메뉴 건너뛰기




Volumn 52, Issue 6, 2009, Pages 1768-1772

Design, synthesis, and biological evaluation of (2R,αS)-3,4-dihydro- 2-[3-(1,1,2,2-tetrafluoroet-hoxy)phenyl]-5-[3-(trifluoromethoxy)-phenyl] -a-(trifluoromethyl)-1(2H)-quinolineethanol as potent and orally active cholesteryl ester transfer protein inhibitor

Author keywords

[No Author keywords available]

Indexed keywords

3,4 DIHYDRO 2 [3 (1,1,2,2 TETRAFLUOROETHOXY)PHENYL] 5 [3 (TRIFLUOROMETHOXY)PHENYL]ALPHA (TRIFLUOROMETHYL) 1(2H) QUIOLINEETHANOL; CHOLESTEROL ESTER TRANSFER PROTEIN INHIBITOR; TORCETRAPIB; UNCLASSIFIED DRUG;

EID: 64349124065     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm801319d     Document Type: Article
Times cited : (41)

References (22)
  • 1
    • 0242490816 scopus 로고    scopus 로고
    • Pharmacotheraphy for dyslipidemia-current therapies and future agents
    • Bays, H.; Stein, E. A. Pharmacotheraphy for dyslipidemia-current therapies and future agents. Expert Opin.pharmacother. 2003, 4 (11), 1901-1938.
    • (2003) Expert Opin.pharmacother , vol.4 , Issue.11 , pp. 1901-1938
    • Bays, H.1    Stein, E.A.2
  • 2
    • 17144380822 scopus 로고    scopus 로고
    • The metabolic syndrome
    • Eckel, R. H.; Grundy, S. M.; Zimmet, P. Z. The metabolic syndrome. Lancet 2005, 365, 11415-11428.
    • (2005) Lancet , vol.365 , pp. 11415-11428
    • Eckel, R.H.1    Grundy, S.M.2    Zimmet, P.Z.3
  • 3
    • 26244432388 scopus 로고    scopus 로고
    • Efficacy and safety of cholesterol-lowering treatment: Prospective meta-analysis of data from 90056 participants in 14 randomised trials of statins
    • Baigent, C.; Keech, A.; Kearney, P. M.; Blackwell, L.; Buck, G.; Pollicino, C.; Kirby, A.; Sourjina, T.; Peto, R.; Collins, R.; Simes, J. Efficacy and safety of cholesterol-lowering treatment: prospective meta-analysis of data from 90056 participants in 14 randomised trials of statins. Lancet 2005, 366, 1267-1278.
    • (2005) Lancet , vol.366 , pp. 1267-1278
    • Baigent, C.1    Keech, A.2    Kearney, P.M.3    Blackwell, L.4    Buck, G.5    Pollicino, C.6    Kirby, A.7    Sourjina, T.8    Peto, R.9    Collins, R.10    Simes, J.11
  • 4
    • 3042700144 scopus 로고    scopus 로고
    • Medical lipid-regulating therapy: Current evidence, ongoing trials and future developments
    • Evans, M.; Roberts, A.; Davies, S.; Rees, A. Medical lipid-regulating therapy: Current evidence, ongoing trials and future developments. Drugs 2004, 64, 1181-1196.
    • (2004) Drugs , vol.64 , pp. 1181-1196
    • Evans, M.1    Roberts, A.2    Davies, S.3    Rees, A.4
  • 5
    • 0017384270 scopus 로고
    • High density lipoprotein as a protective factor against coronary heart disease. The Framingham study
    • Gordon, T.; Castelli, W. P.; Hjortland, M. C.; Kannel, W. B.; Dawber, T. R. High density lipoprotein as a protective factor against coronary heart disease. The Framingham study. Am. J. Med 1977, 62, 707-714.
    • (1977) Am. J. Med , vol.62 , pp. 707-714
    • Gordon, T.1    Castelli, W.P.2    Hjortland, M.C.3    Kannel, W.B.4    Dawber, T.R.5
  • 7
    • 30444432694 scopus 로고    scopus 로고
    • Oral cholesteryl ester transfer protein (CETP) inhibitors: A potential new approach for treating coronary artery disease
    • Sikorski, J. A. Oral cholesteryl ester transfer protein (CETP) inhibitors: a potential new approach for treating coronary artery disease. J. Med. Chem. 2006, 49 (1), 1-22.
    • (2006) J. Med. Chem , vol.49 , Issue.1 , pp. 1-22
    • Sikorski, J.A.1
  • 8
    • 0036911578 scopus 로고    scopus 로고
    • The yin and yang of cholesteryl ester transfer protein and atherosclerosis
    • Watts, G. F. The yin and yang of cholesteryl ester transfer protein and atherosclerosis. Clin. Sci. 2002, 103, 595-597.
    • (2002) Clin. Sci , vol.103 , pp. 595-597
    • Watts, G.F.1
  • 12
    • 0034699510 scopus 로고    scopus 로고
    • Bis(2-(acylamino)-phenyl)disulfides, 2-(acylamino)benzenethiols, and S-(2-(acylamino)-phenyl)-alkanethioates as novel inhibitors of cho-lesteryl ester transfer protein
    • (a) Shinkai, H.; Maeda, K.; Yamasaki, T.; Okamoto, H.; Uchida, I. Bis(2-(acylamino)-phenyl)disulfides, 2-(acylamino)benzenethiols, and S-(2-(acylamino)-phenyl)-alkanethioates as novel inhibitors of cho-lesteryl ester transfer protein. J. Med. Chem. 2000, 43, 3566-3572.
    • (2000) J. Med. Chem , vol.43 , pp. 3566-3572
    • Shinkai, H.1    Maeda, K.2    Yamasaki, T.3    Okamoto, H.4    Uchida, I.5
  • 13
    • 44449145644 scopus 로고    scopus 로고
    • Spotlight on HDL-raising therapies: Insights from the torcetrapib trials
    • (b) Kontush, A.; Guerin, M.; Chapman, M. J. Spotlight on HDL-raising therapies: insights from the torcetrapib trials. Nat. Clin. Pract. Cardiovasc. Med. 2008, 5, 329-336.
    • (2008) Nat. Clin. Pract. Cardiovasc. Med , vol.5 , pp. 329-336
    • Kontush, A.1    Guerin, M.2    Chapman, M.J.3
  • 14
    • 44449171069 scopus 로고    scopus 로고
    • Anacetrapib: New hope for cholesteryl ester transfer protein inhibitors in the treatment of dyslipidemia
    • Vergeer, M.; Kastelein, J. J. P. Anacetrapib: new hope for cholesteryl ester transfer protein inhibitors in the treatment of dyslipidemia. Nat. Clin. Pract. Cardiovasc. Med. 2008, 5, 302-303.
    • (2008) Nat. Clin. Pract. Cardiovasc. Med , vol.5 , pp. 302-303
    • Vergeer, M.1    Kastelein, J.J.P.2
  • 16
    • 0029119899 scopus 로고
    • 2-and 4-Nitrobenzenesulfona-mides: Exceptionally versatile means for preparation of secondary amines and protection of amines
    • Fukuyama, T.; Jow, C.-K.; Cheung, M. 2-and 4-Nitrobenzenesulfona-mides: Exceptionally versatile means for preparation of secondary amines and protection of amines. Tetrahedron Lett. 1995, 36 (36), 6373-6374.
    • (1995) Tetrahedron Lett , vol.36 , Issue.36 , pp. 6373-6374
    • Fukuyama, T.1    Jow, C.-K.2    Cheung, M.3
  • 17
    • 0036170254 scopus 로고    scopus 로고
    • A mild copper-mediated intramolecular amination of aryl halides
    • Yamada, K.; Kubo, T.; Tokuyama, H.; Fukuyama, T. A mild copper-mediated intramolecular amination of aryl halides. Synlett 2002, 2, 231-234.
    • (2002) Synlett , vol.2 , pp. 231-234
    • Yamada, K.1    Kubo, T.2    Tokuyama, H.3    Fukuyama, T.4
  • 18
    • 0001939466 scopus 로고
    • Chiral synthesis via organoboranes. 40. Selective reductions. 55. A simple one-pot synthesis of the enantiomers of (trifluoromethyl)oxirane. A general synthesis in high optical purities of a-trifluoromethyl secondary alcohols via the ring-cleavage reactions of the epoxide
    • Ramachandran, P. V.; Gong, B.; Brown, H. C. Chiral synthesis via organoboranes. 40. Selective reductions. 55. A simple one-pot synthesis of the enantiomers of (trifluoromethyl)oxirane. A general synthesis in high optical purities of a-trifluoromethyl secondary alcohols via the ring-cleavage reactions of the epoxide. J. Org. Chem. 1995, 60, 41-46.
    • (1995) J. Org. Chem , vol.60 , pp. 41-46
    • Ramachandran, P.V.1    Gong, B.2    Brown, H.C.3
  • 19
    • 64349097121 scopus 로고    scopus 로고
    • Rano, T.; Kuo, G.-H.; Sieber-McMaster, E.; Demarest, K. T.; Pelton, P.; Wang, A. 1,2,3,4-Tetrahydro-quinoline derivatives as CETP inhibitors. U.S. Pat. Appl. Publ. US 2007265304 A1 20071115, 2007.
    • Rano, T.; Kuo, G.-H.; Sieber-McMaster, E.; Demarest, K. T.; Pelton, P.; Wang, A. 1,2,3,4-Tetrahydro-quinoline derivatives as CETP inhibitors. U.S. Pat. Appl. Publ. US 2007265304 A1 20071115, 2007.
  • 21
    • 0037030653 scopus 로고    scopus 로고
    • Molecular properties that influence the oral bioavail-ability of drug candidates
    • Veber, D. F.; Johnson, S. R.; Cheng, H. Y.; Smith, B. R.; Ward, K. W.; Kopple, K. D. Molecular properties that influence the oral bioavail-ability of drug candidates. J. Med. Chem. 2002, 45, 2615-2623.
    • (2002) J. Med. Chem , vol.45 , pp. 2615-2623
    • Veber, D.F.1    Johnson, S.R.2    Cheng, H.Y.3    Smith, B.R.4    Ward, K.W.5    Kopple, K.D.6
  • 22
    • 33644775588 scopus 로고    scopus 로고
    • Description of the torcetrapib series of cholesteryl ester transfer protein inhibitiors, including mechanism of action
    • Clark, R. W.; Ruggeri, R. B.; Cunningham, D.; Bamberger, M. J. Description of the torcetrapib series of cholesteryl ester transfer protein inhibitiors, including mechanism of action. J. Lipid Res. 2006, 47, 537-552.
    • (2006) J. Lipid Res , vol.47 , pp. 537-552
    • Clark, R.W.1    Ruggeri, R.B.2    Cunningham, D.3    Bamberger, M.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.