Deltamethrin (BioDeep_00000008434)

 

Secondary id: BioDeep_00001871289

human metabolite


代谢物信息卡片


(S)-Cyano(3-phenoxyphenyl)methyl (1R,3R)-3-(2,2-dibromoethenyl)-2,2-dimethylcyclopropane-1-carboxylic acid

化学式: C22H19Br2NO3 (502.9732)
中文名称: 乙腈中溴氰菊酯溶液
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1(C(C1C(=O)OC(C#N)C2=CC(=CC=C2)OC3=CC=CC=C3)C=C(Br)Br)C
InChI: InChI=1S/C22H19Br2NO3/c1-22(2)17(12-19(23)24)20(22)21(26)28-18(13-25)14-7-6-10-16(11-14)27-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3/t17-,18+,20-/m0/s1

描述信息

Deltamethrin is a pyrethroid ester insecticide. Deltamethrin plays key role in controlling malaria vectors, and is used in the manufacture of long-lasting insecticidal mosquito nets. It is used as one of a battery of pyrethroid insecticides in control of malarial vectors, particularly Anopheles gambiae, and whilst being the most employed pyrethroid insecticide, can be used in conjunction with, or as an alternative to, permethrin, cypermethrin and other organophosphate-based insecticides, such as malathion and fenthion. Resistance to deltamethrin (and its counterparts) is now extremely widespread and threatens the success of worldwide vector control programmes. Deltamethrin products are among the most popular and widely used insecticides in the world[citation needed] and have become very popular with pest control operators and individuals in the United States. This material is a member of one of the safest classes of pesticides: synthetic pyrethroids. This pesticide is highly toxic to aquatic life, particularly fish, and therefore must be used with extreme caution around water. It is neurotoxic to humans and has been found in human breast milk. Since deltamethrin is a neurotoxin, it attacks the nervous system. Skin contact can lead to tingling or reddening of the skin local to the application. If taken in through the eyes or mouth, a common symptom is facial paraesthesia, which can feel like many different abnormal sensations, including burning, partial numbness, pins and needles, skin crawling, etc. There are no reports indicating that chronic intoxication from pyrethroid insecticides causes motor neuron damage or motor neuron disease. However, in 2011, a case report was published demonstrating pathologically proven motor neuron death in a Japanese woman after acute massive ingestion of pesticides containing pyrethroids and organochlorine. There are many uses for deltamethrin, ranging from agricultural uses to home pest control. Deltamethrin has been instrumental in preventing the spread of diseases carried by tick-infested prairie dogs, rodents and other burrowing animals[citation needed]. It is helpful in eliminating and preventing a wide variety of household pests, especially spiders, fleas, ticks, carpenter ants, carpenter bees, cockroaches and bedbugs. Deltamethrin is also one of the primary ingredients in ant chalk.
P - Antiparasitic products, insecticides and repellents > P03 - Ectoparasiticides, incl. scabicides, insecticides and repellents > P03B - Insecticides and repellents > P03BA - Pyrethrines
D010575 - Pesticides > D007306 - Insecticides > D011722 - Pyrethrins
D016573 - Agrochemicals
Same as: D07785

同义名列表

53 个代谢物同义名

(S)-Cyano(3-phenoxyphenyl)methyl (1R,3R)-3-(2,2-dibromoethenyl)-2,2-dimethylcyclopropane-1-carboxylic acid; (S)-Cyano(3-phenoxyphenyl)methyl (1R,3R)-3-(2,2-dibromoethenyl)-2,2-dimethylcyclopropane-1-carboxylate; (S)-alpha-Cyano-3-phenoxybenzyl (1R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylic acid; (S)-alpha-Cyano-3-phenoxybenzyl (1R,3R)-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylic acid; (S)-Cyano(3-phenoxyphenyl)methyl (1R,3R)-3-(2,2-dibromoethenyl)-2,2-dimethylcyclopropanecarboxylate; (S)-alpha-Cyano-3-phenoxybenzyl (1R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate; (S)-Α-cyano-3-phenoxybenzyl (1R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylic acid; (S)-a-Cyano-3-phenoxybenzyl (1R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylic acid; alpha-Cyano-3-phenoxybenzyl (1R,3R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate; (S)-Α-cyano-3-phenoxybenzyl (1R,3R)-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylic acid; (S)-alpha-Cyano-3-phenoxybenzyl (1R,3R)-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate; (S)-a-Cyano-3-phenoxybenzyl (1R,3R)-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylic acid; (S)-Α-cyano-3-phenoxybenzyl (1R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate; (S)-a-Cyano-3-phenoxybenzyl (1R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate; (S)-Α-cyano-3-phenoxybenzyl (1R,3R)-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate; (S)-a-Cyano-3-phenoxybenzyl (1R,3R)-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate; Decamethrin, (1S-(1alpha(r*),3alpha))-isomer; Decamethrin, (1S-(1alpha(s*),3alpha))-isomer; Decamethrin, (1R-(1alpha(r*),3alpha))-isomer; Decamethrin, (1R-(1alpha(r*),3beta))-isomer; Decamethrin, (1R-(1alpha(s*),3beta))-isomer; Cropro D-sect; Glossinex 200; Decis options; Deltamethrine; Decamethrine; Decis 2.5ulv; Deltamethrin; Decis 0.5ulv; Decis 1.5ulv; Esbecythrin; Deltashield; New musigie; Decamethrin; Dekametrin; Ballistic; Crackdown; Deltagran; Phagase 1; DeltaGard; K-Othrine; stricker; NRDC 161; Scalibor; K-Othrin; Difexon; Suspend; K-Obiol; Zorcis; Cislin; Decis; Butox; Deltamethrin



数据库引用编号

15 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 10 BCL2, BDNF, CAT, CYP1A1, GPX1, HPGDS, NFE2L2, TH, TLR4, TP53
Peripheral membrane protein 3 ACHE, CYP1A1, CYP1B1
Endosome membrane 1 TLR4
Endoplasmic reticulum membrane 3 BCL2, CYP1A1, CYP1B1
Nucleus 7 ACHE, BCL2, KDR, NFE2L2, PLCZ1, TH, TP53
cytosol 9 BCL2, CAT, GPX1, GSR, HPGDS, NFE2L2, PLCZ1, TH, TP53
dendrite 2 BDNF, TH
centrosome 2 NFE2L2, TP53
nucleoplasm 5 HPGDS, NFE2L2, PLCZ1, SCNN1G, TP53
RNA polymerase II transcription regulator complex 1 NFE2L2
Cell membrane 4 ACHE, KDR, TLR4, TNF
Cell projection, axon 1 TH
Multi-pass membrane protein 1 SCNN1G
Synapse 1 ACHE
cell junction 1 KDR
cell surface 3 ACHE, TLR4, TNF
Golgi apparatus 3 ACHE, KDR, NFE2L2
mitochondrial inner membrane 1 CYP1A1
neuromuscular junction 1 ACHE
neuronal cell body 1 TNF
smooth endoplasmic reticulum 1 TH
synaptic vesicle 2 BDNF, TH
Cytoplasm, cytosol 1 NFE2L2
endosome 1 KDR
plasma membrane 7 ACHE, BCHE, KDR, NFE2L2, SCNN1G, TLR4, TNF
terminal bouton 1 TH
Membrane 7 ACHE, BCL2, BDNF, CAT, CYP1B1, TLR4, TP53
apical plasma membrane 1 SCNN1G
axon 2 BDNF, TH
extracellular exosome 3 CAT, GSR, SCNN1G
endoplasmic reticulum 3 BCL2, KDR, TP53
extracellular space 6 ACHE, BCHE, BDNF, CXCL8, IL6, TNF
perinuclear region of cytoplasm 5 ACHE, BDNF, PLCZ1, TH, TLR4
mitochondrion 8 BCL2, CAT, CYP1A1, CYP1B1, GPX1, GSR, TH, TP53
protein-containing complex 3 BCL2, CAT, TP53
intracellular membrane-bounded organelle 4 CAT, CYP1A1, CYP1B1, HPGDS
Microsome membrane 2 CYP1A1, CYP1B1
pronucleus 1 PLCZ1
Single-pass type I membrane protein 1 TLR4
Secreted 5 ACHE, BCHE, BDNF, CXCL8, IL6
extracellular region 8 ACHE, BCHE, BDNF, CAT, CXCL8, IL6, KDR, TNF
cytoplasmic side of plasma membrane 1 TH
Mitochondrion outer membrane 1 BCL2
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 1 BCL2
[Isoform 2]: Secreted 1 KDR
Mitochondrion matrix 1 TP53
mitochondrial matrix 4 CAT, GPX1, GSR, TP53
Extracellular side 1 ACHE
anchoring junction 1 KDR
transcription regulator complex 1 TP53
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 1 TP53
Nucleus membrane 1 BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 1 BCL2
external side of plasma membrane 5 GSR, KDR, SCNN1G, TLR4, TNF
perikaryon 1 TH
cytoplasmic vesicle 1 TH
nucleolus 2 PLCZ1, TP53
Melanosome membrane 1 TH
Early endosome 2 KDR, TLR4
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
Apical cell membrane 1 SCNN1G
Cytoplasm, perinuclear region 2 PLCZ1, TH
Mitochondrion inner membrane 1 CYP1A1
Membrane raft 2 KDR, TNF
pore complex 1 BCL2
Cytoplasm, cytoskeleton 1 TP53
focal adhesion 1 CAT
Peroxisome 1 CAT
basement membrane 1 ACHE
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
Nucleus, PML body 1 TP53
PML body 1 TP53
Cell projection, ruffle 1 TLR4
ruffle 1 TLR4
receptor complex 2 KDR, TLR4
neuron projection 1 TH
chromatin 2 NFE2L2, TP53
mediator complex 1 NFE2L2
phagocytic cup 2 TLR4, TNF
blood microparticle 1 BCHE
Lipid-anchor, GPI-anchor 1 ACHE
site of double-strand break 1 TP53
sorting endosome 1 KDR
sodium channel complex 1 SCNN1G
side of membrane 1 ACHE
germ cell nucleus 1 TP53
replication fork 1 TP53
myelin sheath 1 BCL2
lipopolysaccharide receptor complex 1 TLR4
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 1 CAT
endoplasmic reticulum lumen 3 BCHE, BDNF, IL6
nuclear matrix 1 TP53
transcription repressor complex 1 TP53
nuclear envelope lumen 1 BCHE
[Isoform 1]: Nucleus 1 TP53
synaptic cleft 1 ACHE
protein-DNA complex 1 NFE2L2
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
catalase complex 1 CAT
sperm head 1 PLCZ1
interleukin-6 receptor complex 1 IL6
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle 1 TH
BAD-BCL-2 complex 1 BCL2
[Isoform H]: Cell membrane 1 ACHE
[Neurotrophic factor BDNF precursor form]: Secreted 1 BDNF
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Shenggan Wu, Xuehua An, Dou Wang, Chong Cao, Qiang Wang, Yanhua Wang. Co-exposure to deltamethrin and cyazofamid: variations in enzyme activity and gene transcription in the earthworm (Eisenia fetida). Environmental science and pollution research international. 2024 Apr; 31(20):29174-29184. doi: 10.1007/s11356-024-33146-8. [PMID: 38568309]
  • Tean Zaheer, Rao Zahid Abbas, Tauseef Ur Rehman, Muhammad Kasib Khan, Muhammad Imran Arshad. Novel insights regarding the safety and efficacy of pyrethroid-coated nanoparticles against Hyalomma ticks. Toxicology mechanisms and methods. 2024 Feb; 34(2):148-163. doi: 10.1080/15376516.2023.2263545. [PMID: 37749898]
  • Tarık Balkan, Adem Yağcı, Kenan Kara. Dissipation behaviors of deltamethrin, emamectin benzoate and hexythiazox in grape under field conditions. Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes. 2024; 59(3):123-129. doi: 10.1080/03601234.2024.2308487. [PMID: 38287657]
  • Rania Elbanna, Khaled A Osman, Maher S Salama. Biomarkers of oral subacute toxicity of deltamethrin in exposed male Albino rats. Toxicology and industrial health. 2023 Dec; 39(12):735-753. doi: 10.1177/07482337231209360. [PMID: 37877786]
  • Hao Wu, Jinwei Gao, Zhonggui Xie, Min Xie, Rui Song, Xiping Yuan, Yuanan Wu, Dongsheng Ou. Effect of chronic deltamethrin exposure on brain transcriptome and metabolome of juvenile crucian carp. Environmental toxicology. 2023 Nov; ?(?):. doi: 10.1002/tox.24022. [PMID: 38009670]
  • Fred A Ashu, Caroline Fouet, Marilene M Ambadiang, Véronique Penlap-Beng, Colince Kamdem. Vegetable oil-based surfactants are adjuvants that enhance the efficacy of neonicotinoid insecticides and can bias susceptibility testing in adult mosquitoes. PLoS neglected tropical diseases. 2023 Nov; 17(11):e0011737. doi: 10.1371/journal.pntd.0011737. [PMID: 37976311]
  • Yifan Wang, Xin Wang, Dylan J Brown, Mengru An, Rui-De Xue, Nannan Liu. Insecticide resistance: Status and potential mechanisms in Aedes aegypti. Pesticide biochemistry and physiology. 2023 Sep; 195(?):105577. doi: 10.1016/j.pestbp.2023.105577. [PMID: 37666603]
  • Mary Kefi, Vasileia Balabanidou, Chara Sarafoglou, Jason Charamis, Gareth Lycett, Hilary Ranson, Giorgos Gouridis, John Vontas. ABCH2 transporter mediates deltamethrin uptake and toxicity in the malaria vector Anopheles coluzzii. PLoS pathogens. 2023 Aug; 19(8):e1011226. doi: 10.1371/journal.ppat.1011226. [PMID: 37585450]
  • Chengyong Jia, Gaokun Qiu, Hao Wang, Shiyang Zhang, Jun An, Xu Cheng, Peiwen Li, Wending Li, Xin Zhang, Handong Yang, Kun Yang, Tao Jing, Huan Guo, Xiaomin Zhang, Tangchun Wu, Meian He. Lipid metabolic links between serum pyrethroid levels and the risk of incident type 2 diabetes: A mediation study in the prospective design. Journal of hazardous materials. 2023 Jul; 459(?):132082. doi: 10.1016/j.jhazmat.2023.132082. [PMID: 37473566]
  • Natalia Salmazo Pereira, Gustavo Vinícios Munhoz-Garcia, Vanessa Takeshita, Rodrigo Floriano Pimpinato, Valdemar Luiz Tornisielo, Kassio Ferreira Mendes. Egeria densa remediates the aquatic environment and reduces 14C-deltamethrin bioaccumulation in Danio rerio. Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes. 2023 Jul; ?(?):1-6. doi: 10.1080/03601234.2023.2232277. [PMID: 37430469]
  • Olukayode James Adelaja, Adedayo Olatubosun Oduola, Adeolu Taiwo Ande, Oyindamola Olajumoke Abiodun, Abisayo Ruth Adelaja. Toxicity of insecticidal plant oils on the larval and adult stages of a major malaria vector (Anopheles gambiae Giles 1920). Parasitology research. 2023 May; 122(5):1071-1078. doi: 10.1007/s00436-023-07806-6. [PMID: 36890296]
  • Xiaoya Sun, Wenbin Liu, Yuanyuan Peng, Lingfei Meng, Junyu Zhang, Yahan Pan, Deyu Wang, Junhao Zhu, Chengyan Wang, Chuncai Yan. Genome-wide analyses of Glutathione S-transferase gene family and expression profiling under deltamethrin exposure in non-biting midge Propsilocerus akamusi. Comparative biochemistry and physiology. Part D, Genomics & proteomics. 2023 Apr; 46(?):101081. doi: 10.1016/j.cbd.2023.101081. [PMID: 37150092]
  • Judith Kochmann, Melanie Laier, Sven Klimpel, Arne Wick, Uwe Kunkel, Jörg Oehlmann, Jonas Jourdan. Infection with acanthocephalans increases tolerance of Gammarus roeselii (Crustacea: Amphipoda) to pyrethroid insecticide deltamethrin. Environmental science and pollution research international. 2023 Mar; ?(?):. doi: 10.1007/s11356-023-26193-0. [PMID: 36897452]
  • Tarık Balkan, Kenan Kara. Dissipation kinetics of some pesticides applied singly or in mixtures in/on grape leaf. Pest management science. 2023 Mar; 79(3):1234-1242. doi: 10.1002/ps.7299. [PMID: 36416723]
  • Marziyeh Majidpour, Nariman Maroofpour, Mojtaba Ghane-Jahromi. Potential demographic impact of the insecticide mixture between thiacloprid and deltamethrin on the cotton aphid and two of its natural enemies. Bulletin of entomological research. 2023 Feb; 113(1):37-48. doi: 10.1017/s0007485322000281. [PMID: 35899961]
  • Antonio Gugliuzzo, Gaetano Giuliano, Roberto Rizzo, Giovanna Tropea Garzia, Antonio Biondi. Lethal and sublethal effects of synthetic and bioinsecticides toward the invasive ambrosia beetle Xylosandrus compactus. Pest management science. 2023 Jan; ?(?):. doi: 10.1002/ps.7365. [PMID: 36654525]
  • Xiping Yuan, Hao Wu, Jinwei Gao, Xiangchang Geng, Min Xie, Rui Song, Jiaomei Zheng, Yuanan Wu, Dongsheng Ou. Acute deltamethrin exposure induces oxidative stress, triggers endoplasmic reticulum stress, and impairs hypoxic resistance of crucian carp. Comparative biochemistry and physiology. Toxicology & pharmacology : CBP. 2023 Jan; 263(?):109508. doi: 10.1016/j.cbpc.2022.109508. [PMID: 36368507]
  • Alev Yüksel Aydar, Tuba Aydın, Alican Karaiz, Furkan Alabey, Anjineyulu Kothakota, António Raposo, Najla Abdullah Albaridi, R Pandiselvam. Effect of ultrasound assisted cleaning on pesticide removal and quality characteristics of Vitis vinifera leaves. Ultrasonics sonochemistry. 2023 Jan; 92(?):106279. doi: 10.1016/j.ultsonch.2022.106279. [PMID: 36580835]
  • Christopher C Hayes, Coby Schal. Behavioral interactions of bed bugs with long-lasting pyrethroid-treated bed nets: challenges for vector control. Parasites & vectors. 2022 Dec; 15(1):488. doi: 10.1186/s13071-022-05613-z. [PMID: 36572943]
  • Vadavanath Prabhakaran Vineetha, Hemla Naik Tejaswi, Kummari Suresh, Haridas Lekshmi, Kalasseril Girijan Sneha, Chakkalaparambil Gokulan Rakesh, Pillai Devika. Asparagus racemosus improves immune-related parameters in Nile tilapia (Oreochromis niloticus) and mitigates deltamethrin-induced toxicity. Fish & shellfish immunology. 2022 Nov; 130(?):283-293. doi: 10.1016/j.fsi.2022.09.028. [PMID: 36122635]
  • Clara Lago, Daniele Cornara, Serena Anna Minutillo, Aránzazu Moreno, Alberto Fereres. Feeding behaviour and mortality of Philaenus spumarius exposed to insecticides and their impact on Xylella fastidiosa transmission. Pest management science. 2022 Nov; 78(11):4841-4849. doi: 10.1002/ps.7105. [PMID: 35908181]
  • Saijie Song, Minghui Wan, Yi Luo, He Shen, Jian Shen. Carboxymethyl Chitosan-Modified Graphene Oxide as a Multifunctional Vector for Deltamethrin Delivery and pH-Responsive Controlled Release, Enhanced Leaf Affinity, and Improved Mosquito-Killing Activity. Langmuir : the ACS journal of surfaces and colloids. 2022 10; 38(40):12148-12156. doi: 10.1021/acs.langmuir.2c01669. [PMID: 36166331]
  • Yifan Wang, Mengru An, Kelly M Stevens, Nannan Liu. Insecticide Resistance in Alabama Populations of the Mosquito Aedes albopictus. Journal of medical entomology. 2022 09; 59(5):1678-1686. doi: 10.1093/jme/tjac085. [PMID: 35851609]
  • Anandha R Ravula, Suresh Yenugu. Effect of a mixture of pyrethroids at doses similar to human exposure through food in the Indian context. Journal of biochemical and molecular toxicology. 2022 Jun; ?(?):e23132. doi: 10.1002/jbt.23132. [PMID: 35678313]
  • Nan Zhang, Jiaping Wei, Heng Jiang, Huichen Ge, Yang Zheng, Xiangkun Meng, Kun Qian, Jianjun Wang. Knockdown or inhibition of arginine kinases enhances susceptibility of Tribolium castaneum to deltamethrin. Pesticide biochemistry and physiology. 2022 May; 183(?):105080. doi: 10.1016/j.pestbp.2022.105080. [PMID: 35430070]
  • Xin Xu, Nan Zhang, Xiangkun Meng, Heng Jiang, Huichen Ge, Yang Zheng, Kun Qian, Jianjun Wang. FOXO acts as a positive regulator of CncC and deltamethrin tolerance in the red flour beetle, Tribolium castaneum. Pest management science. 2022 May; 78(5):1938-1945. doi: 10.1002/ps.6811. [PMID: 35085425]
  • Poonam Singh, Pradeep Kumar, Veena Pande, Virendra Kumar, Ramesh C Dhiman. Untargeted metabolomics-based response analysis of temperature and insecticide exposure in Aedes aegypti. Scientific reports. 2022 02; 12(1):2066. doi: 10.1038/s41598-022-05630-z. [PMID: 35136077]
  • Ali Allam, Ahmed Abdeen, Hari Prasad Devkota, Samar S Ibrahim, Gehan Youssef, Ahmed Soliman, Mohamed M Abdel-Daim, Khalid J Alzahrani, Khaled Shoghy, Samah F Ibrahim, Mohamed Aboubakr. N-Acetylcysteine Alleviated the Deltamethrin-Induced Oxidative Cascade and Apoptosis in Liver and Kidney Tissues. International journal of environmental research and public health. 2022 01; 19(2):. doi: 10.3390/ijerph19020638. [PMID: 35055458]
  • Yibin Yang, Xia Zhu, Ying Huang, Hongyu Zhang, Yongtao Liu, Ning Xu, Guihong Fu, Xiaohui Ai. RNA-Seq and 16S rRNA Analysis Revealed the Effect of Deltamethrin on Channel Catfish in the Early Stage of Acute Exposure. Frontiers in immunology. 2022; 13(?):916100. doi: 10.3389/fimmu.2022.916100. [PMID: 35747138]
  • İsmail Azar, Nabi Alper Kumral. Validation of LC-MS/MS method for simultaneous determination of chlorpyrifos, deltamethrin, imidacloprid and some of their metabolites in maize silage. Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes. 2022; 57(2):125-132. doi: 10.1080/03601234.2022.2029275. [PMID: 35060839]
  • Jiao Shang, Yong-Sheng Yao, Lu-Lu Chen, Xiang-Zhen Zhu, Lin Niu, Xue-Ke Gao, Jun-Yu Luo, Ji-Chao Ji, Jin-Jie Cui. Sublethal Exposure to Deltamethrin Stimulates Reproduction and Alters Symbiotic Bacteria in Aphis gossypii. Journal of agricultural and food chemistry. 2021 Dec; 69(50):15097-15107. doi: 10.1021/acs.jafc.1c05070. [PMID: 34902254]
  • Tijana B Radovanović, Branka R Gavrilović, Tamara G Petrović, Svetlana G Despotović, Jelena P Gavrić, Ana Kijanović, Marko Mirč, Nataša Tomašević Kolarov, Caterina Faggio, Marko D Prokić. Impact of desiccation pre-exposure on deltamethrin-induced oxidative stress in Bombina variegata juveniles. Comparative biochemistry and physiology. Toxicology & pharmacology : CBP. 2021 Dec; 250(?):109191. doi: 10.1016/j.cbpc.2021.109191. [PMID: 34536572]
  • Shun Zhou, Jing Dong, Yongtao Liu, Qiuhong Yang, Ning Xu, Yibin Yang, Xiaohui Ai. Effects of acute deltamethrin exposure on kidney transcriptome and intestinal microbiota in goldfish (Carassius auratus). Ecotoxicology and environmental safety. 2021 Dec; 225(?):112716. doi: 10.1016/j.ecoenv.2021.112716. [PMID: 34478975]
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