메뉴 건너뛰기




Volumn 30, Issue 11, 2011, Pages 2431-2439

Structure-activity relationship study on the binding of PBDEs with thyroxine transport proteins

Author keywords

Comparative molecular similarity indices analysis; Ligand receptor interaction mechanism; Surflex dock; Thyroid hormone disrupting activity; Transthyretin

Indexed keywords

COMPARATIVE-MOLECULAR-SIMILARITY-INDICES ANALYSIS; LIGAND-RECEPTOR INTERACTIONS; SURFLEX-DOCK; THYROID HORMONE-DISRUPTING ACTIVITY; TRANSTHYRETIN;

EID: 80054093702     PISSN: 07307268     EISSN: 15528618     Source Type: Journal    
DOI: 10.1002/etc.645     Document Type: Article
Times cited : (40)

References (28)
  • 2
    • 33745087223 scopus 로고    scopus 로고
    • Partitioning of polybrominated diphenyl ether (PBDE) congeners in human blood and milk
    • Schecter A, Papke O, Harris TR, Tung KC. 2006. Partitioning of polybrominated diphenyl ether (PBDE) congeners in human blood and milk. Toxicol Environ Chem 88: 319-324.
    • (2006) Toxicol Environ Chem , vol.88 , pp. 319-324
    • Schecter, A.1    Papke, O.2    Harris, T.R.3    Tung, K.C.4
  • 3
    • 22344443193 scopus 로고    scopus 로고
    • Polybrominated diphenyl ethers and polychlorinated biphenyls in human adipose tissue from New York
    • Johnson-Restrepo B, Kannan K, Rapaport DP, Rodan BD. 2005. Polybrominated diphenyl ethers and polychlorinated biphenyls in human adipose tissue from New York. Environ Sci Technol 39: 5177-5182.
    • (2005) Environ Sci Technol , vol.39 , pp. 5177-5182
    • Johnson-Restrepo, B.1    Kannan, K.2    Rapaport, D.P.3    Rodan, B.D.4
  • 4
    • 55949090982 scopus 로고    scopus 로고
    • Hydroxylated metabolites of the polybrominated diphenyl ether mixture DE-71 are weak estrogen receptor-alpha ligands
    • Mercado-Feliciano M, Bigsby RM. 2008. Hydroxylated metabolites of the polybrominated diphenyl ether mixture DE-71 are weak estrogen receptor-alpha ligands. Environ Health Perspect 116: 1315-1321.
    • (2008) Environ Health Perspect , vol.116 , pp. 1315-1321
    • Mercado-Feliciano, M.1    Bigsby, R.M.2
  • 6
    • 40849102532 scopus 로고    scopus 로고
    • Polybrominated diphenyl ethers (PBDEs) and bioaccumulative hydroxylated PBDE metabolites in young humans from Managua, Nicaragua
    • Athanasiadou M, Cuadra SN, Marsh G, Bergman A, Jakobsson K. 2008. Polybrominated diphenyl ethers (PBDEs) and bioaccumulative hydroxylated PBDE metabolites in young humans from Managua, Nicaragua. Environ Health Perspect 116: 400-408.
    • (2008) Environ Health Perspect , vol.116 , pp. 400-408
    • Athanasiadou, M.1    Cuadra, S.N.2    Marsh, G.3    Bergman, A.4    Jakobsson, K.5
  • 7
    • 38749154214 scopus 로고    scopus 로고
    • Inhibition of human placental aromatase activity by hydroxylated polybrominated diphenyl ethers (OH-PBDEs)
    • Cantón RF, Scholten DEA, Marsh G, De Jong PC, van den Berg M. 2008. Inhibition of human placental aromatase activity by hydroxylated polybrominated diphenyl ethers (OH-PBDEs). Toxicol Appl Pharmacol 227: 68-75.
    • (2008) Toxicol Appl Pharmacol , vol.227 , pp. 68-75
    • Cantón, R.F.1    Scholten, D.E.A.2    Marsh, G.3    De Jong, P.C.4    van den Berg, M.5
  • 8
    • 58049089932 scopus 로고    scopus 로고
    • Occurrence and congener specific profiles of polybrominated diphenyl ethers and their hydroxylated and methoxylated derivatives in breast milk from Catalonia
    • Lacorte S, Ikonomou MG. 2009. Occurrence and congener specific profiles of polybrominated diphenyl ethers and their hydroxylated and methoxylated derivatives in breast milk from Catalonia. Chemosphere 74: 412-420.
    • (2009) Chemosphere , vol.74 , pp. 412-420
    • Lacorte, S.1    Ikonomou, M.G.2
  • 9
    • 60749103207 scopus 로고    scopus 로고
    • Hydroxylated metabolites of polybrominated diphenyl ethers in human blood samples from the United States
    • Qiu XH, Bigsby RM, Hites RA. 2009. Hydroxylated metabolites of polybrominated diphenyl ethers in human blood samples from the United States. Environ Health Perspect 117: 93-98.
    • (2009) Environ Health Perspect , vol.117 , pp. 93-98
    • Qiu, X.H.1    Bigsby, R.M.2    Hites, R.A.3
  • 11
    • 61449211223 scopus 로고    scopus 로고
    • Polybrominated diphenyl ether (PBDE) levels in dust from previously owned automobiles at United States dealerships
    • Lagalante AF, Oswald TD, Calvosa FC. 2009. Polybrominated diphenyl ether (PBDE) levels in dust from previously owned automobiles at United States dealerships. Environ Int 35: 539-544.
    • (2009) Environ Int , vol.35 , pp. 539-544
    • Lagalante, A.F.1    Oswald, T.D.2    Calvosa, F.C.3
  • 12
    • 0036222972 scopus 로고    scopus 로고
    • A perspective on the potential health risks of PBDEs
    • McDonald TA. 2002. A perspective on the potential health risks of PBDEs. Chemosphere 46: 745-755.
    • (2002) Chemosphere , vol.46 , pp. 745-755
    • McDonald, T.A.1
  • 15
    • 0242287838 scopus 로고    scopus 로고
    • Are brominated flame retardants endocrine disruptors?
    • Legler J, Brouwer A. 2003. Are brominated flame retardants endocrine disruptors? Environ Int 29: 879-885.
    • (2003) Environ Int , vol.29 , pp. 879-885
    • Legler, J.1    Brouwer, A.2
  • 16
    • 41949131790 scopus 로고    scopus 로고
    • Biotransformation of brominated flame retardants into potentially endocrine-disrupting metabolites, with special attention to 2,2',4,4'-tetrabromodiphenyl ether (BDE-47)
    • Hamers T, Kamstra JH, Sonneveld E, Murk AJ, Visser TJ, Van Velzen MJM, Brouwer A, Bergman Å. 2008. Biotransformation of brominated flame retardants into potentially endocrine-disrupting metabolites, with special attention to 2, 2', 4, 4'-tetrabromodiphenyl ether (BDE-47). Mol Nutr Food Res 52: 284-298.
    • (2008) Mol Nutr Food Res , vol.52 , pp. 284-298
    • Hamers, T.1    Kamstra, J.H.2    Sonneveld, E.3    Murk, A.J.4    Visser, T.J.5    Van Velzen, M.J.M.6    Brouwer, A.7    Bergman, A.8
  • 17
    • 77952353333 scopus 로고    scopus 로고
    • QSAR modeling and prediction of the endocrine-disrupting potencies of brominated flame retardants
    • Papa E, Kovarich S, Gramatica P. 2010. QSAR modeling and prediction of the endocrine-disrupting potencies of brominated flame retardants. Chem Res Toxicol 23: 946-954.
    • (2010) Chem Res Toxicol , vol.23 , pp. 946-954
    • Papa, E.1    Kovarich, S.2    Gramatica, P.3
  • 18
    • 79956156043 scopus 로고    scopus 로고
    • QSAR classification models for the prediction of endocrine disrupting activity of brominated flame retardants
    • Kovarich S, Papa E, Gramatica P. 2011. QSAR classification models for the prediction of endocrine disrupting activity of brominated flame retardants. J Hazard Mater 190: 106-112.
    • (2011) J Hazard Mater , vol.190 , pp. 106-112
    • Kovarich, S.1    Papa, E.2    Gramatica, P.3
  • 19
    • 51849109110 scopus 로고    scopus 로고
    • Only subtle protein conformational adaptations are required for ligand binding to thyroid hormone receptors: simulations using a novel multipoint steered molecular dynamics approach
    • Martinez L, Polikarpov I, Skaf MS. 2008. Only subtle protein conformational adaptations are required for ligand binding to thyroid hormone receptors: simulations using a novel multipoint steered molecular dynamics approach. J Phys Chem B 112: 10741-10751.
    • (2008) J Phys Chem B , vol.112 , pp. 10741-10751
    • Martinez, L.1    Polikarpov, I.2    Skaf, M.S.3
  • 20
    • 0037837211 scopus 로고    scopus 로고
    • Development of biologically active compounds by combining 3D QSAR and structure-based design methods
    • Sippl W. 2002. Development of biologically active compounds by combining 3D QSAR and structure-based design methods. J Comput Aided Mol Des 16: 825-830.
    • (2002) J Comput Aided Mol Des , vol.16 , pp. 825-830
    • Sippl, W.1
  • 21
    • 13944264638 scopus 로고    scopus 로고
    • Three-dimensional structure-activity relationships of nonsteroidal ligands in complex with androgen receptor ligand-binding domain
    • Soderholm AA, Lehtovuori PT, Nyronen TH. 2005. Three-dimensional structure-activity relationships of nonsteroidal ligands in complex with androgen receptor ligand-binding domain. J Med Chem 48: 917-925.
    • (2005) J Med Chem , vol.48 , pp. 917-925
    • Soderholm, A.A.1    Lehtovuori, P.T.2    Nyronen, T.H.3
  • 22
    • 34247515897 scopus 로고    scopus 로고
    • Quantitative structure-activity relationship modeling on in vitro endocrine effects and metabolic stability involving 26 selected brominated flame retardants
    • Harju M, Hamers T, Kamstra JH, Sonneveld E, Boon JP, Tysklind M, Andersson PL. 2007. Quantitative structure-activity relationship modeling on in vitro endocrine effects and metabolic stability involving 26 selected brominated flame retardants. Environ Toxicol Chem 26: 816-826.
    • (2007) Environ Toxicol Chem , vol.26 , pp. 816-826
    • Harju, M.1    Hamers, T.2    Kamstra, J.H.3    Sonneveld, E.4    Boon, J.P.5    Tysklind, M.6    Andersson, P.L.7
  • 23
    • 0032474873 scopus 로고    scopus 로고
    • Three-dimensional quantitative similarity-activity relationships (3D QSAR) from SEAL similarity matrices
    • Kubinyi H, Hamprecht FA, Mietzner T. 1998. Three-dimensional quantitative similarity-activity relationships (3D QSAR) from SEAL similarity matrices. J Med Chem 41: 2553-2564.
    • (1998) J Med Chem , vol.41 , pp. 2553-2564
    • Kubinyi, H.1    Hamprecht, F.A.2    Mietzner, T.3
  • 24
    • 33845277149 scopus 로고    scopus 로고
    • QSAR prediction of estrogen activity for a large set of diverse chemicals under the guidance of OECD principles
    • Liu HX, Papa E, Gramatica P. 2006. QSAR prediction of estrogen activity for a large set of diverse chemicals under the guidance of OECD principles. Chem Res Toxicol 19: 1540-1548.
    • (2006) Chem Res Toxicol , vol.19 , pp. 1540-1548
    • Liu, H.X.1    Papa, E.2    Gramatica, P.3
  • 27
    • 0037424603 scopus 로고    scopus 로고
    • QSAR models in receptor-mediated effects: the nuclear receptor superfamily
    • Fang H, Tong WD, Welsh WJ, Sheehan DM. 2003. QSAR models in receptor-mediated effects: the nuclear receptor superfamily. J Mol Struct (Theochem) 622: 113-125.
    • (2003) J Mol Struct (Theochem) , vol.622 , pp. 113-125
    • Fang, H.1    Tong, W.D.2    Welsh, W.J.3    Sheehan, D.M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.