naphthalene (BioDeep_00000697052)

Main id: BioDeep_00000003286

 

natural product


代谢物信息卡片


naphthalene

化学式: C10H8 (128.0626)
中文名称: 萘, 萘-1-13C, 萘-13C10
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC=C2C=CC=CC2=C1
InChI: InChI=1S/C10H8/c1-2-6-10-8-4-3-7-9(10)5-1/h1-8H

描述信息

An aromatic hydrocarbon comprising two fused benzene rings. It occurs in the essential oils of numerous plant species e.g. magnolia.

同义名列表

3 个代谢物同义名

naphthalene; Naphthalene; Naphthalene



数据库引用编号

21 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(1)

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)

229 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 14 AHR, AKT1, ALB, CAT, CYP2A6, EGFR, G6PD, HPGDS, NFE2L2, NQO1, PMP2, SCGB1A1, TP53, TUBB4B
Peripheral membrane protein 2 FDXR, G6PD
Endosome membrane 1 EGFR
Endoplasmic reticulum membrane 3 CYP1A2, CYP2A6, EGFR
Nucleus 9 AHR, AKT1, ALB, EGFR, NFE2L2, NQO1, PMP2, TP53, TUBB4B
cytosol 12 AHR, AKT1, ALB, CAT, G6PD, GPT, HPGDS, NFE2L2, NQO1, PMP2, TP53, TUBB4B
dendrite 1 NQO1
centrosome 3 ALB, NFE2L2, TP53
nucleoplasm 6 AHR, AKT1, CD2, HPGDS, NFE2L2, TP53
RNA polymerase II transcription regulator complex 1 NFE2L2
Cell membrane 3 AKT1, CD2, EGFR
lamellipodium 1 AKT1
ruffle membrane 1 EGFR
Early endosome membrane 1 EGFR
Synapse 1 NQO1
cell cortex 1 AKT1
cell junction 1 EGFR
cell surface 2 CD2, EGFR
glutamatergic synapse 2 AKT1, EGFR
Golgi apparatus 4 ALB, ATRN, CD2, NFE2L2
Golgi membrane 1 EGFR
mitochondrial inner membrane 1 FDXR
neuronal cell body 1 NQO1
postsynapse 1 AKT1
Cytoplasm, cytosol 3 G6PD, NFE2L2, NQO1
endosome 1 EGFR
plasma membrane 5 AKT1, ATRN, CD2, EGFR, NFE2L2
Membrane 7 AKT1, CAT, CYP2A6, EGFR, G6PD, NQO1, TP53
apical plasma membrane 1 EGFR
basolateral plasma membrane 1 EGFR
extracellular exosome 8 ALB, ATRN, CAT, G6PD, GPT, PMP2, SCGB1A1, TUBB4B
endoplasmic reticulum 2 ALB, TP53
extracellular space 4 ALB, ATRN, EGFR, SCGB1A1
perinuclear region of cytoplasm 1 EGFR
mitochondrion 3 CAT, FDXR, TP53
protein-containing complex 7 AHR, AKT1, ALB, CAT, CD2, EGFR, TP53
intracellular membrane-bounded organelle 5 CAT, CYP1A2, CYP2A6, G6PD, HPGDS
Microsome membrane 1 CYP1A2
Single-pass type I membrane protein 3 ATRN, CD2, EGFR
Secreted 2 ALB, SCGB1A1
extracellular region 5 ALB, CAT, CD2, SCGB1A1, TUBB4B
cytoplasmic side of plasma membrane 2 CD2, G6PD
[Isoform 2]: Secreted 1 ATRN
Mitochondrion matrix 1 TP53
mitochondrial matrix 3 CAT, FDXR, TP53
anchoring junction 1 ALB
transcription regulator complex 2 AHR, TP53
centriolar satellite 1 G6PD
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 1 TP53
nuclear membrane 1 EGFR
external side of plasma membrane 1 CD2
Extracellular vesicle 1 TUBB4B
microtubule cytoskeleton 2 AKT1, TUBB4B
nucleolus 1 TP53
cell-cell junction 2 AKT1, CD2
vesicle 1 AKT1
Mitochondrion inner membrane 1 FDXR
Membrane raft 1 EGFR
Cytoplasm, cytoskeleton 2 TP53, TUBB4B
focal adhesion 2 CAT, EGFR
microtubule 1 TUBB4B
spindle 1 AKT1
Peroxisome 1 CAT
intracellular vesicle 1 EGFR
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
Nucleus, PML body 1 TP53
PML body 1 TP53
Mitochondrion intermembrane space 1 AKT1
mitochondrial intermembrane space 1 AKT1
secretory granule 1 SCGB1A1
receptor complex 1 EGFR
ciliary basal body 2 AKT1, ALB
chromatin 3 AHR, NFE2L2, TP53
mediator complex 1 NFE2L2
mitotic spindle 1 TUBB4B
cytoskeleton 1 TUBB4B
centriole 1 ALB
spindle pole 1 ALB
blood microparticle 1 ALB
site of double-strand break 1 TP53
[Isoform 3]: Secreted 1 ATRN
intercellular bridge 1 TUBB4B
Cytoplasm, cytoskeleton, flagellum axoneme 1 TUBB4B
sperm flagellum 1 TUBB4B
nuclear envelope 1 SCGB1A1
axonemal microtubule 1 TUBB4B
aryl hydrocarbon receptor complex 1 AHR
germ cell nucleus 1 TP53
replication fork 1 TP53
myelin sheath 1 PMP2
basal plasma membrane 1 EGFR
synaptic membrane 1 EGFR
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 1 CAT
endoplasmic reticulum lumen 1 ALB
nuclear matrix 1 TP53
transcription repressor complex 1 TP53
platelet alpha granule lumen 1 ALB
azurophil granule lumen 1 TUBB4B
clathrin-coated endocytic vesicle membrane 1 EGFR
[Isoform 1]: Nucleus 1 TP53
cytoplasmic microtubule 1 CYP2A6
protein-DNA complex 1 NFE2L2
[Isoform 1]: Cell membrane 1 ATRN
multivesicular body, internal vesicle lumen 1 EGFR
Shc-EGFR complex 1 EGFR
catalase complex 1 CAT
nuclear aryl hydrocarbon receptor complex 1 AHR
cytosolic aryl hydrocarbon receptor complex 1 AHR
ciliary transition fiber 1 ALB


文献列表

  • Xuecheng Li, Changyi Li, Ziyu Chen, Jiahui Wang, Jie Sun, Jun Yao, Ke Chen, Zhenghui Li, Hengpeng Ye. High-resolution mass spectrometry-based non-targeted metabolomics reveals toxicity of naphthalene on tall fescue and intrinsic molecular mechanisms. Ecotoxicology and environmental safety. 2024 Feb; 271(?):115975. doi: 10.1016/j.ecoenv.2024.115975. [PMID: 38244514]
  • Q Q Wang, J Cui, C Zhang, M Yuan, H M Yu, X L Zhou. [Benchmark dose estimation of polycyclic aromatic hydrocarbons exposure base on Bayesian kernel machine regression]. Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases. 2023 Oct; 41(10):814-820. doi: 10.3760/cma.j.cn121094-20220907-00446. [PMID: 37935546]
  • Diane L Brinkman, Florita Flores, Heidi M Luter, F Mikaela Nordborg, Maxime Brooks, Thomas F Parkerton, Andrew P Negri. Sensitivity of the Indo-Pacific coral Acropora millepora to aromatic hydrocarbons. Environmental pollution (Barking, Essex : 1987). 2023 Sep; 332(?):121963. doi: 10.1016/j.envpol.2023.121963. [PMID: 37286027]
  • Dan Chen, Xinyu Lou, Junsong Bao, Ying Wang, Yuhao Fan, Qianhui Chen, Jun Jin, Limei Chen. Polychlorinated naphthalene concentrations and temporal trends in serum from the general Chinese adult population and effects of polychlorinated naphthalenes on thyroid function. Environmental research. 2023 Sep; 232(?):116309. doi: 10.1016/j.envres.2023.116309. [PMID: 37301498]
  • Yan Li, Ziquan Wang, Haixia Tian, Mallavarapu Megharaj, Hanzhong Jia, Wenxiang He. Using soil enzyme Vmax as an indicator to evaluate the ecotoxicity of lower-ring polycyclic aromatic hydrocarbons in soil: Evidence from fluorescein diacetate hydrolase kinetics. The Science of the total environment. 2023 May; 874(?):162521. doi: 10.1016/j.scitotenv.2023.162521. [PMID: 36868272]
  • Chao Wang, Wanjun Wang, Weiqiang Deng, Shu Zhang, Shaobin Shao, Meicheng Wen, Guiying Li, Taicheng An. Distribution characteristics, air-water exchange, ozone formation potential and health risk assessments of VOCs emitted from typical coking wastewater treatment process. The Science of the total environment. 2023 Mar; 862(?):160845. doi: 10.1016/j.scitotenv.2022.160845. [PMID: 36526193]
  • Susri Nayak, Lipika Patnaik. Histopathological and Biochemical Changes in the Gills of Anabas testudineus on Exposure to Polycyclic Aromatic Hydrocarbon Naphthalene. Applied biochemistry and biotechnology. 2022 Nov; ?(?):. doi: 10.1007/s12010-022-04214-x. [PMID: 36383310]
  • Kartik Dhar, Logeshwaran Panneerselvan, Suresh R Subashchandrabose, Kadiyala Venkateswarlu, Mallavarapu Megharaj. Anaerobic Degradation of Naphthalene and Pyrene by Sulfate-Reducing Cultures Enriched from Former Manufactured Gas Plant Soil. Microbial ecology. 2022 May; ?(?):. doi: 10.1007/s00248-022-02042-4. [PMID: 35610382]
  • Yunpeng Sun, Jun Chi, Lvjun Zhang, Siyuan Wang, Zhenhao Chen, Hao Zhang, Lingyi Kong, Jun Luo. Sarglaromatics A-E: A Class of Naphthalene-Like Architecture Fused Norlindenane Sesquiterpene Dimers from Sarcandra glabra. The Journal of organic chemistry. 2022 03; 87(6):4323-4332. doi: 10.1021/acs.joc.2c00014. [PMID: 35230123]
  • Zean Zhao, Jin Liu, Peihua Kuang, Jian Luo, Goverdhan Surineni, Xiaolin Cen, Ting Wu, Ying Cao, Pingzheng Zhou, Jianxin Pang, Qun Zhang, Jianjun Chen. Discovery of novel verinurad analogs as dual inhibitors of URAT1 and GLUT9 with improved Druggability for the treatment of hyperuricemia. European journal of medicinal chemistry. 2022 Feb; 229(?):114092. doi: 10.1016/j.ejmech.2021.114092. [PMID: 34998055]
  • Shijie Wang, Jingxi Jin, Chen Guo, Zhigang Li, Tong Xu, Xinyu Wen, Jicheng Hu, Ying Wang, Yongjie Wei, Jun Jin. Polychlorinated naphthalene concentrations in human serum caused by unintentional production and emissions, and potential effects of polychlorinated naphthalenes on thyroid hormones. The Science of the total environment. 2022 Feb; 806(Pt 1):150546. doi: 10.1016/j.scitotenv.2021.150546. [PMID: 34582862]
  • Jun Liu, Jinhua Wang, Shuang Si, Jinyi Xu, Peng Xue. Hydrogean Peroxide Inducible Acid-Activatable Prodrug for Targeted Cancer Treatment. ChemMedChem. 2021 10; 16(20):3231-3235. doi: 10.1002/cmdc.202100354. [PMID: 34288492]
  • Valentina Pirota, Enrico Lunghi, Alessandra Benassi, Emmanuele Crespan, Mauro Freccero, Filippo Doria. Selective Binding and Redox-Activity on Parallel G-Quadruplexes by Pegylated Naphthalene Diimide-Copper Complexes. Molecules (Basel, Switzerland). 2021 Aug; 26(16):. doi: 10.3390/molecules26165025. [PMID: 34443620]
  • Dhulfiqar Ali Abed, Sumi Lee, Xia Wen, Ahmed R Ali, Vaibhav Mangipudy, Lauren M Aleksunes, Longqin Hu. Optimization of 1,4-bis(arylsulfonamido)naphthalene-N,N'-diacetic acids as inhibitors of Keap1-Nrf2 protein-protein interaction to suppress neuroinflammation. Bioorganic & medicinal chemistry. 2021 08; 44(?):116300. doi: 10.1016/j.bmc.2021.116300. [PMID: 34252790]
  • Kirsten Sucker, Wolfgang Zschiesche, Mohammed Aziz, Tanja Drews, Thomas Hummel, Monika Raulf, Tobias Weiss, Daniel Bury, Dietmar Breuer, Silke Werner, Claudia Friedrich, Jürgen Bünger, Dirk Pallapies, Thomas Brüning. Naphthalene: irritative and inflammatory effects on the airways. International archives of occupational and environmental health. 2021 Jul; 94(5):889-899. doi: 10.1007/s00420-020-01636-0. [PMID: 33462664]
  • Jong Min An, Heejo Moon, Yejin Kim, Sangrim Kang, Youngseo Kim, Yuna Jung, Sungnam Park, Peter Verwilst, B Moon Kim, Jae Seung Kang, Dokyoung Kim. Visualizing mitochondria and mouse intestine with a fluorescent complex of a naphthalene-based dipolar dye and serum albumin. Journal of materials chemistry. B. 2020 09; 8(34):7642-7651. doi: 10.1039/d0tb01314e. [PMID: 32724984]
  • Muhammad Farooq Khan, Fahd A Nasr, Omar M Noman, Nouf Abdulaziz Alyhya, Iftikhar Ali, Mohamad Saoud, Robert Rennert, Mthandazo Dube, Wahid Hussain, Ivan R Green, Omer Ahmed M Basudan, Riaz Ullah, Shamsa Hilal Anazi, Hidayat Hussain. Cichorins D-F: Three New Compounds from Cichorium intybus and Their Biological Effects. Molecules (Basel, Switzerland). 2020 Sep; 25(18):. doi: 10.3390/molecules25184160. [PMID: 32932909]
  • Lulu Chai, Lu Yang, Yizhe Zhang, Yuhong Zhou, Feng Wang, Zhonghua Wu. Antagonism or synergism? Responses of Hydrocharis dubia (Bl.) Backer to linear alkylbenzene sulfonate, naphthalene and their joint exposure. Ecotoxicology and environmental safety. 2020 Sep; 200(?):110747. doi: 10.1016/j.ecoenv.2020.110747. [PMID: 32460052]
  • Ahmed Alalaiwe, Yin-Ku Lin, Chih-Hung Lin, Pei-Wen Wang, Jie-Yu Lin, Jia-You Fang. The absorption of polycyclic aromatic hydrocarbons into the skin to elicit cutaneous inflammation: The establishment of structure-permeation and in silico-in vitro-in vivo relationships. Chemosphere. 2020 Sep; 255(?):126955. doi: 10.1016/j.chemosphere.2020.126955. [PMID: 32416390]
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  • Brendan T Freitas, Ian A Durie, Jackelyn Murray, Jaron E Longo, Holden C Miller, David Crich, Robert Jeff Hogan, Ralph A Tripp, Scott D Pegan. Characterization and Noncovalent Inhibition of the Deubiquitinase and deISGylase Activity of SARS-CoV-2 Papain-Like Protease. ACS infectious diseases. 2020 08; 6(8):2099-2109. doi: 10.1021/acsinfecdis.0c00168. [PMID: 32428392]
  • Zi-Jian Chen, Xi-Xia Liu, Zhi-Li Xiao, Hui-Jun Fu, Yu-Ping Huang, Shu-Yi Huang, Yu-Dong Shen, Fan He, Xing-Xing Yang, Bruce Hammock, Zhen-Lin Xu. Production of a specific monoclonal antibody for 1-naphthol based on novel hapten strategy and development of an easy-to-use ELISA in urine samples. Ecotoxicology and environmental safety. 2020 Jun; 196(?):110533. doi: 10.1016/j.ecoenv.2020.110533. [PMID: 32247241]
  • Stefano Bonaglia, Elias Broman, Björn Brindefalk, Erika Hedlund, Tomas Hjorth, Carl Rolff, Francisco J A Nascimento, Klas Udekwu, Jonas S Gunnarsson. Activated carbon stimulates microbial diversity and PAH biodegradation under anaerobic conditions in oil-polluted sediments. Chemosphere. 2020 Jun; 248(?):126023. doi: 10.1016/j.chemosphere.2020.126023. [PMID: 32007777]
  • Masoud Khosravipour, Hadis Khosravipour. The association between urinary metabolites of polycyclic aromatic hydrocarbons and diabetes: A systematic review and meta-analysis study. Chemosphere. 2020 May; 247(?):125680. doi: 10.1016/j.chemosphere.2019.125680. [PMID: 32069705]
  • Jong Cheol Shon, Young Ji Noh, Young Sang Kwon, Jong-Hwan Kim, Zhexue Wu, Jong-Su Seo. The impact of phenanthrene on membrane phospholipids and its biodegradation by Sphingopyxis soli. Ecotoxicology and environmental safety. 2020 Apr; 192(?):110254. doi: 10.1016/j.ecoenv.2020.110254. [PMID: 32007746]
  • Kenneth W Fent, Christine Toennis, Deborah Sammons, Shirley Robertson, Stephen Bertke, Antonia M Calafat, Joachim D Pleil, M Ariel Geer Wallace, Steve Kerber, Denise Smith, Gavin P Horn. Firefighters' absorption of PAHs and VOCs during controlled residential fires by job assignment and fire attack tactic. Journal of exposure science & environmental epidemiology. 2020 03; 30(2):338-349. doi: 10.1038/s41370-019-0145-2. [PMID: 31175324]
  • Peng Zhang, Peng Huang, Hongwen Sun, Jianli Ma, Beixing Li. The structure of agricultural microplastics (PT, PU and UF) and their sorption capacities for PAHs and PHE derivates under various salinity and oxidation treatments. Environmental pollution (Barking, Essex : 1987). 2020 Feb; 257(?):113525. doi: 10.1016/j.envpol.2019.113525. [PMID: 31761592]
  • Dan Ji, Zhen Mao, Jian He, Sihan Peng, Hongyu Wen. Characterization and genomic function analysis of phenanthrene-degrading bacterium Pseudomonas sp. Lphe-2. Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering. 2020; 55(5):549-562. doi: 10.1080/10934529.2019.1711352. [PMID: 31913782]
  • Amrita Singh, Surendra H Bodakhe. Resveratrol delay the cataract formation against naphthalene-induced experimental cataract in the albino rats. Journal of biochemical and molecular toxicology. 2020 Jan; 34(1):e22420. doi: 10.1002/jbt.22420. [PMID: 31746523]
  • Shimin Wu, Guangyi Gong, Kai Yan, Yaqing Sun, Limin Zhang. Polycyclic aromatic hydrocarbons in edible oils and fatty foods: Occurrence, formation, analysis, change and control. Advances in food and nutrition research. 2020; 93(?):59-112. doi: 10.1016/bs.afnr.2020.02.001. [PMID: 32711866]
  • Nataliia Kovalchuk, Qing-Yu Zhang, Jacklyn Kelty, Laura Van Winkle, Xinxin Ding. Toxicokinetic Interaction between Hepatic Disposition and Pulmonary Bioactivation of Inhaled Naphthalene Studied Using Cyp2abfgs-Null and CYP2A13/2F1-Humanized Mice with Deficient Hepatic Cytochrome P450 Activity. Drug metabolism and disposition: the biological fate of chemicals. 2019 12; 47(12):1469-1478. doi: 10.1124/dmd.119.088930. [PMID: 31594800]
  • Tobie D Lee, Olivia W Lee, Kyle R Brimacombe, Lu Chen, Rajarshi Guha, Sabrina Lusvarghi, Bethilehem G Tebase, Carleen Klumpp-Thomas, Robert W Robey, Suresh V Ambudkar, Min Shen, Michael M Gottesman, Matthew D Hall. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Molecular pharmacology. 2019 11; 96(5):629-640. doi: 10.1124/mol.119.115964. [PMID: 31515284]
  • Giselle Torres-Farradá, Ana M Manzano-León, François Rineau, Miguel Ramos Leal, Sofie Thijs, Inge Jambon, Jenny Put, Jan Czech, Gilda Guerra Rivera, Robert Carleer, Jaco Vangronsveld. Biodegradation of polycyclic aromatic hydrocarbons by native Ganoderma sp. strains: identification of metabolites and proposed degradation pathways. Applied microbiology and biotechnology. 2019 Sep; 103(17):7203-7215. doi: 10.1007/s00253-019-09968-9. [PMID: 31256229]
  • Xiang-Yin Lou, Peng-Ran Wu, Ying Guo. Urinary metabolites of polycyclic aromatic hydrocarbons in pregnant women and their association with a biomarker of oxidative stress. Environmental science and pollution research international. 2019 Sep; 26(26):27281-27290. doi: 10.1007/s11356-019-05855-y. [PMID: 31325095]
  • Sarah A Carratt, Nataliia Kovalchuk, Xinxin Ding, Laura S Van Winkle. Metabolism and Lung Toxicity of Inhaled Naphthalene: Effects of Postnatal Age and Sex. Toxicological sciences : an official journal of the Society of Toxicology. 2019 08; 170(2):536-548. doi: 10.1093/toxsci/kfz100. [PMID: 31020322]
  • Katrin Klotz, Tobias Weiß, Melanie Zobel, Daniel Bury, Dietmar Breuer, Silke Werner, Kirsten Sucker, Wolfgang Zschiesche, Thomas Göen, Thomas Brüning, Hans Drexler. Validity of different biomonitoring parameters in human urine for the assessment of occupational exposure to naphthalene. Archives of toxicology. 2019 08; 93(8):2185-2195. doi: 10.1007/s00204-019-02468-9. [PMID: 31222524]
  • Lalit Goswami, Natarajan Arul Manikandan, Jebathomas Christon Ringle Taube, Kannan Pakshirajan, Gopal Pugazhenthi. Novel waste-derived biochar from biomass gasification effluent: preparation, characterization, cost estimation, and application in polycyclic aromatic hydrocarbon biodegradation and lipid accumulation by Rhodococcus opacus. Environmental science and pollution research international. 2019 Aug; 26(24):25154-25166. doi: 10.1007/s11356-019-05677-y. [PMID: 31256397]
  • Yasuhiro Terasaki, Tetsuya Suzuki, Kozue Tonaki, Mika Terasaki, Naomi Kuwahara, Jumi Ohsiro, Masumi Iketani, Mayumi Takahashi, Makoto Hamanoue, Yusuke Kajimoto, Seisuke Hattori, Hideo Kawaguchi, Akira Shimizu, Ikuroh Ohsawa. Molecular hydrogen attenuates gefitinib-induced exacerbation of naphthalene-evoked acute lung injury through a reduction in oxidative stress and inflammation. Laboratory investigation; a journal of technical methods and pathology. 2019 06; 99(6):793-806. doi: 10.1038/s41374-019-0187-z. [PMID: 30710119]
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  • Jisheng Nie, Jinyu Li, Lin Cheng, Yanning Li, Yunjun Deng, Zhiwei Yan, Lei Duan, Qiao Niu, Frederica Perera, Deliang Tang. Maternal urinary 2-hydroxynaphthalene and birth outcomes in Taiyuan, China. Environmental health : a global access science source. 2018 12; 17(1):91. doi: 10.1186/s12940-018-0436-4. [PMID: 30572877]
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  • Shujun Dong, Xiaomin Li, Peilong Wang, Xiaoou Su. Polychlorinated naphthalene concentrations and distribution in feed raw materials. Chemosphere. 2018 Nov; 211(?):912-917. doi: 10.1016/j.chemosphere.2018.08.037. [PMID: 30223339]
  • Roland C Wilhelm, Buck T Hanson, Subhash Chandra, Eugene Madsen. Community dynamics and functional characteristics of naphthalene-degrading populations in contaminated surface sediments and hypoxic/anoxic groundwater. Environmental microbiology. 2018 10; 20(10):3543-3559. doi: 10.1111/1462-2920.14309. [PMID: 30051558]
  • Mohammad Hoseini, Ramin Nabizadeh, Juana Maria Delgado-Saborit, Ata Rafiee, Kamyar Yaghmaeian, Saeid Parmy, Sasan Faridi, Mohammad Sadegh Hassanvand, Masud Yunesian, Kazem Naddafi. Environmental and lifestyle factors affecting exposure to polycyclic aromatic hydrocarbons in the general population in a Middle Eastern area. Environmental pollution (Barking, Essex : 1987). 2018 Sep; 240(?):781-792. doi: 10.1016/j.envpol.2018.04.077. [PMID: 29778814]
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  • Hongshan Chen, Lianxi Sheng, Zhiyuan Gong, Shaoguo Ru, Hongfeng Bian. Investigation of the molecular mechanisms of hepatic injury upon naphthalene exposure in zebrafish (Danio rerio). Ecotoxicology (London, England). 2018 Aug; 27(6):650-660. doi: 10.1007/s10646-018-1943-3. [PMID: 29748829]
  • Xiaomin Zhu, Yinshan Wang, Yuecan Zhang, Baoliang Chen. Reduced bioavailability and plant uptake of polycyclic aromatic hydrocarbons from soil slurry amended with biochars pyrolyzed under various temperatures. Environmental science and pollution research international. 2018 Jun; 25(17):16991-17001. doi: 10.1007/s11356-018-1874-9. [PMID: 29627960]
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