 PPOX
Intermembrane side 1 PPOX
multimeric ribonuclease P complex 1 POP1
nucleolar ribonuclease P complex 1 POP1
ribonuclease MRP complex 1 POP1
catalase complex 1 CAT
glycinergic synapse 1 GLRA2
photoreceptor ribbon synapse 1 ATP2B1
cell projection membrane 1 POP1
ciliary transition fiber 1 ALB


文献列表

  • Chunxia Ding, Can Ye, Wei Zhu, Guangyong Zeng, Xuemei Yao, Yu Ouyang, Jie Rong, Yaping Tao, Xiangying Liu, Yaocheng Deng. Engineered hydrochar from waste reed straw for peroxymonosulfate activation to degrade quinclorac and improve solanaceae plants growth. Journal of environmental management. 2023 Oct; 347(?):119090. doi: 10.1016/j.jenvman.2023.119090. [PMID: 37793289]
  • Siyuan Lu, Jing Chen, Junyuan Wang, Donghui Wu, Hongfeng Bian, Haibo Jiang, Lianxi Sheng, Chunguang He. Toxicological effects and transcriptome mechanisms of rice (Oryza sativa L.) under stress of quinclorac and polystyrene nanoplastics. Ecotoxicology and environmental safety. 2023 Jan; 249(?):114380. doi: 10.1016/j.ecoenv.2022.114380. [PMID: 36508812]
  • Mei-E Zhong, Gongsong Tong, Jingchun Sun, Nan Zhou, Chunxia Ding, Xiangying Liu, Austin Merchant, Xuguo Zhou. Low-Temperature Reduction Synthesis of γ-Fe2O3-x@biochar Catalysts and Their Combining with Peroxymonosulfate for Quinclorac Degradation. International journal of environmental research and public health. 2022 12; 19(24):. doi: 10.3390/ijerph192416790. [PMID: 36554671]
  • Jingyu Zhao, Shuo Tan, Hui Li, Yao Wang, Ting Yao, Lejun Liu, Kailin Liu. Multi-walled Carbon Nanotubes Remediate the Phytotoxicity of Quinclorac to Tomato. Bulletin of environmental contamination and toxicology. 2022 Sep; 109(3):477-483. doi: 10.1007/s00128-022-03582-8. [PMID: 35849168]
  • Linhan Li, Ting Zhou, Linyu Zhong, Qian Zhou, Gang Gu, Mengjun Hu, Fengping Chen, Sheng Lin. Bioremediation of quinclorac injury on tobacco by a rhizosphere bacterium. World journal of microbiology & biotechnology. 2022 Jul; 38(9):147. doi: 10.1007/s11274-022-03329-x. [PMID: 35773599]
  • Lan Yang, Xingyan Ye, Xiating Li, Zhihong Huang, Fengping Chen, Weijuan Yang, Zongwen Wang. Colorimetric aptasensor for sensitive detection of quinclorac based on exonuclease III-assisted cyclic release of phosphorodiamidate morpholino oligomer mimic enzyme strategy. Analytica chimica acta. 2022 May; 1207(?):339815. doi: 10.1016/j.aca.2022.339815. [PMID: 35491044]
  • Gulab Rangani, Christopher E Rouse, Christopher Saski, Rooksana E Noorai, Vijay Shankar, Amy L Lawton-Rauh, Isabel S Werle, Nilda Roma-Burgos. High Resistance to Quinclorac in Multiple-Resistant Echinochloa colona Associated with Elevated Stress Tolerance Gene Expression and Enriched Xenobiotic Detoxification Pathway. Genes. 2022 03; 13(3):. doi: 10.3390/genes13030515. [PMID: 35328069]
  • Zhengbo Wang, Hao Wang, Jun Li, Jiaxing Yu, Hongyan Lin, Liyao Dong. Comparison of quintrione and quinclorac on mechanism of action. Pesticide biochemistry and physiology. 2022 Feb; 181(?):105007. doi: 10.1016/j.pestbp.2021.105007. [PMID: 35082030]
  • Xia Yang, Heping Han, Jingjing Cao, Yongfeng Li, Qin Yu, Stephen B Powles. Exploring quinclorac resistance mechanisms in Echinochloa crus-pavonis from China. Pest management science. 2021 Jan; 77(1):194-201. doi: 10.1002/ps.6007. [PMID: 32652760]
  • Kassio Ferreira Mendes, Bruno Aguiar Maset, Kamila Cabral Mielke, Rodrigo Nogueira de Sousa, Bianca Assis Barbosa Martins, Valdemar Luiz Tornisielo. Phytoremediation of quinclorac and tebuthiuron-polluted soil by green manure plants. International journal of phytoremediation. 2021; 23(5):474-481. doi: 10.1080/15226514.2020.1825329. [PMID: 33000969]
  • Ruyang Zhang, Xiaohan Bai, Jihai Shao, Anwei Chen, Haiyong Wu, Si Luo. Effects of zero-valent iron nanoparticles and quinclorac coexposure on the growth and antioxidant system of rice (Oryza sativa L.). Ecotoxicology and environmental safety. 2020 Oct; 203(?):111054. doi: 10.1016/j.ecoenv.2020.111054. [PMID: 32888616]
  • Jing-Jing Cao, Qiong Peng, Xia Yang, Qian Yang, Lian-Yang Bai, Yong-Feng Li, Zi-Chang Zhang, Tao Gu. [Differences in exogenous methyl jasmonate-induced quinclorac resistance between resistant and sensitive barnyardgrass and the underlying mechanism]. Ying yong sheng tai xue bao = The journal of applied ecology. 2020 Jul; 31(7):2293-2298. doi: 10.13287/j.1001-9332.202007.038. [PMID: 32715694]
  • Pattarasuda Chayapakdee, Yukari Sunohara, Masaki Endo, Takuya Yamaguchi, Longjiang Fan, Akira Uchino, Hiroshi Matsumoto, Satoshi Iwakami. Quinclorac resistance in Echinochloa phyllopogon is associated with reduced ethylene synthesis rather than enhanced cyanide detoxification by β-cyanoalanine synthase. Pest management science. 2020 Apr; 76(4):1195-1204. doi: 10.1002/ps.5660. [PMID: 31659851]
  • Muhammad Zia Ul Haq, Zheng Zhang, Jiajia Wei, Sheng Qiang. Ethylene Biosynthesis Inhibition Combined with Cyanide Degradation Confer Resistance to Quinclorac in Echinochloa crus-galli var. mitis. International journal of molecular sciences. 2020 Feb; 21(5):. doi: 10.3390/ijms21051573. [PMID: 32106618]
  • Yuan Gao, Xukun Pan, Xutao Sun, Jun Li, Liyao Dong. Is the protection of photosynthesis related to the mechanism of quinclorac resistance in Echinochloa crus-galli var. zelayensis?. Gene. 2019 Jan; 683(?):133-148. doi: 10.1016/j.gene.2018.10.022. [PMID: 30316919]
  • La-Mei Wu, Yong Fang, Hao-Na Yang, Lian-Yang Bai. Effects of drought-stress on seed germination and growth physiology of quinclorac-resistant Echinochloa crusgalli. PloS one. 2019; 14(4):e0214480. doi: 10.1371/journal.pone.0214480. [PMID: 30947307]
  • Qiuzan Zhong, Shuqing Wan, Changyou Shen, Yi Liu. Decay of Quinclorac in Acidic Paddy Soil and Risk Evaluation to the Subsequent Crop, Tobacco (Nicotiana tabacum L.). Bulletin of environmental contamination and toxicology. 2018 Aug; 101(2):284-287. doi: 10.1007/s00128-018-2372-y. [PMID: 29947913]
  • Zhe Lang, Dan Qi, Jianjiang Dong, Liwei Ren, Qifa Zhu, Weiwei Huang, Yongmin Liu, Diannan Lu. Isolation and characterization of a quinclorac-degrading Actinobacteria Streptomyces sp. strain AH-B and its implication on microecology in contaminated soil. Chemosphere. 2018 May; 199(?):210-217. doi: 10.1016/j.chemosphere.2018.01.133. [PMID: 29438948]
  • Yuan Gao, Jun Li, Xukun Pan, Dingrong Liu, Richard Napier, Liyao Dong. Quinclorac resistance induced by the suppression of the expression of 1-aminocyclopropane-1-carboxylic acid (ACC) synthase and ACC oxidase genes in Echinochloa crus-galli var. zelayensis. Pesticide biochemistry and physiology. 2018 Apr; 146(?):25-32. doi: 10.1016/j.pestbp.2018.02.005. [PMID: 29626989]
  • Yuan Gao, Lang Pan, Yu Sun, Teng Zhang, Liyao Dong, Jun Li. Resistance to quinclorac caused by the enhanced ability to detoxify cyanide and its molecular mechanism in Echinochloa crus-galli var. zelayensis. Pesticide biochemistry and physiology. 2017 Nov; 143(?):231-238. doi: 10.1016/j.pestbp.2017.08.009. [PMID: 29183597]
  • Jian Wang, Faisal Islam, Lan Li, Meijuan Long, Chong Yang, Xiaoli Jin, Basharat Ali, Bizeng Mao, Weijun Zhou. Complementary RNA-Sequencing Based Transcriptomics and iTRAQ Proteomics Reveal the Mechanism of the Alleviation of Quinclorac Stress by Salicylic Acid in Oryza sativa ssp. japonica. International journal of molecular sciences. 2017 Sep; 18(9):. doi: 10.3390/ijms18091975. [PMID: 28906478]
  • Tanilene Sotero Pinto Persch, Rodrigo Nizolli Weimer, Betânia Souza Freitas, Guendalina Turcato Oliveira. Metabolic parameters and oxidative balance in juvenile Rhamdia quelen exposed to rice paddy herbicides: Roundup®, Primoleo®, and Facet®. Chemosphere. 2017 May; 174(?):98-109. doi: 10.1016/j.chemosphere.2017.01.092. [PMID: 28160682]
  • Yingying Li, Wu Chen, Yunsheng Wang, Kun Luo, Yue Li, Lianyang Bai, Feng Luo. Identifying and sequencing a Mycobacterium sp. strain F4 as a potential bioremediation agent for quinclorac. PloS one. 2017; 12(10):e0185721. doi: 10.1371/journal.pone.0185721. [PMID: 28968436]
  • Jian Wang, Mengting Lv, Faisal Islam, Rafaqat A Gill, Chong Yang, Basharat Ali, Guijun Yan, Weijun Zhou. Salicylic acid mediates antioxidant defense system and ABA pathway related gene expression in Oryza sativa against quinclorac toxicity. Ecotoxicology and environmental safety. 2016 Nov; 133(?):146-56. doi: 10.1016/j.ecoenv.2016.07.002. [PMID: 27448955]
  • Asier Largo-Gosens, María de Castro, Ana Alonso-Simón, Penélope García-Angulo, José L Acebes, Antonio Encina, Jesús M Álvarez. Quinclorac-habituation of bean (Phaseolus vulgaris) cultured cells is related to an increase in their antioxidant capacity. Plant physiology and biochemistry : PPB. 2016 Oct; 107(?):257-263. doi: 10.1016/j.plaphy.2016.06.011. [PMID: 27318799]
  • M F Dornelles, G T Oliveira. Toxicity of atrazine, glyphosate, and quinclorac in bullfrog tadpoles exposed to concentrations below legal limits. Environmental science and pollution research international. 2016 Jan; 23(2):1610-20. doi: 10.1007/s11356-015-5388-4. [PMID: 26381782]
  • Michele Flores Dornelles, Guendalina Turcato Oliveira. Effect of atrazine, glyphosate and quinclorac on biochemical parameters, lipid peroxidation and survival in bullfrog tadpoles (Lithobates catesbeianus). Archives of environmental contamination and toxicology. 2014 Apr; 66(3):415-29. doi: 10.1007/s00244-013-9967-4. [PMID: 24276472]
  • Charlene Menezes, Ignacio Ruiz-Jarabo, Juan Antonio Martos-Sitcha, Jossiele Leitemperger, Bernardo Baldisserotto, Juan Miguel Mancera, Denis Broock Rosemberg, Vania Lucia Loro. Diet with diphenyl diselenide mitigates quinclorac toxicity in silver catfish (Rhamdia quelen). PloS one. 2014; 9(12):e114233. doi: 10.1371/journal.pone.0114233. [PMID: 25469630]
  • Min Liu, Kun Luo, Yunsheng Wang, Aiping Zeng, Xiaomao Zhou, Feng Luo, Lianyang Bai. Isolation, identification and characteristics of an endophytic quinclorac degrading bacterium Bacillus megaterium Q3. PloS one. 2014; 9(9):e108012. doi: 10.1371/journal.pone.0108012. [PMID: 25244184]
  • Jiangyan Xu, Bo Lv, Qiong Wang, Jun Li, Liyao Dong. A resistance mechanism dependent upon the inhibition of ethylene biosynthesis. Pest management science. 2013 Dec; 69(12):1407-14. doi: 10.1002/ps.3524. [PMID: 23457050]
  • Gang Li, Shenggan Wu, Leiming Cai, Qiang Wang, Xueping Zhao, Changxing Wu. Identification and mRNA expression profile of glutamate receptor-like gene in quinclorac-resistant and susceptible Echinochloa crus-galli. Gene. 2013 Dec; 531(2):489-95. doi: 10.1016/j.gene.2013.09.013. [PMID: 24036427]
  • Xia Yang, Xin-Yan Yu, Yong-Feng Li. De novo assembly and characterization of the Barnyardgrass (Echinochloa crus-galli) transcriptome using next-generation pyrosequencing. PloS one. 2013; 8(7):e69168. doi: 10.1371/journal.pone.0069168. [PMID: 23874903]
  • Penélope García-Angulo, Ana Alonso-Simón, Antonio Encina, Jesús M Álvarez, José L Acebes. Cellulose biosynthesis inhibitors: comparative effect on bean cell cultures. International journal of molecular sciences. 2012; 13(3):3685-3702. doi: 10.3390/ijms13033685. [PMID: 22489176]
  • Lewis H Ziska, David R Gealy, Martha B Tomecek, Aaron K Jackson, Howard L Black. Recent and projected increases in atmospheric CO2 concentration can enhance gene flow between wild and genetically altered rice (Oryza sativa). PloS one. 2012; 7(5):e37522. doi: 10.1371/journal.pone.0037522. [PMID: 22649533]
  • Hagai Yasuor, Marco Milan, James W Eckert, Albert J Fischer. Quinclorac resistance: a concerted hormonal and enzymatic effort in Echinochloa phyllopogon. Pest management science. 2012 Jan; 68(1):108-15. doi: 10.1002/ps.2230. [PMID: 21717565]
  • Maidul Hossain, Asma Yasmeen Khan, Gopinatha Suresh Kumar. Interaction of the anticancer plant alkaloid sanguinarine with bovine serum albumin. PloS one. 2011 Apr; 6(4):e18333. doi: 10.1371/journal.pone.0018333. [PMID: 21494677]
  • Alexandra Pretto, Vania Lucia Loro, Charlene Menezes, Bibiana Silveira Moraes, Geovane Boschmann Reimche, Renato Zanella, Luis Antonio de Ávila. Commercial formulation containing quinclorac and metsulfuron-methyl herbicides inhibit acetylcholinesterase and induce biochemical alterations in tissues of Leporinus obtusidens. Ecotoxicology and environmental safety. 2011 Mar; 74(3):336-41. doi: 10.1016/j.ecoenv.2010.10.003. [PMID: 21036398]
  • Xiao-Le Han, Ping Mei, Yi Liu, Qi Xiao, Feng-Lei Jiang, Ran Li. Binding interaction of quinclorac with bovine serum albumin: a biophysical study. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 2009 Oct; 74(3):781-7. doi: 10.1016/j.saa.2009.08.018. [PMID: 19729340]
  • Michael L Lovelace, Robert E Hoagland, Ronald E Talbert, Eric F Scherder. Influence of simulated Quinclorac drift on the accumulation and movement of herbicide in tomato (Lycopersicon esculentum) plants. Journal of agricultural and food chemistry. 2009 Jul; 57(14):6349-55. doi: 10.1021/jf803845p. [PMID: 19537789]
  • Kwok Wai Lai, Chi Ping Yau, Yu Chung Tse, Liwen Jiang, Wing Kin Yip. Heterologous expression analyses of rice OsCAS in Arabidopsis and in yeast provide evidence for its roles in cyanide detoxification rather than in cysteine synthesis in vivo. Journal of experimental botany. 2009; 60(3):993-1008. doi: 10.1093/jxb/ern343. [PMID: 19181864]
  • Yukari Sunohara, Hiroshi Matsumoto. Quinclorac-induced cell death is accompanied by generation of reactive oxygen species in maize root tissue. Phytochemistry. 2008 Sep; 69(12):2312-9. doi: 10.1016/j.phytochem.2008.06.012. [PMID: 18674787]
  • Thimmaraju Rudrappa, Robert E Splaine, Meredith L Biedrzycki, Harsh P Bais. Cyanogenic pseudomonads influence multitrophic interactions in the rhizosphere. PloS one. 2008 Apr; 3(4):e2073. doi: 10.1371/journal.pone.0002073. [PMID: 18446201]
  • Bibiana Silveira Moraes, Vania Lúcia Loro, Lissandra Glusczak, Alexandra Pretto, Charlene Menezes, Enio Marchezan, Sérgio de Oliveira Machado. Effects of four rice herbicides on some metabolic and toxicology parameters of teleost fish (Leporinus obtusidens). Chemosphere. 2007 Jul; 68(8):1597-601. doi: 10.1016/j.chemosphere.2007.03.006. [PMID: 17451783]
  • Tosapon Pornprom, Parnuwat Mahatamnuchoke, Kenji Usui. The role of altered acetyl-CoA carboxylase in conferring resistance to fenoxaprop-P-ethyl in Chinese sprangletop (Leptochloa chinensis (L.) Nees). Pest management science. 2006 Nov; 62(11):1109-15. doi: 10.1002/ps.1287. [PMID: 16964592]
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