Bisphenol F (BioDeep_00000001724)

 

Secondary id: BioDeep_00000397408

human metabolite PANOMIX_OTCML-2023 blood metabolite Industrial Pollutants natural product


代谢物信息卡片


4,4-Methylenebis(phenol), disodium salt

化学式: C13H12O2 (200.0837)
中文名称: 4,4-二羟基二苯基甲烷, 4,4'-二羟基二苯甲烷, 双酚 F
谱图信息: 最多检出来源 Homo sapiens(blood) 33.69%

分子结构信息

SMILES: C1=CC(=CC=C1CC2=CC=C(C=C2)O)O
InChI: InChI=1S/C13H12O2/c14-12-5-1-10(2-6-12)9-11-3-7-13(15)8-4-11/h1-8,14-15H,9H2

描述信息

4,4'-Dihydroxydiphenylmethane is a phenolic derivative with antioxidant activities[1].
4,4'-Dihydroxydiphenylmethane is a phenolic derivative with antioxidant activities[1].

同义名列表

19 个代谢物同义名

4,4-Methylenebis(phenol), disodium salt; 4-[(4-hydroxyphenyl)methyl]phenol; para-(para-hydroxybenzyl)phenol; bis(para-hydroxyphenyl)methane; p,p-Bis(hydroxyphenyl)methane; 4,4-Dihydroxydiphenylmethane; Bis(4-hydroxyphenyl)methane; BIS(P-HYDROXYPHENYL)METHANE; p-(p-Hydroxybenzyl)phenol; p-Hydroxydiphenylmethane; 4,4-Methylenebis(phenol); 4,4-Methylenediphenol; 4,4-bisphenol F; bisphenol F; 650-92-8; BPF; 4,4'-Dihydroxydiphenylmethane; BPF; Bis(4-hydroxyphenyl)methane



数据库引用编号

17 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)

26 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 14 ADIG, AR, CASP3, CASP8, CASP9, CAT, ESR1, FABP4, GPER1, HPGDS, OLIG2, PIK3CA, PPARG, SRPX2
Peripheral membrane protein 1 ESR1
Endoplasmic reticulum membrane 1 GPER1
Mitochondrion membrane 1 GPER1
Nucleus 13 ADIG, AR, CASP3, CASP8, CASP9, ESR1, ESR2, FABP4, GABPA, GPER1, OLIG2, PPARA, PPARG
cytosol 11 AR, CASP3, CASP8, CASP9, CAT, ESR1, FABP4, GPER1, HPGDS, PIK3CA, PPARG
dendrite 1 GPER1
mitochondrial membrane 1 GPER1
trans-Golgi network 1 GPER1
nucleoplasm 10 AR, CASP3, CASP8, ESR1, ESR2, GABPA, GPER1, HPGDS, PPARA, PPARG
RNA polymerase II transcription regulator complex 1 PPARG
Cell membrane 2 ESR1, TNF
Cytoplasmic side 1 ESR1
lamellipodium 2 CASP8, PIK3CA
Cell projection, axon 1 GPER1
Multi-pass membrane protein 2 CACNA1I, GPER1
Golgi apparatus membrane 1 GPER1
Synapse 1 SRPX2
cell surface 2 SRPX2, TNF
dendritic shaft 1 GPER1
glutamatergic synapse 2 CASP3, SRPX2
Golgi apparatus 2 ESR1, GPER1
Golgi membrane 2 GPER1, INS
neuronal cell body 2 CASP3, TNF
presynaptic membrane 1 GPER1
plasma membrane 6 AR, CACNA1I, ESR1, GPER1, PIK3CA, TNF
presynaptic active zone 1 GPER1
Membrane 6 ADIG, AR, CACNA1I, CAT, ESR1, GPER1
axon 1 GPER1
extracellular exosome 2 CAT, FABP4
endoplasmic reticulum 1 GPER1
extracellular space 3 INS, SRPX2, TNF
perinuclear region of cytoplasm 3 GPER1, PIK3CA, PPARG
intercalated disc 1 PIK3CA
mitochondrion 4 CASP8, CASP9, CAT, ESR2
protein-containing complex 5 AR, CASP8, CASP9, CAT, ESR1
intracellular membrane-bounded organelle 5 CAT, ESR2, GPER1, HPGDS, PPARG
postsynaptic density 2 CASP3, GPER1
Secreted 3 ADIG, INS, SRPX2
extracellular region 4 ADIG, CAT, INS, TNF
Single-pass membrane protein 1 ADIG
mitochondrial outer membrane 1 CASP8
excitatory synapse 1 SRPX2
hippocampal mossy fiber to CA3 synapse 1 GPER1
mitochondrial matrix 1 CAT
transcription regulator complex 1 ESR1
external side of plasma membrane 1 TNF
nucleolus 1 GPER1
Early endosome 1 GPER1
recycling endosome 2 GPER1, TNF
Single-pass type II membrane protein 1 TNF
Cell projection, lamellipodium 1 CASP8
Membrane raft 1 TNF
focal adhesion 1 CAT
Peroxisome 1 CAT
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
collagen-containing extracellular matrix 1 SRPX2
nuclear speck 1 AR
receptor complex 1 PPARG
chromatin 7 AR, ESR1, ESR2, GABPA, OLIG2, PPARA, PPARG
phagocytic cup 1 TNF
cytoskeleton 1 CASP8
nuclear envelope 1 GPER1
endosome lumen 1 INS
Lipid droplet 2 ADIG, FABP4
Cytoplasmic vesicle membrane 1 GPER1
Cell projection, dendrite 1 GPER1
euchromatin 1 ESR1
cell body 1 CASP8
synaptic membrane 1 SRPX2
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 2 CAT, INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 1 INS
axon terminus 1 GPER1
voltage-gated calcium channel complex 1 CACNA1I
phosphatidylinositol 3-kinase complex 1 PIK3CA
phosphatidylinositol 3-kinase complex, class IA 1 PIK3CA
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
apoptosome 1 CASP9
[Isoform 1]: Nucleus 1 ESR1
CD95 death-inducing signaling complex 1 CASP8
death-inducing signaling complex 2 CASP3, CASP8
ripoptosome 1 CASP8
keratin filament 1 GPER1
dendritic spine head 1 GPER1
Cell projection, dendritic spine membrane 1 GPER1
dendritic spine membrane 1 GPER1
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
catalase complex 1 CAT
phosphatidylinositol 3-kinase complex, class IB 1 PIK3CA
caspase complex 1 CASP9
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Yun Fan, Shiqi Li, Xiancheng Yang, Shengjun Bai, Min Tang, Xueer Zhang, Chuncheng Lu, Chenbo Ji, Guizhen Du, Yufeng Qin. Multi-omics approach characterizes the role of Bisphenol F in disrupting hepatic lipid metabolism. Environment international. 2024 May; 187(?):108690. doi: 10.1016/j.envint.2024.108690. [PMID: 38685157]
  • 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]
  • Xinjing Wang, Linlin Wu, Jingxian Tao, Heyong Ye, Jun Wang, Rong Gao, Wenwei Liu. A lipidomic approach to bisphenol F-induced non-alcoholic fatty liver disease-like changes: altered lipid components in a murine model. Environmental science and pollution research international. 2023 Oct; ?(?):. doi: 10.1007/s11356-023-30306-0. [PMID: 37837594]
  • Linwei Zhang, Xuexue Xie, Jingxian Tao, Sizhe Wang, Miaoyang Hu, Xi Wang, Zheng Yu, Liuting Xu, Yuxin Lin, Weilan Wu, Jie Cheng, Linlin Wu, Wenwei Liu, Rong Gao, Jun Wang. Mystery of bisphenol F-induced nonalcoholic fatty liver disease-like changes: Roles of Drp1-mediated abnormal mitochondrial fission in lipid droplet deposition. The Science of the total environment. 2023 Sep; 904(?):166831. doi: 10.1016/j.scitotenv.2023.166831. [PMID: 37683851]
  • Beatriz Linillos-Pradillo, Lisa Rancan, Julio García Murias, Margret Schlumpf, Walter Lichtensteiger, J A F Tresguerres, Elena Vara, Sergio D Paredes. Oxidative stress increases in liver of lactating rats after BPF-low-dose exposure: perinatal effects in the offspring. Scientific reports. 2023 07; 13(1):11229. doi: 10.1038/s41598-023-38434-w. [PMID: 37433837]
  • 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]
  • 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]
  • 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]
  • Gabin Thierry M Bitchagno, Anja Schüffler, Jonathan Gross, Matthias Krumb, Pierre Tane, Till Opatz. Sesquiterpene Lactones from Vernonia tufnelliae: Structural Characterization and Biological Evaluation. Journal of natural products. 2022 07; 85(7):1681-1690. doi: 10.1021/acs.jnatprod.2c00055. [PMID: 35704432]
  • Linus Wiklund, Anna Beronius. Systematic evaluation of the evidence for identification of endocrine disrupting properties of Bisphenol F. Toxicology. 2022 Jul; 476(?):153255. doi: 10.1016/j.tox.2022.153255. [PMID: 35811010]
  • Xiyan Mu, Suzhen Qi, Hui Wang, Lilai Yuan, Chengju Wang, Yingren Li, Jing Qiu. Bisphenol analogues induced metabolic effects through eliciting intestinal cell heterogeneous response. Environment international. 2022 07; 165(?):107287. doi: 10.1016/j.envint.2022.107287. [PMID: 35598417]
  • Elize Aparecida Santos Musachio, Marcia Rósula Poetini, Dieniffer Espinosa Janner, Luana Barreto Meichtry, Ketnne Hanna Poleto, Eliana Jardim Fernandes, Gustavo Petri Guerra, Marina Prigol. Sex-specific changes in oxidative stress parameters and longevity produced by Bisphenol F and S compared to Bisphenol A in Drosophila melanogaster. Comparative biochemistry and physiology. Toxicology & pharmacology : CBP. 2022 Jul; 257(?):109329. doi: 10.1016/j.cbpc.2022.109329. [PMID: 35318128]
  • Tasnia Sharin, Doug Crump, Jason M O'Brien. Toxicity screening of bisphenol A replacement compounds: cytotoxicity and mRNA expression in LMH 3D spheroids. Environmental science and pollution research international. 2022 Jun; 29(29):44769-44778. doi: 10.1007/s11356-022-18812-z. [PMID: 35138540]
  • 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]
  • Gui Yu, Suzhen Huang, Xingzhang Luo, Wei Zhao, Zheng Zheng. Single and combined toxicity effects of nanoplastics and bisphenol F on submerged the macrophyte Hydrilla verticillata. The Science of the total environment. 2022 Mar; 814(?):152564. doi: 10.1016/j.scitotenv.2021.152564. [PMID: 34952055]
  • Huiling Chen, Jiangbin Li, Yanchao Zhang, Wei Zhang, Xing Li, Huanwen Tang, Yungang Liu, Tianlan Li, Haoqi He, Bohai Du, Li Li, Ming Shi. Bisphenol F suppresses insulin-stimulated glucose metabolism in adipocytes by inhibiting IRS-1/PI3K/AKT pathway. Ecotoxicology and environmental safety. 2022 Feb; 231(?):113201. doi: 10.1016/j.ecoenv.2022.113201. [PMID: 35051757]
  • 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]
  • Tomasz Tuzimski, Szymon Szubartowski. Application of d-SPE before SPE and HPLC-FLD to Analyze Bisphenols in Human Breast Milk Samples. Molecules (Basel, Switzerland). 2021 Aug; 26(16):. doi: 10.3390/molecules26164930. [PMID: 34443517]
  • Anna Marqueño, Elisabet Pérez-Albaladejo, Nancy D Denslow, John A Bowden, Cinta Porte. Untargeted lipidomics reveals the toxicity of bisphenol A bis(3-chloro-2- hydroxypropyl) ether and bisphenols A and F in zebrafish liver cells. Ecotoxicology and environmental safety. 2021 Aug; 219(?):112311. doi: 10.1016/j.ecoenv.2021.112311. [PMID: 33993092]
  • 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]
  • Isabel C Cohen, Emry R Cohenour, Kristen G Harnett, Sonya M Schuh. BPA, BPAF and TMBPF Alter Adipogenesis and Fat Accumulation in Human Mesenchymal Stem Cells, with Implications for Obesity. International journal of molecular sciences. 2021 May; 22(10):. doi: 10.3390/ijms22105363. [PMID: 34069744]
  • Handan Aykut, Burak Kaptaner. In vitro effects of bisphenol F on antioxidant system indicators in the isolated hepatocytes of rainbow trout (Oncorhyncus mykiss). Molecular biology reports. 2021 Mar; 48(3):2591-2599. doi: 10.1007/s11033-021-06310-3. [PMID: 33791906]
  • Jun Wang, Pengfei Yu, Xuexue Xie, Linlin Wu, Manfei Zhou, Fei Huan, Lei Jiang, Rong Gao. Bisphenol F induces nonalcoholic fatty liver disease-like changes: Involvement of lysosome disorder in lipid droplet deposition. Environmental pollution (Barking, Essex : 1987). 2021 Feb; 271(?):116304. doi: 10.1016/j.envpol.2020.116304. [PMID: 33401208]
  • Elisabet Pérez-Albaladejo, Alejandra Solís, Ilaria Bani, Cinta Porte. PLHC-1 topminnow liver cells: An alternative model to investigate the toxicity of plastic additives in the aquatic environment. Ecotoxicology and environmental safety. 2021 Jan; 208(?):111746. doi: 10.1016/j.ecoenv.2020.111746. [PMID: 33396072]
  • Qian Liu, Wentao Shao, Zhenkun Weng, Xin Zhang, Guipeng Ding, Cheng Xu, Jin Xu, Zhaoyan Jiang, Aihua Gu. In vitro evaluation of the hepatic lipid accumulation of bisphenol analogs: A high-content screening assay. Toxicology in vitro : an international journal published in association with BIBRA. 2020 Oct; 68(?):104959. doi: 10.1016/j.tiv.2020.104959. [PMID: 32763284]
  • 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]
  • Marie-Katherin Zühlke, Rabea Schlüter, Annett Mikolasch, Ann-Kristin Henning, Martin Giersberg, Michael Lalk, Gotthard Kunze, Thomas Schweder, Tim Urich, Frieder Schauer. Biotransformation of bisphenol A analogues by the biphenyl-degrading bacterium Cupriavidusbasilensis - a structure-biotransformation relationship. Applied microbiology and biotechnology. 2020 Apr; 104(8):3569-3583. doi: 10.1007/s00253-020-10406-4. [PMID: 32125477]
  • 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]
  • 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]
  • Chao Zhao, Zhi Tang, Peisi Xie, Kaili Lin, Arthur Chi Kong Chung, Zongwei Cai. Immunotoxic Potential of Bisphenol F Mediated through Lipid Signaling Pathways on Macrophages. Environmental science & technology. 2019 Oct; 53(19):11420-11428. doi: 10.1021/acs.est.8b07314. [PMID: 31453682]
  • 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]
  • Si-Yue Chen, Chang-An Geng, Yun-Bao Ma, Xiao-Yan Huang, Xiao-Tong Yang, Li-Hua Su, Xiao-Feng He, Tian-Ze Li, Zhen-Tao Deng, Zhen Gao, Xue-Mei Zhang, Ji-Jun Chen. Polybenzyls from Gastrodia elata, their agonistic effects on melatonin receptors and structure-activity relationships. Bioorganic & medicinal chemistry. 2019 08; 27(15):3299-3306. doi: 10.1016/j.bmc.2019.06.008. [PMID: 31204226]
  • Asad Ullah, Madeeha Pirzada, Tayyaba Afsar, Suhail Razak, Ali Almajwal, Sarwat Jahan. Effect of bisphenol F, an analog of bisphenol A, on the reproductive functions of male rats. Environmental health and preventive medicine. 2019 Jun; 24(1):41. doi: 10.1186/s12199-019-0797-5. [PMID: 31182008]
  • Taya Huang, Lesley-Ann Danaher, Beat J Brüschweiler, George E N Kass, Caroline Merten. Naturally occurring bisphenol F in plants used in traditional medicine. Archives of toxicology. 2019 06; 93(6):1485-1490. doi: 10.1007/s00204-019-02442-5. [PMID: 31055636]
  • Zuzana Drobna, Alzbeta Talarovicova, Hannah E Schrader, Timothy R Fennell, Rodney W Snyder, Emilie F Rissman. Bisphenol F has different effects on preadipocytes differentiation and weight gain in adult mice as compared with Bisphenol A and S. Toxicology. 2019 05; 420(?):66-72. doi: 10.1016/j.tox.2019.03.016. [PMID: 30959087]
  • Zhiyuan Meng, Sinuo Tian, Jin Yan, Ming Jia, Sen Yan, Ruisheng Li, Renke Zhang, Wentao Zhu, Zhiqiang Zhou. Effects of perinatal exposure to BPA, BPF and BPAF on liver function in male mouse offspring involving in oxidative damage and metabolic disorder. Environmental pollution (Barking, Essex : 1987). 2019 Apr; 247(?):935-943. doi: 10.1016/j.envpol.2019.01.116. [PMID: 30823348]
  • Sangwoo Lee, Cheolmin Kim, Hyesoo Shin, Younglim Kho, Kyungho Choi. Comparison of thyroid hormone disruption potentials by bisphenols A, S, F, and Z in embryo-larval zebrafish. Chemosphere. 2019 Apr; 221(?):115-123. doi: 10.1016/j.chemosphere.2019.01.019. [PMID: 30639807]
  • Zhiyuan Meng, Dezhen Wang, Sen Yan, Ruisheng Li, Jin Yan, Miaomiao Teng, Zhiqiang Zhou, Wentao Zhu. Effects of perinatal exposure to BPA and its alternatives (BPS, BPF and BPAF) on hepatic lipid and glucose homeostasis in female mice adolescent offspring. Chemosphere. 2018 Dec; 212(?):297-306. doi: 10.1016/j.chemosphere.2018.08.076. [PMID: 30145421]
  • Asad Ullah, Madeeha Pirzada, Sarwat Jahan, Hizb Ullah, Naheed Turi, Waheed Ullah, Mariyam Fatima Siddiqui, Muhammad Zakria, Kinza Zafar Lodhi, Muhammad Munir Khan. Impact of low-dose chronic exposure to bisphenol A and its analogue bisphenol B, bisphenol F and bisphenol S on hypothalamo-pituitary-testicular activities in adult rats: A focus on the possible hormonal mode of action. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2018 Nov; 121(?):24-36. doi: 10.1016/j.fct.2018.08.024. [PMID: 30120946]
  • Asad Ullah, Madeeha Pirzada, Sarwat Jahan, Hizb Ullah, Ghazala Shaheen, Humaira Rehman, Mariyam Fatima Siddiqui, Maisra Azhar Butt. Bisphenol A and its analogs bisphenol B, bisphenol F, and bisphenol S: Comparative in vitro and in vivo studies on the sperms and testicular tissues of rats. Chemosphere. 2018 Oct; 209(?):508-516. doi: 10.1016/j.chemosphere.2018.06.089. [PMID: 29940534]
  • Chao Zhao, Peisi Xie, Hailin Wang, Zongwei Cai. Liquid chromatography-mass spectrometry-based metabolomics and lipidomics reveal toxicological mechanisms of bisphenol F in breast cancer xenografts. Journal of hazardous materials. 2018 09; 358(?):503-507. doi: 10.1016/j.jhazmat.2018.05.010. [PMID: 29759594]
  • Xiaoli Sun, Junyu Peng, Muhua Wang, Jincheng Wang, Chunlan Tang, Luoxing Yang, Hua Lei, Fang Li, Xueli Wang, Jiping Chen. Determination of nine bisphenols in sewage and sludge using dummy molecularly imprinted solid-phase extraction coupled with liquid chromatography tandem mass spectrometry. Journal of chromatography. A. 2018 Jun; 1552(?):10-16. doi: 10.1016/j.chroma.2018.04.004. [PMID: 29678407]
  • Yanping Xian, Yuluan Wu, Hao Dong, Xindong Guo, Bin Wang, Li Wang. Dispersive micro solid phase extraction (DMSPE) using polymer anion exchange (PAX) as the sorbent followed by UPLC-MS/MS for the rapid determination of four bisphenols in commercial edible oils. Journal of chromatography. A. 2017 Sep; 1517(?):35-43. doi: 10.1016/j.chroma.2017.08.067. [PMID: 28859891]
  • Aneta Maćczak, Monika Cyrkler, Bożena Bukowska, Jaromir Michałowicz. Bisphenol A, bisphenol S, bisphenol F and bisphenol AF induce different oxidative stress and damage in human red blood cells (in vitro study). Toxicology in vitro : an international journal published in association with BIBRA. 2017 Jun; 41(?):143-149. doi: 10.1016/j.tiv.2017.02.018. [PMID: 28259788]
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