BRPI1014821A2 - "inibidores de replicação de hiv" - Google Patents

"inibidores de replicação de hiv"

Info

Publication number
BRPI1014821A2
BRPI1014821A2 BRPI1014821A BRPI1014821A BRPI1014821A2 BR PI1014821 A2 BRPI1014821 A2 BR PI1014821A2 BR PI1014821 A BRPI1014821 A BR PI1014821A BR PI1014821 A BRPI1014821 A BR PI1014821A BR PI1014821 A2 BRPI1014821 A2 BR PI1014821A2
Authority
BR
Brazil
Prior art keywords
hiv replication
replication inhibitors
inhibitors
hiv
replication
Prior art date
Application number
BRPI1014821A
Other languages
English (en)
Inventor
Anne-Marie Faucher
Christiane Yoakim
Claudio Sturino
Clint James
Eric Malenfant
Jean-Eric Lacoste
Joannie Minville
Louis Morency
Martin Duplessis
Martin Tremblay
Patrick Deroy
Paul J Edwards
Sebastien Morin
Teddy Halmos
Original Assignee
Boehringer Ingelheim Int
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 Boehringer Ingelheim Int filed Critical Boehringer Ingelheim Int
Publication of BRPI1014821A2 publication Critical patent/BRPI1014821A2/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic 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
    • C07D491/02Heterocyclic 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
    • C07D491/04Ortho-condensed systems
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/048Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic 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
    • C07D491/12Heterocyclic 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 three hetero rings
    • C07D491/14Ortho-condensed systems
    • C07D491/147Ortho-condensed systems the condensed system containing one ring with oxygen as ring hetero atom and two rings with nitrogen as ring hetero atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
BRPI1014821A 2009-04-09 2010-04-07 "inibidores de replicação de hiv" BRPI1014821A2 (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US16803209P 2009-04-09 2009-04-09
US26368909P 2009-11-23 2009-11-23
PCT/CA2010/000478 WO2010115264A1 (en) 2009-04-09 2010-04-07 Inhibitors of hiv replication

Publications (1)

Publication Number Publication Date
BRPI1014821A2 true BRPI1014821A2 (pt) 2016-04-05

Family

ID=42934876

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI1014821A BRPI1014821A2 (pt) 2009-04-09 2010-04-07 "inibidores de replicação de hiv"

Country Status (15)

Country Link
US (1) US8349839B2 (pt)
EP (1) EP2417140B1 (pt)
JP (1) JP5643290B2 (pt)
KR (1) KR20120034592A (pt)
CN (1) CN102388051A (pt)
AR (1) AR076252A1 (pt)
AU (1) AU2010234241A1 (pt)
BR (1) BRPI1014821A2 (pt)
CA (1) CA2758149A1 (pt)
CL (1) CL2011002258A1 (pt)
EA (1) EA201101397A1 (pt)
IL (1) IL214606A0 (pt)
MX (1) MX2011010582A (pt)
TW (1) TW201103940A (pt)
WO (1) WO2010115264A1 (pt)

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US9399645B2 (en) * 2011-12-20 2016-07-26 Boehringer Ingelheim International Gmbh Inhibitors of HIV replication
EP3233797B1 (en) * 2015-01-18 2019-05-08 SRI International Inc. Map4k4 (hgk) inhibitors
MX2020003488A (es) 2015-02-02 2022-05-24 Forma Therapeutics Inc Acidos 3-alquil-4-amido-biciclico [4,5,0] hidroxamicos como inhibidores de histona desacetilasas (hdac).
AR103598A1 (es) 2015-02-02 2017-05-24 Forma Therapeutics Inc Ácidos bicíclicos[4,6,0]hidroxámicos como inhibidores de hdac
EP3472131B1 (en) 2016-06-17 2020-02-19 Forma Therapeutics, Inc. 2-spiro-5- and 6-hydroxamic acid indanes as hdac inhibitors
US11667651B2 (en) 2017-12-22 2023-06-06 Hibercell, Inc. Aminopyridine derivatives as phosphatidylinositol phosphate kinase inhibitors
WO2020028482A1 (en) * 2018-07-31 2020-02-06 The Trustees Of The University Of Pennsylvania Small molecules that sensitize hiv-1 infected cells to antibody dependent cellular cytotoxicity
CN111560022A (zh) * 2020-05-13 2020-08-21 深圳职业技术学院 四氢苯并呋喃[3,2-d]嘧啶类衍生物及其制备方法及应用
CN116332947A (zh) * 2021-12-24 2023-06-27 上海海和药物研究开发股份有限公司 具有mat2a抑制活性的嘧啶-2(1h)-酮并二环类化合物及其用途

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US8016A (en) * 1851-04-01 Improvement in the manufacture of india-rubber
JPH06172365A (ja) * 1992-12-11 1994-06-21 Yamasa Shoyu Co Ltd 10−チアイソアロキサジン誘導体およびその用途
JPH06220059A (ja) * 1993-01-28 1994-08-09 Tanabe Seiyaku Co Ltd 縮合ピリミジン誘導体及びその製法
US6593337B1 (en) * 1999-10-19 2003-07-15 Bristol-Myers Squibb Pharma Company Tricyclic compounds useful as HIV reverse transcriptase inhibitors
EP1209158A1 (en) 2000-11-18 2002-05-29 Aventis Pharma Deutschland GmbH Substituted beta-carbolines
TWI270547B (en) * 2000-06-16 2007-01-11 Boehringer Ingelheim Ca Ltd Non-nucleoside reverse transcriptase inhibitors
WO2003099206A2 (en) 2002-05-21 2003-12-04 Bristol-Myers Squibb Company Indole compounds useful as impdh inhibitors
US20030139427A1 (en) * 2002-08-23 2003-07-24 Osi Pharmaceuticals Inc. Bicyclic pyrimidinyl derivatives and methods of use thereof
WO2004046163A1 (ja) 2002-11-08 2004-06-03 Kaneka Corporation エルゴステロールの分離方法
KR20050084621A (ko) 2002-11-15 2005-08-26 티보텍 파마슈티칼즈 리미티드 항­감염성 화합물로서의 치환된 인돌피리디늄
US7642277B2 (en) 2002-12-04 2010-01-05 Boehringer Ingelheim International Gmbh Non-nucleoside reverse transcriptase inhibitors
WO2004096807A2 (en) * 2003-04-28 2004-11-11 Tibotec Pharmaceuticals Ltd. Hiv integrase inhibitors
US20060074124A1 (en) * 2003-09-12 2006-04-06 Andrew Napper Methods of treating a disorder
JP2007509149A (ja) * 2003-10-20 2007-04-12 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として有用なヒドロキシピリドピロロピラジンジオン化合物
WO2005076861A2 (en) * 2004-02-04 2005-08-25 University Of Virginia Patent Foundation Compounds that inhibit hiv particle formation
AR049340A1 (es) 2004-05-17 2006-07-19 Tibotec Pharm Ltd 1- heterociclil - l, 5- dihidro- pirido (3,2-b) indol - 2- onas
ES2351702T3 (es) 2004-05-17 2011-02-09 Tibotec Pharmaceuticals 1-fenil-1,5-dihidro-pirido[3,2-b]indol-2-onas 6,7,8,9-sustituidas útiles como agentes farmacéuticos antiinfecciosos.
CN1953978B (zh) 2004-05-17 2010-09-29 泰博特克药品有限公司 作为抗病毒剂的5-取代的1-苯基-1,5-二氢-吡啶并[3,2-b]吲哚-2-酮及其类似物
EA200602136A1 (ru) * 2004-05-17 2007-04-27 Тиботек Фармасьютикалз Лтд. Комбинации замещенных 1-фенил-1,5-дигидропиридо[3,2-b] индол-2-онов и других ингибиторов вич
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EP1773840B1 (de) * 2004-07-23 2010-01-20 The Medicines Company (Leipzig) GmbH Substituierte pyrido[3',2':4,5]thieno[3,2-d]pyrimidine und pyrido[3',2':4,5]furo[3,2-d]-pyrimidine zur verwendung als inhibitoren der pda-4 und/oder tnf-alpha freisetzung
DE602005025900D1 (de) 2004-09-30 2011-02-24 Boehringer Ingelheim Pharma Alkynilbasierte derivate von benzophenonen als nichtnukleoside reverse-transkriptase-inhibitoren
JP2008515982A (ja) 2004-10-13 2008-05-15 メルク エンド カムパニー インコーポレーテッド 高眼圧症を治療するための眼科組成物
BRPI0517211B8 (pt) 2004-12-17 2021-05-25 Glenmark Pharmaceuticals Sa composto, composição farmacêutica e seu uso.
US20060276440A1 (en) 2005-01-03 2006-12-07 An Wenqian F Treatment of inflammatory disorders
US20070049591A1 (en) 2005-08-25 2007-03-01 Kalypsys, Inc. Inhibitors of MAPK/Erk Kinase
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DE102006062203A1 (de) * 2006-12-22 2008-06-26 Curacyte Discovery Gmbh Substituierte 5H-Pyrimido[5,4-b]indole als Induktoren der Apoptose bei B-CLL Zellen
SI2125792T1 (sl) 2007-02-19 2011-03-31 Glaxosmithkline Llc Purinski derivati kot imunomodulatorji
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EA201001030A1 (ru) 2007-12-19 2011-02-28 Амген Инк. Конденсированные соединения пиридина, пиримидина и триазина в качестве ингибиторов клеточного цикла

Also Published As

Publication number Publication date
EP2417140A4 (en) 2013-02-20
TW201103940A (en) 2011-02-01
EP2417140A1 (en) 2012-02-15
US20100261714A1 (en) 2010-10-14
JP5643290B2 (ja) 2014-12-17
EA201101397A1 (ru) 2012-05-30
WO2010115264A1 (en) 2010-10-14
CN102388051A (zh) 2012-03-21
MX2011010582A (es) 2011-10-19
AU2010234241A1 (en) 2011-09-08
KR20120034592A (ko) 2012-04-12
JP2012523380A (ja) 2012-10-04
IL214606A0 (en) 2011-09-27
EP2417140B1 (en) 2014-11-26
CA2758149A1 (en) 2010-10-14
AR076252A1 (es) 2011-05-26
CL2011002258A1 (es) 2012-02-10
US8349839B2 (en) 2013-01-08

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Legal Events

Date Code Title Description
B11A Dismissal acc. art.33 of ipl - examination not requested within 36 months of filing
B11Y Definitive dismissal - extension of time limit for request of examination expired [chapter 11.1.1 patent gazette]