MA28519B1 - Inhibiteurs de l'integrase du vih - Google Patents

Inhibiteurs de l'integrase du vih

Info

Publication number
MA28519B1
MA28519B1 MA29370A MA29370A MA28519B1 MA 28519 B1 MA28519 B1 MA 28519B1 MA 29370 A MA29370 A MA 29370A MA 29370 A MA29370 A MA 29370A MA 28519 B1 MA28519 B1 MA 28519B1
Authority
MA
Morocco
Prior art keywords
inhibitors
hiv integrase
integrase
hiv
Prior art date
Application number
MA29370A
Other languages
English (en)
Inventor
Wei Han
Melissa Egbertson
John S Wai
Linghang Zhuang
Rowena D Ruzek
Debra S Perlow
Vanessa E Obligado
Original Assignee
Merck & Co Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Merck & Co Inc filed Critical Merck & Co Inc
Publication of MA28519B1 publication Critical patent/MA28519B1/fr

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)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Virology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Engineering & Computer Science (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • AIDS & HIV (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
MA29370A 2004-03-09 2006-10-05 Inhibiteurs de l'integrase du vih MA28519B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US55162504P 2004-03-09 2004-03-09
US63313404P 2004-12-03 2004-12-03

Publications (1)

Publication Number Publication Date
MA28519B1 true MA28519B1 (fr) 2007-04-03

Family

ID=34962221

Family Applications (1)

Application Number Title Priority Date Filing Date
MA29370A MA28519B1 (fr) 2004-03-09 2006-10-05 Inhibiteurs de l'integrase du vih

Country Status (15)

Country Link
US (1) US7598264B2 (fr)
EP (1) EP1725556A1 (fr)
JP (1) JP4625838B2 (fr)
KR (1) KR20070026414A (fr)
CN (1) CN1930160B (fr)
AU (1) AU2005222391B2 (fr)
CA (1) CA2558026C (fr)
CR (1) CR8569A (fr)
EA (1) EA200601654A1 (fr)
EC (1) ECSP066826A (fr)
IL (1) IL177858A0 (fr)
MA (1) MA28519B1 (fr)
NO (1) NO20064555L (fr)
NZ (1) NZ549449A (fr)
WO (2) WO2005087767A1 (fr)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
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
WO2005087766A1 (fr) * 2004-03-09 2005-09-22 Istituto Di Ricerche Di Biologia Molecolare P Angeletti Spa Inhibiteurs de l'intégrase du vih
CN101014574A (zh) * 2004-03-09 2007-08-08 默克公司 Hiv整合酶抑制剂
JP2007528394A (ja) * 2004-03-09 2007-10-11 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薬
CA2566094A1 (fr) 2004-05-26 2005-12-08 Eisai R & D Management Co., Ltd. Compose de cinnamide
AU2005297966B2 (en) 2004-10-26 2010-12-23 Eisai R & D Management Co., Ltd. Amorphous object of cinnamide compound
WO2006066414A1 (fr) * 2004-12-23 2006-06-29 Virochem Pharma Inc. Hydroxydihydropyridopy razine-1,8-diones et procedes d’inhibition de l’integrase du vih
WO2006121831A2 (fr) * 2005-05-10 2006-11-16 Merck & Co., Inc. Inhibiteurs de l'intégrase du vih
ES2615083T3 (es) * 2005-09-20 2017-06-05 Jitsubo Co., Ltd. Vehículo de separación, método de separación de un compuesto, y método de síntesis del péptido utilizando el vehículo
US7939537B2 (en) * 2005-10-04 2011-05-10 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. HIV integrase inhibitors
JP2009513640A (ja) * 2005-10-27 2009-04-02 メルク エンド カムパニー インコーポレーテッド Ｈｉｖインテグラーゼインヒビター
CN101309916A (zh) * 2005-11-18 2008-11-19 卫材R&D管理有限公司 制备肉桂酰胺衍生物的方法
TWI378091B (en) 2006-03-09 2012-12-01 Eisai R&D Man Co Ltd Multi-cyclic cinnamide derivatives
WO2007109160A2 (fr) 2006-03-16 2007-09-27 Renovis, Inc. Composés de bicyclohétéroaryle en tant que modulateurs de p2x7 et leurs utilisations
US20100216834A1 (en) * 2006-10-18 2010-08-26 Isaacs Richard C A Hiv integrase inhibitors
CL2008000582A1 (es) 2007-02-28 2008-06-27 Eisai R&D Man Co Ltd Compuestos ciclicos derivados de oximorfolina condensados; farmacos que comprenden a dichos compuestos; y su uso para tratar enfermedad de alzheimer, demencia senil, sindrome de down o amiloidosis.
WO2009009531A2 (fr) 2007-07-09 2009-01-15 Concert Pharmaceuticals Inc. Nouveaux dérivés de pyrimidinecarboxamide
US7935815B2 (en) 2007-08-31 2011-05-03 Eisai R&D Management Co., Ltd. Imidazoyl pyridine compounds and salts thereof
CA2694401C (fr) 2007-08-31 2012-12-04 Eisai R&D Management Co., Ltd. Compose polycyclique
US8283366B2 (en) 2010-01-22 2012-10-09 Ambrilia Biopharma, Inc. Derivatives of pyridoxine for inhibiting HIV integrase
US9107922B2 (en) 2010-07-16 2015-08-18 Concert Pharmaceuticals, Inc. Pyrimidinecarboxamide derivatives
CN103608346B (zh) * 2011-02-02 2016-06-15 菲布罗根有限公司 作为缺氧诱导因子(hif)羟化酶抑制剂的萘啶衍生物
CN104185420B (zh) 2011-11-30 2017-06-09 埃默里大学 用于治疗或预防逆转录病毒和其它病毒感染的抗病毒jak抑制剂
EP2877469A4 (fr) * 2012-07-25 2016-04-06 Merck Sharp & Dohme Dérivés de naphthyridinedione substitués en tant qu'inhibiteurs de l'intégrase du vih
HUE036384T2 (hu) * 2013-05-17 2018-07-30 Merck Sharp & Dohme Fúzionált triciklusos heterociklikus vegyületek mint HIV integráz inhibitorok
AU2014324829B2 (en) 2013-09-27 2017-09-07 Merck Sharp & Dohme Corp. Substituted Quinolizine Derivatives useful as HIV integrase inhibitors
US10081647B2 (en) 2015-03-26 2018-09-25 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 (fr) * 2021-10-08 2023-04-13 Vrise Therapeutics, Inc. Petites molécules pour le traitement du cancer
US20250051361A1 (en) * 2021-12-10 2025-02-13 Vrise Therapeutics, Inc. 5,6,7,8-tetrahydro-2,6-naphthyridine derivatives as cancer therapeutics

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6380249B1 (en) 1998-06-03 2002-04-30 Merck & Co., Inc. HIV integrase inhibitors
US6306891B1 (en) 1998-06-03 2001-10-23 Merck & Co., Inc. HIV integrase inhibitors
US6262055B1 (en) 1998-06-03 2001-07-17 Merck & Co., Inc. HIV integrase inhibitors
AU5880600A (en) 1999-06-25 2001-01-31 Merck & Co., Inc. 1-(aromatic- or heteroaromatic-substituted)-3-(heteroaromatic substituted)-1,3-propanediones and uses thereof
WO2002030931A2 (fr) 2000-10-12 2002-04-18 Merck & Co., Inc. Aza-naphtalenyle carboxamides et polyaza-naphtalenyle carboxamides utiles en tant qu'inhibiteurs de l'integrase du vih
CA2425625A1 (fr) 2000-10-12 2002-07-18 Merck & Co., Inc. Aza- et polyaza-naphthalenyl carboxamides convenant comme inhibiteurs de l'integrase du vih
CA2425067A1 (fr) 2000-10-12 2002-05-10 Merck & Co., Inc. Aza- et polyaza-naphtalenyl cetones utiles en tant qu'inhibiteurs de l'integrase du vih
DE60128936T2 (de) 2000-10-12 2008-04-10 Merck & Co, Inc. Aza- und polyaza-naphthalenylcarbonsäureamide als hiv-integrase-hemmer
CZ20032332A3 (cs) * 2001-03-01 2003-11-12 Shionogi & Co., Ltd. Heteroarylové sloučeniny obsahující dusík, které mají inhibiční aktivitu proti HIV integrase
JP4338192B2 (ja) 2001-08-10 2009-10-07 塩野義製薬株式会社 抗ウイルス剤
HU230248B1 (hu) 2001-10-26 2015-11-30 Msd Italia S.R.L. N-szubsztituált hidroxipirimidinon-karboxamid HIV-integráz inhibitorok
ATE355064T1 (de) 2001-10-26 2006-03-15 Angeletti P Ist Richerche Bio Dihydroxypyrimidin-carbonsäueramid-hemmer der hiv-integrase
CA2472372C (fr) * 2002-01-17 2010-08-17 Melissa Egbertson Carboxamides hydroxynaphthyridinone utiles comme inhibiteurs de l'integrase du vih
WO2003077857A2 (fr) * 2002-03-15 2003-09-25 Merck & Co., Inc. N-(benzyl substitue)-8-hydroxy-1,6-naphtyridine-7-carboxamides utiles comme inhibiteurs de l'integrase du vih
AU2003248872A1 (en) 2002-07-09 2004-01-23 Bristol-Myers Squibb Company Hiv integrase inhibitors
WO2004014866A1 (fr) * 2002-08-13 2004-02-19 Warner-Lambert Company Llc Derives d'azaisoquinoline utilises comme inhibiteurs de metalloproteases matricielles
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
CN101014574A (zh) 2004-03-09 2007-08-08 默克公司 Hiv整合酶抑制剂
WO2005087766A1 (fr) 2004-03-09 2005-09-22 Istituto Di Ricerche Di Biologia Molecolare P Angeletti Spa Inhibiteurs de l'intégrase du vih
JP2007528394A (ja) 2004-03-09 2007-10-11 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薬
WO2006121831A2 (fr) 2005-05-10 2006-11-16 Merck & Co., Inc. Inhibiteurs de l'intégrase du vih

Also Published As

Publication number Publication date
CN1930160A (zh) 2007-03-14
WO2005087768A1 (fr) 2005-09-22
NZ549449A (en) 2009-05-31
EA200601654A1 (ru) 2007-02-27
CR8569A (es) 2007-08-28
US7598264B2 (en) 2009-10-06
EP1725556A1 (fr) 2006-11-29
CA2558026C (fr) 2010-12-14
CN1930160B (zh) 2011-11-16
JP4625838B2 (ja) 2011-02-02
AU2005222391A1 (en) 2005-09-22
IL177858A0 (en) 2006-12-31
ECSP066826A (es) 2006-11-24
KR20070026414A (ko) 2007-03-08
US20070179196A1 (en) 2007-08-02
AU2005222391B2 (en) 2010-11-11
CA2558026A1 (fr) 2005-09-22
JP2007528401A (ja) 2007-10-11
NO20064555L (no) 2006-12-04
WO2005087767A1 (fr) 2005-09-22

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