Acetochlor (BioDeep_00000001136)

 

Secondary id: BioDeep_00001871708

human metabolite blood metabolite


代谢物信息卡片


2-chloranyl-N-(ethoxymethyl)-N-(2-ethyl-6-methyl-phenyl)ethanamide

化学式: C14H20ClNO2 (269.1182)
中文名称: 乙草胺
谱图信息: 最多检出来源 Homo sapiens(blood) 21.38%

分子结构信息

SMILES: CCC1=CC=CC(=C1N(COCC)C(=O)CCl)C
InChI: InChI=1S/C14H20ClNO2/c1-4-12-8-6-7-11(3)14(12)16(10-18-5-2)13(17)9-15/h6-8H,4-5,9-10H2,1-3H3

描述信息

CONFIDENCE standard compound; INTERNAL_ID 1174; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9499; ORIGINAL_PRECURSOR_SCAN_NO 9495
CONFIDENCE standard compound; INTERNAL_ID 1174; DATASET 20200303_ENTACT_RP_MIX503; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9451; ORIGINAL_PRECURSOR_SCAN_NO 9447
CONFIDENCE standard compound; INTERNAL_ID 1174; DATASET 20200303_ENTACT_RP_MIX503; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9445; ORIGINAL_PRECURSOR_SCAN_NO 9442
CONFIDENCE standard compound; INTERNAL_ID 1174; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9479; ORIGINAL_PRECURSOR_SCAN_NO 9474
CONFIDENCE standard compound; INTERNAL_ID 1174; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9585; ORIGINAL_PRECURSOR_SCAN_NO 9582
CONFIDENCE standard compound; INTERNAL_ID 1174; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9473; ORIGINAL_PRECURSOR_SCAN_NO 9469
CONFIDENCE standard compound; EAWAG_UCHEM_ID 104
CONFIDENCE standard compound; INTERNAL_ID 8482
CONFIDENCE standard compound; INTERNAL_ID 3221
D010575 - Pesticides > D006540 - Herbicides
D016573 - Agrochemicals

同义名列表

8 个代谢物同义名

2-chloranyl-N-(ethoxymethyl)-N-(2-ethyl-6-methyl-phenyl)ethanamide; 2-chloro-N-(ethoxymethyl)-N-(2-ethyl-6-methylphenyl)acetamide; 2-Chloro-2-methyl-6-ethyl-N-ethoxymethylacetanilide; 2-Chloro-N-(ethoxymethyl)-6-ethyl-O-acetotoluidide; 2-Chloro-N-(ethoxymethyl)-6-ethylacet-O-toluidide; Acetochlore; acetochlor; Acetochlor



数据库引用编号

41 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, CASP3, CASP9, CAT, CYP3A4, ESR1, HPGDS, PRKAA2, SLC5A5, SREBF1
Peripheral membrane protein 3 ACHE, CYP1B1, ESR1
Endoplasmic reticulum membrane 5 BCL2, CYP1A2, CYP1B1, CYP3A4, SREBF1
Nucleus 11 ACHE, BCL2, CASP3, CASP9, ESR1, PARP1, PRKAA2, SLC5A5, SREBF1, THRA, THRB
cytosol 10 BCL2, CASP3, CASP9, CAT, ESR1, HPGDS, PARP1, PRKAA2, SREBF1, THRA
dendrite 1 PRKAA2
nuclear body 2 PARP1, THRB
nucleoplasm 8 CASP3, ESR1, HPGDS, PARP1, PRKAA2, SREBF1, THRA, THRB
RNA polymerase II transcription regulator complex 2 THRA, THRB
Cell membrane 5 ACHE, ESR1, SLC38A3, SLC38A5, SLC5A5
Cytoplasmic side 1 ESR1
Multi-pass membrane protein 4 SLC38A3, SLC38A5, SLC5A5, SREBF1
Golgi apparatus membrane 1 SREBF1
Synapse 1 ACHE
cell surface 1 ACHE
glutamatergic synapse 1 CASP3
Golgi apparatus 3 ACHE, ESR1, PRKAA2
Golgi membrane 1 SREBF1
neuromuscular junction 1 ACHE
neuronal cell body 2 CASP3, PRKAA2
Cytoplasm, cytosol 1 PARP1
Lysosome 1 SGSH
plasma membrane 5 ACHE, ESR1, SLC38A3, SLC38A5, SLC5A5
Membrane 11 ACHE, BCL2, CAT, CYP1B1, CYP3A4, ESR1, PARP1, PRKAA2, SLC38A3, SLC38A5, SLC5A5
apical plasma membrane 1 SLC38A3
axon 1 PRKAA2
basolateral plasma membrane 1 SLC38A3
extracellular exosome 3 CAT, SGSH, SLC5A5
endoplasmic reticulum 2 BCL2, SREBF1
extracellular space 2 ACHE, BMP15
lysosomal lumen 1 SGSH
perinuclear region of cytoplasm 1 ACHE
mitochondrion 5 BCL2, CASP9, CAT, CYP1B1, PARP1
protein-containing complex 6 BCL2, CASP9, CAT, ESR1, PARP1, SREBF1
intracellular membrane-bounded organelle 5 CAT, CYP1A2, CYP1B1, CYP3A4, HPGDS
Microsome membrane 3 CYP1A2, CYP1B1, CYP3A4
postsynaptic density 1 CASP3
Secreted 2 ACHE, BMP15
extracellular region 3 ACHE, BMP15, CAT
Mitochondrion outer membrane 1 BCL2
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 1 BCL2
mitochondrial matrix 1 CAT
Extracellular side 1 ACHE
transcription regulator complex 2 ESR1, PARP1
Nucleus membrane 1 BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 1 BCL2
Extracellular vesicle 1 SLC5A5
nucleolus 1 PARP1
pore complex 1 BCL2
focal adhesion 1 CAT
Peroxisome 1 CAT
basement membrane 1 ACHE
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
nuclear speck 1 PRKAA2
chromatin 5 ESR1, PARP1, SREBF1, THRA, THRB
Chromosome 1 PARP1
Nucleus, nucleolus 1 PARP1
nuclear replication fork 1 PARP1
chromosome, telomeric region 1 PARP1
Basolateral cell membrane 1 SLC38A3
Lipid-anchor, GPI-anchor 1 ACHE
site of double-strand break 1 PARP1
nuclear envelope 2 PARP1, SREBF1
Cytoplasmic vesicle membrane 1 SREBF1
cytoplasmic stress granule 1 PRKAA2
euchromatin 1 ESR1
side of membrane 1 ACHE
myelin sheath 1 BCL2
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 1 CAT
endoplasmic reticulum lumen 1 BMP15
ER to Golgi transport vesicle membrane 1 SREBF1
apoptosome 1 CASP9
[Isoform 1]: Nucleus 1 ESR1
synaptic cleft 1 ACHE
protein-DNA complex 1 PARP1
death-inducing signaling complex 1 CASP3
nucleotide-activated protein kinase complex 1 PRKAA2
Cytoplasmic vesicle, COPII-coated vesicle membrane 1 SREBF1
site of DNA damage 1 PARP1
catalase complex 1 CAT
[Poly [ADP-ribose] polymerase 1, processed N-terminus]: Chromosome 1 PARP1
[Poly [ADP-ribose] polymerase 1, processed C-terminus]: Cytoplasm 1 PARP1
BAD-BCL-2 complex 1 BCL2
[Isoform Alpha-2]: Cytoplasm 1 THRA
[Isoform H]: Cell membrane 1 ACHE
[Sterol regulatory element-binding protein 1]: Endoplasmic reticulum membrane 1 SREBF1
[Processed sterol regulatory element-binding protein 1]: Nucleus 1 SREBF1
[Isoform SREBP-1aDelta]: Nucleus 1 SREBF1
[Isoform SREBP-1cDelta]: Nucleus 1 SREBF1
caspase complex 1 CASP9


文献列表

  • Yuzhao Hu, Shuai Wu, Changcai Wu, Zhimin Wei, Jun Ning, Dongmei She. Risk assessment of airborne agricultural pesticide exposure in humans in rural China. Environmental geochemistry and health. 2024 Mar; 46(4):117. doi: 10.1007/s10653-024-01882-y. [PMID: 38478119]
  • Xin Wang, Bo Peng, Cheng Zhang, Mengqi Wu, Wenping Xu, Jiagao Cheng, Liming Tao, Zhong Li, Yang Zhang. Hepatic effects of acetochlor chiral isomers in zebrafish and L02 cells. The Science of the total environment. 2024 Feb; 913(?):169781. doi: 10.1016/j.scitotenv.2023.169781. [PMID: 38176547]
  • Wei Wang, Pingping Wang, Chi Wu, Lan Zhang, Liangang Mao, Lizhen Zhu, Hongyun Jiang, Yongquan Zheng, Xingang Liu. Adsorption of acetochlor-contaminated water systems using novel P-doped biochar: Effects, application, and mechanism. Chemosphere. 2024 Feb; 350(?):141027. doi: 10.1016/j.chemosphere.2023.141027. [PMID: 38142880]
  • Jingjing Ma, Chunhua Lu, Luyao Bai, Jingyu Zhang, Yuemao Shen. Phytotoxic phenols from the needles of Cedrus deodara. Phytochemistry. 2024 Jan; 219(?):113977. doi: 10.1016/j.phytochem.2024.113977. [PMID: 38215813]
  • Xin Wang, Fan Chen, Jian Lu, Mengqi Wu, Jiagao Cheng, Wenping Xu, Zhong Li, Yang Zhang. Developmental and cardiovascular toxicities of acetochlor and its chiral isomers in zebrafish embryos through oxidative stress. The Science of the total environment. 2023 Jul; 896(?):165296. doi: 10.1016/j.scitotenv.2023.165296. [PMID: 37406693]
  • Wei-Guo Wang, Mu-Yao Li, Lin Diao, Cheng Zhang, Li-Ming Tao, Wei-Xing Zhou, Wen-Ping Xu, Yang Zhang. The health risk of acetochlor metabolite CMEPA is associated with lipid accumulation induced liver injury. Environmental pollution (Barking, Essex : 1987). 2023 May; ?(?):121857. doi: 10.1016/j.envpol.2023.121857. [PMID: 37245791]
  • Khair Un Nisa, Attiq Ur Rehman Kakar, Muhammad Asghar, Sami Ullah, Naqeeb Ullah, Niamat Ullah, Arif Shah. Flow injection chemiluminescence determination of acetochlor and cartap-HCl in freshwater samples employing acidic KMnO4 -Rhodamine-B reaction system. Luminescence : the journal of biological and chemical luminescence. 2023 Mar; ?(?):. doi: 10.1002/bio.4493. [PMID: 36967642]
  • Wei Wang, Yanli Man, Jun Xie, Zhi Zhang, Pingping Wang, Xingang Liu. Occurrence and risk assessment of three chloroamide herbicides in water and soil environment in northeastern, eastern and southern China. Environmental research. 2023 02; 219(?):115104. doi: 10.1016/j.envres.2022.115104. [PMID: 36565672]
  • Shenggan Wu, Xinzong Zhou, Weiwei Qin, Xuehua An, Feidi Wang, Lu Lv, Tao Tang, Xinju Liu, Yueping He. Prostaglandin Metabolome Profiles in Zebrafish (Danio rerio) Exposed to Acetochlor and Butachlor. International journal of molecular sciences. 2023 Feb; 24(4):. doi: 10.3390/ijms24043488. [PMID: 36834899]
  • P V Silva, B F Schedenffeldt, E S Medeiros, D Z Molina, M K Pagliarini, P A V Salmazo, M Mauad, P A Monquero, F C Munaro, L Y Shirota, G P Silva, M S Monteiro, R D C Dias, R P N Borges. Selectivity of herbicides used in corn on Crotalaria ochroleuca G. Don. Brazilian journal of biology = Revista brasleira de biologia. 2023; 83(?):e277798. doi: 10.1590/1519-6984.277798. [PMID: 38126645]
  • Bartosz Zieliński, Piotr Miądlicki, Jacek Przepiórski. Development of activated carbon for removal of pesticides from water: case study. Scientific reports. 2022 12; 12(1):20869. doi: 10.1038/s41598-022-25247-6. [PMID: 36460673]
  • Qingxiang Lu, Zhen Shen, Kaiyuan Zheng, Qing Chang, Jiaying Xue, Xiangwei Wu. Estimating the bioavailability of acetochlor to wheat using in situ pore water and passive sampling. The Science of the total environment. 2022 Aug; 833(?):155239. doi: 10.1016/j.scitotenv.2022.155239. [PMID: 35421494]
  • M Y Chen, H Zhang, Z L Huo, H Chen, J R Dou, B L Zhu, F Zhang. [Determination of acetochlor and its metabolites in urine using liquid chromatography-tandem mass spectrometry]. Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases. 2022 May; 40(5):373-377. doi: 10.3760/cma.j.cn121094-20210917-00464. [PMID: 35680583]
  • Xia Zhao, Xu Shi, Qingqing Liu, Xiaojing Li. Tea polyphenols alleviates acetochlor-induced apoptosis and necroptosis via ROS/MAPK/NF-κB signaling in Ctenopharyngodon idellus kidney cells. Aquatic toxicology (Amsterdam, Netherlands). 2022 May; 246(?):106153. doi: 10.1016/j.aquatox.2022.106153. [PMID: 35381412]
  • Yalei Liu, Kuan Fang, Xiaolian Zhang, Tong Liu, Xiuguo Wang. Enantioselective toxicity and oxidative stress effects of acetochlor on earthworms (Eisenia fetida) by mediating the signaling pathway. The Science of the total environment. 2021 Apr; 766(?):142630. doi: 10.1016/j.scitotenv.2020.142630. [PMID: 33069465]
  • Ying Feng, Xuemei Zhong, Yuhan Yao, Zhensheng Shi, Fenghai Li, Hongwei Wang, Xiangling Lv, Wanli Du, Min Zhu, Hu Yang, Dexuan Meng. Photosynthetic and physiological responses to acetochlor in paired near-isogenic lines of waxy maize (Zea mays L.). Environmental science and pollution research international. 2021 Apr; 28(15):19298-19309. doi: 10.1007/s11356-020-12043-w. [PMID: 33394398]
  • Yingying Zhang, Wen Xue, Runze Long, Hui Yang, Wenzhi Wei. Acetochlor affects zebrafish ovarian development by producing estrogen effects and inducing oxidative stress. Environmental science and pollution research international. 2020 Aug; 27(22):27688-27696. doi: 10.1007/s11356-020-09050-2. [PMID: 32394252]
  • Yiming Chang, Liangang Mao, Lan Zhang, Yanning Zhang, Hongyun Jiang. Combined toxicity of imidacloprid, acetochlor, and tebuconazole to zebrafish (Danio rerio): acute toxicity and hepatotoxicity assessment. Environmental science and pollution research international. 2020 Apr; 27(10):10286-10295. doi: 10.1007/s11356-020-07653-3. [PMID: 31933089]
  • Chao Ju, Hongchao Zhang, Ruilin Wu, Suxia Dong, Shijie Yao, Feiyan Wang, Duantao Cao, Shiji Xu, Hua Fang, Yunlong Yu. Upward translocation of acetochlor and atrazine in wheat plants depends on their distribution in roots. The Science of the total environment. 2020 Feb; 703(?):135636. doi: 10.1016/j.scitotenv.2019.135636. [PMID: 31771841]
  • Xiang Ning Su, Jing Jing Zhang, Jin Tong Liu, Nan Zhang, Li Ya Ma, Feng Fan Lu, Zhao Jie Chen, Zhan Shi, Wen Jing Si, Chang Liu, Hong Yang. Biodegrading Two Pesticide Residues in Paddy Plants and the Environment by a Genetically Engineered Approach. Journal of agricultural and food chemistry. 2019 May; 67(17):4947-4957. doi: 10.1021/acs.jafc.8b07251. [PMID: 30994343]
  • Jingqian Xie, Ming Chu, Lu Zhao, Kai Liu, Weiping Liu. Enantiomeric impacts of two amide chiral herbicides on Echinochloa crus-galli physiology and gene transcription. The Science of the total environment. 2019 Mar; 656(?):1365-1372. doi: 10.1016/j.scitotenv.2018.11.355. [PMID: 30625665]
  • Qian Yu, Ping Zhang, Yuhan He, Zhifeng Xu, Xiulong He, Yuan Hu, Hongjun Zhang, Lin He. Dissipation Dynamics and Residue of Four Herbicides in Paddy Fields Using HPLC-MS/MS and GC-MS. International journal of environmental research and public health. 2019 01; 16(2):. doi: 10.3390/ijerph16020236. [PMID: 30650669]
  • Yao Li, Xingang Liu, Xiaohu Wu, Fengshou Dong, Jun Xu, Xinglu Pan, Yongquan Zheng. Effects of biochars on the fate of acetochlor in soil and on its uptake in maize seedling. Environmental pollution (Barking, Essex : 1987). 2018 Oct; 241(?):710-719. doi: 10.1016/j.envpol.2018.05.079. [PMID: 29906765]
  • Guiling Yang, Chen Chen, Yijun Yu, Huiyu Zhao, Wen Wang, Yanhua Wang, Leiming Cai, Yueping He, Xinquan Wang. Combined effects of four pesticides and heavy metal chromium (Ⅵ) on the earthworm using avoidance behavior as an endpoint. Ecotoxicology and environmental safety. 2018 Aug; 157(?):191-200. doi: 10.1016/j.ecoenv.2018.03.067. [PMID: 29621711]
  • Nathalie Bonvallot, Cécile Canlet, Florence Blas-Y-Estrada, Roselyne Gautier, Marie Tremblay-Franco, Sylvie Chevolleau, Sylvaine Cordier, Jean-Pierre Cravedi. Metabolome disruption of pregnant rats and their offspring resulting from repeated exposure to a pesticide mixture representative of environmental contamination in Brittany. PloS one. 2018; 13(6):e0198448. doi: 10.1371/journal.pone.0198448. [PMID: 29924815]
  • Yu-hui Chen, Hong-bo Xi, Dong Yu, Yue-xi Zhou, Xue-min Chen, Xiao-yong Fu. [The Study on the Characteristics of Organic Pollution in Typical Herbicide Plant Wastewater]. Guang pu xue yu guang pu fen xi = Guang pu. 2015 Dec; 35(12):3444-9. doi: . [PMID: 26964227]
  • Ruiyu Jiang, Mingqing Wang, Jianliang Xue, Ning Xu, Guihua Hou, Wubing Zhang. Cytotoxicity of sulfurous acid on cell membrane and bioactivity of Nitrosomonas europaea. Chemosphere. 2015 Jan; 119(?):896-901. doi: 10.1016/j.chemosphere.2014.08.040. [PMID: 25240954]
  • Wei Tan, Ting Liang, Qingliang Li, Yuanpeng Du, Heng Zhai. The phenotype of grape leaves caused by acetochlor or fluoroglycofen, and effects of latter herbicide on grape leaves. Pesticide biochemistry and physiology. 2014 Sep; 114(?):102-7. doi: 10.1016/j.pestbp.2014.06.007. [PMID: 25175657]
  • Cécile Chevrier, Tania Serrano, Rémi Lecerf, Gwendolina Limon, Claire Petit, Christine Monfort, Laurence Hubert-Moy, Gaël Durand, Sylvaine Cordier. Environmental determinants of the urinary concentrations of herbicides during pregnancy: the PELAGIE mother-child cohort (France). Environment international. 2014 Feb; 63(?):11-8. doi: 10.1016/j.envint.2013.10.010. [PMID: 24246238]
  • Joanna Bernasinska, Piotr Duchnowicz, Maria Koter-Michalak, Aneta Koceva-Chyla. Effect of safeners on damage of human erythrocytes treated with chloroacetamide herbicides. Environmental toxicology and pharmacology. 2013 Sep; 36(2):368-377. doi: 10.1016/j.etap.2013.04.010. [PMID: 23732483]
  • X Li, W Miao, C Gong, H Jiang, W Ma, S Zhu. Effects of prometryn and acetochlor on arbuscular mycorrhizal fungi and symbiotic system. Letters in applied microbiology. 2013 Aug; 57(2):122-8. doi: 10.1111/lam.12084. [PMID: 23593967]
  • Zhen Bai, Hui-Juan Xu, Hong-Bo He, Li-Chen Zheng, Xu-Dong Zhang. Alterations of microbial populations and composition in the rhizosphere and bulk soil as affected by residual acetochlor. Environmental science and pollution research international. 2013 Jan; 20(1):369-79. doi: 10.1007/s11356-012-1061-3. [PMID: 22811047]
  • Wei Tan, Ting Liang, Heng Zhai. [Effects of acetochlor on the photosynthetic and fluorescence characteristics and chloroplast structure of grape leaves]. Ying yong sheng tai xue bao = The journal of applied ecology. 2012 Aug; 23(8):2185-90. doi: ". [PMID: 23189697]
  • Stéphane Bouchonnet, Sophie Bourcier, Yasmine Souissi, Christophe Genty, Michel Sablier, Pascal Roche, Véronique Boireau, Valérie Ingrand. GC-MS(n) and LC-MS/MS couplings for the identification of degradation products resulting from the ozonation treatment of Acetochlor. Journal of mass spectrometry : JMS. 2012 Apr; 47(4):439-52. doi: 10.1002/jms.2056. [PMID: 22689619]
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  • Jing-jin Zhao, Shu-ming DU, Yao-xin Zhang. [Determination of acetochlor in human serum with gas chromatography]. Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases. 2010 Aug; 28(8):620-1. doi: NULL. [PMID: 21126463]
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