BR9810841A - Inibidores de metaloprotease alicìclicos - Google Patents
Inibidores de metaloprotease alicìclicosInfo
- Publication number
- BR9810841A BR9810841A BR9810841-7A BR9810841A BR9810841A BR 9810841 A BR9810841 A BR 9810841A BR 9810841 A BR9810841 A BR 9810841A BR 9810841 A BR9810841 A BR 9810841A
- Authority
- BR
- Brazil
- Prior art keywords
- alicyclic
- inhibitors
- metalloprotease inhibitors
- pharmaceutical compositions
- metalloprotease
- Prior art date
Links
- 239000003475 metalloproteinase inhibitor Substances 0.000 title abstract 2
- 125000002723 alicyclic group Chemical group 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 2
- 102000005741 Metalloproteases Human genes 0.000 abstract 1
- 108010006035 Metalloproteases Proteins 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 150000003949 imides Chemical class 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 230000003287 optical effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members 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
- C07D207/36—Oxygen or sulfur atoms
- C07D207/40—2,5-Pyrrolidine-diones
- C07D207/404—2,5-Pyrrolidine-diones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. succinimide
- C07D207/408—Radicals containing only hydrogen and carbon atoms attached to ring carbon atoms
- C07D207/412—Acyclic radicals containing more than six carbon atoms
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- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D335/00—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom
- C07D335/02—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/30—Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
- C07F9/36—Amides thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- 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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Abstract
Patente de Invenção: <B>"INIBIDORES DE METALOPROTEASE ALICìCLICOS"<D>. A invenção provê compostos de fórmula (I) conforme descrito nas reivindicações, ou um seu isómero, diastereómero ou enantiómero óptico, ou um seu sal farmaceuticamente aceitável, ou amida, éster ou imida bioidrolisável que são úteis como inibidores de metaloproteases. Também são descritas composições farmacêuticas e métodos de tratamento de doenças, distúrbios e condições caracterizadas pela atividade de metaloprotease usando esses compostos ou as composições farmacêuticas que os contêm.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5434897P | 1997-07-31 | 1997-07-31 | |
| PCT/IB1998/001139 WO1999006340A2 (en) | 1997-07-31 | 1998-07-27 | Sulfonylamino substituted hydroxamic acid derivatives as metalloprotease inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BR9810841A true BR9810841A (pt) | 2001-07-10 |
Family
ID=21990439
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR9810841-7A BR9810841A (pt) | 1997-07-31 | 1998-07-27 | Inibidores de metaloprotease alicìclicos |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US6218389B1 (pt) |
| EP (1) | EP1009737A2 (pt) |
| JP (1) | JP2001513484A (pt) |
| KR (1) | KR100352316B1 (pt) |
| CN (1) | CN1265647A (pt) |
| AR (1) | AR012264A1 (pt) |
| AU (1) | AU746877B2 (pt) |
| BR (1) | BR9810841A (pt) |
| CA (1) | CA2298617A1 (pt) |
| HU (1) | HUP0004595A3 (pt) |
| IL (1) | IL134273A0 (pt) |
| NO (1) | NO20000464L (pt) |
| NZ (1) | NZ503945A (pt) |
| PE (1) | PE115399A1 (pt) |
| WO (1) | WO1999006340A2 (pt) |
| ZA (1) | ZA986835B (pt) |
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| US6281245B1 (en) | 1996-10-28 | 2001-08-28 | Versicor, Inc. | Methods for solid-phase synthesis of hydroxylamine compounds and derivatives, and combinatorial libraries thereof |
| EP1024134A4 (en) | 1997-10-09 | 2003-05-14 | Ono Pharmaceutical Co | DERIVATIVES OF AMINOBUTANIC ACID |
| JP4750272B2 (ja) * | 1998-02-04 | 2011-08-17 | ノバルティス アーゲー | マトリックス分解メタロプロテイナーゼを阻害するスルホニルアミノ誘導体 |
| US6410580B1 (en) | 1998-02-04 | 2002-06-25 | Novartis Ag | Sulfonylamino derivatives which inhibit matrix-degrading metalloproteinases |
| US6846478B1 (en) | 1998-02-27 | 2005-01-25 | The Procter & Gamble Company | Promoting whole body health |
| IL138725A0 (en) | 1998-04-03 | 2001-10-31 | Sankyo Co | Sulfonamide derivatives and pharmaceutical compositions containing the same |
| US6300341B1 (en) | 1998-09-30 | 2001-10-09 | The Procter & Gamble Co. | 2-substituted heterocyclic sulfonamides |
| BR9914196A (pt) * | 1998-09-30 | 2001-06-19 | Procter & Gamble | Processo de tratamento da perda de cabelo |
| BR0008716A (pt) * | 1999-03-03 | 2002-09-24 | Procter & Gamble | Inibidores de metaloprotease contendo alquenil ou alquinil |
| MXPA01008857A (es) | 1999-03-03 | 2002-07-02 | Procter & Gamble | Inhibidores de metaloproteasa dihetero sustituidos. |
| HN2000000052A (es) * | 1999-05-28 | 2001-02-02 | Pfizer Prod Inc | Hidroxiamidas de acidos 3- (arilsulfonilamino)- tetrahidrofuran-3-carboxilicos. |
| US6294694B1 (en) * | 1999-06-04 | 2001-09-25 | Wisconsin Alumni Research Foundation | Matrix metalloproteinase inhibitors and method of using same |
| GB9918684D0 (en) * | 1999-08-09 | 1999-10-13 | Novartis Ag | Organic compounds |
| AU7450300A (en) * | 1999-09-29 | 2001-04-30 | Sankyo Company Limited | Sulfonamide derivatives |
| WO2001027084A1 (en) * | 1999-10-14 | 2001-04-19 | The Procter & Gamble Company | Beta disubstituted metalloprotease inhibitors |
| US6696456B1 (en) * | 1999-10-14 | 2004-02-24 | The Procter & Gamble Company | Beta disubstituted metalloprotease inhibitors |
| JP2003519119A (ja) * | 1999-12-24 | 2003-06-17 | スミスクライン ビーチャム パブリック リミテッド カンパニー | (ヘテロ)ビシクリルメタンスルホニルアミノ置換ヒドロキサム酸誘導体 |
| NZ520657A (en) | 2000-03-21 | 2004-11-26 | Procter & Gamble | Heterocyclic side chain containing, N-substituted metalloprotease inhibitors |
| WO2001070682A2 (en) * | 2000-03-21 | 2001-09-27 | The Procter & Gamble Company | Carbocyclic side chain containing metalloprotease inhibitors |
| WO2001070693A2 (en) | 2000-03-21 | 2001-09-27 | The Procter & Gamble Company | Difluorobutyric acid derivatives and their use as metalloprotease inhibitors |
| NZ520656A (en) * | 2000-03-21 | 2004-05-28 | Procter & Gamble | Heterocyclic side chain containing metalloprotease inhibitors |
| US8283135B2 (en) | 2000-06-30 | 2012-10-09 | The Procter & Gamble Company | Oral care compositions containing combinations of anti-bacterial and host-response modulating agents |
| MXPA03000043A (es) | 2000-06-30 | 2003-10-15 | Procter & Gamble | Promocion de la salud en todo el cuerpo. |
| AU1401902A (en) * | 2000-10-17 | 2002-04-29 | Applied Research Systems | Pharmaceutically active sulfanilide derivatives |
| GB0103303D0 (en) | 2001-02-09 | 2001-03-28 | Novartis Ag | Organic compounds |
| AU2002256672A1 (en) * | 2001-03-14 | 2002-09-24 | Novartis Ag | Azacycloalkyl substituted acetic acid derivatives for use as mmp inhibitors. |
| KR100701811B1 (ko) | 2002-05-29 | 2007-04-02 | 머크 앤드 캄파니 인코포레이티드 | 탄저병의 치료 및 치사 인자의 억제에 유용한 화합물 |
| GB0219961D0 (en) * | 2002-08-28 | 2002-10-02 | Pfizer Ltd | Oxytocin inhibitors |
| KR101076018B1 (ko) * | 2003-01-08 | 2011-10-21 | 유니버시티 오브 워싱톤 | 항균제 |
| US7842835B2 (en) | 2003-07-07 | 2010-11-30 | Georgetown University | Histone deacetylase inhibitors and methods of use thereof |
| AU2005250351A1 (en) | 2004-05-11 | 2005-12-15 | Merck & Co., Inc. | Process for making n-sulfonated-amino acid derivatives |
| JP2008508348A (ja) * | 2004-08-02 | 2008-03-21 | ジェンメディカ・セラピューティックス・ソシエダッド・リミターダ | 銅含有アミンオキシダーゼを阻害するための化合物およびその使用 |
| ITFI20040174A1 (it) * | 2004-08-03 | 2004-11-03 | Protera S R L | Derivati arilsolfonammidici dell'acido idrossammico ad azione inibitoria di metalloproteinasi |
| WO2006038265A1 (ja) * | 2004-09-30 | 2006-04-13 | Yutaka Imauchi | 耳硬化症治療のための医薬組成物 |
| US20100003276A1 (en) * | 2004-12-07 | 2010-01-07 | Hermes Jeffery D | Methods for treating anthrax and inhibiting lethal factor |
| DE102004060229A1 (de) * | 2004-12-15 | 2006-06-29 | Sanofi-Aventis Deutschland Gmbh | Neue zyklische Harnstoffe als Inhibitoren von Metallproteasen |
| JP2009520695A (ja) * | 2005-12-15 | 2009-05-28 | ヴィキュロン ファーマシューティカルズ インコーポレイテッド | 抗菌活性を有するn−ヒドロキシアミド誘導体 |
| AU2008259804B2 (en) * | 2007-06-05 | 2013-04-18 | Sanofi-Aventis | Substituted benzoylamino-indan-2-carboxylic acids and related compounds |
| TWI519508B (zh) * | 2007-06-12 | 2016-02-01 | Achaogen Inc | 抗菌劑 |
| EP2326619B1 (en) | 2008-08-01 | 2019-02-27 | Bioxiness Pharmaceuticals, Inc. | Methionine analogs and methods of using same |
| SG176085A1 (en) * | 2009-05-15 | 2011-12-29 | Stichting Nl Kanker Inst | Lysine compounds and their use in site- and chemoselective modification of peptides and proteins |
| EP2847168A1 (en) | 2012-05-10 | 2015-03-18 | Achaogen, Inc. | Antibacterial agents |
| CN106892845B (zh) * | 2017-02-28 | 2018-10-30 | 四川同晟生物医药有限公司 | 一种2,4-二氨基丁酸衍生物及其制备方法 |
| CN108821999A (zh) * | 2018-04-26 | 2018-11-16 | 南昌大学 | 一种氨基酸异羟肟酸类氨肽酶n抑制剂及制备方法 |
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| ATE226573T1 (de) | 1996-08-28 | 2002-11-15 | Procter & Gamble | Heterozyklische metalloproteaseinhibitoren |
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-
1998
- 1998-07-27 CA CA002298617A patent/CA2298617A1/en not_active Abandoned
- 1998-07-27 WO PCT/IB1998/001139 patent/WO1999006340A2/en not_active Ceased
- 1998-07-27 JP JP2000505105A patent/JP2001513484A/ja not_active Withdrawn
- 1998-07-27 HU HU0004595A patent/HUP0004595A3/hu unknown
- 1998-07-27 IL IL13427398A patent/IL134273A0/xx unknown
- 1998-07-27 KR KR1020007001085A patent/KR100352316B1/ko not_active Expired - Fee Related
- 1998-07-27 CN CN98807746A patent/CN1265647A/zh active Pending
- 1998-07-27 EP EP98932460A patent/EP1009737A2/en not_active Withdrawn
- 1998-07-27 AU AU82376/98A patent/AU746877B2/en not_active Ceased
- 1998-07-27 NZ NZ503945A patent/NZ503945A/xx unknown
- 1998-07-27 BR BR9810841-7A patent/BR9810841A/pt not_active IP Right Cessation
- 1998-07-30 ZA ZA986835A patent/ZA986835B/xx unknown
- 1998-07-31 AR ARP980103788A patent/AR012264A1/es not_active Application Discontinuation
- 1998-07-31 PE PE1998000686A patent/PE115399A1/es not_active Application Discontinuation
- 1998-07-31 US US09/127,678 patent/US6218389B1/en not_active Expired - Fee Related
-
2000
- 2000-01-28 NO NO20000464A patent/NO20000464L/no unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2298617A1 (en) | 1999-02-11 |
| AU8237698A (en) | 1999-02-22 |
| NO20000464L (no) | 2000-03-30 |
| PE115399A1 (es) | 2000-02-02 |
| AU746877B2 (en) | 2002-05-02 |
| ZA986835B (en) | 1999-02-01 |
| KR100352316B1 (ko) | 2002-09-12 |
| AR012264A1 (es) | 2000-09-27 |
| WO1999006340A3 (en) | 1999-09-30 |
| HUP0004595A2 (hu) | 2001-08-28 |
| IL134273A0 (en) | 2001-04-30 |
| KR20010022499A (ko) | 2001-03-15 |
| WO1999006340A2 (en) | 1999-02-11 |
| EP1009737A2 (en) | 2000-06-21 |
| JP2001513484A (ja) | 2001-09-04 |
| HUP0004595A3 (en) | 2001-12-28 |
| CN1265647A (zh) | 2000-09-06 |
| NZ503945A (en) | 2002-11-26 |
| NO20000464D0 (no) | 2000-01-28 |
| US6218389B1 (en) | 2001-04-17 |
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