(12) United States Patent (10) Patent No.: US 8,003,783 B2 Vicker Et Al

(12) United States Patent (10) Patent No.: US 8,003,783 B2 Vicker Et Al

USO08003783B2 (12) United States Patent (10) Patent No.: US 8,003,783 B2 Vicker et al. (45) Date of Patent: Aug. 23, 2011 (54) 17B-HYDROXYSTEROID DEHYDROGENASE OTHER PUBLICATIONS INHIBITORS Martin R. Tremblay, et al "Overview of a Rational Approach to (75) Inventors: Nigel Vicker, Slough (GB); Harshani DesignType I 17 B-Hydroxysteroid Dehydrogenase Inhibitors With Rithma Ruchiranani Lawrence, Slough out Estrogenic Activity: Chemical Synthesis and Biological Evalua (GB); Gillian Margaret Allan, Slough tion” 66(4) J. Steroid Biochem (1998): 179-191. (GB); Christian Bubert, Slough (GB); (Continued) Delphine Sophie Marion Fischer, Slough (GB); Atul Purohit, Slough Primary Examiner — Barbara P. Badio (GB); Michael John Reed, Slough Assistant Examiner — Sara E Townsley (GB); Barry Victor Lloyd Potter, (74) Attorney, Agent, or Firm — Frommer Lawrence & Slough (GB) Haug LLP; Sandra Kuzmich; Russell A. Garman (73) Assignee: Sterix Limited, Slough, Berkshire (GB) (57) ABSTRACT (*) Notice: Subject to any disclaimer, the term of this There is provided a compound of Formula (III) patent is extended or adjusted under 35 U.S.C. 154(b) by 1622 days. 3 Formula (III) (21) Appl. No.: 11/234,868 R (22) Filed: Sep. 23, 2005 RI (65) Prior Publication Data US 2006/OO74060 A1 Apr. 6, 2006 N Related U.S. Application Data 3 yCa (63) Continuation-in-part of application No. R2 PCT/GB2004/001234, filed on Mar. 22, 2004. R4 (51) Int. Cl. wherein A6 IK3I/58 (2006.01) R" is a selected from an alkyloxyalkyl group, a nitrile group, CO7I 71/00 (2006.01) alkylaryl group, alkenylaryl group, alkylheteroaryl group, (52) U.S. Cl. .......................................... 540/49; 514/176 alkenylheteroaryl group, =N-O-alkyl or =N-O H (58) Field of Classification Search .................... 540/49; group, branched alkenylalkyl-alcohol group, amide or 514f176 alkylamide or —CHO so that R together with R provide See application file for complete search history. the enol tautomer or R together with R form a pyrazole, wherein(a)R’ is =N O-alkylor=N-O-H group, (b) (56) References Cited the pyrazole is substituted with one of alkyl-OH group, alkyl ester group, alkyloxyalkyl group, branched alkyl U.S. PATENT DOCUMENTS group, and an amide and/or (c) the 2-position is Substituted with a group selected from —OH and —O-hydrocarbyl or 3,047,568 A T. 1962 Kissman et al. a heteroaryl ring; (Continued) R’ is selected from —OH and a sulphamate group; and R is selected from —OH or =O; wherein the ring system FOREIGN PATENT DOCUMENTS may be further substituted with one or more hydroxyl, DE 1176 131 T 1961 alkyl, alkoxy, alkinyl or halo Substituents. (Continued) 19 Claims, 1 Drawing Sheet SS HOSO ES El E. E. Tyge at al 2. 8 2. res, set r US 8,003,783 B2 Page 2 U.S. PATENT DOCUMENTS Gorski J., et al., Hormones receptors: Studies on the interaction of 3,163,641 A 12, 1964 Christiansen et al. estrogens with uterus, Recent Prog. Horm. Res., 1968, vol. 24, p. 3,398,140 A 8, 1968 Clinton 45-80. 5,585,405 A * 12/1996 Labrie et al. .................. 514,733 Gupta, et al., Synthesis and biological activity of Some D-ring modi 5,880,115 A 3/1999 Li et al. fied oestrone derivative, Ind. J. Chem. 1999, vol. 38B, p. 563-571. 6,046,186 A 4/2000 Tanabe et al. Heer, et al., Uber Steroide, Marrianol-und Doisynoisaure, Uber FOREIGN PATENT DOCUMENTS oestrogene carbonsauren II. Heiv. Chim. Acta. 1945, vol. 28, p. 156-165. GB 1033520 6, 1966 GB 1096732 12/1967 Horiuchi, et al., Regioselective 2-Iodination of Estradiol, Estriol & GB 233.1987 6, 1999 Oestrone, J. Chem. Soc. Chem. Commun., 1982, p. 671-672. WO WO O2, 16392 2, 2002 Holli K., et al. Lumpectomy with or without postoperative radio WO O2,32409 4/2002 therapy for breast cancer with favourable prognostic features: results WO WO O2/O58634 8, 2002 ofa randomized study, Br. J. Cancer, 2001, vol. 84. No. 2, p. 164-169. Horwitz K. B., et al., Nuclear mechanism of estrogen action: effects OTHER PUBLICATIONS of oestradiol and anti-estrogens on estrogens receptors and nuclear Maninder Minu, et al. “Synthesis and Biological Activity of receptor processing, J. Biol. Chem., 1978, vol. 253, p. 8185-8192. 16-arylidene derivatives of Estrone and Estrone Methyl Ether'42 (1) Horwitz, K.B. et al. Oestrogen control of progesterone receptor in human breast cancer; role of oestradiol and antiestrogen, Endocri Indian Journal of Chemistry Section B (2003): 166-172. nology, 1978, vol. 103, p. 1742-1751. Donald Poirier, et al. "A Multidetachable Sulfamate Linker Success Jin J.-Z. et al., Human estrogenic 17 -hydroxysteroid fully Used in a Solid-Phase Strategy to Generate Libraries of dehydrogenase : predominance of oestrone reduction and its induc Sulfamate and Phenol Derivatives' 12 Bioorganic & Medicinal tion by NADPH, Biochem, Biophys. Res., 1999, 259, p. 489-493. Chemistry Letters (2002) 2833-2838. Jordan V.C.. The Strategic use of antiestrogens to control the devel Tremblay et al., “Synthesis of 16-(Bromoalkyl)-Estradiols having opment and growth of breast cancer, Cancer, 1992, vol. 70, p. 977 Inhibitory Effect on Human Placental Estradiol 17B-Hydroxysteroid 982. Dehydrogenase (173-HSD Type 1)”. Bioorganic and Medicinal Kaae S., et al., Does simple mastectomy followed by irradiation offer Chemistry, vol. 3, No. 5, pp. 505-523 (1995). the Survival comparable to radical procedures. International Journal Liviu Constantin Ciobanu et al., “Nonsteroidal compounds designed of Radiation Oncology, Biology, Physics, 1977, vol. 2, p. 1163-1166. to mimic potent steroid sulfatase inhibitors”, Journal of Steroid Bio Labrie F. At the cutting edge, Intracrinology, Mol. Cell. Endocrinolo., chemistry & Molecular Biology, vol. 80, pp. 339-353, (2002). 1991, 78, C113-118. Adamski, et al., Molecular cloning of a novel widely expressed Lebail et al., Aromatase and 173-hydroxysteroid dehydrogenase human 80 kDa 17B-hydroxysteroid dehydrogenase IV, Biochem. J., inhibition by flavinoids, Cancer Lett., 1998, vol. 133, p. 101-106. 1995, vol. 311, p. 437-443. Li P.-K. et al., Development of potent non-estrogenic oestrone Agnusdei D., et la. B. Ann. Endocrinol, 1999, vol. 60, No. 3, p. Sulphatase inhibitors, Steroids, 1998, 63, p. 425-432. 242-246. Lin et al., 3D structure of human estrogenic 17 B-HSD: binding with Appeletal. Uberdashydrazidosulpfamid, Chem. Ber, 1958, vol.91. various steroids, J. Steroid. Biochem. Mol. Biol., 1999, vol. 69, p. p. 1339-1341. 425-429. Breton, et al., The structure of a complex of human 17 Loev et al., Alkylphenols related to the poison ivy principle, An B-hydroxysteroid dehydrogenase with oestradiol and NADP8 iden improved method of synthesis involving the Na-Butanol cleavage of tifies two principal targets for the design of inhibitors, Structure benzyl ethers, J. Am. Chem. Soc., 1956, vol. 78 p. 6095-6101. (Lond.), 1996, vol. 4, p. 905-915. Makela, et al., Inhibition of 17 beta-hydroxysteroid oxidoreductase Castiglione-Gertsch J. New aromatase inhibitors: more selectivity, by flavonids in breast and prostate cancer cells, Proc. Soc. Exp. Biol. less toxicity, unfortunately, the same activity, Eur, J. Cancer, 1996, Med. 1998, vol. 217, p. 310-316. vol. 32A, p. 393-395. Malini B., et al., Inhibition of steroid Sulphatase activity by tricyclic Claussner A. et al., J. Steroid. Biochem, 1992, vol. 41, p. 609-614. coumarin sulfamates, J. Steroid Biochem. Molecular Biol., 2000, vol. Coldham et al. A possible mechanism for increased breast cell pro 75, p. 253–258. liferation by progestins through increased reductive 17 Matkovics, et al., Rearrangement of steroids, VII, Schmidt reaction B-hydroxysteroid dehydrogenase activity, Int. J. Cancer, 1990, vol. and Beckmann rearrangement of oestrone and its derivatives, Acta 45, p. 174-178. Chim. Acad. Scien. Hung. 1974, vol. 80, p. 79-87. Collins et al., The estrogenic and anti-Oestrogenic activities of Miller B.A., et al. (eds), Racial/Ethnic patterns of Cancer in the phytochemicals with the human estrogen receptor expressed in yeast, United States, 1988-1992, National Cancer Institute, 1996. Steroids, 1997, vol. 62, p. 365-372. Miller W.R., Aromatase Inhibitors—where are we now?, Br. J. Can Coulson C.J., Steroid biosynthesis and action, 2" edition, Molecular cer, 1996, vol. 73, p. 415-417. Mechanism of Drug Action, 1994, p. 95-122. Nicholls P.J., Breast Cancer Management: Science and Care Deyashiki, et al., Molecular cloning and characterization of mouse Together, Pharm.J. 1997, vol. 259, p. 459-470. oestradiol 17 f-dehydrogenase (A-specific), a member of the Numazawa, et al., J. Chem. Soc. Chem. Commun., 1983, vol. 9 p. aldoketoreductase family, J. Biol. chem., 1995, vol. 270, p. 10461 533. 10467. Okada et al. Efficient general method for sulfamoylation of a Duncan, et al. Inhibition of oestrone Sulphatase activity by estrone hydroxyl group, Tet. Lett., 2000, vol. 41, p. 7047-7051. 3-methyl-thiophosphonate: a potential therapeutic agent in breast Peltoketo H., et al., Complete amino acid sequence of human placen cancer, Cancer Res., 1993, vol. 53, p. 298-303. tal 17B-hydroxysteroid dehydrogenase deduced from cDNA, FEBS Early Breast Cancer Trialists' Collaborative Group. Effects of adju Lett., 1988, vol. 239, No. 1, p. 73-77. vant Tamoxifen and of cytotoxic therapy on mortality in early breast Peltoketo H., et al., 17B-hydroxysteroid dehydrogenase (HSD)/ 17 cancer, N. Eng. J. Med., 1988, vol. 319, p. 1681-1692. ketosteroid reductase (KSR) family, nomenclature and main charac Geissler et al., Male pseudohermaphroditism caused by mutation of teristics of the 17 HSD/KSR enzymes, J. Mol. Endocrinol. 1999, vol. testicular 17 B-hydroxysteroid dehydrogenase 3, Nat. Genet., 1994, 23, No. 1, p. 1-11. vol. 7, p. 34-39. Penning T.M., Molecular endocrinology of hydroxysteroid Ghosh, et al., Structure of the human estrogenic 17 beta dehydrogenases, Endocrine Reviews, 1997, vol.

View Full Text

Details

  • File Type
    pdf
  • Upload Time
    -
  • Content Languages
    English
  • Upload User
    Anonymous/Not logged-in
  • File Pages
    134 Page
  • File Size
    -

Download

Channel Download Status
Express Download Enable

Copyright

We respect the copyrights and intellectual property rights of all users. All uploaded documents are either original works of the uploader or authorized works of the rightful owners.

  • Not to be reproduced or distributed without explicit permission.
  • Not used for commercial purposes outside of approved use cases.
  • Not used to infringe on the rights of the original creators.
  • If you believe any content infringes your copyright, please contact us immediately.

Support

For help with questions, suggestions, or problems, please contact us