OA11550A - Succinamide inhibitors of interleukin-1beta converting enzyme. - Google Patents
Succinamide inhibitors of interleukin-1beta converting enzyme. Download PDFInfo
- Publication number
- OA11550A OA11550A OA1200000305A OA1200000305A OA11550A OA 11550 A OA11550 A OA 11550A OA 1200000305 A OA1200000305 A OA 1200000305A OA 1200000305 A OA1200000305 A OA 1200000305A OA 11550 A OA11550 A OA 11550A
- Authority
- OA
- OAPI
- Prior art keywords
- methyl
- oxo
- butyrylamino
- hept
- dimethyl
- Prior art date
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- 239000003112 inhibitor Substances 0.000 title description 15
- 108090000426 Caspase-1 Proteins 0.000 title description 6
- SNCZNSNPXMPCGN-UHFFFAOYSA-N butanediamide Chemical compound NC(=O)CCC(N)=O SNCZNSNPXMPCGN-UHFFFAOYSA-N 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 89
- 238000000034 method Methods 0.000 claims abstract description 73
- 208000027866 inflammatory disease Diseases 0.000 claims abstract description 14
- 206010040070 Septic Shock Diseases 0.000 claims abstract description 12
- 230000036303 septic shock Effects 0.000 claims abstract description 12
- 208000024827 Alzheimer disease Diseases 0.000 claims abstract description 10
- 208000004429 Bacillary Dysentery Diseases 0.000 claims abstract description 10
- 206010040550 Shigella infections Diseases 0.000 claims abstract description 10
- 201000005113 shigellosis Diseases 0.000 claims abstract description 10
- 201000006417 multiple sclerosis Diseases 0.000 claims abstract description 8
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims abstract description 6
- 206010039073 rheumatoid arthritis Diseases 0.000 claims abstract description 5
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 4
- -1 hydrogên Chemical group 0.000 claims description 102
- 229910052739 hydrogen Inorganic materials 0.000 claims description 26
- 239000001257 hydrogen Substances 0.000 claims description 25
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 23
- 239000002253 acid Substances 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 19
- 102000004190 Enzymes Human genes 0.000 claims description 13
- 108090000790 Enzymes Proteins 0.000 claims description 13
- 230000005764 inhibitory process Effects 0.000 claims description 11
- JOOXCMJARBKPKM-UHFFFAOYSA-N laevulinic acid Natural products CC(=O)CCC(O)=O JOOXCMJARBKPKM-UHFFFAOYSA-N 0.000 claims description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 7
- 150000002431 hydrogen Chemical group 0.000 claims description 7
- 230000006378 damage Effects 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 208000027418 Wounds and injury Diseases 0.000 claims description 5
- 208000014674 injury Diseases 0.000 claims description 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 5
- 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- OMUHWSWPEYIRFO-UHFFFAOYSA-N 3-[[4-[2-(1-methylindol-3-yl)ethylamino]-4-oxo-2-propan-2-ylbutanoyl]amino]-4-oxobutanoic acid Chemical compound C1=CC=C2C(CCNC(=O)CC(C(C)C)C(=O)NC(CC(O)=O)C=O)=CN(C)C2=C1 OMUHWSWPEYIRFO-UHFFFAOYSA-N 0.000 claims description 3
- FYCCIUJXABECOW-UHFFFAOYSA-N 3-[[4-[2-(benzimidazol-1-yl)ethylamino]-4-oxo-2-propan-2-ylbutanoyl]amino]-4-oxobutanoic acid Chemical compound C1=CC=C2N(CCNC(=O)CC(C(C)C)C(=O)NC(CC(O)=O)C=O)C=NC2=C1 FYCCIUJXABECOW-UHFFFAOYSA-N 0.000 claims description 3
- WTFFVGDFKJYHDS-UHFFFAOYSA-N ethyl 4-oxo-3-[[4-oxo-4-(2-phenoxyethylamino)-2-propan-2-ylbutanoyl]amino]butanoate Chemical compound CCOC(=O)CC(C=O)NC(=O)C(C(C)C)CC(=O)NCCOC1=CC=CC=C1 WTFFVGDFKJYHDS-UHFFFAOYSA-N 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 125000001041 indolyl group Chemical class 0.000 claims description 3
- 230000002401 inhibitory effect Effects 0.000 claims description 3
- UXUNULFUFXVARP-UHFFFAOYSA-N 3-[(4-amino-4-oxo-2-propan-2-ylbutanoyl)amino]-4-oxo-5-(2-phenylethylsulfonylamino)pentanoic acid Chemical compound NC(=O)CC(C(C)C)C(=O)NC(CC(O)=O)C(=O)CNS(=O)(=O)CCC1=CC=CC=C1 UXUNULFUFXVARP-UHFFFAOYSA-N 0.000 claims description 2
- CFORYPHSPKDMEB-UHFFFAOYSA-N 3-[(4-amino-4-oxo-2-propan-2-ylbutanoyl)amino]-5-[(7,7-dimethyl-3-oxo-4-bicyclo[2.2.1]heptanyl)methylsulfonylamino]-4-oxopentanoic acid Chemical compound C1CC2CC(=O)C1(CS(=O)(=O)NCC(=O)C(CC(O)=O)NC(=O)C(CC(N)=O)C(C)C)C2(C)C CFORYPHSPKDMEB-UHFFFAOYSA-N 0.000 claims description 2
- XRUJXLILCDQUBR-UHFFFAOYSA-N 3-[[4-(2-indazol-1-ylethylamino)-4-oxo-2-propan-2-ylbutanoyl]amino]-4-oxobutanoic acid Chemical compound C1=CC=C2N(CCNC(=O)CC(C(C)C)C(=O)NC(CC(O)=O)C=O)N=CC2=C1 XRUJXLILCDQUBR-UHFFFAOYSA-N 0.000 claims description 2
- XBMQWXWDFFGISD-UHFFFAOYSA-N 3-[[4-[2-(5,6-dimethylbenzimidazol-1-yl)ethyl-methylamino]-4-oxo-2-propan-2-ylbutanoyl]amino]-4-oxobutanoic acid Chemical compound CC1=C(C)C=C2N(CCN(C)C(=O)CC(C(C)C)C(=O)NC(CC(O)=O)C=O)C=NC2=C1 XBMQWXWDFFGISD-UHFFFAOYSA-N 0.000 claims description 2
- ZRBDUXYZPRRPED-UHFFFAOYSA-N 3-[[4-[2-(5-fluoro-1-methylindol-3-yl)ethylamino]-4-oxo-2-propan-2-ylbutanoyl]amino]-4-oxobutanoic acid Chemical compound C1=C(F)C=C2C(CCNC(=O)CC(C(C)C)C(=O)NC(CC(O)=O)C=O)=CN(C)C2=C1 ZRBDUXYZPRRPED-UHFFFAOYSA-N 0.000 claims description 2
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- VLNYIOYVRRRCER-UHFFFAOYSA-N 5-[3-(1h-imidazol-2-yl)naphthalen-2-yl]oxy-4-oxo-3-[[4-oxo-4-(3-phenylpropylamino)-2-propan-2-ylbutanoyl]amino]pentanoic acid Chemical compound C=1C2=CC=CC=C2C=C(C=2NC=CN=2)C=1OCC(=O)C(CC(O)=O)NC(=O)C(C(C)C)CC(=O)NCCCC1=CC=CC=C1 VLNYIOYVRRRCER-UHFFFAOYSA-N 0.000 claims description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 claims description 2
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 claims description 2
- MZUVURCHWDQBDF-UHFFFAOYSA-N 3-[[2-methyl-4-oxo-4-(2-phenylethylamino)butanoyl]amino]-4-oxo-5-(2-phenylethylsulfonylamino)pentanoic acid Chemical compound C=1C=CC=CC=1CCS(=O)(=O)NCC(=O)C(CC(O)=O)NC(=O)C(C)CC(=O)NCCC1=CC=CC=C1 MZUVURCHWDQBDF-UHFFFAOYSA-N 0.000 claims 1
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- XGKBLVBCTNGOIU-UHFFFAOYSA-N 5-[(7,7-dimethyl-3-oxo-4-bicyclo[2.2.1]heptanyl)methylsulfonylamino]-3-[[2-ethyl-4-oxo-4-(3-phenylpropylamino)butanoyl]amino]-4-oxopentanoic acid Chemical compound C1CC(C2(C)C)CC(=O)C12CS(=O)(=O)NCC(=O)C(CC(O)=O)NC(=O)C(CC)CC(=O)NCCCC1=CC=CC=C1 XGKBLVBCTNGOIU-UHFFFAOYSA-N 0.000 claims 1
- ZDWCTMZEINUOOA-UHFFFAOYSA-N 5-[(7,7-dimethyl-3-oxo-4-bicyclo[2.2.1]heptanyl)methylsulfonylamino]-3-[[4-(3-naphthalen-2-ylpropylamino)-4-oxo-2-propan-2-ylbutanoyl]amino]-4-oxopentanoic acid Chemical compound C1=CC=CC2=CC(CCCNC(=O)CC(C(C)C)C(=O)NC(CC(O)=O)C(=O)CNS(=O)(=O)CC34C(CC(CC3)C4(C)C)=O)=CC=C21 ZDWCTMZEINUOOA-UHFFFAOYSA-N 0.000 claims 1
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- 125000000814 indol-3-yl group Chemical group [H]C1=C([H])C([H])=C2N([H])C([H])=C([*])C2=C1[H] 0.000 claims 1
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Classifications
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- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
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- C07C233/46—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
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- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
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- C07C311/12—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings
- C07C311/13—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings the carbon skeleton containing six-membered aromatic rings
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- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
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- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
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- C07D249/18—Benzotriazoles
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- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
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- C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
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- C07D307/32—Oxygen atoms
- C07D307/33—Oxygen atoms in position 2, the oxygen atom being in its keto or unsubstituted enol form
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- C07D311/06—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2
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- C07C2602/00—Systems containing two condensed rings
- C07C2602/36—Systems containing two condensed rings the rings having more than two atoms in common
- C07C2602/42—Systems containing two condensed rings the rings having more than two atoms in common the bicyclo ring system containing seven carbon atoms
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Peptides Or Proteins (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Furan Compounds (AREA)
- Pyrane Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Quinoline Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US8432098P | 1998-05-05 | 1998-05-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| OA11550A true OA11550A (en) | 2004-06-04 |
Family
ID=22184211
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| OA1200000305A OA11550A (en) | 1998-05-05 | 1999-04-30 | Succinamide inhibitors of interleukin-1beta converting enzyme. |
Country Status (27)
| Country | Link |
|---|---|
| EP (1) | EP1082127B1 (de) |
| JP (1) | JP2002513766A (de) |
| KR (1) | KR20010052307A (de) |
| CN (1) | CN1308542A (de) |
| AP (1) | AP2000001992A0 (de) |
| AT (1) | ATE298242T1 (de) |
| AU (1) | AU758120B2 (de) |
| BG (1) | BG105002A (de) |
| BR (1) | BR9911010A (de) |
| CA (1) | CA2327507A1 (de) |
| DE (1) | DE69925914T2 (de) |
| EA (1) | EA200001152A1 (de) |
| EE (1) | EE200000644A (de) |
| ES (1) | ES2242394T3 (de) |
| HR (1) | HRP20000744A2 (de) |
| HU (1) | HUP0101963A3 (de) |
| ID (1) | ID30124A (de) |
| IL (1) | IL139416A0 (de) |
| IS (1) | IS5674A (de) |
| NO (1) | NO20005537L (de) |
| OA (1) | OA11550A (de) |
| PL (1) | PL343837A1 (de) |
| SK (1) | SK16732000A3 (de) |
| TR (1) | TR200003252T2 (de) |
| WO (1) | WO1999056765A1 (de) |
| YU (1) | YU67900A (de) |
| ZA (1) | ZA200006881B (de) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002538151A (ja) | 1999-03-02 | 2002-11-12 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | カテプシンの可逆的インヒビターとして有用な化合物 |
| JP2002541237A (ja) | 1999-04-09 | 2002-12-03 | サイトビア インコーポレイテッド | カスパーゼインヒビターおよびその使用 |
| WO2001009110A1 (en) * | 1999-07-30 | 2001-02-08 | Boehringer Ingelheim Pharmaceuticals, Inc. | Novel succinate derivative compounds useful as cysteine protease inhibitors |
| CN1235875C (zh) | 1999-08-27 | 2006-01-11 | 西托维亚公司 | 取代的α-羟基酸天冬氨酸特异性半胱氨酸蛋白酶抑制剂及其用途 |
| US6420364B1 (en) | 1999-09-13 | 2002-07-16 | Boehringer Ingelheim Pharmaceuticals, Inc. | Compound useful as reversible inhibitors of cysteine proteases |
| US20020052323A1 (en) * | 2000-08-30 | 2002-05-02 | Jinhai Wang | Quinoline-(C=O)-(multiple amino acids)-leaving group compounds for pharmaceutical compositions and reagents |
| CA2447999C (en) * | 2001-05-23 | 2011-04-26 | Vertex Pharmaceuticals Incorporated | Caspase inhibitors and uses thereof |
| JP2005508979A (ja) | 2001-10-29 | 2005-04-07 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | システインプロテアーゼの可逆性インヒビターとして有用な化合物 |
| WO2003103599A2 (en) | 2002-06-05 | 2003-12-18 | Sunesis Pharmaceuticals, Inc. | Caspase-1 inhibitors and methods for their use |
| US7297714B2 (en) * | 2003-10-21 | 2007-11-20 | Irm Llc | Inhibitors of cathepsin S |
| MXPA06013256A (es) | 2004-05-15 | 2007-02-08 | Vertex Pharma | Tratamiento de crisis convulsivas utilizando inhibidores ice. |
| CA2567080A1 (en) | 2004-05-27 | 2005-12-15 | Vertex Pharmaceuticals Incorporated | Ice inhibitors for the treatment of autoinflammatory diseases |
| US7671069B2 (en) | 2006-03-30 | 2010-03-02 | Chemocentryx, Inc. | Tricyclic, heteroaromatic compounds modulating CXCR4 and/ or CXCR7 |
| US7807704B2 (en) | 2006-03-30 | 2010-10-05 | Chemocentryx, Inc. | Bicyclic, nitrogen-containing compounds modulating CXCR4 and/or CCXCKR2 |
| US9365612B2 (en) | 2010-01-29 | 2016-06-14 | United States Of America As Represented By The Secretary, Department Of Health And Human Services | Caspase inhibitors |
| US9116157B2 (en) | 2010-11-05 | 2015-08-25 | Brandeis University | Ice-cleaved alpha-synuclein as a biomarker |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW394760B (en) * | 1993-09-07 | 2000-06-21 | Hoffmann La Roche | Novel Carboxamides, process for their preparation and pharmaceutical composition containing the same |
-
1999
- 1999-04-30 SK SK1673-2000A patent/SK16732000A3/sk unknown
- 1999-04-30 OA OA1200000305A patent/OA11550A/en unknown
- 1999-04-30 AU AU36730/99A patent/AU758120B2/en not_active Ceased
- 1999-04-30 ES ES99918930T patent/ES2242394T3/es not_active Expired - Lifetime
- 1999-04-30 CN CN99808265A patent/CN1308542A/zh active Pending
- 1999-04-30 ID IDW20002501A patent/ID30124A/id unknown
- 1999-04-30 TR TR2000/03252T patent/TR200003252T2/xx unknown
- 1999-04-30 YU YU67900A patent/YU67900A/sh unknown
- 1999-04-30 KR KR1020007012300A patent/KR20010052307A/ko not_active Withdrawn
- 1999-04-30 IL IL13941699A patent/IL139416A0/xx unknown
- 1999-04-30 AP APAP/P/2000/001992A patent/AP2000001992A0/en unknown
- 1999-04-30 PL PL99343837A patent/PL343837A1/xx not_active Application Discontinuation
- 1999-04-30 EE EEP200000644A patent/EE200000644A/xx unknown
- 1999-04-30 HR HR20000744A patent/HRP20000744A2/hr not_active Application Discontinuation
- 1999-04-30 AT AT99918930T patent/ATE298242T1/de not_active IP Right Cessation
- 1999-04-30 EA EA200001152A patent/EA200001152A1/ru unknown
- 1999-04-30 DE DE69925914T patent/DE69925914T2/de not_active Expired - Fee Related
- 1999-04-30 BR BR9911010-5A patent/BR9911010A/pt not_active IP Right Cessation
- 1999-04-30 HU HU0101963A patent/HUP0101963A3/hu unknown
- 1999-04-30 EP EP99918930A patent/EP1082127B1/de not_active Expired - Lifetime
- 1999-04-30 JP JP2000546789A patent/JP2002513766A/ja active Pending
- 1999-04-30 WO PCT/US1999/009463 patent/WO1999056765A1/en not_active Ceased
- 1999-04-30 CA CA002327507A patent/CA2327507A1/en not_active Abandoned
-
2000
- 2000-10-20 IS IS5674A patent/IS5674A/is unknown
- 2000-11-02 NO NO20005537A patent/NO20005537L/no not_active Application Discontinuation
- 2000-11-23 ZA ZA200006881A patent/ZA200006881B/en unknown
- 2000-11-29 BG BG105002A patent/BG105002A/bg unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PL343837A1 (en) | 2001-09-10 |
| DE69925914T2 (de) | 2006-05-11 |
| ES2242394T3 (es) | 2005-11-01 |
| JP2002513766A (ja) | 2002-05-14 |
| CA2327507A1 (en) | 1999-11-11 |
| HRP20000744A2 (en) | 2001-06-30 |
| TR200003252T2 (tr) | 2001-04-20 |
| DE69925914D1 (de) | 2005-07-28 |
| AU3673099A (en) | 1999-11-23 |
| EP1082127A1 (de) | 2001-03-14 |
| SK16732000A3 (sk) | 2001-06-11 |
| AP2000001992A0 (en) | 2000-12-31 |
| ZA200006881B (en) | 2002-05-25 |
| YU67900A (sh) | 2002-12-10 |
| EP1082127A4 (de) | 2002-10-09 |
| WO1999056765A1 (en) | 1999-11-11 |
| BG105002A (bg) | 2001-07-31 |
| AU758120B2 (en) | 2003-03-13 |
| KR20010052307A (ko) | 2001-06-25 |
| IL139416A0 (en) | 2001-11-25 |
| CN1308542A (zh) | 2001-08-15 |
| ID30124A (id) | 2001-11-08 |
| HUP0101963A3 (en) | 2003-07-28 |
| HUP0101963A2 (hu) | 2001-10-28 |
| ATE298242T1 (de) | 2005-07-15 |
| EE200000644A (et) | 2002-04-15 |
| EP1082127B1 (de) | 2005-06-22 |
| EA200001152A1 (ru) | 2001-06-25 |
| NO20005537L (no) | 2000-12-20 |
| IS5674A (is) | 2000-10-20 |
| BR9911010A (pt) | 2005-12-06 |
| NO20005537D0 (no) | 2000-11-02 |
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