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Volumn 9, Issue 11, 2009, Pages 1272-1283

Inhibitors of HMG-CoA reductase: Current and future prospects

Author keywords

asarone; 3 hydroxy 3 methylglutaryl coenzyme A reductase; Cardiovascular disease; Cholesterol; Low density lipoproteins; Side effects; Statins; Structure based drug design

Indexed keywords

ALPHA ASARONE; ATORVASTATIN; FLUINDOSTATIN; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE INHIBITOR; MEVINOLIN; NICOTINIC ACID; PRAVASTATIN; PROBUCOL; ROSUVASTATIN; SIMVASTATIN;

EID: 73349085890     PISSN: 13895575     EISSN: None     Source Type: Journal    
DOI: 10.2174/138955709789878105     Document Type: Short Survey
Times cited : (26)

References (131)
  • 1
    • 73349129902 scopus 로고    scopus 로고
    • Accessed July 28, 2009
    • American Heart Association. http://www.americanheart.org (Accessed July 28, 2009).
  • 2
    • 60449094498 scopus 로고    scopus 로고
    • Lloyd-Jones, D.; Adams, R.; Carnethon, M.; De Simone, G.; Ferguson, T.B.; Flegal, K.; Ford, E.; Furie, K.; Go, A.; Greenlund, K.; Haase, N.; Hailpern, S.; Ho, M.; Howard, V.; Kissela, B.; Kittner, S.; Lackland, D.; Lisabeth, L.; Marelli, A.; McDermott, M.; Meigs, J.; Mozaffarian, D.; Nichol, G.; O'Donnell, C.; Roger, V.; Rosamond, W.; Sacco, R.; Sorlie, P.; Stafford, R.; Steinberger, J.; Thom, T.; Wasserthiel-Smoller, S.; Wong, N.; Wylie-Rosett, J.; Hong, Y. Heart disease and stroke statistics - 2009 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Circulation, 2009, 119, e21-181.
    • Lloyd-Jones, D.; Adams, R.; Carnethon, M.; De Simone, G.; Ferguson, T.B.; Flegal, K.; Ford, E.; Furie, K.; Go, A.; Greenlund, K.; Haase, N.; Hailpern, S.; Ho, M.; Howard, V.; Kissela, B.; Kittner, S.; Lackland, D.; Lisabeth, L.; Marelli, A.; McDermott, M.; Meigs, J.; Mozaffarian, D.; Nichol, G.; O'Donnell, C.; Roger, V.; Rosamond, W.; Sacco, R.; Sorlie, P.; Stafford, R.; Steinberger, J.; Thom, T.; Wasserthiel-Smoller, S.; Wong, N.; Wylie-Rosett, J.; Hong, Y. Heart disease and stroke statistics - 2009 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Circulation, 2009, 119, e21-181.
  • 3
    • 0030983708 scopus 로고    scopus 로고
    • Mortality by cause for eight regions of the world: Global Burden of Disease Study
    • Murray, C.J.; Lopez, A.D. Mortality by cause for eight regions of the world: Global Burden of Disease Study. Lancet, 1997, 349, 1269-76.
    • (1997) Lancet , vol.349 , pp. 1269-1276
    • Murray, C.J.1    Lopez, A.D.2
  • 5
    • 33749233854 scopus 로고    scopus 로고
    • Life after statin patent expiries
    • Kidd, J. Life after statin patent expiries. Nat. Rev. Drug Discov., 2006, 5, 813-4.
    • (2006) Nat. Rev. Drug Discov , vol.5 , pp. 813-814
    • Kidd, J.1
  • 6
    • 0032851111 scopus 로고    scopus 로고
    • Sterols and isoprenoids: Signaling molecules derived from the cholesterol biosynthetic pathway
    • Edwards, P.A.; Ericsson, J. Sterols and isoprenoids: signaling molecules derived from the cholesterol biosynthetic pathway. Annu. Rev. Biochem., 1999, 68, 157-85.
    • (1999) Annu. Rev. Biochem , vol.68 , pp. 157-185
    • Edwards, P.A.1    Ericsson, J.2
  • 7
    • 0025120211 scopus 로고
    • Regulation of the mevalonate pathway
    • Goldstein, J.L.; Brown, M.S. Regulation of the mevalonate pathway. Nature, 1990, 343, 425-30.
    • (1990) Nature , vol.343 , pp. 425-430
    • Goldstein, J.L.1    Brown, M.S.2
  • 8
    • 0037126729 scopus 로고    scopus 로고
    • Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report
    • Third Report of the National Cholesterol Education Program NCEP
    • Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report. Circulation, 2002, 106, 3143-421.
    • (2002) Circulation , vol.106 , pp. 3143-3421
  • 9
    • 0032802253 scopus 로고    scopus 로고
    • The mammalian low-density lipoprotein receptor family
    • Hussain, M.M.; Strickland, D.K.; Bakillah, A. The mammalian low-density lipoprotein receptor family. Annu. Rev. Nutr., 1999, 19, 141-72.
    • (1999) Annu. Rev. Nutr , vol.19 , pp. 141-172
    • Hussain, M.M.1    Strickland, D.K.2    Bakillah, A.3
  • 10
    • 0033045079 scopus 로고    scopus 로고
    • The low-density lipoprotein receptor gene family: Multiple roles in lipid metabolism
    • Willnow, T.E. The low-density lipoprotein receptor gene family: multiple roles in lipid metabolism. J. Mol. Med., 1999, 77, 306-15.
    • (1999) J. Mol. Med , vol.77 , pp. 306-315
    • Willnow, T.E.1
  • 12
    • 0036251153 scopus 로고    scopus 로고
    • SREBPs: Activators of the complete program of cholesterol and fatty acid synthesis in the liver
    • Horton, J.D.; Goldstein, J.L.; Brown, M.S. SREBPs: activators of the complete program of cholesterol and fatty acid synthesis in the liver. J. Clin. Invest., 2002, 109, 1125-31.
    • (2002) J. Clin. Invest , vol.109 , pp. 1125-1131
    • Horton, J.D.1    Goldstein, J.L.2    Brown, M.S.3
  • 13
    • 0022549920 scopus 로고
    • A receptor-mediated pathway for cholesterol homeostasis
    • Brown, M.S.; Goldstein, J.L. A receptor-mediated pathway for cholesterol homeostasis. Science, 1986, 232, 34-47.
    • (1986) Science , vol.232 , pp. 34-47
    • Brown, M.S.1    Goldstein, J.L.2
  • 14
    • 73349084191 scopus 로고    scopus 로고
    • Decision Resources, Inc, Accessed July 28, 2009
    • Decision Resources, Inc. http://www.decisionresources.com (Accessed July 28, 2009).
  • 15
    • 15444368643 scopus 로고    scopus 로고
    • Drug-induced hepatotoxicity: 2005
    • Maddrey, W.C. Drug-induced hepatotoxicity: 2005. J. Clin. Gastroenterol., 2005, 39, S83-9.
    • (2005) J. Clin. Gastroenterol , vol.39
    • Maddrey, W.C.1
  • 16
    • 0033984436 scopus 로고    scopus 로고
    • Current perspectives on statins
    • Maron, D.J.; Fazio, S.; Linton, M.F. Current perspectives on statins. Circulation, 2000, 101, 207-13.
    • (2000) Circulation , vol.101 , pp. 207-213
    • Maron, D.J.1    Fazio, S.2    Linton, M.F.3
  • 17
    • 3242785011 scopus 로고    scopus 로고
    • Isoprenoids: Remarkable diversity of form and function
    • Holstein, S.A.; Hohl, R.J. Isoprenoids: remarkable diversity of form and function. Lipids., 2004, 39, 293-309.
    • (2004) Lipids , vol.39 , pp. 293-309
    • Holstein, S.A.1    Hohl, R.J.2
  • 18
    • 0038004785 scopus 로고    scopus 로고
    • Lovastatin and beyond: The history of the HMG-CoA reductase inhibitors
    • Tobert, J.A. Lovastatin and beyond: the history of the HMG-CoA reductase inhibitors. Nat. Rev. Drug Discov., 2003, 2, 517-26.
    • (2003) Nat. Rev. Drug Discov , vol.2 , pp. 517-526
    • Tobert, J.A.1
  • 19
    • 19744382332 scopus 로고    scopus 로고
    • The 3-hydroxy-3-methylglutaryl coenzyme-A (HMG-CoA) reductases
    • Friesen, J.A.; Rodwell, V.W. The 3-hydroxy-3-methylglutaryl coenzyme-A (HMG-CoA) reductases. Genome Biol., 2004, 5, 248.
    • (2004) Genome Biol , vol.5 , pp. 248
    • Friesen, J.A.1    Rodwell, V.W.2
  • 20
    • 0032789945 scopus 로고    scopus 로고
    • Sequence comparisons reveal two classes of 3-hydroxy-3-methylglutaryl coenzyme A reductase
    • Bochar, D.A.; Stauffacher, C.V.; Rodwell, V.W. Sequence comparisons reveal two classes of 3-hydroxy-3-methylglutaryl coenzyme A reductase. Mol. Genet. Metab., 1999, 66, 122-7.
    • (1999) Mol. Genet. Metab , vol.66 , pp. 122-127
    • Bochar, D.A.1    Stauffacher, C.V.2    Rodwell, V.W.3
  • 21
    • 1642300400 scopus 로고    scopus 로고
    • Class II 3-hydroxy-3-methylglutaryl coenzyme A reductases
    • Hedl, M.; Tabernero, L.; Stauffacher, C.V.; Rodwell, V.W. Class II 3-hydroxy-3-methylglutaryl coenzyme A reductases. J. Bacteriol., 2004, 186, 1927-32.
    • (2004) J. Bacteriol , vol.186 , pp. 1927-1932
    • Hedl, M.1    Tabernero, L.2    Stauffacher, C.V.3    Rodwell, V.W.4
  • 22
    • 0035843962 scopus 로고    scopus 로고
    • Structural mechanism for statin inhibition of HMG-CoA reductase
    • Istvan, E.S.; Deisenhofer, J. Structural mechanism for statin inhibition of HMG-CoA reductase. Science, 2001, 292, 1160-4.
    • (2001) Science , vol.292 , pp. 1160-1164
    • Istvan, E.S.1    Deisenhofer, J.2
  • 23
    • 0034161543 scopus 로고    scopus 로고
    • Crystal structure of the catalytic portion of human HMG-CoA reductase: Insights into regulation of activity and catalysis
    • Istvan, E.S.; Palnitkar, M.; Buchanan, S.K.; Deisenhofer, J. Crystal structure of the catalytic portion of human HMG-CoA reductase: insights into regulation of activity and catalysis. EMBO J., 2000, 19, 819-30.
    • (2000) EMBO J , vol.19 , pp. 819-830
    • Istvan, E.S.1    Palnitkar, M.2    Buchanan, S.K.3    Deisenhofer, J.4
  • 25
    • 37849017426 scopus 로고    scopus 로고
    • Pfefferkorn, J.A.; Choi, C.; Larsen, S.D.; Auerbach, B.; Hutchings, R.; Park, W.; Askew, V.; Dillon, L.; Hanselman, J.C.; Lin, Z.; Lu, G.H.; Robertson, A.; Sekerke, C.; Harris, M.S.; Pavlovsky, A.; Bainbridge, G.; Caspers, N.; Kowala, M.; Tait, B.D. Substituted pyrazoles as hepatoselective HMG-CoA reductase inhibitors: discovery of (3R,5R)-7-[2-(4-fluoro-phenyl)-4-isopropyl-5- (4-methylbenzylcarbamoyl)-2H -pyrazol-3-yl]-3,5-dihydroxyheptanoic acid (PF-3052334) as a candidate for the treatment of hypercholesterolemia. J. Med. Chem., 2008, 51, 31-45.
    • Pfefferkorn, J.A.; Choi, C.; Larsen, S.D.; Auerbach, B.; Hutchings, R.; Park, W.; Askew, V.; Dillon, L.; Hanselman, J.C.; Lin, Z.; Lu, G.H.; Robertson, A.; Sekerke, C.; Harris, M.S.; Pavlovsky, A.; Bainbridge, G.; Caspers, N.; Kowala, M.; Tait, B.D. Substituted pyrazoles as hepatoselective HMG-CoA reductase inhibitors: discovery of (3R,5R)-7-[2-(4-fluoro-phenyl)-4-isopropyl-5- (4-methylbenzylcarbamoyl)-2H -pyrazol-3-yl]-3,5-dihydroxyheptanoic acid (PF-3052334) as a candidate for the treatment of hypercholesterolemia. J. Med. Chem., 2008, 51, 31-45.
  • 27
    • 34447331951 scopus 로고    scopus 로고
    • Pfefferkorn, J.A.; Song, Y.; Sun, K.L.; Miller, S.R.; Trivedi, B.K.; Choi, C.; Sorenson, R.J.; Bratton, L.D.; Unangst, P.C.; Larsen, S.D.; Poel, T.J.; Cheng, X.M.; Lee, C.; Erasga, N.; Auerbach, B.; Askew, V.; Dillon, L.; Hanselman, J.C.; Lin, Z.; Lu, G.; Robertson, A.; Olsen, K.; Mertz, T.; Sekerke, C.; Pavlovsky, A.; Harris, M.S.; Bainbridge, G.; Caspers, N.; Chen, H.; Eberstadt, M. Design and synthesis of hepatoselective, pyrrole-based HMG-CoA reductase inhibitors. Bioorg. Med. Chem. Lett., 2007, 17, 4538-44.
    • Pfefferkorn, J.A.; Song, Y.; Sun, K.L.; Miller, S.R.; Trivedi, B.K.; Choi, C.; Sorenson, R.J.; Bratton, L.D.; Unangst, P.C.; Larsen, S.D.; Poel, T.J.; Cheng, X.M.; Lee, C.; Erasga, N.; Auerbach, B.; Askew, V.; Dillon, L.; Hanselman, J.C.; Lin, Z.; Lu, G.; Robertson, A.; Olsen, K.; Mertz, T.; Sekerke, C.; Pavlovsky, A.; Harris, M.S.; Bainbridge, G.; Caspers, N.; Chen, H.; Eberstadt, M. Design and synthesis of hepatoselective, pyrrole-based HMG-CoA reductase inhibitors. Bioorg. Med. Chem. Lett., 2007, 17, 4538-44.
  • 29
    • 0033595021 scopus 로고    scopus 로고
    • Substrate-induced closure of the flap domain in the ternary complex structures provides insights into the mechanism of catalysis by 3-hydroxy-3-methylglutaryl- CoA reductase
    • Tabernero, L.; Bochar, D.A.; Rodwell, V.W.; Stauffacher, C.V. Substrate-induced closure of the flap domain in the ternary complex structures provides insights into the mechanism of catalysis by 3-hydroxy-3-methylglutaryl- CoA reductase. Proc. Natl. Acad. Sci. USA, 1999, 96, 7167-71.
    • (1999) Proc. Natl. Acad. Sci. USA , vol.96 , pp. 7167-7171
    • Tabernero, L.1    Bochar, D.A.2    Rodwell, V.W.3    Stauffacher, C.V.4
  • 30
    • 0038504101 scopus 로고    scopus 로고
    • Crystal structure of a statin bound to a class II hydroxymethylglutaryl-CoA reductase
    • Tabernero, L.; Rodwell, V.W.; Stauffacher, C.V. Crystal structure of a statin bound to a class II hydroxymethylglutaryl-CoA reductase. J. Biol. Chem., 2003, 278, 19933-8.
    • (2003) J. Biol. Chem , vol.278 , pp. 19933-19938
    • Tabernero, L.1    Rodwell, V.W.2    Stauffacher, C.V.3
  • 31
    • 0035693327 scopus 로고    scopus 로고
    • Bacterial and mammalian HMG-CoA reductases: Related enzymes with distinct architectures
    • Istvan, E.S. Bacterial and mammalian HMG-CoA reductases: related enzymes with distinct architectures. Curr. Opin. Struct. Biol., 2001, 11, 746-51.
    • (2001) Curr. Opin. Struct. Biol , vol.11 , pp. 746-751
    • Istvan, E.S.1
  • 32
    • 0028213166 scopus 로고
    • Regulated degradation of HMG-CoA reductase, an integral membrane protein of the endoplasmic reticulum, in yeast
    • Hampton, R.Y.; Rine, J. Regulated degradation of HMG-CoA reductase, an integral membrane protein of the endoplasmic reticulum, in yeast. J. Cell Biol., 1994, 125, 299-312.
    • (1994) J. Cell Biol , vol.125 , pp. 299-312
    • Hampton, R.Y.1    Rine, J.2
  • 33
    • 0026681612 scopus 로고
    • Regulated degradation of 3-hydroxy-3- methylglutaryl-coenzyme A reductase in permeabilized cells
    • Meigs, T.E.; Simoni, R.D. Regulated degradation of 3-hydroxy-3- methylglutaryl-coenzyme A reductase in permeabilized cells. J. Biol. Chem., 1992, 267, 13547-52.
    • (1992) J. Biol. Chem , vol.267 , pp. 13547-13552
    • Meigs, T.E.1    Simoni, R.D.2
  • 34
    • 0031239831 scopus 로고    scopus 로고
    • Farnesol as a regulator of HMG-CoA reductase degradation: Characterization and role of farnesyl pyrophosphatase
    • Meigs, T.E.; Simoni, R.D. Farnesol as a regulator of HMG-CoA reductase degradation: characterization and role of farnesyl pyrophosphatase. Arch. Biochem. Biophys., 1997, 345, 1-9.
    • (1997) Arch. Biochem. Biophys , vol.345 , pp. 1-9
    • Meigs, T.E.1    Simoni, R.D.2
  • 35
    • 0017894322 scopus 로고
    • Induction of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in human fibroblasts incubated with compactin (ML-236B), a competitive inhibitor of the reductase
    • Brown, M.S.; Faust, J.R.; Goldstein, J.L.; Kaneko, I.; Endo, A. Induction of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in human fibroblasts incubated with compactin (ML-236B), a competitive inhibitor of the reductase. J. Biol. Chem., 1978, 253, 1121-8.
    • (1978) J. Biol. Chem , vol.253 , pp. 1121-1128
    • Brown, M.S.1    Faust, J.R.2    Goldstein, J.L.3    Kaneko, I.4    Endo, A.5
  • 36
    • 0017043554 scopus 로고
    • Competitive inhibition of 3-hydroxy-3-methylglutaryl coenzyme A reductase by ML-236A and ML-236B fungal metabolites, having hypocholesterolemic activity
    • Endo, A.; Kuroda, M.; Tanzawa, K. Competitive inhibition of 3-hydroxy-3-methylglutaryl coenzyme A reductase by ML-236A and ML-236B fungal metabolites, having hypocholesterolemic activity. FEBS Lett., 1976, 72, 323-6.
    • (1976) FEBS Lett , vol.72 , pp. 323-326
    • Endo, A.1    Kuroda, M.2    Tanzawa, K.3
  • 37
    • 0017055252 scopus 로고
    • ML-236A, ML-236B, and ML-236C, new inhibitors of cholesterogenesis produced by Penicillium citrinium
    • Endo, A.; Kuroda, M.; Tsujita, Y. ML-236A, ML-236B, and ML-236C, new inhibitors of cholesterogenesis produced by Penicillium citrinium. J. Antibiot. (Tokyo), 1976, 29, 1346-8.
    • (1976) J. Antibiot. (Tokyo) , vol.29 , pp. 1346-1348
    • Endo, A.1    Kuroda, M.2    Tsujita, Y.3
  • 38
    • 0018500225 scopus 로고
    • Kinetic analysis of the reaction catalyzed by rat-liver 3-hydroxy-3-methylglutaryl-coenzyme-A reductase using two specific inhibitors
    • Tanzawa, K.; Endo, A. Kinetic analysis of the reaction catalyzed by rat-liver 3-hydroxy-3-methylglutaryl-coenzyme-A reductase using two specific inhibitors. Eur. J. Biochem., 1979, 98, 195-201.
    • (1979) Eur. J. Biochem , vol.98 , pp. 195-201
    • Tanzawa, K.1    Endo, A.2
  • 39
    • 0018939225 scopus 로고    scopus 로고
    • Alberts, A.W.; Chen, J.; Kuron, G.; Hunt, V.; Huff, J.; Hoffman, C.; Rothrock, J.; Lopez, M.; Joshua, H.; Harris, E.; Patchett, A.; Monaghan, R.; Currie, S.; Stapley, E.; Albers-Schonberg, G.; Hensens, O.; Hirshfield, J.; Hoogsteen, K.; Liesch, J.; Springer, J. Mevinolin: a highly potent competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase and a cholesterol-lowering agent. Proc. Natl. Acad. Sci. USA, 1980, 77, 3957-61.
    • Alberts, A.W.; Chen, J.; Kuron, G.; Hunt, V.; Huff, J.; Hoffman, C.; Rothrock, J.; Lopez, M.; Joshua, H.; Harris, E.; Patchett, A.; Monaghan, R.; Currie, S.; Stapley, E.; Albers-Schonberg, G.; Hensens, O.; Hirshfield, J.; Hoogsteen, K.; Liesch, J.; Springer, J. Mevinolin: a highly potent competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase and a cholesterol-lowering agent. Proc. Natl. Acad. Sci. USA, 1980, 77, 3957-61.
  • 40
    • 73349111507 scopus 로고    scopus 로고
    • Willard, A.K. 6(R)-[2-(8-Hydroxy-2,6-dimethylpolyhydronaphthyl-1)-e thyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-ones. U.S. Patent 4,293,496. 1981.
    • Willard, A.K. 6(R)-[2-(8-Hydroxy-2,6-dimethylpolyhydronaphthyl-1)-e thyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-ones. U.S. Patent 4,293,496. 1981.
  • 41
    • 0022485201 scopus 로고
    • CS-514, a competitive inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase: Tissue-selective inhibition of sterol synthesis and hypolipidemic effect on various animal species
    • Tsujita, Y.; Kuroda, M.; Shimada, Y.; Tanzawa, K.; Arai, M.; Kaneko, I.; Tanaka, M.; Masuda, H.; Tarumi, C.; Watanabe, Y.; et al. CS-514, a competitive inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase: tissue-selective inhibition of sterol synthesis and hypolipidemic effect on various animal species. Biochim. Biophys. Acta, 1986, 877, 50-60.
    • (1986) Biochim. Biophys. Acta , vol.877 , pp. 50-60
    • Tsujita, Y.1    Kuroda, M.2    Shimada, Y.3    Tanzawa, K.4    Arai, M.5    Kaneko, I.6    Tanaka, M.7    Masuda, H.8    Tarumi, C.9    Watanabe, Y.10
  • 42
    • 73349130669 scopus 로고
    • Intermediates in the synthesis of indole analogs of mevalonolactone and derivatives thereof
    • U.S. Patent 4,739,073
    • Kathawala, F.G. Intermediates in the synthesis of indole analogs of mevalonolactone and derivatives thereof. U.S. Patent 4,739,073. 1988.
    • (1988)
    • Kathawala, F.G.1
  • 43
    • 0025794258 scopus 로고
    • HMG-CoA reductase inhibitors: An exciting development in the treatment of hyperlipoproteinemia
    • Kathawala, F.G. HMG-CoA reductase inhibitors: an exciting development in the treatment of hyperlipoproteinemia. Med. Res. Rev., 1991, 11, 121-46.
    • (1991) Med. Res. Rev , vol.11 , pp. 121-146
    • Kathawala, F.G.1
  • 44
    • 73349111175 scopus 로고    scopus 로고
    • Roth, B.D. Trans-6-[2-(3- or 4-carboxamido-substituted pyrrol-1-yl)alkyl]-4-hydroxypyran-2-one inhibitors of cholesterol synthesis. U.S. Patent 4,681,893. 1987
    • Roth, B.D. Trans-6-[2-(3- or 4-carboxamido-substituted pyrrol-1-yl)alkyl]-4-hydroxypyran-2-one inhibitors of cholesterol synthesis. U.S. Patent 4,681,893. 1987.
  • 45
    • 0029980255 scopus 로고    scopus 로고
    • Effect of the new HMG-CoA reductase inhibitor cerivastatin (BAY W 6228)on migration, proliferation and cholesterol synthesis in arterial myocytes
    • Corsini, A.; Arnaboldi, L.; Raiteri, M.; Quarato, P.; Faggiotto, A.; Paoletti, R.; Fumagalli, R. Effect of the new HMG-CoA reductase inhibitor cerivastatin (BAY W 6228)on migration, proliferation and cholesterol synthesis in arterial myocytes. Pharmacol. Res., 1996, 33, 55-61.
    • (1996) Pharmacol. Res , vol.33 , pp. 55-61
    • Corsini, A.1    Arnaboldi, L.2    Raiteri, M.3    Quarato, P.4    Faggiotto, A.5    Paoletti, R.6    Fumagalli, R.7
  • 46
    • 0031081522 scopus 로고    scopus 로고
    • Synthesis and biological activity of methanesulfonamide pyrimidine-and N-methanesulfonyl pyrrole-substituted 3,5-dihydroxy-6-heptenoates, a novel series of HMG-CoA reductase inhibitors
    • Watanabe, M.; Koike, H.; Ishiba, T.; Okada, T.; Seo, S.; Hirai, K. Synthesis and biological activity of methanesulfonamide pyrimidine-and N-methanesulfonyl pyrrole-substituted 3,5-dihydroxy-6-heptenoates, a novel series of HMG-CoA reductase inhibitors. Bioorg. Med. Chem., 1997, 5, 437-44.
    • (1997) Bioorg. Med. Chem , vol.5 , pp. 437-444
    • Watanabe, M.1    Koike, H.2    Ishiba, T.3    Okada, T.4    Seo, S.5    Hirai, K.6
  • 47
    • 0027987849 scopus 로고
    • Randomised trial of cholesterol lowering in 4444 patients with coronary heart disease: The Scandinavian Simvastatin Survival Study (4S)
    • Randomised trial of cholesterol lowering in 4444 patients with coronary heart disease: the Scandinavian Simvastatin Survival Study (4S). Lancet, 1994, 344, 1383-9.
    • (1994) Lancet , vol.344 , pp. 1383-1389
  • 49
    • 0032487931 scopus 로고    scopus 로고
    • Prevention of cardiovascular events and death with pravastatin in patients with coronary heart disease and a broad range of initial cholesterol levels. The Long-Term Intervention with Pravastatin in Ischaemic Disease (LIPID) Study Group. N. Engl. J. Med, 1998, 339, 1349-57
    • Prevention of cardiovascular events and death with pravastatin in patients with coronary heart disease and a broad range of initial cholesterol levels. The Long-Term Intervention with Pravastatin in Ischaemic Disease (LIPID) Study Group. N. Engl. J. Med., 1998, 339, 1349-57.
  • 50
    • 0028883828 scopus 로고
    • Prevention of coronary heart disease with pravastatin in men with hypercholesterolemia. West of Scotland Coronary Prevention Study Group
    • Shepherd, J.; Cobbe, S.M.; Ford, I.; Isles, C.G.; Lorimer, A.R.; MacFarlane, P.W.; McKillop, J.H.; Packard, C.J. Prevention of coronary heart disease with pravastatin in men with hypercholesterolemia. West of Scotland Coronary Prevention Study Group. N. Engl. J. Med., 1995, 333, 1301-7.
    • (1995) N. Engl. J. Med , vol.333 , pp. 1301-1307
    • Shepherd, J.1    Cobbe, S.M.2    Ford, I.3    Isles, C.G.4    Lorimer, A.R.5    MacFarlane, P.W.6    McKillop, J.H.7    Packard, C.J.8
  • 51
    • 0032572086 scopus 로고    scopus 로고
    • Primary prevention of acute coronary events with lovastatin in men and women with average cholesterol levels: Results of AFCAPS/TexCAPS. Air Force/Texas Coronary Atherosclerosis Prevention Study
    • Downs, J.R.; Clearfield, M.; Weis, S.; Whitney, E.; Shapiro, D.R.; Beere, P.A.; Langendorfer, A.; Stein, E.A.; Kruyer, W.; Gotto, A.M., Jr. Primary prevention of acute coronary events with lovastatin in men and women with average cholesterol levels: results of AFCAPS/TexCAPS. Air Force/Texas Coronary Atherosclerosis Prevention Study. JAMA, 1998, 279, 1615-22.
    • (1998) JAMA , vol.279 , pp. 1615-1622
    • Downs, J.R.1    Clearfield, M.2    Weis, S.3    Whitney, E.4    Shapiro, D.R.5    Beere, P.A.6    Langendorfer, A.7    Stein, E.A.8    Kruyer, W.9    Gotto Jr., A.M.10
  • 54
    • 24344452953 scopus 로고    scopus 로고
    • Binding thermodynamics of statins to HMG-CoA reductase
    • Carbonell, T.; Freire, E. Binding thermodynamics of statins to HMG-CoA reductase. Biochemistry (Mosc), 2005, 44, 11741-8.
    • (2005) Biochemistry (Mosc) , vol.44 , pp. 11741-11748
    • Carbonell, T.1    Freire, E.2
  • 56
    • 0037527704 scopus 로고    scopus 로고
    • Molecular mechanism for inhibition of 3-hydroxy-3-methylglutaryl CoA (HMG-CoA) reductase by rosuvastatin
    • Holdgate, G.A.; Ward, W.H.; McTaggart, F. Molecular mechanism for inhibition of 3-hydroxy-3-methylglutaryl CoA (HMG-CoA) reductase by rosuvastatin. Biochem. Soc. Trans., 2003, 31, 528-31.
    • (2003) Biochem. Soc. Trans , vol.31 , pp. 528-531
    • Holdgate, G.A.1    Ward, W.H.2    McTaggart, F.3
  • 57
    • 0036915094 scopus 로고    scopus 로고
    • Structural mechanism for statin inhibition of 3-hydroxy-3-methylglutaryl coenzyme A reductase
    • Istvan, E.S. Structural mechanism for statin inhibition of 3-hydroxy-3-methylglutaryl coenzyme A reductase. Am. Heart J., 2002, 144, S27-32.
    • (2002) Am. Heart J , vol.144
    • Istvan, E.S.1
  • 58
    • 23944466455 scopus 로고    scopus 로고
    • Intermolecular differences of 3-hydroxy-3-methylglutaryl coenzyme a reductase inhibitors contribute to distinct pharmacologic and pleiotropic actions
    • Mason, R.P.; Walter, M.F.; Day, C.A.; Jacob, R.F. Intermolecular differences of 3-hydroxy-3-methylglutaryl coenzyme a reductase inhibitors contribute to distinct pharmacologic and pleiotropic actions. Am. J. Cardiol., 2005, 96, 11F-23F.
    • (2005) Am. J. Cardiol , vol.96
    • Mason, R.P.1    Walter, M.F.2    Day, C.A.3    Jacob, R.F.4
  • 59
    • 16244386522 scopus 로고    scopus 로고
    • Three-dimensional quantitative structure (3-D QSAR) activity relationship studies on imidazolyl and N-pyrrolyl heptenoates as 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR) inhibitors by comparative molecular similarity indices analysis (CoMSIA)
    • Thilagavathi, R.; Kumar, R.; Aparna, V.; Sobhia, M.E.; Gopalakrishnan, B.; Chakraborti, A.K. Three-dimensional quantitative structure (3-D QSAR) activity relationship studies on imidazolyl and N-pyrrolyl heptenoates as 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR) inhibitors by comparative molecular similarity indices analysis (CoMSIA). Bioorg. Med. Chem. Lett., 2005, 15, 1027-32.
    • (2005) Bioorg. Med. Chem. Lett , vol.15 , pp. 1027-1032
    • Thilagavathi, R.1    Kumar, R.2    Aparna, V.3    Sobhia, M.E.4    Gopalakrishnan, B.5    Chakraborti, A.K.6
  • 61
    • 0036708020 scopus 로고    scopus 로고
    • A review of the pharmacologic and pharmacokinetic aspects of rosuvastatin
    • White, C.M. A review of the pharmacologic and pharmacokinetic aspects of rosuvastatin. J. Clin. Pharmacol., 2002, 42, 963-70.
    • (2002) J. Clin. Pharmacol , vol.42 , pp. 963-970
    • White, C.M.1
  • 62
    • 73349134202 scopus 로고    scopus 로고
    • Accessed July 28, 2009
    • Consumer Health Reports. http://www.consumerreports.org/health/ resources/pdf/best-buy-drugs/StatinsUpdate-FINAL.pdf (Accessed July 28, 2009).
    • Consumer Health Reports
  • 64
    • 84921706374 scopus 로고    scopus 로고
    • New light on statin side effects. What recent research on the cholesterol drugs means to you. Heart Advis., 2005, 8, 3.
    • New light on statin side effects. What recent research on the cholesterol drugs means to you. Heart Advis., 2005, 8, 3.
  • 65
    • 59549089180 scopus 로고    scopus 로고
    • Statin adverse effects : A review of the literature and evidence for a mitochondrial mechanism
    • Golomb, B.A.; Evans, M.A. Statin adverse effects : a review of the literature and evidence for a mitochondrial mechanism. Am. J. Cardiovasc. Drugs, 2008, 8, 373-418.
    • (2008) Am. J. Cardiovasc. Drugs , vol.8 , pp. 373-418
    • Golomb, B.A.1    Evans, M.A.2
  • 67
    • 85044704005 scopus 로고    scopus 로고
    • Drug induced pancreatitis might be a class effect of statin drugs
    • author reply -1
    • Singh, S. Drug induced pancreatitis might be a class effect of statin drugs. J. Pancreas, 2005, 6, 380; author reply -1.
    • (2005) J. Pancreas , vol.6 , pp. 380
    • Singh, S.1
  • 68
    • 41349113141 scopus 로고    scopus 로고
    • Statin induced myotoxicity: The lactone forms are more potent than the acid forms in human skeletal muscle cells in vitro
    • Skottheim, I.B.; Gedde-Dahl, A.; Hejazifar, S.; Hoel, K.; Asberg, A. Statin induced myotoxicity: the lactone forms are more potent than the acid forms in human skeletal muscle cells in vitro. Eur. J. Pharm. Sci., 2008, 33, 317-25.
    • (2008) Eur. J. Pharm. Sci , vol.33 , pp. 317-325
    • Skottheim, I.B.1    Gedde-Dahl, A.2    Hejazifar, S.3    Hoel, K.4    Asberg, A.5
  • 69
    • 33646095764 scopus 로고    scopus 로고
    • An overview of statin-associated proteinuria
    • Tiwari, A. An overview of statin-associated proteinuria. Drug Discov. Today, 2006, 11, 458-64.
    • (2006) Drug Discov. Today , vol.11 , pp. 458-464
    • Tiwari, A.1
  • 71
    • 2142773128 scopus 로고    scopus 로고
    • Modulatory effects of HMG-CoA reductase inhibitors in diabetic microangiopathy
    • Danesh, F.R.; Kanwar, Y.S. Modulatory effects of HMG-CoA reductase inhibitors in diabetic microangiopathy. FASEB J., 2004, 18, 805-15.
    • (2004) FASEB J , vol.18 , pp. 805-815
    • Danesh, F.R.1    Kanwar, Y.S.2
  • 72
    • 2942720515 scopus 로고    scopus 로고
    • Beneficial cardiovascular pleiotropic effects of statins
    • Davignon, J. Beneficial cardiovascular pleiotropic effects of statins. Circulation, 2004, 109, III39-43.
    • (2004) Circulation , vol.109
    • Davignon, J.1
  • 73
    • 33645094374 scopus 로고    scopus 로고
    • Statins: Potential new indications in inflammatory conditions
    • Endres, M. Statins: potential new indications in inflammatory conditions. Atheroscler. Suppl., 2006, 7, 31-5.
    • (2006) Atheroscler. Suppl , vol.7 , pp. 31-35
    • Endres, M.1
  • 74
    • 38049175023 scopus 로고    scopus 로고
    • Statins: A new insight into their mechanisms of action and consequent pleiotropic effects
    • Jasinska, M.; Owczarek, J.; Orszulak-Michalak, D. Statins: a new insight into their mechanisms of action and consequent pleiotropic effects. Pharmacol. Rep., 2007, 59, 483-99.
    • (2007) Pharmacol. Rep , vol.59 , pp. 483-499
    • Jasinska, M.1    Owczarek, J.2    Orszulak-Michalak, D.3
  • 76
    • 0036829777 scopus 로고    scopus 로고
    • Beyond lipid lowering: The role of statins in vascular protection
    • Liao, J.K. Beyond lipid lowering: the role of statins in vascular protection. Int. J. Cardiol., 2002, 86, 5-18.
    • (2002) Int. J. Cardiol , vol.86 , pp. 5-18
    • Liao, J.K.1
  • 77
    • 23944445364 scopus 로고    scopus 로고
    • Effects of statins on 3-hydroxy-3-methylglutaryl coenzyme a reductase inhibition beyond low-density lipoprotein cholesterol
    • Liao, J.K. Effects of statins on 3-hydroxy-3-methylglutaryl coenzyme a reductase inhibition beyond low-density lipoprotein cholesterol. Am. J. Cardiol., 2005, 96, 24F-33F.
    • (2005) Am. J. Cardiol , vol.96
    • Liao, J.K.1
  • 79
    • 38049034068 scopus 로고    scopus 로고
    • Pleiotropic effects of statin therapy: Molecular mechanisms and clinical results
    • Wang, C.Y.; Liu, P.Y.; Liao, J.K. Pleiotropic effects of statin therapy: molecular mechanisms and clinical results. Trends Mol. Med., 2008, 14, 37-44.
    • (2008) Trends Mol. Med , vol.14 , pp. 37-44
    • Wang, C.Y.1    Liu, P.Y.2    Liao, J.K.3
  • 80
    • 0036805674 scopus 로고    scopus 로고
    • Statins as anti-inflammatory agents
    • Weitz-Schmidt, G. Statins as anti-inflammatory agents. Trends Pharmacol. Sci., 2002, 23, 482-6.
    • (2002) Trends Pharmacol. Sci , vol.23 , pp. 482-486
    • Weitz-Schmidt, G.1
  • 82
    • 0036189904 scopus 로고    scopus 로고
    • 3-Hydroxy-3-methylglutaryl coenzyme A reductase inhibitors and rhabdomyolysis: Considerations in the renal failure patient
    • Sica, D.A.; Gehr, T.W. 3-Hydroxy-3-methylglutaryl coenzyme A reductase inhibitors and rhabdomyolysis: considerations in the renal failure patient. Curr. Opin. Nephrol. Hypertens, 2002, 11, 123-33.
    • (2002) Curr. Opin. Nephrol. Hypertens , vol.11 , pp. 123-133
    • Sica, D.A.1    Gehr, T.W.2
  • 83
    • 0036139706 scopus 로고    scopus 로고
    • Rosuvastatin: A highly efficacious statin for the treatment of dyslipidaemia
    • Davidson, M.H. Rosuvastatin: a highly efficacious statin for the treatment of dyslipidaemia. Expert Opin. Investig. Drugs, 2002, 11, 125-41.
    • (2002) Expert Opin. Investig. Drugs , vol.11 , pp. 125-141
    • Davidson, M.H.1
  • 85
    • 33751183978 scopus 로고    scopus 로고
    • Molecular basis of differences among statins and a comparison with antioxidant vitamins
    • Mason, R.P. Molecular basis of differences among statins and a comparison with antioxidant vitamins. Am. J. Cardiol., 2006, 98, 34P-41P.
    • (2006) Am. J. Cardiol , vol.98
    • Mason, R.P.1
  • 86
    • 0038171260 scopus 로고    scopus 로고
    • Uptake of rosuvastatin by isolated rat hepatocytes: Comparison with pravastatin
    • Nezasa, K.; Higaki, K.; Takeuchi, M.; Nakano, M.; Koike, M. Uptake of rosuvastatin by isolated rat hepatocytes: comparison with pravastatin. Xenobiotica, 2003, 33, 379-88.
    • (2003) Xenobiotica , vol.33 , pp. 379-388
    • Nezasa, K.1    Higaki, K.2    Takeuchi, M.3    Nakano, M.4    Koike, M.5
  • 87
    • 13444251203 scopus 로고    scopus 로고
    • Chemical, pharmacokinetic and pharmacodynamic properties of statins: An update
    • Schachter, M. Chemical, pharmacokinetic and pharmacodynamic properties of statins: an update. Fundam. Clin. Pharmacol., 2005, 19, 117-25.
    • (2005) Fundam. Clin. Pharmacol , vol.19 , pp. 117-125
    • Schachter, M.1
  • 88
    • 2942705774 scopus 로고    scopus 로고
    • Safety of statins: Focus on clinical pharmacokinetics and drug interactions
    • Bellosta, S.; Paoletti, R.; Corsini, A. Safety of statins: focus on clinical pharmacokinetics and drug interactions. Circulation, 2004, 109, III50-7.
    • (2004) Circulation , vol.109
    • Bellosta, S.1    Paoletti, R.2    Corsini, A.3
  • 89
    • 0030993910 scopus 로고    scopus 로고
    • Effect of micellar beta-sitosterol on cholesterol metabolism in CaCo-2 cells
    • Field, F.J.; Born, E.; Mathur, S.N. Effect of micellar beta-sitosterol on cholesterol metabolism in CaCo-2 cells. J. Lipid Res., 1997, 38, 348-60.
    • (1997) J. Lipid Res , vol.38 , pp. 348-360
    • Field, F.J.1    Born, E.2    Mathur, S.N.3
  • 91
    • 0036308901 scopus 로고    scopus 로고
    • O, K. Cholestin inhibits cholesterol synthesis and secretion in hepatic cells (HepG2)
    • Man, R.Y.; Lynn, E.G.; Cheung, F.; Tsang, P.S.; O, K. Cholestin inhibits cholesterol synthesis and secretion in hepatic cells (HepG2). Mol. Cell. Biochem., 2002, 233, 153-8.
    • (2002) Mol. Cell. Biochem , vol.233 , pp. 153-158
    • Man, R.Y.1    Lynn, E.G.2    Cheung, F.3    Tsang, P.S.4
  • 92
    • 34547945104 scopus 로고    scopus 로고
    • Diosgenin, a naturally occurring steroid [corrected] saponin suppresses 3-hydroxy-3-methylglutaryl CoA reductase expression and induces apoptosis in HCT-116 human colon carcinoma cells
    • Raju, J.; Bird, R.P. Diosgenin, a naturally occurring steroid [corrected] saponin suppresses 3-hydroxy-3-methylglutaryl CoA reductase expression and induces apoptosis in HCT-116 human colon carcinoma cells. Cancer Lett., 2007, 255, 194-204.
    • (2007) Cancer Lett , vol.255 , pp. 194-204
    • Raju, J.1    Bird, R.P.2
  • 93
    • 0036270621 scopus 로고    scopus 로고
    • S-alk(en)yl cysteines of garlic inhibit cholesterol synthesis by deactivating HMG-CoA reductase in cultured rat hepatocytes
    • Liu, L.; Yeh, Y.Y. S-alk(en)yl cysteines of garlic inhibit cholesterol synthesis by deactivating HMG-CoA reductase in cultured rat hepatocytes. J. Nutr., 2002, 132, 1129-34.
    • (2002) J. Nutr , vol.132 , pp. 1129-1134
    • Liu, L.1    Yeh, Y.Y.2
  • 94
    • 0027288196 scopus 로고
    • Tocotrienols regulate cholesterol production in mammalian cells by post-transcriptional suppression of 3-hydroxy-3-methylglutarylcoenzyme A reductase
    • Parker, R.A.; Pearce, B.C.; Clark, R.W.; Gordon, D.A.; Wright, J.J. Tocotrienols regulate cholesterol production in mammalian cells by post-transcriptional suppression of 3-hydroxy-3-methylglutarylcoenzyme A reductase. J. Biol. Chem., 1993, 268, 11230-8.
    • (1993) J. Biol. Chem , vol.268 , pp. 11230-11238
    • Parker, R.A.1    Pearce, B.C.2    Clark, R.W.3    Gordon, D.A.4    Wright, J.J.5
  • 95
    • 0033857172 scopus 로고    scopus 로고
    • Isolation and identification of novel tocotrienols from rice bran with hypocholesterolemic, antioxidant, and antitumor properties
    • Qureshi, A.A.; Mo, H.; Packer, L.; Peterson, D.M. Isolation and identification of novel tocotrienols from rice bran with hypocholesterolemic, antioxidant, and antitumor properties. J. Agric. Food Chem., 2000, 48, 3130-40.
    • (2000) J. Agric. Food Chem , vol.48 , pp. 3130-3140
    • Qureshi, A.A.1    Mo, H.2    Packer, L.3    Peterson, D.M.4
  • 96
    • 0033993858 scopus 로고    scopus 로고
    • Consumption of fermented and nonfermented dairy products: Effects on cholesterol concentrations and metabolism
    • St-Onge, M.P.; Farnworth, E.R.; Jones, P.J. Consumption of fermented and nonfermented dairy products: effects on cholesterol concentrations and metabolism. Am. J. Clin. Nutr., 2000, 71, 674-81.
    • (2000) Am. J. Clin. Nutr , vol.71 , pp. 674-681
    • St-Onge, M.P.1    Farnworth, E.R.2    Jones, P.J.3
  • 97
    • 4544232864 scopus 로고    scopus 로고
    • Isoflavones inhibit 3-hydroxy-3-methylglutaryl coenzyme A reductase in vitro
    • Sung, J.H.; Lee, S.J.; Park, K.H.; Moon, T.W. Isoflavones inhibit 3-hydroxy-3-methylglutaryl coenzyme A reductase in vitro. Biosci. Biotechnol. Biochem., 2004, 68, 428-32.
    • (2004) Biosci. Biotechnol. Biochem , vol.68 , pp. 428-432
    • Sung, J.H.1    Lee, S.J.2    Park, K.H.3    Moon, T.W.4
  • 98
    • 43949111954 scopus 로고    scopus 로고
    • Sphingolipids and cellular cholesterol homeostasis. Effect of ceramide on cholesterol trafficking and HMG CoA reductase activity
    • Subbaiah, P.V.; Sowa, J.M.; Singh, D.K. Sphingolipids and cellular cholesterol homeostasis. Effect of ceramide on cholesterol trafficking and HMG CoA reductase activity. Arch. Biochem. Biophys., 2008, 474, 32-8.
    • (2008) Arch. Biochem. Biophys , vol.474 , pp. 32-38
    • Subbaiah, P.V.1    Sowa, J.M.2    Singh, D.K.3
  • 99
    • 69749123336 scopus 로고    scopus 로고
    • Green and black tea extracts inhibit HMG-CoA reductase and activate AMP kinase to decrease cholesterol synthesis in hepatoma cells
    • in press doi:10.1016/j.jnutbio.2008.07.011
    • Singh, D.K.; Banerjee, S.; Porter, T.D. Green and black tea extracts inhibit HMG-CoA reductase and activate AMP kinase to decrease cholesterol synthesis in hepatoma cells. J. Nutr. Biochem., 2008. in press (doi:10.1016/j.jnutbio.2008.07.011).
    • (2008) J. Nutr. Biochem
    • Singh, D.K.1    Banerjee, S.2    Porter, T.D.3
  • 100
    • 0028285272 scopus 로고
    • Non-sterol compounds that regulate cholesterogenesis. Analogues of farnesyl pyrophosphate reduce 3-hydroxy-3-methylglutaryl-coenzyme A reductase levels
    • Bradfute, D.L.; Simoni, R.D. Non-sterol compounds that regulate cholesterogenesis. Analogues of farnesyl pyrophosphate reduce 3-hydroxy-3-methylglutaryl-coenzyme A reductase levels. J. Biol. Chem., 1994, 269, 6645-50.
    • (1994) J. Biol. Chem , vol.269 , pp. 6645-6650
    • Bradfute, D.L.1    Simoni, R.D.2
  • 101
    • 0025038640 scopus 로고
    • Effect of ketanserin tartrate on HMG CoA reductase and LDL receptor activity in cultured human skin fibroblasts
    • Suzukawa, M.; Nakamura, H. Effect of ketanserin tartrate on HMG CoA reductase and LDL receptor activity in cultured human skin fibroblasts. Eur. J. Clin. Pharmacol., 1990, 39, 217-20.
    • (1990) Eur. J. Clin. Pharmacol , vol.39 , pp. 217-220
    • Suzukawa, M.1    Nakamura, H.2
  • 102
    • 0028819192 scopus 로고
    • Response of 3-hydroxy-3-methylglutaryl CoA reductase to l-triiodothyronine in cultured fibroblasts from FH homozygotes
    • Harada-Shiba, M.; Tajima, S.; Yamamoto, A. Response of 3-hydroxy-3-methylglutaryl CoA reductase to l-triiodothyronine in cultured fibroblasts from FH homozygotes. Atherosclerosis, 1995, 113, 91-8.
    • (1995) Atherosclerosis , vol.113 , pp. 91-98
    • Harada-Shiba, M.1    Tajima, S.2    Yamamoto, A.3
  • 103
    • 0025915504 scopus 로고
    • Inhibition of degradation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase in vivo by cysteine protease inhibitors
    • Inoue, S.; Bar-Nun, S.; Roitelman, J.; Simoni, R.D. Inhibition of degradation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase in vivo by cysteine protease inhibitors. J. Biol. Chem., 1991, 266, 13311-7.
    • (1991) J. Biol. Chem , vol.266 , pp. 13311-13317
    • Inoue, S.1    Bar-Nun, S.2    Roitelman, J.3    Simoni, R.D.4
  • 104
    • 0020579446 scopus 로고
    • Effect of tunicamycin on 3-hydroxy-3- methylglutaryl coenzyme A reductase in C-6 glial cells
    • Volpe, J.J.; Goldberg, R.I. Effect of tunicamycin on 3-hydroxy-3- methylglutaryl coenzyme A reductase in C-6 glial cells. J. Biol. Chem., 1983, 258, 9220-6.
    • (1983) J. Biol. Chem , vol.258 , pp. 9220-9226
    • Volpe, J.J.1    Goldberg, R.I.2
  • 105
    • 0022905095 scopus 로고
    • Regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity and cholesterol biosynthesis by oxylanosterols
    • Panini, S.R.; Sexton, R.C.; Gupta, A.K.; Parish, E.J.; Chitrakorn, S.; Rudney, H. Regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity and cholesterol biosynthesis by oxylanosterols. J. Lipid Res., 1986, 27, 1190-204.
    • (1986) J. Lipid Res , vol.27 , pp. 1190-1204
    • Panini, S.R.1    Sexton, R.C.2    Gupta, A.K.3    Parish, E.J.4    Chitrakorn, S.5    Rudney, H.6
  • 106
    • 0027525579 scopus 로고
    • Modulation of 3-hydroxy-3-methylglutaryl-CoA reductase by 15 alpha-fluorolanost-7-en-3 beta-ol. A mechanism-based inhibitor of cholesterol biosynthesis
    • Trzaskos, J.M.; Magolda, R.L.; Favata, M.F.; Fischer, R.T.; Johnson, P.R.; Chen, H.W.; Ko, S.S.; Leonard, D.A.; Gaylor, J.L. Modulation of 3-hydroxy-3-methylglutaryl-CoA reductase by 15 alpha-fluorolanost-7-en-3 beta-ol. A mechanism-based inhibitor of cholesterol biosynthesis. J. Biol. Chem., 1993, 268, 22591-9.
    • (1993) J. Biol. Chem , vol.268 , pp. 22591-22599
    • Trzaskos, J.M.1    Magolda, R.L.2    Favata, M.F.3    Fischer, R.T.4    Johnson, P.R.5    Chen, H.W.6    Ko, S.S.7    Leonard, D.A.8    Gaylor, J.L.9
  • 107
    • 0024477730 scopus 로고
    • Effect of vitamin D3 derivatives on cholesterol synthesis and HMG-CoA reductase activity in cultured cells
    • Gupta, A.K.; Sexton, R.C.; Rudney, H. Effect of vitamin D3 derivatives on cholesterol synthesis and HMG-CoA reductase activity in cultured cells. J. Lipid Res., 1989, 30, 379-86.
    • (1989) J. Lipid Res , vol.30 , pp. 379-386
    • Gupta, A.K.1    Sexton, R.C.2    Rudney, H.3
  • 108
    • 15844402429 scopus 로고    scopus 로고
    • The novel cholesterol-lowering drug SR-12813 inhibits cholesterol synthesis via an increased degradation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase
    • Berkhout, T.A.; Simon, H.M.; Patel, D.D.; Bentzen, C.; Niesor, E.; Jackson, B.; Suckling, K.E. The novel cholesterol-lowering drug SR-12813 inhibits cholesterol synthesis via an increased degradation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase. J. Biol. Chem., 1996, 271, 14376-82.
    • (1996) J. Biol. Chem , vol.271 , pp. 14376-14382
    • Berkhout, T.A.1    Simon, H.M.2    Patel, D.D.3    Bentzen, C.4    Niesor, E.5    Jackson, B.6    Suckling, K.E.7
  • 110
    • 0009472268 scopus 로고
    • Separation of the hypnotic potentiating principles from the essential oil of Acorus calamus L. of Indian origin by liquid-gas chromatography
    • Baxter, R.M.; Dandiya, P.C.; Kandel, S.I.; Okany, A.; Walker, G.C. Separation of the hypnotic potentiating principles from the essential oil of Acorus calamus L. of Indian origin by liquid-gas chromatography. Nature, 1960, 185, 466-67.
    • (1960) Nature , vol.185 , pp. 466-467
    • Baxter, R.M.1    Dandiya, P.C.2    Kandel, S.I.3    Okany, A.4    Walker, G.C.5
  • 112
    • 0037870337 scopus 로고    scopus 로고
    • Alpha-asarone inhibits HMG-CoA reductase, lowers serum LDL-cholesterol levels and reduces biliary CSI in hypercholesterolemic rats
    • Rodriguez-Paez, L.; Juarez-Sanchez, M.; Antunez-Solis, J.; Baeza, I.; Wong, C. Alpha-asarone inhibits HMG-CoA reductase, lowers serum LDL-cholesterol levels and reduces biliary CSI in hypercholesterolemic rats. Phytomedicine, 2003, 10, 397-404.
    • (2003) Phytomedicine , vol.10 , pp. 397-404
    • Rodriguez-Paez, L.1    Juarez-Sanchez, M.2    Antunez-Solis, J.3    Baeza, I.4    Wong, C.5
  • 116
    • 0242299718 scopus 로고    scopus 로고
    • Hypolipidemic Activity of New Phenoxyacetic Derivatives Related to alpha-Asarone with Minimal Pharmacophore Features
    • Cruz, M.D.C.; Salazar, M.; Garciafigueroa, Y.; Hernandez, D.; Diaz, F.; Chamorro, G.; Tamariz, J. Hypolipidemic Activity of New Phenoxyacetic Derivatives Related to alpha-Asarone with Minimal Pharmacophore Features. Drug Dev. Res., 2003, 60, 186-95.
    • (2003) Drug Dev. Res , vol.60 , pp. 186-195
    • Cruz, M.D.C.1    Salazar, M.2    Garciafigueroa, Y.3    Hernandez, D.4    Diaz, F.5    Chamorro, G.6    Tamariz, J.7
  • 119
    • 33846601387 scopus 로고    scopus 로고
    • Structure-based rational quest for potential novel inhibitors of human HMG-CoA reductase by combining CoMFA 3D QSAR modeling and virtual screening
    • Zhang, Q.Y.; Wan, J.; Xu, X.; Yang, G.F.; Ren, Y.L.; Liu, J.J.; Wang, H.; Guo, Y. Structure-based rational quest for potential novel inhibitors of human HMG-CoA reductase by combining CoMFA 3D QSAR modeling and virtual screening. J. Comb. Chem., 2007, 9, 131-8.
    • (2007) J. Comb. Chem , vol.9 , pp. 131-138
    • Zhang, Q.Y.1    Wan, J.2    Xu, X.3    Yang, G.F.4    Ren, Y.L.5    Liu, J.J.6    Wang, H.7    Guo, Y.8
  • 121
    • 41249099180 scopus 로고    scopus 로고
    • Use of virtual screening, flexible docking, and molecular interaction fields to design novel HMG-CoA reductase inhibitors for the treatment of hypercholesterolemia
    • da Silva, V.B.; Taft, C.A.; Silva, C.H. Use of virtual screening, flexible docking, and molecular interaction fields to design novel HMG-CoA reductase inhibitors for the treatment of hypercholesterolemia. J. Phys. Chem. A., 2008, 112, 2007-11.
    • (2008) J. Phys. Chem. A , vol.112 , pp. 2007-2011
    • da Silva, V.B.1    Taft, C.A.2    Silva, C.H.3
  • 123
    • 33749166233 scopus 로고    scopus 로고
    • Development of pharmacophoric model of condensed pyridine and pyrimidine analogs as hydroxymethyl glutaryl coenzyme A reductase inhibitors
    • Saxena, M.; Soni, L.K.; Gupta, A.K.; Wakode, S.R.; Saxena, A.K.; Kaskhedikar, S.G. Development of pharmacophoric model of condensed pyridine and pyrimidine analogs as hydroxymethyl glutaryl coenzyme A reductase inhibitors. Indian J. Biochem. Biophys., 2006, 43, 32-6.
    • (2006) Indian J. Biochem. Biophys , vol.43 , pp. 32-36
    • Saxena, M.1    Soni, L.K.2    Gupta, A.K.3    Wakode, S.R.4    Saxena, A.K.5    Kaskhedikar, S.G.6
  • 124
    • 0035927241 scopus 로고    scopus 로고
    • Synthesis and biological evaluations of condensed pyridine and condensed pyrimidine-based HMG-CoA reductase inhibitors
    • Suzuki, M.; Iwasaki, H.; Fujikawa, Y.; Sakashita, M.; Kitahara, M.; Sakoda, R. Synthesis and biological evaluations of condensed pyridine and condensed pyrimidine-based HMG-CoA reductase inhibitors. Bioorg. Med. Chem. Lett., 2001, 11, 1285-8.
    • (2001) Bioorg. Med. Chem. Lett , vol.11 , pp. 1285-1288
    • Suzuki, M.1    Iwasaki, H.2    Fujikawa, Y.3    Sakashita, M.4    Kitahara, M.5    Sakoda, R.6
  • 126
    • 33845583653 scopus 로고    scopus 로고
    • Peptide design of a competitive inhibitor for HMG-CoA reductase based on statin structure
    • Pak, V.V.; Kim, S.H.; Koo, M.; Lee, N.; Shakhidoyatov, K.M.; Kwon, D.Y. Peptide design of a competitive inhibitor for HMG-CoA reductase based on statin structure. Biopolymers, 2006, 84, 586-94.
    • (2006) Biopolymers , vol.84 , pp. 586-594
    • Pak, V.V.1    Kim, S.H.2    Koo, M.3    Lee, N.4    Shakhidoyatov, K.M.5    Kwon, D.Y.6
  • 127
    • 47649114218 scopus 로고    scopus 로고
    • Modeling an active conformation for linear peptides and design of a competitive inhibitor for HMG-CoA reductase
    • Pak, V.V.; Koo, M.; Kim, M.J.; Yang, H.J.; Yun, L.; Kwon, D.Y. Modeling an active conformation for linear peptides and design of a competitive inhibitor for HMG-CoA reductase. J. Mol. Recognit., 2008, 21, 224-32.
    • (2008) J. Mol. Recognit , vol.21 , pp. 224-232
    • Pak, V.V.1    Koo, M.2    Kim, M.J.3    Yang, H.J.4    Yun, L.5    Kwon, D.Y.6
  • 128
    • 38849098428 scopus 로고    scopus 로고
    • Binding effect and design of a competitive inhibitory peptide for HMG-CoA reductase through modeling of an active peptide backbone
    • Pak, V.V.; Koo, M.; Kim, M.J.; Yun, L.; Kwon, D.Y. Binding effect and design of a competitive inhibitory peptide for HMG-CoA reductase through modeling of an active peptide backbone. Bioorg. Med. Chem., 2008, 16, 1309-18.
    • (2008) Bioorg. Med. Chem , vol.16 , pp. 1309-1318
    • Pak, V.V.1    Koo, M.2    Kim, M.J.3    Yun, L.4    Kwon, D.Y.5
  • 129
    • 34447499912 scopus 로고    scopus 로고
    • Recognized sequence and conformation in design of linear peptides as a competitive inhibitor for HMG-CoA reductase
    • Pak, V.V.; Koo, M.; Yun, L.; Kwon, D.Y. Recognized sequence and conformation in design of linear peptides as a competitive inhibitor for HMG-CoA reductase. J. Mol. Recognit., 2007, 20, 197-203.
    • (2007) J. Mol. Recognit , vol.20 , pp. 197-203
    • Pak, V.V.1    Koo, M.2    Yun, L.3    Kwon, D.Y.4
  • 130
    • 0028962803 scopus 로고
    • In vitro myotoxicity of the 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors, pravastatin, lovastatin, and simvastatin, using neonatal rat skeletal myocytes
    • Masters, B.A.; Palmoski, M.J.; Flint, O.P.; Gregg, R.E.; Wang-Iverson, D.; Durham, S.K. In vitro myotoxicity of the 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors, pravastatin, lovastatin, and simvastatin, using neonatal rat skeletal myocytes. Toxicol. Appl. Pharmacol., 1995, 131, 163-74.
    • (1995) Toxicol. Appl. Pharmacol , vol.131 , pp. 163-174
    • Masters, B.A.1    Palmoski, M.J.2    Flint, O.P.3    Gregg, R.E.4    Wang-Iverson, D.5    Durham, S.K.6
  • 131
    • 42949151357 scopus 로고    scopus 로고
    • Ahmad, S.; Madsen, C.S.; Stein, P.D.; Janovitz, E.; Huang, C.; Ngu, K.; Bisaha, S.; Kennedy, L.J.; Chen, B.C.; Zhao, R.; Sitkoff, D.; Monshizadegan, H.; Yin, X.; Ryan, C.S.; Zhang, R.; Giancarli, M.; Bird, E.; Chang, M.; Chen, X.; Setters, R.; Search, D.; Zhuang, S.; Nguyen-Tran, V.; Cuff, C.A.; Harrity, T.; Darienzo, C.J.; Li, T.; Reeves, R.A.; Blanar, M.A.; Barrish, J.C.; Zahler, R.; Robl, J.A. (3R,5S,E)-7-(4-(4-fluorophenyl)-6-isopropyl-2-(methyl(1-methyl-1h-1, 2,4-triazol-5-yl)amino)pyrimidin-5-yl)-3,5-dihydroxyhept-6-enoic acid (BMS-644950): a rationally designed orally efficacious 3-hydroxy-3- methylglutaryl coenzyme-a reductase inhibitor with reduced myotoxicity potential. J. Med. Chem., 2008, 51, 2722-33.
    • Ahmad, S.; Madsen, C.S.; Stein, P.D.; Janovitz, E.; Huang, C.; Ngu, K.; Bisaha, S.; Kennedy, L.J.; Chen, B.C.; Zhao, R.; Sitkoff, D.; Monshizadegan, H.; Yin, X.; Ryan, C.S.; Zhang, R.; Giancarli, M.; Bird, E.; Chang, M.; Chen, X.; Setters, R.; Search, D.; Zhuang, S.; Nguyen-Tran, V.; Cuff, C.A.; Harrity, T.; Darienzo, C.J.; Li, T.; Reeves, R.A.; Blanar, M.A.; Barrish, J.C.; Zahler, R.; Robl, J.A. (3R,5S,E)-7-(4-(4-fluorophenyl)-6-isopropyl-2-(methyl(1-methyl-1h-1, 2,4-triazol-5-yl)amino)pyrimidin-5-yl)-3,5-dihydroxyhept-6-enoic acid (BMS-644950): a rationally designed orally efficacious 3-hydroxy-3- methylglutaryl coenzyme-a reductase inhibitor with reduced myotoxicity potential. J. Med. Chem., 2008, 51, 2722-33.


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