JP2005514334A5 - - Google Patents
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- Publication number
- JP2005514334A5 JP2005514334A5 JP2003535802A JP2003535802A JP2005514334A5 JP 2005514334 A5 JP2005514334 A5 JP 2005514334A5 JP 2003535802 A JP2003535802 A JP 2003535802A JP 2003535802 A JP2003535802 A JP 2003535802A JP 2005514334 A5 JP2005514334 A5 JP 2005514334A5
- Authority
- JP
- Japan
- Prior art keywords
- benzamide
- prop
- ynyl
- phenyl
- benzyl
- 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
- -1 3- (4-methoxy-phenyl) -prop-1-ynyl Chemical group 0.000 claims 24
- 150000003839 salts Chemical class 0.000 claims 10
- 150000001875 compounds Chemical class 0.000 claims 9
- 125000001072 heteroaryl group Chemical group 0.000 claims 7
- 125000003118 aryl group Chemical group 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 4
- 125000003107 substituted aryl group Chemical group 0.000 claims 4
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 239000000825 pharmaceutical preparation Substances 0.000 claims 3
- 229940127557 pharmaceutical product Drugs 0.000 claims 3
- 239000003085 diluting agent Substances 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 201000008482 osteoarthritis Diseases 0.000 claims 2
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 206010039073 rheumatoid arthritis Diseases 0.000 claims 2
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- XLBCEMUGMYDSRN-UHFFFAOYSA-N 3-(2-phenylethynyl)-n-[(4-sulfamoylphenyl)methyl]benzamide Chemical compound C1=CC(S(=O)(=O)N)=CC=C1CNC(=O)C1=CC=CC(C#CC=2C=CC=CC=2)=C1 XLBCEMUGMYDSRN-UHFFFAOYSA-N 0.000 claims 1
- 125000006275 3-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C([H])C(*)=C1[H] 0.000 claims 1
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims 1
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims 1
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims 1
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 1
- GQKUGTWMEZWVAM-UHFFFAOYSA-N 4-[[[3-(3-pyridin-3-ylprop-1-ynyl)benzoyl]amino]methyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1CNC(=O)C1=CC=CC(C#CCC=2C=NC=CC=2)=C1 GQKUGTWMEZWVAM-UHFFFAOYSA-N 0.000 claims 1
- VAMZQGYMTJNWBX-UHFFFAOYSA-N 4-[[[3-(3-pyridin-4-ylprop-1-ynyl)benzoyl]amino]methyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1CNC(=O)C1=CC=CC(C#CCC=2C=CN=CC=2)=C1 VAMZQGYMTJNWBX-UHFFFAOYSA-N 0.000 claims 1
- MZGJMFQQVDXRTB-UHFFFAOYSA-N 4-[[[3-[3-(2-methoxypyridin-4-yl)prop-1-ynyl]benzoyl]amino]methyl]benzoic acid Chemical compound C1=NC(OC)=CC(CC#CC=2C=C(C=CC=2)C(=O)NCC=2C=CC(=CC=2)C(O)=O)=C1 MZGJMFQQVDXRTB-UHFFFAOYSA-N 0.000 claims 1
- WVQMWJAOKFFFEQ-UHFFFAOYSA-N 4-[[[3-[3-(4-chlorophenyl)prop-1-ynyl]benzoyl]amino]methyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1CNC(=O)C1=CC=CC(C#CCC=2C=CC(Cl)=CC=2)=C1 WVQMWJAOKFFFEQ-UHFFFAOYSA-N 0.000 claims 1
- NFICNNZYWGKBEK-UHFFFAOYSA-N 4-[[[3-[3-(4-fluorophenyl)prop-1-ynyl]benzoyl]amino]methyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1CNC(=O)C1=CC=CC(C#CCC=2C=CC(F)=CC=2)=C1 NFICNNZYWGKBEK-UHFFFAOYSA-N 0.000 claims 1
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims 1
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 claims 1
- ZPCOCTGRERLUOF-UHFFFAOYSA-N 4-ethynyl-2-methyl-3-(2-phenylethyl)-n-pyridin-4-ylbenzamide Chemical compound CC1=C(C(=O)NC=2C=CN=CC=2)C=CC(C#C)=C1CCC1=CC=CC=C1 ZPCOCTGRERLUOF-UHFFFAOYSA-N 0.000 claims 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 1
- 239000005711 Benzoic acid Substances 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 claims 1
- VNWSHLWRKWRHEV-UHFFFAOYSA-N n-[(4-cyanophenyl)methyl]-3-(2-phenylethynyl)benzamide Chemical compound C=1C=CC(C#CC=2C=CC=CC=2)=CC=1C(=O)NCC1=CC=C(C#N)C=C1 VNWSHLWRKWRHEV-UHFFFAOYSA-N 0.000 claims 1
- KSJYWNSZYXHQMB-UHFFFAOYSA-N n-[(4-cyanophenyl)methyl]-3-[3-(1,2,4-triazol-1-yl)prop-1-ynyl]benzamide Chemical compound C=1C=CC(C#CCN2N=CN=C2)=CC=1C(=O)NCC1=CC=C(C#N)C=C1 KSJYWNSZYXHQMB-UHFFFAOYSA-N 0.000 claims 1
- IHHZCYSICNZRTD-UHFFFAOYSA-N n-[(4-cyanophenyl)methyl]-3-[3-(triazol-1-yl)prop-1-ynyl]benzamide Chemical compound C=1C=CC(C#CCN2N=NC=C2)=CC=1C(=O)NCC1=CC=C(C#N)C=C1 IHHZCYSICNZRTD-UHFFFAOYSA-N 0.000 claims 1
- OUEIAOCZSKBRSX-UHFFFAOYSA-N n-[(4-methylsulfonylphenyl)methyl]-3-(3-pyridin-3-ylprop-1-ynyl)benzamide Chemical compound C1=CC(S(=O)(=O)C)=CC=C1CNC(=O)C1=CC=CC(C#CCC=2C=NC=CC=2)=C1 OUEIAOCZSKBRSX-UHFFFAOYSA-N 0.000 claims 1
- JAGGBXDPVUHPSM-UHFFFAOYSA-N n-[(4-methylsulfonylphenyl)methyl]-3-(3-pyridin-4-ylprop-1-ynyl)benzamide Chemical compound C1=CC(S(=O)(=O)C)=CC=C1CNC(=O)C1=CC=CC(C#CCC=2C=CN=CC=2)=C1 JAGGBXDPVUHPSM-UHFFFAOYSA-N 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 1
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US32921601P | 2001-10-12 | 2001-10-12 | |
| US60/329,216 | 2001-10-12 | ||
| PCT/IB2002/003057 WO2003032999A1 (en) | 2001-10-12 | 2002-08-02 | Alkyne matrix metalloproteinase inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005514334A JP2005514334A (ja) | 2005-05-19 |
| JP2005514334A5 true JP2005514334A5 (https=) | 2005-12-22 |
| JP4164028B2 JP4164028B2 (ja) | 2008-10-08 |
Family
ID=23284384
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003535802A Expired - Fee Related JP4164028B2 (ja) | 2001-10-12 | 2002-08-02 | アルキンマトリックスメタロプロテイナーゼ阻害剤 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US6849648B2 (https=) |
| EP (1) | EP1434585A1 (https=) |
| JP (1) | JP4164028B2 (https=) |
| BR (1) | BR0213233A (https=) |
| CA (1) | CA2462442A1 (https=) |
| DO (1) | DOP2002000473A (https=) |
| GT (1) | GT200200210A (https=) |
| HN (1) | HN2002000291A (https=) |
| MX (1) | MXPA04002537A (https=) |
| PA (1) | PA8556201A1 (https=) |
| PE (1) | PE20030607A1 (https=) |
| PY (1) | PY0224080A (https=) |
| SV (1) | SV2004001291A (https=) |
| UY (1) | UY27481A1 (https=) |
| WO (1) | WO2003032999A1 (https=) |
Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PA8539501A1 (es) | 2001-02-14 | 2002-09-30 | Warner Lambert Co | Compuestos triazolo como inhibidores de mmp |
| WO2002064571A1 (en) | 2001-02-14 | 2002-08-22 | Warner-Lambert Company Llc | Pyrimidine matrix metalloproteinase inhibitors |
| DOP2002000334A (es) * | 2001-02-14 | 2002-08-30 | Warner Lambert Co | Pirimidinas biciclicas como inhibidores de metaloproteinasas de matriz |
| US6924276B2 (en) | 2001-09-10 | 2005-08-02 | Warner-Lambert Company | Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors |
| US6962922B2 (en) | 2001-10-12 | 2005-11-08 | Warner-Lambert Company Llc | Alkynylated quinazoline compounds |
| US6894057B2 (en) | 2002-03-08 | 2005-05-17 | Warner-Lambert Company | Oxo-azabicyclic compounds |
| US20040006077A1 (en) * | 2002-06-25 | 2004-01-08 | Bernard Gaudilliere | Thiazine and oxazine derivatives as MMP-13 inhibitors |
| AU2003281168A1 (en) * | 2002-07-17 | 2004-02-02 | Warner-Lambert Company Llc | Combination of an allosteric alkyne inhibitor of matrix metalloproteinase-13 with a selective inhibitor of cyclooxygenase-2 that is not celecoxib or valdecoxib |
| BR0312943A (pt) * | 2002-07-17 | 2005-07-12 | Warner Lambert Co | Combinação de um inibidor alostérico de matriz metaloproteinase-13 com um inibidor seletivo de ciclooxigenase-2 que não é celecoxib ou valdecoxib |
| WO2004006914A1 (en) * | 2002-07-17 | 2004-01-22 | Warner-Lambert Company Llc | Combination of an allosteric alkyne inhibitor of matrix metalloproteinase-13 with celecoxib or valdecoxib |
| MXPA05000729A (es) * | 2002-07-17 | 2005-04-08 | Warner Lambert Co | Combinacion de un inhibidor alosterico de metaloproteinasa-13 de matriz con celecoxib o valdecoxib. |
| AU2003249477A1 (en) * | 2002-08-13 | 2004-02-25 | Warner-Lambert Company Llc | Heterobicylcic metalloproteinase inhibitors |
| EP1539709A1 (en) | 2002-08-13 | 2005-06-15 | Warner-Lambert Company LLC | Azaisoquinoline derivatives as matrix metalloproteinase inhibitors |
| JP2006500350A (ja) * | 2002-08-13 | 2006-01-05 | ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー | マトリックスメタロプロテイナーゼ阻害剤としてのイソキノリン誘導体 |
| AU2003250470A1 (en) * | 2002-08-13 | 2004-02-25 | Warner-Lambert Company Llc | Pyrimidinone fused bicyclic metalloproteinase inhibitors |
| JP2005539020A (ja) | 2002-08-13 | 2005-12-22 | ワーナー−ランバート カンパニー リミティド ライアビリティー カンパニー | マトリクスメタロプロテイナーゼ阻害物質としてのクロモン誘導体 |
| AU2003249539A1 (en) * | 2002-08-13 | 2004-02-25 | Warner-Lambert Company Llc | Cyclic compounds containing zinc binding groups as matrix metalloproteinase inhibitors |
| WO2004014375A2 (en) | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | Fused bicyclic metalloproteinase inhibitors |
| WO2004014909A1 (en) | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | Fused tetrahydropyridine derivatives as matrix metalloproteinase inhibitors |
| AU2003249535A1 (en) * | 2002-08-13 | 2004-02-25 | Warner-Lambert Company Llc | 1,6-fused uracil derivatives as matrix metalloproteinase inhibitors |
| WO2004014892A1 (en) | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | Monocyclic derivatives as matrix metalloproteinase inhibitors |
| AU2003250475A1 (en) * | 2002-08-13 | 2004-02-25 | Warner-Lambert Company Llc | 5,6-fused 3,4-dihydropyrimidine-2-one derivatives as matrix metalloproteinase inhibitors |
| AU2003250482A1 (en) * | 2002-08-13 | 2004-02-25 | Warner-Lambert Company Llc | Phthalimide derivatives as matrix metalloproteinase inhibitors |
| EP1394159A1 (fr) * | 2002-08-13 | 2004-03-03 | Warner-Lambert Company LLC | Nouveaux dérivés de thiophène, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent |
| WO2004014378A1 (en) | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | 3-isoquinolinone derivatives as matrix metalloproteinase inhiitors |
| WO2004014916A1 (en) * | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | Pyrimidine fused bicyclic metalloproteinase inhibitors |
| MXPA05001783A (es) | 2002-08-13 | 2005-04-25 | Warner Lambert Co | Derivados de pirimidina-2,4-diona como inhibidores de las metaloproteinasas de matriz. |
| WO2004014388A1 (en) * | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | 6,6-fused heteroaryl derivatives as matrix metalloproteinase inhibitors |
| PA8578101A1 (es) * | 2002-08-13 | 2004-05-07 | Warner Lambert Co | Derivados de heterobiarilo como inhibidores de metaloproteinasa de la matriz |
| US20040142950A1 (en) * | 2003-01-17 | 2004-07-22 | Bunker Amy Mae | Amide and ester matrix metalloproteinase inhibitors |
| WO2005002585A1 (en) * | 2003-07-02 | 2005-01-13 | Warner-Lambert Company Llc | Combination of an allosteric inhibitor of matrix metalloproteinase-13 and a ligand to an alpha-2-delta receptor |
| WO2005016926A1 (en) * | 2003-08-19 | 2005-02-24 | Warner-Lambert Company Llc | Pyrido [3,4-d] pyrimidine derivatives as matrix metalloproteinase-13 inhibitors |
| US20060247231A1 (en) * | 2003-12-18 | 2006-11-02 | Warner-Lambert Company Llc | Amide and ester matrix metalloproteinase inhibitors |
| BRPI0508790A (pt) * | 2004-04-07 | 2007-09-04 | Applied Research Systems | ácido carboxìlicos, uso de um ácido carboxìlico, composto farmacêutico, método de preparação de ácido carboxìlico e composto intermediário |
| RS56037B1 (sr) | 2004-06-24 | 2017-09-29 | Vertex Pharma | Modulatori atp-vezujućih kasetnih transportera |
| US8354427B2 (en) | 2004-06-24 | 2013-01-15 | Vertex Pharmaceutical Incorporated | Modulators of ATP-binding cassette transporters |
| WO2006061715A2 (en) * | 2004-12-08 | 2006-06-15 | Warner-Lambert Company Llc | Methylene inhibitors of matrix metalloproteinase |
| PT1904048E (pt) * | 2005-07-15 | 2011-12-19 | Merck Serono Sa | Inibidores de glepp-1 no tratamento de distúrbios autoimunes e/ou inflamatórios |
| EP1979367A2 (en) * | 2005-12-24 | 2008-10-15 | Vertex Pharmaceuticals Incorporated | Quinolin-4-one derivatives as modulators of abc transporters |
| EP3219705B1 (en) | 2005-12-28 | 2020-03-11 | Vertex Pharmaceuticals Incorporated | Pharmaceutical compositions of the amorphous form of n-[2,4-bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide |
| US12458635B2 (en) | 2008-08-13 | 2025-11-04 | Vertex Pharmaceuticals Incorporated | Pharmaceutical composition and administrations thereof |
| US20100074949A1 (en) | 2008-08-13 | 2010-03-25 | William Rowe | Pharmaceutical composition and administration thereof |
| JP4831190B2 (ja) * | 2009-03-09 | 2011-12-07 | パナソニック株式会社 | ドラム式洗濯機 |
| PL2408750T3 (pl) | 2009-03-20 | 2016-02-29 | Vertex Pharma | Sposób otrzymywania modulatorów błonowego regulatora przewodnictwa swoistego dla mukowiscydozy |
| US8802700B2 (en) | 2010-12-10 | 2014-08-12 | Vertex Pharmaceuticals Incorporated | Modulators of ATP-Binding Cassette transporters |
| JP2015511583A (ja) | 2012-02-27 | 2015-04-20 | バーテックス ファーマシューティカルズ インコーポレイテッドＶｅｒｔｅｘ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ Ｉｎｃｏｒｐｏｒａｔｅｄ | 薬学的組成物およびその投与 |
| PL3087051T3 (pl) * | 2013-12-24 | 2021-02-22 | Oncotartis Inc. | Związki benzamidowe i nikotynamidowe oraz sposoby ich stosowania |
| WO2015130922A2 (en) * | 2014-02-26 | 2015-09-03 | The Trustees Of The University Of Pennsylvania | Small molecule hsp70 inhibitors |
| CN107250113B (zh) | 2014-10-07 | 2019-03-29 | 弗特克斯药品有限公司 | 囊性纤维化跨膜传导调节蛋白的调节剂的共晶 |
| CN113773277B (zh) * | 2021-09-18 | 2023-12-05 | 兰州大学 | 一种4h-1,2,4-苯并噻二嗪-1,1-二氧化物衍生物的合成方法 |
Family Cites Families (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3655679A (en) * | 1969-06-25 | 1972-04-11 | Merck & Co Inc | Certain aryl pyridine carboxylic acid derivatives |
| EP0041476B1 (de) * | 1980-05-31 | 1985-07-24 | Ciba-Geigy Ag | Neue Aryl-Phenyl-Acetylen-Verbindungen |
| US4818819A (en) | 1986-10-20 | 1989-04-04 | The Trustees Of Princeton University | Process for the preparation of fused pyridine compounds |
| US4902796A (en) | 1986-10-20 | 1990-02-20 | The Trustees Of Princeton University | 6-alkenyl and ethynyl derivatives of 2-amino-4-hydroxypyrido[2,3-d]pyrimidines |
| DE3931432A1 (de) | 1989-09-21 | 1991-04-04 | Hoechst Ag | Pyrimidin-4,6-dicarbonsaeurediamide, verfahren zu deren herstellung sowie verwendung derselben sowie arzneimittel auf basis dieser verbindungen |
| DE4020570A1 (de) | 1990-06-28 | 1992-01-02 | Hoechst Ag | 2,4- und 2,5-substituierte pyridin-n-oxide, verfahren zu deren herstellung sowie deren verwendung |
| US5389631A (en) * | 1991-10-29 | 1995-02-14 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| US5608082A (en) | 1994-07-28 | 1997-03-04 | Agouron Pharmaceuticals, Inc. | Compounds useful as antiproliferative agents and GARFT inhibitors |
| JPH08143568A (ja) | 1994-11-22 | 1996-06-04 | Terumo Corp | ピリドピリミジン誘導体及びそれを含有する医薬組成物 |
| ES2193205T3 (es) * | 1994-11-24 | 2003-11-01 | Basilea Pharmaceutica Ag | Nuevas bencil pirimidinas. |
| DE69616993T2 (de) * | 1995-03-14 | 2002-07-04 | Novartis Ag, Basel | Trisubstituierte phenyl derivate |
| AU5347496A (en) * | 1995-04-21 | 1996-11-07 | Daiichi Pharmaceutical Co., Ltd. | Ethynylthiazole derivative |
| AU6526896A (en) * | 1995-07-22 | 1997-02-18 | Rhone-Poulenc Rorer Limited | Substituted aromatic compounds and their pharmaceutical use |
| US5929097A (en) * | 1996-10-16 | 1999-07-27 | American Cyanamid Company | Preparation and use of ortho-sulfonamido aryl hydroxamic acids as matrix metalloproteinase and tace inhibitors |
| AU743901B2 (en) * | 1996-10-16 | 2002-02-07 | Wyeth Holdings Corporation | Ortho-sulfonamido bicyclic heteroaryl hydroxamic acids as matrix metalloprote inase and tace inhibitors |
| JPH10195063A (ja) * | 1996-10-21 | 1998-07-28 | Dai Ichi Seiyaku Co Ltd | エチニルチアゾール誘導体 |
| US6008243A (en) | 1996-10-24 | 1999-12-28 | Agouron Pharmaceuticals, Inc. | Metalloproteinase inhibitors, pharmaceutical compositions containing them, and their use |
| CA2263886A1 (en) | 1996-12-09 | 1998-06-18 | Warner-Lambert Company | Method for treating and preventing heart failure and ventricular dilatation |
| TW544448B (en) * | 1997-07-11 | 2003-08-01 | Novartis Ag | Pyridine derivatives |
| JPH11199512A (ja) | 1997-10-24 | 1999-07-27 | Pfizer Prod Inc | 変形性関節症および他のｍｍｐ媒介疾患の治療のためのｍｍｐ−１３選択的阻害剤の使用 |
| EP1103548A4 (en) * | 1998-08-03 | 2002-05-08 | Sumitomo Chemical Co | TRIAZOLONE DERIVATIVES, THEIR USE AND INTERMEDIATE CONNECTION THEREFOR |
| UA59453C2 (uk) | 1998-08-12 | 2003-09-15 | Пфайзер Продактс Інк. | Похідні гідроксипіпеколат гідроксамової кислоти як інгібітори матричних металопротеїназ |
| PT1149092E (pt) * | 1998-12-17 | 2004-03-31 | Hoffmann La Roche | 4- e 5-alciniloxindois e 4- e 5-alceniloxindois |
| US6248739B1 (en) * | 1999-01-08 | 2001-06-19 | Pharmacia & Upjohn Company | Quinolinecarboxamides as antiviral agents |
| US6225311B1 (en) * | 1999-01-27 | 2001-05-01 | American Cyanamid Company | Acetylenic α-amino acid-based sulfonamide hydroxamic acid tace inhibitors |
| DE19903757A1 (de) * | 1999-01-30 | 2000-08-24 | Ruetgers Automotive Ag | Verfahren und Vorrichtung zum Vermindern bzw. Vermeiden der Geräuschentwicklung von Reibungsbremsen und -kupplungen |
| HN2000000137A (es) | 1999-08-12 | 2001-02-02 | Pfizer Prod Inc | Pirimidina-2,4,6-trionas inhibidores de metaloproteinasas |
| HN2001000008A (es) * | 2000-01-21 | 2003-12-11 | Inc Agouron Pharmaceuticals | Compuesto de amida y composiciones farmaceuticas para inhibir proteinquinasas, y su modo de empleo |
| US6727266B2 (en) * | 2000-01-26 | 2004-04-27 | Shionogi & Co., Ltd. | Substituted tryptophan derivatives |
| US6934639B1 (en) | 2000-02-25 | 2005-08-23 | Wyeth | Methods for designing agents that interact with MMP-13 |
| EP1138680A1 (en) | 2000-03-29 | 2001-10-04 | Pfizer Products Inc. | Gem substituted sulfonyl hydroxamic acids as MMP inhibitors |
| US6682892B2 (en) * | 2000-07-13 | 2004-01-27 | Pharmacia & Upjohn Company | Method for treating herpes viruses |
| CN1501937A (zh) | 2000-10-26 | 2004-06-02 | �Ʒ� | 螺-嘧啶-2,4,6-三酮金属蛋白酶抑制剂 |
| HUP0302337A3 (en) | 2000-10-26 | 2004-01-28 | Pfizer Prod Inc | Pyrimidine-2,4,6-trione metalloproteinase inhibitors, pharmaceutical compositions containing them and their use |
| DOP2002000334A (es) | 2001-02-14 | 2002-08-30 | Warner Lambert Co | Pirimidinas biciclicas como inhibidores de metaloproteinasas de matriz |
| PA8539301A1 (es) | 2001-02-14 | 2002-09-30 | Warner Lambert Co | Inhibidores de la metaloproteinasa de la matriz |
| PA8539401A1 (es) | 2001-02-14 | 2002-10-28 | Warner Lambert Co | Quinazolinas como inhibidores de mmp-13 |
| WO2002064571A1 (en) | 2001-02-14 | 2002-08-22 | Warner-Lambert Company Llc | Pyrimidine matrix metalloproteinase inhibitors |
| DOP2002000332A (es) | 2001-02-14 | 2002-08-30 | Warner Lambert Co | Inhibidores de piridina de metaloproteinasas de la matriz |
| PA8539501A1 (es) | 2001-02-14 | 2002-09-30 | Warner Lambert Co | Compuestos triazolo como inhibidores de mmp |
| BR0207865A (pt) | 2001-02-14 | 2004-03-23 | Warner Lambert Co | Benzotiadiazinas inibidores de metaloproteinases de matriz |
| CA2433778A1 (en) | 2001-02-14 | 2002-08-22 | William Glen Harter | Thieno'2,3-d pyrimidindione derivatives as matrix metalloproteinase inhibitors |
| DOP2002000333A (es) | 2001-02-14 | 2002-09-30 | Warner Lambert Co | Derivados de acido isoftalico como inhibidores de metaloproteinasas de la matriz |
| SV2003001289A (es) | 2001-10-12 | 2003-06-24 | Warner Lambert Co | Compuestos pirimidina de anillo fusionado alquinilado |
| US6962922B2 (en) | 2001-10-12 | 2005-11-08 | Warner-Lambert Company Llc | Alkynylated quinazoline compounds |
| DE10160357A1 (de) | 2001-12-08 | 2003-06-18 | Aventis Pharma Gmbh | Verwendung von Pyridin-2,4-dicarbonsäurediamiden und Pyrimidin-4,6-dicarbonsäurediamiden zur selektiven Inhibierung von Kollagenasen |
| AU2003249539A1 (en) | 2002-08-13 | 2004-02-25 | Warner-Lambert Company Llc | Cyclic compounds containing zinc binding groups as matrix metalloproteinase inhibitors |
| PA8578101A1 (es) | 2002-08-13 | 2004-05-07 | Warner Lambert Co | Derivados de heterobiarilo como inhibidores de metaloproteinasa de la matriz |
| WO2004014892A1 (en) | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | Monocyclic derivatives as matrix metalloproteinase inhibitors |
| MXPA05001783A (es) | 2002-08-13 | 2005-04-25 | Warner Lambert Co | Derivados de pirimidina-2,4-diona como inhibidores de las metaloproteinasas de matriz. |
-
2002
- 2002-08-02 BR BR0213233-8A patent/BR0213233A/pt not_active IP Right Cessation
- 2002-08-02 JP JP2003535802A patent/JP4164028B2/ja not_active Expired - Fee Related
- 2002-08-02 CA CA002462442A patent/CA2462442A1/en not_active Abandoned
- 2002-08-02 MX MXPA04002537A patent/MXPA04002537A/es active IP Right Grant
- 2002-08-02 EP EP02751510A patent/EP1434585A1/en not_active Withdrawn
- 2002-08-02 WO PCT/IB2002/003057 patent/WO2003032999A1/en not_active Ceased
- 2002-09-27 DO DO2002000473A patent/DOP2002000473A/es unknown
- 2002-10-01 PY PY200200224080A patent/PY0224080A/es unknown
- 2002-10-04 US US10/264,764 patent/US6849648B2/en not_active Expired - Fee Related
- 2002-10-09 HN HN2002000291A patent/HN2002000291A/es unknown
- 2002-10-09 UY UY27481A patent/UY27481A1/es not_active Application Discontinuation
- 2002-10-11 PA PA20028556201A patent/PA8556201A1/es unknown
- 2002-10-11 PE PE2002001006A patent/PE20030607A1/es not_active Application Discontinuation
- 2002-10-11 SV SV2002001291A patent/SV2004001291A/es not_active Application Discontinuation
- 2002-10-11 GT GT200200210A patent/GT200200210A/es unknown
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