Nonsteroidal aromatase inhibitors: Recent advances
暂无分享,去创建一个
[1] S. Moslemi,et al. Aromatase inhibitors: past, present and future , 2001, Molecular and Cellular Endocrinology.
[2] A. Buzdar. Endocrine therapy in the treatment of metastatic breast cancer. , 2001, Seminars in oncology.
[3] R. Gil,et al. Aromatase inhibition by an 11,13-dihydroderivative of a sesquiterpene lactone. , 2001, The Journal of pharmacology and experimental therapeutics.
[4] A. Purohit,et al. Aromatase regulation and breast cancer , 2001, Clinical endocrinology.
[5] M. Dowsett,et al. Recent advances in the clinical application of aromatase inhibitors , 2001, The Journal of Steroid Biochemistry and Molecular Biology.
[6] G. Chetrite,et al. The selective estrogen enzyme modulator (SEEM) in breast cancer , 2001, The Journal of Steroid Biochemistry and Molecular Biology.
[7] P. Goss,et al. Aromatase inhibitors in the treatment and prevention of breast cancer. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[8] A. Cavalli,et al. A new class of nonsteroidal aromatase inhibitors: design and synthesis of chromone and xanthone derivatives and inhibition of the P450 enzymes aromatase and 17 alpha-hydroxylase/C17,20-lyase. , 2001, Journal of medicinal chemistry.
[9] C. Pouget,et al. Chalcones are potent inhibitors of aromatase and 17β-hydroxysteroid dehydrogenase activities , 2001 .
[10] A. Cavalli,et al. Linking CoMFA and protein homology models of enzyme-inhibitor interactions: an application to non-steroidal aromatase inhibitors. , 2000, Bioorganic & medicinal chemistry.
[11] E. Simpson,et al. Role of aromatase in sex steroid action. , 2000, Journal of molecular endocrinology.
[12] A. Buzdar. Exemestane in advanced breast cancer , 2000, Anti-cancer drugs.
[13] O. Pelkonen,et al. Synthesis of new potent and selective aromatase inhibitors based on long-chained diarylalkylimidazole and diarylalkyltriazole molecule skeletons. , 2000, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[14] S. Davis,et al. The Role of Local Estrogen Biosynthesis in Males and Females , 2000, Trends in Endocrinology & Metabolism.
[15] J Guillon,et al. New aromatase inhibitors. Synthesis and biological activity of aryl-substituted pyrrolizine and indolizine derivatives. , 2000, Bioorganic & medicinal chemistry.
[16] R. Hartmann,et al. 1-imidazolyl(alkyl)-substituted di- and tetrahydroquinolines and analogues: syntheses and evaluation of dual inhibitors of thromboxane A(2) synthase and aromatase. , 2000, Journal of medicinal chemistry.
[17] V. Njar,et al. Aromatase inhibitors and their application in breast cancer treatment☆ , 2000, Steroids.
[18] G H Loew,et al. Role of the heme active site and protein environment in structure, spectra, and function of the cytochrome p450s. , 2000, Chemical reviews.
[19] H. Sasano,et al. Aromatase as a Therapeutic Target in Endometriosis , 2000, Trends in Endocrinology & Metabolism.
[20] G. Chetrite,et al. Comparison of estrogen concentrations, estrone sulfatase and aromatase activities in normal, and in cancerous, human breast tissues , 2000, The Journal of Steroid Biochemistry and Molecular Biology.
[21] P. Mak,et al. A yeast screen system for aromatase inhibitors and ligands for androgen receptor: yeast cells transformed with aromatase and androgen receptor. , 1999, Environmental health perspectives.
[22] N. Zilembo,et al. Aromatase Inhibitors in the Treatment of Postmenopausal Breast Cancer , 1999, Drugs & aging.
[23] F. Holsboer,et al. Neuroactive steroids: mechanisms of action and neuropsychopharmacological perspectives , 1999, Trends in Neurosciences.
[24] C. Simons,et al. 1-[(Benzofuran-2-yl)phenylmethyl]-triazoles and -tetrazoles - potent competitive inhibitors of aromatase. , 1999, Bioorganic & medicinal chemistry letters.
[25] S. Rault,et al. MR 20492 and MR 20494: two indolizinone derivatives that strongly inhibit human aromatase , 1999, The Journal of Steroid Biochemistry and Molecular Biology.
[26] C. Osborne,et al. Aromatase inhibitors in relation to other forms of endocrine therapy for breast cancer. , 1999, Endocrine-related cancer.
[27] G. Braunstein. Aromatase and gynecomastia. , 1999, Endocrine-related cancer.
[28] D. Merke,et al. Use of aromatase inhibitors in precocious puberty. , 1999, Endocrine-related cancer.
[29] A. Brodie,et al. Aromatase and its inhibitors , 1999, The Journal of Steroid Biochemistry and Molecular Biology.
[30] M. Piccart,et al. The third-generation non-steroidal aromatase inhibitors: a review of their clinical benefits in the second-line hormonal treatment of advanced breast cancer. , 1999, Annals of oncology : official journal of the European Society for Medical Oncology.
[31] R. Whomsley,et al. Inhibition of Aromatase (P450Arom) by some 1‐(Benzofuran‐2‐ylmethyl)imidazoles , 1999, The Journal of pharmacy and pharmacology.
[32] R. Hartmann,et al. New selective nonsteroidal aromatase inhibitors: synthesis and inhibitory activity of 2,3 or 5-(alpha-azolylbenzyl)-1H-indoles. , 1999, Bioorganic & medicinal chemistry letters.
[33] J. Le Bail,et al. Aromatase and 17beta-hydroxysteroid dehydrogenase inhibition by flavonoids. , 1998, Cancer letters.
[34] G. Khodarahmi,et al. Medicinal Chemistry: Enantioselectivity of Some 1‐(Benzofuran‐2‐yl)‐1‐(1‐H‐imidazol‐1‐yl) Alkanes as Inhibitors of P450Arom , 1998 .
[35] L. Wiseman,et al. Anastrozole. A review of its use in the management of postmenopausal women with advanced breast cancer. , 1998, Drugs & aging.
[36] N. Harada,et al. Intratumoral aromatase in human breast, endometrial, and ovarian malignancies. , 1998, Endocrine reviews.
[37] V. Njar,et al. Aromatase inhibitors in advanced breast cancer: mechanism of action and clinical implications , 1998, The Journal of Steroid Biochemistry and Molecular Biology.
[38] S. Rault,et al. Evidence for new non-steroidal human aromatase inhibitors and comparison with equine aromatase inhibition for an understanding of the mammalian active site , 1998 .
[39] G. Ball,et al. New insights into the regulation and function of brain estrogen synthase (aromatase) , 1998, Trends in Neurosciences.
[40] J. Valentine,et al. Mimicking Cytochrome P-450 2B4 and Aromatase: Aromatization of a Substrate Analogue by a Peroxo Fe(III) Porphyrin Complex , 1998 .
[41] J Guillon,et al. Design and synthesis of a new type of non steroidal human aromatase inhibitors. , 1998, Bioorganic & medicinal chemistry letters.
[42] A. Cavalli,et al. Comparative molecular field analysis of non-steroidal aromatase inhibitors: an extended model for two different structural classes. , 1998, Bioorganic & medicinal chemistry.
[43] Nico P. E. Vermeulen,et al. Ab initio calculations on iron-porphyrin model systems for intermediates in the oxidative cycle of cytochrome P450s , 1998, J. Comput. Aided Mol. Des..
[44] Ji-ping Wang,et al. In situ aromatization enhances breast tumor estradiol levels and cellular proliferation. , 1998, Cancer research.
[45] C. Laughton,et al. Molecular basis of the inhibition of human aromatase (estrogen synthetase) by flavone and isoflavone phytoestrogens: A site-directed mutagenesis study. , 1998, Environmental health perspectives.
[46] Y. Isomura,et al. Studies on aromatase inhibitors. IV. Synthesis and biological evaluation of N,N-disubstituted-5-aminopyrimidine derivatives. , 1997, Chemical & pharmaceutical bulletin.
[47] B. Masters,et al. Three-dimensional structure of NADPH-cytochrome P450 reductase: prototype for FMN- and FAD-containing enzymes. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[48] F. Labrie,et al. Physiological changes in dehydroepiandrosterone are not reflected by serum levels of active androgens and estrogens but of their metabolites: intracrinology. , 1997, The Journal of clinical endocrinology and metabolism.
[49] R. Gil,et al. A novel activity for a group of sesquiterpene lactones: inhibition of aromatase , 1997, FEBS letters.
[50] C. Laughton,et al. Binding characteristics of aromatase inhibitors and phytoestrogens to human aromatase , 1997, The Journal of Steroid Biochemistry and Molecular Biology.
[51] S. Ahmed. The mechanism of a P-450 enzyme-aromatase; a molecular modelling perspective for the removal of the C(19) methyl and aromatisation of the steroid A ring. , 1997, Journal of enzyme inhibition.
[52] Y. Isomura,et al. Studies on aromatase inhibitors. III. Synthesis and biological evaluation of [(4-bromobenzyl)(4-cyanophenyl)amino]azoles and their azine analogs. , 1997, Chemical & pharmaceutical bulletin.
[53] Y. Isomura,et al. Studies on aromatase inhibitors. II. Synthesis and biological evaluation of 1-amino-1H-1,2,4-triazole derivatives. , 1997, Chemical & pharmaceutical bulletin.
[54] M Okada,et al. Studies on aromatase inhibitors. I. Synthesis and biological evaluation of 4-amino-4H-1,2,4-triazole derivatives. , 1996, Chemical & pharmaceutical bulletin.
[55] L. Wiseman,et al. Formestane. A review of its pharmacological properties and clinical efficacy in the treatment of postmenopausal breast cancer. , 1996, Drugs & aging.
[56] R. Hartmann,et al. Synthesis and Evaluation of Azole‐Substituted Tetrahydronaphthalenes as Inhibitors of P450 arom, P450 17, and P450 TxA2 , 1996, Archiv der Pharmazie.
[57] C. Laughton,et al. Binding characteristics of seven inhibitors of human aromatase: a site-directed mutagenesis study. , 1996, Cancer research.
[58] M. J. Coon,et al. Cytochrome P450 2: peroxidative reactions of diversozymes. , 1996, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[59] R. Hartmann,et al. Tetrahydronaphthalenes: influence of heterocyclic substituents on inhibition of steroid enzymes P450 arom and P450 17. , 1996, Journal of medicinal chemistry.
[60] R. Brueggemeier,et al. Development of Steroidal and Nonsteroidal Inhibitors of Aromatase for the Treatment of Hormone-Dependent Breast Cancer , 1996, Current Medicinal Chemistry.
[61] Maurizio Recanatini,et al. Comparative molecular field analysis of non-steroidal aromatase inhibitors related to fadrozole , 1996, J. Comput. Aided Mol. Des..
[62] J. H. Smith,et al. Synthesis and biological evaluation of imidazole based compounds as cytochrome P-450 inhibitors. , 1995, Drug design and discovery.
[63] R. Hartmann,et al. Pyridyl-substituted tetrahydrocyclopropa[a]naphthalenes: highly active and selective inhibitors of P450 arom. , 1995, Journal of medicinal chemistry.
[64] L. Koymans,et al. A molecular model for the interaction between vorozole and other non-steroidal inhibitors and human cytochrome P450 19 (P450 Aromatase) , 1995, The Journal of Steroid Biochemistry and Molecular Biology.
[65] E. Simpson,et al. A three‐dimensional model of aromatase cytochrome P450 , 1995, Protein science : a publication of the Protein Society.
[66] K. Korzekwa,et al. Mutagenesis study at a postulated hydrophobic region near the active site of aromatase cytochrome P450. , 1994, The Journal of biological chemistry.
[67] Y. Ito,et al. Aromatase cytochrome P450, the enzyme responsible for estrogen biosynthesis. , 1994, Endocrine reviews.
[68] R. Hartmann,et al. Aromatase inhibitors. Syntheses and structure-activity studies of novel pyridyl-substituted indanones, indans, and tetralins. , 1994, Journal of medicinal chemistry.
[69] J Deisenhofer,et al. Crystal structure and refinement of cytochrome P450terp at 2.3 A resolution. , 1994, Journal of molecular biology.
[70] E. Simpson,et al. Functional domains of human aromatase cytochrome P450 characterized by linear alignment and site-directed mutagenesis. , 1993, Molecular endocrinology.
[71] J Deisenhofer,et al. Crystal structure of hemoprotein domain of P450BM-3, a prototype for microsomal P450's. , 1993, Science.
[72] P. Furet,et al. Aromatase inhibitors: synthesis, biological activity, and binding mode of azole-type compounds. , 1993, Journal of medicinal chemistry.
[73] S. Neidle,et al. A detailed molecular model for human aromatase , 1993, The Journal of Steroid Biochemistry and Molecular Biology.
[74] W. Trager,et al. Studies on the mechanism of aromatase and other cytochrome P450 mediated deformylation reactions , 1993, Journal of Steroid Biochemistry and Molecular Biology.
[75] H. J. Smith,et al. Substituted 1-[(benzofuran-2-YL)-phenylmethyl]-imidazoles as potent inhibitors of aromatase in vitro and in female rats in vivo , 1993, The Journal of Steroid Biochemistry and Molecular Biology.
[76] V. Njar,et al. Mechanistic studies on aromatase and related CC bond cleaving P-450 enzymes , 1993, The Journal of Steroid Biochemistry and Molecular Biology.
[77] P. Furet,et al. Structure-activity relationships and binding model of novel aromatase inhibitors , 1993, The Journal of Steroid Biochemistry and Molecular Biology.
[78] C. Mendelson,et al. Structure-function relationships of human aromatase cytochrome P-450 using molecular modeling and site-directed mutagenesis. , 1991, The Journal of biological chemistry.
[79] W. Trager,et al. Theoretical studies on the mechanism of conversion of androgens to estrogens by aromatase. , 1991, Biochemistry.
[80] M. Lang,et al. Highly selective inhibition of estrogen biosynthesis by CGS 20267, a new non-steroidal aromatase inhibitor , 1990, The Journal of Steroid Biochemistry and Molecular Biology.
[81] P. Cole,et al. Mechanism and inhibition of cytochrome P-450 aromatase. , 1990, Journal of medicinal chemistry.
[82] D. Pompon,et al. Stable expression of human aromatase complementary DNA in mammalian cells: a useful system for aromatase inhibitor screening. , 1990, Cancer research.
[83] P. Janssen,et al. R 76713 and enantiomers: selective, nonsteroidal inhibitors of the cytochrome P450-dependent oestrogen synthesis. , 1990, Biochemical pharmacology.
[84] Y. Abul-Hajj,et al. Aromatase inhibition by flavonoids , 1990, The Journal of Steroid Biochemistry and Molecular Biology.
[85] P. Cole,et al. Conversion of a 3-desoxysteroid to 3-desoxyestrogen by human placental aromatase. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[86] R. Cramer,et al. Comparative molecular field analysis (CoMFA). 1. Effect of shape on binding of steroids to carrier proteins. , 1988, Journal of the American Chemical Society.
[87] P. Cole,et al. Peroxide model reaction for placental aromatase , 1988 .
[88] H. L. Carrell,et al. Metabolism of 19-methyl-substituted steroids by human placental aromatase. , 1987, Biochemistry.
[89] H. L. Carrell,et al. Metabolism of 19-methyl substituted steroids and a proposal for the third aromatase monooxygenation , 1987, Steroids.
[90] Leslie J. Browne,et al. In vitro and in vivo studies demonstrating potent and selective estrogen inhibition with the nonsteroidal aromatase inhibitor CGS 16949A , 1987, Steroids.
[91] T. Poulos,et al. High-resolution crystal structure of cytochrome P450cam. , 1987, Journal of molecular biology.
[92] J. Mason,et al. Imidazole antimycotics: inhibitors of steroid aromatase. , 1985, Biochemical pharmacology.
[93] J. Kellis,et al. Inhibition of human estrogen synthetase (aromatase) by flavones. , 1984, Science.
[94] M. Calder,et al. Mechanistic studies on C-19 demethylation in oestrogen biosynthesis. , 1982, The Biochemical journal.
[95] P. Graves,et al. Stereoselective inhibition of aromatase by enantiomers of aminoglutethimide. , 1979, Endocrinology.
[96] A. Brodie,et al. The effect of an aromatase inhibitor, 4-hydroxy-4-androstene-3,17-dione, on estrogen-dependent processes in reproduction and breast cancer. , 1977, Endocrinology.
[97] Thompson Ea,et al. Utilization of oxygen and reduced nicotinamide adenine dinucleotide phosphate by human placental microsomes during aromatization of androstenedione. , 1974 .
[98] H. Brodie,et al. Studies on the mechanism of estrogen biosynthesis. 8. The development of inhibitors of the enzyme system in human placenta. , 1973, Endocrinology.
[99] D. Parke,et al. Inhibition studies on the aromatization of androst-4-ene-3,17-dione by human placental microsomal preparations. , 1972, The Biochemical journal.
[100] S. Skinner,et al. The stereospecific removal of a C-19 hydrogen atom in oestrogen biosynthesis. , 1969, The Biochemical journal.
[101] S. Skinner,et al. The intermediary role of a 19-oxoandrogen in the biosynthesis of oestrogen. , 1968, The Biochemical journal.
[102] L. Koymans,et al. Aromatase inhibitors — mechanisms for non-steroidal inhibitors , 2004, Breast Cancer Research and Treatment.
[103] I. Smith,et al. Fadrozole and letrozole in advanced breast cancer: Clinical and biochemical effects , 2004, Breast Cancer Research and Treatment.
[104] P. Lønning,et al. Pharmacological and clinical profile of anastrozole , 2004, Breast Cancer Research and Treatment.
[105] P. Lønning. Pharmacological profiles of exemestane and formestane, steroidal aromatase inhibitors used for treatment of postmenopausal breast cancer , 2004, Breast Cancer Research and Treatment.
[106] C. Osborne,et al. Steroid hormone receptors in breast cancer management , 2004, Breast Cancer Research and Treatment.
[107] K. Korzekwa,et al. Evaluation of the mechanism of aromatase cytochrome P450. A site-directed mutagenesis study. , 2001, European journal of biochemistry.
[108] A. Buzdar,et al. Complete Estrogen Blockade for the Treatment of Metastatic and Early Stage Breast Cancer , 2000, Drugs & aging.
[109] R. Hartmann,et al. Synthesis and In Vitro Evaluation of 3‐(1‐Azolylmethyl)‐1H‐indoles and 3‐(1‐Azolyl‐1‐phenylmethyl)‐1H‐indoles as Inhibitors of P450 arom , 1997, Archiv der Pharmazie.
[110] S. Bulun,et al. Aromatase expression in health and disease. , 1997, Recent progress in hormone research.
[111] L. Banting. Inhibition of aromatase. , 1996, Progress in medicinal chemistry.
[112] Takaaki Kobayashi,et al. Prevention of experimental hepatic metastasis with thromboxne synthase inhibitor , 1995, Research in experimental medicine. Zeitschrift fur die gesamte experimentelle Medizin einschliesslich experimenteller Chirurgie.
[113] H. J. Smith,et al. Recent developments in aromatase inhibition as a potential treatment for oestrogen-dependent breast cancer. , 1989, Progress in medicinal chemistry.
[114] A. Meyer. Conversion of 19-hydroxy-Δ4-androstene-3,17-dione to estrone by endocrine tissue , 1955 .