Bisphenol S (BioDeep_00000002710)

 

Secondary id: BioDeep_00001873826

human metabolite blood metabolite Exogenous Industrial Pollutants natural product


代谢物信息卡片


4-(4-hydroxybenzenesulfonyl)phenol

化学式: C12H10O4S (250.03)
中文名称: 双酚S, 双酚 S
谱图信息: 最多检出来源 Homo sapiens(blood) 16.18%

Reviewed

Last reviewed on 2024-08-06.

Cite this Page

Bisphenol S. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/bisphenol_s (retrieved 2024-12-23) (BioDeep RN: BioDeep_00000002710). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: C1=CC(=CC=C1O)S(=O)(=O)C2=CC=C(C=C2)O
InChI: InChI=1S/C12H10O4S/c13-9-1-5-11(6-2-9)17(15,16)12-7-3-10(14)4-8-12/h1-8,13-14H

描述信息

CONFIDENCE standard compound; INTERNAL_ID 551; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7059; ORIGINAL_PRECURSOR_SCAN_NO 7056
CONFIDENCE standard compound; INTERNAL_ID 551; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3374; ORIGINAL_PRECURSOR_SCAN_NO 3371
CONFIDENCE standard compound; INTERNAL_ID 551; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3401; ORIGINAL_PRECURSOR_SCAN_NO 3398
CONFIDENCE standard compound; INTERNAL_ID 551; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3420; ORIGINAL_PRECURSOR_SCAN_NO 3416
CONFIDENCE standard compound; INTERNAL_ID 551; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7124; ORIGINAL_PRECURSOR_SCAN_NO 7120
CONFIDENCE standard compound; INTERNAL_ID 551; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3421; ORIGINAL_PRECURSOR_SCAN_NO 3419
CONFIDENCE standard compound; INTERNAL_ID 551; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7099; ORIGINAL_PRECURSOR_SCAN_NO 7095
CONFIDENCE standard compound; INTERNAL_ID 551; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3383; ORIGINAL_PRECURSOR_SCAN_NO 3380
CONFIDENCE standard compound; INTERNAL_ID 551; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7143; ORIGINAL_PRECURSOR_SCAN_NO 7141
CONFIDENCE standard compound; INTERNAL_ID 551; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7085; ORIGINAL_PRECURSOR_SCAN_NO 7082
CONFIDENCE standard compound; INTERNAL_ID 551; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7120; ORIGINAL_PRECURSOR_SCAN_NO 7116
CONFIDENCE standard compound; INTERNAL_ID 551; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3402; ORIGINAL_PRECURSOR_SCAN_NO 3400
CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 1086
CONFIDENCE standard compound; INTERNAL_ID 4240
CONFIDENCE standard compound; INTERNAL_ID 8644
CONFIDENCE standard compound; INTERNAL_ID 2370

同义名列表

18 个代谢物同义名

4-(4-hydroxybenzenesulfonyl)phenol; 4-(4-Hydroxyphenyl)sulphonylphenol; 1,1-Sulphonylbis(4-hydroxybenzene); 1,1-Sulfonylbis(4-hydroxybenzene); 4,4-Dihydroxydiphenyl sulphone; Bis(4-hydroxyphenyl) sulphone; 4,4-Dihydroxydiphenyl sulfone; Bis(p-hydroxyphenyl) sulphone; Bis(4-hydroxyphenyl) sulfone; Bis(p-hydroxyphenyl) sulfone; Bis(4-hydroxyphenyl)sulfone; 4,4`-sulphonyldiphenol; 4,4-Sulphonyldiphenol; 4,4-Sulfonyldiphenol; Bisphenol S; DHDPHS; BPS; 4,4'-Sulfonyldiphenol



数据库引用编号

50 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)

8 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 12 ADIG, AR, CASP3, CAT, EGFR, ESR1, FABP4, FASN, GPER1, NFE2L2, NR3C1, PPARG
Peripheral membrane protein 2 CYP11A1, ESR1
Endosome membrane 1 EGFR
Endoplasmic reticulum membrane 4 CYP17A1, CYP19A1, EGFR, GPER1
Mitochondrion membrane 2 CYP11A1, GPER1
Nucleus 13 ADIG, AR, CASP3, EGFR, ESR1, ESR2, FABP4, GPER1, NFE2L2, NR3C1, PPARA, PPARG, THRB
cytosol 10 AR, CASP3, CAT, ESR1, FABP4, FASN, GPER1, NFE2L2, NR3C1, PPARG
dendrite 1 GPER1
mitochondrial membrane 1 GPER1
nuclear body 1 THRB
trans-Golgi network 1 GPER1
centrosome 2 NFE2L2, NR3C1
nucleoplasm 10 AR, CASP3, ESR1, ESR2, GPER1, NFE2L2, NR3C1, PPARA, PPARG, THRB
RNA polymerase II transcription regulator complex 3 NFE2L2, PPARG, THRB
Cell membrane 2 EGFR, ESR1
Cytoplasmic side 1 ESR1
ruffle membrane 1 EGFR
Cell projection, axon 1 GPER1
Early endosome membrane 1 EGFR
Multi-pass membrane protein 2 CYP19A1, GPER1
Golgi apparatus membrane 1 GPER1
Synapse 1 NR3C1
cell junction 1 EGFR
cell surface 1 EGFR
dendritic shaft 1 GPER1
glutamatergic synapse 2 CASP3, EGFR
Golgi apparatus 4 ESR1, FASN, GPER1, NFE2L2
Golgi membrane 3 EGFR, GPER1, INS
mitochondrial inner membrane 1 CYP11A1
neuronal cell body 2 CASP3, CYP17A1
presynaptic membrane 1 GPER1
Cytoplasm, cytosol 1 NFE2L2
endosome 1 EGFR
plasma membrane 6 AR, EGFR, ESR1, FASN, GPER1, NFE2L2
presynaptic active zone 1 GPER1
Membrane 10 ADIG, AR, CAT, CYP11A1, CYP19A1, EGFR, ESR1, FASN, GPER1, NR3C1
apical plasma membrane 1 EGFR
axon 2 CYP17A1, GPER1
basolateral plasma membrane 1 EGFR
extracellular exosome 3 CAT, FABP4, FASN
endoplasmic reticulum 3 CYP17A1, CYP19A1, GPER1
extracellular space 3 EGFR, IL6, INS
perinuclear region of cytoplasm 3 EGFR, GPER1, PPARG
mitochondrion 4 CAT, CYP11A1, ESR2, NR3C1
protein-containing complex 5 AR, CAT, EGFR, ESR1, NR3C1
intracellular membrane-bounded organelle 4 CAT, ESR2, GPER1, PPARG
Microsome membrane 2 CYP17A1, CYP19A1
postsynaptic density 2 CASP3, GPER1
Single-pass type I membrane protein 1 EGFR
Secreted 3 ADIG, IL6, INS
extracellular region 4 ADIG, CAT, IL6, INS
Single-pass membrane protein 1 ADIG
hippocampal mossy fiber to CA3 synapse 1 GPER1
mitochondrial matrix 3 CAT, CYP11A1, NR3C1
transcription regulator complex 1 ESR1
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 1 NR3C1
nuclear membrane 1 EGFR
nucleolus 1 GPER1
Early endosome 1 GPER1
recycling endosome 1 GPER1
Mitochondrion inner membrane 1 CYP11A1
Membrane raft 1 EGFR
Cytoplasm, cytoskeleton, spindle 1 NR3C1
focal adhesion 2 CAT, EGFR
spindle 1 NR3C1
Peroxisome 1 CAT
intracellular vesicle 1 EGFR
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
nuclear speck 2 AR, NR3C1
receptor complex 2 EGFR, PPARG
chromatin 8 AR, ESR1, ESR2, NFE2L2, NR3C1, PPARA, PPARG, THRB
mediator complex 1 NFE2L2
Chromosome 1 NR3C1
nuclear envelope 1 GPER1
endosome lumen 1 INS
Lipid droplet 2 ADIG, FABP4
Cytoplasmic vesicle membrane 1 GPER1
Nucleus, nucleoplasm 1 NR3C1
Cell projection, dendrite 1 GPER1
Melanosome 1 FASN
euchromatin 1 ESR1
basal plasma membrane 1 EGFR
synaptic membrane 1 EGFR
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 2 CAT, INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 IL6, INS
axon terminus 1 GPER1
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
clathrin-coated endocytic vesicle membrane 1 EGFR
[Isoform 1]: Nucleus 1 ESR1
protein-DNA complex 1 NFE2L2
death-inducing signaling complex 1 CASP3
keratin filament 1 GPER1
dendritic spine head 1 GPER1
Cell projection, dendritic spine membrane 1 GPER1
dendritic spine membrane 1 GPER1
[Isoform Alpha]: Cytoplasm 1 NR3C1
multivesicular body, internal vesicle lumen 1 EGFR
Shc-EGFR complex 1 EGFR
catalase complex 1 CAT
[Isoform Beta]: Nucleus 1 NR3C1
[Isoform Alpha-B]: Nucleus 1 NR3C1
interleukin-6 receptor complex 1 IL6
glycogen granule 1 FASN


文献列表

  • Yulang Chi, Lin Zhu, Yihui Wang, Cai Peng, Yi Lin, Shouping Ji, Jie Wei. Long-term Bisphenol S exposure induced gut microbiota dysbiosis, obesity, hepatic lipid accumulation, intestinal lesions and dyslipidemia in mice. Toxicology. 2024 May; 504(?):153798. doi: 10.1016/j.tox.2024.153798. [PMID: 38588857]
  • Jiali Li, Ze Li, Yaxuan Zhu, Hongyuan Peng, Zehui Du, Shaoguo Ru, Weiwei Wang. Bisphenol S remodels red blood cell membrane lipids by altering plasma lipid levels, causing the risk of venous thrombosis in SD rats and zebrafish embryos. Environment international. 2023 Dec; 182(?):108331. doi: 10.1016/j.envint.2023.108331. [PMID: 37995390]
  • Jaqueline da Silva Santos, Montcharles da Silva Pontes, Matheus Bispo de Souza, Simone Yasuda Fernandes, Ricardo Antunes Azevedo, Gilberto José de Arruda, Etenaldo Felipe Santiago. Toxicity of bisphenol A (BPA) and its analogues BPF and BPS on the free-floating macrophyte Salvinia biloba. Chemosphere. 2023 Dec; 343(?):140235. doi: 10.1016/j.chemosphere.2023.140235. [PMID: 37734497]
  • Ze Li, Shaoguo Ru, Jiali Li, Yunjia Yang, Weiwei Wang. Continuous exposure to bisphenol S increases the accumulation of endogenous metabolic toxicants by obstructing the glucuronic acid pathway. Environmental pollution (Barking, Essex : 1987). 2023 Sep; 336(?):122433. doi: 10.1016/j.envpol.2023.122433. [PMID: 37659633]
  • Rui Zhang, Jingyao Guo, Yupeng Wang, Rundong Sun, Guangzhu Dong, Xinru Wang, Guizhen Du. Prenatal bisphenol S exposure induces hepatic lipid deposition in male mice offspring through downregulation of adipose-derived exosomal miR-29a-3p. Journal of hazardous materials. 2023 07; 453(?):131410. doi: 10.1016/j.jhazmat.2023.131410. [PMID: 37088024]
  • Radha D Singh, Jessica L Wager, Taylor B Scheidl, Liam T Connors, Sarah H Easson, Mikyla A Callaghan, Samuel Alatorre-Hinojosa, Lucy H Swift, Pina Colarusso, Anshul Jadli, Tim Shutt, Vaibhav Patel, Jennifer Thompson. Potentiation of Adipogenesis by Reactive Oxygen Species is a Unifying Mechanism in the Pro-adipogenic Properties of Bisphenol A and its New Structural Analogues. Antioxidants & redox signaling. 2023 May; ?(?):. doi: 10.1089/ars.2022.0150. [PMID: 37154733]
  • Yiguang Qian, Zhiwei Ye, Yueyue Wu, Dingxin Wang, Xintong Xie, Tengda Ding, Lili Zhang, Juying Li. Bioaccumulation, internal distribution and toxicity of bisphenol S in the earthworm Eisenia fetida. The Science of the total environment. 2023 Apr; 867(?):161169. doi: 10.1016/j.scitotenv.2022.161169. [PMID: 36581266]
  • Elize A Santos Musachio, Marcia Rósula Poetini, Dieniffer Espinosa Janner, Eliana Jardim Fernandes, Luana Barreto Meichtry, Mustafa Munir Mustafa Dahleh, Gustavo Petri Guerra, Marina Prigol. Safer alternatives? Bisphenol F and Bisphenol S induce oxidative stress in Drosophila melanogaster larvae and trigger developmental damage. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2023 Feb; ?(?):113701. doi: 10.1016/j.fct.2023.113701. [PMID: 36863561]
  • Xindong Yang, Juan Wu, Qinghua Zhou, Haofeng Zhu, Anping Zhang, Jianqiang Sun, Jay Gan. Congener-Specific Uptake and Metabolism of Bisphenols in Carrot Cells: Dissipation Kinetics, Biotransformation, and Enzyme Responses. Journal of agricultural and food chemistry. 2023 Feb; 71(4):1896-1906. doi: 10.1021/acs.jafc.2c08197. [PMID: 36649116]
  • Yanan Pan, Liqiao Han, Xiang Chen, Xin Wei, Xiaoyue Zhou, Dingshan Liang, Renli Yin, Xiaoyang Jiao, Huashou Li, Adela Jing Li, Rongliang Qiu. Occurrence of emerging bisphenol S analogues in urine from five occupational populations in South China. Environment international. 2023 02; 172(?):107773. doi: 10.1016/j.envint.2023.107773. [PMID: 36736027]
  • Weiwei Wang, Ze Li, Xiaona Zhang, Jie Zhang, Shaoguo Ru. Bisphenol S Impairs Behaviors through Disturbing Endoplasmic Reticulum Function and Reducing Lipid Levels in the Brain of Zebrafish. Environmental science & technology. 2023 01; 57(1):582-594. doi: 10.1021/acs.est.2c07828. [PMID: 36520979]
  • Muhammad Muddassir Ali, Areej Fatima, Sadia Nawaz, Abdul Rehman, Maryam Javed, Asif Nadeem. Cytotoxic and genotoxic evaluation of bisphenol S on onion root tips by Allium cepa and comet tests. Environmental science and pollution research international. 2022 Dec; 29(59):88803-88811. doi: 10.1007/s11356-022-21888-2. [PMID: 35836054]
  • Ying Han, Yuxuan Liu, Mingxin Wang, Yingang Xue. Effects of BPZ, BPC, BPF, and BPS Exposure on Adult Zebrafish (Danio rerio): Accumulation, Oxidative Stress, and Gene Expression. International journal of environmental research and public health. 2022 11; 19(23):. doi: 10.3390/ijerph192315784. [PMID: 36497860]
  • Zhen Liu, Shuying Pan, Fei Xu, Zhiwei Wang, Chao Zhao, Xing Xu, Baoyu Gao, Qian Li. Revealing the fundamental role of MoO2 in promoting efficient and stable activation of persulfate by iron carbon based catalysts: Efficient Fe2+/Fe3+ cycling to generate reactive species. Water research. 2022 Oct; 225(?):119142. doi: 10.1016/j.watres.2022.119142. [PMID: 36179430]
  • Liping Hao, Shaoguo Ru, Jingyu Qin, Weiwei Wang, Jie Zhang, Shuhui Wei, Jun Wang, Xiaona Zhang. Transgenerational effects of parental bisphenol S exposure on zebrafish (Danio rerio) reproduction. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2022 Jul; 165(?):113142. doi: 10.1016/j.fct.2022.113142. [PMID: 35595038]
  • Kapil Mandrah, Veena Jain, Shagun Shukla, Jamal Ahmad Ansari, Pankaj Jagdale, Anjaneya Ayanur, Vikas Srivastava, Somendu Kumar Roy. A study on bisphenol S induced nephrotoxicity and assessment of altered downstream kidney metabolites using gas chromatography-mass spectrometry based metabolomics. Environmental toxicology and pharmacology. 2022 Jul; 93(?):103883. doi: 10.1016/j.etap.2022.103883. [PMID: 35550874]
  • Iris Reina-Pérez, Alicia Olivas-Martínez, Vicente Mustieles, Elena Salamanca-Fernández, José Manuel Molina-Molina, Nicolás Olea, Mariana F Fernández. The Mixture of Bisphenol-A and Its Substitutes Bisphenol-S and Bisphenol-F Exerts Obesogenic Activity on Human Adipose-Derived Stem Cells. Toxics. 2022 May; 10(6):. doi: 10.3390/toxics10060287. [PMID: 35736896]
  • Melanie A Rehder Silinski, Brenda L Fletcher, Reshan A Fernando, Veronica G Robinson, Suramya Waidyanatha. Development and Validation of an Analytical Method for Quantitation of Bisphenol S in Rodent Plasma, Amniotic Fluid and Fetuses by UPLC-MS-MS. Journal of analytical toxicology. 2022 Mar; 46(3):277-284. doi: 10.1093/jat/bkab008. [PMID: 33512500]
  • Weiwei Wang, Jie Zhang, Ze Li, Jie Gu, Jingyu Qin, Jiali Li, Xiaona Zhang, Shaoguo Ru. Bisphenol S exposure accelerates the progression of atherosclerosis in zebrafish embryo-larvae. Journal of hazardous materials. 2022 03; 426(?):128042. doi: 10.1016/j.jhazmat.2021.128042. [PMID: 34942454]
  • Weili Mao, Lingling Mao, Nan Zhao, Yingying Zhang, Meirong Zhao, Hangbiao Jin. Disposition of Bisphenol S metabolites in Sprague-Dawley rats. The Science of the total environment. 2022 Mar; 811(?):152288. doi: 10.1016/j.scitotenv.2021.152288. [PMID: 34902425]
  • S Irem Kaya, M Emin Corman, Lokman Uzun, Sibel A Ozkan. A porous molecularly imprinted electrochemical sensor for specific determination of bisphenol S from human serum and bottled water samples in femtomolar level. Analytical and bioanalytical chemistry. 2022 Mar; 414(8):2775-2785. doi: 10.1007/s00216-022-03928-5. [PMID: 35112148]
  • Min Jang, Hyemin Yang, Huichan Lee, Kwang Seon Lee, Joo Yeon Oh, Hyeonyeol Jeon, Yong Sik Ok, Sung Yeon Hwang, Jeyoung Park, Dongyeop X Oh. A sensitive environmental forensic method that determines bisphenol S and A exposure within receipt-handling through fingerprint analysis. Journal of hazardous materials. 2022 02; 424(Pt B):127410. doi: 10.1016/j.jhazmat.2021.127410. [PMID: 34634704]
  • Yun Jeong Lee, Youn-Hee Lim, Choong Ho Shin, Bung-Nyun Kim, Johanna Inhyang Kim, Yun-Chul Hong, Yong Min Cho, Young Ah Lee. Relationship between bisphenol A, bisphenol S, and bisphenol F and serum uric acid concentrations among school-aged children. PloS one. 2022; 17(6):e0268503. doi: 10.1371/journal.pone.0268503. [PMID: 35709251]
  • Alice Desmarchais, Ophélie Téteau, Nathalie Kasal-Hoc, Juliette Cognié, Olivier Lasserre, Pascal Papillier, Marlène Lacroix, Claire Vignault, Peggy Jarrier-Gaillard, Virginie Maillard, Aurélien Binet, Maria-Teresa Pellicer-Rubio, Sandrine Fréret, Sebastien Elis. Chronic low BPS exposure through diet impairs in vitro embryo production parameters according to metabolic status in the ewe. Ecotoxicology and environmental safety. 2022 Jan; 229(?):113096. doi: 10.1016/j.ecoenv.2021.113096. [PMID: 34952380]
  • Ophélie Téteau, Philippe Liere, Antoine Pianos, Alice Desmarchais, Olivier Lasserre, Pascal Papillier, Claire Vignault, Marie-Emilie Lebachelier de la Riviere, Virginie Maillard, Aurélien Binet, Svetlana Uzbekova, Marie Saint-Dizier, Sebastien Elis. Bisphenol S Alters the Steroidome in the Preovulatory Follicle, Oviduct Fluid and Plasma in Ewes With Contrasted Metabolic Status. Frontiers in endocrinology. 2022; 13(?):892213. doi: 10.3389/fendo.2022.892213. [PMID: 35685208]
  • Xinghua Zhou, Jie Li, Xiaowei Zhang, Caiqin Zhang, Juan Bai, Yansheng Zhao, Ying Zhu, Jiayan Zhang, Xiang Xiao. Bisphenol S promotes fat storage in multiple generations of Caenorhabditis elegans in a daf-16/nhr-49 dependent manner. Comparative biochemistry and physiology. Toxicology & pharmacology : CBP. 2021 Dec; 250(?):109175. doi: 10.1016/j.cbpc.2021.109175. [PMID: 34464736]
  • Marilin Profita, Elena Fabbri, Enzo Spisni, Paola Valbonesi. Comparing effects and action mechanisms of BPA and BPS on HTR-8/SVneo placental cells†. Biology of reproduction. 2021 11; 105(5):1355-1364. doi: 10.1093/biolre/ioab139. [PMID: 34270681]
  • Alexandra Schaffert, Laura Krieg, Juliane Weiner, Rita Schlichting, Elke Ueberham, Isabel Karkossa, Mario Bauer, Kathrin Landgraf, Kristin M Junge, Martin Wabitsch, Jörg Lehmann, Beate I Escher, Ana C Zenclussen, Antje Körner, Matthias Blüher, John T Heiker, Martin von Bergen, Kristin Schubert. Alternatives for the worse: Molecular insights into adverse effects of bisphenol a and substitutes during human adipocyte differentiation. Environment international. 2021 11; 156(?):106730. doi: 10.1016/j.envint.2021.106730. [PMID: 34186270]
  • Haiyan An, Henan Yu, Yibo Wei, Feng Liu, Jinshao Ye. Disrupted metabolic pathways and potential human diseases induced by bisphenol S. Environmental toxicology and pharmacology. 2021 Nov; 88(?):103751. doi: 10.1016/j.etap.2021.103751. [PMID: 34624477]
  • Kangyu Hao, Jia Luo, Jing Sun, Honghan Ge, Zhaoguo Wang. Associations of urinary bisphenol A and its alternatives bisphenol S and F concentrations with depressive symptoms among adults. Chemosphere. 2021 Sep; 279(?):130573. doi: 10.1016/j.chemosphere.2021.130573. [PMID: 33878692]
  • Yu Zhang, Vicente Mustieles, Paige L Williams, Jennifer Yland, Irene Souter, Joseph M Braun, Antonia M Calafat, Russ Hauser, Carmen Messerlian. Prenatal urinary concentrations of phenols and risk of preterm birth: exploring windows of vulnerability. Fertility and sterility. 2021 09; 116(3):820-832. doi: 10.1016/j.fertnstert.2021.03.053. [PMID: 34238571]
  • Angela Christina Saleh, Reem Sabry, Gabriela Fabiana Mastromonaco, Laura Alessandra Favetta. BPA and BPS affect the expression of anti-Mullerian hormone (AMH) and its receptor during bovine oocyte maturation and early embryo development. Reproductive biology and endocrinology : RB&E. 2021 Aug; 19(1):119. doi: 10.1186/s12958-021-00773-6. [PMID: 34344364]
  • Jing-Yu Qin, Shaoguo Ru, Weiwei Wang, Liping Hao, Shuhui Wei, Jie Zhang, Jiu-Qiang Xiong, Jun Wang, Xiaona Zhang. Unraveling the mechanism of long-term bisphenol S exposure disrupted ovarian lipids metabolism, oocytes maturation, and offspring development of zebrafish. Chemosphere. 2021 Aug; 277(?):130304. doi: 10.1016/j.chemosphere.2021.130304. [PMID: 33798965]
  • S Shehna Mahim, V R Anjali, V S Remya, S Reshmi, C Aruna Devi. Oxidative stress responses of a freshwater fish, Labeo rohita, to a xenobiotic, bisphenol S. Journal of biochemical and molecular toxicology. 2021 Aug; 35(8):e22820. doi: 10.1002/jbt.22820. [PMID: 34075651]
  • Fatma Eldefrawy, Hannah Shibo Xu, Elizabeth Pusch, Ashraf Karkoura, Mohamed Alsafy, Samir Elgendy, Susan M Williams, Kristen Navara, Tai L Guo. Modulation of folliculogenesis in adult laying chickens by bisphenol A and bisphenol S: Perspectives on ovarian morphology and gene expression. Reproductive toxicology (Elmsford, N.Y.). 2021 08; 103(?):181-190. doi: 10.1016/j.reprotox.2021.06.010. [PMID: 34147626]
  • Lingling Mao, Shuhong Fang, Meirong Zhao, Weiping Liu, Hangbiao Jin. Effects of Bisphenol A and Bisphenol S Exposure at Low Doses on the Metabolome of Adolescent Male Sprague-Dawley Rats. Chemical research in toxicology. 2021 06; 34(6):1578-1587. doi: 10.1021/acs.chemrestox.1c00018. [PMID: 34019419]
  • Iris Reina-Pérez, Alicia Olivas-Martínez, Vicente Mustieles, Francisco Javier Ruiz-Ojeda, José Manuel Molina-Molina, Nicolás Olea, Mariana F Fernández. Bisphenol F and bisphenol S promote lipid accumulation and adipogenesis in human adipose-derived stem cells. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2021 Jun; 152(?):112216. doi: 10.1016/j.fct.2021.112216. [PMID: 33865937]
  • Ashish Kumar Sonker, Manisha Bhateria, Kajal Karsauliya, Sheelendra Pratap Singh. Investigating the glucuronidation and sulfation pathways contribution and disposition kinetics of Bisphenol S and its metabolites using LC-MS/MS-based nonenzymatic hydrolysis method. Chemosphere. 2021 Jun; 273(?):129624. doi: 10.1016/j.chemosphere.2021.129624. [PMID: 33515962]
  • Chalana M Sol, Charissa van Zwol-Janssens, Elise M Philips, Alexandros G Asimakopoulos, Maria-Pilar Martinez-Moral, Kurunthachalam Kannan, Vincent W V Jaddoe, Leonardo Trasande, Susana Santos. Maternal bisphenol urine concentrations, fetal growth and adverse birth outcomes: A population-based prospective cohort. Environmental health : a global access science source. 2021 05; 20(1):60. doi: 10.1186/s12940-021-00747-6. [PMID: 33992119]
  • Cindy Peillex, Anthony Kerever, Asmaa Lachhab, Martin Pelletier. Bisphenol A, bisphenol S and their glucuronidated metabolites modulate glycolysis and functional responses of human neutrophils. Environmental research. 2021 05; 196(?):110336. doi: 10.1016/j.envres.2020.110336. [PMID: 33091430]
  • Hizb Ullah, Faizan Ullah, Owais Rehman, Sarwat Jahan, Tayyaba Afsar, Dara Al-Disi, Ali Almajwal, Suhail Razak. Chronic exposure of bisphenol S (BPS) affect hypothalamic-pituitary-testicular activities in adult male rats: possible in estrogenic mode of action. Environmental health and preventive medicine. 2021 Mar; 26(1):31. doi: 10.1186/s12199-021-00954-0. [PMID: 33678156]
  • Jitendra Kumar, Rakesh Verma, Chandana Haldar. Melatonin ameliorates Bisphenol S induced testicular damages by modulating Nrf-2/HO-1 and SIRT-1/FOXO-1 expressions. Environmental toxicology. 2021 Mar; 36(3):396-407. doi: 10.1002/tox.23045. [PMID: 33098627]
  • Xiang Xiao, Xiaowei Zhang, Juan Bai, Jie Li, Caiqin Zhang, Yansheng Zhao, Ying Zhu, Jiayan Zhang, Xinghua Zhou. Bisphenol S increases the obesogenic effects of a high-glucose diet through regulating lipid metabolism in Caenorhabditis elegans. Food chemistry. 2021 Mar; 339(?):127813. doi: 10.1016/j.foodchem.2020.127813. [PMID: 32916401]
  • Lesliam Quirós-Alcalá, Nadia N Hansel, Meredith McCormack, Antonia M Calafat, Xiaoyun Ye, Roger D Peng, Elizabeth C Matsui. Exposure to bisphenols and asthma morbidity among low-income urban children with asthma. The Journal of allergy and clinical immunology. 2021 02; 147(2):577-586.e7. doi: 10.1016/j.jaci.2020.05.031. [PMID: 32736870]
  • Axelle Brulport, Ludovic Le Corre, Guillaume Maquart, Virginie Barbet, Aurélie Dastugue, Isabelle Severin, Daniel Vaiman, Marie-Christine Chagnon. Multigenerational study of the obesogen effects of bisphenol S after a perinatal exposure in C57BL6/J mice fed a high fat diet. Environmental pollution (Barking, Essex : 1987). 2021 Feb; 270(?):116243. doi: 10.1016/j.envpol.2020.116243. [PMID: 33326921]
  • Suramya Waidyanatha, Sherry R Black, Claire R Croutch, Bradley J Collins, Melanie A R Silinski, Season Kerns, Vicki Sutherland, Veronica G Robinson, Kristin Aillon, Reshan A Fernando, Esra Mutlu, Timothy R Fennell. Comparative toxicokinetics of bisphenol S and bisphenol AF in male rats and mice following repeated exposure via feed. Xenobiotica; the fate of foreign compounds in biological systems. 2021 Feb; 51(2):210-221. doi: 10.1080/00498254.2020.1829171. [PMID: 32985913]
  • Jeremy Gingrich, David Filipovic, Rory Conolly, Sudin Bhattacharya, Almudena Veiga-Lopez. Pregnancy-specific physiologically-based toxicokinetic models for bisphenol A and bisphenol S. Environment international. 2021 02; 147(?):106301. doi: 10.1016/j.envint.2020.106301. [PMID: 33360411]
  • Gillian England-Mason, Jiaying Liu, Jonathan W Martin, Gerald F Giesbrecht, Nicole Letourneau, Deborah Dewey. Postnatal BPA is associated with increasing executive function difficulties in preschool children. Pediatric research. 2021 02; 89(3):686-693. doi: 10.1038/s41390-020-0922-6. [PMID: 32408341]
  • Y Y Gu, Y Mei, Y M Ren, J Han. [Determination of bisphenol S in urine by vortex-assisted liquid-liquid microextraction with high performance liquid chromatography]. Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases. 2021 Jan; 39(1):51-54. doi: 10.3760/cma.j.cn121094-20191010-00484. [PMID: 33535342]
  • Jun Zeng, Junli Li, Sishangyu Liu, Zhiqiang Yang, Yue Zhong, Xiaomei Chen, Guiling Li, Jia Li. Lipidome disturbances in preadipocyte differentiation associated with bisphenol A and replacement bisphenol S exposure. The Science of the total environment. 2021 Jan; 753(?):141949. doi: 10.1016/j.scitotenv.2020.141949. [PMID: 32891999]
  • Matthew V Gomez, Moumita Dutta, Alexander Suvorov, Xiaojian Shi, Haiwei Gu, Sridhar Mani, Julia Yue Cui. Early Life Exposure to Environmental Contaminants (BDE-47, TBBPA, and BPS) Produced Persistent Alterations in Fecal Microbiome in Adult Male Mice. Toxicological sciences : an official journal of the Society of Toxicology. 2021 01; 179(1):14-30. doi: 10.1093/toxsci/kfaa161. [PMID: 33078840]
  • Marta Diana Komarowska, Kamil Grubczak, Jan Czerniecki, Adam Hermanowicz, Justyna Magdalena Hermanowicz, Wojciech Debek, Ewa Matuszczak. Identification of the Bisphenol A (BPA) and the Two Analogues BPS and BPF in Cryptorchidism. Frontiers in endocrinology. 2021; 12(?):694669. doi: 10.3389/fendo.2021.694669. [PMID: 34335471]
  • Giada Frenzilli, Joan Martorell-Ribera, Margherita Bernardeschi, Vittoria Scarcelli, Elisabeth Jönsson, Nadia Diano, Martina Moggio, Patrizia Guidi, Joachim Sturve, Noomi Asker. Bisphenol A and Bisphenol S Induce Endocrine and Chromosomal Alterations in Brown Trout. Frontiers in endocrinology. 2021; 12(?):645519. doi: 10.3389/fendo.2021.645519. [PMID: 33776939]
  • Axelle Brulport, Corinne Lencina, Marie-Christine Chagnon, Ludovic Le Corre, Laurence Guzylack-Piriou. Transgenerational effects on intestinal inflammation status in mice perinatally exposed to bisphenol S. Chemosphere. 2021 Jan; 262(?):128009. doi: 10.1016/j.chemosphere.2020.128009. [PMID: 33182144]
  • Lulin Wang, Lulu Song, Bingqing Liu, Mingyang Wu, Yunyun Liu, Jianing Bi, Qing Liu, Kai Chen, Zhongqiang Cao, Shunqing Xu, Aifen Zhou, Yaohua Tian, Youjie Wang. Prenatal exposure to bisphenol S and altered newborn mitochondrial DNA copy number in a baby cohort study: Sex-specific associations. Chemosphere. 2021 Jan; 263(?):128019. doi: 10.1016/j.chemosphere.2020.128019. [PMID: 33297043]
  • Yoonyoung Jang, Yoon-Jung Choi, Youn-Hee Lim, Kyung-Shin Lee, Bung-Nyun Kim, Choong Ho Shin, Young Ah Lee, Johanna Inhyang Kim, Yun-Chul Hong. Associations Between Thyroid Hormone Levels and Urinary Concentrations of Bisphenol A, F, and S in 6-Year-old Children in Korea. Journal of preventive medicine and public health = Yebang Uihakhoe chi. 2021 Jan; 54(1):37-45. doi: 10.3961/jpmph.20.310. [PMID: 33618498]
  • Axelle Brulport, Daniel Vaiman, Elias Bou-Maroun, Marie-Christine Chagnon, Ludovic Le Corre. Hepatic transcriptome and DNA methylation patterns following perinatal and chronic BPS exposure in male mice. BMC genomics. 2020 Dec; 21(1):881. doi: 10.1186/s12864-020-07294-3. [PMID: 33297965]
  • Sunmi Kim, Inae Lee, Jae-Eun Lim, Aram Lee, Hyo-Bang Moon, Jeongim Park, Kyungho Choi. Dietary contribution to body burden of bisphenol A and bisphenol S among mother-children pairs. The Science of the total environment. 2020 Nov; 744(?):140856. doi: 10.1016/j.scitotenv.2020.140856. [PMID: 32721674]
  • Suramya Waidyanatha, Sherry R Black, Melanie Silinski, Vicki Sutherland, Brenda L Fletcher, Reshan A Fernando, Timothy R Fennell. Comparative toxicokinetics of bisphenol S in rats and mice following gavage administration. Toxicology and applied pharmacology. 2020 11; 406(?):115207. doi: 10.1016/j.taap.2020.115207. [PMID: 32853628]
  • Min Jeong Jo, Jae-Hong Park, Kyung-A An, Heeju Choi, Yun-Sook Kang, Myungsil Hwang. Quantification of bisphenols in Korean urine using online solid-phase extraction-high-performance liquid chromatography-tandem mass spectrometry. Environmental toxicology and pharmacology. 2020 Nov; 80(?):103491. doi: 10.1016/j.etap.2020.103491. [PMID: 32942124]
  • Fan Liang, Xiaona Huo, Wei Wang, Yan Li, Jun Zhang, Yan Feng, Yan Wang. Association of bisphenol A or bisphenol S exposure with oxidative stress and immune disturbance among unexplained recurrent spontaneous abortion women. Chemosphere. 2020 Oct; 257(?):127035. doi: 10.1016/j.chemosphere.2020.127035. [PMID: 32702804]
  • Yann Malaisé, Corinne Lencina, Christel Cartier, Maïwenn Olier, Sandrine Ménard, Laurence Guzylack-Piriou. Perinatal oral exposure to low doses of bisphenol A, S or F impairs immune functions at intestinal and systemic levels in female offspring mice. Environmental health : a global access science source. 2020 08; 19(1):93. doi: 10.1186/s12940-020-00614-w. [PMID: 32867778]
  • Jingyu Qin, Shaoguo Ru, Weiwei Wang, Liping Hao, Yiran Ru, Jun Wang, Xiaona Zhang. Long-term bisphenol S exposure aggravates non-alcoholic fatty liver by regulating lipid metabolism and inducing endoplasmic reticulum stress response with activation of unfolded protein response in male zebrafish. Environmental pollution (Barking, Essex : 1987). 2020 Aug; 263(Pt B):114535. doi: 10.1016/j.envpol.2020.114535. [PMID: 32283406]
  • Jun Liang, Shun Liu, Tao Liu, Chunxiu Yang, Yanan Wu, Hui Juan Jennifer Tan, Bincai Wei, Xiaoyun Ma, Baoying Feng, Qunjiao Jiang, Dongping Huang, Xiaoqiang Qiu. Association of prenatal exposure to bisphenols and birth size in Zhuang ethnic newborns. Chemosphere. 2020 Aug; 252(?):126422. doi: 10.1016/j.chemosphere.2020.126422. [PMID: 32199162]
  • Chunfeng Xie, Miaomiao Ge, Jianliang Jin, Haie Xu, Li Mao, Shanshan Geng, Jieshu Wu, Jianyun Zhu, Xiaoting Li, Caiyun Zhong. Mechanism investigation on Bisphenol S-induced oxidative stress and inflammation in murine RAW264.7 cells: The role of NLRP3 inflammasome, TLR4, Nrf2 and MAPK. Journal of hazardous materials. 2020 07; 394(?):122549. doi: 10.1016/j.jhazmat.2020.122549. [PMID: 32283380]
  • Kapil Mandrah, Veena Jain, Jamal Ahmad Ansari, Somendu Kumar Roy. Metabolomic perturbation precedes glycolytic dysfunction and procreates hyperglycemia in a rat model due to bisphenol S exposure. Environmental toxicology and pharmacology. 2020 Jul; 77(?):103372. doi: 10.1016/j.etap.2020.103372. [PMID: 32203925]
  • Yin-Feng Zhang, Chan Shan, Yu Wang, Li-Li Qian, Dong-Dong Jia, Yi-Fei Zhang, Xiao-Dan Hao, Hai-Ming Xu. Cardiovascular toxicity and mechanism of bisphenol A and emerging risk of bisphenol S. The Science of the total environment. 2020 Jun; 723(?):137952. doi: 10.1016/j.scitotenv.2020.137952. [PMID: 32213405]
  • Weiwei Wang, Shaoguo Ru, Liangliang Wang, Jingyu Qin, Yiran Ru, Jie Zhang, Xiaona Zhang. Bisphenol S Induces Ectopic Angiogenesis in Embryos via VEGFR2 Signaling, Leading to Lipid Deposition in Blood Vessels of Larval Zebrafish. Environmental science & technology. 2020 06; 54(11):6822-6831. doi: 10.1021/acs.est.9b07080. [PMID: 32348130]
  • M Á Martínez, J Blanco, J Rovira, V Kumar, J L Domingo, M Schuhmacher. Bisphenol A analogues (BPS and BPF) present a greater obesogenic capacity in 3T3-L1 cell line. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2020 Jun; 140(?):111298. doi: 10.1016/j.fct.2020.111298. [PMID: 32220626]
  • Cecilie N Ramskov Tetzlaff, Terje Svingen, Anne M Vinggaard, Anna K Rosenmai, Camilla Taxvig. Bisphenols B, E, F, and S and 4-cumylphenol induce lipid accumulation in mouse adipocytes similarly to bisphenol A. Environmental toxicology. 2020 May; 35(5):543-552. doi: 10.1002/tox.22889. [PMID: 31820560]
  • Hua Zhang, Qiang Quan, Mingyue Zhang, Nan Zhang, Wu Zhang, Meixiao Zhan, Weiguo Xu, Ligong Lu, Jun Fan, Qian Wang. Occurrence of bisphenol A and its alternatives in paired urine and indoor dust from Chinese university students: Implications for human exposure. Chemosphere. 2020 May; 247(?):125987. doi: 10.1016/j.chemosphere.2020.125987. [PMID: 32069736]
  • Yangqian Jiang, Jiufeng Li, Shunqing Xu, Yanqiu Zhou, Hongzhi Zhao, Yuanyuan Li, Chao Xiong, Xiaojie Sun, Hongxiu Liu, Wenyu Liu, Yang Peng, Chen Hu, Zongwei Cai, Wei Xia. Prenatal exposure to bisphenol A and its alternatives and child neurodevelopment at 2 years. Journal of hazardous materials. 2020 04; 388(?):121774. doi: 10.1016/j.jhazmat.2019.121774. [PMID: 32001102]
  • Wei Huang, Lin Zhu, Chao Zhao, Xiangfeng Chen, Zongwei Cai. Integration of proteomics and metabolomics reveals promotion of proliferation by exposure of bisphenol S in human breast epithelial MCF-10A cells. The Science of the total environment. 2020 Apr; 712(?):136453. doi: 10.1016/j.scitotenv.2019.136453. [PMID: 31945527]
  • Angelico Mendy, Pӓivi M Salo, Jesse Wilkerson, Lydia Feinstein, Kelly K Ferguson, Michael B Fessler, Peter S Thorne, Darryl C Zeldin. Association of urinary levels of bisphenols F and S used as bisphenol A substitutes with asthma and hay fever outcomes. Environmental research. 2020 04; 183(?):108944. doi: 10.1016/j.envres.2019.108944. [PMID: 31911000]
  • Cecile Karrer, Monica Andreassen, Natalie von Goetz, Friederike Sonnet, Amrit Kaur Sakhi, Konrad Hungerbühler, Hubert Dirven, Trine Husøy. The EuroMix human biomonitoring study: Source-to-dose modeling of cumulative and aggregate exposure for the bisphenols BPA, BPS, and BPF and comparison with measured urinary levels. Environment international. 2020 03; 136(?):105397. doi: 10.1016/j.envint.2019.105397. [PMID: 31884417]
  • Lara Ferreira Azevedo, Maria Fernanda Hornos Carneiro, Carlos Roberto Porto Dechandt, Juliana Silva Cassoli, Luciane Carla Alberici, Fernando Barbosa. Global liver proteomic analysis of Wistar rats chronically exposed to low-levels of bisphenol A and S. Environmental research. 2020 03; 182(?):109080. doi: 10.1016/j.envres.2019.109080. [PMID: 31901629]
  • Francisco M Peinado, Inmaculada Lendínez, Rafael Sotelo, Luz M Iribarne-Durán, Jorge Fernández-Parra, Fernando Vela-Soria, Nicolás Olea, Mariana F Fernández, Carmen Freire, Josefa León, Beatriz Pérez-Cabrera, Olga Ocón-Hernández, Francisco Artacho-Cordón. Association of Urinary Levels of Bisphenols A, F, and S with Endometriosis Risk: Preliminary Results of the EndEA Study. International journal of environmental research and public health. 2020 02; 17(4):. doi: 10.3390/ijerph17041194. [PMID: 32069886]
  • Chao Zhao, Ting Yong, Yinbin Zhang, Yaofeng Jin, Yu Xiao, Hailin Wang, Bin Zhao, Zongwei Cai. Evaluation of the splenic injury following exposure of mice to bisphenol S: A mass spectrometry-based lipidomics and imaging analysis. Environment international. 2020 02; 135(?):105378. doi: 10.1016/j.envint.2019.105378. [PMID: 31838264]
  • Axelle Brulport, Daniel Vaiman, Marie-Christine Chagnon, Ludovic Le Corre. Obesogen effect of bisphenol S alters mRNA expression and DNA methylation profiling in male mouse liver. Chemosphere. 2020 Feb; 241(?):125092. doi: 10.1016/j.chemosphere.2019.125092. [PMID: 31683443]
  • Elise M Philips, Susana Santos, Eric A P Steegers, Alexandros G Asimakopoulos, Kurunthachalam Kannan, Leonardo Trasande, Vincent W V Jaddoe. Maternal bisphenol and phthalate urine concentrations and weight gain during pregnancy. Environment international. 2020 02; 135(?):105342. doi: 10.1016/j.envint.2019.105342. [PMID: 31864031]
  • Beata Wyżga, Karolina Połeć, Karolina Olechowska, Katarzyna Hąc-Wydro. The impact of toxic bisphenols on model human erythrocyte membranes. Colloids and surfaces. B, Biointerfaces. 2020 Feb; 186(?):110670. doi: 10.1016/j.colsurfb.2019.110670. [PMID: 31812800]
  • Eurídice Martínez Steele, Neha Khandpur, Maria Laura da Costa Louzada, Carlos Augusto Monteiro. Association between dietary contribution of ultra-processed foods and urinary concentrations of phthalates and bisphenol in a nationally representative sample of the US population aged 6 years and older. PloS one. 2020; 15(7):e0236738. doi: 10.1371/journal.pone.0236738. [PMID: 32735599]
  • Saman Ijaz, Asad Ullah, Ghazala Shaheen, Sarwat Jahan. Exposure of BPA and its alternatives like BPB, BPF, and BPS impair subsequent reproductive potentials in adult female Sprague Dawley rats. Toxicology mechanisms and methods. 2020 Jan; 30(1):60-72. doi: 10.1080/15376516.2019.1652873. [PMID: 31424294]
  • Pingshi Gao, Lei Wang, Nanfei Yang, Jingjing Wen, Mengshu Zhao, Guanyong Su, Jianfa Zhang, Dan Weng. Peroxisome proliferator-activated receptor gamma (PPARγ) activation and metabolism disturbance induced by bisphenol A and its replacement analog bisphenol S using in vitro macrophages and in vivo mouse models. Environment international. 2020 01; 134(?):105328. doi: 10.1016/j.envint.2019.105328. [PMID: 31778932]
  • Hanne Frederiksen, Ole Nielsen, Holger M Koch, Niels E Skakkebaek, Anders Juul, Niels Jørgensen, Anna-Maria Andersson. Changes in urinary excretion of phthalates, phthalate substitutes, bisphenols and other polychlorinated and phenolic substances in young Danish men; 2009-2017. International journal of hygiene and environmental health. 2020 01; 223(1):93-105. doi: 10.1016/j.ijheh.2019.10.002. [PMID: 31669154]
  • Véronique Gayrard, Marlène Z Lacroix, Clémence A Gély, Flore C Grandin, Roger Léandri, Michèle Bouchard, Béatrice Roques, Pierre-Louis Toutain, Nicole Picard-Hagen. Toxicokinetics of bisphenol S in rats for predicting human bisphenol S clearance from allometric scaling. Toxicology and applied pharmacology. 2020 01; 386(?):114845. doi: 10.1016/j.taap.2019.114845. [PMID: 31786412]
  • Yue Shen, Tingyan Liu, Yuanyuan Shi, Feng Zhuang, Jianxin Lu, Qiuyu Zhu, Feng Ding. Bisphenol A analogs in patients with chronic kidney disease and dialysis therapy. Ecotoxicology and environmental safety. 2019 Dec; 185(?):109684. doi: 10.1016/j.ecoenv.2019.109684. [PMID: 31541948]
  • Arash Derakhshan, Huan Shu, Robin P Peeters, Andreas Kortenkamp, Christian H Lindh, Barbara Demeneix, Carl-Gustaf Bornehag, Tim I M Korevaar. Association of urinary bisphenols and triclosan with thyroid function during early pregnancy. Environment international. 2019 12; 133(Pt A):105123. doi: 10.1016/j.envint.2019.105123. [PMID: 31521814]
  • Sha Huang, Jiufeng Li, Shunqing Xu, Hongzhi Zhao, Yuanyuan Li, Yanqiu Zhou, Jing Fang, Jiaqiang Liao, Zongwei Cai, Wei Xia. Bisphenol A and bisphenol S exposures during pregnancy and gestational age - A longitudinal study in China. Chemosphere. 2019 Dec; 237(?):124426. doi: 10.1016/j.chemosphere.2019.124426. [PMID: 31362131]
  • Ramy Abou Ghayda, Paige L Williams, Jorge E Chavarro, Jennifer B Ford, Irene Souter, Antonia M Calafat, Russ Hauser, Lidia Mínguez-Alarcón. Urinary bisphenol S concentrations: Potential predictors of and associations with semen quality parameters among men attending a fertility center. Environment international. 2019 10; 131(?):105050. doi: 10.1016/j.envint.2019.105050. [PMID: 31376593]
  • Fanny Rancière, Jérémie Botton, Rémy Slama, Marlène Z Lacroix, Laurent Debrauwer, Marie Aline Charles, Ronan Roussel, Beverley Balkau, Dianna J Magliano. Exposure to Bisphenol A and Bisphenol S and Incident Type 2 Diabetes: A Case-Cohort Study in the French Cohort D.E.S.I.R. Environmental health perspectives. 2019 10; 127(10):107013. doi: 10.1289/ehp5159. [PMID: 31663775]
  • Lara Ferreira Azevedo, Carlos Roberto Porto Dechandt, Cecília Cristina de Souza Rocha, Maria Fernanda Hornos Carneiro, Luciane Carla Alberici, Fernando Barbosa. Long-term exposure to bisphenol A or S promotes glucose intolerance and changes hepatic mitochondrial metabolism in male Wistar rats. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2019 Oct; 132(?):110694. doi: 10.1016/j.fct.2019.110694. [PMID: 31344369]
  • Jie Hu, Hongzhi Zhao, Joseph M Braun, Tongzhang Zheng, Bin Zhang, Wei Xia, Wenxin Zhang, Jiufeng Li, Yanqiu Zhou, Han Li, Jun Li, Aifen Zhou, Yiming Zhang, Stephen L Buka, Simin Liu, Yang Peng, Chuansha Wu, Minmin Jiang, Wenqian Huo, Yingshuang Zhu, Kunchong Shi, Yuanyuan Li, Zongwei Cai, Shunqing Xu. Associations of Trimester-Specific Exposure to Bisphenols with Size at Birth: A Chinese Prenatal Cohort Study. Environmental health perspectives. 2019 10; 127(10):107001. doi: 10.1289/ehp4664. [PMID: 31573832]
  • Melanie H Jacobson, Miriam Woodward, Wei Bao, Buyun Liu, Leonardo Trasande. Urinary Bisphenols and Obesity Prevalence Among U.S. Children and Adolescents. Journal of the Endocrine Society. 2019 Sep; 3(9):1715-1726. doi: 10.1210/js.2019-00201. [PMID: 31528831]
  • Yovana Sanchis, Clara Coscollà, Vicent Yusà. Analysis of four parabens and bisphenols A, F, S in urine, using dilute and shoot and liquid chromatography coupled to mass spectrometry. Talanta. 2019 Sep; 202(?):42-50. doi: 10.1016/j.talanta.2019.04.048. [PMID: 31171203]
  • Beatriz Souza da Silva, Carla Bruna Pietrobon, Iala Milene Bertasso, Bruna Pereira Lopes, Janaine Cavalcanti Carvalho, Nayara Peixoto-Silva, Tatianne Rosa Santos, Sylvio Claudio-Neto, Alex Christian Manhães, Elaine Oliveira, Egberto Gaspar de Moura, Patrícia Cristina Lisboa. Short and long-term effects of bisphenol S (BPS) exposure during pregnancy and lactation on plasma lipids, hormones, and behavior in rats. Environmental pollution (Barking, Essex : 1987). 2019 Jul; 250(?):312-322. doi: 10.1016/j.envpol.2019.03.100. [PMID: 31003143]
  • Véronique Gayrard, Marlène Z Lacroix, Flore C Grandin, Séverine H Collet, Hanna Mila, Catherine Viguié, Clémence A Gély, Blandine Rabozzi, Michèle Bouchard, Roger Léandri, Pierre-Louis Toutain, Nicole Picard-Hagen. Oral Systemic Bioavailability of Bisphenol A and Bisphenol S in Pigs. Environmental health perspectives. 2019 07; 127(7):77005. doi: 10.1289/ehp4599. [PMID: 31313948]
  • Zhiyuan Meng, Dezhen Wang, Wan Liu, Ruisheng Li, Sen Yan, Ming Jia, Luyao Zhang, Zhiqiang Zhou, Wentao Zhu. Perinatal exposure to Bisphenol S (BPS) promotes obesity development by interfering with lipid and glucose metabolism in male mouse offspring. Environmental research. 2019 06; 173(?):189-198. doi: 10.1016/j.envres.2019.03.038. [PMID: 30921577]
  • Jiaying Liu, Jonathan W Martin. Comparison of Bisphenol A and Bisphenol S Percutaneous Absorption and Biotransformation. Environmental health perspectives. 2019 06; 127(6):67008. doi: 10.1289/ehp5044. [PMID: 31199677]