EP1173213A1 - Compositions containing benzimidazolones and progestogens - Google Patents
Compositions containing benzimidazolones and progestogensInfo
- Publication number
- EP1173213A1 EP1173213A1 EP00932006A EP00932006A EP1173213A1 EP 1173213 A1 EP1173213 A1 EP 1173213A1 EP 00932006 A EP00932006 A EP 00932006A EP 00932006 A EP00932006 A EP 00932006A EP 1173213 A1 EP1173213 A1 EP 1173213A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- substituted
- alkyl
- phase
- antiprogestm
- pharmaceutically acceptable
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000000583 progesterone congener Substances 0.000 title claims abstract description 44
- 239000000203 mixture Substances 0.000 title description 59
- 150000008641 benzimidazolones Chemical class 0.000 title description 2
- 229940095055 progestogen systemic hormonal contraceptives Drugs 0.000 title description 2
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 68
- 238000000034 method Methods 0.000 claims abstract description 64
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 46
- 150000003839 salts Chemical class 0.000 claims abstract description 38
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract description 32
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 29
- 125000003118 aryl group Chemical group 0.000 claims abstract description 27
- 150000002367 halogens Chemical class 0.000 claims abstract description 27
- 125000000304 alkynyl group Chemical group 0.000 claims abstract description 23
- 239000000262 estrogen Substances 0.000 claims abstract description 22
- 229940011871 estrogen Drugs 0.000 claims abstract description 22
- 125000001424 substituent group Chemical group 0.000 claims abstract description 21
- -1 indoline derivative compounds Chemical class 0.000 claims abstract description 19
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 18
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 16
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract description 10
- 125000004103 aminoalkyl group Chemical group 0.000 claims abstract description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 8
- 125000004426 substituted alkynyl group Chemical group 0.000 claims abstract description 6
- 150000001875 compounds Chemical class 0.000 claims description 145
- WWYNJERNGUHSAO-XUDSTZEESA-N (+)-Norgestrel Chemical compound O=C1CC[C@@H]2[C@H]3CC[C@](CC)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 WWYNJERNGUHSAO-XUDSTZEESA-N 0.000 claims description 43
- 229960004400 levonorgestrel Drugs 0.000 claims description 43
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 35
- 230000001072 progestational effect Effects 0.000 claims description 28
- VOXZDWNPVJITMN-ZBRFXRBCSA-N 17β-estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 VOXZDWNPVJITMN-ZBRFXRBCSA-N 0.000 claims description 24
- 229960005309 estradiol Drugs 0.000 claims description 24
- 229930182833 estradiol Natural products 0.000 claims description 24
- 239000000902 placebo Substances 0.000 claims description 23
- 229940068196 placebo Drugs 0.000 claims description 23
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 17
- 125000003107 substituted aryl group Chemical group 0.000 claims description 15
- 125000005309 thioalkoxy group Chemical group 0.000 claims description 13
- 230000000708 anti-progestin effect Effects 0.000 claims description 12
- 239000003418 antiprogestin Substances 0.000 claims description 12
- 239000003795 chemical substances by application Substances 0.000 claims description 12
- 125000005842 heteroatom Chemical group 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 6
- FQFILJKFZCVHNH-UHFFFAOYSA-N tert-butyl n-[3-[(5-bromo-2-chloropyrimidin-4-yl)amino]propyl]carbamate Chemical compound CC(C)(C)OC(=O)NCCCNC1=NC(Cl)=NC=C1Br FQFILJKFZCVHNH-UHFFFAOYSA-N 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- GCKFUYQCUCGESZ-BPIQYHPVSA-N etonogestrel Chemical compound O=C1CC[C@@H]2[C@H]3C(=C)C[C@](CC)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 GCKFUYQCUCGESZ-BPIQYHPVSA-N 0.000 claims description 4
- 229960005352 gestodene Drugs 0.000 claims description 4
- SIGSPDASOTUPFS-XUDSTZEESA-N gestodene Chemical compound O=C1CC[C@@H]2[C@H]3CC[C@](CC)([C@](C=C4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 SIGSPDASOTUPFS-XUDSTZEESA-N 0.000 claims description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 3
- 229940022663 acetate Drugs 0.000 claims description 3
- UWFYSQMTEOIJJG-FDTZYFLXSA-N cyproterone acetate Chemical compound C1=C(Cl)C2=CC(=O)[C@@H]3C[C@@H]3[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(C)=O)(OC(=O)C)[C@@]1(C)CC2 UWFYSQMTEOIJJG-FDTZYFLXSA-N 0.000 claims description 3
- 229960000978 cyproterone acetate Drugs 0.000 claims description 3
- 229960000417 norgestimate Drugs 0.000 claims description 3
- KIQQMECNKUGGKA-NMYWJIRASA-N norgestimate Chemical compound O/N=C/1CC[C@@H]2[C@H]3CC[C@](CC)([C@](CC4)(OC(C)=O)C#C)[C@@H]4[C@@H]3CCC2=C\1 KIQQMECNKUGGKA-NMYWJIRASA-N 0.000 claims description 3
- 229960004976 desogestrel Drugs 0.000 claims description 2
- RPLCPCMSCLEKRS-BPIQYHPVSA-N desogestrel Chemical compound C1CC[C@@H]2[C@H]3C(=C)C[C@](CC)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 RPLCPCMSCLEKRS-BPIQYHPVSA-N 0.000 claims description 2
- 229960003309 dienogest Drugs 0.000 claims description 2
- AZFLJNIPTRTECV-FUMNGEBKSA-N dienogest Chemical compound C1CC(=O)C=C2CC[C@@H]([C@H]3[C@@](C)([C@](CC3)(O)CC#N)CC3)C3=C21 AZFLJNIPTRTECV-FUMNGEBKSA-N 0.000 claims description 2
- METQSPRSQINEEU-UHFFFAOYSA-N dihydrospirorenone Natural products CC12CCC(C3(CCC(=O)C=C3C3CC33)C)C3C1C1CC1C21CCC(=O)O1 METQSPRSQINEEU-UHFFFAOYSA-N 0.000 claims description 2
- 229960004845 drospirenone Drugs 0.000 claims description 2
- METQSPRSQINEEU-HXCATZOESA-N drospirenone Chemical compound C([C@]12[C@H]3C[C@H]3[C@H]3[C@H]4[C@@H]([C@]5(CCC(=O)C=C5[C@@H]5C[C@@H]54)C)CC[C@@]31C)CC(=O)O2 METQSPRSQINEEU-HXCATZOESA-N 0.000 claims description 2
- 229960004911 nomegestrol Drugs 0.000 claims description 2
- KZUIYQJTUIACIG-YBZCJVABSA-N nomegestrol Chemical compound C1=C(C)C2=CC(=O)CC[C@@H]2[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(=O)C)(O)[C@@]1(C)CC2 KZUIYQJTUIACIG-YBZCJVABSA-N 0.000 claims description 2
- ZLLOIFNEEWYATC-XMUHMHRVSA-N osaterone Chemical compound C1=C(Cl)C2=CC(=O)OC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(=O)C)(O)[C@@]1(C)CC2 ZLLOIFNEEWYATC-XMUHMHRVSA-N 0.000 claims description 2
- 229950006466 osaterone Drugs 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 230000000694 effects Effects 0.000 abstract description 24
- 102000003998 progesterone receptors Human genes 0.000 abstract description 23
- 108090000468 progesterone receptors Proteins 0.000 abstract description 23
- 239000005557 antagonist Substances 0.000 abstract description 17
- 230000002265 prevention Effects 0.000 abstract description 8
- 229910052717 sulfur Inorganic materials 0.000 abstract description 8
- 210000000481 breast Anatomy 0.000 abstract description 6
- 210000001072 colon Anatomy 0.000 abstract description 5
- 210000001672 ovary Anatomy 0.000 abstract description 5
- 210000002307 prostate Anatomy 0.000 abstract description 5
- 229910052760 oxygen Inorganic materials 0.000 abstract description 4
- 230000000740 bleeding effect Effects 0.000 abstract description 3
- 125000004122 cyclic group Chemical group 0.000 abstract description 3
- 230000037406 food intake Effects 0.000 abstract description 3
- 235000012631 food intake Nutrition 0.000 abstract description 3
- 201000010065 polycystic ovary syndrome Diseases 0.000 abstract description 3
- 201000000736 Amenorrhea Diseases 0.000 abstract description 2
- 206010001928 Amenorrhoea Diseases 0.000 abstract description 2
- 231100000540 amenorrhea Toxicity 0.000 abstract description 2
- 230000002175 menstrual effect Effects 0.000 abstract description 2
- 201000009030 Carcinoma Diseases 0.000 abstract 1
- 201000009273 Endometriosis Diseases 0.000 abstract 1
- 208000009956 adenocarcinoma Diseases 0.000 abstract 1
- 238000002648 combination therapy Methods 0.000 abstract 1
- 210000004696 endometrium Anatomy 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 109
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 86
- 229910001868 water Inorganic materials 0.000 description 68
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 64
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 36
- 235000019439 ethyl acetate Nutrition 0.000 description 35
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 34
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 31
- 239000000243 solution Substances 0.000 description 31
- RJKFOVLPORLFTN-LEKSSAKUSA-N Progesterone Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](C(=O)C)[C@@]1(C)CC2 RJKFOVLPORLFTN-LEKSSAKUSA-N 0.000 description 30
- 238000005481 NMR spectroscopy Methods 0.000 description 29
- 239000002253 acid Substances 0.000 description 26
- 239000002904 solvent Substances 0.000 description 26
- 210000004027 cell Anatomy 0.000 description 25
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
- 238000010992 reflux Methods 0.000 description 22
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 20
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 20
- 229910052757 nitrogen Inorganic materials 0.000 description 20
- 239000000186 progesterone Substances 0.000 description 20
- 239000007787 solid Substances 0.000 description 20
- 239000012071 phase Substances 0.000 description 19
- 231100000673 dose–response relationship Toxicity 0.000 description 18
- 239000002609 medium Substances 0.000 description 18
- 229910000027 potassium carbonate Inorganic materials 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 17
- 239000012044 organic layer Substances 0.000 description 17
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 16
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
- 229960003387 progesterone Drugs 0.000 description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 13
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 238000003556 assay Methods 0.000 description 12
- 239000003153 chemical reaction reagent Substances 0.000 description 12
- 238000005160 1H NMR spectroscopy Methods 0.000 description 11
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 11
- 239000000556 agonist Substances 0.000 description 11
- 230000001911 anti-progestational effect Effects 0.000 description 11
- 239000012298 atmosphere Substances 0.000 description 11
- 239000000284 extract Substances 0.000 description 11
- VKHAHZOOUSRJNA-GCNJZUOMSA-N mifepristone Chemical compound C1([C@@H]2C3=C4CCC(=O)C=C4CC[C@H]3[C@@H]3CC[C@@]([C@]3(C2)C)(O)C#CC)=CC=C(N(C)C)C=C1 VKHAHZOOUSRJNA-GCNJZUOMSA-N 0.000 description 11
- 238000012360 testing method Methods 0.000 description 11
- 229910052786 argon Inorganic materials 0.000 description 10
- 239000005089 Luciferase Substances 0.000 description 9
- 241001465754 Metazoa Species 0.000 description 9
- 229940123788 Progesterone receptor antagonist Drugs 0.000 description 9
- 238000004458 analytical method Methods 0.000 description 9
- 239000001963 growth medium Substances 0.000 description 9
- 239000003981 vehicle Substances 0.000 description 9
- 239000002585 base Substances 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 239000003446 ligand Substances 0.000 description 8
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- 125000000547 substituted alkyl group Chemical group 0.000 description 8
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 7
- 239000012267 brine Substances 0.000 description 7
- 239000012043 crude product Substances 0.000 description 7
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 7
- CFHGBZLNZZVTAY-UHFFFAOYSA-N lawesson's reagent Chemical compound C1=CC(OC)=CC=C1P1(=S)SP(=S)(C=2C=CC(OC)=CC=2)S1 CFHGBZLNZZVTAY-UHFFFAOYSA-N 0.000 description 7
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 7
- 239000008194 pharmaceutical composition Substances 0.000 description 7
- 239000002244 precipitate Substances 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 7
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 6
- WOVKYSAHUYNSMH-RRKCRQDMSA-N 5-bromodeoxyuridine Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(Br)=C1 WOVKYSAHUYNSMH-RRKCRQDMSA-N 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
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- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- 102220497176 Small vasohibin-binding protein_T47D_mutation Human genes 0.000 description 6
- 230000037396 body weight Effects 0.000 description 6
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 6
- 229940088597 hormone Drugs 0.000 description 6
- 239000005556 hormone Substances 0.000 description 6
- 229910000104 sodium hydride Inorganic materials 0.000 description 6
- SDEAGACSNFSZCU-UHFFFAOYSA-N (3-chlorophenyl)boronic acid Chemical compound OB(O)C1=CC=CC(Cl)=C1 SDEAGACSNFSZCU-UHFFFAOYSA-N 0.000 description 5
- HJCMDXDYPOUFDY-WHFBIAKZSA-N Ala-Gln Chemical compound C[C@H](N)C(=O)N[C@H](C(O)=O)CCC(N)=O HJCMDXDYPOUFDY-WHFBIAKZSA-N 0.000 description 5
- 229930182555 Penicillin Natural products 0.000 description 5
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 5
- 102000004160 Phosphoric Monoester Hydrolases Human genes 0.000 description 5
- 108090000608 Phosphoric Monoester Hydrolases Proteins 0.000 description 5
- 241000700159 Rattus Species 0.000 description 5
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 5
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- 102000027411 intracellular receptors Human genes 0.000 description 5
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- 235000019341 magnesium sulphate Nutrition 0.000 description 5
- 229960002985 medroxyprogesterone acetate Drugs 0.000 description 5
- PSGAAPLEWMOORI-PEINSRQWSA-N medroxyprogesterone acetate Chemical compound C([C@@]12C)CC(=O)C=C1[C@@H](C)C[C@@H]1[C@@H]2CC[C@]2(C)[C@@](OC(C)=O)(C(C)=O)CC[C@H]21 PSGAAPLEWMOORI-PEINSRQWSA-N 0.000 description 5
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- 239000011734 sodium Substances 0.000 description 5
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- ZNRGSYUVFVNSAW-UHFFFAOYSA-N 3-nitrophenylboronic acid Chemical compound OB(O)C1=CC=CC([N+]([O-])=O)=C1 ZNRGSYUVFVNSAW-UHFFFAOYSA-N 0.000 description 4
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
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- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 206010046798 Uterine leiomyoma Diseases 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 125000003282 alkyl amino group Chemical group 0.000 description 3
- 238000000540 analysis of variance Methods 0.000 description 3
- 238000013459 approach Methods 0.000 description 3
- 125000005110 aryl thio group Chemical group 0.000 description 3
- 239000012131 assay buffer Substances 0.000 description 3
- 150000001555 benzenes Chemical class 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 201000011510 cancer Diseases 0.000 description 3
- PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000004113 cell culture Methods 0.000 description 3
- 238000001516 cell proliferation assay Methods 0.000 description 3
- 238000004587 chromatography analysis Methods 0.000 description 3
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/18—Feminine contraceptives
Definitions
- This invention relates to regimens of administering compounds which are antagonists of the progesterone receptor
- Intracellular receptors form a class of structurally related gene regulators known as "ligand dependent transcription factors" (R M Evans, Science, 240, 889, 1988)
- the steroid receptor family is a subset of the IR family, including progesterone receptor (PR), estrogen receptor (ER), androgen receptor (AR), glucocorticoid receptor (GR), and mineralocorticoid receptor (MR)
- the natural hormone, or ligand, for the PR is the steroid progesterone, but synthetic compounds, such as medroxyprogesterone acetate or levonorgestrel, have been made which also serve as ligands
- a ligand is present in the fluid surrounding a cell, it passes through the membrane via passive diffusion, and binds to the IR to create a receptor/hgand complex
- This complex binds to specific gene promoters present in the cell's DNA Once bound to the DNA the complex modulates the production of mRNA and protein encoded by that gene
- a compound that binds to an IR and mimics the action of the natural hormone is termed an agonist, whilst a compound which inhibits the effect of the hormone is an antagonist
- PR agonists are known to play an important role in the health of women PR agonists are used in birth control formulations, typically in the presence of an ER agonist ER agonists are used to treat the symptoms of menopause, but have been associated with a prohferative effect on the uterus which can lead to an increased risk of uterine cancers
- Co-administration of a PR agonist reduces/ablates PR antagonists may also be used in contraception In this context they may be administered alone (Ulmann, et ai, Ann N Y Ac ⁇ d Sci , 261, 248, 1995), in combination with a PR agonist (Kekkonen, et al, Fertility and Sterility, 60, 610, 1993) or in combination with a partial ER antagonist such as tamoxifen (WO 96/19997 Al July 4, 1996) PR antagonists may also be useful for the treatment of hormone dependent breast cancers (Horwitz, et al, Horm Cancer, 283, pub Birkhaeuser, Boston, Mass
- Ueda et al claimed benzothiazoline and benzoxazoline compounds of formula A as the inhibitors of aldose reductase
- the benzimidazolmone derivatives such as compound B were disclosed by Hara et al (EP 454330) and claimed as lung surfactant secretion promoters
- Bru-Magniez et al synthesized the benzoimidazohnones such as compound C.
- U S Patent No 5,521,166 teaches cyclophasic hormonal regimens comprising an antiprogestm and a progestm wherem the progestm is admmistered m the alternating presence and absence of an antiprogestm
- the disclosed regimens also provide for use of an estrogen for a period of from 2-4 days to prevent breakthrough bleeding
- This mvention provides combmation therapies and dosmg regimens utilizing antiprogestational agents in combmation with one or more progestational agents
- This mvention further provides methods of treatment and dosmg regimens further utilizing m combmation with these antiprogestins and progestins, an estrogen, such as ethmyl estradiol
- regimens and combmations may be admmistered to a mammal to induce contraception or for the treatment and/or prevention of secondary amenorrhea, dysfunctional bleedmg, uterme leiomyomata, endomet ⁇ osis, polycystic ovary syndrome, carcmomas and adenocarcmomas of the endomet ⁇ um, ovary, breast, colon, prostate Additional uses of the invention mclude stimulation of food intake
- the uses herem for the treatment and/or prevention of the conditions or diseases described above includes the continuous administration or periodic discontinuation of administration of the mvention to allow for minimization of effect dose or minimization of side effects or cyclic menstrual bleedmg
- this mvention for contraception includes administration, preferably orally, to a female of child bearing age an antiprogestm m combination with an estrogen or progestm or both These administration regimens are preferably carried out over 28 consecutive days, with a terminal portion of the cyc * *j containing administration of no progestins, estrogens or anti-pro gestms
- the progestms of these combmations may be administered alone or m combination with an estrogen for the first 14 to 24 days of the cycle, the progestins being admmistered at a dosage range equal m progestational activity to about 35 ⁇ g to about 150 ⁇ g levonorgestrel per day, preferably equal m activity to from about 35 ⁇ g to about 100 ⁇ g levonorgestrel per day
- An antiprogestm may then be administered alone or m combmation with an estrogen for a period of 1 to 11 days to begm on any cycle day between day 14 and 24
- the anti-pro gestm m these combmations may be admmistered at a dose of from about 2 ⁇ g to about 50 ⁇ g per day and the estrogen may be administered at a dose of from about 10 ⁇ g to about 35 ⁇ g per day
- a package or kit containing 28 tablets will include a placebo tablet on those days when the antiprogestm or progestm or estrogen is
- the progestins of this mvention may be admmistered alone or m combmation with estrogen for the initial 18 to 21 days of a 28-day cycle, followed by administration of an antiprogestm, alone or m combmation with an estrogen, for from 1 to 7 days
- the estrogen to be used m the combmations and formulations of this mvention is preferably ethmyl estradiol
- Progestational agents useful with this mvention include, but are not limited to, levonorgestrel, norgestrel, desogestrel, 3-ketodesogestrel, norethmdrone, gestodene, norethmdrone acetate, norgestimate, osaterone, cyproterone acetate, t ⁇ megestone, dienogest, drospirenone, nomegestrol, or (17-deacetyl)norgest ⁇ mate
- the preferred progestins for use in the combinations of this mvention are levonorgestrel, gestodene and t ⁇ megestone
- Examples of orally admmistered regimens of this mvention over a 28 day cycle mclude admmistration of a progestational agent solely for the first 21 days at a daily dose equal m progestational activity to from about 35 to about 100 ⁇ g of levonorgestrel
- a progestational agent may be coadministered for the first 21 days at a daily dose equal m progestational activity to from about 35 to about 150 ⁇ g levonorgestrel, preferably equal m activity to from about 35 to about 100 ⁇ g levonorgestrel, with an estrogen, such as ethmyl estradiol, at a daily dose range of from about 10 to about 35 ⁇ g
- an antiprogestm admmistered at a daily dose of from about 2 to 50 mg from day 22 to day 24, followed by no admmistration or admmistration of a placebo for days 25 to 28
- Still another regimen withm the scope of this mvention will mclude coadministration from days 1 to 21 of a progestational agent, the progestational agent, preferably levonorgestrel, bemg administered at a daily dose equal m progestational activity to from about 35 to about 100 ⁇ g levonorgestrel, and
- one 28-day kit may comprise a) an initial phase of from 14 to 21 daily dosage units of a progestational agent equal m progestational activity to about 35 to about 150 ⁇ g levonorgestrel, preferably equal m progestational activity to about 35 to about 100 ⁇ g levonorgestrel, b) a second phase of from 1 to 11 daily dosage units of an antiprogestm compound of this invention, each daily dosage unit containing an antiprogestm compound at a daily dosage of from about 2 to 50 mg, and c) optionally, a third phase of an orally and pharmaceutically acceptable placebo for the remaining days of the cycle in which no antiprogestm, progestm or estrogen is administered
- a preferred embodiment of this kit may comprise a) an initial phase of 21 daily dosage units of a progestational agent equal m progestational activity to about 35 to about 150 ⁇ g levonorgestrel, preferably equal in progestational activity to about 35 to about 100 ⁇ g levonorgestrel, b) a second phase of 3 daily dosage units for days 22 to 24 of an antiprogestm compound of this mvention, each daily dosage unit containing an antiprogestm compound at a daily dosage of from about 2 to 50 mg, and c) optionally, a third phase of 4 daily units of an orally and pharmaceutically acceptable placebo for each of days 25 to 28
- Another 28-day cycle packagmg regimen or kit of this invention comprises a) a first phase of from 18 to 21 daily dosage units of a progestational agent equal m progestational activity to about 35 to about 150 ⁇ g levonorgestrel, preferably equal in activity to from about 35 to about 100 ⁇ g levonorgestrel, and, as an estrogen, ethmyl estradiol at a daily dose range of from about 10 to about 35 ⁇ g, and b) a second phase of from 1 to 7 daily dosage units of an antiprogestm of this mvention at a daily dose of from about 2 to 50 mg, and c) optionally, an orally and pharmaceutically acceptable placebo for each of the remaining 0-9 days m the 28-day cycle m which no progestational agent, estrogen or antiprogestm is admmistered
- kits descnbed above may comprise a) a first phase of 21 daily dosage units of a progestational agent equal in progestational activity to about 35 to about 150 ⁇ g levonorgestrel, preferably equal m activity to from about 35 to about 100 ⁇ g levonorgestrel, and, as an estrogen, ethmyl estradiol at a daily dose range of from about 10 to about 35 ⁇ g, and b) a second phase of 3 daily dosage units for days 22 to 24 of an antiprogestm admmistered at a daily dose of from about 2 to 50 mg, and c) optionally, a third phase of 4 daily dose units of an orally and pharmaceutically acceptable placebo for each of days 25 to 28
- a further 28-day packaged regimen or kit of this mvention comprises a) a first phase of from 18 to 21 daily dosage units, each containing a progestational agent of this mvention at a daily dose equal m progestational activity to about 35 to about 150 ⁇ g levonorgestrel, preferably equal in activity to from about 35 to about 100 ⁇ g levonorgestrel, and ethmyl estradiol at a daily dose range of from about 10 to about 35 ⁇ g, b) a second phase of from 1 to 7 daily dose units, each daily dose unit containing an antiprogestm of this mvention at a concentration of from 2 to 50 mg, and ethmyl estradiol at a concentration of from about 10 to about 35 ⁇ g, and c) optionally, an orally and pharmaceutically acceptable placebo for each of the remainmg 0-9 days m the 28-day cycle m which no progestational agent, estrogen or antiprogestm is admmistered
- a prefe ⁇ ed embodiment of the package or kit just described comprises a) a first phase of 21 daily dosage units, each containing a progestational agent of this mvention at a daily dose equal m progestational activity to about 35 to about 150 ⁇ g levonorgestrel, preferably from about 35 to about 100 ⁇ g levonorgestrel, and ethmyl estradiol at a daily dose range of from about 10 to about 35 ⁇ g, b) a second phase of 3 daily dose units for days 22 to 24, each dose unit containing an antiprogestm of this mvention at a concentration oi ⁇ om 2 to 50 mg, and ethmyl estradiol at a concentration of from about 10 to about 35 ⁇ g, and c) optionally, a third phase of 4 daily units of an orally and pharmaceutically acceptable placebo for each of days 25 to 28
- each pharmaceutically active component of the regimen remam fixed m each particular phase m which it is administered
- the daily dose units described are to be admmistered in the order described, with the first phase followed m order by the second and third phases
- the kits contain the placebo described for the final days of the cycle
- each package or kit comprise a pharmaceutically acceptable package havmg mdicators for each day of the 28-day cycle, such as a labeled blister package or dial dispenser packages known in the art
- anti-progestational agents anti-progestational agents
- anti-progestins anti-progestins
- progesterone receptor antagonists are understood to be synonymous
- progestms, progestational agents and progesterone receptor agonists are understood to refer to compounds of the same activity
- dosage regimens may be adjusted to provide the optimal therapeutic response
- several divided doses of each component may be admmistered daily or the dose may be proportionally mcreased or reduced as mdicated by the exigencies of the therapeutic situation
- reference to a daily dosage unit may also include divided units which are admmistered over the course of each day of the cycle contemplated
- R 1 is selected from H, OH, NH 2 , C, to C 6 alkyl, substituted C, to C 6 alkyl, C 3 to C 6 alkenyl, substituted Ci to C 6 alkenyl, alkynyl, substituted alkynyl, or COR A ,
- R A is selected from H, Ci to C 3 alkyl, substituted C, to C 3 alkyl, aryl, substituted aryl, C* to C 3 alkoxy, substituted Ci to C 3 alkoxy, Ci to C 3 ammoalkyl, or substituted C- to C3 ammoalkyl,
- R 2 is selected from H, halogen, CN, N0 2 , C- to C 6 alkyl, substituted C- to C 6 alkyl, Ci to C 6 alkoxy, substituted Ci to C 6 alkoxy, Ci to C 6 ammoalkyl, or substituted Ci to C 6 ammoalkyl,
- R 3 is selected from a) or b) a) R 3 is a trisubstituted benzene rmg containing the substituents X,
- X is selected from the group of halogen, CN, d to C 3 alkyl, substituted Ci to C 3 alkyl, Ci to C 3 alkoxy, substituted Ci to C alkoxy, Ci to C 3 thioalkoxy, substituted Ci to C 3 thioalkoxy, Ci to C 3 ammoalkyl, substituted Ci to C 3 ammoalkyl, N0 2 , Ci to C 3 perfluoroalkyl, 5 or 6 membered heterocychc rmg containing 1 to 3 heteroatoms, COR B , OCOR B , or NR c COR B ,
- R B is H, Ci to C alkyl, substituted Ci to C 3 alkyl, aryl, substituted aryl, Ci to C 3 alkoxy, substituted Ci to C 3 alkoxy, Ci to C 3 aminoalkyl, or substituted Ci to C 3 aminoalkyl,
- R c is H, Ci to C 3 alkyl, or substituted Ci to C 3 alkyl,
- Y and Z are mdependent substituents taken from the group mcludmg H, halogen, CN, N0 2 , Ci to C alkoxy, Ci to C alkyl, or Ci to C 3 thioalkoxy, or b)
- R 3 is a five or six membered rmg with 1 , 2, or 3 heteroatoms from the group mcludmg O S, SO, S0 2 or NR 7 and containing one or two mdependent substituents from the group of H, halogen, CN, N0 2 and Ci to C 3 alkyl, Ci to C 3 alkoxy, Ci to C 3 ammoalkyl, COR D , or NR E COR D , R D is H, Ci to C 3 alkyl, substituted Ci to C 3 alkyl, aryl, substituted aryl, Ci to
- R E is H, Ci to C 3 alkyl, or substituted d to C alkyl,
- R 7 is H, or C, to C 3 alkyl, or a pharmaceutically acceptable salt thereof
- Preferred anti-pro gestational compounds of this mvention include those of the general formula described above wherein
- A is O, S, or NR 4 ,
- R 4 , R 5 , R 6 are mdependent substituents from the group mcludmg H, Ci to C 6 alkyl, substituted Ci to C 6 alkyl, C 2 to C 6 alkenyl, substituted C 2 to C 6 alkenyl, C 2 to C 6 alkynyl, substituted C 2 to C 6 alkynyl, C 3 to C 8 cycloalkyl, substituted C 3 to C 8 cycloalkyl, aryl, substituted aryl, heterocychc, substituted heterocychc, or cyclic alkyl constructed by fusing R 4 and R 5 to from a 5 to 7 membered ring, R 1 is H, OH, NH 2 , Ci to C 6 alkyl, substituted Ci to C 6 alkyl, or COR A ,
- R A is H, Ci to C 4 alkyl, C, to C 4 alkoxy,
- R 2 is H, halogen, N0 2 , Ci to C 3 alkyl, or substituted Ci to C 3 alkyl,
- R 3 is a disubstituted benzene rmg containing the substituents X and Y as shown below
- X is taken from the group of halogen, CN, Ci to C 3 alkoxy, Ci to C 3 alkyl, NO 2 , Ci to C3 perfluoroalkyl, 5 membered heterocychc ring containing 1 to 3 heteroatoms, or d to C 3 thioalkoxy,
- Y is a substituent on the 4' or 5' position from the group of H, halogen, CN, N0 , Ci to C 3 alkoxy, Ci to C alkyl, or Ci to C thioalkoxy, or
- R 3 is a five membered rmg with the structure
- R 7 is H, C, to C 3 alkyl, or C, to C 4 C0 2 alkyl,
- X' is selected from the group of halogen, CN, N0 , Ci to C 3 alkyl or Ci to C 3 alkoxy,
- Y' is H or Ci to C 4 alkyl
- R is a six membered ring with the structure
- X 1 is halogen, CN or N0 2 ,
- Another preferred progesterone receptor antagonist subgroup of this invention comprises compounds of the general formula
- R 1 is selected from H, OH, NH 2 , Ci to C 6 alkyl, substituted C, to C 6 alkyl, C 3 to C 6 alkenyl, substituted Ci to C 6 alkenyl, alkynyl, substituted alkynyl, or COR A ,
- R A is selected from H, Ci to C 3 alkyl, substituted Ci to C 3 alkyl, aryl, substituted aryl, Ci to C 3 alkoxy, substituted Ci to O* alkoxy, Ci to C 3 ammoalkyl, or substituted Ci to C3 ammoalkyl,
- R 4 is H, Ci to C 6 alkyl, substituted Ci to C 6 alkyl, C 2 to C 6 alkenyl, substituted C 2 to C 6 alkenyl, C 2 to C 6 alkynyl, substituted C 2 to C 6 alkynyl, C 3 to C 8 cycloalkyl, substituted C3 to C 8 cycloalkyl, benzyl, or substituted benzyl, and
- R 3 is selected from halogen or a disubstituted benzene rmg contammg the substituents X and Y as shown below
- X is taken from the group of halogen, CN, G to C 3 alkoxy, Ci to C 3 alkyl, N0 2 , Ci to C 3 perfluoroalkyl, or Ci to C thioalkoxy,
- Y is a substituent on the 4' or 5' position from the group of H, halogen, CN, N0 2 , Ci to C 3 alkoxy, G to C 4 alkyl, or G to C 3 thioalkoxy, or a pharmaceutically acceptable salt thereof
- the anti-pro gestational compounds of this mvention may contam an asymmet ⁇ c carbon atom and some of the compounds of this mvention may contam one or more asymmetric centers and may thus give rise to optical isomers and diastereomers While shown without respect to stereochemistry m Formula I, II. and III, the present mvention mcludes such optical isomers and diastereomers of these compounds, as well as the racemic and resolved, enantiomerically pure R and S stereoisomers, as well as other mixtures of the R and S stereo isomers and pharmaceutically acceptable salts thereof
- alkyl is used herein to refer to both straight- and branched-chain saturated aliphatic hydrocarbon groups havmg one to eight carbon atoms, preferably one to six carbon atoms
- alkenyl is mtended to include both straight- and branched- chain alkyl group with at least one carbon-carbon double bond and two to eight carbon atoms, preferably two to six carbon atoms
- alkynyl is mtended to cover both straight- and branched-chain alkyl group with at least one carbon-carbon triple bond and two to eight carbon atoms, preferably two to six carbon atoms
- substituted alkyl refers to alkyl, alkenyl, and alkynyl as just described having one or more substituents from the group mcludmg halogen, CN, OH, N0 2 , ammo, aryl, heterocychc, substituted aryl, substituted heterocychc, alkoxy, aryloxy, substituted alkyloxy, alkylcarbonyl, alkylcarboxy, alkylamino, arylthio
- substituents may be attached to any carbon of alkyl, alkenyl, or alkynyl group provided that the attachment constitutes a stable chemical moiety
- aryl is used herem to refer to an aromatic system which may be a smgle ring or multiple aromatic rmgs fused or linked together as such that at least one part of the fused or linked rings forms the conjugated aromatic system.
- the anti-pro gestm compounds of the present mvention can be prepared as described m the following schemes Sc eme I
- the anti-progestin compounds of this mvention, 5 can be easily prepared usmg an appropriate sulfur reagent such as Lawesson's reagent or P 2 Ss in a suitable solvent such as toluene, xylene, chlorobenzene at reflux under an inert atmosphere such as nitrogen or argon Scheme
- 5-aryl benzothiazolinones 7 can be readily effected from an appropriate 5-bromo-benzoth ⁇ azolmone 6 and a suitable electrophile such as aryl boronic acid, aryl tin reagent, or aryl zmc reagent via a suitable couplmg reaction as described for the synthesis of benzimidazo nones 4
- Conversion of 7 into 7a can be effected usmg an appropriate sulfur reagent such as Lawesson's reagent or P 2 Ss in a suitable solvent such as toluene, xylene, chlorobenzene at reflux under an inert atmosphere such as nitrogen or argon
- Compounds 14 and 17 can be prepared as shown m schemes V and VI from compound 4 and 7 using a strong basic condition such as heatmg the compound m a mixture of potassium hydroxide and ethylene glycol at 165 °C under an mert atmosphere such as argon or nitrogen
- alkyl or substituted alkyl derivatives 20 can be effected by treatment of compound A with a suitable base such as sodium hydride m suitable solvent such as DMF under an mert atmosphere such as argon or nitrogen followed by addition of an appropriate electrophile such as alkyl or substituted alkyl bromide, iodide, or inflate
- a suitable base such as sodium hydride m suitable solvent such as DMF
- an appropriate electrophile such as alkyl or substituted alkyl bromide, iodide, or inflate
- Such transformation of A at position- 1 can also be effected usmg a biphasic condition as mdicated m scheme VII m which alkylation is executed using a biphasic catalyst such as t ⁇ butylammonium bromide in a suitable solvent such as acetonit ⁇ le
- a biphasic catalyst such as t ⁇ butylammonium bromide in a suitable solvent such as acetonit
- the acylation or carboxylation of the compound A at position- 1 to give compound 21 can be readily effected by treatment of A with a suitable acylating or carboxylatmg reagent such as di-t-butyl dicarbonate m the presence of a suitable basic catalyst such as DMAP in a suitable solvent such as acetonit ⁇ le under an mert atmosphere such as argon or nitrogen
- a suitable acylating or carboxylatmg reagent such as di-t-butyl dicarbonate m the presence of a suitable basic catalyst such as DMAP in a suitable solvent such as acetonit ⁇ le under an mert atmosphere such as argon or nitrogen
- the animation of position- 1 of compound A to give compound 22 can be furnished usmg a suitable aminating reagent such as chloroamine m the presence of a suitable base such as sodium hydride in a suitable solvent such as THF or diethyl ether following the literature procedure (Metlesics et al J Or
- Scheme IX illustrates an approach to prepare the benzothiazinones
- an appropriately substituted o-amino benzenethiol 28 is treated with an appropriately substituted ⁇ -bromoacetate m a suitable solvent such as ethanol to afford compound 29 which can be readily coupled with an appropriate aryl boronic acid following the protocol of compound 9 to afford the compounds of this mvention, 30
- SO to 31 can be earned out using a suitable sulfur reagent such as Lawesson's reagent according to procedure of compounds 11a
- the compounds of the present mvention can be used m the form of salts derived from pharmaceutically or physiologically acceptable acids or bases
- These salts mclude, but are not limited to, the following salts with inorganic acids such as hydrochloric acid, sulfunc acid, nit ⁇ c acid, phosphoric acid and, as the case may be, such organic acids as acetic acid, oxalic acid, succinic acid, and maleic acid
- Other salts mclude salts with alkali metals or alkaline earth metals, such as sodium, potassium, calcium or magnesium m the form of esters, carbamates and other conventional "pro-drug" forms, which, when admmistered in such form, convert to the active moiety in vivo
- This mvention includes pharmaceutical compositions compnsmg one or more compounds of this invention, preferably m combmation with one or more pharmaceutically acceptable earners and/or excipients
- the mvention also mcludes methods of contraception and methods of treatmg or preventing maladies associated with the progesterone receptor, the methods compnsmg administering to a mammal m need thereof a pharmaceutically effective amount of one or more compounds as described above wherem Q is oxygen as antagonists of the progesterone receptor
- the mvention further provides comparable methods and compositions which utilize one or more compounds herein wherem Q is S, NR 6 , or CR 7 R 8 as agonists of the progesterone receptor
- the progesterone receptor antagonists of this mvention can be utilized m methods of contraception and the treatment and/or prevention of benign and malignant neoplastic disease
- Specific uses of the compounds and pharmaceutical compositions of mvention mclude the treatment and/or prevention of uterme myomet ⁇ al fibroids, endomet ⁇ osis, benign prostatic hypertrophy, carcmomas and adenocarcmomas of the endomet ⁇ um, ovary, breast, colon, prostate, pituitary, meningioma and other hormone-dependent tumors
- Additional uses of the present progesterone receptor antagonists mclude the synchronization of the estrus m livestock
- the progesterone receptor antagonists of the current mvention may be used either alone m a contmuous administration of between 0 1 and 500 mg per day, or alternatively used in a different regimen which would entail 2-4 days of treatment with the progesterone receptor antagonist after 21 days of a progestm
- this regimen between 0 1 and 500 mg daily doses of the progestm (e g levonorgestrel, t ⁇ megestone, gestodene, norethistrone acetate, norgestimate or cyproterone acetate) would be followed by between 0 1 and 500 mg daily doses of the progesterone receptor antagonists of the current mvention
- the progesterone receptor antagonists of this mvention can also be utilized in methods of treatment and/or prevention of benign and malignant neoplastic disease
- Specific uses of the compounds and pharmaceutical compositions of mvention include the treatment and/or prevention of uterme myometnal fibroids, endometnosis, benign prostatic hypertrophy, carcinomas and adenocarcmomas of the endomet ⁇ um, ovary, breast, colon, prostate, pituitary, memngioma and other hormone-dependent tumors
- Additional uses of the present progesterone receptor antagonists mclude the synchronization of the estrus m livestock
- the progesterone receptor agonists of this mvention used alone or in combination, can be utilized m methods of contraception and the treatment and/or prevention of dysfunctional bleeding, uterine leiomyomata, endometnosis, polycystic ovary syndrome, carcmomas and adenocarcmomas of the endomet ⁇ um,
- active compounds may be administered orally as well as by intravenous, intramuscular, or subcutaneous routes
- Solid earners mclude starch, lactose, dicalcium phosphate, microcrystalhne cellulose, sucrose and kaolm
- liquid carriers mclude ste ⁇ le water, polyethylene glycols, non-ionic surfactants and edible oils such as corn, peanut and sesame oils, as are appropriate to the nature of the active mgredient and the particular form of admmistration desired
- Adjuvants customarily employed m the preparation of pharmaceutical compositions may be advantageously included, such as flavormg agents, colormg agents, preservmg agents, and antioxidants, for example, vitamin E, ascorbic acid, BHT and BHA
- compositions from the standpoint of ease of preparation and administration are solid compositions, particularly tablets and hard- filled or hquid-filled capsules Oral admmistration of the compounds is preferred
- active compounds may also be administered parenterally or mtrape ⁇ toneally
- Solutions or suspensions of these active compounds as a free base or pharmacologically acceptable salt can be prepared in water suitably mixed with a surfactant such as hydroxypropylcellulose Dispersions can also be prepared m glycerol, liquid, polyethylene glycols and mixtures thereof m oils Under ordinary conditions of storage and use, these preparations contam a preservative to prevent the growth of microorganisms
- the pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions
- the form must be sterile and must be fluid to the extent that easy syrmge ability exits It must be stable under conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacterial and fungi
- the carrier can be a solvent or dispersion medium contammg, for example, water, ethanol (e g , glycerol, propylene glycol and liquid polyethylene glycol), suitable mixtures thereof, and vegetable oil
- the compounds of this invention were tested m the relevant assay as described below and their potency are m the range of 0 01 nM to 5 mM m the in vitro assays and 0 001 to 300 mg/kg m the in vivo assays The selected examples are listed in Table 1 and 2
- This assay is the determination of progestational and antiprogestational potency by usmg a cell proliferation assay m T47D cells A compound's effect on DNA synthesis in T47D cells is measured
- the materials and methods used m this assay are as follows a Growth medium DMEM F12 (1 1) (GIBCO, BRL) supplemented with 10% (v/v) fetal bovme serum (not heat- mactivated), lOOU/ml penicillin, lOOmg/ml streptomycin, and 2 mM GlutaMax (GIBCO, BRL) b Treatment medium Minimum Essential
- T ⁇ megestone and medroxyprogesterone acetate (MPA) are reference progestms and RU486 is the reference antiprogestm All reference compounds are run m full dose-response curves and the EC 50 or IC 50 values are calculated
- this procedure is used to evaluate the effect of progestms and antiprogestms on rat uterme decidualization and compare the relative potencies of various test compounds
- the materials and methods used m this assay are as follows a Methods: Test compounds are dissolved in 100% ethanol and mixed with corn oil (vehicle) Stock solutions of the test compounds m oil
- Ova ⁇ ectomized mature female Sprague-Dawley rats ( ⁇ 60-day old and 230g) are obtained from Tacorac (Taconic Farms, NY) following surgery Ova ⁇ ectomy is performed at least 10 days prior to treatment to reduce circulating sex steroids Animals are housed under 12 hr light/dark cycle and given standard rat chow and water ad libitum c Treatment
- Rats are weighed and randomly assigned to groups of 4 or 5 before treatment
- Test compounds in 0 2 ml vehicle are admmistered by subcutaneous injection m the nape of the neck or by gavage usmg 0 5 ml
- the animals are treated once daily for seven days
- testmg antiprogestins animals are given the test compounds and a EC50 dose of progesterone (5 6 mg/kg) during the first three days of treatment
- Folio wmg decidual stimulation animals contmue to receive progesterone until necropsy four days later d
- Doses are prepared based upon mg/kg mean group body weight In all studies, a control group receiving vehicle is included Determination of dose-response curves is carried out using doses with half log mcreases (e g 0 1, 0 3, 1 0, 3 0 mg/kg ) e Decidual mduction
- decidualization is induced in one of the uterme horns by scratching the antimesomet ⁇ al luminal epithehum with a blunt 21 G needle The contralateral horn is not scratched and serves as an unstimulated control
- rats are sacrificed by C ⁇ 2 asphyxiation and body weight measured Uteri are removed and trimmed of fat Decidualized (D-horn) and control (C-horn) uterme horns are weighed separately f Analysis of Results
- the mcrease in weight of the decidualized uterme horn is calculated by D-horn/C-horn and logarithmic transformation is used to maximize normality and homogeneity of variance
- the Huber M-estimator is used to down weight the outlymg transformed observations for both dose-response curve fitting and one-way analysis of variance JMP software (SAS Institute, Inc ) is used for both oneway ANOVA and non-hnear dose-response analyses g Reference Compounds
- Concentration Compound concentration m assay (default-mg/kg body weight) Route of admmistration Route the compound is administered to the animals Body weight Mean total animal body weight (default-kg)
- Progestational activity Compounds that mduce decidualization significantly (p ⁇ 0 05) compared to vehicle control are considered active
- Antiprogestational activity Compounds that decrease EC 0 progesterone induced decidualization significantly (p ⁇ 0 05)
- the object of this assay is to determine a compound's progestational or antiprogestational potency based on its effect on PRE-luciferase reporter activity m CV-1 cells co-transfected with human PR and PRE-luciferase plasmids
- the materials methods used in the assay are as follows a Growth medium DMEM (BioWhittaker) containing 10% (v/v) fetal bovme serum (heat mactivated), 0 1 mM MEM non- essential ammo acids, lOOU/ml penicillin, lOOmg/ml streptomycm, and 2 mM GlutaMax (GIBCO, BRL) Experimental medium DMEM (BioWhittaker), phenol red-free, contammg 10% (v/v) charcoal-stnpped fetal bovine serum (heat-mactivated), 0 1 mM MEM non-essential ammo acids, lOOU/ml penicillin, lOOm
- Each treatment consists of at least 4 replicates Log transformed data are used for analysis of variance and nonlinear dose response curve fittmg for both agonist and antagonist modes Huber weightmg is used to downweight the effects of outliers EC 50 or IC 50 values are calculated from the retransformed values JMP software (SAS Institute, Inc ) is used for both one-way analysis of variance and non-linear response analyses d Reference Compounds
- Progesterone and t ⁇ megestone are reference progestms and RU486 is the reference antiprogestm All reference compounds are run m full dose- response curves and the EC 5 o or IC 50 values are calculated
- Progestational activity Compounds that mcrease PRE-luciferase activity significantly (p ⁇ 0 05) compared to vehicle control are considered active
- Antiprogestational activity Compounds that decrease 3 nM progesterone mduced PRE-luciferase activity significantly (p ⁇ 0 05)
- this assay is to identif) progestins or antiprogestins by determmmg a compound's effect on alkalme phosphatase activity m T47D cells
- the matenals and methods used in this assay are as follows a. Culture medium DMEM F12 (1 1) (GIBCO, BRL) supplemented with 5% (v/v) charcoal stripped fetal bovme serum (not heat-mactivated), lOOU/ml penicillin, 100 ⁇ g/ml streptomycm, and 2 mM GlutaMax (GIBCO, BRL) b Alkalme phosphatase assay buffer
- Frozen T47D cells were thawed m a 37°C water bath and diluted to 280,000 cells/ml m culture medium.
- a 96-well plate (Falcon, Becton Dickinson Labware)
- 180 ⁇ l of diluted cell suspension was added
- Twenty ⁇ l of reference or test compounds diluted m the culture medium was then added to each well
- testmg for progestm antagorast activity reference antiprogestins or test compounds were added m the presence of 1 nM progesterone
- the cells were mcubated at 37°C in a 5% C0 2 /hum ⁇ d ⁇ fied atmosphere for 24 hr d Alkalme Phosphatase Enzyme Assay
- the medium was removed from the plate and fifty ⁇ l of assay buffer I was added to each well
- the plates were shaken m a titer plate shaker for 15 min
- 150 ⁇ l of assay buffer II was added to each well
- a dose response curve is generated for dose (X-axis) vs the rate of enzyme reaction (slope) (Y-axis)
- Square root-transformed data are used for analysis of variance and nonlinear dose response curve fittmg for both agonist and antagonist modes
- Huber weighting is used to downweight the effects of outliers
- EC50 or IC50 values are calculated from the retransformed values
- JMP software SAS Institute, Inc
- Reference Compounds Progesterone and tnmegestone are reference progestms and RU486 is the reference antiprogestm All reference compounds are run m full dose response curves and the EC50 or IC 50 values are calculated Table 10.
- Progesterone 1 0 839 0 030 0 706 0 996
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- Gynecology & Obstetrics (AREA)
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- Endocrinology (AREA)
- Reproductive Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
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Abstract
Description
Claims
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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US198249P | 1999-05-04 | ||
US552355 | 2000-04-19 | ||
US09/552,355 US6423699B1 (en) | 1999-05-04 | 2000-04-19 | Combination therapies using benzimidazolones |
PCT/US2000/011845 WO2000066168A1 (en) | 1999-05-04 | 2000-05-01 | Compositions containing benzimidazolones and progestogens |
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EP00932006A Withdrawn EP1173213A1 (en) | 1999-05-04 | 2000-05-01 | Compositions containing benzimidazolones and progestogens |
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EP (1) | EP1173213A1 (en) |
AU (1) | AU4980100A (en) |
WO (1) | WO2000066168A1 (en) |
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WO2004033459A1 (en) | 2002-10-11 | 2004-04-22 | Ligand Pharmaceuticals Incorporated | 5-(1',1'-CYCLOALKYL/ALKENYL)METHYLIDENE 1,2-DIHYDRO-5H-CHROMENO[3,4-f]QUINOLINES AS SELECTIVE PROGESTERONE RECEPTOR MODULATOR COMPOUNDS |
JP2006508076A (en) | 2002-10-11 | 2006-03-09 | リガンド・ファーマシューティカルズ・インコーポレイテッド | 5-Cycloalkenyl 5H-chromeno [3,4-f] quinoline derivatives as selective progesterone receptor modulator compounds |
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Publication number | Priority date | Publication date | Assignee | Title |
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DE3733478A1 (en) * | 1987-10-01 | 1989-04-13 | Schering Ag | ANTIGESTAGEN AND ANTIOOTROGENIC COMPOUNDS FOR THE INTRODUCTION OF BIRTH AND PREGNANCY, AND THE TREATMENT OF GYNAECOLOGICAL DISORDER AND HORMONE-RELATED TUMORS |
DE4330234A1 (en) * | 1993-09-02 | 1995-03-09 | Schering Ag | The use of progestogens and competitive progesterone antagonists for the production of pharmaceuticals for female fertility control and compositions comprising a progestogen and a competitive progesterone antagonist |
DE4344463A1 (en) * | 1993-12-22 | 1995-06-29 | Schering Ag | Combination product for contraception |
PT792152E (en) * | 1994-11-22 | 2004-07-30 | Balance Pharmaceuticals Inc | METHODS OF CONTRACEPTION |
US5521166A (en) * | 1994-12-19 | 1996-05-28 | Ortho Pharmaceitical Corporation | Antiprogestin cyclophasic hormonal regimen |
US5688808A (en) * | 1994-12-22 | 1997-11-18 | Ligand Pharmaceuticals Incorporated | Steroid receptor modulator compounds and methods |
TR199802705T2 (en) * | 1996-06-25 | 1999-03-22 | Akzo Nobel N.V. | Progestogens-anti-progestogens k�r� |
-
2000
- 2000-05-01 EP EP00932006A patent/EP1173213A1/en not_active Withdrawn
- 2000-05-01 WO PCT/US2000/011845 patent/WO2000066168A1/en not_active Application Discontinuation
- 2000-05-01 AU AU49801/00A patent/AU4980100A/en not_active Abandoned
Non-Patent Citations (1)
Title |
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See references of WO0066168A1 * |
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WO2000066168A1 (en) | 2000-11-09 |
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