EA200601654A1 - Ингибиторы интегразы вич - Google Patents
Ингибиторы интегразы вичInfo
- Publication number
- EA200601654A1 EA200601654A1 EA200601654A EA200601654A EA200601654A1 EA 200601654 A1 EA200601654 A1 EA 200601654A1 EA 200601654 A EA200601654 A EA 200601654A EA 200601654 A EA200601654 A EA 200601654A EA 200601654 A1 EA200601654 A1 EA 200601654A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- compounds
- hiv
- integrase inhibitors
- hiv integrase
- prevent
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Гидрокси(тетра- или гекса-)гидронафтиридиндионовые соединения формулы I являются ингибиторами интегразы ВИЧ и ингибиторами репликации ВИЧ, где значения Х, X, Rи Rопределены в описании. Соединения могут быть использованы для предупреждения и лечения заражения ВИЧ и для предупреждения, замедления наступления и лечения СПИДа. Соединения используются против заражения ВИЧ и СПИД как сами по себе, так и в виде фармацевтически приемлемых солей. Соединения и их соли могут быть использованы как ингредиенты в фармацевтических композициях, необязательно в комбинации с другими противовирусными агентами, иммуномодуляторами, антибиотиками или вакцинами.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US55162504P | 2004-03-09 | 2004-03-09 | |
US63313404P | 2004-12-03 | 2004-12-03 | |
PCT/US2005/007730 WO2005087767A1 (en) | 2004-03-09 | 2005-03-09 | Hiv integrase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
EA200601654A1 true EA200601654A1 (ru) | 2007-02-27 |
Family
ID=34962221
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200601654A EA200601654A1 (ru) | 2004-03-09 | 2005-03-09 | Ингибиторы интегразы вич |
Country Status (15)
Country | Link |
---|---|
US (1) | US7598264B2 (ru) |
EP (1) | EP1725556A1 (ru) |
JP (1) | JP4625838B2 (ru) |
KR (1) | KR20070026414A (ru) |
CN (1) | CN1930160B (ru) |
AU (1) | AU2005222391B2 (ru) |
CA (1) | CA2558026C (ru) |
CR (1) | CR8569A (ru) |
EA (1) | EA200601654A1 (ru) |
EC (1) | ECSP066826A (ru) |
IL (1) | IL177858A0 (ru) |
MA (1) | MA28519B1 (ru) |
NO (1) | NO20064555L (ru) |
NZ (1) | NZ549449A (ru) |
WO (2) | WO2005087768A1 (ru) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW200510425A (en) | 2003-08-13 | 2005-03-16 | Japan Tobacco Inc | Nitrogen-containing fused ring compound and use thereof as HIV integrase inhibitor |
US20070161639A1 (en) * | 2004-03-09 | 2007-07-12 | Philip Jones | Hiv integrase inhibitors |
US7619086B2 (en) * | 2004-03-09 | 2009-11-17 | Merck & Co., Inc. | HIV integrase inhibitors |
CA2557785A1 (en) * | 2004-03-09 | 2005-10-06 | Merck & Co. Inc. | Hiv integrase inhibitors |
KR100966749B1 (ko) | 2004-05-26 | 2010-06-30 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 신나미드 화합물 |
CN100577657C (zh) | 2004-10-26 | 2010-01-06 | 卫材R&D管理有限公司 | 肉桂酰胺化合物的无定形物 |
WO2006066414A1 (en) * | 2004-12-23 | 2006-06-29 | Virochem Pharma Inc. | Hydroxydihydropyridopy razine-1,8-diones and methods for inhibiting hiv integrase |
AU2006244424B2 (en) * | 2005-05-10 | 2011-09-22 | Merck Sharp & Dohme Corp. | HIV integrase inhibitors |
DK1927584T3 (en) * | 2005-09-20 | 2017-02-20 | Jitsubo Co Ltd | CARRIER FOR SEPARATION, PROCEDURE FOR SEPARATION OF CONNECTION AND PROCEDURE FOR SYNTHESIS OF PEPTIDE USING THE CARRIER |
CA2622639C (en) * | 2005-10-04 | 2012-01-03 | Istituto Di Recerche Di Biologia Molecolare P. Angeletti S.P.A. | Hiv integrase inhibitors |
EP1942736A2 (en) * | 2005-10-27 | 2008-07-16 | Merck & Co., Inc. | Hiv integrase inhibitors |
AU2006316005A1 (en) * | 2005-11-18 | 2007-05-24 | Eisai R & D Management Co., Ltd. | Process for production of cinnamamide derivative |
TWI378091B (en) | 2006-03-09 | 2012-12-01 | Eisai R&D Man Co Ltd | Multi-cyclic cinnamide derivatives |
BRPI0709596A2 (pt) | 2006-03-16 | 2011-07-19 | Renovis Inc | compostos bicicloeteroarila como moduladores de p2x7 e seus usos |
JP2010506913A (ja) * | 2006-10-18 | 2010-03-04 | メルク エンド カムパニー インコーポレーテッド | Hivインテグラーゼ阻害剤 |
TW200848054A (en) | 2007-02-28 | 2008-12-16 | Eisai R&D Man Co Ltd | Two cyclic oxomorpholine derivatives |
CA2702317A1 (en) | 2007-07-09 | 2009-01-15 | Concert Pharmaceuticals, Inc. | Novel pyrimidinecarboxamide derivatives |
AR068121A1 (es) | 2007-08-31 | 2009-11-04 | Eisai R&D Man Co Ltd | Compuestos multiciclicos para tratar enfermedades neurodegenerativas |
US7935815B2 (en) | 2007-08-31 | 2011-05-03 | Eisai R&D Management Co., Ltd. | Imidazoyl pyridine compounds and salts thereof |
US8283366B2 (en) | 2010-01-22 | 2012-10-09 | Ambrilia Biopharma, Inc. | Derivatives of pyridoxine for inhibiting HIV integrase |
WO2012009446A1 (en) | 2010-07-16 | 2012-01-19 | Concert Pharmaceuticals Inc. | Novel pyrimidinecarboxamide derivatives |
WO2012106472A1 (en) * | 2011-02-02 | 2012-08-09 | Fibrogen, Inc. | Naphthyridine derivatives as inhibitors of hypoxia inducible factor (hif) hydroxylase |
EP2785184B1 (en) | 2011-11-30 | 2020-06-10 | Emory University | Compositions comprising jak inhibitors and haart drugs for use in the prevention or treatment of hiv |
EP2877469A4 (en) * | 2012-07-25 | 2016-04-06 | Merck Sharp & Dohme | SUBSTITUTED NAPHTHYRIDINEDIONE DERIVATIVES AS INHIBITORS OF HIV INTEGRASE |
HUE036384T2 (hu) * | 2013-05-17 | 2018-07-30 | Merck Sharp & Dohme | Fúzionált triciklusos heterociklikus vegyületek mint HIV integráz inhibitorok |
AP2016009157A0 (en) * | 2013-09-27 | 2016-04-30 | Merck Sharp & Dohme | Substituted quinolizine derivatives useful as hiv integrase inhibitors |
EP3285582B1 (en) * | 2015-03-26 | 2020-11-11 | Merck Sharp & Dohme Corp. | Phosphate-substituted quinolizine derivatives useful as hiv integrase inhibitors |
KR102613659B1 (ko) * | 2017-10-02 | 2023-12-15 | 노파르티스 아게 | 제약 제품의 제조 방법 |
WO2023057985A1 (en) * | 2021-10-08 | 2023-04-13 | Vrise Therapeutics, Inc. | Small molecules for treatement of cancer |
TW202342471A (zh) * | 2021-12-10 | 2023-11-01 | 美商薇瑞絲生物製藥公司 | 作為癌症治療藥物的小分子 |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6306891B1 (en) | 1998-06-03 | 2001-10-23 | Merck & Co., Inc. | HIV integrase inhibitors |
US6380249B1 (en) | 1998-06-03 | 2002-04-30 | Merck & Co., Inc. | HIV integrase inhibitors |
US6262055B1 (en) | 1998-06-03 | 2001-07-17 | Merck & Co., Inc. | HIV integrase inhibitors |
WO2001000578A1 (en) | 1999-06-25 | 2001-01-04 | Merck & Co., Inc. | 1-(aromatic- or heteroaromatic-substituted)-3-(heteroaromatic substituted)-1,3-propanediones and uses thereof |
EP1333831A2 (en) | 2000-10-12 | 2003-08-13 | Merck & Co., Inc. | Aza-and polyaza-naphthalenyl ketones useful as hiv integrase inhibitors |
DE60128936T2 (de) | 2000-10-12 | 2008-04-10 | Merck & Co, Inc. | Aza- und polyaza-naphthalenylcarbonsäureamide als hiv-integrase-hemmer |
AU2002246499B2 (en) | 2000-10-12 | 2005-12-22 | Merck & Co., Inc. | Aza-and polyaza-naphthalenyl carboxamides useful as HIV integrase inhibitors |
DE60138635D1 (de) | 2000-10-12 | 2009-06-18 | Merck & Co Inc | Aza- und polyaza naphthalenyl karboxamide als inhibitoren der hiv-integrase |
EP1375486B1 (en) * | 2001-03-01 | 2008-10-15 | Shionogi & Co., Ltd. | Nitrogen-containing heteroaryl compounds having hiv integrase inhibitory activity |
ATE530520T1 (de) | 2001-08-10 | 2011-11-15 | Shionogi & Co | Antivirales mittel |
CA2463975A1 (en) | 2001-10-26 | 2003-05-01 | Maria Emilia Di Francesco | Dihydroxypyrimidine carboxamide inhibitors of hiv integrase |
CA2463976C (en) | 2001-10-26 | 2007-02-13 | Benedetta Crescenzi | N-substituted hydroxypyrimidinone carboxamide inhibitors of hiv integrase |
CA2472372C (en) * | 2002-01-17 | 2010-08-17 | Melissa Egbertson | Hydroxynaphthyridinone carboxamides useful as hiv integrase inhibitors |
CA2478310A1 (en) * | 2002-03-15 | 2003-09-25 | Merck & Co., Inc. | N-(substituted benzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamides useful as hiv integrase inhibitors |
WO2004004657A2 (en) | 2002-07-09 | 2004-01-15 | Bristol-Myers Squibb Company | Hiv integrase inhibitors |
MXPA05001786A (es) * | 2002-08-13 | 2005-04-25 | Warner Lambert Co | Derivados de azaisoquinolina como inhibidores de la metaloproteinasa de matriz. |
JP2006232849A (ja) * | 2003-08-13 | 2006-09-07 | Japan Tobacco Inc | 含窒素縮合環化合物及びそのhivインテグラーゼ阻害剤としての利用 |
TW200510425A (en) | 2003-08-13 | 2005-03-16 | Japan Tobacco Inc | Nitrogen-containing fused ring compound and use thereof as HIV integrase inhibitor |
US20070161639A1 (en) | 2004-03-09 | 2007-07-12 | Philip Jones | Hiv integrase inhibitors |
US7619086B2 (en) | 2004-03-09 | 2009-11-17 | Merck & Co., Inc. | HIV integrase inhibitors |
CA2557785A1 (en) | 2004-03-09 | 2005-10-06 | Merck & Co. Inc. | Hiv integrase inhibitors |
AU2006244424B2 (en) | 2005-05-10 | 2011-09-22 | Merck Sharp & Dohme Corp. | HIV integrase inhibitors |
-
2005
- 2005-03-09 JP JP2007502960A patent/JP4625838B2/ja not_active Expired - Fee Related
- 2005-03-09 CN CN2005800074042A patent/CN1930160B/zh not_active Expired - Fee Related
- 2005-03-09 US US10/587,682 patent/US7598264B2/en not_active Expired - Fee Related
- 2005-03-09 WO PCT/US2005/007772 patent/WO2005087768A1/en not_active Application Discontinuation
- 2005-03-09 EA EA200601654A patent/EA200601654A1/ru unknown
- 2005-03-09 NZ NZ549449A patent/NZ549449A/en unknown
- 2005-03-09 WO PCT/US2005/007730 patent/WO2005087767A1/en active Application Filing
- 2005-03-09 KR KR1020067018481A patent/KR20070026414A/ko not_active Application Discontinuation
- 2005-03-09 AU AU2005222391A patent/AU2005222391B2/en not_active Ceased
- 2005-03-09 CA CA2558026A patent/CA2558026C/en not_active Expired - Fee Related
- 2005-03-09 EP EP05725120A patent/EP1725556A1/en not_active Ceased
-
2006
- 2006-08-24 CR CR8569A patent/CR8569A/es unknown
- 2006-09-03 IL IL177858A patent/IL177858A0/en unknown
- 2006-09-06 EC EC2006006826A patent/ECSP066826A/es unknown
- 2006-10-05 MA MA29370A patent/MA28519B1/fr unknown
- 2006-10-06 NO NO20064555A patent/NO20064555L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
CN1930160B (zh) | 2011-11-16 |
US20070179196A1 (en) | 2007-08-02 |
AU2005222391A1 (en) | 2005-09-22 |
KR20070026414A (ko) | 2007-03-08 |
WO2005087768A1 (en) | 2005-09-22 |
JP4625838B2 (ja) | 2011-02-02 |
JP2007528401A (ja) | 2007-10-11 |
NZ549449A (en) | 2009-05-31 |
US7598264B2 (en) | 2009-10-06 |
CA2558026A1 (en) | 2005-09-22 |
IL177858A0 (en) | 2006-12-31 |
AU2005222391B2 (en) | 2010-11-11 |
CR8569A (es) | 2007-08-28 |
CA2558026C (en) | 2010-12-14 |
CN1930160A (zh) | 2007-03-14 |
ECSP066826A (es) | 2006-11-24 |
WO2005087767A1 (en) | 2005-09-22 |
NO20064555L (no) | 2006-12-04 |
MA28519B1 (fr) | 2007-04-03 |
EP1725556A1 (en) | 2006-11-29 |
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