Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 105

1.

Molecular docking and molecular dynamics studies on the interactions of hydroxylated polybrominated diphenyl ethers to estrogen receptor alpha.

Lu Q, Cai Z, Fu J, Luo S, Liu C, Li X, Zhao D.

Ecotoxicol Environ Saf. 2014 Mar;101:83-9. doi: 10.1016/j.ecoenv.2013.12.018. Epub 2014 Jan 11.

PMID:
24507131
2.

Molecular docking, molecular dynamics simulation, and structure-based 3D-QSAR studies on estrogenic activity of hydroxylated polychlorinated biphenyls.

Li X, Ye L, Wang X, Wang X, Liu H, Qian X, Zhu Y, Yu H.

Sci Total Environ. 2012 Dec 15;441:230-8. doi: 10.1016/j.scitotenv.2012.08.072. Epub 2012 Nov 6.

PMID:
23137989
3.

Nuclear hormone receptor activity of polybrominated diphenyl ethers and their hydroxylated and methoxylated metabolites in transactivation assays using Chinese hamster ovary cells.

Kojima H, Takeuchi S, Uramaru N, Sugihara K, Yoshida T, Kitamura S.

Environ Health Perspect. 2009 Aug;117(8):1210-8. doi: 10.1289/ehp.0900753. Epub 2009 Apr 28.

4.

Structure-dependent activities of hydroxylated polybrominated diphenyl ethers on human estrogen receptor.

Li X, Gao Y, Guo LH, Jiang G.

Toxicology. 2013 Jul 5;309:15-22. doi: 10.1016/j.tox.2013.04.001. Epub 2013 Apr 18.

PMID:
23603053
5.

Molecular modeling and molecular dynamics simulation studies on the interactions of hydroxylated polychlorinated biphenyls with estrogen receptor-β.

Li X, Ye L, Wang X, Shi W, Qian X, Zhu Y, Yu H.

Arch Environ Contam Toxicol. 2013 Oct;65(3):357-67. doi: 10.1007/s00244-013-9916-2. Epub 2013 May 28.

PMID:
23712771
6.

Exploring the binding features of polybrominated diphenyl ethers as estrogen receptor antagonists: docking studies.

Yang WH, Wang ZY, Liu HL, Yu HX.

SAR QSAR Environ Res. 2010 Apr;21(3-4):351-67. doi: 10.1080/10629361003773971.

PMID:
20544555
7.

Insights into the structural and conformational requirements of polybrominated diphenyl ethers and metabolites as potential estrogens based on molecular docking.

Yang W, Wei S, Liu H, Yu H.

Chemosphere. 2011 Jun;84(3):328-35. doi: 10.1016/j.chemosphere.2011.04.010. Epub 2011 May 20.

PMID:
21601234
8.

Combined 3D-QSAR, molecular docking and molecular dynamics study on thyroid hormone activity of hydroxylated polybrominated diphenyl ethers to thyroid receptors β.

Li X, Ye L, Wang X, Wang X, Liu H, Zhu Y, Yu H.

Toxicol Appl Pharmacol. 2012 Dec 15;265(3):300-7. doi: 10.1016/j.taap.2012.08.030. Epub 2012 Sep 6.

PMID:
22982074
9.

Hormone activity of hydroxylated polybrominated diphenyl ethers on human thyroid receptor-beta: in vitro and in silico investigations.

Li F, Xie Q, Li X, Li N, Chi P, Chen J, Wang Z, Hao C.

Environ Health Perspect. 2010 May;118(5):602-6. doi: 10.1289/ehp.0901457.

10.

Different photolysis kinetics and photooxidation reactivities of neutral and anionic hydroxylated polybrominated diphenyl ethers.

Xie Q, Chen J, Zhao H, Qiao X, Cai X, Li X.

Chemosphere. 2013 Jan;90(2):188-94. doi: 10.1016/j.chemosphere.2012.06.033. Epub 2012 Jul 23.

PMID:
22832336
11.

Modeling and predicting pKa values of mono-hydroxylated polychlorinated biphenyls (HO-PCBs) and polybrominated diphenyl ethers (HO-PBDEs) by local molecular descriptors.

Yu H, Wondrousch D, Yuan Q, Lin H, Chen J, Hong H, Schüürmann G.

Chemosphere. 2015 Nov;138:829-36. doi: 10.1016/j.chemosphere.2015.08.012. Epub 2015 Aug 24.

PMID:
26295542
12.

Hydroxylated metabolites of the polybrominated diphenyl ether mixture DE-71 are weak estrogen receptor-alpha ligands.

Mercado-Feliciano M, Bigsby RM.

Environ Health Perspect. 2008 Oct;116(10):1315-21. doi: 10.1289/ehp.11343. Epub 2008 May 27.

13.

Molecular docking and comparative molecular similarity indices analysis of estrogenicity of polybrominated diphenyl ethers and their analogues.

Yang W, Liu X, Liu H, Wu Y, Giesy JP, Yu H.

Environ Toxicol Chem. 2010 Mar;29(3):660-8. doi: 10.1002/etc.70.

PMID:
20821492
14.

Production of hydroxylated polybrominated diphenyl ethers from bromophenols by bromoperoxidase-catalyzed dimerization.

Lin K, Gan J, Liu W.

Environ Sci Technol. 2014 Oct 21;48(20):11977-83. doi: 10.1021/es502854e. Epub 2014 Oct 1.

PMID:
25229997
15.

Hydroxylated polybrominated diphenyl ethers exhibit different activities on thyroid hormone receptors depending on their degree of bromination.

Ren XM, Guo LH, Gao Y, Zhang BT, Wan B.

Toxicol Appl Pharmacol. 2013 May 1;268(3):256-63. doi: 10.1016/j.taap.2013.01.026. Epub 2013 Feb 8.

PMID:
23402801
16.

Structure-dependent activities of polybrominated diphenyl ethers and hydroxylated metabolites on zebrafish retinoic acid receptor.

Zhao J, Zhu X, Xu T, Yin D.

Environ Sci Pollut Res Int. 2015 Feb;22(3):1723-30. doi: 10.1007/s11356-014-3364-z. Epub 2014 Aug 1.

PMID:
25077655
17.

Structure-based investigation on the binding interaction of hydroxylated polybrominated diphenyl ethers with thyroxine transport proteins.

Cao J, Lin Y, Guo LH, Zhang AQ, Wei Y, Yang Y.

Toxicology. 2010 Nov 9;277(1-3):20-8. doi: 10.1016/j.tox.2010.08.012. Epub 2010 Sep 8.

PMID:
20804816
19.

Effects of HO-/MeO-PBDEs on androgen receptor: in vitro investigation and helix 12-involved MD simulation.

Wang X, Yang H, Hu X, Zhang X, Zhang Q, Jiang H, Shi W, Yu H.

Environ Sci Technol. 2013 Oct 15;47(20):11802-9. doi: 10.1021/es4029364. Epub 2013 Oct 2.

PMID:
24044724
20.

Analysis of Ah receptor binding affinities of polybrominated diphenyl ethers via in silico molecular docking and 3D-QSAR.

Li X, Wang X, Shi W, Liu H, Yu H.

SAR QSAR Environ Res. 2013 Jan;24(1):75-87. doi: 10.1080/1062936X.2012.729225. Epub 2012 Nov 5.

PMID:
23121134

Supplemental Content

Support Center