Triazophos (BioDeep_00000001958)

 

Secondary id: BioDeep_00001867853

human metabolite blood metabolite


代谢物信息卡片


Diethoxy-[(1-phenyl-1,2,4-triazol-3-yl)oxy]-sulphanylidene-$l^{5}-phosphane

化学式: C12H16N3O3PS (313.065)
中文名称: 三唑磷
谱图信息: 最多检出来源 Homo sapiens(blood) 17.14%

分子结构信息

SMILES: CCOP(=S)(OCC)OC1=NN(C=N1)C1=CC=CC=C1
InChI: InChI=1S/C12H16N3O3PS/c1-3-16-19(20,17-4-2)18-12-13-10-15(14-12)11-8-6-5-7-9-11/h5-10H,3-4H2,1-2H3

描述信息

CONFIDENCE standard compound; INTERNAL_ID 1193; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9355; ORIGINAL_PRECURSOR_SCAN_NO 9354
CONFIDENCE standard compound; INTERNAL_ID 1193; DATASET 20200303_ENTACT_RP_MIX503; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9217; ORIGINAL_PRECURSOR_SCAN_NO 9214
CONFIDENCE standard compound; INTERNAL_ID 1193; DATASET 20200303_ENTACT_RP_MIX503; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9286; ORIGINAL_PRECURSOR_SCAN_NO 9281
CONFIDENCE standard compound; INTERNAL_ID 1193; DATASET 20200303_ENTACT_RP_MIX503; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9227; ORIGINAL_PRECURSOR_SCAN_NO 9226
CONFIDENCE standard compound; INTERNAL_ID 1193; DATASET 20200303_ENTACT_RP_MIX503; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9231; ORIGINAL_PRECURSOR_SCAN_NO 9228
CONFIDENCE standard compound; INTERNAL_ID 1193; DATASET 20200303_ENTACT_RP_MIX503; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9272; ORIGINAL_PRECURSOR_SCAN_NO 9270
C471 - Enzyme Inhibitor > C47792 - Acetylcholinesterase Inhibitor

同义名列表

14 个代谢物同义名

Diethoxy-[(1-phenyl-1,2,4-triazol-3-yl)oxy]-sulphanylidene-$l^{5}-phosphane; Phosphorothioic acid, O,O-diethyl O-(1-phenyl-1H-1,2,4-triazol-3-yl) ester; Phosphorothioate, O,O-diethyl O-(1-phenyl-1H-1,2,4-triazol-3-yl) ester; O,O-Diethyl O-(1-phenyl-1H-1,2,4-triazol-3-yl) thiophosphoric acid; O,O-diethyl O-1-phenyl-1H-1,2,4-triazol-3-yl phosphorothioate; 1-Phenyl-1,2,4-triazolyl-3-(O,O-diethylthionophosphoric acid); O,O-Diethyl O-(1-phenyl-1H-1,2,4-triazol-3-yl) thiophosphate; 1-Phenyl-1,2,4-triazolyl-3-(O,O-diethylthionophosphate); 1-Phenyl-3-(O,O-diethylthiophosphoryl)-1,2,4- triazole; Hostathion; Triazophos; Methoxone; Triazofos; Triazophos



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 12 ABCB1, APAF1, AR, BCL2, CASP3, CASP9, CAT, HPGDS, NR3C1, PGR, POMC, SOD1
Peripheral membrane protein 2 ACHE, CYP1B1
Endoplasmic reticulum membrane 3 BCL2, CYP1B1, DIO1
Nucleus 9 ACHE, APAF1, AR, BCL2, CASP3, CASP9, NR3C1, PGR, SOD1
cytosol 10 APAF1, AR, BCL2, CASP3, CASP9, CAT, HPGDS, NR3C1, PGR, SOD1
centrosome 1 NR3C1
nucleoplasm 6 AR, CASP3, HPGDS, NR3C1, PGR, SOD1
Cell membrane 3 ABCB1, ACHE, ADRB3
Multi-pass membrane protein 2 ABCB1, ADRB3
Synapse 2 ACHE, NR3C1
cell surface 2 ABCB1, ACHE
glutamatergic synapse 1 CASP3
Golgi apparatus 1 ACHE
Golgi membrane 1 INS
neuromuscular junction 1 ACHE
neuronal cell body 2 CASP3, SOD1
plasma membrane 7 ABCB1, ACHE, ADRB3, AR, BCHE, DIO1, PGR
Membrane 9 ABCB1, ACHE, APAF1, AR, BCL2, CAT, CYP1B1, DIO1, NR3C1
apical plasma membrane 1 ABCB1
extracellular exosome 5 ABCB1, APAF1, CAT, SOD1, SOD2
endoplasmic reticulum 1 BCL2
extracellular space 5 ACHE, BCHE, INS, POMC, SOD1
perinuclear region of cytoplasm 1 ACHE
mitochondrion 7 BCL2, CASP9, CAT, CYP1B1, NR3C1, SOD1, SOD2
protein-containing complex 7 APAF1, AR, BCL2, CASP9, CAT, NR3C1, SOD1
intracellular membrane-bounded organelle 3 CAT, CYP1B1, HPGDS
Microsome membrane 1 CYP1B1
postsynaptic density 1 CASP3
Secreted 4 ACHE, BCHE, INS, POMC
extracellular region 7 ACHE, APAF1, BCHE, CAT, INS, POMC, SOD1
Mitochondrion outer membrane 1 BCL2
Single-pass membrane protein 2 BCL2, DIO1
mitochondrial outer membrane 2 BCL2, PGR
Mitochondrion matrix 1 SOD2
mitochondrial matrix 4 CAT, NR3C1, SOD1, SOD2
Extracellular side 1 ACHE
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 1 NR3C1
Nucleus membrane 1 BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 1 BCL2
cytoplasmic vesicle 1 SOD1
axon cytoplasm 1 SOD1
Apical cell membrane 1 ABCB1
pore complex 1 BCL2
Cytoplasm, cytoskeleton, spindle 1 NR3C1
focal adhesion 1 CAT
spindle 1 NR3C1
mitochondrial nucleoid 1 SOD2
Peroxisome 2 CAT, SOD1
basement membrane 1 ACHE
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
mitochondrial intermembrane space 1 SOD1
secretory granule 1 POMC
nuclear speck 2 AR, NR3C1
dendrite cytoplasm 1 SOD1
receptor complex 1 ADRB3
chromatin 3 AR, NR3C1, PGR
Chromosome 1 NR3C1
blood microparticle 1 BCHE
Lipid-anchor, GPI-anchor 1 ACHE
Endomembrane system 1 DIO1
endosome lumen 1 INS
Nucleus, nucleoplasm 1 NR3C1
side of membrane 1 ACHE
myelin sheath 1 BCL2
ficolin-1-rich granule lumen 2 APAF1, CAT
secretory granule lumen 4 APAF1, CAT, INS, POMC
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 BCHE, INS
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
nuclear envelope lumen 1 BCHE
apoptosome 2 APAF1, CASP9
synaptic cleft 1 ACHE
external side of apical plasma membrane 1 ABCB1
death-inducing signaling complex 1 CASP3
[Isoform Alpha]: Cytoplasm 1 NR3C1
catalase complex 1 CAT
[Isoform Beta]: Nucleus 1 NR3C1
[Isoform Alpha-B]: Nucleus 1 NR3C1
[Isoform 4]: Mitochondrion outer membrane 1 PGR
BAD-BCL-2 complex 1 BCL2
[Isoform H]: Cell membrane 1 ACHE
caspase complex 1 CASP9


文献列表

  • K S Suhas, Shubham Vijapure, Supriya Yadav, Madhu Ramesh, M Saminathan, Kaveri Jambagi, Bindu Suresh, C L Madhu, Ajay Kumar, Vikash Chandra, Avinash G Telang. Nano-quercetin mitigates triazophos-induced testicular toxicity in rats by suppressing oxidative stress and apoptosis. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2024 Jan; 183(?):114331. doi: 10.1016/j.fct.2023.114331. [PMID: 38061569]
  • Linbao Zhang, Wei Sun, Zhe Zhang, Fei Tian, Haigang Chen. Sex-specific metabolic dysregulation in digestive glands of green mussels following exposure to triazophos. Pesticide biochemistry and physiology. 2023 Aug; 194(?):105514. doi: 10.1016/j.pestbp.2023.105514. [PMID: 37532329]
  • Qi Su, Juan Zheng, Jiejun Xi, Jing Yang, Lixin Wang, Dongmei Xiong. Evaluation of the acute toxic response induced by triazophos to the non-target green algae Chlorella pyrenoidosa. Pesticide biochemistry and physiology. 2022 Mar; 182(?):105036. doi: 10.1016/j.pestbp.2022.105036. [PMID: 35249646]
  • Guangyue Song, Lianrun Huang, Yue Huang, Weimei Liu, Minghua Wang, Xiude Hua. Electrofusion preparation of anti-triazophos monoclonal antibodies for development of an indirect competitive enzyme-linked immunosorbent assay. Journal of immunological methods. 2022 01; 500(?):113184. doi: 10.1016/j.jim.2021.113184. [PMID: 34808129]
  • Rakesh Kumar Chandra, Ajay Kumar Bhardwaj, Manish Kumar Tripathi. Evaluation of triazophos induced immunotoxicity of spleen and head kidney in fresh water teleost, Channa punctata. Comparative biochemistry and physiology. Toxicology & pharmacology : CBP. 2021 Jul; 245(?):109029. doi: 10.1016/j.cbpc.2021.109029. [PMID: 33722765]
  • Fang-Wei Yang, Bing Fang, Guo-Fang Pang, Ming Zhang, Fa-Zheng Ren. Triazophos and its metabolite diethyl phosphate have different effects on endocrine hormones and gut health in rats. Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes. 2021; 56(6):566-576. doi: 10.1080/03601234.2021.1922042. [PMID: 34038317]
  • Mahesh Kumar Mummadi, Raghavendra Pandurangi, J J Babu Geddam, Sukesh Narayan Sinha, Ananthan Rajendran, Sivaperumal P, Naveen K Ramachandrappa, Sree Ramakrishna K, Pagidoju Sreenu. Investigation of an acute neurological outbreak in Eluru, India, 2020. PloS one. 2021; 16(11):e0259192. doi: 10.1371/journal.pone.0259192. [PMID: 34748567]
  • João Vitor Ferreira Rodrigues, Anna Paula Perin Vidigal, Vítor Sampaio Minassa, Thatiany Jardim Batista, Randriely Merscher Sobreira de Lima, Vinícius Rafael Funck, Leandro S Antero, Leonardo Barbosa Moraes Resstel, Juliana Barbosa Coitinho, Leandro Jose Bertoglio, Karla Nívea Sampaio, Vanessa Beijamini. A single dose of the organophosphate triazophos induces fear extinction deficits accompanied by hippocampal acetylcholinesterase inhibition. Neurotoxicology and teratology. 2020 Nov; 82(?):106929. doi: 10.1016/j.ntt.2020.106929. [PMID: 33031921]
  • Zhihe Qing, Yacheng Li, Younan Li, Guoyan Luo, Jinlei Hu, Zhen Zou, Yanli Lei, Juewen Liu, Ronghua Yang. Thiol-suppressed I2-etching of AuNRs: acetylcholinesterase-mediated colorimetric detection of organophosphorus pesticides. Mikrochimica acta. 2020 08; 187(9):497. doi: 10.1007/s00604-020-04486-2. [PMID: 32803418]
  • Gang Xu, Yu Jiang, Nannan Zhang, Fang Liu, Guoqing Yang. Triazophos-induced vertical transmission of rice stripe virus is associated with host vitellogenin in the small brown planthopper Laodelphax striatellus. Pest management science. 2020 May; 76(5):1949-1957. doi: 10.1002/ps.5729. [PMID: 31858699]
  • Guihua Wang, Dongmei Xiong, Manni Wu, Lixin Wang, Jing Yang. Induction of time- and dose-dependent oxidative stress of triazophos to brain and liver in zebrafish (Danio rerio). Comparative biochemistry and physiology. Toxicology & pharmacology : CBP. 2020 Feb; 228(?):108640. doi: 10.1016/j.cbpc.2019.108640. [PMID: 31654829]
  • Reetu Bhanot, Gurinder Kaur Sangha. Effect of in utero and lactational exposure of triazophos on reproductive system functions in male offsprings, Rattus norvegicus. Drug and chemical toxicology. 2019 Sep; 42(5):519-525. doi: 10.1080/01480545.2018.1457048. [PMID: 29681207]
  • Fang-Wei Yang, Bing Fang, Guo-Fang Pang, Fa-Zheng Ren. Organophosphorus pesticide triazophos: A new endocrine disruptor chemical of hypothalamus-pituitary-adrenal axis. Pesticide biochemistry and physiology. 2019 Sep; 159(?):91-97. doi: 10.1016/j.pestbp.2019.05.021. [PMID: 31400790]
  • Mengmeng Yan, Ge Chen, Yongxin She, Jun Ma, Sihui Hong, Yong Shao, A M Abd El-Aty, Miao Wang, Shanshan Wang, Jing Wang. Sensitive and Simple Competitive Biomimetic Nanozyme-Linked Immunosorbent Assay for Colorimetric and Surface-Enhanced Raman Scattering Sensing of Triazophos. Journal of agricultural and food chemistry. 2019 Aug; 67(34):9658-9666. doi: 10.1021/acs.jafc.9b03401. [PMID: 31381330]
  • Tehseen Yaseen, Hongbin Pu, Da-Wen Sun. Rapid detection of multiple organophosphorus pesticides (triazophos and parathion-methyl) residues in peach by SERS based on core-shell bimetallic Au@Ag NPs. Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment. 2019 May; 36(5):762-778. doi: 10.1080/19440049.2019.1582806. [PMID: 30943113]
  • Lin-Quan Ge, Hao-Tian Gu, Xin Li, Sui Zheng, Ze Zhou, Hong Miao, Jin-Cai Wu. Silencing of triazophos-induced Hexokinase-1-like reduces fecundity in Nilaparvata lugens (Stål) (Hemiptera: Delphacidae). Pesticide biochemistry and physiology. 2019 Jan; 153(?):176-184. doi: 10.1016/j.pestbp.2018.11.016. [PMID: 30744893]
  • Xian Zhang, Jun Ding, Bing Xu, Lin-Quan Ge, Guo-Qing Yang, Jin-Cai Wu. Long chain fatty acid coenzyme A ligase (FACL) regulates triazophos-induced stimulation of reproduction in the small brown planthopper (SBPH), Laodelphax striatellus (Fallen). Pesticide biochemistry and physiology. 2018 Jun; 148(?):81-86. doi: 10.1016/j.pestbp.2018.04.002. [PMID: 29891382]
  • Lin-Quan Ge, Bo Huang, Xin Li, Hao-Tian Gu, Sui Zheng, Ze Zhou, Hong Miao, Jin-Cai Wu. Silencing pyruvate kinase (NlPYK) leads to reduced fecundity in brown planthoppers, Nilaparvata lugens (Stål) (Hemiptera: Delphacidae). Archives of insect biochemistry and physiology. 2017 Dec; 96(4):. doi: 10.1002/arch.21429. [PMID: 29114912]
  • Juan Wu, Zhu Li, Liang Wu, Fei Zhong, Naxin Cui, Yanran Dai, Shuiping Cheng. Triazophos (TAP) removal in horizontal subsurface flow constructed wetlands (HSCWs) and its accumulation in plants and substrates. Scientific reports. 2017 07; 7(1):5468. doi: 10.1038/s41598-017-05874-0. [PMID: 28710370]
  • Lin-Lin You, You Wu, Bing Xu, Jun Ding, Lin-Quan Ge, Guo-Qin Yang, Qi-Sheng Song, David Stanley, Jin-Cai Wu. Driving Pest Insect Populations: Agricultural Chemicals Lead to an Adaptive Syndrome in Nilaparvata Lugens Stål (Hemiptera: Delphacidae). Scientific reports. 2016 11; 6(?):37430. doi: 10.1038/srep37430. [PMID: 27876748]
  • Lin-Quan Ge, Ting Xia, Bo Huang, Qi-Sheng Song, Hong-Wei Zhang, David Stanley, Guo-Qing Yang, Jin-Cai Wu. Suppressing male spermatogenesis-associated protein 5-like gene expression reduces vitellogenin gene expression and fecundity in Nilaparvata lugens Stål. Scientific reports. 2016 06; 6(?):28111. doi: 10.1038/srep28111. [PMID: 27305948]
  • Rui Liu, Xiao Liang, Dandan Xiang, Yirong Guo, Yihua Liu, Guonian Zhu. Expression and Functional Properties of an Anti-Triazophos High-Affinity Single-Chain Variable Fragment Antibody with Specific Lambda Light Chain. International journal of molecular sciences. 2016 Jun; 17(6):. doi: 10.3390/ijms17060823. [PMID: 27338340]
  • Juan Wu, Yuqin Feng, Yanran Dai, Naxin Cui, Bruce Anderson, Shuiping Cheng. Biological mechanisms associated with triazophos (TAP) removal by horizontal subsurface flow constructed wetlands (HSFCW). The Science of the total environment. 2016 May; 553(?):13-19. doi: 10.1016/j.scitotenv.2016.02.067. [PMID: 26897579]
  • Zong-Yu Liu, Yi-Ping Jiang, Lei Li, Lin-Lin You, You Wu, Bin Xu, Lin-Quan Ge, Jin-Cai Wu. Silencing of ACO decreases reproduction and energy metabolism in triazophos-treated female brown plant hoppers, Nilaparvata lugens Stål (Hemiptera: Delphacidae). Pesticide biochemistry and physiology. 2016 Mar; 128(?):76-81. doi: 10.1016/j.pestbp.2015.09.014. [PMID: 26969443]
  • Irani Mukherjee, Ashok Kumar, Aman Kumar. Dissipation of deltamethrin, triazophos, and endosulfan in ready mix formulations in tomato (Lycopersicon esculentum L.) and Egg plant (Solanum melongena L.). Environmental science and pollution research international. 2015 Sep; 22(18):14169-77. doi: 10.1007/s11356-015-4637-x. [PMID: 25966882]
  • Lei Liu, Bin Zhu, Yu-Xin Gong, Guang-Lu Liu, Gao-Xue Wang. Neurotoxic effect of triazophos on goldfish (Carassius auratus) and tissue specific antioxidant responses. Ecotoxicology and environmental safety. 2015 Jun; 116(?):68-75. doi: 10.1016/j.ecoenv.2015.03.001. [PMID: 25768424]
  • Baoju Wang, Ying Wang, Yang Zhang, Ping Han, Fei Li, Zhaojun Han. Genome-wide analysis of esterase-like genes in the striped rice stem borer, Chilo suppressalis. Genome. 2015 Jun; 58(6):323-31. doi: 10.1139/gen-2014-0082. [PMID: 26285093]
  • Guang-Hua Luo, Xiao-Huan Li, Zhi-Chun Zhang, Bao-Sheng Liu, Shui-Jin Huang, Ji-Chao Fang. Cloning of Two Acetylcholinesterase Genes and Analysis of Point Mutations Putatively Associated with Triazophos Resistance in Chilo auricilius (Lepidoptera: Pyralidae). Journal of economic entomology. 2015 Jun; 108(3):1289-97. doi: 10.1093/jee/tov086. [PMID: 26470257]
  • Lin-Quan Ge, Yu-Cheng Sun, Fang Ouyang, Jin-Cai Wu, Feng Ge. The effects of triazophos applied to transgenic Bt rice on the nutritional indexes, Nlvg expression, and population growth of Nilaparvata lugens Stål under elevated CO₂. Pesticide biochemistry and physiology. 2015 Feb; 118(?):50-7. doi: 10.1016/j.pestbp.2014.11.010. [PMID: 25752430]
  • Dharmender Sharma, Gurinder Kaur Sangha, Kuldeep Singh Khera. Triazophos-induced oxidative stress and histomorphological changes in ovary of female Wistar rats. Pesticide biochemistry and physiology. 2015 Jan; 117(?):9-18. doi: 10.1016/j.pestbp.2014.09.004. [PMID: 25619906]
  • Zhan-Fei Zhu, Jia Cheng, Xiu-Li Lu, Xin Li, Lin-Quan Ge, Ji-Chao Fang, Jin-Cai Wu. Comparisons of topical and spray applications of two pesticides, triazophos and jinggangmycin, on the protein content in the ovaries and fat bodies of the brown planthopper Nilaparvata lugens Stål (Hemiptera:Delphacidae). Pesticide biochemistry and physiology. 2014 Sep; 114(?):97-101. doi: 10.1016/j.pestbp.2014.06.008. [PMID: 25175656]
  • Mohineesh, Jaya Raj, A C Rajvanshi, T D Dogra, Anupuma Raina. Effect of acute exposure of triazophos on oxidative stress and histopathological alterations in liver, kidney and brain of Wistar rats. Indian journal of experimental biology. 2014 Aug; 52(8):814-9. doi: . [PMID: 25141545]
  • Tao Gu, Li Na Sun, Jun Zhang, Xin Hua Sui, Shun Peng Li. Rhizobium flavum sp. nov., a triazophos-degrading bacterium isolated from soil under the long-term application of triazophos. International journal of systematic and evolutionary microbiology. 2014 Jun; 64(Pt 6):2017-2022. doi: 10.1099/ijs.0.061523-0. [PMID: 24639241]
  • Qing Chen, Li-Na Sun, Xiao-Xia Zhang, Jian He, Soon-Wo Kwon, Jun Zhang, Shun-Peng Li, Jin-Gang Gu. Roseomonas rhizosphaerae sp. nov., a triazophos-degrading bacterium isolated from soil. International journal of systematic and evolutionary microbiology. 2014 Apr; 64(Pt 4):1127-1133. doi: 10.1099/ijs.0.057000-0. [PMID: 24408520]
  • Jia Cheng, Liu-Juan Huang, Zhan-Fei Zhu, Li-Ben Jiang, Lin-Quan Ge, Jin-Cai Wu. Heat-dependent fecundity enhancement observed in Nilaparvata lugens (Hemiptera: Delphacidae) after treatment with triazophos. Environmental entomology. 2014 Apr; 43(2):474-81. doi: 10.1603/en13249. [PMID: 24763100]
  • Dharmender Sharma, Gurinder Kaur Sangha. Triazophos induced oxidative stress and histomorphological changes in liver and kidney of female albino rats. Pesticide biochemistry and physiology. 2014 Mar; 110(?):71-80. doi: 10.1016/j.pestbp.2014.03.003. [PMID: 24759054]
  • Zhu Li, Huiping Xiao, Shuiping Cheng, Liping Zhang, Xiaolong Xiel, Zhenbin Wu. A comparison on the phytoremediation ability of triazophos by different macrophytes. Journal of environmental sciences (China). 2014 Feb; 26(2):315-22. doi: 10.1016/s1001-0742(13)60417-9. [PMID: 25077355]
  • Lin-Quan Ge, Liu-Juan Huang, Guo-Qin Yang, Qi-Sheng Song, David Stanley, G M Gurr, Jin-Cai Wu. Molecular basis for insecticide-enhanced thermotolerance in the brown planthopper Nilaparvata lugens Stål (Hemiptera:Delphacidae). Molecular ecology. 2013 Nov; 22(22):5624-34. doi: 10.1111/mec.12502. [PMID: 24303791]
  • Stephen Chan Teck Leong, Fatimah Abang, Andrew Beattie, Roland Jui Heng Kueh, Sing King Wong. Impacts of horticultural mineral oils and two insecticide practices on population fluctuation of Diaphorina citri and spread of Huanglongbing in a citrus orchard in Sarawak. TheScientificWorldJournal. 2012; 2012(?):651416. doi: 10.1100/2012/651416. [PMID: 22629178]
  • Lin-Quan Ge, Yao Cheng, Jin-Cai Wu, Gary C Jahn. Proteomic analysis of insecticide triazophos-induced mating-responsive proteins of Nilaparvata lugens Stål (Hemiptera: Delphacidae). Journal of proteome research. 2011 Oct; 10(10):4597-612. doi: 10.1021/pr200414g. [PMID: 21800909]
  • Smita Jain, S Mythily, Rafat S Ahmed, Vinod K Arora, B D Banerjee. Induction of oxidative stress and histopathological changes by sub-chronic doses of triazophos. Indian journal of biochemistry & biophysics. 2010 Dec; 47(6):388-92. doi: . [PMID: 21355424]
  • Hari C Meher, Vijay T Gajbhiye, Ghanendra Singh, Anju Kamra, Gautam Chawla. Persistence and nematicidal efficacy of carbosulfan, cadusafos, phorate, and triazophos in soil and uptake by chickpea and tomato crops under tropical conditions. Journal of agricultural and food chemistry. 2010 Feb; 58(3):1815-22. doi: 10.1021/jf903609d. [PMID: 20085277]
  • Hari C Meher, Vijay T Gajbhiye, Gautam Chawla, Ghanendra Singh. Virulence development and genetic polymorphism in Meloidogyne incognita (Kofoid & White) Chitwood after prolonged exposure to sublethal concentrations of nematicides and continuous growing of resistant tomato cultivars. Pest management science. 2009 Nov; 65(11):1201-7. doi: 10.1002/ps.1810. [PMID: 19562824]
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