BRPI0922912A2 - peptídeos de 4-amino-4-oxobutanoil como inibidores de replicação viral - Google Patents
peptídeos de 4-amino-4-oxobutanoil como inibidores de replicação viralInfo
- Publication number
- BRPI0922912A2 BRPI0922912A2 BRPI0922912A BRPI0922912A BRPI0922912A2 BR PI0922912 A2 BRPI0922912 A2 BR PI0922912A2 BR PI0922912 A BRPI0922912 A BR PI0922912A BR PI0922912 A BRPI0922912 A BR PI0922912A BR PI0922912 A2 BRPI0922912 A2 BR PI0922912A2
- Authority
- BR
- Brazil
- Prior art keywords
- amino
- viral replication
- replication inhibitors
- oxobutanoyl peptides
- oxobutanoyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—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
- C07D207/04—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 no double bonds between ring members or between ring members and non-ring members
- C07D207/10—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 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
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- 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
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- 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
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 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
- C07D471/08—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/08—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/18—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/113—Spiro-condensed systems with two or more oxygen atoms as ring hetero atoms in the oxygen-containing ring
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12137808P | 2008-12-10 | 2008-12-10 | |
US22631709P | 2009-07-17 | 2009-07-17 | |
PCT/US2009/067506 WO2010068760A2 (en) | 2008-12-10 | 2009-12-10 | New 4-amino-4-oxobutanoyl peptides as inhibitors of viral replication |
Publications (2)
Publication Number | Publication Date |
---|---|
BRPI0922912A2 true BRPI0922912A2 (pt) | 2016-01-26 |
BRPI0922912A8 BRPI0922912A8 (pt) | 2018-01-02 |
Family
ID=42243312
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BRPI0922912A BRPI0922912A8 (pt) | 2008-12-10 | 2009-12-10 | peptídeos de 4-amino-4-oxobutanoil como inibidores de replicação viral |
Country Status (20)
Country | Link |
---|---|
US (2) | US8614180B2 (pt) |
EP (1) | EP2364309B1 (pt) |
JP (1) | JP5723783B2 (pt) |
KR (1) | KR101762842B1 (pt) |
CN (1) | CN102245599B (pt) |
AU (1) | AU2009324643B2 (pt) |
BR (1) | BRPI0922912A8 (pt) |
CA (1) | CA2746264C (pt) |
CY (1) | CY1116254T1 (pt) |
DK (1) | DK2364309T3 (pt) |
EA (1) | EA022134B1 (pt) |
ES (1) | ES2527166T3 (pt) |
HK (1) | HK1156623A1 (pt) |
IL (1) | IL212786A (pt) |
MX (1) | MX2011006244A (pt) |
NZ (1) | NZ592668A (pt) |
PL (1) | PL2364309T3 (pt) |
PT (1) | PT2364309E (pt) |
SI (1) | SI2364309T1 (pt) |
WO (1) | WO2010068760A2 (pt) |
Families Citing this family (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008008502A1 (en) | 2006-07-13 | 2008-01-17 | Achillion Pharmaceuticals, Inc. | 4-amino-4-oxobutanoyl peptides as inhibitors of viral replication |
EP2125113A2 (en) * | 2007-02-26 | 2009-12-02 | Achillion Pharmaceuticals, Inc. | Tertiary amine substituted peptides useful as inhibitors of hcv replication |
MX2011006244A (es) * | 2008-12-10 | 2011-06-27 | Achillion Pharmaceuticals Inc | Nuevos peptidos de 4-amino-4-oxobutanoilo como inhibidores de replica viral. |
NZ592705A (en) * | 2008-12-10 | 2013-02-22 | Achillion Pharmaceuticals Inc | 4-amino-4-oxobutanoyl peptide cyclic analogues, inhibitors of viral replication |
US8957203B2 (en) | 2011-05-05 | 2015-02-17 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
JP6198721B2 (ja) | 2011-05-27 | 2017-09-20 | アキリオン ファーマシューティカルズ,インコーポレーテッド | Hcv感染症を治療するのに有用な置換されたアリファン、シクロファン、ヘテラファン、ヘテロファン、ヘテロ−ヘテラファンおよびメタロセン |
US8492386B2 (en) | 2011-10-21 | 2013-07-23 | Abbvie Inc. | Methods for treating HCV |
US8466159B2 (en) | 2011-10-21 | 2013-06-18 | Abbvie Inc. | Methods for treating HCV |
ES2572328B1 (es) | 2011-10-21 | 2017-08-24 | Abbvie Inc. | Combinación de al menos dos agentes antivirales de acción directa y ribavirina pero no interferón, para su uso en el tratamiento del vhc |
EP2583680A3 (en) | 2011-10-21 | 2013-06-12 | Abbvie Inc. | Mono (PSI-7977) or combination treatment of DAAs for use in treating HCV |
JP6154474B2 (ja) | 2012-10-19 | 2017-06-28 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | C型肝炎ウイルス阻害剤 |
US9643999B2 (en) | 2012-11-02 | 2017-05-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
WO2014070964A1 (en) | 2012-11-02 | 2014-05-08 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
WO2014071007A1 (en) | 2012-11-02 | 2014-05-08 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
US9409943B2 (en) | 2012-11-05 | 2016-08-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US20140135270A1 (en) * | 2012-11-09 | 2014-05-15 | Ensemble Therapeutics Corp. | Macrocyclic compounds for inhibition of inhibitors of apoptosis |
US9580463B2 (en) | 2013-03-07 | 2017-02-28 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
BR112015023343A2 (pt) | 2013-03-14 | 2017-07-18 | Achillion Pharmaceuticals Inc | método para preparar sovaprevir, método de preparar um composto da fórmula (c), método de preparação do composto f-2, composto, processo, método de preparação de uma forma amorfa pura de sovaprevir, e,forma cristalina de sovaprevir |
KR20160005686A (ko) | 2013-03-15 | 2016-01-15 | 아칠리온 파르마세우티칼스 인코포레이티드 | 소바프레비르 다형체들 및 이의 제조 방법 |
US9006423B2 (en) * | 2013-03-15 | 2015-04-14 | Achillion Pharmaceuticals Inc. | Process for making a 4-amino-4-oxobutanoyl peptide cyclic analogue, an inhibitor of viral replication, and intermediates thereof |
US9085607B2 (en) | 2013-03-15 | 2015-07-21 | Achillion Pharmaceuticals, Inc. | ACH-0142684 sodium salt polymorph, composition including the same, and method of manufacture thereof |
JP2016522172A (ja) | 2013-04-12 | 2016-07-28 | アキリオン ファーマシューティカルズ,インコーポレーテッド | Hcvを治療するのに有用な重水素化されたヌクレオシドプロドラッグ |
CN103396351B (zh) * | 2013-08-09 | 2015-10-21 | 山东大学 | 吡咯烷类Bcl-2蛋白小分子抑制剂化合物及其制备、药物组合物与制药用途 |
EP3448392A4 (en) | 2016-04-28 | 2020-01-15 | Emory University | ALCYNE-CONTAINING NUCLEOTIDES AND NUCLEOSIDES THERAPEUTIC COMPOSITIONS AND USES THEREOF |
WO2017197036A1 (en) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | Spirocyclic degronimers for target protein degradation |
CN109641874A (zh) | 2016-05-10 | 2019-04-16 | C4医药公司 | 用于靶蛋白降解的c3-碳连接的戊二酰亚胺降解决定子体 |
CN109562107A (zh) | 2016-05-10 | 2019-04-02 | C4医药公司 | 用于靶蛋白降解的杂环降解决定子体 |
Family Cites Families (59)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE93526T1 (de) | 1989-07-19 | 1993-09-15 | Upjohn Co | Peptide mit diaminoglycolen als uebergangszustandmimik. |
JP2668003B2 (ja) | 1992-06-12 | 1997-10-27 | ファイザー インク. | ヒトの心臓キマーゼを含むアンギオテンシンiキマーゼに関する阻害剤 |
EP0674513B1 (en) | 1992-12-29 | 1996-09-25 | Abbott Laboratories | Retroviral protease inhibiting compounds |
UA74546C2 (en) | 1999-04-06 | 2006-01-16 | Boehringer Ingelheim Ca Ltd | Macrocyclic peptides having activity relative to hepatitis c virus, a pharmaceutical composition and use of the pharmaceutical composition |
US6608027B1 (en) * | 1999-04-06 | 2003-08-19 | Boehringer Ingelheim (Canada) Ltd | Macrocyclic peptides active against the hepatitis C virus |
ES2263687T3 (es) | 2000-11-20 | 2006-12-16 | Bristol-Myers Squibb Company | Inhibidores tripeptidicos de la hepatitis c. |
US6867185B2 (en) | 2001-12-20 | 2005-03-15 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
US7119072B2 (en) | 2002-01-30 | 2006-10-10 | Boehringer Ingelheim (Canada) Ltd. | Macrocyclic peptides active against the hepatitis C virus |
WO2004032827A2 (en) | 2002-05-20 | 2004-04-22 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
MY140680A (en) * | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
DE60334205D1 (en) | 2002-05-20 | 2010-10-28 | Bristol Myers Squibb Co | Heterocyclische sulfonamid-hepatitis-c-virus-hemmer |
US20060199773A1 (en) | 2002-05-20 | 2006-09-07 | Sausker Justin B | Crystalline forms of (1R,2S)-N-[(1,1-dimethylethoxy)carbonyl]-3-methyl-L-valyl-(4R)-4-[(6-methoxy-1-isoquinolinyl)oxy]-L-prolyl-1-amino-N-(cyclopropylsulfonyl)-2-ethenyl-cyclopropanecarboxamide, monopotassium salt |
ATE413411T1 (de) | 2002-05-20 | 2008-11-15 | Bristol Myers Squibb Co | Substituierte cycloalkyl p1' hepatitis c virus inhibitoren |
EP1408031A1 (en) | 2002-10-09 | 2004-04-14 | 3 D Gene Pharma | Pyrolidine derivatives useful in treatment of hepatitis C virus infection |
US7601709B2 (en) * | 2003-02-07 | 2009-10-13 | Enanta Pharmaceuticals, Inc. | Macrocyclic hepatitis C serine protease inhibitors |
JP2007524576A (ja) | 2003-02-07 | 2007-08-30 | エナンタ ファーマシューティカルズ インコーポレイテッド | 大環状のc型肝炎セリンプロテアーゼ阻害剤 |
ATE486889T1 (de) * | 2003-03-05 | 2010-11-15 | Boehringer Ingelheim Int | Peptidanaloga mit inhibitorischer wirkung auf hepatitis c |
ES2386161T3 (es) | 2003-04-16 | 2012-08-10 | Bristol-Myers Squibb Company | Proceso para separar una mezcla de enantiómeros de éster alquílico usando una enzima |
US7176208B2 (en) | 2003-04-18 | 2007-02-13 | Enanta Pharmaceuticals, Inc. | Quinoxalinyl macrocyclic hepatitis C serine protease inhibitors |
ES2297424T3 (es) | 2003-05-21 | 2008-05-01 | Boehringer Ingelheim International Gmbh | Compuestos inhibidores de la hepatitis c. |
WO2004113365A2 (en) | 2003-06-05 | 2004-12-29 | Enanta Pharmaceuticals, Inc. | Hepatitis c serine protease tri-peptide inhibitors |
AU2004257288A1 (en) | 2003-07-18 | 2005-01-27 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly HCV NS3-NS4A protease |
BRPI0414571A (pt) | 2003-09-22 | 2006-11-07 | Boehringer Ingelheim Int | peptìdeos macrocìclicos ativos contra o vìrus da hepatite c |
JP4584260B2 (ja) | 2003-10-14 | 2010-11-17 | インターミューン・インコーポレーテッド | Hcv複製阻害剤としての大環状カルボン酸およびアシルスルホンアミド |
US7132504B2 (en) | 2003-11-12 | 2006-11-07 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US7135462B2 (en) | 2003-11-20 | 2006-11-14 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US7309708B2 (en) | 2003-11-20 | 2007-12-18 | Birstol-Myers Squibb Company | Hepatitis C virus inhibitors |
CA2549851C (en) | 2004-01-21 | 2012-09-11 | Boehringer Ingelheim International Gmbh | Macrocyclic peptides active against the hepatitis c virus |
DE602005017582D1 (en) | 2004-01-30 | 2009-12-24 | Medivir Ab | Hcv ns-3 serine protease inhibitoren |
JP4654239B2 (ja) | 2004-03-15 | 2011-03-16 | 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 | C型肝炎ウィルス感染症の治療に適した大環状ジペプチドの調製方法 |
CA2560897C (en) | 2004-03-30 | 2012-06-12 | Intermune, Inc. | Macrocyclic compounds as inhibitors of viral replication |
EP1767010B1 (en) | 2004-06-15 | 2015-11-11 | Tekelec Global, Inc. | Method, system, and computer program products for content-based screening of MMS messages |
PL1778702T3 (pl) | 2004-07-16 | 2011-12-30 | Gilead Sciences Inc | Związki przeciwwirusowe |
UY29016A1 (es) | 2004-07-20 | 2006-02-24 | Boehringer Ingelheim Int | Analogos de dipeptidos inhibidores de la hepatitis c |
ATE512971T1 (de) * | 2004-07-20 | 2011-07-15 | Boehringer Ingelheim Int | Peptidanaloga als hepatitis c-hemmer |
CN101039947A (zh) * | 2004-08-09 | 2007-09-19 | 布里斯托尔-迈尔斯斯奎布公司 | Hcv复制抑制剂 |
US7153848B2 (en) * | 2004-08-09 | 2006-12-26 | Bristol-Myers Squibb Company | Inhibitors of HCV replication |
JP2008513454A (ja) | 2004-09-17 | 2008-05-01 | 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 | 大環状hcvプロテアーゼインヒビターの調製方法 |
US7659263B2 (en) | 2004-11-12 | 2010-02-09 | Japan Tobacco Inc. | Thienopyrrole compound and use thereof as HCV polymerase inhibitor |
US7323447B2 (en) | 2005-02-08 | 2008-01-29 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
DK1863833T3 (da) | 2005-03-08 | 2013-12-02 | Boehringer Ingelheim Int | Fremgangsmåde til fremstilling af makrocykliske forbindelser |
US7592336B2 (en) | 2005-05-10 | 2009-09-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
PL1891089T3 (pl) | 2005-06-02 | 2015-05-29 | Merck Sharp & Dohme | Inhibitory proteazy HCV w połączeniu z pokarmem |
US7608592B2 (en) | 2005-06-30 | 2009-10-27 | Virobay, Inc. | HCV inhibitors |
US7601686B2 (en) | 2005-07-11 | 2009-10-13 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
TWI389908B (zh) | 2005-07-14 | 2013-03-21 | Gilead Sciences Inc | 抗病毒化合物類 |
US20080200497A1 (en) | 2005-07-20 | 2008-08-21 | Bailey Murray D | Hepatitis C Inhibitor Peptide Analogs |
JP5249028B2 (ja) | 2005-07-25 | 2013-07-31 | インターミューン・インコーポレーテッド | C型肝炎ウイルス複製の新規大環状阻害剤 |
PE20070343A1 (es) | 2005-07-29 | 2007-05-12 | Medivir Ab | Inhibidores macrociclicos del virus de la hepatitis c |
JO2768B1 (en) | 2005-07-29 | 2014-03-15 | تيبوتيك فارماسيوتيكالز ليمتد | Large cyclic inhibitors of hepatitis C virus |
JP5190364B2 (ja) | 2005-09-09 | 2013-04-24 | 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 | 大環状ペプチドの調製の為の閉環メタセシス工程 |
DK1999129T3 (da) | 2005-10-11 | 2011-02-07 | Intermune Inc | Forbindelser og fremgangsmåder til inhibering af replikationen af hepatitis C-virus |
US7772183B2 (en) | 2005-10-12 | 2010-08-10 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US7741281B2 (en) | 2005-11-03 | 2010-06-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
WO2008008502A1 (en) * | 2006-07-13 | 2008-01-17 | Achillion Pharmaceuticals, Inc. | 4-amino-4-oxobutanoyl peptides as inhibitors of viral replication |
EP1881002A1 (en) | 2006-07-20 | 2008-01-23 | Tibotec Pharmaceuticals Ltd. | HCV NS-3 serine protease inhibitors |
KR20090101372A (ko) | 2007-01-08 | 2009-09-25 | 페노믹스 코포레이션 | 매크로시클릭 c형 간염 프로테아제 억제제 |
WO2008095058A1 (en) | 2007-02-01 | 2008-08-07 | Taigen Biotechnology Co. Ltd. | Hcv protease inhibitors |
MX2011006244A (es) * | 2008-12-10 | 2011-06-27 | Achillion Pharmaceuticals Inc | Nuevos peptidos de 4-amino-4-oxobutanoilo como inhibidores de replica viral. |
-
2009
- 2009-12-10 MX MX2011006244A patent/MX2011006244A/es active IP Right Grant
- 2009-12-10 CA CA2746264A patent/CA2746264C/en not_active Expired - Fee Related
- 2009-12-10 PT PT98325418T patent/PT2364309E/pt unknown
- 2009-12-10 ES ES09832541.8T patent/ES2527166T3/es active Active
- 2009-12-10 BR BRPI0922912A patent/BRPI0922912A8/pt not_active Application Discontinuation
- 2009-12-10 DK DK09832541T patent/DK2364309T3/en active
- 2009-12-10 EP EP20090832541 patent/EP2364309B1/en not_active Not-in-force
- 2009-12-10 NZ NZ59266809A patent/NZ592668A/en not_active IP Right Cessation
- 2009-12-10 JP JP2011540889A patent/JP5723783B2/ja not_active Expired - Fee Related
- 2009-12-10 KR KR1020117015962A patent/KR101762842B1/ko active IP Right Grant
- 2009-12-10 WO PCT/US2009/067506 patent/WO2010068760A2/en active Application Filing
- 2009-12-10 PL PL09832541T patent/PL2364309T3/pl unknown
- 2009-12-10 SI SI200931098T patent/SI2364309T1/sl unknown
- 2009-12-10 AU AU2009324643A patent/AU2009324643B2/en not_active Ceased
- 2009-12-10 CN CN200980149528.2A patent/CN102245599B/zh not_active Expired - Fee Related
- 2009-12-10 EA EA201100928A patent/EA022134B1/ru not_active IP Right Cessation
- 2009-12-10 US US12/635,270 patent/US8614180B2/en active Active
-
2011
- 2011-05-09 IL IL21278611A patent/IL212786A/en not_active IP Right Cessation
- 2011-10-17 HK HK11111013.7A patent/HK1156623A1/xx not_active IP Right Cessation
-
2013
- 2013-12-23 US US14/139,196 patent/US9133115B2/en not_active Expired - Fee Related
-
2014
- 2014-12-22 CY CY20141101077T patent/CY1116254T1/el unknown
Also Published As
Publication number | Publication date |
---|---|
CA2746264C (en) | 2017-11-14 |
MX2011006244A (es) | 2011-06-27 |
EA022134B1 (ru) | 2015-11-30 |
EP2364309A4 (en) | 2012-08-29 |
WO2010068760A2 (en) | 2010-06-17 |
KR101762842B1 (ko) | 2017-08-04 |
AU2009324643A1 (en) | 2010-06-17 |
DK2364309T3 (en) | 2015-01-12 |
CN102245599A (zh) | 2011-11-16 |
JP5723783B2 (ja) | 2015-05-27 |
PL2364309T3 (pl) | 2015-03-31 |
CA2746264A1 (en) | 2010-06-17 |
US9133115B2 (en) | 2015-09-15 |
CN102245599B (zh) | 2014-05-14 |
EP2364309A2 (en) | 2011-09-14 |
SI2364309T1 (sl) | 2015-03-31 |
KR20110114566A (ko) | 2011-10-19 |
NZ592668A (en) | 2013-12-20 |
BRPI0922912A8 (pt) | 2018-01-02 |
JP2012511587A (ja) | 2012-05-24 |
AU2009324643B2 (en) | 2014-08-28 |
IL212786A0 (en) | 2011-07-31 |
US20140113890A1 (en) | 2014-04-24 |
EP2364309B1 (en) | 2014-10-01 |
CY1116254T1 (el) | 2017-02-08 |
ES2527166T3 (es) | 2015-01-21 |
US20100216725A1 (en) | 2010-08-26 |
PT2364309E (pt) | 2015-01-14 |
HK1156623A1 (en) | 2012-06-15 |
EA201100928A1 (ru) | 2011-12-30 |
IL212786A (en) | 2014-11-30 |
WO2010068760A3 (en) | 2010-10-14 |
US8614180B2 (en) | 2013-12-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BRPI0922912A8 (pt) | peptídeos de 4-amino-4-oxobutanoil como inibidores de replicação viral | |
LTC2410844I2 (lt) | Hepatito C viruso replikacijos inhibitoriai | |
BRPI0913879A2 (pt) | fenilpirazinonas como inibidores de quinase | |
DE112009004699A5 (de) | Elektrochirurgisches System | |
BRPI0920135A2 (pt) | imidazopiridazinacarbonitrilos úteis como inibidores de quinase | |
BRPI1014084A2 (pt) | inibidores do vírus da hepatite c | |
BRPI1013393A2 (pt) | inibidores do vírus da hepatite c | |
BRPI1007836A2 (pt) | Inibidores do vírus c da hepatite | |
BRPI1008846A2 (pt) | inibidores do vírus da hepatite c | |
BRPI0922913A2 (pt) | Análogos cíclicos de peptídeo 4-amino-4-oxobutanoil inibidores de replicação viral | |
BR112012005382A2 (pt) | inibidores de jak | |
DK2310613T3 (da) | Forbedret brudled til stigrør | |
BRPI1010661A2 (pt) | peptídeo | |
BR112012006603A2 (pt) | braçadeira de fixação | |
ITPD20090053U1 (it) | Paradordi per banchine | |
IT1395137B1 (it) | Nuovi peptidi antipatogeni | |
FR2949371B3 (fr) | Agrafeuse | |
IT1397994B1 (it) | Morsetto | |
FR2943455B1 (fr) | Declencheur magnetothermique | |
FI20096202A0 (fi) | Biologinen regeneraatti | |
IT1393503B1 (it) | Spaccalegna | |
FI20095179A (fi) | Tasoelektrodijärjestelmä | |
ES1070576Y (es) | Bionda perfeccionada | |
FI9141U1 (fi) | Apuväline | |
FI8739U1 (fi) | Polttolaite |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE A 3A ANUIDADE. |
|
B08H | Application fees: decision cancelled [chapter 8.8 patent gazette] |
Free format text: REFERENTE AO DESPACHO 8.6 PUBLICADO NA RPI 2385 DE 20/09/2016. |
|
B07D | Technical examination (opinion) related to article 229 of industrial property law [chapter 7.4 patent gazette] | ||
B06F | Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette] | ||
B07E | Notification of approval relating to section 229 industrial property law [chapter 7.5 patent gazette] |
Free format text: NOTIFICACAO DE ANUENCIA RELACIONADA COM O ART 229 DA LPI |
|
B06U | Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette] | ||
B11B | Dismissal acc. art. 36, par 1 of ipl - no reply within 90 days to fullfil the necessary requirements |