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Volumn 73, Issue 6, 2008, Pages 681-688

Synthesis and biological evaluation of some new A,B-ring modified steroidal d-lactones

Author keywords

Aromatase inhibitor; In vitro cytotoxicity; Steroidal epoxides; Steroidal lactones; X ray analysis

Indexed keywords

17A HOMOLACTONE DERIVATIVE; 3 CHLOROPERBENZOIC ACID; 4ALPHA EPOXIDE; 4BETA EPOXIDE; 5ALPHA EPOXIDE; 5BETA EPOXIDE; LACTONE DERIVATIVE; STEROIDAL DEXTRO LACTONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 41649097931     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2008.02.006     Document Type: Article
Times cited : (37)

References (17)
  • 2
    • 0043239221 scopus 로고    scopus 로고
    • Inhibition of aromatase: insights from recent studies
    • Santen R.J. Inhibition of aromatase: insights from recent studies. Steroids 68 (2003) 559-567
    • (2003) Steroids , vol.68 , pp. 559-567
    • Santen, R.J.1
  • 3
    • 0025372326 scopus 로고
    • Endocrine treatment of breast cancer in women
    • Santen R.J., Manni A., Harvey H., and Redmond C. Endocrine treatment of breast cancer in women. Endocr Rev 11 (1990) 221-265
    • (1990) Endocr Rev , vol.11 , pp. 221-265
    • Santen, R.J.1    Manni, A.2    Harvey, H.3    Redmond, C.4
  • 4
    • 0041826100 scopus 로고    scopus 로고
    • Aromatase inhibitors in breast cancer
    • Robertson J.F.R., Nicholson R.I., and Hayes D.F. (Eds), Martin Dunitz Ltd. Publishers, London, England
    • Yue W., Mor G., Naftolin F., Pauley R., Shim W.-S., Harvey H.A., et al. Aromatase inhibitors in breast cancer. In: Robertson J.F.R., Nicholson R.I., and Hayes D.F. (Eds). Endocrine therapy of breast cancer (2002), Martin Dunitz Ltd. Publishers, London, England 75-106
    • (2002) Endocrine therapy of breast cancer , pp. 75-106
    • Yue, W.1    Mor, G.2    Naftolin, F.3    Pauley, R.4    Shim, W.-S.5    Harvey, H.A.6
  • 5
    • 0026666565 scopus 로고
    • 4-Hydroxyandrostenedione: a new treatment for postmenopausal patients with breast cancer
    • Coombes R.C., Hughes S.W., and Dowsett M. 4-Hydroxyandrostenedione: a new treatment for postmenopausal patients with breast cancer. Eur J Cancer 28A (1992) 1941-1945
    • (1992) Eur J Cancer , vol.28 A , pp. 1941-1945
    • Coombes, R.C.1    Hughes, S.W.2    Dowsett, M.3
  • 6
    • 0032979982 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of 6-phenylaliphatic-substituted C19 steroids having a 1,4-diene, 4,6-diene or 1,4,6-triene structure as aromatase inhibitors
    • Numazawa M., and Yamaguchi S. Synthesis and structure-activity relationships of 6-phenylaliphatic-substituted C19 steroids having a 1,4-diene, 4,6-diene or 1,4,6-triene structure as aromatase inhibitors. Steroids 64 (2001) 187-196
    • (2001) Steroids , vol.64 , pp. 187-196
    • Numazawa, M.1    Yamaguchi, S.2
  • 7
    • 0035935681 scopus 로고    scopus 로고
    • Role of hydrophilic interaction in binding of hydroxylated 3-deoxy C19 steroids to the active site of aromatase
    • Numazawa M., Yamada K., Nitta S., Sasaki C., and Kidokoro K. Role of hydrophilic interaction in binding of hydroxylated 3-deoxy C19 steroids to the active site of aromatase. J Med Chem 44 (2001) 4277-4283
    • (2001) J Med Chem , vol.44 , pp. 4277-4283
    • Numazawa, M.1    Yamada, K.2    Nitta, S.3    Sasaki, C.4    Kidokoro, K.5
  • 8
    • 0042167222 scopus 로고    scopus 로고
    • Structure-activity relationships of 3-deoxy androgens as aromatase inhibitors, synthesis and biochemical studies of 4-substituted 4-ene and 5-ene steroids
    • Nagaoka M., Watari Y., Yajima H., Tsukioka K., Muroi Y., Yamada K., et al. Structure-activity relationships of 3-deoxy androgens as aromatase inhibitors, synthesis and biochemical studies of 4-substituted 4-ene and 5-ene steroids. Steroids 68 (2003) 533-542
    • (2003) Steroids , vol.68 , pp. 533-542
    • Nagaoka, M.1    Watari, Y.2    Yajima, H.3    Tsukioka, K.4    Muroi, Y.5    Yamada, K.6
  • 9
    • 26444502089 scopus 로고    scopus 로고
    • Structure-activity relationships of new A,D-ring modified steroids as aromatase inhibitors: design, synthesis, and biological activity evaluation
    • Cepa M.M.D.S., Tavares da Silva E.J., Correia-da-Silva G., Roleira F.M.F., and Teixeira N.A.A. Structure-activity relationships of new A,D-ring modified steroids as aromatase inhibitors: design, synthesis, and biological activity evaluation. J Med Chem 48 (2005) 6379-6385
    • (2005) J Med Chem , vol.48 , pp. 6379-6385
    • 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
  • 12
    • 0036689758 scopus 로고    scopus 로고
    • Novel cytotoxic oxigenated C29 sterols from the Colombian marine sponge Polymastia tenax
    • Santafé G., Paz V., Rodríguez J., and Jiménez C. Novel cytotoxic oxigenated C29 sterols from the Colombian marine sponge Polymastia tenax. J Nat Prod 65 (2002) 1161-1164
    • (2002) J Nat Prod , vol.65 , pp. 1161-1164
    • Santafé, G.1    Paz, V.2    Rodríguez, J.3    Jiménez, C.4
  • 13
    • 0004150157 scopus 로고    scopus 로고
    • University of Göttingrn, Germany
    • Sheldrick G.M. SHELX97 (1997), University of Göttingrn, Germany
    • (1997) SHELX97
    • Sheldrick, G.M.1
  • 16
    • 0036159042 scopus 로고    scopus 로고
    • Experimental application of the median-effect principle for in vitro quantification of the combined inhibitory activities of clavulanic acid and imipenem against IRT-4 β-lactamase
    • Sotto A., Foulongne V., Sirot D., Labia R., and Jourdan J. Experimental application of the median-effect principle for in vitro quantification of the combined inhibitory activities of clavulanic acid and imipenem against IRT-4 β-lactamase. Int J Antimicrob Agents 19 (2002) 75-78
    • (2002) Int J Antimicrob Agents , vol.19 , pp. 75-78
    • Sotto, A.1    Foulongne, V.2    Sirot, D.3    Labia, R.4    Jourdan, J.5
  • 17
    • 0141452964 scopus 로고    scopus 로고
    • WinGX suite for small-molecule single-crystal crystallography
    • Farrugia L.J. WinGX suite for small-molecule single-crystal crystallography. J Appl Crystallogr 32 (1999) 837-838
    • (1999) J Appl Crystallogr , vol.32 , pp. 837-838
    • Farrugia, L.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.