WO2010062506A2 - Decahydro-1h-indenoquinolinone and decahydro-3h-cyclopentaphenanthridinone cyp17 inhibitors - Google Patents
Decahydro-1h-indenoquinolinone and decahydro-3h-cyclopentaphenanthridinone cyp17 inhibitors Download PDFInfo
- Publication number
- WO2010062506A2 WO2010062506A2 PCT/US2009/061550 US2009061550W WO2010062506A2 WO 2010062506 A2 WO2010062506 A2 WO 2010062506A2 US 2009061550 W US2009061550 W US 2009061550W WO 2010062506 A2 WO2010062506 A2 WO 2010062506A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- optionally substituted
- decahydro
- dimethyl
- indeno
- quinolin
- Prior art date
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- 229940124766 Cyp17 inhibitor Drugs 0.000 title description 6
- 150000001875 compounds Chemical class 0.000 claims abstract description 408
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 78
- 239000003098 androgen Substances 0.000 claims abstract description 48
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 47
- 230000001419 dependent effect Effects 0.000 claims abstract description 32
- 208000035475 disorder Diseases 0.000 claims abstract description 24
- -1 carbonyl Chemical group 0.000 claims description 222
- 239000001257 hydrogen Substances 0.000 claims description 188
- 229910052739 hydrogen Inorganic materials 0.000 claims description 188
- 125000001072 heteroaryl group Chemical group 0.000 claims description 128
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 113
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 97
- 229910052736 halogen Inorganic materials 0.000 claims description 96
- 150000002367 halogens Chemical group 0.000 claims description 96
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 81
- 125000000217 alkyl group Chemical group 0.000 claims description 76
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 76
- 238000000034 method Methods 0.000 claims description 76
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 73
- 229910052799 carbon Inorganic materials 0.000 claims description 72
- 150000003839 salts Chemical class 0.000 claims description 69
- 125000001188 haloalkyl group Chemical group 0.000 claims description 67
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 66
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 63
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 63
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- 206010028980 Neoplasm Diseases 0.000 claims description 60
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 60
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- 125000000304 alkynyl group Chemical group 0.000 claims description 56
- 201000011510 cancer Diseases 0.000 claims description 56
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 55
- 229910052760 oxygen Inorganic materials 0.000 claims description 55
- 239000012453 solvate Substances 0.000 claims description 51
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 50
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 claims description 48
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- 125000003107 substituted aryl group Chemical group 0.000 claims description 48
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- 125000005842 heteroatom Chemical group 0.000 claims description 41
- 229910052757 nitrogen Inorganic materials 0.000 claims description 37
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 35
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- 208000000236 Prostatic Neoplasms Diseases 0.000 claims description 32
- 125000003545 alkoxy group Chemical group 0.000 claims description 29
- 125000005415 substituted alkoxy group Chemical group 0.000 claims description 29
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- 125000001424 substituent group Chemical group 0.000 claims description 27
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 26
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- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 24
- 229910052717 sulfur Inorganic materials 0.000 claims description 23
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 22
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 21
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims description 21
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 20
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 18
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- 125000003341 7 membered heterocyclic group Chemical group 0.000 claims description 16
- 208000026310 Breast neoplasm Diseases 0.000 claims description 16
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical group C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 16
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 16
- 125000004426 substituted alkynyl group Chemical group 0.000 claims description 16
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 15
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 15
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 claims description 15
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Chemical group C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims description 14
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- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical group C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims description 10
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims description 10
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 claims description 10
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical group C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 claims description 10
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- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical group C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims description 6
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- FYADHXFMURLYQI-UHFFFAOYSA-N 1,2,4-triazine Chemical compound C1=CN=NC=N1 FYADHXFMURLYQI-UHFFFAOYSA-N 0.000 claims description 5
- FKASFBLJDCHBNZ-UHFFFAOYSA-N 1,3,4-oxadiazole Chemical group C1=NN=CO1 FKASFBLJDCHBNZ-UHFFFAOYSA-N 0.000 claims description 5
- FLBAYUMRQUHISI-UHFFFAOYSA-N 1,8-naphthyridine Chemical compound N1=CC=CC2=CC=CN=C21 FLBAYUMRQUHISI-UHFFFAOYSA-N 0.000 claims description 5
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 claims description 5
- UXGVMFHEKMGWMA-UHFFFAOYSA-N 2-benzofuran Chemical compound C1=CC=CC2=COC=C21 UXGVMFHEKMGWMA-UHFFFAOYSA-N 0.000 claims description 5
- VHMICKWLTGFITH-UHFFFAOYSA-N 2H-isoindole Chemical compound C1=CC=CC2=CNC=C21 VHMICKWLTGFITH-UHFFFAOYSA-N 0.000 claims description 5
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- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 5
- 239000012964 benzotriazole Substances 0.000 claims description 5
- WCZVZNOTHYJIEI-UHFFFAOYSA-N cinnoline Chemical compound N1=NC=CC2=CC=CC=C21 WCZVZNOTHYJIEI-UHFFFAOYSA-N 0.000 claims description 5
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- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims description 5
- HOBCFUWDNJPFHB-UHFFFAOYSA-N indolizine Chemical compound C1=CC=CN2C=CC=C21 HOBCFUWDNJPFHB-UHFFFAOYSA-N 0.000 claims description 5
- ZLTPDFXIESTBQG-UHFFFAOYSA-N isothiazole Chemical group C=1C=NSC=1 ZLTPDFXIESTBQG-UHFFFAOYSA-N 0.000 claims description 5
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical group C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 claims description 5
- LFSXCDWNBUNEEM-UHFFFAOYSA-N phthalazine Chemical compound C1=NN=CC2=CC=CC=C21 LFSXCDWNBUNEEM-UHFFFAOYSA-N 0.000 claims description 5
- CPNGPNLZQNNVQM-UHFFFAOYSA-N pteridine Chemical compound N1=CN=CC2=NC=CN=C21 CPNGPNLZQNNVQM-UHFFFAOYSA-N 0.000 claims description 5
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 claims description 5
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- 229960005026 toremifene Drugs 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- ODLHGICHYURWBS-LKONHMLTSA-N trappsol cyclo Chemical compound CC(O)COC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)COCC(O)C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1COCC(C)O ODLHGICHYURWBS-LKONHMLTSA-N 0.000 description 1
- 229960000575 trastuzumab Drugs 0.000 description 1
- 229960003181 treosulfan Drugs 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- GYUURHMITDQTRU-UHFFFAOYSA-N tributyl(pyridin-2-yl)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)C1=CC=CC=N1 GYUURHMITDQTRU-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
- 229940029284 trichlorofluoromethane Drugs 0.000 description 1
- 125000005423 trihalomethanesulfonamido group Chemical group 0.000 description 1
- 125000005152 trihalomethanesulfonyl group Chemical group 0.000 description 1
- UORVGPXVDQYIDP-UHFFFAOYSA-N trihydridoboron Substances B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 1
- KVJXBPDAXMEYOA-CXANFOAXSA-N trilostane Chemical compound OC1=C(C#N)C[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CC[C@@]32O[C@@H]31 KVJXBPDAXMEYOA-CXANFOAXSA-N 0.000 description 1
- 229960001670 trilostane Drugs 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- 229910000404 tripotassium phosphate Inorganic materials 0.000 description 1
- VXKHXGOKWPXYNA-PGBVPBMZSA-N triptorelin Chemical compound C([C@@H](C(=O)N[C@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1[C@@H](CCC1)C(=O)NCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H]1NC(=O)CC1)C1=CC=C(O)C=C1 VXKHXGOKWPXYNA-PGBVPBMZSA-N 0.000 description 1
- 229960004824 triptorelin Drugs 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 210000005239 tubule Anatomy 0.000 description 1
- 229940046728 tumor necrosis factor alpha inhibitor Drugs 0.000 description 1
- 239000002451 tumor necrosis factor inhibitor Substances 0.000 description 1
- 229940121358 tyrosine kinase inhibitor Drugs 0.000 description 1
- 239000005483 tyrosine kinase inhibitor Substances 0.000 description 1
- 229950009811 ubenimex Drugs 0.000 description 1
- 229960002004 valdecoxib Drugs 0.000 description 1
- LNPDTQAFDNKSHK-UHFFFAOYSA-N valdecoxib Chemical compound CC=1ON=C(C=2C=CC=CC=2)C=1C1=CC=C(S(N)(=O)=O)C=C1 LNPDTQAFDNKSHK-UHFFFAOYSA-N 0.000 description 1
- 229960000653 valrubicin Drugs 0.000 description 1
- ZOCKGBMQLCSHFP-KQRAQHLDSA-N valrubicin Chemical compound O([C@H]1C[C@](CC2=C(O)C=3C(=O)C4=CC=CC(OC)=C4C(=O)C=3C(O)=C21)(O)C(=O)COC(=O)CCCC)[C@H]1C[C@H](NC(=O)C(F)(F)F)[C@H](O)[C@H](C)O1 ZOCKGBMQLCSHFP-KQRAQHLDSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 229960003895 verteporfin Drugs 0.000 description 1
- ZQFGRJWRSLZCSQ-ZSFNYQMMSA-N verteporfin Chemical compound C=1C([C@@]2([C@H](C(=O)OC)C(=CC=C22)C(=O)OC)C)=NC2=CC(C(=C2C=C)C)=NC2=CC(C(=C2CCC(O)=O)C)=NC2=CC2=NC=1C(C)=C2CCC(=O)OC ZQFGRJWRSLZCSQ-ZSFNYQMMSA-N 0.000 description 1
- KDQAABAKXDWYSZ-PNYVAJAMSA-N vinblastine sulfate Chemical compound OS(O)(=O)=O.C([C@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](OC(C)=O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(=O)OC)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1NC1=CC=CC=C21 KDQAABAKXDWYSZ-PNYVAJAMSA-N 0.000 description 1
- 229960004982 vinblastine sulfate Drugs 0.000 description 1
- OGWKCGZFUXNPDA-XQKSVPLYSA-N vincristine Chemical compound C([N@]1C[C@@H](C[C@]2(C(=O)OC)C=3C(=CC4=C([C@]56[C@H]([C@@]([C@H](OC(C)=O)[C@]7(CC)C=CCN([C@H]67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)C[C@@](C1)(O)CC)CC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-XQKSVPLYSA-N 0.000 description 1
- 229960004528 vincristine Drugs 0.000 description 1
- OGWKCGZFUXNPDA-UHFFFAOYSA-N vincristine Natural products C1C(CC)(O)CC(CC2(C(=O)OC)C=3C(=CC4=C(C56C(C(C(OC(C)=O)C7(CC)C=CCN(C67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)CN1CCC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-UHFFFAOYSA-N 0.000 description 1
- UGGWPQSBPIFKDZ-KOTLKJBCSA-N vindesine Chemical compound C([C@@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(N)=O)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1N=C1[C]2C=CC=C1 UGGWPQSBPIFKDZ-KOTLKJBCSA-N 0.000 description 1
- 229960004355 vindesine Drugs 0.000 description 1
- IQDSXWRQCKDBMW-NSFJATOBSA-N vintriptol Chemical compound C([C@@H](C[C@@](O)(CC)C1)C[C@@]2(C3=C(OC)C=C4N(C)[C@H]5[C@@]([C@@H]([C@]6(CC)C=CCN7CC[C@]5([C@H]67)C4=C3)O)(O)C(=O)N[C@@H](CC=3C4=CC=CC=C4NC=3)C(=O)OCC)C(=O)OC)N1CCC1=C2NC2=CC=CC=C12 IQDSXWRQCKDBMW-NSFJATOBSA-N 0.000 description 1
- 229950003415 vintriptol Drugs 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229950005839 vinzolidine Drugs 0.000 description 1
- 150000002266 vitamin A derivatives Chemical class 0.000 description 1
- 235000019166 vitamin D Nutrition 0.000 description 1
- 239000011710 vitamin D Substances 0.000 description 1
- 150000003710 vitamin D derivatives Chemical class 0.000 description 1
- 229940046008 vitamin d Drugs 0.000 description 1
- 229920003176 water-insoluble polymer Polymers 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229940100445 wheat starch Drugs 0.000 description 1
- 229960000523 zalcitabine Drugs 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- FBTUMDXHSRTGRV-ALTNURHMSA-N zorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(\C)=N\NC(=O)C=1C=CC=CC=1)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 FBTUMDXHSRTGRV-ALTNURHMSA-N 0.000 description 1
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Classifications
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- C07J—STEROIDS
- C07J73/00—Steroids in which the cyclopenta[a]hydrophenanthrene skeleton has been modified by substitution of one or two carbon atoms by hetero atoms
- C07J73/001—Steroids in which the cyclopenta[a]hydrophenanthrene skeleton has been modified by substitution of one or two carbon atoms by hetero atoms by one hetero atom
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- C07J73/003—Steroids in which the cyclopenta[a]hydrophenanthrene skeleton has been modified by substitution of one or two carbon atoms by hetero atoms by one hetero atom by oxygen as hetero atom
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- C07J73/005—Steroids in which the cyclopenta[a]hydrophenanthrene skeleton has been modified by substitution of one or two carbon atoms by hetero atoms by one hetero atom by nitrogen as hetero atom
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Definitions
- Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat androgen-dependent diseases or conditions.
- CYP 17 is a bifunctional enzyme which possess both a C ⁇ o-lyase activity and a C17- hydroxylase activity. These two alternative enzymatic activities of CYP 17 result in the formation of critically different intermediates in steroid biosynthesis and each activity appear to be differentially and developmentally regulated.
- compounds, compositions and methods for inhibiting the CYP 17 enzyme are also described herein.
- compounds provided herein have the structure of Formula (I), (II) or (III) and pharmaceutically acceptable salts, solvates, esters, acids and prodrugs thereof.
- isomers and chemically protected forms of compounds having a structure represented by Formula (I), (II), and (III) are also provided.
- X is O or NR 1 ;
- A is a heteroaryl optionally substituted with 1, 2, 3, or 4 R 8 ; ⁇ Ms a single or double bond;
- R 1 is selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl; wherein the alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl groups are optionally substituted with 1 , 2, or 3 substituents independently selected from the group consisting of halogen, alkenyl, alkoxy, alkoxycarbonyl, hydroxyl, hydroxyalkyl, alkynyl, cyano, haloalkoxy, haloalkyl, nitro, NR A R B , (NR A R B )carbonyl;
- R A and R B are independently selected from the group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl, optionally substituted alkoxyalkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl; or R A and R B taken together with the nitrogen atom to which they are attached form an optionally substituted 4 to 7 membered heterocyclic ring having one or two heteroatoms;
- R is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, nitro, optionally substituted alkoxy, optionally substituted alkoxyalkyl, optionally substituted haloalkoxy, optionally substituted haloalkoxyalkyl, hydroxyl, optionally substituted hydroxyalkyl and optionally substituted alkylcarbonyloxy;
- R 3 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkynyl, cyano, optionally substituted haloalkoxy, optionally substituted haloalkyl, hydroxyl, optionally substituted hydroxyalkyl, nitro, R A carbonyl, NR A R B , and (NR A R B )carbonyl; and R 5 and R 6 are each independently hydrogen, halogen, nitro, cyano, hydroxyl, optionally substituted alkyl, optionally substituted cycloalkyl, perfluoroalkyl, optionally substituted heteroalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl;
- R 7 is hydrogen or an optionally substituted alkyl
- R 8 is each independently selected from the group consisting of halogen, cyano, hydroxyl, optionally substituted alkoxy, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, COR A , NR A R B carbonyl, or NR A R B ; or a pharmaceutically acceptable salt or solvate thereof.
- X is O or NR 1 ;
- L is a direct bond or >K qvvX
- A is a heteroaryl optionally substituted with 1, 2, 3, or 4 R 8 ;
- R 1 is selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl; wherein the alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl groups are optionally substituted with 1 , 2, or 3 substituents independently selected from the group consisting of halogen, alkenyl, alkoxy, alkoxycarbonyl, hydroxyl, hydroxyalkyl, alkynyl, cyano, haloalkoxy, haloalkyl, nitro, NR A R B , (NR A R B )carbonyl; R A andR B are independently selected from the group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl, optionally substituted
- R A and R B taken together with the nitrogen atom to which they are attached form an optionally substituted 4 to 7 membered heterocyclic ring having one or two heteroatoms;
- R 2 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, nitro, optionally substituted alkoxy, optionally substituted alkoxyalkyl, optionally substituted haloalkoxy, optionally substituted haloalkoxyalkyl, hydroxyl, optionally substituted hydroxyalkyl and optionally substituted alkylcarbonyloxy;
- R 3 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkynyl, cyano, optionally substituted haloalkoxy, optionally substituted haloalkyl, hydroxyl, optionally substituted hydroxyalkyl, nitro, R A carbonyl, NR A R B , and (NR A R B )carbonyl; and
- R 5 and R 6 are each independently hydrogen, halogen, nitro, cyano, hydroxyl, optionally substituted alkyl, optionally substituted cycloalkyl, perfluoroalkyl, optionally substituted heteroalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl;
- R 7 is hydrogen or an optionally substituted alkyl
- R 8 is each independently selected from the group consisting of halogen, cyano, hydroxy 1, optionally substituted alkoxy, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, COR A , NR A R B carbonyl, or NR A R B ; or a pharmaceutically acceptable salt or solvate thereof.
- R 8 is each independently selected from the group consisting of halogen, cyano, hydroxy 1, optionally substituted alkoxy, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, COR A , NR A R B carbonyl, or NR A R B ; or a pharmaceutically acceptable salt or solvate thereof.
- A is a heteroaryl optionally substituted with 1, 2, 3, or 4 R 8 ;
- R 1 is selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl; wherein the alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl groups are optionally substituted with 1 , 2, or 3 substituents independently selected from the group consisting of halogen, alkenyl, alkoxy, alkoxycarbonyl, hydroxyl, hydroxyalkyl, alkynyl, cyano, haloalkoxy, haloalkyl, nitro, NR A R B , (NR A R B )carbonyl;
- R A andR B are independently selected from the group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl, optionally substituted alkoxyalkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl; or
- R A and R B taken together with the nitrogen atom to which they are attached form an optionally substituted 4 to 7 membered heterocyclic ring having one or two heteroatoms;
- R 2 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, nitro, optionally substituted alkoxy, optionally substituted alkoxyalkyl, optionally substituted haloalkoxy, optionally substituted haloalkoxyalkyl, hydroxyl, optionally substituted hydroxyalkyl and optionally substituted alkylcarbonyloxy;
- R 3 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkynyl, cyano, optionally substituted haloalkoxy, optionally substituted haloalkyl, hydroxyl, optionally substituted hydroxyalkyl, nitro, R A carbonyl, NR A R B , and (NR A R B )carbonyl;
- R 4 is selected from the group consisting of hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted haloalkyl, optionally substituted hydroxyalkyl, R A carbonyl, (NR A R B )alkyl, and (NR A R B )carbonyl; and R 5 and R 6 are each independently hydrogen, halogen, nitro, cyano, hydroxyl, optionally substituted alkyl, optionally substituted cycloalkyl, perfluoroalkyl, optionally substituted heteroalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl;
- R 7 is hydrogen or an optionally substituted alkyl
- R 8 is each independently selected from the group consisting of halogen, cyano, hydroxyl, optionally substituted alkoxy, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, COR A , NR A R B carbonyl, or NR A R B ; or a pharmaceutically acceptable salt or solvate thereof.
- Formula (IA) or a pharmaceutically acceptable salt or solvate thereof.
- Formula (IB) is a compound having the structure of Formula (IB):
- Formula (IB) or a pharmaceutically acceptable salt or solvate thereof.
- Formula (HA) or a pharmaceutically acceptable salt or solvate thereof.
- HB a compound having the structure of Formula (HB):
- Formula (HB) or a pharmaceutically acceptable salt or solvate thereof.
- A is an optionally substituted heteroaryl.
- A is a compound having the structure of Formula (I), (II) or (III) wherein the heteroaryl is selected from the group consisting of pyridine, pyrimidine, pyrazine, pyrazole, oxazole, thiazole, isoxazole, isothiazole, 1,3,4 -oxadiazole, pyridazine, 1,3,5-trazine,
- the heteroaryl is pyridine.
- [0018] is a compound having the structure of Formula (I), (II) or (III) wherein the heteroaryl is benzimidazole.
- in yet another embodiment is a compound having the structure of Formula (I), (II) or (III) wherein the heteroaryl is selected from the group consisting of pyrazine and pyrimidine.
- a further embodiment is a compound having the structure of Formula (I), (II) or (III) wherein R 1 is hydrogen, alkyl, cycloalkyl and wherein the alkyl and cycloalkyl groups are optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, alkenyl, alkoxy, alkoxycarbonyl, hydroxyl, hydroxyalkyl, alkynyl, cyano, haloalkoxy, haloalkyl, nitro, NR A R B , and (NR A R B )carbonyl.
- R 1 is hydrogen, alkyl, cycloalkyl and wherein the alkyl and cycloalkyl groups are optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, alkenyl, alkoxy, alkoxycarbonyl, hydroxyl, hydroxyalkyl, alkynyl, cyano, haloalkoxy,
- R 2 is selected from the group consisting of hydrogen, halogen, hydroxyl, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, or nitro.
- R 3 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, hydroxyl, or nitro.
- R 4 is selected from the group consisting of hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl or R A carbonyl.
- L is a direct bond.
- L is a direct bond.
- L is ; Y is a direct bond; R and R are independently hydrogen, and q is 0-4.
- composition comprising a compound having a structure of Formula (I), (II) or (III) and a pharmaceutically acceptable carrier, excipient or binder thereof.
- a method for treating cancer in a subject comprising administering to a subject in need a therapeutically acceptable amount of a compound having the structure of Formula (I), (II) or (III) or a pharmaceutically acceptable salt or solvate thereof.
- a method for treating cancer in a subject comprising administering to a subject in need a therapeutically acceptable amount of a compound having the structure of Formula (I), (II) or (III) or a pharmaceutically acceptable salt or solvate thereof.
- a method for treating cancer in a subject comprising administering to a subject in need a therapeutically acceptable amount of a compound having the structure of
- the cancer is selected from the group consisting of bladder cancer, brain cancer, breast cancer, cervical cancer, colorectal cancer, endometrial cancer, gastric cancer, glioblastoma, head and neck cancer, Kaposi's sarcoma, kidney cancer, leiomyosarcoma, leukemia, liver cancer, lung
- in another embodiment is a method for treating cancer in a subject comprising administering to a subject in need a therapeutically acceptable amount of a compound having the structure of Formula (I), (II) or (III) or a pharmaceutically acceptable salt or solvate thereof wherein the cancer is prostate cancer.
- a method for treating cancer in a subject comprising administering to a subject in need a therapeutically acceptable amount of a compound having the structure of Formula (I), (II) or (III) or a pharmaceutically acceptable salt or solvate thereof wherein the cancer is breast cancer.
- the method of treating cancer further comprises providing to the subject in need an additional therapy selected from the group consisting of surgery, radiation therapy, chemotherapy, gene therapy, immunotherapy, or a combination thereof.
- the additional therapy is surgery.
- providing chemotherapy to the subject in need comprises administering a therapeutically effective amount of at least one anti- androgenic agent.
- the at least one anti-androgenic agent is selected from the group consisting of flutamide, nicalutamide, bicalutamide, inhibitors of 17 ⁇ -hydroxylase/C 17-20 lyase, luteinizing hormone-releasing hormone agonists, luteinizing hormone-releasing hormone antagonists, and 5 ⁇ -reductase type 1 and/or type 2 and combinations thereof.
- a method of inhibiting CYP 17 enzyme comprising contacting a compound having the structure of Formula (I), (II) or (III) or a pharmaceutically acceptable salt or solvate thereof with a CYP 17 enzyme.
- the contacting step is in vivo.
- a method of treating an androgen-dependent disorder in a subject comprising administering to a subject in need a therapeutically acceptable amount of a compound having the structure of Formula (I), (II) or (III) or a pharmaceutically acceptable salt or solvate thereof.
- the androgen-dependent disorder is selected from the group consisting of prostate cancer, benign prostatic hyperplasia, prostatic intraepithelial neoplasia, hirsutism, acne, androgenic alopecia, and polycystic ovary syndrome.
- the androgen-dependent disorder is prostate cancer.
- a method of treating a proliferative disease comprising administering to a subject in need a therapeutically effective amount of a compound having the structure of Formula (I), (II) or (III) or a pharmaceutically acceptable salt or solvate thereof.
- the method further comprises administering a therapeutically effective amount of at least one agent or therapy selected from the group consisting of a chemotherapeutic agent, a biological agent, surgery, and radiation therapy.
- the administration is performed concurrently or sequentially.
- an article of manufacture comprising packaging material, a compound having the structure of Formula (I), (II) or (III), and a label, wherein the compound is effective for the treatment of an androgen dependent disorder, wherein the compound is packaged within the packaging material, and wherein the label indicates that the compound, or pharmaceutically acceptable salt or solvate thereof is used for the treatment of an androgen dependent disorder.
- a compound having the structure of Formula (I), (II) or (III) or a pharmaceutically acceptable salt or solvate thereof for the manufacture of a medicament for the treatment of prostate cancer.
- CYP17 is a key enzyme in the biosynthesis of androgens, and converts the C 21 steroids (pregnenolone and progesterone) to the Ci9 androgens, dehydroepiandrosterone (DHEA), androstenediol (A-diol), testosterone, and androstenedione in the testes and adrenals.
- DHEA dehydroepiandrosterone
- A-diol testosterone
- DHEA and androstenedione lyase products are key intermediates in the synthesis of not only the androgens testosterone and dihydrotestosterone (DHT), but also the estrogens 17 ⁇ -estradiol and estrone.
- Adrenal and ovarian estrogens are the main sources of estrogens in postmenopausal women.
- the C ⁇ -hydroxylase activity of CYP 17 catalyzes the conversion of the common intermediate progesterone to 17-hydroxyprogesterone, a precursor of Cortisol.
- the C ⁇ -hydroxylase activity promotes the formation of glucocorticoids while the Ci 7;2 o-lyase activity promotes the formation of sex hormones — particularly androgens including testosterone as well as estrogens.
- Prostate cancer is the most common malignancy and age-related cause of cancer death worldwide. Apart from lung cancer, prostate cancer is the most common form of cancer in men and the second leading cause of death in American men. During the period of 1992 to 1999, the average annual incidence of prostate cancer among African American men was 59% higher than among Caucasian men, and the average annual death rate was more than twice that of Caucasian men (American Cancer Society — Cancer Facts and Figures 2003).
- Androgens play an important role in the development, growth, and progression of prostate cancer.
- Two important androgens in this regard are testosterone and dihydrotestosterone (DHT).
- DHT dihydrotestosterone
- the testes synthesize about 90% of testosterone and the rest (10%) is synthesized by the adrenal glands.
- Testosterone is further converted to the more potent androgen DHT by the enzyme steroid 5 ⁇ - reductase that is localized primarily in the prostate.
- prostate cancer is typically androgen-dependent, the reduction of androgen production via surgical or pharmacological castration is the major treatment option for this indication. Androgen deprivation has been used as therapy for advanced and metastatic prostate cancer.
- orchidectomy remains the standard treatment option for most prostate cancer patients.
- Medical and surgical orchidectomy reduces or eliminates androgen production by the testes but does not affect androgen synthesis in the adrenal glands.
- orchidectomy therapy and treatment with anti-androgens to inhibit the action of adrenal androgens significantly prolongs the survival of prostate cancer patients.
- testosterone and DHT occur in recurrent prostate cancer tissues at levels sufficient to activate androgen receptor.
- ketoconazole an active imidazole fungicide has been used to reduce testosterone biosynthesis in the treatment of patients with advanced prostatic cancer.
- side-effects including liver damage, inhibition of several other cytochrome P 450 steroidogenic enzymes, and reduction of Cortisol production.
- Potent and selective inhibitors of CYP 17 as potential prostate cancer treatments have been the subject of previous studies.
- Finasteride a 5 ⁇ -reductatse inhibitor, is an approved treatment for benign prostatic hyperplasia (BPH), although it is only effective with patients exhibiting minimal disease. While finasteride reduces serum DHT levels, it increases testosterone levels and may therefore be insufficient for prostate cancer treatment.
- CYP 17 inhibitors will find utility for the indication of breast cancer, more particularly, estrogen-dependent breast cancer.
- treatment with high doses of ketoconazole resulted in suppression of both testosterone and estradiol levels, implicating CYP 17 as a potential target for hormone therapy.
- CYP 17 is a potential target for hormone therapy.
- X is O or NR 1 ;
- L is a direct bond or ;
- ⁇ - is a single or double bond
- R 1 is selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl; wherein the alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl groups are optionally substituted with 1 , 2, or 3 substituents independently selected from the group consisting of halogen, alkenyl, alkoxy, alkoxycarbonyl, hydroxyl, hydroxyalkyl, alkynyl, cyano, haloalkoxy, haloalkyl, nitro, NR A R B , (NR A R B )carbonyl;
- R A and R B are independently selected from the group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl, optionally substituted alkoxyalkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl; or
- R A and R B taken together with the nitrogen atom to which they are attached form an optionally substituted 4 to 7 membered heterocyclic ring having one or two heteroatoms;
- R is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, nitro, optionally substituted alkoxy, optionally substituted alkoxyalkyl, optionally substituted haloalkoxy, optionally substituted haloalkoxyalkyl, hydroxyl, optionally substituted hydroxyalkyl and optionally substituted alkylcarbonyloxy;
- R is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkynyl, cyano, optionally substituted haloalkoxy, optionally substituted haloalkyl, hydroxyl, optionally substituted hydroxyalkyl, nitro, R A carbonyl, NR A R B , and (NR A R B )carbonyl; and
- R 5 and R 6 are each independently hydrogen, halogen, nitro, cyano, hydroxyl, optionally substituted alkyl, optionally substituted cycloalkyl, perfluoroalkyl, optionally substituted heteroalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl;
- R 7 is hydrogen or an optionally substituted alkyl
- R 8 is each independently selected from the group consisting of halogen, cyano, hydroxyl, optionally substituted alkoxy, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, COR A , NR A R B carbonyl, or NR A R B ; or a pharmaceutically acceptable salt or solvate thereof.
- Formula (IA) or a pharmaceutically acceptable salt or solvate thereof.
- Formula (IB) or a pharmaceutically acceptable salt or solvate thereof.
- A is a compound having the structure of Formula (I), (IA), or (IB) wherein A is an optionally substituted heteroaryl.
- A is an optionally substituted heteroaryl group.
- the heteroaryl group consists of one, two, three, or four heteroatoms selected from N, S, and O.
- the heteroaryl group is selected from pyridine, imidazole, benzimidazole, pyrrole, pyrazole, pyrimidine, pyrazine, and pyridazine.
- the heteroaryl group is pyridine.
- the heteroaryl group is benzimidazole.
- the heteroaryl group is imidazole.
- the heteroaryl group is pyrazine.
- A is an optionally substituted benzoimidazole group, wherein the benzoimidazole
- L is a direct bond
- benzoimidazole group is attached directly to the steroid scaffold, .
- A is an optionally substituted pyridine group, wherein the pyridine group is
- L is a direct bond such that the pyridine
- L is a direct bond.
- Y is a direct bond
- O, C O, C(O)O, S(O) 11 , NR 1 , or NR 7 C(O)
- q is an integer from O to 4
- u is an integer from O to 2
- R 5 and R 6 are each independently hydrogen, hal
- R 5 R 6 L is wherein Y is a direct bond and q is O.
- Y is a direct bond; q is 1-4; and R 5 and R 6 are both hydrogen.
- L is -CH 2 -.
- L is -CH 2 CH 2 -.
- Y is -O- and q is 0-4.
- Y is NH. In another embodiment, Y is -N(Ci-C 6 alkyl)-. [0070] In one embodiment, is a compound having the structure of Formula (I), (IA) or (IB), wherein R 2 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, nitro, optionally substituted alkoxy, optionally substituted alkoxyalkyl, optionally substituted haloalkoxy, optionally substituted haloalkoxyalkyl, hydroxyl, optionally substituted hydroxyalkyl and optionally substituted alkylcarbonyloxy.
- R 2 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, nitro, optionally substituted alkoxy, optionally substituted alkoxyalkyl, optionally substituted haloalkoxy, optionally substituted haloalk
- R 2 is selected from a group consisting of hydrogen, optionally substituted Ci-C 6 alkyl; optionally substituted Ci-C 8 cycloalkyl, cyano, halogen, or nitro.
- R 2 is hydrogen or Ci-C 6 alkyl.
- R is hydrogen.
- R is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkynyl, cyano, optionally substituted haloalkoxy, optionally substituted haloalkyl, hydroxyl, optionally substituted hydroxyalkyl, nitro, R A carbonyl, NR A R B , and (NR A R B )carbonyl.
- R 3 is R A carbonyl, wherein R A is hydrogen.
- R 3 is selected from a group consisting of hydrogen, optionally substituted Ci-C 6 alkyl; optionally substituted Ci-C 8 cycloalkyl, cyano, halogen, or nitro. In a further embodiment, R 3 is hydrogen or Ci-C 6 alkyl. In yet a further embodiment, R 3 is hydrogen.
- R 1 is selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl; wherein the alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl groups are optionally substituted with 1 , 2, or 3 substituents independently selected from the group consisting of halogen, alkenyl, alkoxy, alkoxycarbonyl, hydroxyl, hydroxyalkyl, alkynyl, cyano, haloalkoxy, haloalkyl, nitro, NR A R B , (NR A R B )carbonyl; R A andR B are independently selected from the group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl;
- R A and R B taken together with the nitrogen atom to which they are attached form an optionally substituted 4 to 7 membered heterocyclic ring having one or two heteroatoms.
- R 1 is selected from the group consisting of hydrogen, optionally substituted alkyl or optionally substituted cycloalkyl.
- R 1 is hydrogen or Ci-C 6 alkyl.
- R 1 is hydrogen.
- R 1 is -CH 3 .
- X is O or NR 1 ;
- L is a direct bond or ;
- q is an integer from 0 to 4;
- u is an integer from O to 2;
- A is a heteroaryl optionally substituted with 1, 2, 3, or 4 R 8 ;
- R 1 is selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl; wherein the alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl groups are optionally substituted with 1 , 2, or 3 substituents independently selected from the group consisting of halogen, alkenyl, alkoxy, alkoxycarbonyl, hydroxyl, hydroxyalkyl, alkynyl, cyano, haloalkoxy, haloalkyl, nitro, NR A R B , (NR A R B )carbonyl;
- R A and R B are independently selected from the group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl, optionally substituted alkoxyalkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl; or
- R A and R B taken together with the nitrogen atom to which they are attached form an optionally substituted 4 to 7 membered heterocyclic ring having one or two heteroatoms;
- R 2 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, nitro, optionally substituted alkoxy, optionally substituted alkoxyalkyl, optionally substituted haloalkoxy, optionally substituted haloalkoxyalkyl, hydroxyl, optionally substituted hydroxyalkyl and optionally substituted alkylcarbonyloxy;
- R 3 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkynyl, cyano, optionally substituted haloalkoxy, optionally substituted haloalkyl, hydroxyl, optionally substituted hydroxyalkyl, nitro, R A carbonyl, NR A R B , and (NR A R B )carbonyl; and
- R 5 and R 6 are each independently hydrogen, halogen, nitro, cyano, hydroxyl, optionally substituted alkyl, optionally substituted cycloalkyl, perfluoroalkyl, optionally substituted heteroalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl;
- R 7 is hydrogen or an optionally substituted alkyl
- R 8 is each independently selected from the group consisting of halogen, cyano, hydroxyl, optionally substituted alkoxy, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, COR A , NR A R B carbonyl, or NR A R B ; or a pharmaceutically acceptable salt or solvate thereof.
- Formula (HB); or a pharmaceutically acceptable salt or solvate thereof is a compound having the structure of Formula (II), (HA), or (HB) wherein A is an optionally substituted heteroaryl.
- A is an optionally substituted heteroaryl group.
- the heteroaryl group consists of one, two, three, or four heteroatoms selected from N, S, and O.
- the heteroaryl group is selected from pyridine, imidazole, benzimidazole, pyrrole, pyrazole, pyrimidine, pyrazine, and pyridazine.
- the heteroaryl group is pyridine.
- the heteroaryl group is benzimidazole.
- the heteroaryl group is imidazole.
- the heteroaryl group is pyrazine.
- A is an optionally substituted benzoimidazole group, J*? wherein the benzoimidazole group is attached to L at a nitrogen atom, ⁇ - .
- L is a direct bond such that the benzoimidazole group is attached directly to the steroid scaffold,
- A is an optionally substituted pyridine group, " ⁇ f" wherein the pyridine
- L is a direct bond such that the
- pyridine group is attached directly to the steroid scaffold
- L is a direct bond.
- Y is a direct bond
- O, C O, C(O)O, S(O) 11 , NR 1 , or NR 7 C(O)
- q is an integer from O to 4
- u is an integer from O to 2
- R 5 and R 6 are each independently hydrogen, hal
- Y is NH. In another embodiment, Y is -N(Ci-C 6 alkyl)-
- R is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, nitro, optionally substituted alkoxy, optionally substituted alkoxyalkyl, optionally substituted haloalkoxy, optionally substituted haloalkoxyalkyl, hydroxyl, optionally substituted hydroxyalkyl and optionally substituted alkylcarbonyloxy.
- R is selected from a group consisting of hydrogen, optionally substituted Ci-Ce alkyl; optionally substituted Ci-Cg cycloalkyl, cyano, halogen, or nitro.
- R 2 is hydrogen or Ci-C 6 alkyl. In yet a further embodiment, R 2 is hydrogen.
- R is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkynyl, cyano, optionally substituted haloalkoxy, optionally substituted haloalkyl, hydroxyl, optionally substituted hydroxyalkyl, nitro, R A carbonyl, NR A R B , and (NR A R B )carbonyl.
- R 3 is R A carbonyl, wherein R A is hydrogen.
- R 3 is selected from a group consisting of hydrogen, optionally substituted Ci-C 6 alkyl; optionally substituted Ci-C 8 cycloalkyl, cyano, halogen, or nitro. In a further embodiment, R 3 is hydrogen or Ci-C 6 alkyl. In yet a further embodiment, R 3 is hydrogen.
- R 1 is selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl; wherein the alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl groups are optionally substituted with 1 , 2, or 3 substituents independently selected from the group consisting of halogen, alkenyl, alkoxy, alkoxycarbonyl, hydroxyl, hydroxyalkyl, alkynyl, cyano, haloalkoxy, haloalkyl, nitro, NR A R B , (NR A R B )carbonyl;
- R A and R B are independently selected from the group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl, optionally substituted alkoxyalkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl; or R A and R B taken together with the nitrogen atom to which they are attached form an optionally substituted 4 to 7 membered heterocyclic ring having one or two heteroatoms.
- R 1 is selected from the group consisting of hydrogen, optionally substituted alkyl or optionally substituted cycloalkyl.
- R 1 is hydrogen or Ci-C 6 alkyl.
- R 1 is hydrogen.
- A is a heteroaryl optionally substituted with 1, 2, 3, or 4 R 8 ;
- R 1 is selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl; wherein the alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl groups are optionally substituted with 1 , 2, or 3 substituents independently selected from the group consisting of halogen, alkenyl, alkoxy, alkoxycarbonyl, hydroxyl, hydroxyalkyl, alkynyl, cyano, haloalkoxy, haloalkyl, nitro, NR A R B , (NR A R B )carbonyl;
- R A andR B are independently selected from the group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl, optionally substituted alkoxyalkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl; or
- R A and R B taken together with the nitrogen atom form an optionally substituted 4 to 7 membered heterocyclic ring having one or two heteroatoms;
- R is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, nitro, optionally substituted alkoxy, optionally substituted alkoxyalkyl, optionally substituted haloalkoxy, optionally substituted haloalkoxyalkyl, hydroxyl, optionally substituted hydroxyalkyl and optionally substituted alkylcarbonyloxy;
- R is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkynyl, cyano, optionally substituted haloalkoxy, optionally substituted haloalkyl, hydroxyl, optionally substituted hydroxyalkyl, nitro, R A carbonyl, NR A R B , and (NR A R B )carbonyl;
- R 4 is selected from the group consisting of hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted haloalkyl, optionally substituted hydroxyalkyl, R A carbonyl, (NR A R B )alkyl, and (NR A R B )carbonyl; and R 5 and R 6 are each independently hydrogen, halogen, nitro, cyano, hydroxyl, optionally substituted alkyl, optionally substituted cycloalkyl, perfluoroalkyl, optionally substituted heteroalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl; R 7 is hydrogen or an optionally substituted alkyl;
- R 8 is each independently selected from the group consisting of halogen, cyano, hydroxyl, optionally substituted alkoxy, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, COR A , NR A R B carbonyl, or NR A R B ; or a pharmaceutically acceptable salt or solvate thereof.
- A is a compound having the structure of Formula (III) wherein A is an optionally substituted heteroaryl.
- A is an optionally substituted heteroaryl group.
- the heteroaryl group consists of one, two, three, or four heteroatoms selected from N, S, and O.
- the heteroaryl group is selected
- the heteroaryl group is selected from pyridine, imidazole, benzimidazole, pyrrole, pyrazole, pyrimidine, pyrazine, and pyridazine.
- the heteroaryl group is pyridine.
- the heteroaryl group is benzimidazole.
- the heteroaryl group is imidazole.
- the heteroaryl group is pyrazine.
- A is an optionally substituted heteroaryl attached to L at a heteroatom of the heteroaryl group.
- A is an optionally substituted heteroaryl attached to L at a heteroatom of the heteroaryl group.
- A is an optionally substituted heteroaryl attached to L at a heteroatom of the heteroaryl group.
- A is an optionally substituted heteroaryl attached to L at a heteroatom of the heteroaryl group.
- A is an optionally substituted heteroaryl attached to L at a heteroatom of the heteroaryl group.
- A is an optionally substituted heteroary
- L is a direct bond such that the benzoimidazole group is attached directly to the steroid scaffold, .
- A is an optionally substituted heteroaryl attached to L at a carbon atom of the heteroaryl group. Also by way of example only, A is an
- L is a direct bond such that the pyridine group is attached
- the heterocycloalkyl group is selected from the group consisting of pyrrolidine, imidazolidine, piperidine, piperazine, pyrazolidine, tetrahydrofuran, tetrahydrothiophene, 1,3-oxathiolane, indoline, isoindoline, morpholine, and pyrazoline.
- L is a direct bond.
- Y is a direct bond
- O, C O, C(O)O, S(O) 11 , NR 1 , or NR 7 C(O)
- q is an integer from 0 to 4
- u is an integer from 0 to 2
- R 5 and R 6 are each independently
- L is wherein Y is a direct bond and q is 0.
- Y is a direct bond; q is 1-4; and R 5 and R 6 are both hydrogen.
- L is -CH 2 -.
- L is -CH 2 CH 2 -.
- Y is -O- and q is 0-4.
- Y is NH. In another embodiment, Y is -N(Ci-C 6 alkyl)-. [0087] In one embodiment, is a compound having the structure of Formula (III), wherein R 2 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, nitro, optionally substituted alkoxy, optionally substituted alkoxyalkyl, optionally substituted haloalkoxy, optionally substituted haloalkoxyalkyl, hydroxyl, optionally substituted hydroxyalkyl and optionally substituted alkylcarbonyloxy.
- R 2 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, nitro, optionally substituted alkoxy, optionally substituted alkoxyalkyl, optionally substituted haloalkoxy, optionally substituted haloalkoxyalkyl, hydroxyl,
- R 2 is selected from a group consisting of hydrogen, optionally substituted Ci-C 6 alkyl; optionally substituted Ci-Cg cycloalkyl, cyano, halogen, or nitro.
- R is hydrogen or Ci-C 6 alkyl.
- R 2 is hydrogen.
- R is a compound having the structure of Formula (III), wherein R is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkynyl, cyano, optionally substituted haloalkoxy, optionally substituted haloalkyl, hydroxyl, optionally substituted hydroxyalkyl, nitro, R A carbonyl, NR A R B , and (NR A R B )carbonyl.
- R is R A carbonyl.
- R 3 is R A carbonyl wherein R A is hydrogen or Ci-C 6 alkyl.
- R 3 is CHO.
- R 3 is selected from a group consisting of hydrogen, optionally substituted Q- C 6 alkyl; optionally substituted Ci-C 8 cycloalkyl, cyano, halogen, or nitro. In a further embodiment, R 3 is hydrogen or Ci-C 6 alkyl. In yet a further embodiment, R 3 is hydrogen.
- R 1 is selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl; wherein the alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl groups are optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, alkenyl, alkoxy, alkoxycarbonyl, hydroxyl, hydroxyalkyl, alkynyl, cyano, haloalkoxy, haloalkyl, nitro, NR A R B , (NR A R B )carbonyl;
- R A and R B are independently selected from the group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl, optionally substituted alkoxyalkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl; or R A and R B taken together with the nitrogen atom form an optionally substituted 4 to 7 membered heterocyclic ring having one or two heteroatoms.
- R 1 is selected from the group consisting of hydrogen, optionally substituted alkyl or optionally substituted cycloalkyl.
- R 1 is hydrogen or Ci-C 6 alkyl.
- R 1 is hydrogen. In yet a further embodiment, R 1 is -CH 3 .
- R 4 is selected from the group consisting of hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted haloalkyl, optionally substituted hydroxyalkyl, R A carbonyl, (NR A R B )alkyl, and (NR A R B )carbonyl.
- R 4 is selected from a group consisting of hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl and R A carbonyl. In one embodiment, R 4 is hydrogen.
- R 4 is R A carbonyl wherein R A is selected from a group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl, optionally substituted alkoxyalkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl.
- R A is Ci-Ce alkyl or hydrogen.
- R A is -CH 3 .
- L is a direct bond or ;
- R 1 is selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl; wherein the alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl groups are optionally substituted with 1 , 2, or 3 substituents independently selected from the group consisting of halogen, alkenyl, alkoxy, alkoxycarbonyl, hydroxyl, hydroxyalkyl, alkynyl, cyano, haloalkoxy, haloalkyl, nitro, NR A R B , (NR A R B )carbonyl;
- R A and R B are independently selected from the group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl, optionally substituted alkoxyalkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl; or R A and R B taken together with the nitrogen atom to which they are attached form an optionally substituted 4 to 7 membered heterocyclic ring having one or two heteroatoms;
- R 2 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, nitro, optionally substituted alkoxy, optionally substituted alkoxyalkyl, optionally substituted haloalkoxy, optionally substituted haloalkoxyalkyl, hydroxyl, optionally substituted hydroxyalkyl and optionally substituted alkylcarbonyloxy;
- R 3 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkynyl, cyano, optionally substituted haloalkoxy, optionally substituted haloalkyl, hydroxyl, optionally substituted hydroxyalkyl, nitro, R A carbonyl, NR A R B , and (NR A R B )carbonyl;
- R 4 is selected from the group consisting of hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted haloalkyl, optionally substituted hydroxyalkyl, COR A , (NR A R B )alkyl, and (NR A R B )carbonyl;
- R 5 and R 6 are each independently hydrogen, halogen, nitro, cyano, hydroxyl, optionally substituted alkyl, optionally substituted cycloalkyl, perfluoroalkyl, optionally substituted heteroalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl;
- R 7 is hydrogen or an optionally substituted alkyl
- R 8 is each independently selected from the group consisting of hydrogen, halogen, cyano, hydroxyl, optionally substituted alkoxy, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, COR A , NR A R B carbonyl, or NR A R B ; and m is an integer from 1-4; or a pharmaceutically acceptable salt or solvate thereof.
- L is a direct bond such that the pyridine group is directly attached to the steroid.
- L is attached to the optionally substituted pyridine group at the 1, 2, or 3 -position.
- L is attached to the optionally substituted pyridine group at the 3 -position.
- L is a bond such that the steroid is directly attached to the optionally ring at the 3 -position.
- R 2 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, nitro, optionally substituted alkoxy, optionally substituted alkoxyalkyl, optionally substituted haloalkoxy, optionally substituted haloalkoxyalkyl, hydroxyl, optionally substituted hydroxyalkyl and optionally substituted alkylcarbonyloxy.
- R 2 is selected from a group consisting of hydrogen, optionally substituted Ci-C 6 alkyl; optionally substituted Ci-Cg cycloalkyl, cyano, halogen, or nitro.
- R 2 is hydrogen or Ci-Ce alkyl.
- R is hydrogen.
- R 3 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkynyl, cyano, optionally substituted haloalkoxy, optionally substituted haloalkyl, hydroxyl, optionally substituted hydroxyalkyl, nitro, R A carbonyl, NR A R B , and (NR A R B )carbonyl.
- R 3 is R A carbonyl.
- R 3 is R A carbonyl wherein R A is hydrogen or Ci-C 6 alkyl.
- R 3 is CHO.
- R is selected from a group consisting of hydrogen, optionally substituted Ci-C 6 alkyl; optionally substituted Ci-C 8 cycloalkyl, cyano, halogen, or nitro.
- R is hydrogen or Ci-C 6 alkyl.
- R is hydrogen.
- R 1 is selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl; wherein the alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl groups are optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, alkenyl, alkoxy, alkoxycarbonyl, hydroxyl, hydroxyalkyl, alkynyl, cyano, haloalkoxy, haloalkyl, nitro, NR A R B , (NR A R B )carbonyl;
- R A andR B are independently selected from the group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl, optionally substituted alkoxyalkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl; or
- R A and R B taken together with the nitrogen atom to which they are attached form an optionally substituted 4 to 7 membered heterocyclic ring having one or two heteroatoms.
- R 1 is selected from the group consisting of hydrogen, optionally substituted alkyl or optionally substituted cycloalkyl.
- R 1 is hydrogen or Ci-C 6 alkyl.
- R 1 is hydrogen.
- R 1 is -CH 3 .
- R 4 is selected from the group consisting of hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted haloalkyl, optionally substituted hydroxyalkyl, R A carbonyl, (NR A R B )alkyl, and (NR A R B )carbonyl.
- R 4 is selected from a group consisting of hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl and R A carbonyl.
- R 4 is hydrogen.
- R 4 is R A carbonyl wherein R A is selected from a group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl, optionally substituted alkoxyalkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl.
- R A is Ci-C 6 alkyl or hydrogen.
- R A is -CH 3 .
- each R 8 is independently hydrogen.
- at least one R 8 is halogen.
- at least one R 8 is selected from Cl, Br, or F.
- at least one R 8 is Ci-C 6 alkoxy.
- at least one R 8 is Ci-C 6 alkyl.
- m is an integer from 1-4.
- L is a direct bond or q y> X
- R 1 is selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl; wherein the alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl groups are optionally substituted with 1 , 2, or 3 substituents independently selected from the group consisting of halogen, alkenyl, alkoxy, alkoxycarbonyl, hydroxyl, hydroxyalkyl, alkynyl, cyano, haloalkoxy, haloalkyl, nitro, NR A R B , (NR A R B )carbonyl;
- R A andR B are independently selected from the group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl, optionally substituted alkoxyalkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl; or R A and R B taken together with the nitrogen atom to which they are attached form an optionally substituted 4 to 7 membered heterocyclic ring having one or two heteroatoms;
- R 2 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, nitro, optionally substituted alkoxy, optionally substituted alkoxyalkyl, optionally substituted haloalkoxy, optionally substituted haloalkoxyalkyl, hydroxyl, optionally substituted hydroxyalkyl and optionally substituted alkylcarbonyloxy;
- R 3 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkynyl, cyano, optionally substituted haloalkoxy, optionally substituted haloalkyl, hydroxyl, optionally substituted hydroxyalkyl, nitro, R A carbonyl, NR A R B , and (NR A R B )carbonyl;
- R 4 is selected from the group consisting of hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted haloalkyl, optionally substituted hydroxyalkyl, R A carbonyl, (NR A R B )alkyl, and (NR A R B )carbonyl;
- R 5 and R 6 are each independently hydrogen, halogen, nitro, cyano, hydroxyl, optionally substituted alkyl, optionally substituted cycloalkyl, perfluoroalkyl, optionally substituted heteroalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl;
- R 7 is hydrogen or an optionally substituted alkyl
- R 8 is each independently selected from hydrogen, halogen, cyano, hydroxyl, optionally substituted alkoxy, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, COR A , NR A R B carbonyl, or NR A R B ; and o is an integer from 1-5; or a pharmaceutically acceptable salt or solvate thereof.
- L is a direct bond such that the benzimidazole group is directly attached to the steroid.
- L is attached to the optionally substituted benzimidazole group at a nitrogen atom of the benzimidazole group.
- L is attached to the optionally substituted benzimidazole group at a nitrogen atom.
- L is a bond such that the steroid is attached to the optionally substituted benzimidazole at a nitrogen atom.
- R 2 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, cyano, nitro, optionally substituted alkoxy, optionally substituted alkoxyalkyl, optionally substituted haloalkoxy, optionally substituted haloalkoxyalkyl, hydroxyl, optionally substituted hydroxyalkyl and optionally substituted alkylcarbonyloxy.
- R 2 is selected from a group consisting of hydrogen, optionally substituted Ci-C 6 alkyl; optionally substituted Ci-Cg cycloalkyl, cyano, halogen, or nitro.
- R 2 is hydrogen or Ci-Ce alkyl.
- R is hydrogen.
- R 3 is selected from the group consisting of hydrogen, halogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkynyl, cyano, optionally substituted haloalkoxy, optionally substituted haloalkyl, hydroxyl, optionally substituted hydroxyalkyl, nitro, R A carbonyl, NR A R B , and (NR A R B )carbonyl.
- R 3 is R A carbonyl.
- R 3 is R A carbonyl wherein R A is hydrogen or Ci-C 6 alkyl.
- R 3 is CHO.
- R is selected from a group consisting of hydrogen, optionally substituted Ci-C 6 alkyl; optionally substituted Ci-C 8 cycloalkyl, cyano, halogen, or nitro.
- R is hydrogen or Ci-C 6 alkyl.
- R is hydrogen.
- R 1 is selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl; wherein the alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkoxyalkyl groups are optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, alkenyl, alkoxy, alkoxycarbonyl, hydroxyl, hydroxyalkyl, alkynyl, cyano, haloalkoxy, haloalkyl, nitro, NR A R B , (NR A R B )carbonyl;
- R A andR B are independently selected from the group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl, optionally substituted alkoxyalkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl; or
- R A and R B taken together with the nitrogen atom form an optionally substituted 4 to 7 membered heterocyclic ring having one or two heteroatoms.
- R 1 is selected from the group consisting of hydrogen, optionally substituted alkyl or optionally substituted cycloalkyl.
- R 1 is hydrogen or Ci-C 6 alkyl.
- R 1 is hydrogen.
- R 1 is -CH 3 .
- R 4 is selected from the group consisting of hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted haloalkyl, optionally substituted hydroxyalkyl, R A carbonyl, (NR A R B )alkyl, and (NR A R B )carbonyl.
- R 4 is selected from a group consisting of hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl and R A carbonyl.
- R 4 is hydrogen.
- R 4 is R A carbonyl wherein R A is selected from a group consisting of hydrogen, optionally substituted alkyl, halosubstituted alkyl, optionally substituted alkoxyalkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl.
- R A is Ci-C 6 alkyl or hydrogen.
- R A is -CH 3 .
- each R 8 is independently hydrogen.
- at least one R 8 is halogen.
- at least one R 8 is selected from Cl, Br, or F.
- at least one R 8 is Ci-C 6 alkoxy.
- At least one R 8 is Ci-C 6 alkyl.
- o is an integer from
- compositions comprising of a compound having the structure of Formula (I), (II), (III), or a pharmaceutically acceptable salt, a pharmaceutically acceptable solvate, pharmaceutically acceptable prodrug thereof in combination with a pharmaceutically acceptable carrier, excipient, binder or diluent.
- methods of treating an androgen-dependent disease in a subject in need of such treatment comprising administering to the subject a therapeutically acceptable amount of a compound having a structure of Formula (I), (II), (III) or a therapeutically acceptable salt or solvate thereof.
- [00108] is a method for treating cancer in a subject comprising administering to a subject in need a therapeutically acceptable amount of a compound having the structure of Formula (I), (II) or (III) or a pharmaceutically acceptable salt or solvate thereof.
- CYP 17-associated diseases and disorders examples include, but are not limited to, sex steroid hormone dependent cancers, such as androgen-dependent prostate cancer, which in some embodiments is treated by inhibiting CYP 17-mediated androgen synthesis, and estrogen-dependent breast cancer or ovarian cancer, which in other embodiments is treated by inhibiting CYPl 7-mediated estrogen synthesis.
- sex steroid hormone dependent cancers such as androgen-dependent prostate cancer
- estrogen-dependent breast cancer or ovarian cancer which in other embodiments is treated by inhibiting CYPl 7-mediated estrogen synthesis.
- adenocarcinoma of the prostate is a common disease that causes significant morbidity and mortality in the adult male population (see Han and Nelson, Expert Opin. Pharmacother. 2000, 1, 443-9).
- Hormonal therapy for prostate cancer is considered when a patient fails with initial curative therapy, such as radical prostatectomy or definitive radiation therapy, or if he is found with an advanced disease.
- Hormonal agents have been developed to exploit the fact that prostate cancer growth is dependent on androgen.
- Non-steroidal anti-androgens (NSAAs) block androgen at the cellular level. Castration is another, albeit drastic means of decreasing androgens levels in order to treat or prevent prostate cancer.
- breast cancer such as, by way of example only, breast cancer in postmenopausal women, is treated by administration of a CYP 17 inhibitor described herein since adrenal and ovarian androgens are the main precursors of the estrogens which stimulate the growth of hormone dependent breast cancer.
- breast cancer is treated with CYP 17 inhibitors that inhibit interconversion of estrogens and adrenal and ovarian androgens.
- compositions described herein are suited to treating or preventing hormone-dependent cancers in individuals genetically predisposed to such cancers, particularly those predisposed due to an alteration in the CYP 17 gene.
- a method for treating cancer in a subject comprising administering to a subject in need a therapeutically acceptable amount of a compound having the structure of Formula (I), (II) or (III) or a pharmaceutically acceptable salt or solvate thereof wherein the cancer is selected from the group consisting of bladder cancer, brain cancer, breast cancer, cervical cancer, colorectal cancer, endometrial cancer, gastric cancer, glioblastoma, head and neck cancer, Kaposi's sarcoma, kidney cancer, leiomyosarcoma, leukemia, liver cancer, lung cancer, melanoma, multiple myeloma, Non-Hodgkin lymphoma, ovarian cancer, pancreatic cancer, papillary renal cell carcinoma, prostate cancer, renal cancer, squamous cell cancer, and thoracic cancer.
- the cancer is selected from the group consisting of bladder cancer, brain cancer, breast cancer, cervical cancer, colorectal cancer, endometrial cancer, gastric cancer, glioblastoma,
- [00114] in another embodiment is a method for treating cancer in a subject comprising administering to a subject in need a therapeutically acceptable amount of a compound having the structure of Formula (I), (II) or (III) or a pharmaceutically acceptable salt or solvate thereof wherein the cancer is prostate cancer.
- [00115] in another embodiment is a method for treating cancer in a subject comprising administering to a subject in need a therapeutically acceptable amount of a compound having the structure of Formula (I), (II) or (III) or a pharmaceutically acceptable salt or solvate thereof wherein the cancer is breast cancer.
- the method of treating cancer further comprises providing to the subject in need an additional therapy selected from the group consisting of surgery, radiation therapy, chemotherapy, gene therapy, immunotherapy, or a combination thereof.
- the additional therapy is surgery.
- providing chemotherapy to the subject in need comprises administering a therapeutically effective amount of at least one anti- androgenic agent.
- the at least one anti-androgenic agent is selected from the group consisting of flutamide, nicalutamide, bicalutamide, inhibitors of 17 ⁇ -hydroxylase/C 17-20 lyase, luteinizing hormone-releasing hormone agonists, luteinizing hormone-releasing hormone antagonists, and 5 ⁇ -reductase type 1 and/or type 2 and combinations thereof.
- a method of inhibiting CYP 17 enzyme comprising contacting a compound having the structure of Formula (I), (II) or (III) or a pharmaceutically acceptable salt or solvate thereof with a CYP 17 enzyme.
- the contacting step is in vivo.
- a method of treating an androgen-dependent disorder in a subject comprising administering to a subject in need a therapeutically acceptable amount of a compound having the structure of Formula (I), (II) or (III) or a pharmaceutically acceptable salt or solvate thereof.
- the androgen-dependent disorder is selected from the group consisting of prostate cancer, benign prostatic hyperplasia, prostatic intraepithelial neoplasia, hirsutism, acne, androgenic alopecia, and polycystic ovary syndrome.
- the androgen-dependent disorder is prostate cancer.
- a method of treating a proliferative disease comprising administering to a subject in need a therapeutically effective amount of a compound having the structure of Formula (I), (II) or (III) or a pharmaceutically acceptable salt or solvate thereof.
- the method further comprises administering a therapeutically effective amount of at least one agent or therapy selected from the group consisting of a chemotherapeutic agent, a biological agent, surgery, and radiation therapy.
- the administration is performed concurrently or sequentially.
- a method of treating a disease associated with cancer ameliorated by the inhibition of CYP 17 enzyme comprising administering to a subject in need of treatment a therapeutically-effective amount of a compound having the structure of Formula (I), (II), (III), or a therapeutically acceptable salt or solvate thereof.
- a method for the treatment of or prevention of a disease such as prostate or breast cancer comprising administering to a subject in need of treatment a therapeutically effective amount of a compound having the structure of Formula (I), (II), (III), or a therapeutically acceptable salt or solvate thereof.
- CYP17-associated diseases or disorders amenable to treatment with the compositions and methods of the present disclosure include those associated with mineralocorticoid excess such as hypertension caused by sodium retention at renal tubules.
- a decrease in CYP 17 activity results in an alteration in mineralocorticoid (e.g. aldosterone) biosynthesis.
- the CYP17-associated diseases include those associated with altered levels of aldosterone production (e.g. hypertension, primary adrenal hyperplasia).
- CYP17-associated diseases or disorders contemplated for treatment using a compound having the structure of Formula (I), (II) or (III) are Cushing's disease, prostatic hyperplasia, glucocorticoid deficiency, and endometrial cancer.
- Combination therapies comprise the administration of at least one compound disclosed herein and at least one other pharmaceutically active ingredient.
- second pharmaceutically active agents for combination therapy include anti-cancer agents.
- the active ingredient(s) and pharmaceutically active agents are administered separately or together. In further embodiments, separate administration occurs simultaneously or separately in any order. The amounts of the active ingredients(s) and pharmaceutically active agent(s) and the relative timings of administration will be selected in order to achieve the desired combined therapeutic effect.
- Certain embodiments provide a use of a compound having the structure of Formula (I), (II), (III), or a therapeutically acceptable salt or solvate thereof, to prepare a medicament for treating diseases associated with the CYP 17 enzyme.
- Certain Chemical Terminology [00135] Unless defined otherwise, all technical and scientific terms used herein have the standard meaning pertaining to the claimed subject matter belongs. In the event that there are a plurality of definitions for terms herein, those in this section prevail. Where reference is made to a URL or other such identifier or address, it understood that such identifiers can change and particular information on the internet can come and go, but equivalent information can be found by searching the internet. Reference thereto evidences the availability and public dissemination of such information.
- alkenyl as used herein, means a straight, branched chain, or cyclic (in which case, it would also be known as a "cycloalkenyl") hydrocarbon containing from 2-10 carbons and containing at least one carbon-carbon double bond formed by the removal of two hydrogens.
- an alkenyl group includes a monoradical or a diradical (i.e., an alkenylene group).
- Alkenyl groups include optionally substituted groups.
- alkenyl examples are ethenyl, 2-propenyl, 2-methyl-2-propenyl, 3-butenyl, 4-pentenyl, 5-hexenyl, 2-heptenyl, 2 -methyl- 1 -heptenyl, and 3-cecenyl.
- alkoxy as used herein, means an alkyl group, as defined herein, appended to the parent molecular moiety through an oxygen atom.
- alkoxy are methoxy, ethoxy, propoxy, 2-propoxy, butoxy, tert-butoxy, pentyloxy, and hexyloxy.
- alkyl as used herein, means a straight, branched chain, or cyclic (in this case, it would also be known as “cycloalkyl”) hydrocarbon containing from 1-10 carbon atoms.
- Illustrative examples of alkyl are methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, n-hexyl, 3-methylhexyl, 2,2-dimethylpentyl, 2,3-dimethylhexyl, n-heptyl, n- octyl, n-nonyl, and n-decyl.
- cycloalkyl as used herein, means a monocyclic or polycyclic radical that contains only carbon and hydrogen, and includes those that are saturated, partially unsaturated, or fully unsaturated. Cycloalkyl groups include groups having from 3 to 10 ring atoms. Illustrative examples of cyclic are the following moieties:
- a cycloalkyl group includes a monoradical or a diradical (e.g., a cycloalkylene group).
- cycloalkyl groups refers to groups which are optionally substituted with 1, 2, 3, or 4 substituents selected from alkenyl, alkoxy, alkoxyalkyl, alkoxycarbonyl, alkyl, alkylcarbonyl, alkylcarbonyloxy, alkylthio, alkylthioalkyl, alkynyl, carboxy, cyano, formyl, haloalkoxy, haloalkyl, halogen, hydroxyl, hydroxyalkyl, mercapto, oxo, -NR A R A , and
- cycloalkylalkyl as used herein, means a cycloalkyl group, as defined herein, appended to the parent molecular moiety through an alkyl group, as defined herein.
- Illustrative examples of cycloalkylalkyl are cyclopropylmethyl, 2-cyclobutylethyl, cyclopentylmethyl, cyclohexylmethyl, and 4-cycloheptylbutyl.
- Carbocycle refers to a ring, wherein each of the atoms forming the ring is a carbon atom.
- Carbocyclic rings include those formed by three, four, five, six, seven, eight, nine, or more than nine carbon atoms. Carbocycles are optionally substituted.
- alkoxyalkyl means at least one alkoxy group, as defined herein, appended to the parent molecular moiety through an alkyl group, as defined herein.
- alkoxyalkyl are 2-methoxyethyl, 2-ethoxyethyl, tert-butoxyethyl and methoxymethyl.
- alkoxycarbonyl as used herein, means an alkoxy group, as defined herein, appended to the parent molecular moiety through a carbonyl group, as defined herein.
- alkoxycarbonyl examples include methoxycarbonyl, ethoxycarbonyl, and tert-butoxycarbonyl.
- alkoxycarbonylalkyl means an alkoxycarbonyl group, as defined herein, appended to the parent molecular moiety through an alkyl group, as defined herein.
- alkylcarbonyl as used herein, means an alkyl group, as defined herein, appended to the parent molecular moiety through a carbonyl group, as defined herein.
- alkylcarbonyl examples include acetyl, 1-oxopropyl, 2,2-dimethyl-l-oxopropyl, 1-oxobutyl, and 1-oxopentyl.
- alkylcarbonyloxy means an alkylcarbonyl group, as defined herein, appended to the parent molecular moiety through an oxygen atom.
- alkylcarbonyloxy examples include acetyloxy, ethylcarbonyloxy, and tert-butylcarbonyloxy.
- alkylthio or "thioalkoxy” as used herein, means an alkyl group, as defined herein, appended to the parent molecular moiety through a sulfur atom.
- alkylthio are methylthio, ethylthio, butylthio, tert-butylthio, and hexylthio.
- alkylthioalkyl as used herein, means an alkylthio group, as defined herein, appended to the parent molecular moiety through an alkyl group, as defined herein.
- alkylthioalkyl are methylthiomethyl, 2-(ethylthio)ethyl, butylthiomethyl, and hexylthioethyl.
- alkynyl as used herein, means a straight, branched chain hydrocarbon containing from 2-10 carbons and containing at least one carbon-carbon triple bond. Alkynyl groups are optionally substituted.
- alkynyl are acetylenyl, 1-propynyl, 2-propynyl, 3- butynyl, 2-pentynyl, and 1 -butynyl.
- aromatic refers to a planar ring having a delocalized ⁇ -electron system containing 4n+2 ⁇ electrons, where n is an integer.
- Aromatic rings include those formed by five, six, seven, eight, nine, or more than nine atoms. Aromatics are be optionally substituted.
- the term includes monocyclic or fused-ring polycyclic (i.e., rings which share adjacent pairs of carbon atoms) groups.
- aryl refers to an aromatic ring wherein each of the atoms forming the ring is a carbon atom.
- Aryl rings include those formed by five, six, seven, eight, nine, or more than nine carbon atoms.
- Illustrative examples of aryl groups are phenyl, naphthalenyl, phenanthrenyl, anthracenyl, fluorenyl, and indenyl.
- aryl as used herein means an aryl group that is optionally substituted with one, two, three, four or five substituents independently selected from the group consisting of alkenyl, alkoxy, alkoxyalkyl, alkoxycarbonyl, alkyl, alkylcarbonyl, alkylcarbonyloxy, alkylthio, alkylthioalkyl, alkynyl, carbonyl, cyano, formyl, haloalkoxy, haloalkyl, halogen, hydroxyl, hydroxyalkyl, mercapto, nitro, -NR A R A , and (NR A R B )carbonyl.
- arylalkyl as used herein, means an aryl group, as defined herein, appended to the parent molecular moiety through an alkyl group, as defined herein.
- Illustrative examples of arylalkyl are benzyl, 2-phenylethyl, -phenylpropyl, l-methyl-3-phenylpropyl, and 2-naphth-2-ylethyl.
- carbonyl as used herein, means a -C(O)- group.
- cyano as used herein, means a -CN group.
- nitro as used herein, means a -NO 2 group.
- hydroxy as used herein, means a -OH group.
- bond or “single bond” as used herein, refers to a chemical bond between two atoms, or two moieties when the atoms joined by the bond are considered to be part of larger substructure.
- haloalkyl include alkyl, alkenyl, alkynyl and alkoxy structures in which at least one hydrogen is replaced with a halogen atom. In some embodiments in which two or more hydrogen atoms are replaced with halogen atoms, the halogen atoms are all the same as one another. In other embodiments in which two or more hydrogen atoms are replaced with halogen atoms, the halogen atoms are not all the same as one another.
- fluoroalkyl and fluoroalkoxy include haloalkyl and haloalkoxy groups, respectively, in which the halo is fluorine. In certain embodiments, haloalkyls are optionally substituted.
- amide as used herein, is a chemical moiety with the formula -C(O)NHR or -NHC(O)R, where R is selected from among hydrogen, alkyl, cycloalkyl, aryl, heteroaryl (bonded through a ring carbon) and heteroalicyclic (bonded through a ring carbon).
- An amide moiety includes a linkage between an amino acid or a peptide molecule and a compound described herein, e.g., in a prodrug. Any amine, or carboxyl side chain on the compounds described herein is optionally amidified.
- esters refers to a chemical moiety with formula -COOR, where R is selected from among alkyl, cycloalkyl, aryl, heteroaryl (bonded through a ring carbon) and heteroalicyclic (bonded through a ring carbon). Any hydroxy, or carboxyl side chain on the compounds described herein is optionally esterified.
- heteroalkyl “heteroalkenyl” and “heteroalkynyl” as used herein, include optionally substituted alkyl, alkenyl and alkynyl radicals in which one or more skeletal chain atoms are selected from an atom other than carbon, e.g.
- heteroatom refers to an atom other than carbon or hydrogen. Heteroatoms are typically independently selected from among oxygen, sulfur, nitrogen, silicon and phosphorus, but are not limited to these atoms. In embodiments in which two or more heteroatoms are present, the two or more heteroatoms are the same as one another, or some or all of the two or more heteroatoms are different from the other or others.
- ring refers to any covalently closed structure.
- Rings include, for example, carbocycles (e.g., aryls and cycloalkyls), heterocycles (e.g., heteroaryls and non-aromatic heterocycles), aromatics (e.g. aryls and heteroaryls), and non-aromatics (e.g., cycloalkyls and non- aromatic heterocycles). Rings are optionally substituted. In some instances, rings form part of a ring system.
- carbocycles e.g., aryls and cycloalkyls
- heterocycles e.g., heteroaryls and non-aromatic heterocycles
- aromatics e.g. aryls and heteroaryls
- non-aromatics e.g., cycloalkyls and non- aromatic heterocycles
- ring system refers to two or more rings, wherein two or more of the rings are fused.
- fused refers to structures in which two or more rings share one or more bonds.
- heteroaryl or, alternatively, “heteroaromatic” refers to an aromatic group that includes one or more ring heteroatoms selected from nitrogen, oxygen and sulfur.
- heteroaryl refers to an aromatic group in which at least one of the skeletal atoms of the ring is a nitrogen atom.
- the polycyclic heteroaryl group includes both fused and non-fused groups.
- Illustrative of heteroaryl groups are the following moieties:
- a heteroaryl group includes a monoradical or a diradical (i.e., a heteroarylene group).
- substituted heteroaryl means heteroaryl groups that are substituted with 0, 1, 2, 3, or 4 substituents independently selected from alkenyl, alkoxy, alkoxyalkyl, alkoxycarbonyl, alkyl, alkylcarbonyl, alkylcarbonyloxy, alkylthio, alkylthioalkyl, alynyl, carboxy, cyano, formyl, haloalkoxy, haloalkyl, halogen, hydroxyl, hydroxyalkyl, mercapto, nitro, -NR A R B , and -(NR A R B )carbonyl.
- heteroarylalkyl as used herein, means a heteroaryl, as defined herein, appended to the parent molecular moiety through an alkyl group, as defined herein.
- An illustrative example of heteroarylalkyl is pyridinylmethyl.
- non-aromatic heterocycle refers to a non-aromatic ring wherein one or more atoms forming the ring is a heteroatom.
- a “non-aromatic heterocycle” or “non-aromatic heterocyclic”, “heterocycloalkyl” or “heteroalicyclic” group refers to a cycloalkyl group that includes at least one heteroatom selected from nitrogen, oxygen and sulfur. The radicals include those fused with an aryl or heteroaryl.
- Non-aromatic heterocycle rings include those formed by three, four, five, six, seven, eight, nine, or more than nine atoms. Heterocycloalkyl rings are optionally substituted. In certain embodiments, non-aromatic heterocycles contain one or more carbonyl or thiocarbonyl groups such as, for example, oxo- and thio-containing groups.
- heterocycloalkyls are lactams, lactones, cyclic imides, cyclic thioimides, cyclic carbamates, tetrahydrothiopyran, 4H- pyran, tetrahydropyran, piperidine, 1,3-dioxin, 1,3-dioxane, 1,4-dioxin, 1,4-dioxane, piperazine, 1,3- oxathiane, 1 ,4-oxathiin, 1 ,4-oxathiane, tetrahydro- 1 ,4-thiazine, 2H-l,2-oxazine , maleimide, succinimide, barbituric acid, thiobarbituric acid, dioxopiperazine, hydantoin, dihydrouracil, morpholine, trioxane, hexahydro-l,3,5-triazine, tetrahydr
- heteroalicyclic also includes all ring forms of the carbohydrates, including but not limited to the monosaccharides, the disaccharides and the oligosaccharides.
- heterocycle refers to heteroaromatic and heteroalicyclic used herein, refers to groups containing one to four heteroatoms each selected from O, S and N, wherein each heterocyclic group has from 4 to 10 atoms in its ring system, and with the proviso that the ring of said group does not contain two adjacent O or S atoms.
- a heterocycle e.g., Ci-C 6 heterocycle
- the heteroatom must be present in the ring.
- Designations such as “Ci-C 6 heterocycle” refer only to the number of carbon atoms in the ring and do not refer to the total number of atoms in the ring.
- heterocyclic ring optionally has additional heteroatoms in the ring.
- Designations such as "4-6 membered heterocycle” refer to the total number of atoms that are contained in the ring (i.e., a four, five, or six membered ring, in which at least one atom is a carbon atom, at least one atom is a heteroatom and the remaining two to four atoms are either carbon atoms or heteroatoms).
- those two or more heteroatoms are the same or different from one another.
- Heterocycles are optionally substituted. Binding to a heterocycle is at a heteroatom or at a carbon atom.
- Non-aromatic heterocyclic groups include groups having only 4 atoms in their ring system, but aromatic heterocyclic groups must have at least 5 atoms in their ring system.
- the heterocyclic groups include benzo-fused ring systems.
- An example of a 4-membered heterocyclic group is azetidinyl (derived from azetidine).
- An example of a 5-membered heterocyclic group is thiazolyl.
- An example of a 6-membered heterocyclic group is pyridyl, and an example of a 10-membered heterocyclic group is quinolinyl.
- non-aromatic heterocyclic groups are pyrrolidinyl, tetrahydrofuranyl, dihydrofuranyl, tetrahydrothienyl, tetrahydropyranyl, dihydropyranyl, tetrahydrothiopyranyl, piperidino, morpholino, thiomorpholino, thioxanyl, piperazinyl, azetidinyl, oxetanyl, thietanyl, homopiperidinyl, oxepanyl, thiepanyl, oxazepinyl, diazepinyl, thiazepinyl, 1,2,3,6-tetrahydropyridinyl, 2-pyrrolinyl, 3-pyrrolinyl, indolinyl, 2H- pyranyl, 4H-pyranyl, dioxanyl, 1,3-dioxolanyl, pyrazolinyl, di
- aromatic heterocyclic groups are pyridinyl, imidazolyl, pyrimidinyl, pyrazolyl, triazolyl, pyrazinyl, tetrazolyl, furyl, thienyl, isoxazolyl, thiazolyl, oxazolyl, isothiazolyl, pyrrolyl, quinolinyl, isoquinolinyl, indolyl, benzimidazolyl, benzofuranyl, cinnolinyl, indazolyl, indolizinyl, phthalazinyl, pyridazinyl, triazinyl, isoindolyl, pteridinyl, purinyl, oxadiazolyl, thiadiazolyl, furazanyl, benzofurazanyl, benzothiophenyl, benzothiazolyl, benzoxazolyl, quinazolinyl, quinox
- a group derived from pyrrole includes pyrrol- 1-yl groups (N-attached) or pyrrol-3-yl groups (C-attached).
- a group derived from imidazole includes imidazol- 1 -yl or imidazol-3-yl (both N-attached) or imidazol-2-yl, imidazol-4-yl or imidazol-5-yl (all C-attached) groups.
- a heterocycle group includes a monoradical or a diradical (i.e., a heterocyclene group).
- heterocycles described herein are substituted with 0, 1, 2, 3, or 4 substituents independently selected from alkenyl, alkoxy, alkoxyalkyl, alkoxycarbonyl, alkyl, alkylcarbonyl, alkylcarbonyloxy, alkylthio, alkylthioalkyl, alynyl, carboxy, cyano, formyl, haloalkoxy, haloalkyl, halogen, hydroxyl, hydroxyalkyl, mercapto, nitro, -NR A R B , and -(NR A R B )carbonyl.
- heterocycloalkylalkyl means a heterocycloalkyl, as defined herein, appended to the parent molecular moiety through an alkyl group, as defined herein.
- membered ring embraces any cyclic structure.
- membered is meant to denote the number of skeletal atoms that constitute the ring.
- cyclohexyl, pyridine, pyran and thiopyran are 6-membered rings and cyclopentyl, pyrrole, furan, and thiophene are 5-membered rings.
- non-aromatic 5, 6, 7, 8, 9, 10, 11 or 12- bicyclic heterocycle means a non-aromatic heterocycle, as defined herein, consisting of two carbocyclic rings, fused together at the same carbon atom (forming a spiro structure) or different carbon atoms (in which two rings share one or more bonds), having 5 to 12 atoms in its overall ring system, wherein one or more atoms forming the ring is a heteroatom.
- non-aromatic 5, 6, 7, 8, 9, 10, 11, or 12- bicyclic heterocycle ring are 2- azabicyclo[2.2.1]heptanyl, 7- azabicyclo[2.2.1]heptanyl, 2- azabicyclo[3.2.0]heptanyl, 3- azabicyclo[3.2.0]heptanyl, 4- azaspiro[2.4]heptanyl, 5- azaspiro[2.4]heptanyl, 2-oxa-5- azabicyclo[2.2.1]heptanyl, 4- azaspiro[2.5]octanyl, 5- azaspiro[2.5]octanyl, 5- azaspiro[3.4]octanyl, 6- azaspiro[3.4]octanyl, 4- oxa-7- azaspiro[2.5]octanyl, 2- azabicyclo[2.2.2]octanyl, 1,3- diazabicyclo[2.2.2]octanyl, 5- aza
- hydroxyalkyl are hydroxymethyl, 2-hydroxy-ethyl, 3-hydroxypropyl and 4- hydroxyheptyl.
- NR A R B means two group, R A and R B , as defined herein, which are appended to the parent molecular moiety through a nitrogen atom.
- Illustrative examples of NR A R B are amino, methylamino, acetylamino, and acetylmethylamino.
- (NR A R B )carbonyl as used herein, means a NR A R B , group, as defined herein, which are appended to the parent molecular moiety through a carbonyl group, as defined herein.
- Illustrative examples of (NR A R B )carbonyl are aminocarbonyl, (methylamino)carbonyl, (dimethylamino)carbonyl, and (ethylmethylamino)carbonyl.
- NR C R D as used herein, means two group, Rc and R D , as defined herein which are appended to the parent molecular moiety through a nitrogen atom.
- NR C R D are amino, methylamino, acetylamino, and acetylmethylamino.
- (NR c R D )carbonyl as used herein, means a NR C R D , group, as defined herein, appended to the parent molecular moiety through a carbonyl group, as defined herein.
- Illustrative examples of (NR c R D )carbonyl are aminocarbonyl, (methylamino)carbonyl,
- mercaptyl refers to a (alkyl)S- group.
- moiety refers to a specific segment or functional group of a molecule. Chemical moieties are often recognized chemical entities embedded in or appended to a molecule.
- substituted arylacyl refers to a group or radical of formula -
- R is a substituted aryl group wherein substituted aryl is as defined.
- isocyanato refers to a group of formula -NCO.
- thiocyanato refers to a group of formula -CNS.
- isothiocyanato refers to a group of formula -NCS.
- R the substituent appearing by itself and without a number designation refers to a substituent selected from among from alkyl, cycloalkyl, aryl, heteroaryl (bonded through a ring carbon) and non-aromatic heterocycle (bonded through a ring carbon).
- substituted means that the referenced group is optionally substituted (substituted or unsubstituted) with one or more additional group(s) individually and independently selected from alkyl, cycloalkyl, aryl, heteroaryl, heteroalicyclic, hydroxy, alkoxy, aryloxy, mercapto, alkylthio, arylthio, alkylsulfoxide, arylsulfoxide, alkylsulfone, arylsulfone, cyano, halo, carbonyl, thiocarbonyl, isocyanato, thiocyanato, isothiocyanato, nitro, perhaloalkyl, perfluoroalkyl, silyl, and amino, including mono- and di-substituted amino groups, and the protected derivatives thereof.
- protected-hydroxy refers to a hydroxy group protected with a hydroxy protecting group, as defined above.
- the compounds described herein exist as stereoisomers, wherein asymmetric or chiral centers are present. Stereoisomers are designated (R) or (S) depending on the configuration of substituents around the chiral carbon atom.
- the term (R) and (S) used herein are configurations as defined in IUPAC 1974 Recommendations for Section E, Fundamental Stereochemistry, Pure Appl. Chem., (1976), 45: 13-30, hereby incorporated by reference for this purpose.
- the embodiments described herein specifically includes the various stereoisomers and mixtures thereof.
- Stereoisomers include enantiomers, diastereomers, and mixtures of enantiomers or diastereomers.
- individual stereoisomers of compounds are prepared synthetically from commercially available starting materials which contain asymmetric or chiral centers or by preparation of racemic mixtures followed by resolution. These methods of resolution are exemplified by (1) attachment of a mixture of enantiomers to a chiral axillary, separation of the resulting mixture of diastereomers by recrystallization or chromatography and liberation of the optically pure product from the auxiliary or (2) direct separation of the mixture of optical enantiomers on chiral chromatographic column.
- the methods and formulations described herein include the use of N-oxides, crystalline forms (also known as polymorphs), or pharmaceutically acceptable salts of compounds described herein, as well as active metabolites of these compounds having the same type of activity.
- compounds exist as tautomers. All tautomers are included within the scope of the compounds presented herein.
- the compounds described herein exist in unsolvated as well as solvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like.
- the solvated forms of the compounds presented herein are also considered to be disclosed herein.
- groups and substituents thereof are chosen, in certain embodiments, to provide stable moieties and compounds. Preparation of Compounds
- the compounds described herein are synthesized using any synthetic techniques including standard synthetic techniques and the synthetic processes described herein. In specific embodiments, the following synthetic processes are utilized.
- carbon electrophiles are susceptible to attack by complementary nucleophiles, including carbon nucleophiles, wherein an attacking nueleophile brings an electron pair to the carbon electrophile in order to form a new bond between the nueleophile and the carbon electrophile.
- Suitable carbon nucleophiles include, but are not limited to alkyl, alkenyl, aryl and alkynyl Grignard, organolithium, organozinc, alkyl-, alkenyl , aryl- and alkynyl-tin reagents (organostannanes), alkyl-, alkenyl-, aryl- and alkynyl-borane reagents (organoboranes and organoboronates); these carbon nucleophiles have the advantage of being kinetically stable in water or polar organic solvents.
- Non-carbon nucleophiles suitable for coupling to carbon electrophiles include but are not limited to primary and secondary amines, thiols, thiolates, and thioethers, alcohols, alkoxides, azides, semicarbazides, and the like. These non-carbon nucleophiles, when used in conjunction with carbon electrophiles, typically generate heteroatom linkages (C-X-C), wherein X is a heteroatom, e. g, oxygen or nitrogen.
- protecting group refers to chemical moieties that block some or all reactive moieties and prevent such groups from participating in chemical reactions until the protective group is removed. In specific embodiments, more than one protecting group is utilized. In more specific embodiments, each protective group is removable by a different process. Protective groups that are cleaved under totally disparate reaction conditions fulfill the requirement of differential removal. In various embodiments, protective groups are removed by acid, base, or hydrogenolysis.
- Groups such as trityl, dimethoxytrityl, acetal and t-butyldimethylsilyl are acid labile and are, in some embodiments, used to protect carboxy and hydroxy reactive moieties in the presence of amino groups protected with Cbz groups, which are removable by hydrogenolysis, and Fmoc groups, which are base labile.
- carboxylic acid and hydroxy reactive moieties are blocked with base labile groups such as, without limitation, methyl, ethyl, and acetyl in the presence of amines blocked with acid labile groups such as t-butyl carbamate or with carbamates that are both acid and base stable but hydrolytically removable.
- carboxylic acid and hydroxy reactive moieties are blocked with hydrolytically removable protective groups such as the benzyl group, while, in some embodiments, amine groups capable of hydrogen bonding with acids are blocked with base labile groups such as Fmoc.
- carboxylic acid reactive moieties are protected by conversion to simple ester derivatives as exemplified herein, or they are blocked with oxidatively-removable protective groups such as 2,4-dimethoxybenzyl, while, in some embodiments, co-existing amino groups are blocked with fluoride labile silyl carbamates.
- allyl blocking groups are useful in the presence of acid- and base- protecting groups since the former are stable. In some embodiments, such groups are subsequently removed by metal or pi-acid catalysts.
- an allyl-blocked carboxylic acid is deprotected with a Pd°-catalyzed reaction in the presence of acid labile t-butyl carbamate or base-labile acetate amine protecting groups.
- a protecting group is a resin to which a compound or intermediate is attached. As long as the residue is attached to the resin, that functional group is blocked and cannot react. Once released from the resin, the functional group is available to react.
- blocking/protecting groups are selected from, by way of non- limiting example: allyl Bn Cbz alloc Me
- compounds of Formula (I), (II), and (III) are prepared by various methods, as outlined in Synthetic Schemes I-VI In each scheme, the variables (e.g., R 1 , R 2 , R 3 , and
- R 4 correspond to the same definitions as those recited above.
- compounds are synthesized using methodologies analogous to those described below by the use of appropriate alternative starting materials.
- R 2 and R 3 are other than hydrogen, the appropriate starting material is obtained before subsequent synthetic steps are performed.
- Step 3 Conversion of compound (3) to compound (4) is achieved by using condition as Step 3 which involves the enol triflate formation by the use of triflic anhydride ( trifluoromethanesulfonic anhydride) in the presence of base such as triethylamine and the like.
- triflic anhydride trifluoromethanesulfonic anhydride
- Suzuki coupling reaction on compound (4) with 3-(diethylboryl)pyridine, and (Ph 3 P) 2 PdCl 2 in THF in the presence of a base such as sodium carbonate yields compounds having the structure of Formula (IE) (step 4).
- IE sodium carbonate
- Step 1 of the synthesis requires the hydroxyl protection by the use of triisopropylsilanyl triflate in the presence of an organic base such as 2,6-lutidine and the like to give the 3-triisopropylsilanyloxy derivative compound (8).
- Step 2 involves the ring opening reaction by the use of ozone followed by the treatment with sodium dihydrogen phosphate and sulfamic acid and then sodium chlorite to give compound (9).
- Chlorination of compound (9) with thionyl chloride step 3) gives compound (10).
- Displacement of the acyl chloride of compound (10) with sodium azide provides the compound (11).
- Step 3 and step 4 can be combined by the use of diphenyl phosphoryl azide.
- Step 5 of the synthesis requires the heating of compound (11) in dry toluene followed by the addition of neutral alumina to yield compound (12).
- Treatment of compound (12) with di-tert-butyldicarbonate in pyridine (step 6) gives compound (13).
- Removal of the hydroxyl protection group of compound (13) (step 7) with tetrabutylammonium fluoride yields compound (14).
- Oxidation of the hydroxyl group of compound (14) with N-methylmorphine N- oxide and tetrapropylammonium perruthenate (step 8) gives compound (15).
- step 9 Hydrolysis of the t- butoxycarbonyl group with trifluoroacetic acid (step 9) provides compound (16).
- step 10 Treatment of compound (16) with iodomethane or R-Br in dry DMF and sodium hydride (step 10) yields compound (17).
- step 11 of the synthesis requires the triflate formation of compound (17) by the use of triflic anhydride ( trifluoromethanesulfonic anhydride) in the presence of base such as triethylamine and the like to give the enol triflate compound (18).
- triflic anhydride trifluoromethanesulfonic anhydride
- Step 12 requires the Suzuki coupling reaction on compound (18) with 3-(diethylboryl)pyridine, and (Ph 3 P) 2 PdC ⁇ in THF in the presence of a base such as sodium carbonate yields compounds having the structure of Formula (HE).
- compound (15) can be converted to compound (18) by doing the triflate formation by the use of triflic anhydride ( trifluoromethanesulfonic anhydride) in the presence of base such as triethylamine and the like followed by hydrolysis with trifluoroacetic acid (step 1 IA).
- triflic anhydride trifluoromethanesulfonic anhydride
- Step 1 requires the ring opening reaction on compound (19) by the use of ozone followed by the treatment with sodium dihydrogen phosphate and sulfamic acid and then sodium chlorite to give compound (20).
- Chlorination of compound (20) with thionyl chloride gives compound (21).
- Displacement of the acyl chloride of compound (21) with sodium azide provides the compound (22).
- Step 2 and step 3 can be combined by the use of diphenyl phosphoryl azide.
- Step 4 of the synthesis requires the heating of compound (22) in dry toluene followed by the addition of neutral alumina to yield compound (23).
- Step 5 Treatment of compound (23) with di-tert-butyldicarbonate in pyridine (step 5) gives compound (24).
- Step 6 of the synthesis requires the triflate formation of compound (24) by the use of triflic anhydride (trifluoromethanesulfonic anhydride) in the presence of base such as triethylamine and the like to give the enol triflate compound (25).
- Step 7 requires the Suzuki coupling reaction on compound (25) with 3-(diethylboryl)pyridine, and (Ph 3 P) 2 PdC ⁇ in THF in the presence of a base such as sodium carbonate to yield compound (26).
- Step 1 requires the heating a mixture of compound (2) with methylamine (33% w/w in ethanol) in a sealed vessel for several hours to yield compound (27).
- step 1 can involve the treatment of compound (2) with methylamine in ethanol in the presence of sodium ethoxide at refluxing condition.
- Reaction of compound (27) with phosphoryl trichloride in DMF will yield a mixture of compound (28A) and compound (28B) (step 2).
- step 29) Displacement of the chlorine atom of compound (28) with benzoimidazole in the presence of potassium carbonate in DMF at 80° C yields compound (29) (step 3).
- Step 4 of the synthesis involves the reaction of compound (29) with 10% palladium on carbon in refluxing benzonitrile to yield compounds having the structure of Formula (IG).
- Step 1 requires heating compound (24) with phosphoryl trichloride in DMF to yield compound (30). Displacement of the chlorine atom of compound (30) with benzoimidazole in the presence of potassium carbonate in DMF at 80° C yields compound (31) (step 2).
- Step 3 of the synthesis involves the reaction of compound (31) with 10% palladium on carbon in refluxing benzonitrile to yield compound (32). Treatment of compound (32) with 10% methanolic potassium hydroxide at room temperature yields compounds having the structure of Formula (IIIF).
- selective binding compound refers to a compound that selectively binds to any portion of one or more target proteins.
- selective binds refers to the ability of a selective binding compound to bind to a target protein, such as, for example, CYP 17 enzyme, with greater affinity than it binds to a non-target protein.
- specific binding refers to binding to a target with an affinity that is at least about 10, about 50, about 100, about 250, about 500, about 1000 or more times greater than the affinity for a non-target.
- target protein refers to a molecule or a portion of a protein capable of being bound by a selective binding compound.
- a target protein is the enzyme CYP 17.
- the terms “treating” or “treatment” encompass either or both responsive and prophylaxis measures, e.g., designed to inhibit, slow or delay the onset of a symptom of a disease or disorder, achieve a full or partial reduction of a symptom or disease state, and/or to alleviate, ameliorate, lessen, or cure a disease or disorder and/or its symptoms.
- amelioration of the symptoms of a particular disorder by administration of a particular compound or pharmaceutical composition refers to any lessening of severity, delay in onset, slowing of progression, or shortening of duration, whether permanent or temporary, lasting or transient that can be attributed to or associated with administration of the compound or composition.
- inhibitor refers to a compound that decreases in the magnitude of a certain activity of a target protein or molecule compared to the magnitude of the activity in the absence of the inhibitor.
- selective inhibitor refers to a compound that selectively inhibits a target activity.
- the IC 50 refers to an amount, concentration or dosage of a particular test compound that achieves a 50% inhibition of a maximal response, such as modulation of CYP 17, in an assay that measures such response.
- EC 5O refers to a dosage, concentration or amount of a particular test compound that elicits a dose-dependent response at 50% of maximal expression of a particular response that is induced, provoked or potentiated by the particular test compound.
- toxicity and therapeutic efficacy of the compounds is determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., for determining the LD 50 (the dose lethal to 50% of the population) and the ED 50 (the dose therapeutically effective in 50% of the population).
- the dose ratio between toxic and therapeutic effects is the therapeutic index and is expressed as the ratio LD 50 ZED 50 .
- Compounds which exhibit large therapeutic indices are contemplated herein. While in some embodiments, compounds that exhibit toxic side effects are used, care should be taken to design a delivery system that targets such reagents to the site of affected tissue in order to minimize potential damage to normal cells and, thereby, reduce side effects.
- carrier refers to relatively nontoxic chemical compounds or agents that facilitate the incorporation of a compound into cells or tissues.
- co-administration or the like, as used herein, are meant to encompass administration of the selected therapeutic agents to a single patient, and are intended to include treatment regimens in which the agents are administered by the same or different route of administration or at the same or different time.
- CYP 17 substrate includes any of the various steroid hormones acted upon by a
- CYP 17 or a CYP17-like PzJ 50 enzyme examples include pregnenolone, progesterone and their 17 ⁇ - hydroxylated forms.
- Pregnenolone is converted to DHEA via a CYP 17 C ⁇ o-lyase reaction, but is also subject to C17 ⁇ -hydroxylation via the Ci 7;20 -lyase activity.
- Progesterone is converted to ⁇ 4- androstenedione via a CYP17 Ci 7;2 o-lyase reaction, but is also subject to C17 ⁇ -hydroxylation via the C17-hydroxylase activity to form 17-hydroxy -progesterone, a precursor to hydrocortisone (i.e. Cortisol).
- CYP 17 metabolite-associated disease or disorder refers to a disease or disorder which in some embodiments is treated by alteration of the level of one or more CYP 17 metabolites. Examples include a hormone dependent cancer, such as an androgen-dependent prostate cancer, which in other embodiments is treated by inhibiting CYP 17-mediated androgen synthesis, and an estrogen-dependent breast cancer or ovarian cancer, which in further embodiments is treated by inhibiting CYPl 7-mediated estrogen synthesis.
- the term "diluent” refers to chemical compounds that are used to dilute the compound of interest prior to delivery. Diluents include chemicals used to stabilize compounds because they provide a more stable environment.
- an “effective amount” or “therapeutically effective amount,” as used herein, refer to a sufficient amount of an agent or a compound being administered which will relieve to some extent one or more of the symptoms of the disease or condition being treated. The result includes reduction and/or alleviation of the signs, symptoms, or causes of a disease, or any other desired alteration of a biological system.
- an "effective amount” for therapeutic uses is the amount of the composition comprising a compound as disclosed herein required to provide a clinically significant decrease in disease symptoms.
- An appropriate "effective" amount in any individual case is determined using any suitable technique, such as a dose escalation study.
- the terms “enhance” or “enhancing,” as used herein, means to increase or prolong either in potency or duration a desired effect.
- the term “enhancing” refers to the ability to increase or prolong, either in potency or duration, the effect of other therapeutic agents on a system.
- An “enhancing-effective amount,” as used herein, refers to an amount adequate to enhance the effect of another therapeutic agent in a desired system.
- the term “enzymatically cleavable linker,” as used herein refers to unstable or degradable linkages which are degraded by one or more enzymes.
- kit and “article of manufacture” are used as synonyms.
- a "metabolite” of a compound disclosed herein is a derivative of that compound that is formed when the compound is metabolized.
- active metabolite refers to a biologically active derivative of a compound that is formed when the compound is metabolized.
- metabolism refers to the sum of the processes (including, but not limited to, hydrolysis reactions and reactions catalyzed by enzymes) by which a particular substance is changed by an organism. Thus, in certain instances, enzymes produce specific structural alterations to a compound.
- metabolites of the compounds disclosed herein are identified either by administration of compounds to a host and analysis of tissue samples from the host, or by incubation of compounds with hepatic cells in vitro and analysis of the resulting compounds.
- modulate means to interact with a target either directly or indirectly so as to alter the activity of the target, including, by way of example only, to enhance the activity of the target, to inhibit the activity of the target, to limit the activity of the target, or to extend the activity of the target.
- pharmaceutically acceptable refers a material, such as a carrier or diluent, which does not abrogate the biological activity or properties of the compound, and is relatively nontoxic.
- nontoxic and non-abrogative materials includes materials that when administered to an individual do not cause substantial, undesirable biological effects and/or do not interact in a deleterious manner with any of the components of the composition in which it is contained.
- pharmaceutically acceptable salt or “therapeutically acceptable salt” refers to a formulation of a compound that does not cause significant irritation to an organism to which it is administered and does not abrogate the biological activity and properties of the compound.
- pharmaceutically acceptable salts are obtained by reacting a compound described herein, with acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid and the like.
- acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid and the like.
- pharmaceutically acceptable salts are obtained by reacting a compound having acidic group described herein with a base to form a salt such as an ammonium salt, an alkali metal salt, such as a sodium or a potassium salt, an alkaline earth metal salt, such as a calcium or a magnesium salt, a salt of organic bases such as dicyclohexylamine, N-methyl-D-glucamine, tris(hydroxymethyl)methylamine, and salts with amino acids such as arginine, lysine, and the like, or by other methods known in the art.
- a salt such as an ammonium salt, an alkali metal salt, such as a sodium or a potassium salt, an alkaline earth metal salt, such as a calcium or a magnesium salt, a salt of organic bases such as dicyclohexylamine, N-methyl-D-glucamine, tris(hydroxymethyl)methylamine, and salts with amino acids such as arginine, lysine, and the like, or by other methods known
- the term "pharmaceutical combination” as used herein, means a product that results from the mixing or combining of more than one active ingredient and includes both fixed and non- fixed combinations of the active ingredients.
- the term "fixed combination” means that the active ingredients, e.g. a compound described herein and a co-agent, are both administered to a patient simultaneously in the form of a single entity or dosage.
- non- fixed combination means that the active ingredients, e.g. a compound described herein and a co-agent, are administered to a patient as separate entities either simultaneously, concurrently or sequentially with no specific intervening time limits, wherein such administration provides effective levels of the two compounds in the body of the patient.
- cocktail therapy e.g.
- composition refers to a mixture of a compound described herein with other chemical components, such as carriers, stabilizers, diluents, dispersing agents, suspending agents, thickening agents, and/or excipients.
- the pharmaceutical composition facilitates administration of the compound to an organism. Multiple techniques of administering a compound exist in the art including, but not limited to: intravenous, oral, aerosol, parenteral, ophthalmic, pulmonary and topical administration.
- a prodrug refers to an agent that is converted into the parent drug in vivo. Prodrugs are often useful because, in some situations, they are easier to administer than the parent drug. In certain instances, a prodrug is bioavailable by oral administration whereas the parent is not. In some instances, a prodrug has improved solubility in pharmaceutical compositions over the parent drug.
- An example, without limitation, of a prodrug is a compound described herein, which is administered as an ester (the "prodrug") to facilitate transmittal across a cell membrane where water solubility is detrimental to mobility but which then is metabolically hydrolyzed to the carboxylic acid, the active entity, once inside the cell where water-solubility is beneficial.
- a further example of a prodrug might be a short peptide (polyaminoacid) bonded to an acid or amino group where the peptide is metabolized to reveal the active moiety.
- a prodrug upon in vivo administration, is chemically converted to the biologically, pharmaceutically or therapeutically more active form of the compound.
- a prodrug is enzymatically metabolized by one or more steps or processes to the biologically, pharmaceutically or therapeutically active form of the compound.
- a pharmaceutically active compound is modified such that the active compound will be regenerated upon in vivo administration.
- the prodrug is designed to alter the metabolic stability or the transport characteristics of a drug, to mask side effects or toxicity, to improve the flavor of a drug or to alter other characteristics or properties of a drug.
- the term "subject" or “patient” encompasses mammals and non-mammals. Examples of mammals include, but are not limited to, any member of the Mammalian class: humans, non-human primates such as chimpanzees, and other apes and monkey species; farm animals such as cattle, horses, sheep, goats, swine; domestic animals such as rabbits, dogs, and cats; laboratory animals including rodents, such as rats, mice and guinea pigs, and the like. Examples of non-mammals include, but are not limited to, birds, fish and the like. In one embodiment of the methods and compositions provided herein, the mammal is a human.
- treat include alleviating, abating or ameliorating a disease or condition symptoms, preventing additional symptoms, ameliorating or preventing the underlying metabolic causes of symptoms, inhibiting the disease or condition, e.g., arresting the development of the disease or condition, relieving the disease or condition, causing regression of the disease or condition, relieving a condition caused by the disease or condition, or stopping the symptoms of the disease or condition either prophylactically and/or therapeutically.
- Pharmaceutical Composition/Formulation include alleviating, abating or ameliorating a disease or condition symptoms, preventing additional symptoms, ameliorating or preventing the underlying metabolic causes of symptoms, inhibiting the disease or condition, e.g., arresting the development of the disease or condition, relieving the disease or condition, causing regression of the disease or condition, relieving a condition caused by the disease or condition, or stopping the symptoms of the disease or condition either prophylactically and/or therapeutically.
- compositions are formulated in any manner, including using one or more physiologically acceptable carriers comprising excipients and/or auxiliaries which facilitate processing of the active compounds into pharmaceutical preparations. In some embodiments, proper formulation is dependent upon the route of administration chosen. In various embodiments, any techniques, carriers, and excipients are used as suitable. [00275] Provided herein are pharmaceutical compositions that include a compound described herein and a pharmaceutically acceptable diluent(s), excipient(s), and/or carrier(s). In addition, in some embodiments, the compounds described herein are administered as pharmaceutical compositions in which compounds described herein are mixed with other active ingredients, as in combination therapy.
- a pharmaceutical composition refers to a mixture of a compound described herein with other chemical components, such as carriers, stabilizers, diluents, dispersing agents, suspending agents, thickening agents, and/or excipients.
- a pharmaceutical composition facilitates administration of the compound to an organism.
- practicing the methods of treatment or use provided herein includes administering or using a pharmaceutical composition comprising a therapeutically effective amount of a compound provided herein.
- the methods of treatment provided for herein include administering such a pharmaceutical composition to a mammal having a disease or condition to be treated. In one embodiment, the mammal is a human.
- the therapeutically effective amount varies widely depending on the severity of the disease, the age and relative health of the subject, the potency of the compound used and other factors.
- the compounds described herein are used singly or in combination with one or more therapeutic agents as components of mixtures.
- the pharmaceutical compositions provided herein are formulated for intravenous injections.
- the intravenous injection formulations provided herein are formulated as aqueous solutions, and, in some embodiments, in physiologically compatible buffers such as Hank's solution, Ringer's solution, or physiological saline buffer.
- the pharmaceutical compositions provided herein are formulated for transmucosal administration.
- transmucosal formulations include penetrants appropriate to the barrier to be permeated.
- the pharmaceutical compositions provided herein are formulated for other parenteral injections, appropriate formulations include aqueous or nonaqueous solutions, and in one embodiment, with physiologically compatible buffers or excipients.
- the pharmaceutical compositions provided herein are formulated for oral administration.
- the oral formulations provided herein comprise compounds described herein that are formulated with pharmaceutically acceptable carriers or excipients.
- Such carriers enable the compounds described herein to be formulated as tablets, powders, pills, dragees, capsules, liquids, gels, syrups, elixirs, slurries, suspensions and the like, for oral ingestion by a patient to be treated.
- pharmaceutical preparations for oral use are obtained by mixing one or more solid excipient with one or more of the compounds described herein, optionally grinding the resulting mixture, and processing the mixture of granules, after adding suitable auxiliaries, if desired, to obtain tablets or dragee cores.
- Suitable excipients include, in particular, fillers such as sugars, including lactose, sucrose, mannitol, or sorbitol; cellulose preparations such as: for example, maize starch, wheat starch, rice starch, potato starch, gelatin, gum tragacanth, methylcellulose, microcrystalline cellulose, hydroxypropylmethylcellulose, sodium carboxymethylcellulose; or others such as: polyvinylpyrrolidone (PVP or povidone) or calcium phosphate.
- disintegrating agents are optionally added, such as the cross-linked croscarmellose sodium, polyvinylpyrrolidone, agar, or alginic acid or a salt thereof such as sodium alginate.
- a pharmaceutical composition formulated as dragee cores with suitable coatings is provided herein.
- concentrated sugar solutions are used in forming the suitable coating, and optionally contain gum arabic, talc, polyvinylpyrrolidone, carbopol gel, polyethylene glycol, and/or titanium dioxide, lacquer solutions, and suitable organic solvents or solvent mixtures.
- dyestuffs and/or pigments are added to tablets, dragees and/or the coatings thereof for, e.g., identification or to characterize different combinations of active compound doses.
- pharmaceutical preparations which are used include orally include push- fit capsules made of gelatin, as well as soft, sealed capsules made of gelatin and a plasticizer, such as glycerol or sorbitol.
- the push- fit capsules contain the active ingredients in admixture with filler such as lactose, binders such as starches, and/or lubricants such as talc or magnesium stearate and, optionally, stabilizers.
- the active compounds are dissolved or suspended in suitable liquids, such as fatty oils, liquid paraffin, or liquid polyethylene glycols.
- stabilizers are optionally added.
- the formulations for oral administration are in dosages suitable for such administration.
- the pharmaceutical compositions provided herein are formulated for buccal or sublingual administration.
- buccal or sublingual compositions take the form of tablets, lozenges, or gels formulated in a conventional manner.
- parenteral injections involve bolus injection or continuous infusion.
- formulations for injection are presented in unit dosage form, e.g., in ampoules or in multi-dose containers, with an added preservative.
- the pharmaceutical composition described herein is in a form suitable for parenteral injection as a sterile suspensions, solutions or emulsions in oily or aqueous vehicles, and optionally contains formulatory agents such as suspending, stabilizing and/or dispersing agents.
- compositions for parenteral administration include aqueous solutions of the active compounds in water-soluble form.
- suspensions of the active compounds are prepared as appropriate oily injection suspensions.
- Suitable lipophilic solvents or vehicles include fatty oils such as sesame oil, or synthetic fatty acid esters, such as ethyl oleate or triglycerides, or liposomes.
- aqueous injection suspensions contain substances which increase the viscosity of the suspension, such as sodium carboxymethyl cellulose, sorbitol, or dextran.
- the suspensions also contain suitable stabilizers or agents which increase the solubility of the compounds to allow for the preparation of highly concentrated solutions.
- the active ingredient is in powder form for constitution with a suitable vehicle, e.g., sterile pyrogen- free water, before use.
- the compounds described herein are administered topically.
- the compounds described herein are formulated into a variety of topically administrable compositions, such as solutions, suspensions, lotions, gels, pastes, medicated sticks, balms, creams or ointments.
- Such pharmaceutical compounds optionally contain solubilizers, stabilizers, tonicity enhancing agents, buffers and/or preservatives.
- the pharmaceutical compositions provided herein are formulated for transdermal administration of compounds described herein.
- administration of such compositions employs transdermal delivery devices and transdermal delivery patches.
- the compositions are lipophilic emulsions or buffered, aqueous solutions, dissolved and/or dispersed in a polymer or an adhesive.
- patches include those constructed for continuous, pulsatile, or on demand delivery of pharmaceutical agents.
- transdermal delivery of the compounds described herein is accomplished by use of iontophoretic patches and the like.
- transdermal patches provide controlled delivery of the compounds provided herein, such as, for example, compounds of Formula (I), (II), or (III).
- the rate of absorption is slowed by using rate-controlling membranes or by trapping the compound within a polymer matrix or gel.
- absorption enhancers are optionally used to increase absorption.
- Absorption enhancer and carrier include absorbable pharmaceutically acceptable solvents that assist in passage of the compound through the skin.
- transdermal devices are in the form of a bandage comprising a backing member, a reservoir containing the compound optionally with carriers, optionally a rate controlling barrier to deliver the compound to the skin of the host at a controlled and predetermined rate over a prolonged period of time, and means to secure the device to the skin.
- the pharmaceutical compositions provided herein are formulated for administration by inhalation.
- the compounds described herein are in a form as an aerosol, a mist or a powder.
- pharmaceutical compositions described herein are conveniently delivered in the form of an aerosol spray presentation from pressurized packs or a nebuliser, with the use of a suitable propellant, e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
- the dosage unit is determined by providing a valve to deliver a metered amount.
- capsules and cartridges of, such as, by way of example only, gelatin for use in an inhaler or insufflator is formulated containing a powder mix of the compound described herein and a suitable powder base such as lactose or starch.
- the compounds described herein are formulated in rectal compositions such as enemas, rectal gels, rectal foams, rectal aerosols, suppositories, jelly suppositories, or retention enemas.
- rectal compositions optionally contain conventional suppository bases such as cocoa butter or other glycerides, as well as synthetic polymers such as polyvinylpyrrolidone, PEG, and the like.
- a low-melting wax such as, but not limited to, a mixture of fatty acid glycerides, optionally in combination with cocoa butter is first melted.
- the pharmaceutical compositions are formulated in a conventional manner using one or more physiologically acceptable carriers comprising excipients and auxiliaries which facilitate processing of the active compounds into pharmaceutically acceptable preparations.
- proper formulation is dependent upon the route of administration chosen.
- any of the techniques, carriers, and excipients is used as suitable.
- pharmaceutical compositions comprising a compound described herein are manufactured in a conventional manner, such as, by way of example only, by means of conventional mixing, dissolving, granulating, dragee-making, levigating, emulsifying, encapsulating, entrapping or compression processes.
- the pharmaceutical compositions include at least one pharmaceutically acceptable carrier, diluent or excipient and a compound described herein described herein as an active ingredient in free-acid or free-base form, or in a pharmaceutically acceptable salt form.
- the methods and pharmaceutical compositions described herein include the use of N-oxides, crystalline forms (also known as polymorphs), as well as active metabolites of these compounds having the same type of activity.
- compounds described herein exist as tautomers. All tautomers are included within the scope of the compounds presented herein. Additionally, included herein are the solvated and unsolvated forms of the compounds described herein.
- Solvated compounds include those that are solvated with pharmaceutically acceptable solvents such as water, ethanol, and the like.
- the solvated forms of the compounds presented herein are also considered to be disclosed herein.
- the pharmaceutical compositions described herein include other medicinal or pharmaceutical agents, carriers, adjuvants, such as preserving, stabilizing, wetting or emulsifying agents, solution promoters, salts for regulating the osmotic pressure, and/or buffers.
- the pharmaceutical compositions described herein also contain other therapeutically valuable substances.
- Methods for the preparation of compositions containing the compounds described herein include formulating the compounds with one or more inert, pharmaceutically acceptable excipients or carriers to form a solid, semi-solid or liquid.
- Solid compositions include, but are not limited to, powders, tablets, dispersible granules, capsules, cachets, and suppositories.
- Liquid compositions include solutions in which a compound is dissolved, emulsions comprising a compound, or a solution containing liposomes, micelles, or nanoparticles comprising a compound as disclosed herein.
- Semi-solid compositions include, but are not limited to, gels, suspensions and creams. In various embodiments, the compositions are in liquid solutions or suspensions, solid forms suitable for solution or suspension in a liquid prior to use, or as emulsions.
- compositions optionally contain minor amounts of nontoxic, auxiliary substances, such as wetting or emulsifying agents, pH buffering agents, and so forth.
- a composition comprising a compound described herein takes the form of a liquid where the agents are present in solution, in suspension or both.
- a first portion of the agent is present in solution and a second portion of the agent is present in particulate form, in suspension in a liquid matrix.
- a liquid composition includes a gel formulation.
- the liquid composition is aqueous.
- Useful aqueous suspension optionally contain one or more polymers as suspending agents.
- Useful polymers include water-soluble polymers such as cellulosic polymers, e.g., hydroxypropyl methylcellulose, and water-insoluble polymers such as cross-linked carboxyl-containing polymers.
- Useful compositions optionally comprise an mucoadhesive polymer, selected for example from carboxymethylcellulose, carbomer (acrylic acid polymer), polymethylmethacrylate), polyacrylamide, polycarbophil, acrylic acid/butyl acrylate copolymer, sodium alginate and dextran.
- Useful compositions optionally include solubilizing agents to aid in the solubility of a compound described herein.
- Solubilizing agent generally includes agents that result in formation of a micellar solution or a true solution of the agent.
- Solubilizing agents include certain acceptable nonionic surfactants, for example polysorbate 80, and ophthalmically acceptable glycols, polyglycols, e.g., polyethylene glycol 400, and glycol ethers.
- Useful compositions optionally include one or more pH adjusting agents or buffering agents, including acids such as acetic, boric, citric, lactic, phosphoric and hydrochloric acids; bases such as sodium hydroxide, sodium phosphate, sodium borate, sodium citrate, sodium acetate, sodium lactate and tris-hydroxymethylaminomethane; and buffers such as citrate/dextrose, sodium bicarbonate and ammonium chloride.
- acids such as acetic, boric, citric, lactic, phosphoric and hydrochloric acids
- bases such as sodium hydroxide, sodium phosphate, sodium borate, sodium citrate, sodium acetate, sodium lactate and tris-hydroxymethylaminomethane
- buffers such as citrate/dextrose, sodium bicarbonate and ammonium chloride.
- Such acids, bases and buffers are included in an amount required to maintain pH of the composition in an acceptable range.
- Useful compositions optionally include one or more salts in an amount required to bring osmolality of the composition into an acceptable range.
- Such salts include those having sodium, potassium or ammonium cations and chloride, citrate, ascorbate, borate, phosphate, bicarbonate, sulfate, thiosulfate or bisulfite anions; suitable salts include sodium chloride, potassium chloride, sodium thiosulfate, sodium bisulfite and ammonium sulfate.
- compositions optionally include one or more preservatives to inhibit microbial activity.
- Suitable preservatives include mercury-containing substances such as merfen and thiomersal; stabilized chlorine dioxide; and quaternary ammonium compounds such as benzalkonium chloride, cetyltrimethylammonium bromide and cetylpyridinium chloride.
- Some useful compositions optionally include one or more surfactants to enhance physical stability or for other purposes.
- Suitable nonionic surfactants include polyoxyethylene fatty acid glycerides and vegetable oils, e.g., polyoxyethylene (60) hydrogenated castor oil; and polyoxyethylene alkylethers and alkylphenyl ethers, e.g., octoxynol 10, octoxynol 40.
- Certain useful compositions optionally one or more antioxidants to enhance chemical stability where required. Suitable antioxidants include, by way of example only, ascorbic acid and sodium metabisulfite.
- aqueous suspension compositions are packaged in single-dose non- reclosable containers.
- multiple-dose reclosable containers are used, in which case it is typical to include a preservative in the composition.
- any delivery system for hydrophobic pharmaceutical compounds is employed.
- Liposomes and emulsions are examples of delivery vehicles or carriers for hydrophobic drugs.
- certain organic solvents such as N-methylpyrrolidone are employed.
- the compounds are delivered using a sustained-release system, such as semipermeable matrices of solid hydrophobic polymers containing the therapeutic agent.
- sustained-release materials are utilized in the embodiments herein.
- sustained-release capsules release the compounds for a few weeks up to over 100 days.
- additional strategies for protein stabilization are employed.
- the formulations or compositions described herein benefit from and/or optionally comprise antioxidants, metal chelating agents, thiol containing compounds and other general stabilizing agents.
- stabilizing agents include, but are not limited to: (a) about 0.5% to about 2% w/v glycerol, (b) about 0.1% to about 1% w/v methionine, (c) about 0.1% to about 2% w/v monothioglycerol, (d) about 1 mM to about 10 mM EDTA, (e) about 0.01% to about 2% w/v ascorbic acid, (f) 0.003% to about 0.02% w/v polysorbate 80, (g) 0.001% to about 0.05% w/v.
- polysorbate 20 (h) arginine, (i) heparin, (j) dextran sulfate, (k) cyclodextrins, (1) pentosan polysulfate and other heparinoids, (m) divalent cations such as magnesium and zinc; or (n) combinations thereof.
- the compounds described herein are used in the preparation or manufacture of medicaments for the treatment of diseases or conditions that are mediated by the CYP 17 enzyme. Inhibition of the enzymes ameliorates the disease or condition associated with CYP 17.
- a method for treating any of the diseases or conditions described herein in a subject in need of such treatment involves administration of pharmaceutical compositions containing at least one compound described herein, or a pharmaceutically acceptable salt, pharmaceutically acceptable N-oxide, pharmaceutically active metabolite, pharmaceutically acceptable prodrug, or pharmaceutically acceptable solvate thereof, in therapeutically effective amounts to said subject.
- compositions containing the compound(s) described herein are administered for prophylactic and/or therapeutic treatments.
- the compositions are administered to a patient already suffering from a disease or condition, in an amount sufficient to cure or at least partially arrest the symptoms of the disease or condition.
- amounts effective for this use will depend on the severity and course of the disease or condition, previous therapy, the patient's health status, weight, and response to the drugs, and the judgment of the treating physician.
- compositions containing the compounds described herein are administered to a patient susceptible to or otherwise at risk of a particular disease, disorder or condition.
- the amount administered is defined to be a "prophylactically effective amount or dose.”
- the precise amounts of compound administered depend on the patient's state of health, weight, and the like.
- effective amounts for this use will depend on the severity and course of the disease, disorder or condition, previous therapy, the patient's health status and response to the drugs, and the judgment of the treating physician.
- a patient's condition does not improve or does not significantly improve following administration of a compound or composition described herein and, upon the doctor's discretion the administration of the compounds is optionally administered chronically, that is, for an extended period of time, including throughout the duration of the patient's life in order to ameliorate or otherwise control or limit the symptoms of the patient's disease or condition.
- a maintenance dose is administered if necessary.
- the dosage e.g., of the maintenance dose, or the frequency of administration, or both, are reduced, as a function of the symptoms, to a level at which the improved disease, disorder or condition is retained.
- patients are optionally given intermittent treatment on a long-term basis upon any recurrence of symptoms.
- the amount of a given agent that corresponds to an effective amount varies depending upon factors such as the particular compound, disease or condition and its severity, the identity (e.g., weight) of the subject or host in need of treatment.
- the effective amount is, nevertheless, determined according to the particular circumstances surrounding the case, including, e.g., the specific agent that is administered, the route of administration, the condition being treated, and the subject or host being treated.
- doses employed for adult human treatment is in the range of about 0.02 to about 5000 mg per day.
- dose employment for adult human treatment is about 1 to about 1500 mg per day.
- the desired dose is conveniently presented in a single dose or as divided doses administered simultaneously (or over a short period of time) or at appropriate intervals, for example as two, three, four or more sub-doses per day.
- the pharmaceutical compositions described herein are given at a dose from about 0.01 mg to about 1 g per administration for an adult given once or several times a day orally or in a dosage form of an injection such as intravenous injection and the like.
- an anti-cancer agent is generally required to sustain its effect for a long time, so that can be effective not only for temporary suppression but also for prohibition on a long term basis.
- the compounds described herein are administered on a long term basis.
- the pharmaceutical compositions described herein are in a unit dosage form suitable for single administration of precise dosages.
- the formulation is divided into unit doses containing appropriate quantities of one or more compound.
- the unit dosage is in the form of a package containing discrete quantities of the formulation. Non- limiting examples are packaged tablets or capsules, and powders in vials or ampoules.
- aqueous suspension compositions are packaged in single-dose non-reclosable containers.
- multiple-dose reclosable containers are used, in which case it is typical to include a preservative in the composition.
- formulations for parenteral injection are, in some embodiments, presented in unit dosage form, which include, but are not limited to ampoules, or in multi-dose containers, with an added preservative.
- the daily dosages appropriate for the compounds described herein are from about 0.01 to about 5 mg/kg per body weight.
- an indicated daily dosage in the larger subject including, but not limited to, humans, is in the range from about 0.5 mg to about 1000 mg, conveniently administered in divided doses, including, but not limited to, up to four times a day or in extended release form.
- suitable unit dosage forms for oral administration comprise from about 1 to about 500 mg active ingredient.
- the dosages are altered depending on a number of variables, not limited to the activity of the compound used, the disease or condition to be treated, the mode of administration, the requirements of the individual subject, the severity of the disease or condition being treated, and the judgment of the practitioner.
- toxicity and therapeutic efficacy of such therapeutic regimens are determined by standard pharmaceutical procedures in cell cultures or experimental animals, including, but not limited to, the determination of the LD 50 (the dose lethal to 50% of the population) and the ED 50 (the dose therapeutically effective in 50% of the population).
- the dose ratio between the toxic and therapeutic effects is the therapeutic index and it can be expressed as the ratio between LD 50 and ED 50 .
- compounds exhibiting high therapeutic indices are preferred.
- the data obtained from cell culture assays and animal studies is used in formulating a range of dosage for use in human.
- the dosage of such compounds lies within a range of circulating concentrations that include the ED 50 with minimal toxicity. In certain embodiments, the dosage varies within this range depending upon the dosage form employed and the route of administration utilized.
- Suitable compounds used in combination with a compound having the structure of Formula (I), (II) or (III) include anti-cancer agents, such as for example, hormone ablation agents, anti- androgen agents, differentiating agents, anti-neoplastic agents, kinase inhibitors, anti-metabolite agents, alkylating agents, antibiotic agents, immunological agents, interferon-type agents, intercalating agents, growth factor inhibitors, cell cycle inhibitors, enzymes, topoisomerase inhibitors, biological response modifiers, mitotic inhibitors, matrix metalloprotease inhibitors, genetic therapeutics, and anti-androgens.
- anti-cancer agents such as for example, hormone ablation agents, anti- androgen agents, differentiating agents, anti-neoplastic agents, kinase inhibitors, anti-metabolite agents, alkylating agents, antibiotic agents, immunological agents, interferon-type agents, intercalating agents, growth factor inhibitors, cell cycle inhibitors, enzymes, topoisomerase inhibitors, biological response
- the amount of the additional anti-cancer agent administered to a mammal having cancer is an amount that is sufficient to treat the cancer whether administered alone or in combination with a compound having the structure of Formula (I), (II) or (III).
- a compound having the structure of Formula (I), (II) or (III) is an amount that is sufficient to treat the cancer whether administered alone or in combination with a compound having the structure of Formula (I), (II) or (III).
- Suitable hormonal ablation agents include, but are not limited to, androgen ablation agents and estrogen ablation agents.
- a compound having the structure of Formula (I), (II) or (III) is administered with a hormonal ablation agent, such as deslorelin, leuprolide, goserelin or triptorelin.
- the amount of the hormonal ablation agent administered to a mammal having cancer is an amount that is sufficient to treat the cancer whether administered alone or in combination with a compound having the structure of Formula (I), (II) or (III).
- Suitable anti-androgen agents include but are not limited to bicalutamide, flutamide and nilutamide.
- the amount of the anti-androgen agent administered to a mammal having cancer is an amount that is sufficient to treat the cancer whether administered alone or in combination with a compound having the structure of Formula (I), (II) or (III).
- a compound having the structure of Formula (I), (II) or (III) is administered with a differentiating agent.
- suitable differentiating agents include, but are not limited to, polyamine inhibitors; vitamin D and its analogs, such as, calcitriol, doxercalciferol and seocalcitol; metabolites of vitamin A, such as, ATRA, retinoic acid, retinoids; short-chain fatty acids; phenylbutyrate; and nonsteroidal anti-inflammatory agents.
- the amount of the differentiating agent administered to a mammal having cancer is an amount that is sufficient to treat the cancer whether administered alone or in combination with a compound having the structure of Formula (I), (II) or (III).
- a compound having the structure of Formula (I), (II) or (III) is administered with an anti-neoplastic agent, including, but not limited to, tubulin interacting agents, topoisomerase inhibitors and agents, acitretin, alstonine, amonafide, amphethinile, amsacrine, ankinomycin, anti-neoplaston, aphidicolin glycinate, asparaginase, baccharin, batracylin, benfluron, benzotript, bromofosfamide, caracemide, carmethizole hydrochloride, chlorsulfaquinoxalone, clanfenur, claviridenone, crisnatol, curaderm, cytarabine, cytocytin, dacarbazine, datelliptinium, dihaematoporphyrin ether, dihydrolenperone, dinaline
- the amount of the anti-neoplastic agent administered to a mammal having cancer is an amount that is sufficient to treat the cancer whether administered alone or in combination with a compound having the structure of Formula (I), (II) or (III).
- the compounds described herein such as for example, a compound having the structure of Formula (I), (II) or (III) is used with a kinase inhibitor including p38 inhibitors and CDK inhibitors, TNF inhibitors, metallomatrix proteases inhibitors (MMP), COX-2 inhibitors including celecoxib, rofecoxib, parecoxib, valdecoxib, and etoricoxib, SOD mimics or 0Cv ⁇ 3 inhibitors.
- the amount of the kinase inhibitor administered to a mammal having cancer is an amount that is sufficient to treat the cancer whether administered alone or in combination with a compound having the structure of Formula (I), (II) or (III).
- a compound having the structure of Formula (I), (II) or (III) is administered with an anti-metabolite agent.
- suitable anti-metabolite agents are selected from, but not limited to, 5-FU-fibrinogen, acanthifolic acid, aminothiadiazole, brequinar sodium, carmofur, cyclopentyl cytosine, cytarabine phosphate stearate, cytarabine conjugates, dezaguanine, dideoxycytidine, dideoxyguanosine, didox, doxifluridine, camrabine, floxuridine, fludarabine phosphate, 5-fluorouracil, N-(2'-furanidyl)-5-fluorouracil, isopropyl pyrrolizine, methobenzaprim, methotrexate, norspermidine, pentostatin, piritrexim, plicamycin, thiogu
- a compound having the structure of Formula (I), (II) or (III) is administered with an alkylating agent.
- suitable alkylating agents are selected from, but not limited to, aldo-phosphamide analogues, altretamine, anaxirone, bestrabucil, budotitane, carboplatin, carmustine, chlorambucil, cisplatin, cyclophosphamide, cyplatate, diphenylspiromustine, diplatinum cytostatic, elmustine, estramustine phosphate sodium, fotemustine, hepsul-fam, ifosfamide, iproplatin, lomustine, mafosfamide, mitolactol, oxaliplatin, prednimustine, ranimustine, semustine, spiromustine, tauromustine, temozolomide, teroxirone, tetrap
- the amount of the alkylating agent administered to a mammal having cancer is an amount that is sufficient to treat the cancer whether administered alone or in combination with a compound having the structure of Formula (I), (II) or (III).
- a compound having the structure of Formula (I), (II) or (III) is administered with an antibiotic agent.
- suitable antibiotic agents are selected from, but not limited to, aclarubicin, actinomycin D, actinoplanone, adriamycin, aeroplysinin derivative, amrubicin, anthracycline, azino-mycin-A, bisucaberin, bleomycin sulfate, bryostatin- 1 , calichemycin, chromoximycin, dactinomycin, daunorubicin, ditrisarubicin B, dexamethasone, doxorubicin, doxorubicin-fibrinogen, elsamicin-A, epirubicin, erbstatin, esorubicin, esperamicin-Al, esperamicin-Alb, fostriecin, glidobactin, gregatin-A, grincamycin, herbimycin, corticosteroids such as hydrocortisone, idarubicin, illudin
- the amount of the antibiotic agent administered to a mammal having cancer is an amount that is sufficient to treat the cancer whether administered alone or in combination with a compound having the structure of Formula (I), (II) or (III).
- a compound having the structure of Formula (I), (II) or (III) is used with other anti-cancer agents, including but not limited to, acemannan, aclarubicin, aldesleukin, alemtuzumab, alitretinoin, altretamine, amifostine, amsacrine, anagrelide, anastrozole, ancestim, bexarotene, broxuridine, capecitabine, celmoleukin, cetrorelix, cladribine, clotrimazole, daclizumab, dexrazoxane, dilazep, docosanol, doxifluridine, bromocriptine, carmustine, cytarabine,
- the amount of the anti-cancer agent administered to a mammal having cancer is an amount that is sufficient to treat the cancer whether administered alone or in combination with a compound having the structure of Formula (I), (II) or (III).
- a compound having the structure of Formula (I), (II) or (III) is administered or combined with steroids, such as corticosteroids or glucocorticoids.
- steroids such as corticosteroids or glucocorticoids.
- a compound having the structure of Formula (I), (II) or (III) and the steroid are administered in the same or in different compositions.
- suitable steroids include hydrocortisone, prednisone, or dexamethasone.
- the amount of the steroid administered to a mammal having cancer is an amount that is sufficient to treat the cancer whether administered alone or in combination with a compound having the structure of Formula (I), (II) or (III).
- one of the side effects experienced by a patient upon receiving one of the compounds herein is inflammation, then, in some embodiments, it is appropriate to administer an anti-inflammatory agent in combination with the initial therapeutic agent.
- the therapeutic effectiveness of one of the compounds described herein is enhanced by administration of an adjuvant (i.e., by itself the adjuvant may have minimal therapeutic benefit, but in combination with another therapeutic agent, the overall therapeutic benefit to the patient is enhanced).
- the benefit experienced by a patient is increased by administering one of the compounds described herein with another therapeutic agent (which also includes a therapeutic regimen that also has same therapeutic benefit (e.g. anti-cancer agent against the same enzyme as the compound described herein but of different mode of action) so as to reduce the chance of enzyme resistant development.
- another therapeutic agent which also includes a therapeutic regimen that also has same therapeutic benefit (e.g. anti-cancer agent against the same enzyme as the compound described herein but of different mode of action) so as to reduce the chance of enzyme resistant development.
- the overall benefit experienced by the patient as a result of a combination treatment is additive or synergistic.
- therapeutically-effective dosages vary when the drugs are used in treatment combinations.
- therapeutically-effective dosages of drugs and other agents for use in combination treatment regimens is determined in any suitable manner, e.g., through the use of metronomic dosing, i.e., providing more frequent, lower doses in order to minimize toxic side effects.
- combination treatment regimen described herein encompass treatment regimens in which administration of a compound having the structure of Formula (I), (II) or (III) described herein is initiated prior to, during, or after treatment with a second agent described above, and continues until any time during treatment with the second agent or after termination of treatment with the second agent.
- compositions and methods for combination therapy are provided herein.
- the pharmaceutical compositions disclosed herein are used to in a method of treating a CYP 17 mediated condition or a disease or condition that is ameliorated by inhibition of these enzymes.
- combination therapies described herein are used as part of a specific treatment regimen intended to provide a beneficial effect from the co-action of a compound having the structure of Formula (I), (II) or (III) described herein and a concurrent treatment. It is understood that the dosage regimen to treat, prevent, or ameliorate the condition(s) for which relief is sought, is optionally modified in accordance with a variety of factors.
- dosages of the co-administered compounds vary depending on the type of co-drug employed, on the specific drug employed, on the disease or condition being treated and so forth.
- the compound provided herein when co-administered with one or more biologically active agents, is administered either simultaneously with the biologically active agent(s), or sequentially. In certain aspects wherein the agents are administered sequentially, the attending physician will decide on the appropriate sequence of administering protein in combination with the biologically active agent(s).
- the multiple therapeutic agents are administered in any order or even simultaneously. In certain instances, administration is simultaneous and the multiple therapeutic agents are, optionally, provided in a single, unified form, or in multiple forms (by way of example only, either as a single pill or as two separate pills). In some embodiments, one of the therapeutic agents is given in multiple doses, or both are given as multiple doses.
- administration is not simultaneous and the timing between the multiple doses varies, by way of non- limiting example, from more than zero weeks to less than four weeks.
- combination methods, compositions and formulations are not to be limited to the use of only two agents; the use of multiple therapeutic combinations is also contemplated herein.
- the compounds described herein and combination therapies are administered before, during or after the occurrence of a disease or condition.
- the timing of administering the composition containing a compound varies.
- the compounds are used as a prophylactic and are administered continuously to subjects with a propensity to develop conditions or diseases in order to prevent the occurrence of the disease or condition.
- the compounds and compositions are administered to a subject during or as soon as possible after the onset of the symptoms.
- the initial administration is achieved via any route practical, such as, for example, an intravenous injection, a bolus injection, infusion over 5 minutes to about 5 hours, a pill, a capsule, transdermal patch, buccal delivery, and the like, or combination thereof. Kits/Articles of Manufacture
- kits and articles of manufacture are also described herein.
- such kits comprise a carrier, package, or container that is compartmentalized to receive one or more containers such as vials, tubes, and the like, each of the container(s) comprising one of the separate elements to be used in a method described herein.
- Suitable containers include, for example, bottles, vials, syringes, and test tubes.
- the containers are formed from a variety of materials such as glass or plastic.
- the articles of manufacture provided herein contain packaging materials.
- Packaging materials for use in packaging pharmaceutical products include, but are not limited to, blister packs, bottles, tubes, inhalers, pumps, bags, vials, containers, syringes, bottles, and any packaging material suitable for a selected formulation and intended mode of administration and treatment.
- the container(s) described herein comprise one or more compounds described herein, optionally in a composition or in combination with another agent as disclosed herein.
- the container(s) optionally have a sterile access port (for example the container can be an intravenous solution bag or a vial having a stopper pierceable by a hypodermic injection needle).
- kits optionally comprise a compound with an identifying description or label or instructions relating to its use in the methods described herein.
- a kit will comprises one or more additional containers, each with one or more of various materials (such as reagents, optionally in concentrated form, and/or devices) desirable from a commercial and user standpoint for use of a compound described herein.
- materials include, but are not limited to, buffers, diluents, filters, needles, syringes; carrier, package, container, vial and/or tube labels listing contents and/or instructions for use, and package inserts with instructions for use.
- a set of instructions is optionally included.
- a label is on or associated with the container.
- a label is on a container when letters, numbers or other characters forming the label are attached, molded or etched into the container itself; a label can be associated with a container when it is present within a receptacle or carrier that also holds the container, e.g., as a package insert.
- a label indicates that the contents are to be used for a specific therapeutic application.
- the label indicates directions for use of the contents, such as in the methods described herein.
- the pharmaceutical compositions are presented in a pack or dispenser device which contains one or more unit dosage forms containing a compound provided herein.
- the pack contains a metal or plastic foil, such as a blister pack.
- the pack or dispenser device is optionally accompanied by instructions for administration.
- the pack or dispenser is accompanied with a notice associated with the container in form prescribed by a governmental agency regulating the manufacture, use, or sale of pharmaceuticals, which notice is reflective of approval by the agency of the form of the drug for human or veterinary administration.
- such notice is, for example, the labeling approved by the U.S. Food and Drug Administration for prescription drugs, or the approved product insert.
- compositions containing a compound provided herein are formulated in a compatible pharmaceutical carrier and are placed in an appropriate container labeled for treatment of an indicated condition.
- Example 1 The following Examples are intended as an illustration of the various embodiments as defined in appended claims. In some embodiments, the compounds are prepared by a variety of synthetic routes. Example 1
- Example Ia Parenteral Composition
- a parenteral pharmaceutical composition suitable for administration by injection 100 mg of a water-soluble salt of a compound having the structure of Formula (I), (II) or (III) is mixed with 2-hydroxypropyl- ⁇ -cyclodextrin and then dissolved in 10 mL of 0.9% sterile saline. The mixture is incorporated into a dosage unit form suitable for administration by injection.
- a water-soluble salt of a compound having the structure of Formula (I), (II) or (III) (20 mg) is mixed with lactose (180 mg), microcrystalline cellulose (140 mg) and magnesium stearate (20 mg). The mixture is granulated and the remaining 10 mg of magnesium stearate is added. The content is then sealed in a gelation capsule.
- a water-soluble salt of a compound having the structure of Formula (I), (II) or (III) (20 mg) is mixed with lactose (70 mg), corn starch (300 mg), microcrystalline cellulose (60 mg) and magnesium stearate (10 mg). The mixture is granulated and the remaining 10 mg of microcrystalline cellulose and 2.5 mg of magnesium stearate is added. The mixture is compression formed to give a suitable tablet.
- a compound having the structure of Formula (I), (II), or (III) (15 mg per 5 ml of syrup) is added to a solution of 0.1% benzoic acid, 5% alcohol, citric acid, edetate disodium, ethyl maltol, flavors, glycerin, ammoniated glycyrrhizin, propylene glycol, purified water, sodium saccharin, sucrose, FD&C blue #1 and FD&C red #40.
- Example Ic Sublingual (Hard Lozenge) Composition
- a pharmaceutical composition for buccal delivery such as a hard lozenge
- a pharmaceutical composition for buccal delivery such as a hard lozenge
- 420 mg of powdered sugar mixed with 1.6 mL of light corn syrup, 2.4 mL distilled water, and 0.42 mL mint extract.
- the mixture is gently blended and poured into a mold to form a lozenge suitable for buccal administration.
- Example 1 d Inhalation Composition
- a pharmaceutical composition for inhalation delivery 20 mg of a compound having the structure of Formula (I), (II), or (III) is mixed with 50 mg of anhydrous citric acid and 100 mL of 0.9% sodium chloride solution. The mixture is incorporated into an inhalation delivery unit, such as a nebulizer, which is suitable for inhalation administration.
- an inhalation delivery unit such as a nebulizer
- a pharmaceutical composition for rectal delivery 100 mg of a compound having the structure of Formula (I), (II), or (III) is mixed with 2.5 g of methylcelluose (1500 mPa), 100 mg of methylparapen, 5 g of glycerin and 100 mL of purified water. The resulting gel mixture is then incorporated into rectal delivery units, such as syringes, which are suitable for rectal administration.
- Example 1 f Topical Gel Composition To prepare a pharmaceutical topical gel composition, 100 mg of a compound having the structure of
- Formula (I), (II), or (III) is mixed with 1.75 g of hydroxypropyl cellulose, 10 mL of propylene glycol, 10 mL of isopropyl myristate and 100 mL of purified alcohol USP.
- the resulting gel mixture is then incorporated into containers, such as tubes, which are suitable for topical administration.
- Example 2A 3-((38S, 5aS, 6R, 9aR, 9b£)-3a, 6-dimethyl-3,7-dioxododecahydro-l/7- cyclopenta [a] naphthalen-6-yl)propanoic acid
- Example 2C (4aR ,4bS ,6aS, 9aS, 9b ⁇ )-l,4a,6a-trimethyl-2-oxo-2, 3, 4, 4a, 4b, 5, 6, 6a, 9, 9a,9b,10- dodecahydro-lH-indeno[5,4-f
- Example 3 C 3-((38S, 5aS, 6R, 9aS, 9b£)-3a,6-dimethyl-7-oxo-3-(pyridin-3-yl)-3a,4,5,5a,6,7,8,9,9a,9b- decahydro-lH-cyclopenta [a] naphthalen-6-yl)propanoic acid [00350] To a solution of (AaR,AbS,6aS,9aS,9bR)-tert-butyl 4a,6a-dimethyl-2,7-dioxo- 2,3,4,4a,4b,5,6,6a,7,8,9,9a,9b,10-tetradecahydro-lH-indeno[5,4-/
- Example 4B 2-((3a£; 4R, 5S, 7aS)-5-((lR, 4£)-4-isopropyl-l-methyl-2oxocyclohexyl)-7a-methyl-l- oxooctahydro-lH-inden ⁇ -ylJ-acetic acid compound with diisopropylsilanone (1:1)
- Example 4F (3aS, 3bR, 9aR, 9bS, lla£)-t ⁇ rt-butyl-9a, lla-dimethyl-l,7dioxo-3, 3a, 3b, 4, 7, 8, 9, 9a, 9b, 10, 11 , 1 la-dodecahydro-lH-cyclopenta [i] phenanthridine-5(2H)-carboxylate [00357] A solution of (3 aS, 3bR, IS, 9aR, 9bS, l laS)-terf-butyl-9a, 11 a-dimethyl- l-oxo-7- (triisopropylsilyloxy)-3, 3a, 3b, 4, 7, 8, 9, 9a, 9b, 10, 11, l la-dodecahydro-lH- cyclopenta[i]phenanthridine-5(2H)-carboxylate (30.2 g, 55.3 mmol) in tetrahydr
- the mixture was stirred at room temperature for 1 hour, and was then diluted with dichloromethane and washed water and brine, dried over Na 2 SO 4 . After filtration the filtrate was concentrated to ca. 400 mL, was then added molecular sieves (50 g), followed by N-methylmorpholine N-oxide (9.7 g, 1.5 eq) and tetrapropylammonium perruthenate (1.0 g, 0.05 eq). The mixture was stirred at room temperature for 2 hours.
- PhNTf 2 was added as a solution in T ⁇ F (30 mL). The mixture was stirred at 0 0 C for Ih before quenching with saturated NH 4 Cl, extracted with dichloromethane (3x), dried over Na 2 SO 4 .
- Example 5B (3aS, 3bR, 9aR, 9bS, Ha5)-9a,lla-dimethyl-7-oxo-5-((2-(trimethylsilyl)ethoxy)methyl)-3a, 3b, 4, 5, 7, 8, 9, 9a, 9b, 10, 11, lla-dodecahydro-SH-cyclopentaflphenanthridin-l-yl trifluoromethanesulfonate
- Example 17 N-5((4aR, 4bS, 6aS, 9aS, 9bS)-l, 4a, 6a-Trimethyl-2-oxo-2, 3, 4, 4a, 4b,5, 6, 6a, 9, 9a, 9b, 10- dodecahydro-l//-indeno [5,4-f] quinolin-7-yl)-pyridin-2-yl] -acetamide [00377] Using aR, 4bS, 6aS, 9aS, 9bS>7-(6-methoxypyridin-3-yl)-l,4a, 6a-trimethyl- 1 , 3, 4, 4a, 4b, 5, 6, 6a, 9, 9a, 9b, 10-decahydro-indeno[5,4-f]quinolin-2(3H)-one, replacing 6-methoxypyridin-3-ylboronic acid with 6-acetamidopyridin-3-ylboronic
- the reaction was heated to 80 0 C under N 2 for 5 hours. Then cooled to room temperature and partitioned between ethyl acetate (100 mL) and water (100 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (25 mL x 3). The combined organic layers were dried over Na 2 SOz I .
- the reaction was heated to 80 0 C and stirred at this temperature for 5 hours.
- the reaction was cooled to room temperature and partitioned between ethyl acetate (50 mL) and water (50 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (25 mL x 3).
- the reaction was heated to 120 0 C under N 2 for 6 hours.
- the reaction was cooled to room temperature and partitioned between ethyl acetate (50 mL) and water (50 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (25 mL x 3). The combined organic layers were dried over Na 2 SO 4 .
- the reaction was heated to 80 0 C under N 2 for 0.5 hour.
- the reaction was cooled to room temperature and partitioned between ethyl acetate (50 mL) and water (50 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (25 mL x 3). The combined organic layers were dried over Na 2 SO 4 .
- the reaction was heated to 80 0 C under N 2 for 0.5 hour.
- the reaction was cooled to room temperature and partitioned between ethyl acetate (50 mL) and water (50 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (25 mL x 3). The combined organic layers were dried over Na 2 SO 4 .
- the reaction was heated to 120 0 C and stirred at this temperature for 2 hours.
- the reaction was cooled to room temperature and partitioned between ethyl acetate (50 mL) and water (50 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (25 mL x 3). The combined organic layers were dried over Na 2 SO 4 .
- Pd(dppf)Cl 2 (10 mg, 5% w/w), 5-isoquinolineboronic acid (136 mg, 0.785 mmol) and K 2 CO 3 (287 mg, in 1 mL water, 2.08 mmol) were added consecutively to a stirred solution of (4ai?, AbS, 6aS, 9aS, 9bR)- ⁇ , 4a, 6a-trimethyl-2-oxo-2, 3, 4, 4a, 4b, 5, 6, 6a, 9, 9a, 9b, 10-dodecahydro-lH- indeno [5, 4-f]quinolin-7-yl trifluoromethanesulfonate (200 mg, 0.462 mmol) in 1,4-dioxane (15 mL).
- the reaction was heated to 80 0 C under N 2 for 1.5 hours.
- the reaction was cooled to room temperature and partitioned between ethyl acetate (50 mL) and water (50 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (25 mL x 3). The combined organic layers were dried over Na 2 SOz I .
- the reaction was heated to 80 0 C under N 2 for 3 hours.
- the reaction was cooled to room temperature and partitioned between ethyl acetate (50 mL) and water (50 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (25 mL x 3).
- the reaction is heated to 80 0 C under N 2 for 3 hours.
- the reaction is cooled to room temperature and partitioned between ethyl acetate (50 mL) and water (50 mL).
- the layers are separated and the aqueous layer extracted with ethyl acetate (25 mL x 3).
- the combined organic layers are dried over Na 2 SOzJ.
- the mixture was stirred at 80 0 C under N 2 for 2 hr, and then cooled to room temperature and partitioned with EA (10 mL) and water (10 mL). The aqueous layer was extracted with EA (50 mL x 3). The combined organic layers were dried over Na 2 S ⁇ 4 and concentrated.
- the mixture was stirred at 120 0 C for 2 hrs, and then cooled to room temperature and partitioned with EA (10 mL) and water (10 mL). The aqueous layer was extracted with EA (50 mL x 3). The combined organic layers were dried over Na 2 SO 4 and concentrated.
- the mixture was stirred at 100 0 C under N 2 for 15 min, and then cooled to room temperature and partitioned with EA (10 mL) and water (10 mL). The aqueous layer was extracted with EA (50 mL x 3). The combined organic layers were dried over Na 2 SO 4 and concentrated.
- the mixture was stirred at 120 0 C under N 2 for 3 h, and then cooled to room temperature and partitioned with EA (10 mL) and water (10 mL). The aqueous layer was extracted with EA (50 mL x 3). The combined organic layers were dried over Na 2 SO 4 and concentrated.
- the mixture was stirred at 120 0 C under N 2 for 3 h, and then cooled to room temperature and partitioned with EA (10 mL) and water (10 mL). The aqueous layer was extracted with EA (50 mL x 3). The combined organic layers were dried over Na 2 SC ⁇ and concentrated.
- Example 35 A (4a/?, 4bS, 6aS, 9&S, 9b/?)-l-Cyclopropyl-4a, 6a-dimethyl-4, 4a, 4b, 5, 6, 6a, 9, 9a, 9b, 10- decahydro-1//- indeno [5, 4-f] quinoline-2, 7(3//, 8//)-dione
- Example 35 B (4a/?, AbS, 6aS, 9aS, 9b/?)-l-Cyclopropyl-4a, 6a-dimethyl-2-oxo-2, 3, 4, 4a, 4b, 5, 6, 6a, 9, 9a,
- the mixture was purified by column chromatography on silica gel (PE / EA, 3/1) to give (4aR, 4bS, 6aS, 9aS, 9bR)- 1 -cyclopropyl-4a, 6a-dimethyl-2-oxo-2, 3, 4, 4a, 4b, 5, 6, 6a, 9, 9a, 9b, 10-dodecahydro-lH-indeno [5, 4-f] quinolin-7-yl trifluoromethanesulfonate (500 mg, yield 31%).
- the reaction was heated to 100 0 C under N 2 for 0.5 hour.
- the reaction was cooled to room temperature and partitioned between ethyl acetate (100 mL) and water (100 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (25 mL x 3).
- the mixture was heated to 100 0 C under N 2 for 0.5 hour.
- the reaction was cooled to room temperature and partitioned between ethyl acetate (100 mL) and water (100 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (25 mL x 3).
- the mixture was heated to 80 0 C under N 2 and stirred at this temperature for 5 hours.
- the reaction was cooled to room temperature and partitioned between ethyl acetate (100 mL) and water (100 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (25 mL x 3). The combined organic layers were dried over Na 2 SOz I .
- the mixture was heated to 90 0 C under N 2 for 10 minute. Then cooled to room temperature and partitioned between ethyl acetate (100 mL) and water (100 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (25 mL x 3). The combined organic layers were dried over Na 2 SOz I .
- the mixture was heated to 100 0 C under N 2 for 0.5 hour. Then cooled to room temperature and partitioned between ethyl acetate (50 mL) and water (50 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (25 mL x 3).
- Example 41 (4aR, 4bS, 6aS, 9aS, 9b£)-l-Cyclopropyl-4a, 6a-dimethyl-7-(pyridin-2-yl)-4, 4a, 4b, 5, 6, 6a, 9, 9a, 9b, 10-decahydro-lH-indeno [5, 4-f] quinolin-2(3H)-one [00405] To a mixture of (4aR, 4bS, 6aS, 9aS, 9bR)-l-cyclopropyl-4a,6a-dimethyl-2-oxo-2, 3, 4, 4a, 4b, 5, 6, 6a, 9, 9a, 9b, 10-dodecahydro-lH-indeno[5, 4-f]quinolin-7-yl trifluoromethanesulfonate (200 mg, 0.436 mmol) and 2-(tributylstannyl)pyridine (225 mg, 0.61 mmol) in DMF (2 mL) was added
- the reaction was cooled to room temperature and partitioned between ethyl acetate (100 mL) and water (100 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (25 mL x 3). The combined organic layers were dried over Na 2 SO 4 .
- the mixture was heated to 120 0 C under N 2 for 0.5 hour. Then cooled to room temperature and partitioned between ethyl acetate (50 mL) and water (50 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (15 mL x 3). The combined organic layers were dried over Na 2 SO 4 .
- the mixture was heated to 100 0 C under N 2 for 0.5 hour. Then cooled to room temperature and partitioned between ethyl acetate (50 mL) and water (50 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (25 mL x 3). The combined organic layers were dried over Na 2 SO 4 .
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Abstract
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Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
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AU2009320250A AU2009320250A1 (en) | 2008-10-28 | 2009-10-21 | Decahydro-1H-indenoquinolinone and decahydro-3H-cyclopentaphenanthridinone CYP17 inhibitors |
JP2011534622A JP2012506906A (en) | 2008-10-28 | 2009-10-21 | Decahydro-1H-indenoquinoline and decahydro-3H-cyclopentaphenanthridinone CYP17 inhibitor |
CN2009801527688A CN102282133A (en) | 2008-10-28 | 2009-10-21 | Decahydro-1h-indenoquinolinone and decahydro-3h-cyclopentaphenanthridinone cyp17 inhibitors |
EP09829548A EP2362872A4 (en) | 2008-10-28 | 2009-10-21 | Decahydro-1h-indenoquinolinone and decahydro-3h-cyclopentaphenanthridinone cyp17 inhibitors |
CA2739251A CA2739251A1 (en) | 2008-10-28 | 2009-10-21 | Decahydro-1h-indenoquinolinone and decahydro-3h-cyclopentaphenanthridinone cyp17 inhibitors |
BRPI0920681A BRPI0920681A2 (en) | 2008-10-28 | 2009-10-21 | cyp17 decahidro-1h-indenoquinolinone and decahidro-3h-cyclopentafenantridinone inhibitors |
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US10896608P | 2008-10-28 | 2008-10-28 | |
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US (1) | US20100105700A1 (en) |
EP (1) | EP2362872A4 (en) |
JP (1) | JP2012506906A (en) |
CN (1) | CN102282133A (en) |
AR (1) | AR075474A1 (en) |
AU (1) | AU2009320250A1 (en) |
BR (1) | BRPI0920681A2 (en) |
CA (1) | CA2739251A1 (en) |
GB (1) | GB2464812A (en) |
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Cited By (3)
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WO2011088160A3 (en) * | 2010-01-15 | 2011-10-13 | Biomarin Pharmaceutical Inc. | Novel cyp17 inhibitors |
WO2012009510A1 (en) * | 2010-07-15 | 2012-01-19 | Bristol-Myers Squibb Company | Azaindazole compounds |
WO2012064943A2 (en) | 2010-11-13 | 2012-05-18 | Viamet Pharmaceuticals, Inc. | Metalloenzyme inhibitor compounds |
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US20120295932A1 (en) * | 2011-05-17 | 2012-11-22 | Western Connecticut Health Network, Inc. | Method for the treatment of cancer |
CN103102305B (en) * | 2013-02-05 | 2015-01-21 | 中国科学院新疆理化技术研究所 | Alkaloid of skeleton type 2 in nigella glandulifera preyn and preparation method of alkaloid |
WO2018166855A1 (en) | 2017-03-16 | 2018-09-20 | Basf Se | Heterobicyclic substituted dihydroisoxazoles |
CN109507165A (en) * | 2019-01-10 | 2019-03-22 | 南京师范大学 | A kind of detection method of Fructose in Honey content |
CN111170943B (en) * | 2020-01-22 | 2021-03-26 | 浙江大学 | Benzo [ f ] cyclopentano [ c ] quinoline derivatives and use thereof |
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DE69313114T2 (en) * | 1992-05-20 | 1998-03-19 | Merck & Co Inc | NEW DELTA-17 AND DELTA-20 UNSATURATED AND SATURATED 17 - g (b) -SUBSTITUTED-4-AZA-5-g (a) -ANDROSTAN-3-ON COMPOUNDS AS INHIBITORS OF 5-ALPHA REDUCTASE |
WO1993023039A1 (en) * | 1992-05-20 | 1993-11-25 | Merck & Co., Inc. | Substituted 4-aza-5a-androstan-ones as 5a-reductase inhibitors |
GB9216284D0 (en) * | 1992-07-31 | 1992-09-16 | Erba Carlo Spa | Fluorinated 17beta-substituted 4-aza-5alpha-androstane-3-one derivatives |
HU212459B (en) * | 1992-10-02 | 1996-06-28 | Richter Gedeon Vegyeszet | Process for producing new 17-beta-substituted 4-aza-androstane-derivatives and pharmaceutical compositions containing them |
US5525608A (en) * | 1994-04-20 | 1996-06-11 | Merck & Co., Inc. | 17b-aryl-4-aza-steroid derivatives useful as 5-alpha-reductase inhibitors |
US5516779A (en) * | 1994-06-08 | 1996-05-14 | Merck & Co., Inc. | 17β-substituted-6-azasteroid derivatives useful as 5α-reductase inhibitors |
NZ327041A (en) * | 1996-02-14 | 1999-11-29 | Hoechst Marion Roussel Inc | 17-beta-cyclopropyl(amino/oxy) 4-aza steriods as active inhibitors of testosterone 5-alpha-reductase and C17-20-lyase |
GB9608045D0 (en) * | 1996-04-18 | 1996-06-19 | Pharmacia Spa | Process for preparing steroids having a carboxamide side-chain |
KR100415858B1 (en) * | 2001-09-22 | 2004-01-24 | 한미약품 주식회사 | PROCESS FOR THE PREPARATION OF 17β-(N-TERT-BUTYLCARBAMOYL)-3-ONE STEROID COMPOUND |
KR100483136B1 (en) * | 2003-04-02 | 2005-04-14 | 한미약품 주식회사 | Novel process for preparing high purity finasteride |
KR100508019B1 (en) * | 2003-07-19 | 2005-08-17 | 한미약품 주식회사 | Method for the preparation of highly pure 1-androstene derivatives |
CA2599953C (en) * | 2005-03-02 | 2013-08-13 | Angela Brodie | Novel c-17-heteroaryl steroidal cyp17 inhibitors/antiandrogens: synthesis, in vitro biological activities, pharmacokinetics and antitumor activity |
-
2009
- 2009-10-21 BR BRPI0920681A patent/BRPI0920681A2/en not_active Application Discontinuation
- 2009-10-21 AU AU2009320250A patent/AU2009320250A1/en not_active Abandoned
- 2009-10-21 JP JP2011534622A patent/JP2012506906A/en not_active Withdrawn
- 2009-10-21 WO PCT/US2009/061550 patent/WO2010062506A2/en active Application Filing
- 2009-10-21 CN CN2009801527688A patent/CN102282133A/en active Pending
- 2009-10-21 EP EP09829548A patent/EP2362872A4/en not_active Withdrawn
- 2009-10-21 CA CA2739251A patent/CA2739251A1/en not_active Abandoned
- 2009-10-21 US US12/603,377 patent/US20100105700A1/en not_active Abandoned
- 2009-10-23 GB GB0918601A patent/GB2464812A/en not_active Withdrawn
- 2009-10-27 TW TW098136335A patent/TW201019940A/en unknown
- 2009-10-28 AR ARP090104161A patent/AR075474A1/en unknown
Non-Patent Citations (1)
Title |
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See references of EP2362872A4 * |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011088160A3 (en) * | 2010-01-15 | 2011-10-13 | Biomarin Pharmaceutical Inc. | Novel cyp17 inhibitors |
WO2012009510A1 (en) * | 2010-07-15 | 2012-01-19 | Bristol-Myers Squibb Company | Azaindazole compounds |
US8673922B2 (en) | 2010-07-15 | 2014-03-18 | Bristol-Myers Squibb Company | Azaindazole compounds |
WO2012064943A2 (en) | 2010-11-13 | 2012-05-18 | Viamet Pharmaceuticals, Inc. | Metalloenzyme inhibitor compounds |
EP2638021A2 (en) * | 2010-11-13 | 2013-09-18 | Viamet Pharmaceuticals, Inc. | Metalloenzyme inhibitor compounds |
EP2638021A4 (en) * | 2010-11-13 | 2014-05-07 | Viamet Pharmaceuticals Inc | Metalloenzyme inhibitor compounds |
AU2011326487B2 (en) * | 2010-11-13 | 2017-03-02 | Innocrin Pharmaceuticals, Inc. | Metalloenzyme inhibitor compounds |
EP3483147A1 (en) * | 2010-11-13 | 2019-05-15 | Innocrin Pharmaceuticals, Inc. | Metalloenzyme inhibitor compounds |
Also Published As
Publication number | Publication date |
---|---|
JP2012506906A (en) | 2012-03-22 |
BRPI0920681A2 (en) | 2015-12-29 |
CN102282133A (en) | 2011-12-14 |
US20100105700A1 (en) | 2010-04-29 |
EP2362872A4 (en) | 2012-05-30 |
GB0918601D0 (en) | 2009-12-09 |
WO2010062506A3 (en) | 2010-10-07 |
CA2739251A1 (en) | 2010-06-03 |
EP2362872A2 (en) | 2011-09-07 |
AU2009320250A1 (en) | 2010-06-03 |
AR075474A1 (en) | 2011-04-06 |
GB2464812A (en) | 2010-05-05 |
TW201019940A (en) | 2010-06-01 |
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