Bisphenol B (BioDeep_00001871730)

   

Industrial Pollutants


代谢物信息卡片


p,p-sec-Butylidenediphenol

化学式: C16H18O2 (242.1307)
中文名称: 双酚B, 双酚 B
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CCC(C)(C1=CC=C(C=C1)O)C2=CC=C(C=C2)O
InChI: InChI=1S/C16H18O2/c1-3-16(2,12-4-8-14(17)9-5-12)13-6-10-15(18)11-7-13/h4-11,17-18H,3H2,1-2H3

描述信息

同义名列表

5 个代谢物同义名

p,p-sec-Butylidenediphenol; Bisphenol B; BPB; Bisphenol B; Bisphenol B



数据库引用编号

8 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)

0 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 13 AKT1, AKT2, CAT, CCNB1, CDK2, CDK4, ESR1, GPER1, HSD3B1, PDGFRA, SRPX2, SULT1A1, TYR
Peripheral membrane protein 2 CYP11A1, ESR1
Endoplasmic reticulum membrane 4 GPER1, HSD3B1, PDGFRA, SRD5A1
Mitochondrion membrane 2 CYP11A1, GPER1
Nucleus 10 AKT1, AKT2, CCNB1, CDK2, CDK4, ESR1, GPER1, PCNA, PDGFRA, SOX9
cytosol 9 AKT1, AKT2, CAT, CCNB1, CDK2, CDK4, ESR1, GPER1, SULT1A1
dendrite 1 GPER1
mitochondrial membrane 1 GPER1
nuclear body 1 PCNA
trans-Golgi network 1 GPER1
centrosome 3 CCNB1, CDK2, PCNA
nucleoplasm 10 AKT1, AKT2, CCNB1, CDK2, CDK4, ESR1, GPER1, PCNA, PDGFRA, SOX9
Cell membrane 4 AKT1, ESR1, FSHR, PDGFRA
Cytoplasmic side 1 ESR1
lamellipodium 1 AKT1
ruffle membrane 1 AKT2
Cell projection, axon 1 GPER1
Multi-pass membrane protein 3 FSHR, GPER1, SRD5A1
Golgi apparatus membrane 1 GPER1
Synapse 1 SRPX2
cell cortex 2 AKT1, AKT2
cell junction 1 PDGFRA
cell surface 1 SRPX2
dendritic shaft 1 GPER1
glutamatergic synapse 2 AKT1, SRPX2
Golgi apparatus 3 ESR1, GPER1, PDGFRA
Golgi membrane 1 GPER1
mitochondrial inner membrane 2 CYP11A1, HSD3B1
neuronal cell body 1 SRD5A1
postsynapse 1 AKT1
presynaptic membrane 1 GPER1
Lysosome 1 TYR
endosome 1 CDK2
plasma membrane 6 AKT1, AKT2, ESR1, FSHR, GPER1, PDGFRA
presynaptic active zone 1 GPER1
Membrane 9 AKT1, CAT, CCNB1, CYP11A1, ESR1, FSHR, GPER1, PDGFRA, SRD5A1
axon 1 GPER1
extracellular exosome 3 CAT, PCNA, TTR
endoplasmic reticulum 2 GPER1, HSD3B1
extracellular space 2 SRPX2, TTR
perinuclear region of cytoplasm 3 GPER1, SRD5A1, TYR
bicellular tight junction 1 CDK4
mitochondrion 2 CAT, CYP11A1
protein-containing complex 5 AKT1, CAT, ESR1, PDGFRA, SOX9
intracellular membrane-bounded organelle 5 AKT2, CAT, GPER1, HSD3B1, TYR
postsynaptic density 1 GPER1
Single-pass type I membrane protein 2 PDGFRA, TYR
Secreted 2 SRPX2, TTR
extracellular region 2 CAT, TTR
excitatory synapse 1 SRPX2
hippocampal mossy fiber to CA3 synapse 1 GPER1
mitochondrial matrix 3 CAT, CCNB1, CYP11A1
transcription regulator complex 4 CDK2, CDK4, ESR1, SOX9
Cell projection, cilium 1 PDGFRA
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 1 CDK2
Nucleus membrane 1 CDK4
nuclear membrane 1 CDK4
external side of plasma membrane 1 PDGFRA
microtubule cytoskeleton 1 AKT1
nucleolus 3 CDK4, GPER1, HSD3B1
Melanosome membrane 1 TYR
Early endosome 2 AKT2, GPER1
cell-cell junction 1 AKT1
Golgi-associated vesicle 1 TYR
recycling endosome 1 GPER1
vesicle 1 AKT1
Mitochondrion inner membrane 1 CYP11A1
focal adhesion 1 CAT
spindle 1 AKT1
Peroxisome 1 CAT
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
Mitochondrion intermembrane space 1 AKT1
mitochondrial intermembrane space 2 AKT1, HSD3B1
collagen-containing extracellular matrix 1 SRPX2
receptor complex 2 FSHR, PDGFRA
ciliary basal body 1 AKT1
cilium 1 PDGFRA
chromatin 4 CDK4, ESR1, PCNA, SOX9
spindle pole 1 CCNB1
nuclear replication fork 1 PCNA
chromosome, telomeric region 2 CDK2, PCNA
intercellular bridge 1 HSD3B1
nuclear envelope 2 CDK2, GPER1
microvillus 1 PDGFRA
Cytoplasmic vesicle membrane 1 GPER1
cell body fiber 1 SRD5A1
Cell projection, dendrite 1 GPER1
Melanosome 1 TYR
euchromatin 1 ESR1
Smooth endoplasmic reticulum membrane 1 HSD3B1
replication fork 1 PCNA
synaptic membrane 1 SRPX2
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 1 CAT
male germ cell nucleus 2 CDK2, PCNA
axon terminus 1 GPER1
azurophil granule lumen 1 TTR
outer kinetochore 1 CCNB1
nuclear lamina 1 PCNA
Cajal body 1 CDK2
ribonucleoprotein complex 1 ELAVL3
[Isoform 1]: Nucleus 1 ESR1
keratin filament 1 GPER1
condensed chromosome 1 CDK2
Nucleus, Cajal body 1 CDK2
dendritic spine head 1 GPER1
X chromosome 1 CDK2
Y chromosome 1 CDK2
Cell projection, dendritic spine membrane 1 GPER1
dendritic spine membrane 1 GPER1
cyclin-dependent protein kinase holoenzyme complex 3 CDK2, CDK4, PCNA
cyclin E1-CDK2 complex 1 CDK2
cyclin E2-CDK2 complex 1 CDK2
catalase complex 1 CAT
cyclin B1-CDK1 complex 1 CCNB1
cyclin D1-CDK4 complex 1 CDK4
cyclin D2-CDK4 complex 1 CDK4
cyclin D3-CDK4 complex 1 CDK4
PCNA complex 1 PCNA
PCNA-p21 complex 1 PCNA
replisome 1 PCNA
cyclin A2-CDK2 complex 1 CDK2
cyclin A1-CDK2 complex 1 CDK2


文献列表

  • 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]
  • Yang Li, Haoni Yan, Yige Yu, Cheng Zou, Lili Tian, Xiu Xin, Song Zhang, Zengqiang Li, Feifei Ma, Ren-Shan Ge. Bisphenol B stimulates Leydig cell proliferation but inhibits maturation in late pubertal rats. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2021 Jul; 153(?):112248. doi: 10.1016/j.fct.2021.112248. [PMID: 33940105]
  • 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]
  • 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]
  • Shoeb Ikhlas, Masood Ahmad. Acute and sub-acute bisphenol-B exposures adversely affect sperm count and quality in adolescent male mice. Chemosphere. 2020 Mar; 242(?):125286. doi: 10.1016/j.chemosphere.2019.125286. [PMID: 31896186]
  • 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]
  • 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]
  • T Jambor, E Kovacikova, H Greifova, A Kovacik, L Libova, N Lukac. Assessment of the effective impact of bisphenols on mitochondrial activity and steroidogenesis in a dose-dependency in mice TM3 Leydig cells. Physiological research. 2019 08; 68(4):689-693. doi: 10.33549/physiolres.934200. [PMID: 31342755]
  • Nuria Vela, May Calín, María J Yáñez-Gascón, Isabel Garrido, Gabriel Pérez-Lucas, José Fenoll, Simón Navarro. Photocatalytic oxidation of six endocrine disruptor chemicals in wastewater using ZnO at pilot plant scale under natural sunlight. Environmental science and pollution research international. 2018 Dec; 25(35):34995-35007. doi: 10.1007/s11356-018-1716-9. [PMID: 29558788]
  • 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]
  • 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]
  • Shanjun Song, Mingwu Shao, Weihua Wang, Yajuan He, Xinhua Dai, Huiyu Wang, Liliang Liu, Feng Guo. Development and evaluation of microwave-assisted and ultrasound-assisted methods based on a quick, easy, cheap, effective, rugged, and safe sample preparation approach for the determination of bisphenol analogues in serum and sediments. Journal of separation science. 2017 Dec; 40(23):4610-4618. doi: 10.1002/jssc.201700628. [PMID: 28988464]
  • 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]
  • A L Heffernan, K Thompson, G Eaglesham, S Vijayasarathy, J F Mueller, P D Sly, M J Gomez. Rapid, automated online SPE-LC-QTRAP-MS/MS method for the simultaneous analysis of 14 phthalate metabolites and 5 bisphenol analogues in human urine. Talanta. 2016 May; 151(?):224-233. doi: 10.1016/j.talanta.2016.01.037. [PMID: 26946031]
  • Margherita Fattore, Giacomo Russo, Francesco Barbato, Lucia Grumetto, Stefania Albrizio. Monitoring of bisphenols in canned tuna from Italian markets. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2015 Sep; 83(?):68-75. doi: 10.1016/j.fct.2015.05.010. [PMID: 26070504]
  • Jiajia Yang, Yun Li, Wang Jinchengt, Xiaoli Sun, Jiping Chen. [Preparation of molecularly imprinted polymers using dummy template and the applications in selective solid-phase extraction of seven bisphenols from human urine, bovine serum and beer samples]. Se pu = Chinese journal of chromatography. 2015 May; 33(5):468-74. doi: 10.3724/sp.j.1123.2015.02065. [PMID: 26387203]
  • Huixiao Hong, William S Branham, Hui Wen Ng, Carrie L Moland, Stacey L Dial, Hong Fang, Roger Perkins, Daniel Sheehan, Weida Tong. Human sex hormone-binding globulin binding affinities of 125 structurally diverse chemicals and comparison with their binding to androgen receptor, estrogen receptor, and α-fetoprotein. Toxicological sciences : an official journal of the Society of Toxicology. 2015 Feb; 143(2):333-48. doi: 10.1093/toxsci/kfu231. [PMID: 25349334]
  • S C Cunha, J O Fernandes. Quantification of free and total bisphenol A and bisphenol B in human urine by dispersive liquid-liquid microextraction (DLLME) and heart-cutting multidimensional gas chromatography-mass spectrometry (MD-GC/MS). Talanta. 2010 Nov; 83(1):117-25. doi: 10.1016/j.talanta.2010.08.048. [PMID: 21035651]
  • Luigi Cobellis, Nicola Colacurci, Elisabetta Trabucco, Carmen Carpentiero, Lucia Grumetto. Measurement of bisphenol A and bisphenol B levels in human blood sera from healthy and endometriotic women. Biomedical chromatography : BMC. 2009 Nov; 23(11):1186-90. doi: 10.1002/bmc.1241. [PMID: 19444800]