sulfamethazine (BioDeep_00000397455)

Main id: BioDeep_00000001572

 

natural product


代谢物信息卡片


Sulfadimidin / sulfamethazin

化学式: C12H14N4O2S (278.0837)
中文名称: 磺胺二甲嘧啶
谱图信息: 最多检出来源 Homo sapiens(blood) 28.45%

分子结构信息

SMILES: c1(S(Nc2nc(cc(n2)C)C)(=O)=O)ccc(N)cc1
InChI: InChI=1S/C12H14N4O2S/c1-8-7-9(2)15-12(14-8)16-19(17,18)11-5-3-10(13)4-6-11/h3-7H,13H2,1-2H3,(H,14,15,16)

描述信息

J - Antiinfectives for systemic use > J01 - Antibacterials for systemic use > J01E - Sulfonamides and trimethoprim > J01EB - Short-acting sulfonamides
A sulfonamide consisting of pyrimidine with methyl substituents at the 4- and 6-positions and a 4-aminobenzenesulfonamido group at the 2-position.
C254 - Anti-Infective Agent > C29739 - Sulfonamide Anti-Infective Agent
D000890 - Anti-Infective Agents > D013424 - Sulfanilamides
CONFIDENCE standard compound; INTERNAL_ID 1309; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8847; ORIGINAL_PRECURSOR_SCAN_NO 8846
CONFIDENCE standard compound; INTERNAL_ID 1309; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8855; ORIGINAL_PRECURSOR_SCAN_NO 8853
CONFIDENCE standard compound; INTERNAL_ID 1309; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8878; ORIGINAL_PRECURSOR_SCAN_NO 8876
CONFIDENCE standard compound; INTERNAL_ID 1309; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8904; ORIGINAL_PRECURSOR_SCAN_NO 8903
CONFIDENCE standard compound; INTERNAL_ID 1309; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8916; ORIGINAL_PRECURSOR_SCAN_NO 8915
CONFIDENCE standard compound; INTERNAL_ID 1309; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8901; ORIGINAL_PRECURSOR_SCAN_NO 8900
CONFIDENCE standard compound; INTERNAL_ID 4099
CONFIDENCE standard compound; INTERNAL_ID 8503
CONFIDENCE standard compound; EAWAG_UCHEM_ID 181
CONFIDENCE standard compound; INTERNAL_ID 1008

同义名列表

3 个代谢物同义名

sulfamethazine; Sulfadimidin / sulfamethazin; Sulfamethazine



数据库引用编号

46 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 ALB, CAT, CYP2D6, CYP2E1, DHFR, G6PD, HMGB1, HPGDS, NAT2, PKD2
Peripheral membrane protein 5 ACHE, CYP2E1, G6PD, GBA1, HMGB1
Endoplasmic reticulum membrane 4 CYP1A2, CYP2D6, CYP2E1, PKD2
Nucleus 5 ACHE, ALB, HMGB1, NAT2, PKD2
cytosol 8 ALB, CAT, DHFR, G6PD, HPGDS, NAT1, NAT2, PKD2
trans-Golgi network 1 GBA1
centrosome 1 ALB
nucleoplasm 3 HMGB1, HPGDS, PKD2
Cell membrane 5 ACHE, HMGB1, NAT1, NAT2, PKD2
lamellipodium 1 PKD2
Multi-pass membrane protein 3 NAT1, NAT2, PKD2
Synapse 2 ACHE, NAT1
cell surface 4 ACHE, HMGB1, NAT1, TNR
glutamatergic synapse 1 TNR
Golgi apparatus 4 ACHE, ALB, GBA1, PKD2
Golgi membrane 1 INS
lysosomal membrane 2 GAA, GBA1
mitochondrial inner membrane 1 CYP2E1
neuromuscular junction 1 ACHE
neuronal cell body 1 NAT2
presynaptic membrane 1 NAT1
Cytoplasm, cytosol 1 G6PD
Lysosome 2 GAA, GBA1
endosome 1 HMGB1
plasma membrane 7 ACHE, BTC, GAA, HMGB1, NAT1, NAT2, PKD2
synaptic vesicle membrane 1 NAT1
Membrane 9 ACHE, BTC, CAT, CYP2D6, G6PD, GAA, NAT1, NAT2, PKD2
apical plasma membrane 1 NAT1
axon 2 NAT1, NAT2
basolateral plasma membrane 3 NAT1, NAT2, PKD2
extracellular exosome 7 ALB, CAT, G6PD, GAA, GBA1, NAT2, PKD2
Lysosome membrane 2 GAA, GBA1
Lumenal side 1 GBA1
endoplasmic reticulum 5 ALB, CYP2D6, GBA1, HMGB1, PKD2
extracellular space 8 ACHE, ALB, BTC, GH1, HMGB1, IGF1, INS, TNR
lysosomal lumen 2 GAA, GBA1
perinuclear region of cytoplasm 1 ACHE
Schaffer collateral - CA1 synapse 1 TNR
mitochondrion 3 CAT, CYP2D6, DHFR
protein-containing complex 2 ALB, CAT
intracellular membrane-bounded organelle 7 CAT, CYP1A2, CYP2D6, CYP2E1, G6PD, GAA, HPGDS
Microsome membrane 3 CYP1A2, CYP2D6, CYP2E1
Secreted 7 ACHE, ALB, GAA, GH1, HMGB1, IGF1, INS
extracellular region 10 ACHE, ALB, BTC, CAT, GAA, GH1, HMGB1, IGF1, INS, TNR
cytoplasmic side of plasma membrane 1 G6PD
Single-pass membrane protein 1 CYP2D6
neuronal cell body membrane 1 NAT1
mitochondrial matrix 1 CAT
Extracellular side 2 ACHE, HMGB1
anchoring junction 1 ALB
transcription regulator complex 1 NAT2
Cell projection, cilium 1 PKD2
centriolar satellite 1 G6PD
ciliary membrane 1 PKD2
motile cilium 1 PKD2
Secreted, extracellular space, extracellular matrix 1 TNR
cell-cell junction 1 PKD2
vesicle 1 PKD2
Mitochondrion inner membrane 1 CYP2E1
Membrane raft 1 TNR
focal adhesion 1 CAT
Peroxisome 1 CAT
basement membrane 1 ACHE
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
collagen-containing extracellular matrix 1 TNR
ciliary basal body 2 ALB, PKD2
cilium 1 PKD2
cell projection 1 PKD2
mitotic spindle 1 PKD2
Chromosome 1 HMGB1
centriole 1 ALB
Golgi apparatus, trans-Golgi network 1 PKD2
spindle pole 1 ALB
blood microparticle 1 ALB
non-motile cilium 1 PKD2
Basolateral cell membrane 2 NAT1, PKD2
Lipid-anchor, GPI-anchor 1 ACHE
Endomembrane system 1 PKD2
endosome lumen 2 GH1, INS
monoatomic ion channel complex 1 PKD2
Cytoplasmic vesicle membrane 1 PKD2
tertiary granule membrane 1 GAA
side of membrane 1 ACHE
basal plasma membrane 1 PKD2
exocytic vesicle 1 IGF1
ficolin-1-rich granule lumen 2 CAT, HMGB1
secretory granule lumen 3 CAT, HMGB1, INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 ALB, INS
transcription repressor complex 1 HMGB1
platelet alpha granule lumen 2 ALB, IGF1
transport vesicle 1 INS
azurophil granule membrane 1 GAA
Secreted, extracellular exosome 1 PKD2
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
perineuronal net 1 TNR
clathrin-coated endocytic vesicle membrane 1 BTC
endoplasmic reticulum-Golgi intermediate compartment 1 HMGB1
synaptic cleft 1 ACHE
ficolin-1-rich granule membrane 1 GAA
external side of apical plasma membrane 1 NAT2
lumenal side of endoplasmic reticulum membrane 1 PKD2
condensed chromosome 1 HMGB1
Cell projection, cilium membrane 1 PKD2
basal cortex 1 PKD2
growth hormone receptor complex 1 GH1
catalase complex 1 CAT
alphav-beta3 integrin-IGF-1-IGF1R complex 1 IGF1
insulin-like growth factor binding protein complex 1 IGF1
insulin-like growth factor ternary complex 1 IGF1
alphav-beta3 integrin-HMGB1 complex 1 HMGB1
autolysosome lumen 1 GAA
migrasome 1 PKD2
cytoplasmic side of endoplasmic reticulum membrane 1 PKD2
tenascin complex 1 TNR
[Isoform H]: Cell membrane 1 ACHE
NatA complex 1 NAT2
cation channel complex 1 PKD2
ciliary transition fiber 1 ALB
polycystin complex 1 PKD2


文献列表

  • Xiao-Qiong Zhao, Heng-Hui Zhang, Run-Zhu Zhao, Xin-Mei Zhang. [Effects of Combined Stress of Polyethylene and Sulfamethazine on Seed Germination, Seedling Growth, and Physiological Characteristics of Soybean]. Huan jing ke xue= Huanjing kexue. 2023 Sep; 44(9):5092-5101. doi: 10.13227/j.hjkx.202211033. [PMID: 37699827]
  • Meihong Tan, Wanping Shi, Haifeng Wang, Guanglan Di, Zhengxin Xie, Shisuo Fan, Jun Tang, Fengshou Dong. Effective photodegradation of antibiotics by guest-host synergy between photosensitizer and bismuth vanadate: Underlying mechanism and toxicity assessment. Chemosphere. 2023 Jun; 325(?):138362. doi: 10.1016/j.chemosphere.2023.138362. [PMID: 36905996]
  • Wei Zhang, Pei-Fang Wang, Qiu-Tong Jin, Bin Hu. [Effects of Sulfamethazine in Soil on Rice Growth]. Huan jing ke xue= Huanjing kexue. 2023 Feb; 44(2):1021-1028. doi: 10.13227/j.hjkx.202203003. [PMID: 36775625]
  • Peng Liu, Jiamin Dai, Chunyao Bie, Huang Li, Zixuan Zhang, Xuetao Guo, Lingyan Zhu. Bioaccessibility of Microplastic-Associated Antibiotics in Freshwater Organisms: Highlighting the Impacts of Biofilm Colonization via an In Vitro Protocol. Environmental science & technology. 2022 09; 56(17):12267-12277. doi: 10.1021/acs.est.2c02782. [PMID: 35952376]
  • Yanyan Huang, Zhimin Qiang, Zhe Sun, Mengkai Li. Micropollutant degradation by UV/H2O2 in drinking water: Facilitated prediction through combination of model simulation and portable measurement. Water research. 2022 Aug; 221(?):118794. doi: 10.1016/j.watres.2022.118794. [PMID: 35785695]
  • Jie Wu, Yihe Zhang, Mengyuan Huang, Ziheng Zou, Shumin Guo, Jinyang Wang, Jianwen Zou. Sulfonamide antibiotics alter gaseous nitrogen emissions in the soil-plant system: A mesocosm experiment and meta-analysis. The Science of the total environment. 2022 Jul; 828(?):154230. doi: 10.1016/j.scitotenv.2022.154230. [PMID: 35271923]
  • Linlin Qiu, Jingjing Wu, Yuan Qian, Muhammad Nafees, Jingxian Zhang, Wenchao Du, Ying Yin, Hongyan Guo. Impact of biochar-induced vertical mobilization of dissolved organic matter, sulfamethazine and antibiotic resistance genes variation in a soil-plant system. Journal of hazardous materials. 2021 09; 417(?):126022. doi: 10.1016/j.jhazmat.2021.126022. [PMID: 34229407]
  • Mark J Henderson, Kathleen A Trychta, Shyh-Ming Yang, Susanne Bäck, Adam Yasgar, Emily S Wires, Carina Danchik, Xiaokang Yan, Hideaki Yano, Lei Shi, Kuo-Jen Wu, Amy Q Wang, Dingyin Tao, Gergely Zahoránszky-Kőhalmi, Xin Hu, Xin Xu, David Maloney, Alexey V Zakharov, Ganesha Rai, Fumihiko Urano, Mikko Airavaara, Oksana Gavrilova, Ajit Jadhav, Yun Wang, Anton Simeonov, Brandon K Harvey. A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome. Cell reports. 2021 04; 35(4):109040. doi: 10.1016/j.celrep.2021.109040. [PMID: 33910017]
  • M Conde-Cid, R Cela-Dablanca, G Ferreira-Coelho, D Fernández-Calviño, A Núñez-Delgado, M J Fernández-Sanjurjo, M Arias-Estévez, E Álvarez-Rodríguez. Sulfadiazine, sulfamethazine and sulfachloropyridazine removal using three different porous materials: Pine bark, "oak ash" and mussel shell. Environmental research. 2021 04; 195(?):110814. doi: 10.1016/j.envres.2021.110814. [PMID: 33524329]
  • Ariel E Turcios, Marie Hielscher, Bernardo Duarte, Vanessa F Fonseca, Isabel Caçador, Jutta Papenbrock. Screening of Emerging Pollutants (EPs) in Estuarine Water and Phytoremediation Capacity of Tripolium pannonicum under Controlled Conditions. International journal of environmental research and public health. 2021 01; 18(3):. doi: 10.3390/ijerph18030943. [PMID: 33499038]
  • Changrui Zhou, Qiang Ma, Shuailin Li, Mengmeng Zhu, Zhuqing Xia, Wantai Yu. Toxicological effects of single and joint sulfamethazine and cadmium stress in soil on pakchoi (Brassica chinensis L.). Chemosphere. 2021 Jan; 263(?):128296. doi: 10.1016/j.chemosphere.2020.128296. [PMID: 33297238]
  • Yangyang Zhang, Dan Peng, Yuanyuan Luo, Daofen Huang, Xuetao Guo, Lingyan Zhu. Cellulase modified waste biomass to remove sulfamethazine from aqueous solutions. The Science of the total environment. 2020 Aug; 731(?):138806. doi: 10.1016/j.scitotenv.2020.138806. [PMID: 32413652]
  • Qiaohong Chen, Li Zhang, Yihong Han, Jingyun Fang, Haiying Wang. Degradation and metabolic pathways of sulfamethazine and enrofloxacin in Chlorella vulgaris and Scenedesmus obliquus treatment systems. Environmental science and pollution research international. 2020 Aug; 27(22):28198-28208. doi: 10.1007/s11356-020-09008-4. [PMID: 32415445]
  • Rui Yang, Xiaoming Xia, Jinhua Wang, Lusheng Zhu, Jun Wang, Zulfiqar Ahmad, Lili Yang, Shushuai Mao, Yangyang Chen. Dose and time-dependent response of single and combined artificial contamination of sulfamethazine and copper on soil enzymatic activities. Chemosphere. 2020 Jul; 250(?):126161. doi: 10.1016/j.chemosphere.2020.126161. [PMID: 32092565]
  • M Conde-Cid, D Fernández-Calviño, M J Fernández-Sanjurjo, A Núñez-Delgado, E Álvarez-Rodríguez, M Arias-Estévez. Effects of pine bark amendment on the transport of sulfonamide antibiotics in soils. Chemosphere. 2020 Jun; 248(?):126041. doi: 10.1016/j.chemosphere.2020.126041. [PMID: 32028162]
  • G Douglas Inglis, Jenny F Gusse, Kathaleen E House, Tara G Shelton, Eduardo N Taboada. Clinically Relevant Campylobacter jejuni Subtypes Are Readily Found and Transmitted within the Cattle Production Continuum but Present a Limited Foodborne Risk. Applied and environmental microbiology. 2020 03; 86(6):. doi: 10.1128/aem.02101-19. [PMID: 31862718]
  • Khang Huynh, Dawn Reinhold. Uptake, translocation, and metabolism of sulfamethazine by Arabidopsis thaliana: distinguishing between phytometabolites and abiotic transformation products in the media. International journal of phytoremediation. 2020; 22(4):412-419. doi: 10.1080/15226514.2019.1667952. [PMID: 31549518]
  • Wen Yang, Tongtong Feng, Markus Flury, Baoguo Li, Jianying Shang. Effect of sulfamethazine on surface characteristics of biochar colloids and its implications for transport in porous media. Environmental pollution (Barking, Essex : 1987). 2020 Jan; 256(?):113482. doi: 10.1016/j.envpol.2019.113482. [PMID: 31679872]
  • Allan J Cessna, Sandra L Kuchta, Marley Waiser, Robert B Brua, Jonathan Bailey. Persistence of the antimicrobials lincomycin, chlortetracycline, and sulfamethazine in prairie wetlands. Journal of environmental quality. 2020 Jan; 49(1):236-245. doi: 10.1002/jeq2.20034. [PMID: 33016366]
  • Jiu-Qiang Xiong, Byong-Hun Jeon, Sanjay P Govindwar, Mayur B Kurade, Swapnil M Patil, Jung-Han Park, Ki-Hyun Kim. Plant and microalgae consortium for an enhanced biodegradation of sulfamethazine. Environmental science and pollution research international. 2019 Nov; 26(33):34552-34561. doi: 10.1007/s11356-019-06506-y. [PMID: 31650474]
  • 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]
  • Dapeng Wang, Xian Zhang, Changzhou Yan. Occurrence and removal of sulfonamides and their acetyl metabolites in a biological aerated filter (BAF) of wastewater treatment plant in Xiamen, South China. Environmental science and pollution research international. 2019 Nov; 26(32):33363-33372. doi: 10.1007/s11356-019-06311-7. [PMID: 31522397]
  • Lanjun Wang, Xiaoming Xia, Wenjie Zhang, Jinhua Wang, Lusheng Zhu, Jun Wang, Ziyan Wei, Zulfiqar Ahmad. Separate and joint eco-toxicological effects of sulfadimidine and copper on soil microbial biomasses and ammoxidation microorganisms abundances. Chemosphere. 2019 Aug; 228(?):556-564. doi: 10.1016/j.chemosphere.2019.04.165. [PMID: 31055070]
  • Anne Ostermann, Peter E Mortimer, Rongcai Huang, Lu Ma, Dengpan Bu, Jianchu Xu. Symbiotic Nitrogen Fixation in Soil Contaminated with the Veterinary Antibiotics Oxytetracycline and Sulfamethazine. Journal of environmental quality. 2019 Jul; 48(4):1067-1073. doi: 10.2134/jeq2019.01.0021. [PMID: 31589684]
  • Surased Suraritdechachai, Chayan Charoenpakdee, Iain Young, Simon Maher, Tirayut Vilaivan, Thanit Praneenararat. Rapid Detection of the Antibiotic Sulfamethazine in Pig Body Fluids by Paper Spray Mass Spectrometry. Journal of agricultural and food chemistry. 2019 Mar; 67(10):3055-3061. doi: 10.1021/acs.jafc.9b00500. [PMID: 30799617]
  • A N Ngigi, Y S Ok, S Thiele-Bruhn. Biochar-mediated sorption of antibiotics in pig manure. Journal of hazardous materials. 2019 Feb; 364(?):663-670. doi: 10.1016/j.jhazmat.2018.10.045. [PMID: 30396139]
  • Ariel E Turcios, Jutta Papenbrock. Enzymatic degradation of the antibiotic sulfamethazine by using crude extracts of different halophytic plants. International journal of phytoremediation. 2019; 21(11):1104-1111. doi: 10.1080/15226514.2019.1606782. [PMID: 31037959]
  • Ariel E Turcios, Jutta Papenbrock. Biofiltration of the antibacterial drug sulfamethazine by the species Chenopodium quinoa and its further biodegradation through anaerobic digestion. Journal of environmental sciences (China). 2019 Jan; 75(?):54-63. doi: 10.1016/j.jes.2018.02.022. [PMID: 30473307]
  • Yasuhiro Uno, Norie Murayama, Hiroshi Yamazaki. Molecular and Functional Characterization of N-Acetyltransferases NAT1 and NAT2 in Cynomolgus Macaque. Chemical research in toxicology. 2018 11; 31(11):1269-1276. doi: 10.1021/acs.chemrestox.8b00236. [PMID: 30358977]
  • Md Hasan Turabee, Thavasyappan Thambi, Huu Thuy Trang Duong, Ji Hoon Jeong, Doo Sung Lee. A pH- and temperature-responsive bioresorbable injectable hydrogel based on polypeptide block copolymers for the sustained delivery of proteins in vivo. Biomaterials science. 2018 Feb; 6(3):661-671. doi: 10.1039/c7bm00980a. [PMID: 29423489]
  • Mingyun Jia, Fang Wang, Yongrong Bian, Robert D Stedtfeld, Guangxia Liu, Jinping Yu, Xin Jiang. Sorption of sulfamethazine to biochars as affected by dissolved organic matters of different origin. Bioresource technology. 2018 Jan; 248(Pt B):36-43. doi: 10.1016/j.biortech.2017.08.082. [PMID: 28863989]
  • E I Akogwu, S A Saganuwan, P A Onyeyili. Effects of piroxicam on tissue distribution of sulfadimidine in West African Dwarf male and female goats. Human & experimental toxicology. 2018 Jan; 37(1):61-68. doi: 10.1177/0960327117692135. [PMID: 28176534]
  • Min Pan, L M Chu. Transfer of antibiotics from wastewater or animal manure to soil and edible crops. Environmental pollution (Barking, Essex : 1987). 2017 Dec; 231(Pt 1):829-836. doi: 10.1016/j.envpol.2017.08.051. [PMID: 28866424]
  • Imen Saidi, Florence Fourcade, Didier Floner, Isabelle Soutrel, Nizar Bellakhal, Abdeltif Amrane, Florence Geneste. Sulfamethazine removal by means of a combined process coupling an oxidation pretreatment and activated sludge culture - preliminary results. Environmental technology. 2017 Nov; 38(21):2684-2690. doi: 10.1080/09593330.2016.1273395. [PMID: 27973980]
  • Nishikant Wase, Boqiang Tu, James W Allen, Paul N Black, Concetta C DiRusso. Identification and Metabolite Profiling of Chemical Activators of Lipid Accumulation in Green Algae. Plant physiology. 2017 Aug; 174(4):2146-2165. doi: 10.1104/pp.17.00433. [PMID: 28652262]
  • Sudarshan Kurwadkar, Garrett Struckhoff, Kameron Pugh, Om Singh. Uptake and translocation of sulfamethazine by alfalfa grown under hydroponic conditions. Journal of environmental sciences (China). 2017 Mar; 53(?):217-223. doi: 10.1016/j.jes.2016.04.019. [PMID: 28372746]
  • Xiaoying Guo, Xiaofang Shen, Meng Zhang, Haiyun Zhang, Weixiao Chen, Hui Wang, A A Koelmans, Gerard Cornelissen, Shu Tao, Xilong Wang. Sorption mechanisms of sulfamethazine to soil humin and its subfractions after sequential treatments. Environmental pollution (Barking, Essex : 1987). 2017 Feb; 221(?):266-275. doi: 10.1016/j.envpol.2016.11.073. [PMID: 27955989]
  • Ariel E Turcios, Dirk Weichgrebe, Jutta Papenbrock. Uptake and biodegradation of the antimicrobial sulfadimidine by the species Tripolium pannonicum acting as biofilter and its further biodegradation by anaerobic digestion and concomitant biogas production. Bioresource technology. 2016 Nov; 219(?):687-693. doi: 10.1016/j.biortech.2016.08.047. [PMID: 27544919]
  • Fernanda Garcia Sampaio, Maria Lídia Carra, Claudio Martin Jonsson, Vitoria Teodoro Gonçalves, Genoefa Dal'Bo, Kátia Santos Damacena Nunes, José Henrique Valim, Bruno Stéfano Lima Dallago, Sonia Claudia do Nascimento de Queiroz, Felix Guillermo Reyes Reyes. Effects of Dietary Exposure to Sulfamethazine on the Hematological Parameters and Hepatic Oxidative Stress Biomarkers in Nile Tilapia (Oreochromis niloticus). Bulletin of environmental contamination and toxicology. 2016 Oct; 97(4):528-35. doi: 10.1007/s00128-016-1837-0. [PMID: 27225508]
  • Yaju Zhao, Guoqing Deng, Xiaohui Liu, Liang Sun, Hui Li, Quan Cheng, Kai Xi, Danke Xu. MoS2/Ag nanohybrid: A novel matrix with synergistic effect for small molecule drugs analysis by negative-ion matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Analytica chimica acta. 2016 Sep; 937(?):87-95. doi: 10.1016/j.aca.2016.06.026. [PMID: 27590549]
  • Min Pan, L M Chu. Phytotoxicity of veterinary antibiotics to seed germination and root elongation of crops. Ecotoxicology and environmental safety. 2016 Apr; 126(?):228-237. doi: 10.1016/j.ecoenv.2015.12.027. [PMID: 26773832]
  • I M Tahir, T Iqbal, S Saleem, H Mehboob, N Akhter, M Riaz. Effect of acetaminophen on sulfamethazine acetylation in male volunteers. International journal of immunopathology and pharmacology. 2016 Mar; 29(1):17-22. doi: 10.1177/0394632015593238. [PMID: 26519524]
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