Nothing Special   »   [go: up one dir, main page]

DK2057125T3 - Ikke-nucleosid revers transkriptase-inhibitorer - Google Patents

Ikke-nucleosid revers transkriptase-inhibitorer

Info

Publication number
DK2057125T3
DK2057125T3 DK07802503.8T DK07802503T DK2057125T3 DK 2057125 T3 DK2057125 T3 DK 2057125T3 DK 07802503 T DK07802503 T DK 07802503T DK 2057125 T3 DK2057125 T3 DK 2057125T3
Authority
DK
Denmark
Prior art keywords
reverse transcriptase
transcriptase inhibitors
nucleoside reverse
nucleoside
inhibitors
Prior art date
Application number
DK07802503.8T
Other languages
English (en)
Inventor
Joshua Kennedy-Smith
Wylie Solang Palmer
Zachary Kevin Sweeney
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Application granted granted Critical
Publication of DK2057125T3 publication Critical patent/DK2057125T3/da

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • 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
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/54Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
    • C07D231/56Benzopyrazoles; Hydrogenated benzopyrazoles
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Virology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • AIDS & HIV (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
DK07802503.8T 2006-08-16 2007-08-06 Ikke-nucleosid revers transkriptase-inhibitorer DK2057125T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US83827206P 2006-08-16 2006-08-16
PCT/EP2007/058116 WO2008019968A1 (en) 2006-08-16 2007-08-06 Non-nucleoside reverse transcriptase inhibitors

Publications (1)

Publication Number Publication Date
DK2057125T3 true DK2057125T3 (da) 2011-05-16

Family

ID=38663155

Family Applications (1)

Application Number Title Priority Date Filing Date
DK07802503.8T DK2057125T3 (da) 2006-08-16 2007-08-06 Ikke-nucleosid revers transkriptase-inhibitorer

Country Status (23)

Country Link
US (2) US7713974B2 (da)
EP (1) EP2057125B1 (da)
JP (1) JP5216768B2 (da)
KR (1) KR101401811B1 (da)
CN (1) CN101501002B (da)
AR (1) AR062366A1 (da)
AT (1) ATE503744T1 (da)
AU (1) AU2007286345B2 (da)
BR (1) BRPI0715193A2 (da)
CA (1) CA2658984C (da)
CL (1) CL2007002346A1 (da)
DE (1) DE602007013573D1 (da)
DK (1) DK2057125T3 (da)
ES (1) ES2360893T3 (da)
IL (1) IL196655A (da)
MX (1) MX2009001198A (da)
NO (1) NO20090405L (da)
PE (1) PE20080734A1 (da)
PL (1) PL2057125T3 (da)
PT (1) PT2057125E (da)
RU (1) RU2451676C2 (da)
TW (1) TWI417293B (da)
WO (1) WO2008019968A1 (da)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR057455A1 (es) * 2005-07-22 2007-12-05 Merck & Co Inc Inhibidores de la transcriptasa reversa de vih y composicion farmaceutica
TW200831085A (en) * 2006-12-13 2008-08-01 Merck & Co Inc Non-nucleoside reverse transcriptase inhibitors
WO2008122534A2 (en) * 2007-04-09 2008-10-16 F. Hoffmann-La Roche Ag Non-nucleoside reverse transcriptase inhibitors
WO2009067597A1 (en) * 2007-11-21 2009-05-28 Decode Genetics Ehf 4- (or 5-) substituted catechol derivatives
EP2225239B1 (en) * 2007-12-21 2014-10-22 F. Hoffmann-La Roche AG Heterocyclic antiviral compounds
EP2356116A1 (en) 2008-11-20 2011-08-17 OSI Pharmaceuticals, Inc. Substituted pyrroloý2,3-b¨-pyridines and-pyrazines
AR081039A1 (es) 2010-05-14 2012-05-30 Osi Pharmaceuticals Llc Inhibidores biciclicos fusionados de quinasa
JP2013526570A (ja) * 2010-05-14 2013-06-24 オーエスアイ・ファーマシューティカルズ,エルエルシー 縮合二環式キナーゼ阻害剤
US20120142627A1 (en) * 2010-12-06 2012-06-07 Emory University Monophosphate prodrugs of dapd and analogs thereof
US9487506B2 (en) * 2011-04-13 2016-11-08 Merck Sharp & Dohme Corp. Mineralocorticoid receptor antagonists
WO2012148999A1 (en) 2011-04-26 2012-11-01 The Procter & Gamble Company Bulked absorbent members
CA2871680C (en) 2012-04-25 2018-01-09 The Procter & Gamble Company Corrugated and apertured web
BR112014026584A2 (pt) 2012-04-25 2017-06-27 Procter & Gamble aparelho e processo para abrir e estirar uma manta
WO2014091265A1 (en) 2012-12-11 2014-06-19 Aurigene Discovery Technologies Limited Pyrimidine-2,4-diamine derivatives as kinase inhibitors
JP6321965B2 (ja) 2014-01-09 2018-05-09 富士フイルム株式会社 有機薄膜トランジスタ、有機半導体薄膜および有機半導体材料
CN106614663A (zh) * 2016-12-29 2017-05-10 新沂市中诺新材料科技有限公司 一种新型纳米级吲唑类农药合成方法
CN113511960A (zh) * 2021-08-20 2021-10-19 郑州华赞医药科技有限公司 一种1-氯-3-甲氧基-5-甲基苯的合成方法

Family Cites Families (61)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB427857A (en) 1934-08-02 1935-05-01 Newsum Sons & Company Ltd H A new or improved system of construction for skeleton structures, particularly vehicle body frames and door frames
US4949314A (en) 1966-08-16 1990-08-14 The United States Of America As Represented By The Secretary Of The Navy Method and means for increasing echo-ranging-search rate
US3682932A (en) 1970-11-23 1972-08-08 Hoffmann La Roche 2-chloro-6-hydroxynicotinic acid
US4211771A (en) 1971-06-01 1980-07-08 Robins Ronald K Treatment of human viral diseases with 1-B-D-ribofuranosyl-1,2,4-triazole-3-carboxamide
US4189718A (en) * 1978-03-02 1980-02-19 Carson Manufacturing Company, Inc. Electronic siren
US4518584A (en) 1983-04-15 1985-05-21 Cetus Corporation Human recombinant interleukin-2 muteins
GB8327880D0 (en) 1983-10-18 1983-11-16 Ajinomoto Kk Saccharomyces cerevisiae
US4569790A (en) 1984-03-28 1986-02-11 Cetus Corporation Process for recovering microbially produced interleukin-2 and purified recombinant interleukin-2 compositions
US4530787A (en) 1984-03-28 1985-07-23 Cetus Corporation Controlled oxidation of microbially produced cysteine-containing proteins
US4604377A (en) 1984-03-28 1986-08-05 Cetus Corporation Pharmaceutical compositions of microbially produced interleukin-2
IL76360A0 (en) 1984-09-26 1986-01-31 Takeda Chemical Industries Ltd Mutual separation of proteins
US4752585A (en) 1985-12-17 1988-06-21 Cetus Corporation Oxidation-resistant muteins
US4748234A (en) 1985-06-26 1988-05-31 Cetus Corporation Process for recovering refractile bodies containing heterologous proteins from microbial hosts
AU622926B2 (en) 1988-09-09 1992-04-30 Nippon Kayaku Kabushiki Kaisha Pyrimidine or purine cyclobutane derivatives
US5925643A (en) 1990-12-05 1999-07-20 Emory University Enantiomerically pure β-D-dioxolane-nucleosides
US5464933A (en) 1993-06-07 1995-11-07 Duke University Synthetic peptide inhibitors of HIV transmission
US5489697A (en) 1994-08-03 1996-02-06 Medichem Research, Inc. Method for the preparation of (+)-calanolide A and intermediates thereof
DE69532245T2 (de) 1994-09-26 2004-09-16 Shionogi & Co., Ltd. Imidazolderivat
AU4788396A (en) 1995-02-16 1996-09-04 Children's Medical Center Corporation Inhibition of angiogenesis using interleukin-12
IL117574A0 (en) 1995-04-03 1996-07-23 Bristol Myers Squibb Co Processes for the preparation of cyclobutanone derivatives
WO2000016625A1 (en) 1998-09-23 2000-03-30 University Of Kentucky Research Foundation Antiviral drug compositions containing lithium inorganic salts
FR2783826B1 (fr) 1998-09-29 2002-07-19 Rhodia Chimie Sa Procede de preparation de 4-hydroxyquinoleines et/ou formes tautomeres
US7217714B1 (en) 1998-12-23 2007-05-15 Agouron Pharmaceuticals, Inc. CCR5 modulators
WO2000066559A1 (en) 1999-05-04 2000-11-09 Schering Corporation Piperidine derivatives useful as ccr5 antagonists
CZ20013940A3 (cs) 1999-05-04 2002-04-17 Schering Corporation Piperazinové deriváty uľitečné jako CCR5 antagonisté
CN1279040C (zh) 2000-05-26 2006-10-11 辉瑞大药厂 用于治疗的莨菪烷衍生物
GB0016787D0 (en) 2000-07-07 2000-08-30 Pfizer Ltd Compounds useful in therapy
GB0024795D0 (en) * 2000-10-10 2000-11-22 Hoffmann La Roche Pyrazole derivatives for the treatment of viral diseases
US6620586B2 (en) 2001-02-20 2003-09-16 Applied Gene Technologies, Inc. Methods and compositions for analyzing nucleic acids
GB0107228D0 (en) 2001-03-22 2001-05-16 Astrazeneca Ab Chemical compounds
GB0108046D0 (en) 2001-03-30 2001-05-23 Astrazeneca Ab Chemical compounds
EE05400B1 (et) 2001-04-10 2011-04-15 Pfizer Inc. Prasoolderivaadid, neid v?i nende farmatseutiliselt vastuv?etavaid sooli, solvaate v?i derivaate sisaldavad farmatseutilised kompositsioonid, nende kasutamine ning meetodid nende valmistamiseks
GB0113524D0 (en) 2001-06-04 2001-07-25 Hoffmann La Roche Pyrazole derivatives
GB0127547D0 (en) 2001-11-16 2002-01-09 Astrazeneca Ab Chemical compounds
SE0200919D0 (sv) 2002-03-25 2002-03-25 Astrazeneca Ab Chemical compounds
SE0202483D0 (sv) 2002-08-21 2002-08-21 Astrazeneca Ab Chemical compounds
JP2006505625A (ja) 2002-09-26 2006-02-16 ファイザー・インク Hiv感染症を治療するためのピラゾールアミド
MXPA05003195A (es) 2002-09-26 2005-06-08 Pfizer Derivados de pirazol como inhibidores de la transcriptasa inversa.
GB0223232D0 (en) 2002-10-07 2002-11-13 Pfizer Ltd Chemical compounds
GB0223234D0 (en) 2002-10-07 2002-11-13 Pfizer Ltd Chemical compounds
AR042628A1 (es) 2002-12-20 2005-06-29 Astrazeneca Ab Derivados de piperidina como moduladores del receptor ccr5
TW200423930A (en) * 2003-02-18 2004-11-16 Hoffmann La Roche Non-nucleoside reverse transcriptase inhibitors
TW200505441A (en) * 2003-03-24 2005-02-16 Hoffmann La Roche Non-nucleoside reverse transcriptase inhibitorsⅠ
BRPI0408704A (pt) 2003-03-24 2006-03-07 Hoffmann La Roche benzil-piridazinonas como inibidores de transcriptase reversa
US7220772B2 (en) * 2003-09-05 2007-05-22 Pfizer, Inc. Pyrazole derivatives
BRPI0507586A (pt) 2004-02-10 2007-07-03 Hoffmann La Roche moduladores de receptor de quimiocina ccr5
EP1730120A1 (en) * 2004-03-23 2006-12-13 F.Hoffmann-La Roche Ag Non-nucleoside reverse transcriptase inhibitors
US7625949B2 (en) * 2004-04-23 2009-12-01 Roche Palo Alto Llc Methods for treating retroviral infections
US7166738B2 (en) * 2004-04-23 2007-01-23 Roche Palo Alto Llc Non-nucleoside reverse transcriptase inhibitors
CN101001860A (zh) 2004-06-09 2007-07-18 霍夫曼-拉罗奇有限公司 杂环抗病毒化合物
WO2006010545A1 (en) * 2004-07-27 2006-02-02 F. Hoffmann-La Roche Ag Benzyltriazolone compounds as non-nucleoside reverse transcriptase inhibitors
CA2577144C (en) * 2004-09-30 2011-06-21 Boehringer Ingelheim International Gmbh Alkynyl compounds as non-nucleoside reverse transcriptase inhibitors
US20090264425A1 (en) 2004-12-22 2009-10-22 Pfizer Limited Chemical compounds
CA2600759A1 (en) * 2005-03-24 2006-09-28 F. Hoffmann-La Roche Ag 1,2,4-triazole-5-one compounds as heterocyclic reverse transcriptase inhibitors
AR057455A1 (es) * 2005-07-22 2007-12-05 Merck & Co Inc Inhibidores de la transcriptasa reversa de vih y composicion farmaceutica
DE602006004473D1 (de) * 2005-09-30 2009-02-05 Hoffmann La Roche Nnrt-inhibitoren
DE602006005699D1 (de) * 2005-10-19 2009-04-23 Hoffmann La Roche N-phenyl-phenylacetamid-nichtnukleosidinhibitoren reverser transkriptase
EP1940781A1 (en) * 2005-10-19 2008-07-09 F.Hoffmann-La Roche Ag Phenyl-acetamide nnrt inhibitors
EP2001880A2 (en) * 2006-03-07 2008-12-17 Array Biopharma, Inc. Heterobicyclic pyrazole compounds and methods of use
CN103497185A (zh) * 2007-03-14 2014-01-08 兰贝克赛实验室有限公司 用作磷酸二酯酶抑制剂的吡唑并(3,4-b)吡啶衍生物
WO2010106333A1 (en) * 2009-03-19 2010-09-23 Medical Research Council Technology Compounds

Also Published As

Publication number Publication date
CL2007002346A1 (es) 2008-03-14
ES2360893T3 (es) 2011-06-10
IL196655A (en) 2012-09-24
CA2658984C (en) 2014-12-02
TWI417293B (zh) 2013-12-01
DE602007013573D1 (de) 2011-05-12
AU2007286345A1 (en) 2008-02-21
MX2009001198A (es) 2009-02-11
BRPI0715193A2 (pt) 2013-10-01
WO2008019968A1 (en) 2008-02-21
KR101401811B1 (ko) 2014-05-29
EP2057125A1 (en) 2009-05-13
US20080045511A1 (en) 2008-02-21
JP2010500392A (ja) 2010-01-07
CA2658984A1 (en) 2008-02-21
KR20090040438A (ko) 2009-04-24
US20110059975A1 (en) 2011-03-10
US8063064B2 (en) 2011-11-22
PE20080734A1 (es) 2008-06-14
AR062366A1 (es) 2008-11-05
TW200817397A (en) 2008-04-16
PT2057125E (pt) 2011-05-31
AU2007286345B2 (en) 2012-03-08
JP5216768B2 (ja) 2013-06-19
IL196655A0 (en) 2009-11-18
RU2009109354A (ru) 2010-09-27
EP2057125B1 (en) 2011-03-30
NO20090405L (no) 2009-01-30
RU2451676C2 (ru) 2012-05-27
CN101501002B (zh) 2012-06-27
US7713974B2 (en) 2010-05-11
CN101501002A (zh) 2009-08-05
ATE503744T1 (de) 2011-04-15
PL2057125T3 (pl) 2011-09-30

Similar Documents

Publication Publication Date Title
DK2057125T3 (da) Ikke-nucleosid revers transkriptase-inhibitorer
IL199103A0 (en) Non-nucleoside reverse transcriptase inhibitors
EP2076492A4 (en) NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS
EP2217069A4 (en) INHIBITORS OF NON-NUCLEOSIDE INHIBITORS OF THE REVERSE TRANSCRIPTASE
NO20161397A1 (no) Ikke-nukleosidbaserte revers-transkriptase-inhibitorer
IL205386A0 (en) Non - nucleoside reverse transcriptase inhibitors
BRPI0813269A2 (pt) Inibidores de hiv transcriptase reversa
AP2514A (en) HIV reverse transcriptase inhibitors
CY2017016I1 (el) Αναστολεις πρωτεασωματος
DK2086939T3 (da) Pyridiacarboxamid som II-beta-HSDI-inhibitorer
EP2220091A4 (en) REVERSE transcriptase inhibitors
DK2383271T3 (da) Aminoquinoloner som GSK-3-inhibitorer
ATE425138T1 (de) N-phenyl-phenylacetamid-nichtnukleosidinhibitor n reverser transkriptase
DK2041138T3 (da) Pyrroltriazinkinase-inhibitorer
DK2024375T3 (da) Cyclopropyl-kondenserede indolobenzazepin-HCV-NS5B-hæmmere
DK2099447T3 (da) Imidazotriaziner og imidazopyrimidiner som kinaseinhibitorer
NO20084533L (no) Pyrimidin-derivat som PI3K-inhibitor og bruk av dette
CR10831A (es) INHIBIDORES ESPIRO CETONA DE ACETIL-CoA CARBOXILASA
DK2066662T3 (da) Serinhydrolaseinhibitorer
BRPI0810496A2 (pt) inibidores de transcriptase reversa de não-nucleosídeo
ZA200900071B (en) Non-nucleoside reverse transcriptase inhibitors
BRPI0811645A2 (pt) Inibidores de transcriptase reversa de não-nucleosídeo
EP1899340A4 (en) NON-NUCLEOSIDIC REVERSE TRANSCRIPTASE INHIBITORS
ATE522533T1 (de) Pyrazolopyrimidinonkinaseinhibitor
FI20075320A0 (fi) Uusia käyttökelpoisia inhibiittoreita