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Volumn 14, Issue 6, 2012, Pages 347-351

New diethylsilylacetylenic linker for parallel solid-phase synthesis of libraries of hydroxy acetylenic steroid derivatives with improved metabolic stability

Author keywords

hydroxy acetylenic compounds; library; linker; solid phase synthesis; steroids

Indexed keywords

ALKYNE; STEROID;

EID: 84862155403     PISSN: 21568952     EISSN: None     Source Type: Journal    
DOI: 10.1021/co300034y     Document Type: Article
Times cited : (12)

References (22)
  • 1
    • 84862133618 scopus 로고    scopus 로고
    • Term Paper, Swiss Federal Institude of Technology, Institute of Biogeochemistry and Polluant Dynamics (IBP-ETH), Universitaetsstrasse 16, CH-8092 Zurich
    • Moshet, C.; Hollender, J. Microbial degradation of steroid hormones in the environment and technical systems. Term Paper, Swiss Federal Institude of Technology, Institute of Biogeochemistry and Polluant Dynamics (IBP-ETH), Universitaetsstrasse 16, CH-8092 Zurich, 2009.
    • (2009) Microbial Degradation of Steroid Hormones in the Environment and Technical Systems
    • Moshet, C.1    Hollender, J.2
  • 2
    • 24144485432 scopus 로고    scopus 로고
    • Pharmacology of estrogens and progestogens: Influence of different routes of administration
    • Kuhl, H. Pharmacology of estrogens and progestogens: influence of different routes of administration Climateric 2005, 8 (Suppl 1) 3-63
    • (2005) Climateric , vol.8 , Issue.SUPPL. 1 , pp. 3-63
    • Kuhl, H.1
  • 4
    • 0027521059 scopus 로고
    • Human bilirubin UDP-glucuronosyltransferase catalyses the glucuronidation of ethinylestradiol
    • Ebner, T.; Remmel, R. P.; Burchell, B. Human bilirubin UDP-glucuronosyltransferase catalyses the glucuronidation of ethinylestradiol Mol. Pharmacol. 1993, 43, 649-654
    • (1993) Mol. Pharmacol. , vol.43 , pp. 649-654
    • Ebner, T.1    Remmel, R.P.2    Burchell, B.3
  • 6
    • 4944264475 scopus 로고    scopus 로고
    • Removal of estrogenic activity and formation of oxidation products during ozonation of 17α-ethinylestradiol
    • Huber, M. M.; Ternes, T. A.; Von Gunten, U. Removal of estrogenic activity and formation of oxidation products during ozonation of 17α-ethinylestradiol Environ. Sci. Technol. 2004, 38, 5177-5186
    • (2004) Environ. Sci. Technol. , vol.38 , pp. 5177-5186
    • Huber, M.M.1    Ternes, T.A.2    Von Gunten, U.3
  • 9
    • 0000853115 scopus 로고    scopus 로고
    • Estrogens and progestins
    • In, 9 th ed. Gilman, A. G. Goodman, L. S. Hardman, G. Limbird, L. McGraw-Hill, New York
    • Williams, C. L.; Stancel, G. M. Estrogens and progestins. In The Pharmacological Basis of Therapeutics, 9 th ed.; Gilman, A. G.; Goodman, L. S.; Hardman, G.; Limbird, L., Eds.; McGraw-Hill,: New York, 1996; 1411-1440.
    • (1996) The Pharmacological Basis of Therapeutics , pp. 1411-1440
    • Williams, C.L.1    Stancel, G.M.2
  • 13
    • 79953268949 scopus 로고    scopus 로고
    • Discovery of new rennin inhibitory leads via sequential pharmacophore modeling, QSAR analysis, in silico screening and in vitro evaluation
    • Al-Nadaf, A. H.; Taha, M. O. Discovery of new rennin inhibitory leads via sequential pharmacophore modeling, QSAR analysis, in silico screening and in vitro evaluation J. Mol. Graph. Model. 2011, 29, 843-864
    • (2011) J. Mol. Graph. Model. , vol.29 , pp. 843-864
    • Al-Nadaf, A.H.1    Taha, M.O.2
  • 14
    • 0034736085 scopus 로고    scopus 로고
    • Chiral derivatives of 2-cyclohexylideneperhydro-4,7-methanoindenes, a novel class of nonsteroidal androgen receptor gigan: Synthesis, X-ray analysis and biological activity
    • Burden, P. M.; Ai, T. H.; Lin, H. Q.; Akinci, M.; Costandi, M.; Hambley, T. M.; Johnston, G. A. R. Chiral derivatives of 2-cyclohexylideneperhydro-4,7- methanoindenes, a novel class of nonsteroidal androgen receptor gigan: synthesis, X-ray analysis and biological activity J. Med. Chem. 2000, 43, 4629-4635
    • (2000) J. Med. Chem. , vol.43 , pp. 4629-4635
    • Burden, P.M.1    Ai, T.H.2    Lin, H.Q.3    Akinci, M.4    Costandi, M.5    Hambley, T.M.6    Johnston, G.A.R.7
  • 15
    • 72449181468 scopus 로고    scopus 로고
    • Innovations and opportinities to improve conventional (deoxy)nucleoside and fluoropyrimidine analogs in cancer
    • Adema, A. D.; Bijnsdorp, I. V.; Sandvold, M. L.; Verheul, H. M.; Peters, G. J. Innovations and opportinities to improve conventional (deoxy)nucleoside and fluoropyrimidine analogs in cancer Curr. Med. Chem. 2009, 16, 4632-4643
    • (2009) Curr. Med. Chem. , vol.16 , pp. 4632-4643
    • Adema, A.D.1    Bijnsdorp, I.V.2    Sandvold, M.L.3    Verheul, H.M.4    Peters, G.J.5
  • 17
    • 48949117194 scopus 로고    scopus 로고
    • Cytotoxic nucleoside analogues: Differents strategies to improve their clinical efficacy
    • Galmarini, C. M.; Popowycz, F.; Joseph, B. Cytotoxic nucleoside analogues: differents strategies to improve their clinical efficacy Curr. Med. Chem. 2008, 15, 1072-1082
    • (2008) Curr. Med. Chem. , vol.15 , pp. 1072-1082
    • Galmarini, C.M.1    Popowycz, F.2    Joseph, B.3
  • 18
    • 4344581290 scopus 로고    scopus 로고
    • Tibolone: A selective tissue estrogenic activity regulator (STEAR)
    • Kloosterboer, H. J.; Reed, M. J. Tibolone: a selective tissue estrogenic activity regulator (STEAR) Maturitas 2004, 48 (Suppl. 1) S1-S42
    • (2004) Maturitas , vol.48 , Issue.SUPPL. 1
    • Kloosterboer, H.J.1    Reed, M.J.2
  • 19
    • 8744247081 scopus 로고    scopus 로고
    • The synthesis of tetrahydroquinolines related to virantmycin
    • Francis, C. L.; Williamson, N. M.; Ward, D. A. The synthesis of tetrahydroquinolines related to virantmycin Synthesis 2004, 16, 2685-2691
    • (2004) Synthesis , vol.16 , pp. 2685-2691
    • Francis, C.L.1    Williamson, N.M.2    Ward, D.A.3
  • 20
    • 0001652171 scopus 로고
    • A novel synthesis of spironolactone. An application of the hydroformylation reaction
    • Wuts, P. G. M.; Ritter, A. R. A novel synthesis of spironolactone. An application of the hydroformylation reaction J. Org. Chem. 1989, 54, 5180-5182
    • (1989) J. Org. Chem. , vol.54 , pp. 5180-5182
    • Wuts, P.G.M.1    Ritter, A.R.2
  • 21
    • 34249942380 scopus 로고    scopus 로고
    • 2β-(N -Substituted piperazino)-5α-androstane-3α, 17β-diols: Parallel solid-phase synthesis and antiproliferative activity on human leukemia HL-60 Cells
    • Roy, J.; DeRoy, P.; Poirier, D. 2β-(N -Substituted piperazino)-5α-androstane-3α,17β-diols: parallel solid-phase synthesis and antiproliferative activity on human leukemia HL-60 Cells J. Comb. Chem. 2007, 9, 347-358
    • (2007) J. Comb. Chem. , vol.9 , pp. 347-358
    • Roy, J.1    Deroy, P.2    Poirier, D.3
  • 22
    • 80051573783 scopus 로고    scopus 로고
    • Libraries of 2β-(N -Substituted piperazino)-5α-androstane- 3α,17β-diols: Chemical synthesis and cytotoxic effects on human leukemia HL-60 cells and on normal lymphocytes
    • Roy, J.; Maltais, R.; Jegham, H.; Poirier, D. Libraries of 2β-(N -Substituted piperazino)-5α-androstane-3α,17β-diols: chemical synthesis and cytotoxic effects on human leukemia HL-60 cells and on normal lymphocytes Mol. Diversity 2011, 15, 317-339
    • (2011) Mol. Diversity , vol.15 , pp. 317-339
    • Roy, J.1    Maltais, R.2    Jegham, H.3    Poirier, D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.