Sulfamethoxazole (BioDeep_00000001516)

 

Secondary id: BioDeep_00000397458

human metabolite blood metabolite Chemicals and Drugs natural product


代谢物信息卡片


4-amino-N-(5-methyl-1,2-oxazol-3-yl)benzene-1-sulfonamide

化学式: C10H11N3O3S (253.0521)
中文名称: 磺胺甲基异噁唑, 磺胺甲噁唑
谱图信息: 最多检出来源 Viridiplantae(plant) 14.6%

分子结构信息

SMILES: c1(S(Nc2cc(C)on2)(=O)=O)ccc(N)cc1
InChI: InChI=1S/C10H11N3O3S/c1-7-6-10(12-16-7)13-17(14,15)9-4-2-8(11)3-5-9/h2-6H,11H2,1H3,(H,12,13)

描述信息

Sulfamethoxazole is only found in individuals that have used or taken this drug. It is a bacteriostatic antibacterial agent that interferes with folic acid synthesis in susceptible bacteria. Its broad spectrum of activity has been limited by the development of resistance. (From Martindale, The Extra Pharmacopoeia, 30th ed, p208)Sulfonamides inhibit the enzymatic conversion of pteridine and p-aminobenzoic acid (PABA) to dihydropteroic acid by competing with PABA for binding to dihydrofolate synthetase, an intermediate of tetrahydrofolic acid (THF) synthesis. THF is required for the synthesis of purines and dTMP and inhibition of its synthesis inhibits bacterial growth. Pyrimethamine and trimethoprim inhibit dihydrofolate reductase, another step in THF synthesis, and therefore act synergistically with the sulfonamides.
J - Antiinfectives for systemic use > J01 - Antibacterials for systemic use > J01E - Sulfonamides and trimethoprim > J01EC - Intermediate-acting sulfonamides
COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials
C254 - Anti-Infective Agent > C29739 - Sulfonamide Anti-Infective Agent
D000890 - Anti-Infective Agents > D013424 - Sulfanilamides
CONFIDENCE standard compound; EAWAG_UCHEM_ID 298
CONFIDENCE standard compound; INTERNAL_ID 1018
Corona-virus
Coronavirus
SARS-CoV-2
COVID-19
SARS-CoV
COVID19
SARS2
SARS

同义名列表

44 个代谢物同义名

4-amino-N-(5-methyl-1,2-oxazol-3-yl)benzene-1-sulfonamide; 4-Amino-N-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide; 4-Amino-N-(5-methyl-3-isoxazolyl)benzenesulphonamide; 4-Amino-N-(5-methyl-3-isoxazolyl)-benzenesulfonamide; 4-Amino-N-(5-methyl-3-isoxazolyl)benzenesulfonamide; 3-(Para-aminophenylsulphonamido)-5-methylisoxazole; Ndimethyl1-(5-methyl-3-isoxazolyl)-sulfanilamide; 3-(p-Aminophenylsulphonamido)-5-methylisoxazole; 3-(p-Aminobenzenesulfonamido)-5-methylisoxazole; 3-(p-Aminophenylsulfonamido)-5-methylisoxazole; N^1-(5-methyl-3-isoxazolyl)-sulfanilamide; N1-(5-Methyl-3-isoxazolyl)sulphanilamide; N1-(5-Methyl-3-isoxazolyl)-sulfanilamide; N1-(5-Methyl-3-isoxazolyl)sulfanilamide; N-(5-methyl-3-isoxazolyl)-sulfanilamide; N-(5-methylisoxazol-3-yl)sulphanilamide; N-(5-methyl-3-isoxazolyl)sulfanilamide; N-(5-methyl-3-isoxazole)sulfanilamide; 5-Methyl-3-sulphanil-amidoisoxazole; 3-Sulphanilamido-5-methylisoxazole; 5-Methyl-3-sulfanilamidoisoxazole; 3-Sulfanilamido-5-methylisoxazole; 5-Methyl-3-sulfanylamidoisoxazole; 5-Methyl-3-sulfonylamidoisoxazole; Sulfamethoxazole(usan); Sulphamethylisoxazole; Sulfamethylisoxazole; Sulpha-methoxizole; Sulphamethoxazole; Sulphamethoxazol; sulfamethoxazole; Sulfamethalazole; Sulfamethoxazol; Sulphisomezole; Sulfisomezole; Azo-gantanol; Simsinomin; Gantanol; Metoxal; Bactrim; Radonil; Sinomin; SMX; Sulfamethoxazole



数据库引用编号

48 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)

9 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 8 ALB, CAT, CYP2C9, DHFR, DHPS, HPGDS, NAT2, TBX20
Peripheral membrane protein 3 ACHE, CYP1B1, CYP27A1
Endoplasmic reticulum membrane 3 CD4, CYP1B1, CYP2C9
Mitochondrion membrane 1 CYP27A1
Nucleus 5 ACHE, ALB, MPO, NAT2, TBX20
cytosol 7 ALB, CAT, DHFR, DHPS, HPGDS, NAT1, NAT2
centrosome 1 ALB
nucleoplasm 2 HPGDS, MPO
Cell membrane 6 ACHE, CD4, CD8A, NAT1, NAT2, TNF
Multi-pass membrane protein 2 NAT1, NAT2
Synapse 2 ACHE, NAT1
cell surface 3 ACHE, NAT1, TNF
Golgi apparatus 3 ACHE, ALB, ATRN
mitochondrial inner membrane 1 CYP27A1
neuromuscular junction 1 ACHE
neuronal cell body 2 NAT2, TNF
presynaptic membrane 1 NAT1
Lysosome 1 MPO
plasma membrane 10 ACHE, ATRN, CD4, CD8A, CYP2C9, IFNLR1, IGHE, NAT1, NAT2, TNF
synaptic vesicle membrane 1 NAT1
Membrane 6 ACHE, CAT, CYP1B1, IFNLR1, NAT1, NAT2
apical plasma membrane 1 NAT1
axon 2 NAT1, NAT2
basolateral plasma membrane 2 NAT1, NAT2
extracellular exosome 5 ALB, ATRN, CAT, MPO, NAT2
endoplasmic reticulum 1 ALB
extracellular space 6 ACHE, ALB, ATRN, IGHE, MPO, TNF
perinuclear region of cytoplasm 1 ACHE
mitochondrion 4 CAT, CYP1B1, CYP27A1, DHFR
protein-containing complex 2 ALB, CAT
intracellular membrane-bounded organelle 5 CAT, CYP1B1, CYP2C9, HPGDS, MPO
Microsome membrane 2 CYP1B1, CYP2C9
Single-pass type I membrane protein 5 ATRN, CD4, CD8A, IFNLR1, IGHE
Secreted 3 ACHE, ALB, PRB1
extracellular region 8 ACHE, ALB, CAT, CD8A, IGHE, MPO, PRB1, TNF
neuronal cell body membrane 1 NAT1
[Isoform 2]: Secreted 2 ATRN, CD8A
mitochondrial matrix 2 CAT, CYP27A1
Extracellular side 1 ACHE
anchoring junction 1 ALB
transcription regulator complex 1 NAT2
external side of plasma membrane 3 CD4, CD8A, TNF
Early endosome 1 CD4
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
Mitochondrion inner membrane 1 CYP27A1
Membrane raft 2 CD4, TNF
focal adhesion 1 CAT
Peroxisome 1 CAT
basement membrane 1 ACHE
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
secretory granule 1 MPO
receptor complex 1 CD8A
ciliary basal body 1 ALB
chromatin 1 TBX20
IgE immunoglobulin complex 1 IGHE
phagocytic cup 1 TNF
centriole 1 ALB
spindle pole 1 ALB
blood microparticle 1 ALB
Basolateral cell membrane 1 NAT1
Lipid-anchor, GPI-anchor 1 ACHE
[Isoform 2]: Cell membrane 1 IGHE
[Isoform 3]: Secreted 1 ATRN
side of membrane 1 ACHE
azurophil granule 1 MPO
plasma membrane raft 1 CD8A
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 1 CAT
endoplasmic reticulum lumen 2 ALB, CD4
platelet alpha granule lumen 1 ALB
azurophil granule lumen 1 MPO
clathrin-coated endocytic vesicle membrane 1 CD4
phagocytic vesicle lumen 1 MPO
synaptic cleft 1 ACHE
external side of apical plasma membrane 1 NAT2
[Isoform 1]: Cell membrane 2 ATRN, CD8A
[Isoform 3]: Cell membrane 1 IGHE
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
T cell receptor complex 2 CD4, CD8A
[Isoform 1]: Secreted 1 IGHE
IgE B cell receptor complex 1 IGHE
immunoglobulin complex, circulating 1 IGHE
catalase complex 1 CAT
[Isoform H]: Cell membrane 1 ACHE
NatA complex 1 NAT2
ciliary transition fiber 1 ALB
interleukin-28 receptor complex 1 IFNLR1
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Xuan Wu, Feifei Sun, Siqi Cao, Qilin Wang, Lianhong Wang, Songfeng Wang, Yan He, Boris Alexander Kolvenbach, Philippe Francois-Xavier Corvini, Rong Ji. Maize (Zea mays L.) Plants Alter the Fate and Accumulate Nonextractable Residues of Sulfamethoxazole in Farmland Soil. Environmental science & technology. 2024 May; 58(21):9292-9302. doi: 10.1021/acs.est.3c08954. [PMID: 38752544]
  • Erping Cui, Xiangyang Fan, Bingjian Cui, Shengshu Li, Taotao Chen, Feng Gao, Jianan Li, Zhenchao Zhou. The introduction of influent sulfamethoxazole loads induces changes in the removal pathways of sulfamethoxazole in vertical flow constructed wetlands featuring hematite substrate. Journal of hazardous materials. 2024 May; 469(?):133964. doi: 10.1016/j.jhazmat.2024.133964. [PMID: 38452680]
  • Yujie He, Longxue Jiang, Xuan Wu, Wenhui Zhang, Yao Zong, Jiacheng Wang, Jinmei Chen, Jun Shan, Deyang Kong, Rong Ji. Fate of sulfamethoxazole in wetland sediment under controlled redox conditions. Water research. 2024 May; 254(?):121350. doi: 10.1016/j.watres.2024.121350. [PMID: 38402752]
  • Kan Yu, Yueqiang Song, Nengzheng Wang, Xiaogang Yu, Tong Sun, Huiju Yu, Zhengshang Ruan, Yushu Qiu. Exposure of Danio rerio to environmental sulfamethoxazole may contribute to neurobehavioral abnormalities via gut microbiome disturbance. The Science of the total environment. 2024 Mar; 918(?):170546. doi: 10.1016/j.scitotenv.2024.170546. [PMID: 38309340]
  • Yinghe Jiang, Yinqi Zhao, Yubo Liu, Yihui Ban, Kaiguo Li, Xiaomei Li, Xiangling Zhang, Zhouying Xu. Removal of sulfamethoxazole and Cu, Cd compound pollution by arbuscular mycorrhizal fungi enhanced vertical flow constructed wetlands. Environmental research. 2024 Mar; 245(?):117982. doi: 10.1016/j.envres.2023.117982. [PMID: 38142732]
  • Yuanxiao Jin, Jiang Yu, Jie Yu, Yuerong Wu, Siwei Deng, Yinying Jiang, Zhi Huang, Donghai Wu, Weiwei Zhu. Ce/N @BC prepared based on plant metallurgy strategy: A novel activator of peroxymonosulfate for the degradation of sulfamethoxazole. Environmental pollution (Barking, Essex : 1987). 2024 Mar; 345(?):123558. doi: 10.1016/j.envpol.2024.123558. [PMID: 38355088]
  • Youshuai Fang, Guannan Lin, Ying Liu, Jian Zhang. Advanced treatment of antibiotic-polluted wastewater by a consortium composed of bacteria and mixed cyanobacteria. Environmental pollution (Barking, Essex : 1987). 2024 Mar; 344(?):123293. doi: 10.1016/j.envpol.2024.123293. [PMID: 38184153]
  • Jinlong Zhang, Wenjing Yang, Xingyu Liu, Fan Su, Gang Wang, Sihui Zhan, Yi Li. Iron hydroxyphosphate electro-Fenton catalyst for efficient removal of sulfamethoxazole and resource recycling into slow-release fertiliser ammonium ferrous phosphate. Environmental research. 2024 Mar; 244(?):117908. doi: 10.1016/j.envres.2023.117908. [PMID: 38092238]
  • Érika M L Sousa, Marta Otero, María V Gil, Paula Ferreira, Valdemar I Esteves, Vânia Calisto. Evaluation of different functionalization methodologies for improving the removal of three target antibiotics from wastewater by a brewery waste activated carbon. The Science of the total environment. 2024 Feb; 912(?):169437. doi: 10.1016/j.scitotenv.2023.169437. [PMID: 38128671]
  • Ying Liu, Maozhen Han, Fengmin Li, Na Zhang, Shaoyong Lu, Xiaohui Liu, Fengchang Wu. Performance and mechanism of SMX removal by an electrolysis-integrated ecological floating bed at low temperatures: A new perspective of plant activity, iron plaque, and microbial functions. Journal of hazardous materials. 2024 02; 463(?):132802. doi: 10.1016/j.jhazmat.2023.132802. [PMID: 37922584]
  • Yuzhe He, Lei Liu, Qi Wang, Xiaoqi Dong, Jingfei Huang, Xiaoshan Jia, Xingxing Peng. Bio-degraded of sulfamethoxazole by microbial consortia without addition nutrients: Mineralization, nitrogen removal, and proteomic characterization. Journal of hazardous materials. 2024 Jan; 466(?):133558. doi: 10.1016/j.jhazmat.2024.133558. [PMID: 38262313]
  • Sara Kamanmalek, Jacelyn Rice-Boayue. Development of a national antibiotic multimetric index for identifying watersheds vulnerable to antibiotic pollution. Environmental pollution (Barking, Essex : 1987). 2023 Dec; 339(?):122670. doi: 10.1016/j.envpol.2023.122670. [PMID: 37813143]
  • Aina Queral-Beltran, Marc Marín-García, Silvia Lacorte, Romà Tauler. UV-Vis absorption spectrophotometry and LC-DAD-MS-ESI(+)-ESI(-) coupled to chemometrics analysis of the monitoring of sulfamethoxazole degradation by chlorination, photodegradation, and chlorination/photodegradation. Analytica chimica acta. 2023 Oct; 1276(?):341563. doi: 10.1016/j.aca.2023.341563. [PMID: 37573101]
  • Yanjie Zhang, Weiyang Dong, Congyu Li, Haiyan Wang, Huan Wang, Yu Ling, Guokai Yan, Yang Chang. Effects of antibiotics on corncob supported solid-phase denitrification: Denitrification and antibiotics removal performance, mechanism, and antibiotic resistance genes. Journal of environmental sciences (China). 2023 Aug; 130(?):24-36. doi: 10.1016/j.jes.2022.10.020. [PMID: 37032040]
  • Vinicius Diniz, Susanne Rath. Adsorption of aqueous phase contaminants of emerging concern by activated carbon: Comparative fixed-bed column study and in situ regeneration methods. Journal of hazardous materials. 2023 Jul; 459(?):132197. doi: 10.1016/j.jhazmat.2023.132197. [PMID: 37543021]
  • Mengting Zhao, Jun Li, Shanshan Zhou, Ke Li, Lili Niu, Lu Zhao, Dongmei Xu. Analysis of the effects of sulfamethoxazole on the secondary metabolites and antioxidants in oilseed rape (Brassica napus L.) and the underlying mechanisms. The Science of the total environment. 2023 Jul; ?(?):165768. doi: 10.1016/j.scitotenv.2023.165768. [PMID: 37516166]
  • Han Zhang, Weijia Gong, Ying Xue, Weichen Zeng, Hesong Wang, Jinlong Wang, Xiaobin Tang, Guibai Li, Heng Liang. Municipal wastewater contains antibiotic treatment using O2 transfer membrane based biofilm reactor: Interaction between regular pollutants metabolism and sulfamethoxazole degradation. The Science of the total environment. 2023 Jun; 879(?):163060. doi: 10.1016/j.scitotenv.2023.163060. [PMID: 36966821]
  • Hui Liu, Yue Wang, Xinyu Shi. Co-existing antibiotics alter the enantioselective dissipation characteristics of zoxamide and drive combined impact on soil microenvironment. Journal of environmental management. 2023 Jun; 344(?):118340. doi: 10.1016/j.jenvman.2023.118340. [PMID: 37336018]
  • Katsivelou Eleni, Perruchon Chiara, Karas A Panagiotis, Sarantidou Apostolia, Pappa Eleni, Katsoula Athanasia, Ligda Panagiota, Sotiraki Smaragda, Martin-Laurent Fabrice, Vasileiadis Sotirios, Karpouzas G Dimitrios. Accelerated dissipation, soil microbial toxicity and dispersal of antimicrobial resistance in soils repeatedly exposed to tiamulin, tilmicosin and sulfamethoxazole. The Science of the total environment. 2023 Jun; ?(?):164817. doi: 10.1016/j.scitotenv.2023.164817. [PMID: 37329912]
  • Yuming Zhang, Wenjie Xiu, Miao Yan, Xinrui Guo, Zhihua Ni, Jihai Gu, Ting Tang, Fengsong Liu. Adverse effects of sulfamethoxazole on locomotor behavior and lipid metabolism by inhibiting acetylcholinesterase and lipase in Daphnia magna. The Science of the total environment. 2023 Jun; ?(?):164631. doi: 10.1016/j.scitotenv.2023.164631. [PMID: 37270018]
  • Millaray Sierra-Olea, Simon Kölle, Emil Bein, Thorsten Reemtsma, Oliver J Lechtenfeld, Uwe Hübner. Isotopically labeled ozone: A new approach to elucidate the formation of ozonation products. Water research. 2023 Apr; 233(?):119740. doi: 10.1016/j.watres.2023.119740. [PMID: 36822109]
  • Ilaria Berruti, Samira Nahim-Granados, María Jesús Abeledo-Lameiro, Isabel Oller, María Inmaculada Polo-López. Peroxymonosulfate/Solar process for urban wastewater purification at a pilot plant scale: A techno-economic assessment. The Science of the total environment. 2023 Apr; 881(?):163407. doi: 10.1016/j.scitotenv.2023.163407. [PMID: 37044331]
  • Lei Yang, Ashiwin Vadiveloo, Ai-Jie Chen, Wen-Zhu Liu, Dong-Zhi Chen, Feng Gao. Supplementation of exogenous phytohormones for enhancing the removal of sulfamethoxazole and the simultaneous accumulation of lipid by Chlorella vulgaris. Bioresource technology. 2023 Apr; 378(?):129002. doi: 10.1016/j.biortech.2023.129002. [PMID: 37019415]
  • Nhat Le-Duy, Lan-Anh T Hoang, Trinh Duy Nguyen, Taeyoon Lee. Pd nanoparticles decorated BiVO4 pine architectures for photocatalytic degradation of sulfamethoxazole. Chemosphere. 2023 Apr; 321(?):138118. doi: 10.1016/j.chemosphere.2023.138118. [PMID: 36775029]
  • Youshuai Fang, Ying Liu, Jian Zhang. Mechanisms for the increase in lipid production in cyanobacteria during the degradation of antibiotics. Environmental pollution (Barking, Essex : 1987). 2023 Apr; 322(?):121171. doi: 10.1016/j.envpol.2023.121171. [PMID: 36736559]
  • Jeong-In Hwang, P Chris Wilson. Absorption, translocation, and metabolism of atrazine, carbamazepine, and sulfamethoxazole by the macrophyte Orange King Humbert canna lily (Canna × generalis L.H. Bailey (pro sp.) [glauca × indica]). Environmental science and pollution research international. 2023 Jan; ?(?):. doi: 10.1007/s11356-023-25400-2. [PMID: 36719575]
  • Sanjeeb Mohapatra, Daniel Snow, Patrick Shea, Andy Gálvez-Rodríguez, Manish Kumar, Lokesh P Padhye, Suparna Mukherji. Photodegradation of a mixture of five pharmaceuticals commonly found in wastewater: Experimental and computational analysis. Environmental research. 2023 01; 216(Pt 3):114659. doi: 10.1016/j.envres.2022.114659. [PMID: 36328221]
  • Klaudia Stando, Aleksandra Czyż, Magdalena Gajda, Ewa Felis, Sylwia Bajkacz. Study of the Phytoextraction and Phytodegradation of Sulfamethoxazole and Trimethoprim from Water by Limnobium laevigatum. International journal of environmental research and public health. 2022 12; 19(24):. doi: 10.3390/ijerph192416994. [PMID: 36554877]
  • Anna Barra Caracciolo, Andrea Visca, Jasmin Rauseo, Francesca Spataro, Gian Luigi Garbini, Paola Grenni, Livia Mariani, Valentina Mazzurco Miritana, Giulia Massini, Luisa Patrolecco. Bioaccumulation of antibiotics and resistance genes in lettuce following cattle manure and digestate fertilization and their effects on soil and phyllosphere microbial communities. Environmental pollution (Barking, Essex : 1987). 2022 Dec; 315(?):120413. doi: 10.1016/j.envpol.2022.120413. [PMID: 36243186]
  • Yue Zhang, Ke Song, Juanqin Zhang, Xiaoyun Xu, Geng Ye, Huan Cao, Ming Chen, Shumei Cai, Xinde Cao, Xianqing Zheng, Weiguang Lv. Removal of sulfamethoxazole and antibiotic resistance genes in paddy soil by earthworms (Pheretima guillelmi): Intestinal detoxification and stimulation of indigenous soil bacteria. The Science of the total environment. 2022 Dec; 851(Pt 1):158075. doi: 10.1016/j.scitotenv.2022.158075. [PMID: 35985593]
  • Kan Yu, Yushu Qiu, Yi Shi, Xiaogang Yu, Ting Dong, Yuhang Wu, Huajun Li, Lisu Huang. Association of long-term effects of low-level sulfamethoxazole with ovarian lipid and amino acid metabolism, sex hormone levels, and oocyte maturity in zebrafish. Ecotoxicology and environmental safety. 2022 Dec; 247(?):114234. doi: 10.1016/j.ecoenv.2022.114234. [PMID: 36326554]
  • K Slipko, D Reif, H Schaar, E Saracevic, A Klinger, L Wallmann, J Krampe, M Woegerbauer, P Hufnagl, N Kreuzinger. Advanced wastewater treatment with ozonation and granular activated carbon filtration: Inactivation of antibiotic resistance targets in a long-term pilot study. Journal of hazardous materials. 2022 09; 438(?):129396. doi: 10.1016/j.jhazmat.2022.129396. [PMID: 35785739]
  • P Senthil Kumar, B S Sreeja, K Krishna Kumar, G Padmalaya. Static and dynamic analysis of sulfamethoxazole using GO/ZnO modified glassy carbon electrode by differential pulse voltammetry and amperometry techniques. Chemosphere. 2022 Sep; 302(?):134926. doi: 10.1016/j.chemosphere.2022.134926. [PMID: 35561779]
  • Fan Liu, Jing Ding, Guanshu Zhao, Qingliang Zhao, Kun Wang, Guangzhi Wang, Qingwei Gao. Catalytic pyrolysis of lotus leaves for producing nitrogen self-doping layered graphitic biochar: Performance and mechanism for peroxydisulfate activation. Chemosphere. 2022 Sep; 302(?):134868. doi: 10.1016/j.chemosphere.2022.134868. [PMID: 35533937]
  • Kathryn R Hayden, Matthew Jones, Kyle R Elkin, Michael J Shreve, William Irvin Clees, Shirley Clark, Michael L Mashtare, Tamie L Veith, Herschel A Elliott, John E Watson, Justin Silverman, Thomas L Richard, Andrew F Read, Heather E Preisendanz. Impacts of the COVID-19 pandemic on pharmaceuticals in wastewater treated for beneficial reuse: Two case studies in central Pennsylvania. Journal of environmental quality. 2022 Sep; 51(5):1066-1082. doi: 10.1002/jeq2.20398. [PMID: 35919971]
  • Zhipeng Li, Ruochun Zhang, Peizhe Sun. Simultaneous removal of phosphate and antibiotic from hydrolyzed urine by novel spherical particles. Chemosphere. 2022 Aug; 300(?):134637. doi: 10.1016/j.chemosphere.2022.134637. [PMID: 35439493]
  • Klaudia Stando, Ewa Korzeniewska, Ewa Felis, Monika Harnisz, Sylwia Bajkacz. Uptake of Pharmaceutical Pollutants and Their Metabolites from Soil Fertilized with Manure to Parsley Tissues. Molecules (Basel, Switzerland). 2022 Jul; 27(14):. doi: 10.3390/molecules27144378. [PMID: 35889250]
  • Ellen Edefell, Ola Svahn, Per Falås, Elina Bengtsson, Michael Axelsson, Regine Ullman, Michael Cimbritz. Digging deep into a GAC filter - Temporal and spatial profiling of adsorbed organic micropollutants. Water research. 2022 Jun; 218(?):118477. doi: 10.1016/j.watres.2022.118477. [PMID: 35487159]
  • Noureddine El Messaoudi, Abdelaziz El Mouden, Yasmine Fernine, Mohammed El Khomri, Amal Bouich, Nadia Faska, Zeynep Ciğeroğlu, Juliana Heloisa Pinê Américo-Pinheiro, Amane Jada, Abdellah Lacherai. Green synthesis of Ag2O nanoparticles using Punica granatum leaf extract for sulfamethoxazole antibiotic adsorption: characterization, experimental study, modeling, and DFT calculation. Environmental science and pollution research international. 2022 Jun; ?(?):. doi: 10.1007/s11356-022-21554-7. [PMID: 35729389]
  • Jin Hou, Jinquan Wan, Zhicheng Yan, Yan Wang, Yongwen Ma, Yongchang Xie, Huajian Chen, Yangyang Xue. A novel polydopamine-modified metal organic frameworks catalyst with enhanced catalytic performance for efficient degradation of sulfamethoxazole in wastewater. Chemosphere. 2022 Jun; 297(?):134100. doi: 10.1016/j.chemosphere.2022.134100. [PMID: 35219710]
  • S Keerthanan, Chamila Jayasinghe, Nanthi Bolan, Jörg Rinklebe, Meththika Vithanage. Retention of sulfamethoxazole by cinnamon wood biochar and its efficacy of reducing bioavailability and plant uptake in soil. Chemosphere. 2022 Jun; 297(?):134073. doi: 10.1016/j.chemosphere.2022.134073. [PMID: 35227748]
  • Jian Sun, Jinquan Wan, Yan Wang, Zhicheng Yan, Yongwen Ma, Su Ding, Min Tang, Yongchang Xie. Modulated construction of Fe-based MOF via formic acid modulator for enhanced degradation of sulfamethoxazole:Design, degradation pathways, and mechanism. Journal of hazardous materials. 2022 05; 429(?):128299. doi: 10.1016/j.jhazmat.2022.128299. [PMID: 35077971]
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