MONOCROTOPHOS (BioDeep_00000403345)

Main id: BioDeep_00000002080

 

natural product


代谢物信息卡片


Pesticide1_Monocrotophos_C7H14NO5P_Dimethyl (2E)-4-(methylamino)-4-oxo-2-buten-2-yl phosphate

化学式: C7H14NO5P (223.061)
中文名称: 久效磷, O,O-二甲-O-(1-甲基-2-甲基氨基甲酰基)乙烯基磷酸酯
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C/C(=C\C(=N\C)\O)/OP(=O)(OC)OC
InChI: InChI=1S/C7H14NO5P/c1-6(5-7(9)8-2)13-14(10,11-3)12-4/h5H,1-4H3,(H,8,9)/b6-5+

描述信息

D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D002800 - Cholinesterase Inhibitors
D004791 - Enzyme Inhibitors > D008996 - Monoamine Oxidase Inhibitors
C471 - Enzyme Inhibitor > C47792 - Acetylcholinesterase Inhibitor
D010575 - Pesticides > D007306 - Insecticides
D009676 - Noxae > D009153 - Mutagens
D016573 - Agrochemicals
CONFIDENCE standard compound; INTERNAL_ID 3133

同义名列表

4 个代谢物同义名

MONOCROTOPHOS; Pesticide1_Monocrotophos_C7H14NO5P_Dimethyl (2E)-4-(methylamino)-4-oxo-2-buten-2-yl phosphate; Monocrotophos; Monocrotophos



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)

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 10 ARHGAP45, CASP3, CASP9, CAT, CYP1A1, FASN, FLNA, HPGDS, NFE2L2, TH
Peripheral membrane protein 2 ACHE, CYP1A1
Endoplasmic reticulum membrane 3 CYP19A1, CYP1A1, STAR
Nucleus 8 ACHE, CASP3, CASP9, FLNA, NFE2L2, NR1I2, PPARGC1A, TH
cytosol 12 ARHGAP45, CASP3, CASP9, CAT, FASN, FLNA, GSR, HPGDS, NFE2L2, PPARGC1A, TAT, TH
dendrite 1 TH
nuclear body 1 NR1I2
trans-Golgi network 1 FLNA
centrosome 1 NFE2L2
nucleoplasm 6 ATP2B1, CASP3, HPGDS, NFE2L2, NR1I2, PPARGC1A
RNA polymerase II transcription regulator complex 1 NFE2L2
Cell membrane 3 ACHE, ATP2B1, STAR
ruffle membrane 1 ARHGAP45
Cell projection, axon 1 TH
Cell projection, growth cone 1 FLNA
Multi-pass membrane protein 2 ATP2B1, CYP19A1
Synapse 2 ACHE, ATP2B1
cell surface 1 ACHE
dendritic shaft 1 FLNA
glutamatergic synapse 3 ATP2B1, CASP3, FLNA
Golgi apparatus 3 ACHE, FASN, NFE2L2
Golgi membrane 1 INS
mitochondrial inner membrane 1 CYP1A1
neuromuscular junction 1 ACHE
neuronal cell body 1 CASP3
postsynapse 1 FLNA
presynaptic membrane 1 ATP2B1
smooth endoplasmic reticulum 1 TH
synaptic vesicle 1 TH
Cytoplasm, cytosol 1 NFE2L2
plasma membrane 8 ACHE, ARHGAP45, ATP2B1, BCHE, FASN, FLNA, NFE2L2, STAR
synaptic vesicle membrane 1 ATP2B1
terminal bouton 1 TH
Membrane 7 ACHE, ARHGAP45, ATP2B1, CAT, CYP19A1, FASN, FLNA
axon 1 TH
basolateral plasma membrane 1 ATP2B1
brush border 1 FLNA
extracellular exosome 5 ATP2B1, CAT, FASN, FLNA, GSR
endoplasmic reticulum 1 CYP19A1
extracellular space 3 ACHE, BCHE, INS
perinuclear region of cytoplasm 3 ACHE, FLNA, TH
mitochondrion 6 CASP9, CAT, CYP1A1, GSR, STAR, TH
protein-containing complex 2 CASP9, CAT
intracellular membrane-bounded organelle 4 ATP2B1, CAT, CYP1A1, HPGDS
Microsome membrane 2 CYP19A1, CYP1A1
postsynaptic density 1 CASP3
Single-pass type I membrane protein 1 STAR
Secreted 3 ACHE, BCHE, INS
extracellular region 6 ACHE, ARHGAP45, BCHE, CAT, FLNA, INS
cytoplasmic side of plasma membrane 1 TH
mitochondrial matrix 3 CAT, GSR, STAR
Extracellular side 1 ACHE
transcription regulator complex 1 NR1I2
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 1 ATP2B1
external side of plasma membrane 1 GSR
actin cytoskeleton 1 FLNA
perikaryon 2 FLNA, TH
Z disc 1 FLNA
cytoplasmic vesicle 1 TH
nucleolus 1 FLNA
Melanosome membrane 1 TH
cell-cell junction 1 FLNA
Cell projection, ruffle membrane 1 ARHGAP45
Cytoplasm, perinuclear region 1 TH
Mitochondrion inner membrane 1 CYP1A1
Cytoplasm, cytoskeleton 1 FLNA
focal adhesion 2 CAT, FLNA
Peroxisome 1 CAT
basement membrane 1 ACHE
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
Nucleus, PML body 1 PPARGC1A
PML body 1 PPARGC1A
mitochondrial intermembrane space 1 STAR
lateral plasma membrane 1 ATP2B1
neuron projection 1 TH
chromatin 3 NFE2L2, NR1I2, PPARGC1A
mediator complex 1 NFE2L2
axonal growth cone 1 FLNA
cell projection 1 ATP2B1
Cell projection, podosome 1 FLNA
podosome 1 FLNA
Cytoplasm, cell cortex 1 FLNA
actin filament 1 FLNA
blood microparticle 1 BCHE
Basolateral cell membrane 1 ATP2B1
Lipid-anchor, GPI-anchor 1 ACHE
endosome lumen 1 INS
Melanosome 1 FASN
Presynaptic cell membrane 1 ATP2B1
side of membrane 1 ACHE
intermediate filament cytoskeleton 1 NR1I2
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 3 ARHGAP45, CAT, INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 BCHE, INS
transport vesicle 1 INS
azurophil granule lumen 1 ARHGAP45
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
immunological synapse 1 ATP2B1
nuclear envelope lumen 1 BCHE
apoptosome 1 CASP9
[Isoform 1]: Nucleus 1 PPARGC1A
synaptic cleft 1 ACHE
protein-DNA complex 1 NFE2L2
apical dendrite 1 FLNA
death-inducing signaling complex 1 CASP3
intracellular non-membrane-bounded organelle 1 FLNA
actin filament bundle 1 FLNA
cortical cytoskeleton 1 FLNA
catalase complex 1 CAT
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle 1 TH
glycoprotein Ib-IX-V complex 1 FLNA
Myb complex 1 FLNA
photoreceptor ribbon synapse 1 ATP2B1
[Isoform H]: Cell membrane 1 ACHE
glycogen granule 1 FASN
caspase complex 1 CASP9
[Isoform B4]: Nucleus 1 PPARGC1A
[Isoform B4-8a]: Cytoplasm 1 PPARGC1A
[Isoform B5]: Nucleus 1 PPARGC1A
[Isoform 9]: Nucleus 1 PPARGC1A


文献列表

  • Shazmin, Siti Aqlima Ahmad, Tatheer Alam Naqvi, Muhammad Farooq Hussain Munis, Muhammad Tariq Javed, Hassan Javed Chaudhary. Biodegradation of monocrotophos by Brucella intermedia Msd2 isolated from cotton plant. World journal of microbiology & biotechnology. 2023 Mar; 39(6):141. doi: 10.1007/s11274-023-03575-7. [PMID: 37000294]
  • Mary Isabella Sonali J, K Veena Gayathri, P Senthil Kumar, Gayathri Rangasamy. A study of potent biofertiliser and its degradation ability of monocrotophos and its in silico analysis. Chemosphere. 2023 Jan; 312(Pt 2):137304. doi: 10.1016/j.chemosphere.2022.137304. [PMID: 36410511]
  • Twinkle Dhillon, Amit Kumar, Vijay Kumar. Neuroprotective Effect of N-acetylcysteine Against Monocrotophos-Induced Oxidative Stress in Different Brain Regions of Rats. Applied biochemistry and biotechnology. 2022 Sep; 194(9):4049-4065. doi: 10.1007/s12010-022-03967-9. [PMID: 35587328]
  • C S K Mishra, Suryasikha Samal, Rashmi Rekha Samal, Binayak Prasad Behera, Pragyan Pallavini, Priyadarshini Dash, Satyabrata Brahma, Tanushree Moharana, Stutiprgnya Pradhan, Pratik Acharya. Polyvinylchloride and polypropylene as adsorbents of the pesticide monocrotophos enhance oxidative stress in Eudrillus eugeniae (Kinberg). Chemosphere. 2022 May; 295(?):133837. doi: 10.1016/j.chemosphere.2022.133837. [PMID: 35120958]
  • Shaheen Jafri Ali. Monocrotophos, an organophosphorus insecticide, induces cortical and trabecular bone loss in Swiss albino mice. Chemico-biological interactions. 2020 Sep; 329(?):109112. doi: 10.1016/j.cbi.2020.109112. [PMID: 32360284]
  • R Nagaraju, Akr Joshi, S Vamadeva, P S Rajini. Effect of chronic exposure to monocrotophos on white adipose tissue in rats and its association with metabolic dyshomeostasis. Human & experimental toxicology. 2020 Sep; 39(9):1190-1199. doi: 10.1177/0960327120913080. [PMID: 32207356]
  • Raju Nagaraju, Apurva K R Joshi, Sowmya G Vamadeva, Padmanabhan S Rajini. Deregulation of hepatic lipid metabolism associated with insulin resistance in rats subjected to chronic monocrotophos exposure. Journal of biochemical and molecular toxicology. 2020 Aug; 34(8):e22506. doi: 10.1002/jbt.22506. [PMID: 32267039]
  • Perumal Vivekanandhan, Kannan Swathy, Dharman Kalaimurugan, Marimuthu Ramachandran, Ananthanarayanan Yuvaraj, Arjunan Naresh Kumar, Ayyavu Thendral Manikandan, Neelakandan Poovarasan, Muthugoundar Subramanian Shivakumar, Eliningaya J Kweka. Larvicidal toxicity of Metarhizium anisopliae metabolites against three mosquito species and non-targeting organisms. PloS one. 2020; 15(5):e0232172. doi: 10.1371/journal.pone.0232172. [PMID: 32365106]
  • Durgesh Kumar Jaiswal, Jay Prakash Verma, Ram Krishna, Anand Kumar Gaurav, Janardan Yadav. Molecular characterization of monocrotophos and chlorpyrifos tolerant bacterial strain for enhancing seed germination of vegetable crops. Chemosphere. 2019 May; 223(?):636-650. doi: 10.1016/j.chemosphere.2019.02.053. [PMID: 30798059]
  • Zou Bin, Chu Yanhong, Xia Jiaojiao, Yao Jing. Acetylcholinesterase biosensor based on functionalized surface of carbon nanotubes for monocrotophos detection. Analytical biochemistry. 2018 11; 560(?):12-18. doi: 10.1016/j.ab.2018.08.024. [PMID: 30172744]
  • Xiaona Zhang, Wei Liu, Jun Wang, Hua Tian, Wei Wang, Shaoguo Ru. Quantitative analysis of in-vivo responses of reproductive and thyroid endpoints in male goldfish exposed to monocrotophos pesticide. Comparative biochemistry and physiology. Toxicology & pharmacology : CBP. 2018 Sep; 211(?):41-47. doi: 10.1016/j.cbpc.2018.05.010. [PMID: 29803892]
  • Yun-Xiu Hou, Shi-Wen Liu, Lian-Wen Wang, Shu-Hua Wu. Physiopathology of multiple organ dysfunctions in severely monocrotophos-poisoned rabbits. Chemico-biological interactions. 2017 Dec; 278(?):9-14. doi: 10.1016/j.cbi.2017.08.016. [PMID: 28864276]
  • Xiaona Zhang, Shuman Li, Cuicui Wang, Hua Tian, Wei Wang, Shaoguo Ru. Effects of monocrotophos pesticide on cholinergic and dopaminergic neurotransmitter systems during early development in the sea urchin Hemicentrotus pulcherrimus. Toxicology and applied pharmacology. 2017 08; 328(?):46-53. doi: 10.1016/j.taap.2017.05.003. [PMID: 28479505]
  • Vinay Kumar Tripathi, Vivek Kumar, Ankita Pandey, Pankhi Vatsa, Anupam Dhasmana, Rajat Pratap Singh, Sri Hari Chandan Appikonda, Inho Hwang, Mohtashim Lohani. Monocrotophos Induces the Expression of Xenobiotic Metabolizing Cytochrome P450s (CYP2C8 and CYP3A4) and Neurotoxicity in Human Brain Cells. Molecular neurobiology. 2017 07; 54(5):3633-3651. doi: 10.1007/s12035-016-9938-7. [PMID: 27206429]
  • Hua Tian, Yang Sun, Hui Wang, Xin Bing, Wei Wang, Shaoguo Ru. Monocrotophos pesticide affects synthesis and conversion of sex steroids through multiple targets in male goldfish (Carassius auratus). Scientific reports. 2017 05; 7(1):2306. doi: 10.1038/s41598-017-01935-6. [PMID: 28536437]
  • Madhusudan Reddy Narra, Kodimyala Rajender, R Rudra Reddy, U Suryanarayana Murty, Ghousia Begum. Insecticides induced stress response and recuperation in fish: Biomarkers in blood and tissues related to oxidative damage. Chemosphere. 2017 Feb; 168(?):350-357. doi: 10.1016/j.chemosphere.2016.10.066. [PMID: 27810534]
  • S Binukumari, K Anusiya Devi, J Vasanthi. Applications in environmental risk assessment of biochemical analysis on the Indian fresh water fish, Labeo rohita exposed to monocrotophos pesticide. Environmental toxicology and pharmacology. 2016 Oct; 47(?):200-205. doi: 10.1016/j.etap.2016.08.014. [PMID: 27771501]
  • Shaheen Jafri Ali, Padmanabhan Sharda Rajini. Effect of monocrotophos, an organophosphorus insecticide, on the striatal dopaminergic system in a mouse model of Parkinson's disease. Toxicology and industrial health. 2016 Jul; 32(7):1153-65. doi: 10.1177/0748233714547733. [PMID: 25227224]
  • Xiaona Zhang, Yan Zhong, Hua Tian, Wei Wang, Shaoguo Ru. Impairment of the cortisol stress response mediated by the hypothalamus-pituitary-interrenal (HPI) axis in zebrafish (Danio rerio) exposed to monocrotophos pesticide. Comparative biochemistry and physiology. Toxicology & pharmacology : CBP. 2015 Oct; 176-177(?):10-6. doi: 10.1016/j.cbpc.2015.07.003. [PMID: 26196239]
  • Jun Wang, Wei Wang, Xiaona Zhang, Hua Tian, Shaoguo Ru. Development of a lipovitellin-based goldfish (Carassius auratus) vitellogenin ELISA for detection of environmental estrogens. Chemosphere. 2015 Aug; 132(?):166-71. doi: 10.1016/j.chemosphere.2015.03.038. [PMID: 25855009]
  • Ravneet Kaur Uppal, Mohinder Singh Johal, Madan Lal Sharma. Toxicological effects and recovery of the corneal epithelium in Cyprinus carpio communis Linn. exposed to monocrotophos: an scanning electron microscope study. Veterinary ophthalmology. 2015 May; 18(3):214-20. doi: 10.1111/vop.12134. [PMID: 24373492]
  • Arun Jose, Ratnasamy Selvakumar, John Victor Peter, Gunasekaran Karthik, Denise Helen Fleming, Jude Joseph Fleming. Estimation of Monocrotophos renal elimination half-life in humans. Clinical toxicology (Philadelphia, Pa.). 2015; 53(7):629-32. doi: 10.3109/15563650.2015.1054500. [PMID: 26065438]
  • Raju Nagaraju, Apurva Kumar Ramesh Joshi, Padmanabhan Sharda Rajini. Organophosphorus insecticide, monocrotophos, possesses the propensity to induce insulin resistance in rats on chronic exposure. Journal of diabetes. 2015 Jan; 7(1):47-59. doi: 10.1111/1753-0407.12158. [PMID: 24698518]
  • Jun Wang, Xin Bing, Kun Yu, Hua Tian, Wei Wang, Shaoguo Ru. Preparation of a polyclonal antibody against goldfish (Carassius auratus) vitellogenin and its application to detect the estrogenic effects of monocrotophos pesticide. Ecotoxicology and environmental safety. 2015 Jan; 111(?):109-16. doi: 10.1016/j.ecoenv.2014.10.007. [PMID: 25450922]
  • Xiaona Zhang, Hua Tian, Wei Wang, Shaoguo Ru. Monocrotophos pesticide decreases the plasma levels of total 3,3',5-triiodo-l-thyronine and alters the expression of genes associated with the thyroidal axis in female goldfish (Carassius auratus). PloS one. 2014; 9(9):e108972. doi: 10.1371/journal.pone.0108972. [PMID: 25268935]
  • Xiaona Zhang, Hua Tian, Wei Wang, Shaoguo Ru. Exposure to monocrotophos pesticide causes disruption of the hypothalamic-pituitary-thyroid axis in adult male goldfish (Carassius auratus). General and comparative endocrinology. 2013 Nov; 193(?):158-66. doi: 10.1016/j.ygcen.2013.08.003. [PMID: 23948368]
  • Qin Zhao, Qian Lu, Qiong-Wei Yu, Yu-Qi Feng. Dispersive microextraction based on "magnetic water" coupled to gas chromatography/mass spectrometry for the fast determination of organophosphorus pesticides in cold-pressed vegetable oils. Journal of agricultural and food chemistry. 2013 Jun; 61(22):5397-403. doi: 10.1021/jf400870m. [PMID: 23687955]
  • G Velmurugan, D D Venkatesh Babu, Subbiah Ramasamy. Prolonged monocrotophos intake induces cardiac oxidative stress and myocardial damage in rats. Toxicology. 2013 May; 307(?):103-8. doi: 10.1016/j.tox.2012.11.022. [PMID: 23228476]
  • R Rajasankar, G Manju Gayathry, A Sathiavelu, C Ramalingam, V S Saravanan. Pesticide tolerant and phosphorus solubilizing Pseudomonas sp. strain SGRAJ09 isolated from pesticides treated Achillea clavennae rhizosphere soil. Ecotoxicology (London, England). 2013 May; 22(4):707-17. doi: 10.1007/s10646-013-1062-0. [PMID: 23512438]
  • Vivek Kumar, Vinay K Tripathi, Abhishek K Singh, Mohathshim Lohani, Mohammed Kuddus. Trans-resveratrol restores the damages induced by organophosphate pesticide-monocrotophos in neuronal cells. Toxicology international. 2013 Jan; 20(1):48-55. doi: 10.4103/0971-6580.111571. [PMID: 23833438]
  • A Masoud, R Sandhir. Increased oxidative stress is associated with the development of organophosphate-induced delayed neuropathy. Human & experimental toxicology. 2012 Dec; 31(12):1214-27. doi: 10.1177/0960327112446842. [PMID: 22751200]
  • Ashwin B Patel, Aruna Dewan, Bharat C Kaji. Monocrotophos poisoning through contaminated millet flour. Arhiv za higijenu rada i toksikologiju. 2012 Sep; 63(3):377-83. doi: 10.2478/10004-1254-63-2012-2158. [PMID: 23152387]
  • Lei Xu, Hua Tian, Wei Wang, Shaoguo Ru. Effects of monocrotophos pesticide on serotonin metabolism during early development in the sea urchin, Hemicentrotus pulcherrimus. Environmental toxicology and pharmacology. 2012 Sep; 34(2):537-547. doi: 10.1016/j.etap.2012.06.014. [PMID: 22824501]
  • Madhusudan Reddy Narra, Ghousia Begum, Kodimyala Rajender, J Venkateswara Rao. Toxic impact of two organophosphate insecticides on biochemical parameters of a food fish and assessment of recovery response. Toxicology and industrial health. 2012 May; 28(4):343-52. doi: 10.1177/0748233711412423. [PMID: 21983276]
  • Apurva Kumar Ramesh Joshi, Raju Nagaraju, Padmanabhan Sharda Rajini. Insights into the mechanisms mediating hyperglycemic and stressogenic outcomes in rats treated with monocrotophos, an organophosphorus insecticide. Toxicology. 2012 Mar; 294(1):9-16. doi: 10.1016/j.tox.2012.01.009. [PMID: 22305719]
  • Amajad Iqbal Kazi, Anna Oommen. Monocrotophos induced oxidative damage associates with severe acetylcholinesterase inhibition in rat brain. Neurotoxicology. 2012 Mar; 33(2):156-61. doi: 10.1016/j.neuro.2012.01.008. [PMID: 22285544]
  • Apurva Kumar R Joshi, P S Rajini. Hyperglycemic and stressogenic effects of monocrotophos in rats: evidence for the involvement of acetylcholinesterase inhibition. Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie. 2012 Jan; 64(1-2):115-20. doi: 10.1016/j.etp.2010.07.003. [PMID: 20674316]
  • Khamrunissa Begum, P S Rajini. Augmentation of hepatic and renal oxidative stress and disrupted glucose homeostasis by monocrotophos in streptozotocin-induced diabetic rats. Chemico-biological interactions. 2011 Sep; 193(3):240-5. doi: 10.1016/j.cbi.2011.07.003. [PMID: 21821013]
  • Madhusudan Reddy Narra, Ghousia Begum, Kodimyala Rajender, J Venkateswara Rao. In vivo impact of monocrotophos on biochemical parameters of a freshwater fish during subacute toxicity and following cessation of exposure to the insecticide. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2011 Sep; 66(9-10):507-14. doi: 10.1515/znc-2011-9-1011. [PMID: 22191217]
  • Natalie A Belsey, Sarah F Cordery, Annette L Bunge, Richard H Guy. Assessment of dermal exposure to pesticide residues during re-entry. Environmental science & technology. 2011 May; 45(10):4609-15. doi: 10.1021/es200172q. [PMID: 21510672]
  • Nidhi Dwivedi, Swaran J S Flora. Concomitant exposure to arsenic and organophosphates on tissue oxidative stress in rats. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2011 May; 49(5):1152-9. doi: 10.1016/j.fct.2011.02.007. [PMID: 21349312]
  • Anwar Masoud, Ravi Kiran, Rajat Sandhir. Modulation of dopaminergic system and neurobehavioral functions in delayed neuropathy induced by organophosphates. Toxicology mechanisms and methods. 2011 Jan; 21(1):1-5. doi: 10.3109/15376516.2010.529182. [PMID: 21067471]
  • M P Kashyap, A K Singh, M A Siddiqui, V Kumar, V K Tripathi, V K Khanna, S Yadav, S K Jain, A B Pant. Caspase cascade regulated mitochondria mediated apoptosis in monocrotophos exposed PC12 cells. Chemical research in toxicology. 2010 Nov; 23(11):1663-72. doi: 10.1021/tx100234m. [PMID: 20957986]
  • Hua Tian, Shaoguo Ru, Xin Bing, Wei Wang. Effects of monocrotophos on the reproductive axis in the male goldfish (Carassius auratus): potential mechanisms underlying vitellogenin induction. Aquatic toxicology (Amsterdam, Netherlands). 2010 Jun; 98(1):67-73. doi: 10.1016/j.aquatox.2010.01.011. [PMID: 20149464]
  • Hua Tian, Shaoguo Ru, Wei Wang, Xin Bing. Effects of monocrotophos on the reproductive axis in the female goldfish (Carassius auratus). Comparative biochemistry and physiology. Toxicology & pharmacology : CBP. 2010 Jun; 152(1):107-13. doi: 10.1016/j.cbpc.2010.03.004. [PMID: 20298809]
  • Jérôme Carletto, Thibaud Martin, Flavie Vanlerberghe-Masutti, Thierry Brévault. Insecticide resistance traits differ among and within host races in Aphis gossypii. Pest management science. 2010 Mar; 66(3):301-7. doi: 10.1002/ps.1874. [PMID: 19908228]
  • Nidhi Dwivedi, Yangchen D Bhutia, Vinesh Kumar, Preeti Yadav, Pramod Kushwaha, Harimohan Swarnkar, S J S Flora. Effects of combined exposure to dichlorvos and monocrotophos on blood and brain biochemical variables in rats. Human & experimental toxicology. 2010 Feb; 29(2):121-9. doi: 10.1177/0960327109357212. [PMID: 20026515]
  • Anwar Masoud, Ravi Kiran, Rajat Sandhir. Impaired mitochondrial functions in organophosphate induced delayed neuropathy in rats. Cellular and molecular neurobiology. 2009 Dec; 29(8):1245-55. doi: 10.1007/s10571-009-9420-4. [PMID: 19517227]
  • Hua Tian, Shaoguo Ru, Zhenyu Wang, Wenting Cai, Wei Wang. Estrogenic effects of monocrotophos evaluated by vitellogenin mRNA and protein induction in male goldfish (Carassius auratus). Comparative biochemistry and physiology. Toxicology & pharmacology : CBP. 2009 Aug; 150(2):231-6. doi: 10.1016/j.cbpc.2009.04.014. [PMID: 19439194]
  • Y-H Yang, Y-J Yang, W-Y Gao, J-J Guo, Y-H Wu, Y-D Wu. Introgression of a disrupted cadherin gene enables susceptible Helicoverpa armigera to obtain resistance to Bacillus thuringiensis toxin Cry1Ac. Bulletin of entomological research. 2009 Apr; 99(2):175-81. doi: 10.1017/s0007485308006226. [PMID: 18954492]
  • Daoud Ali, Sudhir Kumar. Long-term genotoxic effect of monocrotophos in different tissues of freshwater fish Channa punctatus (Bloch) using alkaline single cell gel electrophoresis. The Science of the total environment. 2008 Nov; 405(1-3):345-50. doi: 10.1016/j.scitotenv.2008.05.037. [PMID: 18649923]
  • Chandrakala Patil, Ravindra Paul, Malkanna. Neuroendocrine regulation and pesticidal impact on freshwater crab, Barytelphusa guerini (H. Milne Edwards). Journal of environmental biology. 2008 Nov; 29(6):887-92. doi: ". [PMID: 19297986]
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