메뉴 건너뛰기




Volumn 102, Issue , 2015, Pages 375-386

Recent developments in steroidal and nonsteroidal aromatase inhibitors for the chemoprevention of estrogen-dependent breast cancer

Author keywords

Aromatase; Breast cancer; Nonsteroidal aromatase inhibitors; Steroidal aromatase inhibitors

Indexed keywords

16 [3 [3 (IMIDAZOLE 1 YL)PROPOXY]BENZYLIDENE] 4 ANDROSTENE 3,17 DIONE; 16 [4 [3 (IMIDAZOL 1 YL)PROPOXY] 3 METHOXYBENZYLIDENE] 5 ANDROSTENE 3BETA,17BETA DIOL; 16BETA (IMIDAZOL 1 YL) 4 ANDROSTA 1,4 DIENE 3,17 DIONE; 16BETA (IMIDAZOL 1 YL) 4 ANDROSTENE 3,17 DIONE; ANASTROZOLE; ANTINEOPLASTIC AGENT; APIGENIN; AROMATASE; AROMATASE INHIBITOR; ATAMESTANE; BIOCCHANIN A; CHRYSIN; ESTROGEN; EXEMESTANE; FORMESTANE; LETROZOLE; LIAROZOLE; PLOMESTANE; QUERCETIN; RESVERATROL; STEROID; UNCLASSIFIED DRUG; VOROZOLE;

EID: 84939810868     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2015.08.010     Document Type: Short Survey
Times cited : (97)

References (94)
  • 2
    • 65249155440 scopus 로고    scopus 로고
    • State of the evidence: The connection between breast cancer and the environment
    • J. Gray, N. Evans, B. Taylor, L. Rizzo, M. Walker, State of the evidence: the connection between breast cancer and the environment, Int. J. Occup. Environ. Health 15 (1) (2009) 43-78.
    • (2009) Int. J. Occup. Environ. Health , vol.15 , Issue.1 , pp. 43-78
    • Gray, J.1    Evans, N.2    Taylor, B.3    Rizzo, L.4    Walker, M.5
  • 4
    • 0036154287 scopus 로고    scopus 로고
    • Selective estrogen receptor modulators (SERMS) and their roles in breast cancer prevention
    • (a) W.C. Park, V.C. Jordan, Selective estrogen receptor modulators (SERMS) and their roles in breast cancer prevention, Trends Mol. Med. 8 (2) (2002) 82-88;
    • (2002) Trends Mol. Med. , vol.8 , Issue.2 , pp. 82-88
    • Park, W.C.1    Jordan, V.C.2
  • 5
    • 84865483901 scopus 로고    scopus 로고
    • Characterization of a tamoxifen-tethered single-walled carbon nanotube conjugate by using NMR spectroscopy
    • (b) D.J. Nelson, Shagufta, R. Kumar, Characterization of a tamoxifen-tethered single-walled carbon nanotube conjugate by using NMR spectroscopy, Anal. Bioanal. Chem. 404 (2012) 771-776;
    • (2012) Anal. Bioanal. Chem. , vol.404 , pp. 771-776
    • Nelson, D.J.1    Shagufta2    Kumar, R.3
  • 7
    • 1542316334 scopus 로고    scopus 로고
    • Biological rationale for endocrine therapy in breast cancer
    • W.R. Miller, Biological rationale for endocrine therapy in breast cancer, Best. Pract. Res. Clin. Endocrinol. Metab. 18 (1) (2004) 1-32.
    • (2004) Best. Pract. Res. Clin. Endocrinol. Metab. , vol.18 , Issue.1 , pp. 1-32
    • Miller, W.R.1
  • 8
    • 0036238085 scopus 로고    scopus 로고
    • Nonsteroidal aromatase inhibitors: Recent advances
    • M. Recanatini, A. Cavalli, P. Valenti, Nonsteroidal aromatase inhibitors: recent advances, Med. Res. Rev. 22 (3) (2002) 282-304.
    • (2002) Med. Res. Rev. , vol.22 , Issue.3 , pp. 282-304
    • Recanatini, M.1    Cavalli, A.2    Valenti, P.3
  • 10
    • 77952101961 scopus 로고    scopus 로고
    • Pharmacophore modeling strategies for the development of novel nonsteroidal inhibitors of human aromatase (CYP19)
    • Y. Mouftuoglu, G. Mustata, Pharmacophore modeling strategies for the development of novel nonsteroidal inhibitors of human aromatase (CYP19), Bioorg. Med. Chem. Lett. 20 (10) (2010) 3050-3064.
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , Issue.10 , pp. 3050-3064
    • Mouftuoglu, Y.1    Mustata, G.2
  • 12
    • 34250818796 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of (+/-)an-abyssinone II and its analogues as aromatase inhibitors for chemoprevention of breast cancer
    • A. Maiti, M. Cuendet, V.L. Croy, D.C. Endringer, G.M. Pezzuto, M. Cushman, Synthesis and biological evaluation of (+/-)an-abyssinone II and its analogues as aromatase inhibitors for chemoprevention of breast cancer, J. Med. Chem. 50 (2007) 2799-2806.
    • (2007) J. Med. Chem. , vol.50 , pp. 2799-2806
    • Maiti, A.1    Cuendet, M.2    Croy, V.L.3    Endringer, D.C.4    Pezzuto, G.M.5    Cushman, M.6
  • 13
    • 34047171998 scopus 로고    scopus 로고
    • Aromatase inhibitors for the treatment of breast cancer
    • J.R. Benson, O. Ravisekar, Aromatase inhibitors for the treatment of breast cancer, Curr. Cancer Ther. Rev. 3 (2007) 67-79.
    • (2007) Curr. Cancer Ther. Rev. , vol.3 , pp. 67-79
    • Benson, J.R.1    Ravisekar, O.2
  • 14
    • 33845637854 scopus 로고    scopus 로고
    • Non-steroidal anti-estrogens in the treatment of breast cancer
    • S. Barker, Non-steroidal anti-estrogens in the treatment of breast cancer, Curr. Opin. Investig. Drugs 7 (12) (2006) 1085-1091.
    • (2006) Curr. Opin. Investig. Drugs , vol.7 , Issue.12 , pp. 1085-1091
    • Barker, S.1
  • 16
    • 0038210242 scopus 로고    scopus 로고
    • Aromatase inhibitors in breast cancer
    • I.E. Smith, M. Dowsett, Aromatase inhibitors in breast cancer, N. Eng. J. Med. 348 (24) (2003) 2431-2442.
    • (2003) N. Eng. J. Med. , vol.348 , Issue.24 , pp. 2431-2442
    • Smith, I.E.1    Dowsett, M.2
  • 17
    • 0036374410 scopus 로고    scopus 로고
    • Aromatase and its inhibitors: Significance for breast cancer therapy
    • E.R. Simpson, M. Dowsett, Aromatase and its inhibitors: significance for breast cancer therapy, Recent Prog. Horm. Res. 57 (2002) 317-338.
    • (2002) Recent Prog. Horm. Res. , vol.57 , pp. 317-338
    • Simpson, E.R.1    Dowsett, M.2
  • 18
    • 18144387234 scopus 로고    scopus 로고
    • The role of growth factor receptor pathways in human breast cancer cells adapted to long-term estrogen deprivation
    • G.J. Sabnis, D. Jevolac, B. Lomg, A. Brodie, The role of growth factor receptor pathways in human breast cancer cells adapted to long-term estrogen deprivation, Cancer Res. 65 (9) (2005) 3903-3910.
    • (2005) Cancer Res. , vol.65 , Issue.9 , pp. 3903-3910
    • Sabnis, G.J.1    Jevolac, D.2    Lomg, B.3    Brodie, A.4
  • 19
    • 27944468748 scopus 로고    scopus 로고
    • Adaptation of estrogen-regulated genes in long-term estradiol deprived MCF-7 breast cancer cells
    • R.J. Santen, E.K. Lobenhofer, C.A. Afshari, Y. Bao, R.X. Song, Adaptation of estrogen-regulated genes in long-term estradiol deprived MCF-7 breast cancer cells, Breast Cancer Res. Treat. 94 (3) (2005) 213-223.
    • (2005) Breast Cancer Res. Treat. , vol.94 , Issue.3 , pp. 213-223
    • Santen, R.J.1    Lobenhofer, E.K.2    Afshari, C.A.3    Bao, Y.4    Song, R.X.5
  • 20
    • 0017755181 scopus 로고
    • The effect of an aromatase inhibitor 4-hydroxy-4-androstene-3,17-dione, on estrogen-dependent processes in reproduction and breast cancer
    • A.M. Brodie, W.C. Schwarzel, A.A. Shaikh, H.J. Brodie, The effect of an aromatase inhibitor 4-hydroxy-4-androstene-3,17-dione, on estrogen-dependent processes in reproduction and breast cancer, Endocrinology 100 (6) (1977) 1684-1695.
    • (1977) Endocrinology , vol.100 , Issue.6 , pp. 1684-1695
    • Brodie, A.M.1    Schwarzel, W.C.2    Shaikh, A.A.3    Brodie, H.J.4
  • 21
    • 0027504510 scopus 로고
    • Synthesis and aromatase inhibition by potential metabolites of exemestane (6-methylenandrosta-1,4-diene-3,17-dione)
    • F. Buzzetti, E.D. Salle, A. Longo, G. Briatico, Synthesis and aromatase inhibition by potential metabolites of exemestane (6-methylenandrosta-1,4-diene-3,17-dione), Steroids 58 (11) (1993) 527-532.
    • (1993) Steroids , vol.58 , Issue.11 , pp. 527-532
    • Buzzetti, F.1    Salle, E.D.2    Longo, A.3    Briatico, G.4
  • 22
    • 0022550064 scopus 로고
    • 1-Methyl-1,4-androstadiene-3,17-dione (SH 489): Characterization of an irreversible inhibitor of estrogen biosynthesis
    • D. Henderson, G. Norbisrath, U. Kerb, 1-Methyl-1,4-androstadiene-3,17-dione (SH 489): characterization of an irreversible inhibitor of estrogen biosynthesis, J. Steroid Biochem. 24 (1) (1986) 303-306.
    • (1986) J. Steroid Biochem. , vol.24 , Issue.1 , pp. 303-306
    • Henderson, D.1    Norbisrath, G.2    Kerb, U.3
  • 23
    • 0023468902 scopus 로고
    • Biological characterization of 10-(2-propynyl)estr-4-ene-3,17 dione (MDL 18,962), an enzyme-activated inhibitors of aromatase
    • J.O. Johnston, Biological characterization of 10-(2-propynyl)estr-4-ene-3,17 dione (MDL 18,962), an enzyme-activated inhibitors of aromatase, Steroids 50 (1987) 105-120.
    • (1987) Steroids , vol.50 , pp. 105-120
    • Johnston, J.O.1
  • 29
    • 43349097373 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of a series of A,B-ring modified 16,17-secoandrostane derivatives
    • M. Sakac, A. Gakovic, S. Stojanovic, E. Djurendic, V. Kojic, G. Bogdanovic, K.P. Gasi, Synthesis and biological evaluation of a series of A,B-ring modified 16,17-secoandrostane derivatives, Bioorg. Chem. 36 (2008) 128-132.
    • (2008) Bioorg. Chem. , vol.36 , pp. 128-132
    • Sakac, M.1    Gakovic, A.2    Stojanovic, S.3    Djurendic, E.4    Kojic, V.5    Bogdanovic, G.6    Gasi, K.P.7
  • 31
    • 79952427860 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 16E-arylidenosteroids as cytotoxic and anti-aromatase agents
    • R. Bansal, S. Guleria, S. Thota, R.W. Hartmann, C. Zimmer, Synthesis and biological evaluation of 16E-arylidenosteroids as cytotoxic and anti-aromatase agents, Chem. Pharm. Bull. 59 (3) (2011) 327-331.
    • (2011) Chem. Pharm. Bull. , vol.59 , Issue.3 , pp. 327-331
    • Bansal, R.1    Guleria, S.2    Thota, S.3    Hartmann, R.W.4    Zimmer, C.5
  • 32
    • 84867136827 scopus 로고    scopus 로고
    • Synthesis and aromatase inhibitory activity of some new 16E-arylidenosteroids
    • R. Bansal, S. Thota, N. Karkra, M. Minu, C. Zimmer, R.W. Hartmann, Synthesis and aromatase inhibitory activity of some new 16E-arylidenosteroids, Bioorg. Chem. 45 (2012) 36-40.
    • (2012) Bioorg. Chem. , vol.45 , pp. 36-40
    • Bansal, R.1    Thota, S.2    Karkra, N.3    Minu, M.4    Zimmer, C.5    Hartmann, R.W.6
  • 33
    • 84859821802 scopus 로고    scopus 로고
    • Design, synthesis and evaluation of novel 16-imidazolyl substituted steroidal derivatives possessing potent diversified pharmacological properties
    • R. Bansal, S. Guleria, S. Thota, S.L. Bodhankar, M.R. Patwardhan, C. Zimmer, R.W. Hartmann, A.L. Harvey, Design, synthesis and evaluation of novel 16-imidazolyl substituted steroidal derivatives possessing potent diversified pharmacological properties, Steroids 77 (2012) 621-629.
    • (2012) Steroids , vol.77 , pp. 621-629
    • Bansal, R.1    Guleria, S.2    Thota, S.3    Bodhankar, S.L.4    Patwardhan, M.R.5    Zimmer, C.6    Hartmann, R.W.7    Harvey, A.L.8
  • 34
    • 84873987495 scopus 로고    scopus 로고
    • Synthesis of imidazole-derived steroidal hybrids as potent aromatase inhibitors
    • R. Bansal, S. Guleria, S. Thota, R.W. Hartmann, C. Zimmer, Synthesis of imidazole-derived steroidal hybrids as potent aromatase inhibitors, Med. Chem. Res. 22 (2013) 692-698.
    • (2013) Med. Chem. Res. , vol.22 , pp. 692-698
    • Bansal, R.1    Guleria, S.2    Thota, S.3    Hartmann, R.W.4    Zimmer, C.5
  • 37
    • 27744476294 scopus 로고    scopus 로고
    • Structure-activity relationships of 2α-substituted androstenedione analogues as aromatase inhibitors and their aromatization reactions
    • M. Numazawa, W. Handa, C. Hasegawa, M. Takahashi, Structure-activity relationships of 2α-substituted androstenedione analogues as aromatase inhibitors and their aromatization reactions, J. Steroid Biochem. Mol. Biol. 97 (2005) 353-359.
    • (2005) J. Steroid Biochem. Mol. Biol. , vol.97 , pp. 353-359
    • Numazawa, M.1    Handa, W.2    Hasegawa, C.3    Takahashi, M.4
  • 38
    • 51349140489 scopus 로고    scopus 로고
    • Structure-activity relationships of estrogen derivatives as aromatase inhibitors. Effect of heterocyclic substituents
    • M. Numazawa, S. Komatsu, T. Tominaga, K. Yamashita, Structure-activity relationships of estrogen derivatives as aromatase inhibitors. Effect of heterocyclic substituents, Chem. Pharm. Bull. 56 (9) (2008) 1304-1309.
    • (2008) Chem. Pharm. Bull. , vol.56 , Issue.9 , pp. 1304-1309
    • Numazawa, M.1    Komatsu, S.2    Tominaga, T.3    Yamashita, K.4
  • 39
  • 41
    • 55549118561 scopus 로고    scopus 로고
    • Synthesis and biochemical studies of 17-substituted androst-3-enes and 3,4-epoxyandrostanes as aromatase inhibitors
    • M.M.D.S. Cepa, E.J. Tavares da Silva, G. Correia-da-Silva, F.M.F. Roleira, N.A.A. Teixeira, Synthesis and biochemical studies of 17-substituted androst-3-enes and 3,4-epoxyandrostanes as aromatase inhibitors, Steroids 73 (2008) 1409-1415.
    • (2008) Steroids , vol.73 , pp. 1409-1415
    • Cepa, M.M.D.S.1    Tavares Da Silva, E.J.2    Correia-da-Silva, G.3    Roleira, F.M.F.4    Teixeira, N.A.A.5
  • 42
    • 84555189852 scopus 로고    scopus 로고
    • 19 steroidal 17-oxime analogs
    • 19 steroidal 17-oxime analogs, Molecules 16 (2011) 9868-9885.
    • (2011) Molecules , vol.16 , pp. 9868-9885
    • Pokhrel, M.1    Ma, E.2
  • 44
    • 0032790550 scopus 로고    scopus 로고
    • Comprehensive pharmacology and clinical efficacy of aromatase inhibitors
    • V.C.O. Njar, A.M.H. Brodie, Comprehensive pharmacology and clinical efficacy of aromatase inhibitors, Drugs 58 (2) (1999) 233-255.
    • (1999) Drugs , vol.58 , Issue.2 , pp. 233-255
    • Njar, V.C.O.1    Brodie, A.M.H.2
  • 46
    • 33748036987 scopus 로고    scopus 로고
    • Defining the role of aromatase inhibitors in the adjuvant endocrine treatment of early breast cancer
    • A.U. Buzdar, R. Chlebowski, J. Cuzick, S. Duffy, J. Forbes, W. Jonat, P. Ravdin, Defining the role of aromatase inhibitors in the adjuvant endocrine treatment of early breast cancer, Curr. Med. Res. Opin. 22 (8) (2006) 1575-1585.
    • (2006) Curr. Med. Res. Opin. , vol.22 , Issue.8 , pp. 1575-1585
    • Buzdar, A.U.1    Chlebowski, R.2    Cuzick, J.3    Duffy, S.4    Forbes, J.5    Jonat, W.6    Ravdin, P.7
  • 47
    • 33749369815 scopus 로고    scopus 로고
    • Update on the use of aromatase inhibitors in breast cancer
    • R.W. Brueggemeier, Update on the use of aromatase inhibitors in breast cancer, Expert Opin. Pharmacother. 7 (14) (2006) 1919-1930.
    • (2006) Expert Opin. Pharmacother. , vol.7 , Issue.14 , pp. 1919-1930
    • Brueggemeier, R.W.1
  • 48
    • 0038495565 scopus 로고    scopus 로고
    • The current status of aromatase inhibitors in the management of breast cancer
    • M. Baum, A. Buzdar, The current status of aromatase inhibitors in the management of breast cancer, Surg. Clin. North Am. 83 (4) (2003) 973-994.
    • (2003) Surg. Clin. North Am. , vol.83 , Issue.4 , pp. 973-994
    • Baum, M.1    Buzdar, A.2
  • 49
    • 33644557137 scopus 로고    scopus 로고
    • Landmark trials in endocrine adjuvant therapy for breast carcinoma
    • W. Gradishar, Landmark trials in endocrine adjuvant therapy for breast carcinoma, Cancer 106 (5) (2006) 975-981.
    • (2006) Cancer , vol.106 , Issue.5 , pp. 975-981
    • Gradishar, W.1
  • 50
    • 0036514255 scopus 로고    scopus 로고
    • Aromatase inhibitors in breast cancer
    • A. Brodie, Aromatase inhibitors in breast cancer, Trends Endocrinol. Metab. 13 (2) (2002) 61-65.
    • (2002) Trends Endocrinol. Metab. , vol.13 , Issue.2 , pp. 61-65
    • Brodie, A.1
  • 51
    • 0025157171 scopus 로고
    • Estrogen synthetase inhibitors. 2. Comparison of the in vitro aromatase inhibitory activity for a variety of nitrogen heterocycles substituted with diarylmethane or diarylmethanol groups
    • C.D. Jones, M.A. Winter, K.S. Hirsch, N. Stamm, H.M. Taylor, H.E. Holden, J.D. Davenport, E.V. Krumkalns, R.G. Suhr, Estrogen synthetase inhibitors. 2. Comparison of the in vitro aromatase inhibitory activity for a variety of nitrogen heterocycles substituted with diarylmethane or diarylmethanol groups, J. Med. Chem. 33 (1) (1990) 416-429.
    • (1990) J. Med. Chem. , vol.33 , Issue.1 , pp. 416-429
    • Jones, C.D.1    Winter, M.A.2    Hirsch, K.S.3    Stamm, N.4    Taylor, H.M.5    Holden, H.E.6    Davenport, J.D.7    Krumkalns, E.V.8    Suhr, R.G.9
  • 52
    • 0029804614 scopus 로고    scopus 로고
    • Studies on aromatase inhibitors. I. Synthesis and biological evaluation of 4-amino-4H-1,2,4-triazole derivatives
    • M. Okada, T. Yoden, E. Kawaminami, Y. Shimada, M. Kudoh, Y. Isomura, H. Shikama, T. Fujikura, Studies on aromatase inhibitors. I. Synthesis and biological evaluation of 4-amino-4H-1,2,4-triazole derivatives, Chem. Pharm. Bull. 44 (10) (1996) 1871-1879.
    • (1996) Chem. Pharm. Bull. , vol.44 , Issue.10 , pp. 1871-1879
    • Okada, M.1    Yoden, T.2    Kawaminami, E.3    Shimada, Y.4    Kudoh, M.5    Isomura, Y.6    Shikama, H.7    Fujikura, T.8
  • 55
    • 0026050606 scopus 로고
    • New aromatase inhibitors. Synthesis and biological activity of pyridyl-substituted tetralone derivatives
    • H. Bayer, C. Batzl, R.W. Hartmann, A. Mannschreck, New aromatase inhibitors. Synthesis and biological activity of pyridyl-substituted tetralone derivatives, J. Med. Chem. 34 (9) (1991) 2685-2691.
    • (1991) J. Med. Chem. , vol.34 , Issue.9 , pp. 2685-2691
    • Bayer, H.1    Batzl, C.2    Hartmann, R.W.3    Mannschreck, A.4
  • 56
    • 0028305222 scopus 로고
    • Aromatase inhibitors. Syntheses and structure-activity studies of novel pyridyl-substituted indanones, indans, and tetralins
    • R.W. Hartmann, H. Bayer, G. Grun, Aromatase inhibitors. Syntheses and structure-activity studies of novel pyridyl-substituted indanones, indans, and tetralins, J. Med. Chem. 37 (9) (1994) 1275-1281.
    • (1994) J. Med. Chem. , vol.37 , Issue.9 , pp. 1275-1281
    • Hartmann, R.W.1    Bayer, H.2    Grun, G.3
  • 57
    • 0030059847 scopus 로고    scopus 로고
    • Tetrahydro-naphthalenes: Influence of heterocyclic substituents on inhibition of steroidogenic enzymes P450 arom and P450 17
    • G.A. Wachter, R.W. Hartmann, T. Sergejew, G.L. Grun, D. Ledergerber, Tetrahydro-naphthalenes: influence of heterocyclic substituents on inhibition of steroidogenic enzymes P450 arom and P450 17, J. Med. Chem. 39 (1996) 834-841.
    • (1996) J. Med. Chem. , vol.39 , pp. 834-841
    • Wachter, G.A.1    Hartmann, R.W.2    Sergejew, T.3    Grun, G.L.4    Ledergerber, D.5
  • 59
    • 0029044427 scopus 로고
    • Pyridyl-substituted tetrahydrocyclopropa[a]naphthalenes: Highly active and selective inhibitors of P450 arom
    • R.W. Hartmann, H. Bayer, G. Grun, T. Sergejew, U. Bartz, M. Mitrenga, Pyridyl-substituted tetrahydrocyclopropa[a]naphthalenes: highly active and selective inhibitors of P450 arom, J. Med. Chem. 38 (1995) 2103-2111.
    • (1995) J. Med. Chem. , vol.38 , pp. 2103-2111
    • Hartmann, R.W.1    Bayer, H.2    Grun, G.3    Sergejew, T.4    Bartz, U.5    Mitrenga, M.6
  • 60
    • 0034026141 scopus 로고    scopus 로고
    • 1-Imidazolyl (alkyl) substituted di and tetrahydroquinolines and analogs. Synthesis and evaluation of dual inhibitors of P450 TxA 2 and P450 arom
    • C. Jacobs, M. Frotscher, G. Dannhardt, R.W. Hartmann, 1-Imidazolyl (alkyl) substituted di and tetrahydroquinolines and analogs. Synthesis and evaluation of dual inhibitors of P450 TxA 2 and P450 arom, J. Med. Chem. 43 (2000) 1841-1851.
    • (2000) J. Med. Chem. , vol.43 , pp. 1841-1851
    • Jacobs, C.1    Frotscher, M.2    Dannhardt, G.3    Hartmann, R.W.4
  • 62
    • 31344451950 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 5-[(aryl)(1H-imidazol- 1-yl)methyl]-1H-indoles: Potent and selective aromatase inhibitors
    • M.P. Leze, M.L. Borgne, P. Pinson, A. Palusczak, M. Duflos, G.L. Baut, R.W. Hartmann, Synthesis and biological evaluation of 5-[(aryl)(1H-imidazol- 1-yl)methyl]-1H-indoles: potent and selective aromatase inhibitors, Bioorg. Med. Chem. Lett. 16 (2006) 1134-1137.
    • (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 1134-1137
    • Leze, M.P.1    Borgne, M.L.2    Pinson, P.3    Palusczak, A.4    Duflos, M.5    Baut, G.L.6    Hartmann, R.W.7
  • 63
    • 48849094047 scopus 로고    scopus 로고
    • Synthesis of 6- and 4-functionalized indoles via a reductive cyclization approach and evaluation as aromatase inhibitors
    • M.P. Leze, A. Palusczak, R.W. Hartmann, M.L. Borgne, Synthesis of 6- and 4-functionalized indoles via a reductive cyclization approach and evaluation as aromatase inhibitors, Bioorg. Med. Chem. Lett. 18 (2008) 4713-4715.
    • (2008) Bioorg. Med. Chem. Lett. , vol.18 , pp. 4713-4715
    • Leze, M.P.1    Palusczak, A.2    Hartmann, R.W.3    Borgne, M.L.4
  • 64
    • 84874667729 scopus 로고    scopus 로고
    • Design, synthesis and aromatase inhibitory activities of novel indole-imidazole derivatives
    • R. Wang, H.-F. Shi, J.-F. Zhao, Y.-P. He, H.-B. Zhang, J.-P. Liu, Design, synthesis and aromatase inhibitory activities of novel indole-imidazole derivatives, Bioorg. Med. Chem. Lett. 23 (2013) 1760-1762.
    • (2013) Bioorg. Med. Chem. Lett. , vol.23 , pp. 1760-1762
    • Wang, R.1    Shi, H.-F.2    Zhao, J.-F.3    He, Y.-P.4    Zhang, H.-B.5    Liu, J.-P.6
  • 65
    • 0027255772 scopus 로고
    • Substituted 1-[benzofuran-2-yl-phenylmethyl]-imidazoles as potent inhibitors of aromatase in vitro and in female rats in vivo
    • R. Whomsley, E. Fernandez, P.J. Nicholls, H.J. Smith, P. Lombardi, V. Pestellini, Substituted 1-[benzofuran-2-yl)-phenylmethyl]-imidazoles as potent inhibitors of aromatase in vitro and in female rats in vivo, J. Steroid Biochem. Mol. Biol. 44 (4-6) (1993) 675-676.
    • (1993) J. Steroid Biochem. Mol. Biol. , vol.44 , Issue.4-6 , pp. 675-676
    • Whomsley, R.1    Fernandez, E.2    Nicholls, P.J.3    Smith, H.J.4    Lombardi, P.5    Pestellini, V.6
  • 66
    • 0032589131 scopus 로고    scopus 로고
    • Inhibition of aromatase (P450Arom) by some 1-(benzofuran-2-ylmethyl)imidazoles
    • C.P. Owen, P.J. Nicholls, H.J. Smith, R. Whomsley, Inhibition of aromatase (P450Arom) by some 1-(benzofuran-2-ylmethyl)imidazoles, J. Pharm. Pharmacol. 51 (4) (1999) 427-433.
    • (1999) J. Pharm. Pharmacol. , vol.51 , Issue.4 , pp. 427-433
    • Owen, C.P.1    Nicholls, P.J.2    Smith, H.J.3    Whomsley, R.4
  • 67
    • 0031760523 scopus 로고    scopus 로고
    • Medicinal chemistry: Enantioselectivity of some 1-(benzofuran-2-yl)-1-(1-H-imidazol-1-yl) alkanes as inhibitors of P450Arom
    • G.A. Khodarahmi, H.J. Smith, P.J. Nicholls, M. Ahmadi, Medicinal chemistry: enantioselectivity of some 1-(benzofuran-2-yl)-1-(1-H-imidazol-1-yl) alkanes as inhibitors of P450Arom, J. Pharm. Pharmacol. 50 (11) (1998) 1321-1330.
    • (1998) J. Pharm. Pharmacol. , vol.50 , Issue.11 , pp. 1321-1330
    • Khodarahmi, G.A.1    Smith, H.J.2    Nicholls, P.J.3    Ahmadi, M.4
  • 72
    • 18844443185 scopus 로고    scopus 로고
    • Aromatase inhibitors in the treatment of breast cancer
    • (a) R.W. Brueggemeier, J.C. Hackett, E.S. Diaz-Cruz, Aromatase inhibitors in the treatment of breast cancer, Endocr. Rev. 26 (3) (2005) 331-345;
    • (2005) Endocr. Rev. , vol.26 , Issue.3 , pp. 331-345
    • Brueggemeier, R.W.1    Hackett, J.C.2    Diaz-Cruz, E.S.3
  • 73
    • 84875121613 scopus 로고    scopus 로고
    • Novel inhibitor discovery against aromatase through virtual screening and molecular dynamic simulation: A computational approach drug design
    • (b) S. Mirzaie, L. Chupani, E.B. Asadabadi, A.R. Shahverdi, M. Jamalan, Novel inhibitor discovery against aromatase through virtual screening and molecular dynamic simulation: a computational approach drug design, EXCLI J. 12 (2013) 168-183.
    • (2013) EXCLI J , vol.12 , pp. 168-183
    • Mirzaie, S.1    Chupani, L.2    Asadabadi, E.B.3    Shahverdi, A.R.4    Jamalan, M.5
  • 74
    • 84872647271 scopus 로고    scopus 로고
    • A new class of nonsteroidal aromatase Inhibitors: Design and synthesis of chromone and xanthone derivatives and inhibition of the P450 enzymes aromatase and 17α-Hydroxylase/C17,20-Lyase
    • M. Recanatini, A. Bisi, A. Cavalli, F. Belluti, S. Gobbi, A. Rampa, P. Valenti, M. Palzer, A. Palusczak, R.W. Hartmann, A new class of nonsteroidal aromatase Inhibitors: design and synthesis of chromone and xanthone derivatives and inhibition of the P450 enzymes aromatase and 17α-Hydroxylase/C17,20-Lyase, J. Med. Chem. 44 (5) (2001) 672-780.
    • (2001) J. Med. Chem. , vol.44 , Issue.5 , pp. 672-780
    • Recanatini, M.1    Bisi, A.2    Cavalli, A.3    Belluti, F.4    Gobbi, S.5    Rampa, A.6    Valenti, P.7    Palzer, M.8    Palusczak, A.9    Hartmann, R.W.10
  • 75
    • 3242794236 scopus 로고    scopus 로고
    • Synthesis and aromatase inhibitory activity of novel pyridine containing isoflavones
    • Y.W. Kim, J.C. Hackett, R.W. Brueggemeier, Synthesis and aromatase inhibitory activity of novel pyridine containing isoflavones, J. Med. Chem. 47 (2004) 4032-4040.
    • (2004) J. Med. Chem. , vol.47 , pp. 4032-4040
    • Kim, Y.W.1    Hackett, J.C.2    Brueggemeier, R.W.3
  • 76
    • 19444374982 scopus 로고    scopus 로고
    • Synthesis and characterization of azole isoflavone inhibitors of aromatase
    • J.C. Hackett, Y.W. Kim, B. Su, R.W. Brueggemeier, Synthesis and characterization of azole isoflavone inhibitors of aromatase, Bioorg. Med. Chem. 13 (2005) 4063-4070.
    • (2005) Bioorg. Med. Chem. , vol.13 , pp. 4063-4070
    • Hackett, J.C.1    Kim, Y.W.2    Su, B.3    Brueggemeier, R.W.4
  • 77
    • 84859435820 scopus 로고    scopus 로고
    • Development of a new class of aromatase inhibitors: Design, synthesis and inhibitory activity of 3-phenylchroman-4-one (isoflavanone) derivatives
    • K. Bonfield, E. Amato, T. Bankemper, H. Agard, J. Steller, J.M. Keeler, D. Roy, A. McCallum, S. Paula, L. Ma, Development of a new class of aromatase inhibitors: design, synthesis and inhibitory activity of 3-phenylchroman-4-one (isoflavanone) derivatives, Bioorg. Med. Chem. 20 (8) (2012) 2603-2613.
    • (2012) Bioorg. Med. Chem. , vol.20 , Issue.8 , pp. 2603-2613
    • Bonfield, K.1    Amato, E.2    Bankemper, T.3    Agard, H.4    Steller, J.5    Keeler, J.M.6    Roy, D.7    McCallum, A.8    Paula, S.9    Ma, L.10
  • 80
    • 38849089406 scopus 로고    scopus 로고
    • New 7,8-benzoflavanones as potent aromatase inhibitors: Synthesis and biological evaluation
    • S. Yahiaoui, C. Fagnere, C. Pouget, J. Buxeraud, A.-J. Chulia, New 7,8-benzoflavanones as potent aromatase inhibitors: synthesis and biological evaluation, Bioorg. Med. Chem. 16 (2008) 1474-1480.
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 1474-1480
    • Yahiaoui, S.1    Fagnere, C.2    Pouget, C.3    Buxeraud, J.4    Chulia, A.-J.5
  • 83
    • 79952810375 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of imidazolyl derivatives of 4,7-disubstituted coumarins as aromatase inhibitors selective over 17-α-hydroxylase/C17-20 lyase
    • A. Stefanachi, A.D. Favia, O. Nicolotti, F. Leonetti, L. Pisani, M. Catto, C. Zimmer, R.W. Hartmann, A. Carotti, Design, synthesis and biological evaluation of imidazolyl derivatives of 4,7-disubstituted coumarins as aromatase inhibitors selective over 17-α-hydroxylase/C17-20 lyase, J. Med. Chem. 54 (2011) 1613-1625.
    • (2011) J. Med. Chem. , vol.54 , pp. 1613-1625
    • Stefanachi, A.1    Favia, A.D.2    Nicolotti, O.3    Leonetti, F.4    Pisani, L.5    Catto, M.6    Zimmer, C.7    Hartmann, R.W.8    Carotti, A.9
  • 84
    • 77955324216 scopus 로고    scopus 로고
    • Design, synthesis and biological evolution of resveratrol analogues as aromatase and quinone reductase 2 inhibitors for chemoprevention of cancer
    • B. Sun, J. Hoshino, K. Jermihov, L. Marler, J.M. Pezzuto, A.D. Mesecar, M. Cushman, Design, synthesis and biological evolution of resveratrol analogues as aromatase and quinone reductase 2 inhibitors for chemoprevention of cancer, Bioorg. Med. Chem. 18 (14) (2010) 5352-5366.
    • (2010) Bioorg. Med. Chem. , vol.18 , Issue.14 , pp. 5352-5366
    • Sun, B.1    Hoshino, J.2    Jermihov, K.3    Marler, L.4    Pezzuto, J.M.5    Mesecar, A.D.6    Cushman, M.7
  • 87
    • 84879058938 scopus 로고    scopus 로고
    • Synthesis of mixed (E,Z)-, (E)-, and (Z)-norendoxifen with dual aromatase inhibitory and estrogen receptor modulatory activities
    • W. Lv, J. Liu, D. Lu, D.A. Flockhart, M. Cushman, Synthesis of mixed (E,Z)-, (E)-, and (Z)-norendoxifen with dual aromatase inhibitory and estrogen receptor modulatory activities, J. Med. Chem. 56 (11) (2013) 4611-4618.
    • (2013) J. Med. Chem. , vol.56 , Issue.11 , pp. 4611-4618
    • Lv, W.1    Liu, J.2    Lu, D.3    Flockhart, D.A.4    Cushman, M.5
  • 88
    • 84925872644 scopus 로고    scopus 로고
    • Design and synthesis of norendoxifen analogues with dual aromatase inhibitory and estrogen receptor modulatory activities
    • W. Lv, J. Liu, T.C. Skaar, D.A. Flockhart, M. Cushman, Design and synthesis of norendoxifen analogues with dual aromatase inhibitory and estrogen receptor modulatory activities, J. Med. Chem. 58 (2015) 2623-2648.
    • (2015) J. Med. Chem. , vol.58 , pp. 2623-2648
    • Lv, W.1    Liu, J.2    Skaar, T.C.3    Flockhart, D.A.4    Cushman, M.5
  • 89
    • 84901044292 scopus 로고    scopus 로고
    • Synthesis and QSAR studies of benzylimidazole derivatives and benzylcarbazole as potential aromatase inhibitors
    • Y. Dai, Y. Xiao, Q. Wang, S. Wei, X. Zhang, Z. Ma, H. Zheng, M. Hou, T. Zhang, Synthesis and QSAR studies of benzylimidazole derivatives and benzylcarbazole as potential aromatase inhibitors, Asian J. Chem. 26 (8) (2014) 2381-2388.
    • (2014) Asian J. Chem. , vol.26 , Issue.8 , pp. 2381-2388
    • Dai, Y.1    Xiao, Y.2    Wang, Q.3    Wei, S.4    Zhang, X.5    Ma, Z.6    Zheng, H.7    Hou, M.8    Zhang, T.9
  • 90
    • 80054926232 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of callophycin A and analogues as potential chemopreventive anticancer agents
    • L. Shen, E.-J. Park, T.P. Kondratyuk, D. Guendisch, L. Marler, J.M. Pezzuto, A.D. Wright, D. Sun, Design, synthesis and biological evaluation of callophycin A and analogues as potential chemopreventive anticancer agents, Bioorg. Med. Chem. 19 (21) (2011) 6182-6195.
    • (2011) Bioorg. Med. Chem. , vol.19 , Issue.21 , pp. 6182-6195
    • Shen, L.1    Park, E.-J.2    Kondratyuk, T.P.3    Guendisch, D.4    Marler, L.5    Pezzuto, J.M.6    Wright, A.D.7    Sun, D.8
  • 92
    • 79960692837 scopus 로고    scopus 로고
    • Aromatase and dual aromatase-steroid sulfatase inhibitors from the letrozole and vorozole templates
    • P.M. Wood, L.W.L. Woo, M.P. Thomas, M.F. Mahon, A. Purohit, B.V.L. Potter, Aromatase and dual aromatase-steroid sulfatase inhibitors from the letrozole and vorozole templates, Chem. Med. Chem. 6 (2011) 1423-1438.
    • (2011) Chem. Med. Chem. , vol.6 , pp. 1423-1438
    • Wood, P.M.1    Woo, L.W.L.2    Thomas, M.P.3    Mahon, M.F.4    Purohit, A.5    Potter, B.V.L.6
  • 93
    • 79952648555 scopus 로고    scopus 로고
    • Hybrid dual aromatase steroid sulfatase inhibitors with exquisite picomolar inhibitory activity
    • L.W.L. Woo, C. Bubert, A. Purohit, B.V.L. Potter, Hybrid dual aromatase steroid sulfatase inhibitors with exquisite picomolar inhibitory activity, ACS Med. Chem. Lett. 2 (2011) 243-247.
    • (2011) ACS Med. Chem. Lett. , vol.2 , pp. 243-247
    • Woo, L.W.L.1    Bubert, C.2    Purohit, A.3    Potter, B.V.L.4
  • 94
    • 84877074103 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationship studies of derivatives of the dual aromatase-sulfatase inhibitor 4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl) amino]methyl}phenyl sulfamate
    • L.W.L. Woo, P.M. Wood, C. Bubert, M.P. Thomas, A. Purohit, B.V.L. Potter, Synthesis and structure-activity relationship studies of derivatives of the dual aromatase-sulfatase inhibitor 4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl) amino]methyl}phenyl sulfamate, Chem. Med. Chem. 8 (2013) 779-799.
    • (2013) Chem. Med. Chem. , vol.8 , pp. 779-799
    • Woo, L.W.L.1    Wood, P.M.2    Bubert, C.3    Thomas, M.P.4    Purohit, A.5    Potter, B.V.L.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.