JP2005539088A5 - - Google Patents
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- Publication number
- JP2005539088A5 JP2005539088A5 JP2004559025A JP2004559025A JP2005539088A5 JP 2005539088 A5 JP2005539088 A5 JP 2005539088A5 JP 2004559025 A JP2004559025 A JP 2004559025A JP 2004559025 A JP2004559025 A JP 2004559025A JP 2005539088 A5 JP2005539088 A5 JP 2005539088A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- benzo
- formula
- pharmaceutically acceptable
- acceptable salt
- 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.)
- Granted
Links
- 125000000623 heterocyclic group Chemical group 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 6
- 150000003839 salts Chemical class 0.000 claims 4
- 239000011780 sodium chloride Substances 0.000 claims 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- 206010007559 Cardiac failure congestive Diseases 0.000 claims 2
- 206010020772 Hypertension Diseases 0.000 claims 2
- 201000006233 congestive heart failure Diseases 0.000 claims 2
- 230000003205 diastolic Effects 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 125000001475 halogen functional group Chemical group 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 0 CC**1*(C)CC(*C)C([C@@](C(*)(CC)C(CCC(*)CC2)CC*(C)*2N)C2=CCCC(C)(*)CC(C)(*)CCC2*C)=CCCC1 Chemical compound CC**1*(C)CC(*C)C([C@@](C(*)(CC)C(CCC(*)CC2)CC*(C)*2N)C2=CCCC(C)(*)CC(C)(*)CCC2*C)=CCCC1 0.000 description 2
- DWAWUJTUMDEWBR-UHFFFAOYSA-N CC(C)(C)c(cc1)cc2c1[nH]cn2 Chemical compound CC(C)(C)c(cc1)cc2c1[nH]cn2 DWAWUJTUMDEWBR-UHFFFAOYSA-N 0.000 description 1
Description
Claims (5)
- 式:
[式中、
「A」は、
「B」は、
XおよびYは一緒になって、−CH2−CH2−、−CH2−O−または−O−CH2−を表す;
R4〜R7はそれぞれ独立して、水素、ヒドロキシ、ハロ、(C1−C6)アルキル、(C1−C6)アルコキシまたはOR14(ここで、R14は、(C1−C4)アルキル−アリール、(C1−C4)アルキル−置換アリール、(C1−C4)アルキル−複素環または(C1−C4)アルキル−(C3−C7)シクロアルキルを表す)を表す;
R8は、水素、ハロ、(C1−C6)アルキル、ヒドロキシメチル、(C1−C4)アルキル−(C1−C6)アルコキシまたはCOR12(ここで、R12は、(C1−C6)アルコキシ、(C3−C7)シクロアルキル、フェニルまたは置換アリールを表す)を表す]
で示される新規な式Iの化合物またはその医薬的に許容しうる塩。 - 収縮期または拡張期鬱血性心不全または高血圧の治療用医薬の製造のための、請求項1に記載の化合物の使用。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US39199202P | 2002-06-26 | 2002-06-26 | |
PCT/US2003/016213 WO2004052847A2 (en) | 2002-06-26 | 2003-06-13 | Tricyclic steroid hormone nuclear receptor modulators |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2005539088A JP2005539088A (ja) | 2005-12-22 |
JP2005539088A5 true JP2005539088A5 (ja) | 2006-07-27 |
JP4395076B2 JP4395076B2 (ja) | 2010-01-06 |
Family
ID=32507560
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2004559025A Expired - Fee Related JP4395076B2 (ja) | 2002-06-26 | 2003-06-13 | 三環式ステロイドホルモン核内受容体モジュレーター |
Country Status (27)
Country | Link |
---|---|
US (2) | US7411072B2 (ja) |
EP (1) | EP1519915B1 (ja) |
JP (1) | JP4395076B2 (ja) |
KR (1) | KR20050013255A (ja) |
CN (2) | CN101161641A (ja) |
AR (1) | AR044526A1 (ja) |
AT (1) | ATE432257T1 (ja) |
AU (1) | AU2003302220B2 (ja) |
BR (1) | BR0312095A (ja) |
CA (1) | CA2489276C (ja) |
CO (1) | CO5650160A2 (ja) |
CY (1) | CY1109490T1 (ja) |
DE (1) | DE60327767D1 (ja) |
DK (1) | DK1519915T3 (ja) |
EA (1) | EA200500088A1 (ja) |
EC (1) | ECSP045501A (ja) |
ES (1) | ES2325861T3 (ja) |
HR (1) | HRP20041187A2 (ja) |
MX (1) | MXPA04012998A (ja) |
NO (1) | NO20050397L (ja) |
PE (1) | PE20040587A1 (ja) |
PL (1) | PL374708A1 (ja) |
PT (1) | PT1519915E (ja) |
SI (1) | SI1519915T1 (ja) |
TW (1) | TW200400816A (ja) |
WO (1) | WO2004052847A2 (ja) |
ZA (1) | ZA200410293B (ja) |
Families Citing this family (45)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1697350B1 (en) | 2003-12-19 | 2008-06-25 | Eli Lilly And Company | Tricyclic steroid hormone nuclear receptor modulators |
US7482344B2 (en) | 2003-12-19 | 2009-01-27 | Eli Lilly And Company | Tricyclic steroid hormone nuclear receptor modulators |
WO2006008118A1 (en) * | 2004-07-16 | 2006-01-26 | Proteosys Ag | Muscarinic antagonists with parp and sir modulating activity as cytoprotective agents |
KR20070046150A (ko) * | 2004-07-28 | 2007-05-02 | 아이알엠 엘엘씨 | 스테로이드 호르몬 핵 수용체의 조절제로서의 화합물 및조성물 |
MX2007010318A (es) * | 2005-02-25 | 2007-10-17 | Irm Llc | Compuestos y composiciones que contienen espiro como moduladores de los receptores nucleares de hormonas esteroideas. |
DE102005022020A1 (de) * | 2005-05-12 | 2006-11-23 | Merckle Gmbh | Dibenzocycloheptanverbindungen und pharmazeutische Mittel, welche diese Verbindungen enthalten |
PE20070335A1 (es) * | 2005-08-30 | 2007-04-21 | Novartis Ag | Benzimidazoles sustituidos y metodos para su preparacion |
EP1951252A4 (en) * | 2005-10-21 | 2010-03-17 | Merck Sharp & Dohme | INHIBITORS OF TYROSINE KINASES |
EA014695B1 (ru) * | 2006-07-14 | 2010-12-30 | Эли Лилли Энд Компани | Модулятор рецепторов глюкокортикостероидов и его применение |
GB0614947D0 (en) * | 2006-07-27 | 2006-09-06 | Isis Innovation | Epitope reduction therapy |
EA016370B1 (ru) | 2006-10-31 | 2012-04-30 | Пфайзер Продактс Инк. | Пиразолиновые соединения в качестве антагонистов минералокортикоидных рецепторов |
JP4866901B2 (ja) | 2007-02-07 | 2012-02-01 | 協和発酵キリン株式会社 | 3環系化合物 |
TWI431010B (zh) | 2007-12-19 | 2014-03-21 | Lilly Co Eli | 礦皮質素受體拮抗劑及使用方法 |
EA017288B1 (ru) * | 2008-01-11 | 2012-11-30 | Эли Лилли Энд Компани | (E)-N-{3-[1-(8-ФТОР-11Н-10-ОКСА-1-АЗАДИБЕНЗО[a,d]ЦИКЛОГЕПТЕН-5-ИЛИДЕН)ПРОПИЛ]ФЕНИЛ}МЕТАНСУЛЬФОНАМИД В КАЧЕСТВЕ МОДУЛЯТОРА РЕЦЕПТОРОВ ГЛЮКОКОРТИКОИДОВ ДЛЯ ЛЕЧЕНИЯ РЕВМАТИЗМА |
JPWO2010001990A1 (ja) | 2008-07-03 | 2011-12-22 | 協和発酵キリン株式会社 | 四環系化合物 |
US8629135B2 (en) * | 2008-07-14 | 2014-01-14 | Queen's University At Kingston | Pharmaceutical compositions comprising RET inhibitors and methods for the treatment of cancer |
US20110190201A1 (en) * | 2008-07-24 | 2011-08-04 | Searete Llc | Method, device, and kit for maintaining physiological levels of steroid hormone in a subject |
US20100022494A1 (en) * | 2008-07-24 | 2010-01-28 | Searete Llc, A Limited Liability Corporation Of The State Of Delaware | Method, device, and kit for maintaining physiological levels of steroid hormone in a subject |
US20100022497A1 (en) * | 2008-07-24 | 2010-01-28 | Searete Llc, A Limited Liability Corporation Of The State Of Delaware | Method for treating or preventing a cardiovascular disease or condition utilizing estrogen receptor modulators based on APOE allelic profile of a mammalian subject |
US20100022991A1 (en) * | 2008-07-24 | 2010-01-28 | Searete Llc, A Limited Liability Corporation Of The State Of Delaware | System and device for maintaining physiological levels of steroid hormone in a subject |
US20100061976A1 (en) * | 2008-07-24 | 2010-03-11 | Searete Llc, A Limited Liability Corporation Of The State Of Delaware | Method for treating or preventing osteoporosis by reducing follicle stimulating hormone to cyclic physiological levels in a mammalian subject |
US8486980B2 (en) | 2008-08-06 | 2013-07-16 | Kyowa Hakko Kirin Co., Ltd. | Tricyclic compound |
WO2010104721A1 (en) | 2009-03-12 | 2010-09-16 | Eli Lilly And Company | Mineralocorticoid receptor antagonist and methods of use |
WO2011081173A1 (ja) * | 2009-12-29 | 2011-07-07 | 協和発酵キリン株式会社 | 四環系化合物 |
WO2011141456A1 (en) | 2010-05-10 | 2011-11-17 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and compositions for the treatment of fluid accumulation in and/ or under the retina |
EP2569310A1 (en) | 2010-05-11 | 2013-03-20 | Pfizer Inc | Morpholine compounds as mineralocorticoid receptor antagonists |
US9241944B2 (en) | 2010-06-16 | 2016-01-26 | Institut National De La Santé Et De La Recherche Médicale (Inserm) | Methods and compositions for stimulating reepithelialisation during wound healing |
MX2013010576A (es) * | 2011-03-15 | 2014-03-12 | Abbvie Inc | Moduladores de receptores de hormonas nucleares. |
KR20140070550A (ko) | 2011-08-16 | 2014-06-10 | 마운트 시나이 스쿨 오브 메디슨 | 항암제로서의 삼환식 화합물 |
TW201422590A (zh) | 2012-09-07 | 2014-06-16 | Abbvie Inc | 雜環核激素受體調節劑 |
AU2013333938A1 (en) | 2012-10-16 | 2015-04-09 | Almirall, S.A. | Pyrrolotriazinone derivatives as PI3K inhibitors |
WO2014094357A1 (en) | 2012-12-21 | 2014-06-26 | Abbvie Inc. | Heterocyclic nuclear hormone receptor modulators |
US9796717B2 (en) | 2013-02-19 | 2017-10-24 | Icahn School Of Medicine At Mount Sinai | Tricyclic heterocycles as anticancer agents |
JP2017507962A (ja) | 2014-03-11 | 2017-03-23 | アイカーン スクール オブ メディスン アット マウント サイナイIcahn School of Medicine at Mt. Sinai | 限定された三環式スルホンアミド |
JP2017512766A (ja) | 2014-03-11 | 2017-05-25 | アイカーン スクール オブ メディスン アット マウント サイナイIcahn School of Medicine at Mt. Sinai | 抗癌剤としてのトリシクリル−2−アミノシクロアルカノール由来スルホンアミド |
CN104402920B (zh) * | 2014-11-27 | 2018-04-03 | 河南科技学院 | 一种合成2‑卤代‑3‑频那醇硼酸酯‑5‑氯苯胺的方法 |
CN108349943A (zh) | 2015-09-09 | 2018-07-31 | 西奈山伊坎医学院 | 杂环受限三环磺酰胺作为抗癌试剂 |
CA2997784A1 (en) | 2015-09-09 | 2017-03-16 | Icahn School Of Medicine At Mount Sinai | Heterocyclic constrained tricyclic sulfonamides as anti-cancer agents |
JP6835836B2 (ja) | 2015-10-13 | 2021-02-24 | アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル | 脈絡膜血管新生の処置のための方法及び医薬組成物 |
EP3490606B8 (en) | 2016-07-26 | 2024-04-10 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Antagonist of mineralocorticoid receptor for the treatment of osteoarthritis |
TWI811400B (zh) * | 2018-07-20 | 2023-08-11 | 德商歌林達有限公司 | 經進一步取代之三唑并喹噁啉衍生物 |
US20230151425A1 (en) | 2020-03-11 | 2023-05-18 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods of determining whether a subject has or is at risk of having a central serous chorioretinopathy |
CN113101291A (zh) * | 2021-04-14 | 2021-07-13 | 浙江大学 | 磺酰胺类化合物在制备治疗自身免疫性疾病药物中的应用 |
CN113264917B (zh) * | 2021-05-28 | 2022-07-01 | 华南理工大学 | 一种抗乙肝病毒化合物及其制备方法和应用 |
WO2023031277A1 (en) | 2021-08-31 | 2023-03-09 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the treatment of ocular rosacea |
Family Cites Families (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1001822A (en) | 1960-08-26 | 1965-08-18 | Sandoz Ag | Improvements in or relating to homothiaxanthenes |
GB1043158A (en) | 1962-06-07 | 1966-09-21 | Sandoz Ag | Improvements in or relating to piperidylalkidene-5h-dibenzo(a,d)cycloheptenes |
US3205264A (en) | 1962-06-15 | 1965-09-07 | Merck & Co Inc | Process for the preparation of 10, 11-dihydro-5-(gamma-methyl-and dimethyl-amino propylidene)-5h-dibenzo[a, d] cycloheptene |
US3351588A (en) | 1965-09-14 | 1967-11-07 | American Home Prod | Dibenz [b, e] azepine derivative |
US3519621A (en) | 1967-10-16 | 1970-07-07 | American Home Prod | 5h-dibenzo(a,d)cycloheptene derivatives |
GB1242096A (en) | 1968-12-20 | 1971-08-11 | Labaz | Benzobenzofuranooxepine compounds and process for preparing the same |
US3859356A (en) | 1972-07-24 | 1975-01-07 | Sandoz Ag | Benzylidene substituted bicyclic and tricyclic compounds |
FI753701A (ja) | 1975-01-06 | 1976-07-07 | Sumitomo Chemical Co | |
US4282233B1 (en) | 1980-06-19 | 2000-09-05 | Schering Corp | Antihistaminic 11-(4-piperidylidene)-5h-benzoÄ5,6Ü-cyclohepta-Ä1,2Ü-pyridines |
FR2603713B1 (fr) | 1986-09-10 | 1992-07-24 | Canon Kk | Derive nouveau de 5h-dibenzo(a,d)cycloheptane-(ene)ylidene, son procede de production et support electrophotographique photosensible le contenant |
US5151545A (en) | 1987-10-13 | 1992-09-29 | Pfizer Inc. | 3,5-dihydroxy-6,8-nonadienoic acids and derivatives as hypocholesterolemic agents |
JPH01161245A (ja) | 1987-12-18 | 1989-06-23 | Canon Inc | 電子写真感光体 |
JPH01183663A (ja) | 1988-01-14 | 1989-07-21 | Canon Inc | 電子写真感光体 |
US4999363A (en) | 1988-06-09 | 1991-03-12 | Kyowa Hakko Kogyo Co., Ltd. | Tricyclic compounds |
JPH0232358A (ja) | 1988-07-21 | 1990-02-02 | Canon Inc | 電子写真感光体 |
JPH02113258A (ja) | 1988-10-21 | 1990-04-25 | Canon Inc | 電子写真感光体 |
US5093210A (en) | 1989-06-30 | 1992-03-03 | Ricoh Company, Ltd. | Electroluminescent device |
JPH0446352A (ja) | 1990-06-14 | 1992-02-17 | Minolta Camera Co Ltd | 感光体 |
JPH052278A (ja) | 1991-06-24 | 1993-01-08 | Konica Corp | 電子写真感光体 |
US5378701A (en) | 1991-12-27 | 1995-01-03 | Kyowa Hakko Kogyo | Tricyclic compounds |
EP0549352B1 (en) | 1991-12-27 | 2000-03-01 | Kyowa Hakko Kogyo Co., Ltd. | Tricyclic compounds as angiotensin II antagonists |
JPH05281765A (ja) | 1992-03-30 | 1993-10-29 | Kao Corp | 電子写真感光体 |
WO1997011071A1 (en) | 1995-09-19 | 1997-03-27 | Novo Nordisk A/S | Novel heterocyclic compounds |
JPH09101200A (ja) | 1995-10-05 | 1997-04-15 | Canon Inc | イメ−ジセンサ− |
NZ320580A (en) | 1995-10-16 | 1998-12-23 | Kyowa Hakko Kogyo Kk | Tricyclic compounds, preparation and pharmaceutical compositions thereof |
ZA9811898B (en) | 1997-12-29 | 2000-06-28 | Ortho Mcneil Pharm Inc | Anti-Inflammatory Compounds. |
PT1100483E (pt) * | 1998-07-30 | 2005-02-28 | Abbott Lab | Agentes anti-inflamatorios selectivos para glicocorticoide |
EP0984334B1 (en) | 1998-09-04 | 2004-12-01 | Canon Kabushiki Kaisha | Electrophotographic apparatus and process cartridge |
US6362188B1 (en) | 1998-12-18 | 2002-03-26 | Schering Corporation | Farnesyl protein transferase inhibitors |
EP1154997A4 (en) | 1999-01-26 | 2002-11-04 | Dana Farber Cancer Inst Inc | PHARMACEUTICALLY ACTIVE COMPOUNDS AND METHODS OF USE |
JP2001089680A (ja) | 1999-09-22 | 2001-04-03 | Fuji Photo Film Co Ltd | トリアリールアミン構造を有する新規な三置換エチレン系化合物 |
AU1604001A (en) | 2000-06-13 | 2001-12-24 | Pharmacia Corp | Use of an aldosterone antagonist for the treatment or prohpylaxis of aldosterone-mediated pathogenic effects |
CA2415078A1 (en) | 2000-07-27 | 2002-02-07 | Pharmacia Corporation | Aldosterone antagonist and cyclooxygenase-2 inhibitor combination therapy to prevent or treat inflammation-related cardiovascular disorders |
EP1313485B1 (en) | 2000-08-28 | 2005-10-12 | Pharmacia Corporation | Use of an aldosterone receptor antagonist to improve cognitive function |
GB0113232D0 (en) | 2001-05-31 | 2001-07-25 | Glaxo Group Ltd | Chemical process |
EP1697350B1 (en) * | 2003-12-19 | 2008-06-25 | Eli Lilly And Company | Tricyclic steroid hormone nuclear receptor modulators |
-
2003
- 2003-05-30 TW TW092114743A patent/TW200400816A/zh unknown
- 2003-06-13 CN CNA2007101121728A patent/CN101161641A/zh active Pending
- 2003-06-13 ES ES03810038T patent/ES2325861T3/es not_active Expired - Lifetime
- 2003-06-13 KR KR10-2004-7021263A patent/KR20050013255A/ko not_active Application Discontinuation
- 2003-06-13 DK DK03810038T patent/DK1519915T3/da active
- 2003-06-13 PT PT03810038T patent/PT1519915E/pt unknown
- 2003-06-13 EA EA200500088A patent/EA200500088A1/ru unknown
- 2003-06-13 EP EP03810038A patent/EP1519915B1/en not_active Expired - Lifetime
- 2003-06-13 SI SI200331630T patent/SI1519915T1/sl unknown
- 2003-06-13 JP JP2004559025A patent/JP4395076B2/ja not_active Expired - Fee Related
- 2003-06-13 WO PCT/US2003/016213 patent/WO2004052847A2/en active Application Filing
- 2003-06-13 CA CA2489276A patent/CA2489276C/en not_active Expired - Fee Related
- 2003-06-13 DE DE60327767T patent/DE60327767D1/de not_active Expired - Lifetime
- 2003-06-13 BR BR0312095-3A patent/BR0312095A/pt not_active IP Right Cessation
- 2003-06-13 AU AU2003302220A patent/AU2003302220B2/en not_active Expired - Fee Related
- 2003-06-13 PL PL03374708A patent/PL374708A1/xx not_active Application Discontinuation
- 2003-06-13 CN CNB038150980A patent/CN1331848C/zh not_active Expired - Fee Related
- 2003-06-13 US US10/517,010 patent/US7411072B2/en not_active Expired - Fee Related
- 2003-06-13 AT AT03810038T patent/ATE432257T1/de active
- 2003-06-13 MX MXPA04012998A patent/MXPA04012998A/es not_active Application Discontinuation
- 2003-06-25 AR ARP030102283A patent/AR044526A1/es unknown
- 2003-06-26 PE PE2003000645A patent/PE20040587A1/es not_active Application Discontinuation
-
2004
- 2004-12-14 HR HR20041187A patent/HRP20041187A2/hr not_active Application Discontinuation
- 2004-12-21 ZA ZA200410293A patent/ZA200410293B/xx unknown
- 2004-12-21 EC EC2004005501A patent/ECSP045501A/es unknown
- 2004-12-23 CO CO04128011A patent/CO5650160A2/es not_active Application Discontinuation
-
2005
- 2005-01-25 NO NO20050397A patent/NO20050397L/no not_active Application Discontinuation
-
2008
- 2008-07-15 US US12/173,059 patent/US20090149445A1/en not_active Abandoned
-
2009
- 2009-07-28 CY CY20091100806T patent/CY1109490T1/el unknown
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