JP2008524210A5 - - Google Patents
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- Publication number
- JP2008524210A5 JP2008524210A5 JP2007546609A JP2007546609A JP2008524210A5 JP 2008524210 A5 JP2008524210 A5 JP 2008524210A5 JP 2007546609 A JP2007546609 A JP 2007546609A JP 2007546609 A JP2007546609 A JP 2007546609A JP 2008524210 A5 JP2008524210 A5 JP 2008524210A5
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- methyl
- pharmaceutically acceptable
- dione
- 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.)
- Pending
Links
- 150000001875 compounds Chemical class 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 11
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 230000000414 obstructive effect Effects 0.000 claims description 3
- 208000023504 respiratory system disease Diseases 0.000 claims description 3
- 208000006673 asthma Diseases 0.000 claims description 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 4
- 239000002671 adjuvant Substances 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- AOSSJKMXLBALBV-JOCHJYFZSA-N (5s)-5-[[6-(2-cyclobutylpyrimidin-5-yl)-3,4-dihydro-1h-isoquinolin-2-yl]sulfonylmethyl]-5-methylimidazolidine-2,4-dione Chemical compound C1CC2=CC(C=3C=NC(=NC=3)C3CCC3)=CC=C2CN1S(=O)(=O)C[C@@]1(C)NC(=O)NC1=O AOSSJKMXLBALBV-JOCHJYFZSA-N 0.000 claims 1
- KFSHRBYTUSBDGT-OAQYLSRUSA-N (5s)-5-[[6-(2-cyclopropylpyrimidin-5-yl)-3,4-dihydro-1h-2,7-naphthyridin-2-yl]sulfonylmethyl]-5-ethylimidazolidine-2,4-dione Chemical compound C1CC2=CC(C=3C=NC(=NC=3)C3CC3)=NC=C2CN1S(=O)(=O)C[C@@]1(CC)NC(=O)NC1=O KFSHRBYTUSBDGT-OAQYLSRUSA-N 0.000 claims 1
- LDPJXGRNICHPCB-HXUWFJFHSA-N (5s)-5-[[6-(2-cyclopropylpyrimidin-5-yl)-3,4-dihydro-1h-2,7-naphthyridin-2-yl]sulfonylmethyl]-5-methylimidazolidine-2,4-dione Chemical compound C1CC2=CC(C=3C=NC(=NC=3)C3CC3)=NC=C2CN1S(=O)(=O)C[C@@]1(C)NC(=O)NC1=O LDPJXGRNICHPCB-HXUWFJFHSA-N 0.000 claims 1
- GNPKJIOJLOETEO-JOCHJYFZSA-N (5s)-5-[[6-(2-cyclopropylpyrimidin-5-yl)-3,4-dihydro-1h-isoquinolin-2-yl]sulfonylmethyl]-5-ethylimidazolidine-2,4-dione Chemical compound C1CC2=CC(C=3C=NC(=NC=3)C3CC3)=CC=C2CN1S(=O)(=O)C[C@@]1(CC)NC(=O)NC1=O GNPKJIOJLOETEO-JOCHJYFZSA-N 0.000 claims 1
- OEQLCXYTKIRISP-OAQYLSRUSA-N (5s)-5-[[6-(2-cyclopropylpyrimidin-5-yl)-3,4-dihydro-1h-isoquinolin-2-yl]sulfonylmethyl]-5-methylimidazolidine-2,4-dione Chemical compound C1CC2=CC(C=3C=NC(=NC=3)C3CC3)=CC=C2CN1S(=O)(=O)C[C@@]1(C)NC(=O)NC1=O OEQLCXYTKIRISP-OAQYLSRUSA-N 0.000 claims 1
- BMXGUKRYJMVPCE-OAQYLSRUSA-N (5s)-5-[[6-(6-cyclopropylpyridin-3-yl)-3,4-dihydro-1h-2,7-naphthyridin-2-yl]sulfonylmethyl]-5-methylimidazolidine-2,4-dione Chemical compound C1CC2=CC(C=3C=NC(=CC=3)C3CC3)=NC=C2CN1S(=O)(=O)C[C@@]1(C)NC(=O)NC1=O BMXGUKRYJMVPCE-OAQYLSRUSA-N 0.000 claims 1
- LPMNKIDUXUPDBL-QHCPKHFHSA-N (5s)-5-cyclopropyl-5-[[6-(2-cyclopropylpyrimidin-5-yl)-3,4-dihydro-1h-isoquinolin-2-yl]sulfonylmethyl]imidazolidine-2,4-dione Chemical compound N1C(=O)NC(=O)[C@@]1(C1CC1)CS(=O)(=O)N1CC2=CC=C(C=3C=NC(=NC=3)C3CC3)C=C2CC1 LPMNKIDUXUPDBL-QHCPKHFHSA-N 0.000 claims 1
- BIUIDDFOHIEILW-JOCHJYFZSA-N (5s)-5-methyl-5-[[6-[2-(1-methylcyclopropyl)pyrimidin-5-yl]-3,4-dihydro-1h-isoquinolin-2-yl]sulfonylmethyl]imidazolidine-2,4-dione Chemical compound N=1C=C(C=2C=C3CCN(CC3=CC=2)S(=O)(=O)C[C@]2(C)C(NC(=O)N2)=O)C=NC=1C1(C)CC1 BIUIDDFOHIEILW-JOCHJYFZSA-N 0.000 claims 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 claims 1
- 201000001320 Atherosclerosis Diseases 0.000 claims 1
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 235000012501 ammonium carbonate Nutrition 0.000 claims 1
- 239000001099 ammonium carbonate Substances 0.000 claims 1
- 150000001642 boronic acid derivatives Chemical class 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 201000006417 multiple sclerosis Diseases 0.000 claims 1
- 201000008482 osteoarthritis Diseases 0.000 claims 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 206010039073 rheumatoid arthritis Diseases 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 101000990902 Homo sapiens Matrix metalloproteinase-9 Proteins 0.000 description 2
- 102100030412 Matrix metalloproteinase-9 Human genes 0.000 description 2
- 0 *C(CS(I)(=O)=O)(C(N1)=O)NC1=O Chemical compound *C(CS(I)(=O)=O)(C(N1)=O)NC1=O 0.000 description 1
- 101000577881 Homo sapiens Macrophage metalloelastase Proteins 0.000 description 1
- 102100027998 Macrophage metalloelastase Human genes 0.000 description 1
- 208000037273 Pathologic Processes Diseases 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 210000000981 epithelium Anatomy 0.000 description 1
- 210000004969 inflammatory cell Anatomy 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000009545 invasion Effects 0.000 description 1
- 230000033001 locomotion Effects 0.000 description 1
- 210000001161 mammalian embryo Anatomy 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000009054 pathological process Effects 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 210000002993 trophoblast Anatomy 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0403085A SE0403085D0 (sv) | 2004-12-17 | 2004-12-17 | Novel componds |
| PCT/SE2005/001917 WO2006065215A1 (en) | 2004-12-17 | 2005-12-14 | Novel compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008524210A JP2008524210A (ja) | 2008-07-10 |
| JP2008524210A5 true JP2008524210A5 (https=) | 2009-01-29 |
Family
ID=34075235
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007546609A Pending JP2008524210A (ja) | 2004-12-17 | 2005-12-14 | メタロプロテイナーゼ阻害剤としての新規ヒダントイン誘導体 |
Country Status (23)
| Country | Link |
|---|---|
| US (2) | US7655664B2 (https=) |
| EP (1) | EP1831199B1 (https=) |
| JP (1) | JP2008524210A (https=) |
| KR (1) | KR20070090924A (https=) |
| CN (1) | CN101119987A (https=) |
| AR (1) | AR051795A1 (https=) |
| AT (1) | ATE545642T1 (https=) |
| AU (1) | AU2005317286B2 (https=) |
| BR (1) | BRPI0517035A (https=) |
| CA (1) | CA2590845A1 (https=) |
| ES (1) | ES2380670T3 (https=) |
| IL (1) | IL183599A (https=) |
| MX (1) | MX2007007023A (https=) |
| MY (1) | MY147770A (https=) |
| NO (1) | NO20073572L (https=) |
| NZ (1) | NZ555831A (https=) |
| RU (1) | RU2376301C2 (https=) |
| SA (1) | SA05260409B1 (https=) |
| SE (1) | SE0403085D0 (https=) |
| TW (1) | TW200635917A (https=) |
| UA (1) | UA90285C2 (https=) |
| WO (1) | WO2006065215A1 (https=) |
| ZA (1) | ZA200705075B (https=) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE0100902D0 (sv) | 2001-03-15 | 2001-03-15 | Astrazeneca Ab | Compounds |
| SE0202539D0 (sv) | 2002-08-27 | 2002-08-27 | Astrazeneca Ab | Compounds |
| SE0401762D0 (sv) * | 2004-07-05 | 2004-07-05 | Astrazeneca Ab | Novel compounds |
| US7648992B2 (en) * | 2004-07-05 | 2010-01-19 | Astrazeneca Ab | Hydantoin derivatives for the treatment of obstructive airway diseases |
| SE0403085D0 (sv) | 2004-12-17 | 2004-12-17 | Astrazeneca Ab | Novel componds |
| SE0403086D0 (sv) * | 2004-12-17 | 2004-12-17 | Astrazeneca Ab | Compounds |
| EP1859356B1 (en) * | 2005-03-16 | 2019-07-10 | Sensus Metering Systems Inc. | Method, system, apparatus, and computer program product for determining a physical location of a sensor |
| MX2007013595A (es) * | 2005-05-04 | 2008-01-24 | Renovis Inc | Compuestos heterociclicos fusionados y composiciones y usos de estos. |
| TW200740769A (en) * | 2006-03-16 | 2007-11-01 | Astrazeneca Ab | Novel process |
| TW200831488A (en) * | 2006-11-29 | 2008-08-01 | Astrazeneca Ab | Novel compounds |
| KR101271219B1 (ko) * | 2011-01-27 | 2013-06-07 | 광주과학기술원 | 신규한 하이단토인 유도체 및 이의 용도 |
| US9975880B2 (en) * | 2013-12-31 | 2018-05-22 | Ipsen Pharma S.A.S. | Imidazolidine-2,4-dione dervatives |
| US20200268728A1 (en) | 2016-12-20 | 2020-08-27 | Sumitomo Dainippon Pharma Co., Ltd. | Drug targeting cancer stem cell |
| TWI901650B (zh) * | 2020-03-26 | 2025-10-21 | 匈牙利商羅特格登公司 | 啶及吡啶并〔3,4-c〕嗒衍生物 |
| CA3244639A1 (en) | 2021-12-28 | 2025-06-13 | Nippon Shinyaku Co., Ltd. | Indazole compound and pharmaceutical |
| KR20250011204A (ko) * | 2022-05-30 | 2025-01-21 | 시노허브 파마슈티컬 씨오., 엘티디 | 유착 관련 질환을 예방 치료하는 약물의 제조에서 테트라히드로나프티리딘 유도체의 응용 |
Family Cites Families (84)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2327890A (en) * | 1940-04-17 | 1943-08-24 | Parke Davis & Co | Substituted phenoxyalkyl ethers |
| US2745875A (en) * | 1953-06-30 | 1956-05-15 | Hoechst Ag | Preparation of nu-acylamino-phenylpropane diols |
| US3452040A (en) * | 1966-01-05 | 1969-06-24 | American Home Prod | 5,5-disubstituted hydantoins |
| US3529019A (en) | 1968-04-23 | 1970-09-15 | Colgate Palmolive Co | Alkylaryloxy alanines |
| US3849574A (en) * | 1971-05-24 | 1974-11-19 | Colgate Palmolive Co | Alpha-substituted-beta-arylthioalkyl amino-acids,for increasing heart rate |
| US4315031A (en) * | 1977-09-01 | 1982-02-09 | Science Union Et Cie | Thiosubstituted amino acids |
| GB1601310A (en) * | 1978-05-23 | 1981-10-28 | Lilly Industries Ltd | Aryl hydantoins |
| US4529019A (en) * | 1981-07-28 | 1985-07-16 | The Crowell Corporation | Safe tire inflator |
| JPS6172762A (ja) | 1984-09-17 | 1986-04-14 | Kanegafuchi Chem Ind Co Ltd | 光学活性ヒダントイン類の製造法 |
| JPS61212292A (ja) * | 1985-03-19 | 1986-09-20 | Mitsui Toatsu Chem Inc | D−α−アミノ酸の製造方法 |
| CA1325222C (en) | 1985-08-23 | 1993-12-14 | Lederle (Japan), Ltd. | Process for producing 4-biphenylylacetic acid |
| GB8618559D0 (en) | 1986-07-30 | 1986-09-10 | Genetics Int Inc | Rhodococcus bacterium |
| JPH0279879A (ja) | 1988-09-17 | 1990-03-20 | Canon Inc | 画像形成装置 |
| US4983771A (en) * | 1989-09-18 | 1991-01-08 | Hexcel Corporation | Method for resolution of D,L-alpha-phenethylamine with D(-)mandelic acid |
| NL9000386A (nl) | 1990-02-16 | 1991-09-16 | Stamicarbon | Werkwijze voor de bereiding van optisch aktief aminozuuramide. |
| DK161690D0 (da) | 1990-07-05 | 1990-07-05 | Novo Nordisk As | Fremgangsmaade til fremstilling af enantiomere forbindelser |
| IL99957A0 (en) | 1990-11-13 | 1992-08-18 | Merck & Co Inc | Piperidinylcamphorsulfonyl oxytocin antagonists and pharmaceutical compositions containing them |
| PH31245A (en) | 1991-10-30 | 1998-06-18 | Janssen Pharmaceutica Nv | 1,3-Dihydro-2H-imidazoÄ4,5-BÜ-quinolin-2-one derivatives. |
| US5308853A (en) * | 1991-12-20 | 1994-05-03 | Warner-Lambert Company | Substituted-5-methylidene hydantoins with AT1 receptor antagonist properties |
| US5246943A (en) * | 1992-05-19 | 1993-09-21 | Warner-Lambert Company | Substituted 1,2,3,4-tetahydroisoquinolines with angiotensin II receptor antagonist properties |
| NL9201230A (nl) | 1992-07-09 | 1994-02-01 | Dsm Nv | Werkwijze voor de bereiding van optisch aktief methionineamide. |
| EP0640594A1 (en) | 1993-08-23 | 1995-03-01 | Fujirebio Inc. | Hydantoin derivative as metalloprotease inhibitor |
| AU687953B2 (en) | 1993-11-16 | 1998-03-05 | Merck & Co., Inc. | Piperidinylcamphorsulfonyl oxytocin antagonists |
| EP0709375B1 (en) | 1994-10-25 | 2005-05-18 | AstraZeneca AB | Therapeutic heterocycles |
| ZA96211B (en) | 1995-01-12 | 1996-07-26 | Teva Pharma | Compositions containing and methods of using 1- aminoindan and derivatives thereof and process for preparing optically active 1-aminoindan derivatives |
| US5863949A (en) | 1995-03-08 | 1999-01-26 | Pfizer Inc | Arylsulfonylamino hydroxamic acid derivatives |
| US6166041A (en) * | 1995-10-11 | 2000-12-26 | Euro-Celtique, S.A. | 2-heteroaryl and 2-heterocyclic benzoxazoles as PDE IV inhibitors for the treatment of asthma |
| WO1997019075A1 (en) * | 1995-11-22 | 1997-05-29 | Darwin Discovery Limited | Mercaptoalkylpeptidyl compounds having an imidazole substituent and their use as inhibitors of matrix metalloproteinases (mmp) and/or tumour necrosis factor (tnf) |
| GB9616643D0 (en) * | 1996-08-08 | 1996-09-25 | Chiroscience Ltd | Compounds |
| US5919790A (en) * | 1996-10-11 | 1999-07-06 | Warner-Lambert Company | Hydroxamate inhibitors of interleukin-1β converting enzyme |
| ATE212619T1 (de) * | 1996-10-22 | 2002-02-15 | Upjohn Co | Alpha-amino sulfonyl hydroxamsäure als matrix metalloproteinase inhibitoren |
| IL132170A0 (en) * | 1997-05-06 | 2001-03-19 | Novo Nordisk As | Novel heterocyclic compounds |
| DE59802394D1 (de) * | 1997-05-09 | 2002-01-24 | Hoechst Ag | Substituierte Diaminocarbonsäuren |
| NZ501166A (en) | 1997-07-31 | 2001-12-21 | Abbott Lab | Reverse hydroxamate-containing compounds and their use as inhibitors of matrix metalloproteinases |
| TW514634B (en) | 1997-10-14 | 2002-12-21 | Lilly Co Eli | Process to make chiral compounds |
| DE69811111T2 (de) | 1997-11-12 | 2003-07-24 | Darwin Discovery Ltd., Cambridge | Hydroxamsäure- und carbonsäurederivate mit mmp und tnf hemmender wirkung |
| RU2208609C2 (ru) | 1998-02-04 | 2003-07-20 | Новартис Аг | Сульфониламинопроизводные, которые ингибируют разлагающие матрикс металлопротеиназы |
| US6329418B1 (en) * | 1998-04-14 | 2001-12-11 | The Procter & Gamble Company | Substituted pyrrolidine hydroxamate metalloprotease inhibitors |
| EP1077974A1 (en) * | 1998-05-14 | 2001-02-28 | Du Pont Pharmaceuticals Company | Substituted aryl hydroxamic acids as metalloproteinase inhibitors |
| CN1295561A (zh) | 1998-06-03 | 2001-05-16 | Gpinil控股公司 | N-杂环羧酸或羧酸等排物的n-结合氨磺酰 |
| AU4692399A (en) * | 1998-06-17 | 2000-01-05 | Du Pont Pharmaceuticals Company | Cyclic hydroxamic acids as metalloproteinase inhibitors |
| FR2782082B3 (fr) * | 1998-08-05 | 2000-09-22 | Sanofi Sa | Formes cristallines de (r)-(+)-n-[[3-[1-benzoyl-3-(3,4- dichlorophenyl)piperidin-3-yl]prop-1-yl]-4-phenylpiperidin-4 -yl]-n-methylacetamide (osanetant) et procede pour la preparation dudit compose |
| US6339101B1 (en) * | 1998-08-14 | 2002-01-15 | Gpi Nil Holdings, Inc. | N-linked sulfonamides of N-heterocyclic carboxylic acids or isosteres for vision and memory disorders |
| EP1107953A1 (en) | 1998-08-29 | 2001-06-20 | British Biotech Pharmaceuticals Limited | Hydroxamic acid derivatives as proteinase inhibitors |
| GB9919776D0 (en) | 1998-08-31 | 1999-10-27 | Zeneca Ltd | Compoujnds |
| EP1117616B1 (en) | 1998-10-07 | 2003-04-23 | Yazaki Corporation | Sol-gel process using porous mold |
| DK1004578T3 (da) * | 1998-11-05 | 2004-06-28 | Pfizer Prod Inc | 5-oxo-pyrrolidin-2-carboxylsyrehydroxamidderivater |
| WO2000035886A2 (en) | 1998-12-18 | 2000-06-22 | Axys Pharmaceuticals, Inc. | (hetero)aryl-bicyclic heteroaryl derivatives, their preparation and their use as protease inhibitors |
| EP1150975A1 (en) | 1998-12-31 | 2001-11-07 | Aventis Pharmaceuticals Inc. | 1-carboxymethyl-2-oxo-azepan derivatives useful as selective inhibitors of mmp-12 |
| US6340691B1 (en) * | 1999-01-27 | 2002-01-22 | American Cyanamid Company | Alkynyl containing hydroxamic acid compounds as matrix metalloproteinase and tace inhibitors |
| KR100440643B1 (ko) | 1999-01-28 | 2004-07-21 | 쥬가이 세이야쿠 가부시키가이샤 | 치환 페네틸아민 유도체 |
| US6294694B1 (en) | 1999-06-04 | 2001-09-25 | Wisconsin Alumni Research Foundation | Matrix metalloproteinase inhibitors and method of using same |
| GB9916562D0 (en) | 1999-07-14 | 1999-09-15 | Pharmacia & Upjohn Spa | 3-Arylsulfonyl-2-(substituted-methyl) propanoic acid derivatives as matrix metalloproteinase inhibitora |
| US20020006920A1 (en) * | 1999-07-22 | 2002-01-17 | Robinson Ralph Pelton | Arylsulfonylamino hydroxamic acid derivatives |
| US6266453B1 (en) | 1999-07-26 | 2001-07-24 | Computerized Medical Systems, Inc. | Automated image fusion/alignment system and method |
| EP1078923B1 (en) * | 1999-08-02 | 2006-03-08 | F. Hoffmann-La Roche Ag | Process for the preparation of benzothiophene derivatives |
| KR20020060160A (ko) | 1999-08-12 | 2002-07-16 | 파마시아 이탈리아 에스.피.에이. | 3(5)-아미노-피라졸 유도체, 이의 제조 방법 및항종양제로서의 이의 용도 |
| SE9904044D0 (sv) | 1999-11-09 | 1999-11-09 | Astra Ab | Compounds |
| NZ519981A (en) * | 2000-01-20 | 2005-02-25 | Eisai Co Ltd | Nitrogenous cyclic compounds and pharmaceutical compositions containing the same |
| US6525202B2 (en) * | 2000-07-17 | 2003-02-25 | Wyeth | Cyclic amine phenyl beta-3 adrenergic receptor agonists |
| US20020065219A1 (en) * | 2000-08-15 | 2002-05-30 | Naidu B. Narasimhulu | Water soluble thiazolyl peptide derivatives |
| US20020091107A1 (en) * | 2000-09-08 | 2002-07-11 | Madar David J. | Oxazolidinone antibacterial agents |
| EP1191024A1 (en) | 2000-09-22 | 2002-03-27 | Harald Tschesche | Thiadiazines and their use as inhibitors of metalloproteinases |
| SE0100903D0 (sv) * | 2001-03-15 | 2001-03-15 | Astrazeneca Ab | Compounds |
| JP2004527511A (ja) * | 2001-03-15 | 2004-09-09 | アストラゼネカ・アクチエボラーグ | メタロプロテイナーゼ阻害剤 |
| SE0100902D0 (sv) * | 2001-03-15 | 2001-03-15 | Astrazeneca Ab | Compounds |
| US6890915B2 (en) * | 2001-05-25 | 2005-05-10 | Bristol-Myers Squibb Pharma Company | Hydantoins and related heterocycles as inhibitors of matrix metalloproteinases and/or TNF-α converting enzyme (TACE) |
| GB0114004D0 (en) * | 2001-06-08 | 2001-08-01 | Glaxo Group Ltd | Chemical compounds |
| SE0103710D0 (sv) * | 2001-11-07 | 2001-11-07 | Astrazeneca Ab | Compounds |
| JP4485941B2 (ja) | 2002-06-05 | 2010-06-23 | 株式会社カネカ | 光学活性α−メチルシステイン誘導体の製造方法 |
| SE0202539D0 (sv) * | 2002-08-27 | 2002-08-27 | Astrazeneca Ab | Compounds |
| SE0202693D0 (sv) * | 2002-09-11 | 2002-09-11 | Astrazeneca Ab | Compounds |
| GB0221246D0 (en) * | 2002-09-13 | 2002-10-23 | Astrazeneca Ab | Compounds |
| AU2003282920A1 (en) * | 2002-10-04 | 2004-05-04 | Bristol-Myers Squibb Company | Hydantoin derivatives as inhibitors of matrix metalloproteinases and/or tnf-alpha converting enzyme (tace) |
| US7132432B2 (en) * | 2003-06-05 | 2006-11-07 | Bristol-Myers Squibb Company | Hydantoin derivatives as inhibitors of tumor necrosis factor-alpha converting enzyme (TACE) |
| US20040266832A1 (en) * | 2003-06-26 | 2004-12-30 | Li Zheng J. | Crystal forms of 2-(3-difluoromethyl-5-phenyl-pyrazol-1-yl)-5-methanesulfonyl pyridine |
| TWI220073B (en) * | 2003-07-24 | 2004-08-01 | Au Optronics Corp | Method for manufacturing polysilicon film |
| US7648992B2 (en) * | 2004-07-05 | 2010-01-19 | Astrazeneca Ab | Hydantoin derivatives for the treatment of obstructive airway diseases |
| SE0401762D0 (sv) | 2004-07-05 | 2004-07-05 | Astrazeneca Ab | Novel compounds |
| SE0401763D0 (sv) * | 2004-07-05 | 2004-07-05 | Astrazeneca Ab | Compounds |
| SE0403085D0 (sv) | 2004-12-17 | 2004-12-17 | Astrazeneca Ab | Novel componds |
| SE0403086D0 (sv) * | 2004-12-17 | 2004-12-17 | Astrazeneca Ab | Compounds |
| TW200740769A (en) * | 2006-03-16 | 2007-11-01 | Astrazeneca Ab | Novel process |
| TW200831488A (en) * | 2006-11-29 | 2008-08-01 | Astrazeneca Ab | Novel compounds |
-
2004
- 2004-12-17 SE SE0403085A patent/SE0403085D0/sv unknown
-
2005
- 2005-12-14 US US11/721,586 patent/US7655664B2/en not_active Expired - Fee Related
- 2005-12-14 MX MX2007007023A patent/MX2007007023A/es active IP Right Grant
- 2005-12-14 RU RU2007126746/04A patent/RU2376301C2/ru not_active IP Right Cessation
- 2005-12-14 EP EP05815745A patent/EP1831199B1/en not_active Expired - Lifetime
- 2005-12-14 KR KR1020077013489A patent/KR20070090924A/ko not_active Ceased
- 2005-12-14 CA CA002590845A patent/CA2590845A1/en not_active Abandoned
- 2005-12-14 CN CNA2005800481778A patent/CN101119987A/zh active Pending
- 2005-12-14 JP JP2007546609A patent/JP2008524210A/ja active Pending
- 2005-12-14 AU AU2005317286A patent/AU2005317286B2/en not_active Ceased
- 2005-12-14 ES ES05815745T patent/ES2380670T3/es not_active Expired - Lifetime
- 2005-12-14 NZ NZ555831A patent/NZ555831A/en not_active IP Right Cessation
- 2005-12-14 AT AT05815745T patent/ATE545642T1/de active
- 2005-12-14 UA UAA200706657A patent/UA90285C2/ru unknown
- 2005-12-14 WO PCT/SE2005/001917 patent/WO2006065215A1/en not_active Ceased
- 2005-12-14 BR BRPI0517035-4A patent/BRPI0517035A/pt not_active IP Right Cessation
- 2005-12-15 MY MYPI20055915A patent/MY147770A/en unknown
- 2005-12-15 AR ARP050105273A patent/AR051795A1/es not_active Application Discontinuation
- 2005-12-16 TW TW094144602A patent/TW200635917A/zh unknown
- 2005-12-17 SA SA05260409A patent/SA05260409B1/ar unknown
-
2007
- 2007-05-31 IL IL183599A patent/IL183599A/en not_active IP Right Cessation
- 2007-06-12 ZA ZA200705075A patent/ZA200705075B/xx unknown
- 2007-07-10 NO NO20073572A patent/NO20073572L/no not_active Application Discontinuation
-
2010
- 2010-02-01 US US12/697,625 patent/US20100256166A1/en not_active Abandoned
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