AR009990A1 - ORTHOS-SULFONAMIDE HETEROARYL ACIDS BICYCLIC HYDROXAMICS AS MATRIX AND TACE METALOPROTEINASE INHIBITORS, USE OF SUCH COMPOUNDS TO PREPARE MEDICINES, AND CONTAINING PHARMACEUTICAL COMPOSITIONS - Google Patents
ORTHOS-SULFONAMIDE HETEROARYL ACIDS BICYCLIC HYDROXAMICS AS MATRIX AND TACE METALOPROTEINASE INHIBITORS, USE OF SUCH COMPOUNDS TO PREPARE MEDICINES, AND CONTAINING PHARMACEUTICAL COMPOSITIONSInfo
- Publication number
- AR009990A1 AR009990A1 ARP970104749A ARP970104749A AR009990A1 AR 009990 A1 AR009990 A1 AR 009990A1 AR P970104749 A ARP970104749 A AR P970104749A AR P970104749 A ARP970104749 A AR P970104749A AR 009990 A1 AR009990 A1 AR 009990A1
- Authority
- AR
- Argentina
- Prior art keywords
- tace
- disease
- independently selected
- membered heteroaryl
- heteroaryl ring
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- 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
- C07D215/16—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 with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Inhibidores no peptídicos de bajo peso molecular de las metaloproteinasas de matriz (por ejemplo, gelatinasas, estromelisinas y colagenasas) y de laenzima conversora de TNF - alfa (TACE, enzima de conversion de factor alfa de necrosis tumoral) que son utiles para el tratamiento de enfermedades en lascuales intervienen estas enzimas, tales como la artritirs, la metástasis y desarrollo de tumores, alangiogénesis, al ulceracion de tejidos, lacicatrizacion anormal de heridas, enfermedad periodontal, enfermedad osea, proteinuria, enfermedad de aneurisma aortico, pérdida degenerativa de cartílagoposterior a lesion traumática de las articulaciones, enfermedades desmielinizantes del sistema nervioso, rechazo de injertos,caquexia, anorexia,inflamacion, fiebre resistencia a la insulina, choque séptico, insuficiencia cardíaca congestiva, enfermedad inflamatoria del sistema nervioso central,enfermedad inflamatoria intestinal, infeccion por HIV, degeneracion macularasociada a la edad, retinopatía diabética, vitreorretinopatía proliferativa,retinopatía de la prematuridad, inflamacion ocular, queratocono, síndrome de Sjogren, miopía, tumores oculares, angiogénesis/ neovascularizacion ocular. Losácidos orto-sulfonamido arilhidroxámicos inhibidores de TACE y MMP están representados por la formula (I) en la cual la porcion de ácido hidroxámico yla porcion sulfonamido están unidas a los carbonos adyacentes del grupo A donde A es un anillo heteroarilo de 5 a 6 miembros con 1 a 3 heteroátomosindependientemente seleccionados entre N, O y S fusionado o un anillo heteroarilo de 5-6 miembros que tiene de 1 a 3 heteroátomos independientementeseleccionados entre N, O y S fusionado o un anillo heteroarilo de 5-6 miembros que tiene de 1 a 3 heteroátomos independientemente seleccionados entre N, O y SLow-molecular-weight, non-peptidic inhibitors of matrix metalloproteinases (eg, gelatinases, stromelysins, and collagenases) and TNF-alpha converting enzyme (TACE), which are useful for the treatment of Diseases in which these enzymes are involved, such as arthritis, metastasis and development of tumors, alangiogenesis, tissue ulceration, abnormal wound healing, periodontal disease, bone disease, proteinuria, aortic aneurysm disease, degenerative loss of cartilage after injury traumatic joints, demyelinating diseases of the nervous system, graft rejection, cachexia, anorexia, inflammation, insulin resistance fever, septic shock, congestive heart failure, inflammatory disease of the central nervous system, inflammatory bowel disease, HIV infection, degeneration age-related macularas, retin Diabetic Opathy, Proliferative Vitreoretinopathy, Retinopathy of Prematurity, Eye Inflammation, Keratoconus, Sjogren's Syndrome, Myopia, Ocular Tumors, Ocular Angiogenesis / Neovascularization. The ortho-sulfonamido arylhydroxamic acids inhibitors of TACE and MMP are represented by formula (I) in which the portion of hydroxamic acid and the portion of sulfonamido are attached to the adjacent carbons of group A where A is a 5-6 membered heteroaryl ring with 1 to 3 heteroatoms independently selected from fused N, O, and S or a 5-6 membered heteroaryl ring having 1 to 3 independently selected heteroatoms between fused N, O, and S, or a 5-6 membered heteroaryl ring having 1 to 3 heteroatoms independently selected from N, O and S
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US73200496A | 1996-10-16 | 1996-10-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR009990A1 true AR009990A1 (en) | 2000-05-17 |
Family
ID=24941797
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP970104749A AR009990A1 (en) | 1996-10-16 | 1997-10-15 | ORTHOS-SULFONAMIDE HETEROARYL ACIDS BICYCLIC HYDROXAMICS AS MATRIX AND TACE METALOPROTEINASE INHIBITORS, USE OF SUCH COMPOUNDS TO PREPARE MEDICINES, AND CONTAINING PHARMACEUTICAL COMPOSITIONS |
Country Status (4)
Country | Link |
---|---|
AR (1) | AR009990A1 (en) |
AU (1) | AU743901B2 (en) |
WO (1) | WO1998016514A1 (en) |
ZA (1) | ZA979235B (en) |
Families Citing this family (47)
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US6548524B2 (en) * | 1996-10-16 | 2003-04-15 | American Cyanamid Company | Preparation and use of ortho-sulfonamido bicyclic heteroaryl hydroxamic acids as matrix metalloproteinase and TACE inhibitors |
WO1998016520A1 (en) * | 1996-10-16 | 1998-04-23 | American Cyanamid Company | The preparation and use of ortho-sulfonamido heteroaryl hydroxamic acids as matrix metalloproteinase and tace inhibitors |
ATE242768T1 (en) * | 1997-10-06 | 2003-06-15 | Wyeth Corp | PREPARATION AND USE OF ORTHO-SULFONAMIDO BICYCLIC HETEROARYL HYDROXAMIC ACID DERIVATIVES AS MATRIX METALLOPROTEINASE AND TACE INHIBITORS |
US6110929A (en) | 1998-07-28 | 2000-08-29 | 3M Innovative Properties Company | Oxazolo, thiazolo and selenazolo [4,5-c]-quinolin-4-amines and analogs thereof |
GB9919776D0 (en) | 1998-08-31 | 1999-10-27 | Zeneca Ltd | Compoujnds |
US6225311B1 (en) | 1999-01-27 | 2001-05-01 | American Cyanamid Company | Acetylenic α-amino acid-based sulfonamide hydroxamic acid tace inhibitors |
US6277885B1 (en) | 1999-01-27 | 2001-08-21 | American Cyanamid Company | Acetylenic aryl sulfonamide and phosphinic acid amide hydroxamic acid TACE inhibitors |
US6358980B1 (en) | 1999-01-27 | 2002-03-19 | American Cyanamid Company | Alkynyl containing hydroxamic acid compounds as matrix metalloproteinase/tace inhibitors |
US6326516B1 (en) | 1999-01-27 | 2001-12-04 | American Cyanamid Company | Acetylenic β-sulfonamido and phosphinic acid amide hydroxamic acid TACE inhibitors |
US6200996B1 (en) | 1999-01-27 | 2001-03-13 | American Cyanamid Company | Heteroaryl acetylenic sulfonamide and phosphinic acid amide hydroxamic acid tace inhibitors |
US6762178B2 (en) | 1999-01-27 | 2004-07-13 | Wyeth Holdings Corporation | Acetylenic aryl sulfonamide and phosphinic acid amide hydroxamic acid TACE inhibitors |
US6313123B1 (en) | 1999-01-27 | 2001-11-06 | American Cyanamid Company | Acetylenic sulfonamide thiol tace inhibitors |
US6753337B2 (en) | 1999-01-27 | 2004-06-22 | Wyeth Holdings Corporation | Alkynyl containing hydroxamic acid compounds as matrix metalloproteinase/tace inhibitors |
US6946473B2 (en) | 1999-01-27 | 2005-09-20 | Wyeth Holdings Corporation | Preparation and use of acetylenic ortho-sulfonamido and phosphinic acid amido bicyclic heteroaryl hydroxamic acids as TACE inhibitors |
AR035311A1 (en) * | 1999-01-27 | 2004-05-12 | Wyeth Corp | HYDROXAMIC ACID DERIVATIVES CONTAINING ALQUINYL, AS INHIBITORS OF THE METALLOPROTEINAS OF MATRIX AND THE TACE, PHARMACEUTICAL COMPOSITION AND THE USE OF THE SAME FOR THE MANUFACTURE OF A MEDICINAL PRODUCT |
AR022424A1 (en) * | 1999-01-27 | 2002-09-04 | American Cyanamid Co | COMPOUNDS DERIVED FROM ACIDS ORTOSULFONAMIDO ACETYLENE AND HYDROXAMIC HYDROXAMIC HYDROARAMYL AMID OF PHOSPHINIC ACID AS INHIBITORS TACE, COMPOSITION PHARMACEUTICAL THAT UNDERSTANDS AND THE USE OF THE SAME FOR THE MANUFACTURE OF A MEDICATION |
US6340691B1 (en) | 1999-01-27 | 2002-01-22 | American Cyanamid Company | Alkynyl containing hydroxamic acid compounds as matrix metalloproteinase and tace inhibitors |
WO2001062742A1 (en) | 2000-02-21 | 2001-08-30 | Astrazeneca Ab | Piperidine- and piperazine substituted n-hydroxyformamides as inhibitors of metalloproteinases |
WO2001062751A1 (en) * | 2000-02-21 | 2001-08-30 | Astrazeneca Ab | Arylpiperazines and arylpiperidines and their use as metalloproteinase inhibiting agents |
AR027943A1 (en) * | 2000-02-25 | 2003-04-16 | Wyeth Corp | ARIL HYDROXAMIC ORTO-SULPHONAMIDE ACIDS AS MATRIX METALOPROTEINASE INHIBITORS AND PREPARATION OF THE SAME |
US6465508B1 (en) | 2000-02-25 | 2002-10-15 | Wyeth | Preparation and use of ortho-sulfonamido aryl hydroxamic acids as matrix metalloproteinase inhibitors |
WO2001082911A2 (en) * | 2000-04-28 | 2001-11-08 | Gerolymatos P N Sa | TREATMENT OF PATHOLOGICAL CONDITIONS INFLUENCED BY THE ACTION OF MATRIX METALLOPROTEINASES (MMPs) USING CLIOQUINOL |
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US6436629B1 (en) | 2000-10-27 | 2002-08-20 | The Regents Of The University Of California | Modulating angiogenesis |
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US6962922B2 (en) | 2001-10-12 | 2005-11-08 | Warner-Lambert Company Llc | Alkynylated quinazoline compounds |
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CA2464727A1 (en) | 2001-11-01 | 2003-05-08 | Wyeth Holdings Corporation | Allenic aryl sulfonamide hydroxamic acids as matrix metalloproteinase and tace inhibitors |
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MXPA05001642A (en) * | 2002-08-13 | 2005-04-25 | Warner Lambert Co | 4-hydroxyquinoline derivatives as matrix metalloproteinase inhibitors. |
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US20040157836A1 (en) * | 2002-10-08 | 2004-08-12 | Comess Kenneth M. | Sulfonamides having antiangiogenic and anticancer activity |
TW200418825A (en) | 2002-12-16 | 2004-10-01 | Hoffmann La Roche | Novel (R)-and (S) enantiomers of thiophene hydroxamic acid derivatives |
WO2005021489A2 (en) | 2002-12-23 | 2005-03-10 | Wyeth Holdings Corporation | Acetylenic aryl sulfonate hydroxamic acid tace and matrix metalloproteinase inhibitors |
WO2006117660A2 (en) * | 2005-05-04 | 2006-11-09 | Clio Pharmaceutical Corporation | Method for treating cancer, coronary, inflammatory and macular disease, combining the modulation of zinc- and/or copper dependent proteins |
JP5588339B2 (en) * | 2007-06-25 | 2014-09-10 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | New chemical compounds |
JP2012513464A (en) * | 2008-12-23 | 2012-06-14 | ザ トラスティーズ オブ コロンビア ユニヴァーシティ イン ザ シティ オブ ニューヨーク | Phosphodiesterase inhibitors and uses thereof |
FR2947270B1 (en) | 2009-06-30 | 2011-08-26 | Galderma Res & Dev | NOVEL BENZENE-SULFONAMIDE COMPOUNDS, PROCESS FOR THE SYNTHESIS AND THEIR USE IN MEDICINE AND COSMETICS |
FR2947268B1 (en) | 2009-06-30 | 2011-08-26 | Galderma Res & Dev | NOVEL BENZENE-SULFONAMIDE COMPOUNDS, PROCESS FOR THE SYNTHESIS AND THEIR USE IN MEDICINE AND COSMETICS |
WO2011146591A1 (en) | 2010-05-19 | 2011-11-24 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
US20140275108A1 (en) | 2013-03-15 | 2014-09-18 | Galderma Research & Development | Novel benzenesulfonamide compounds, method for synthesizing same, and use thereof in medicine as well as in cosmetics |
IL237852A0 (en) | 2015-03-19 | 2016-03-24 | Yeda Res & Dev | Anti amphiregulin antibodies, compositions comprising same and uses thereof |
US20190008828A1 (en) | 2015-12-28 | 2019-01-10 | The U.S.A., As Represented By The Secretary Department Of Health And Human Services | Methods for inhibiting human immunodeficiency virus (hiv) release from infected cells |
ES2695533T3 (en) | 2016-02-01 | 2019-01-08 | Galderma Res & Dev | Benzenesulfonamide compounds, method for their synthesis and use in medicine and cosmetics |
BR112021006407A8 (en) | 2018-10-04 | 2022-12-06 | Inst Nat Sante Rech Med | use of egfr inhibitors for keratoderms |
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US5455258A (en) * | 1993-01-06 | 1995-10-03 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamic acids |
WO1998016520A1 (en) * | 1996-10-16 | 1998-04-23 | American Cyanamid Company | The preparation and use of ortho-sulfonamido heteroaryl hydroxamic acids as matrix metalloproteinase and tace inhibitors |
-
1997
- 1997-10-08 AU AU49806/97A patent/AU743901B2/en not_active Ceased
- 1997-10-08 WO PCT/US1997/018281 patent/WO1998016514A1/en active Application Filing
- 1997-10-15 ZA ZA979235A patent/ZA979235B/en unknown
- 1997-10-15 AR ARP970104749A patent/AR009990A1/en unknown
Also Published As
Publication number | Publication date |
---|---|
AU4980697A (en) | 1998-05-11 |
WO1998016514A1 (en) | 1998-04-23 |
AU743901B2 (en) | 2002-02-07 |
ZA979235B (en) | 1999-04-15 |
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