LU91528I9 - - Google Patents

Info

Publication number
LU91528I9
LU91528I9 LU91528C LU91528C LU91528I9 LU 91528 I9 LU91528 I9 LU 91528I9 LU 91528 C LU91528 C LU 91528C LU 91528 C LU91528 C LU 91528C LU 91528 I9 LU91528 I9 LU 91528I9
Authority
LU
Luxembourg
Application number
LU91528C
Other versions
LU91528I2 (fr
Inventor
Jan Heeres
Paul Adriaan Jan Janssen
Michael Joseph Kukla
Donald William Ludovici
Corte Bart De
Jonge Marc René De
Chih Yung Ho
Robert W Kavash
Lucien Maria Henricus Koymans
Aken Koen Jeanne Alfons Van
Original Assignee
Janssen Pharmaceutica Nv
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26805159&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=LU91528(I9) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of LU91528I2 publication Critical patent/LU91528I2/fr
Publication of LU91528I9 publication Critical patent/LU91528I9/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/12Heterocyclic 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
    • 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
    • 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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/55131,4-Benzodiazepines, e.g. diazepam or clozapine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • 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
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/47One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/78Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
    • C07D239/80Oxygen atoms

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Communicable Diseases (AREA)
  • Virology (AREA)
  • AIDS & HIV (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
LU91528C 1998-11-10 2009-02-18 "Etravirine sous toutes formes couvertes par le brevet de base" LU91528I2 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US10779298P 1998-11-10 1998-11-10
US14396299P 1999-07-15 1999-07-15
PCT/EP1999/007417 WO2000027825A1 (fr) 1998-11-10 1999-09-24 Pyrimidines inhibant la replication du vih

Publications (2)

Publication Number Publication Date
LU91528I2 LU91528I2 (fr) 2009-04-20
LU91528I9 true LU91528I9 (fr) 2019-01-02

Family

ID=26805159

Family Applications (1)

Application Number Title Priority Date Filing Date
LU91528C LU91528I2 (fr) 1998-11-10 2009-02-18 "Etravirine sous toutes formes couvertes par le brevet de base"

Country Status (41)

Country Link
US (5) US6878717B2 (fr)
EP (2) EP1002795B1 (fr)
JP (1) JP3635238B2 (fr)
KR (1) KR100658489B1 (fr)
CN (1) CN1214013C (fr)
AP (1) AP1683A (fr)
AR (1) AR024227A1 (fr)
AT (2) ATE455107T1 (fr)
AU (2) AU762523C (fr)
BG (1) BG65103B1 (fr)
BR (1) BRPI9915552B8 (fr)
CA (1) CA2350801C (fr)
CY (1) CY2008021I1 (fr)
CZ (1) CZ301367B6 (fr)
DE (3) DE69905683T2 (fr)
DK (1) DK1002795T3 (fr)
EA (1) EA004049B1 (fr)
EE (1) EE05086B1 (fr)
ES (2) ES2193664T3 (fr)
FR (1) FR09C0004I2 (fr)
HK (2) HK1025330A1 (fr)
HR (2) HRP20010161B9 (fr)
HU (2) HU230394B1 (fr)
ID (1) ID28376A (fr)
IL (2) IL143023A0 (fr)
LT (1) LTC1002795I2 (fr)
LU (1) LU91528I2 (fr)
MY (1) MY121108A (fr)
NL (1) NL300373I2 (fr)
NO (3) NO318801B1 (fr)
NZ (1) NZ511116A (fr)
OA (1) OA11674A (fr)
PL (1) PL204427B1 (fr)
PT (1) PT1002795E (fr)
SI (1) SI1002795T1 (fr)
SK (2) SK287269B6 (fr)
TR (1) TR200101306T2 (fr)
TW (1) TWI238161B (fr)
UA (1) UA70966C2 (fr)
WO (1) WO2000027825A1 (fr)
ZA (1) ZA200103769B (fr)

Families Citing this family (125)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CZ301367B6 (cs) * 1998-11-10 2010-02-03 Janssen Pharmaceutica N. V. Derivát pyrimidinu, zpusob a meziprodukty pro jeho prípravu a lécivo pro lécení HIV na jeho bázi
GB9914258D0 (en) * 1999-06-18 1999-08-18 Celltech Therapeutics Ltd Chemical compounds
AU775360B2 (en) 1999-09-24 2004-07-29 Janssen Pharmaceutica N.V. Antiviral compositions
DE19945982A1 (de) 1999-09-24 2001-03-29 Knoll Ag Geschwindigkeitsbestimmte Partikel
WO2001025220A1 (fr) 1999-10-07 2001-04-12 Amgen Inc. Inhibiteurs de triazine kinase
HUP0301117A3 (en) 2000-02-17 2004-01-28 Amgen Inc Thousand Oaks Imidazole derivatives kinase inhibitors, their use, process for their preparation and pharmaceutical compositions containing them
EP1282607B1 (fr) 2000-05-08 2015-11-11 Janssen Pharmaceutica NV Promedicaments a base de pyrimidines inhibant la replication du vih
JP5230050B2 (ja) 2000-05-08 2013-07-10 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ Hiv複製阻害剤
CN100339846C (zh) * 2000-11-01 2007-09-26 斯雷普内姆斯·Com公司 对域名数据的状态变化进行实时监测并即时注册的系统及方法
US6958211B2 (en) 2001-08-08 2005-10-25 Tibotech Bvba Methods of assessing HIV integrase inhibitor therapy
US7638522B2 (en) 2001-08-13 2009-12-29 Janssen Pharmaceutica N.V. Salt of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]amino] benzonitrile
JO3429B1 (ar) 2001-08-13 2019-10-20 Janssen Pharmaceutica Nv مشتقات برميدينات مثبطة فيروس الايدز
US8101629B2 (en) 2001-08-13 2012-01-24 Janssen Pharmaceutica N.V. Salt of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]amino]benzonitrile
US6939874B2 (en) 2001-08-22 2005-09-06 Amgen Inc. Substituted pyrimidinyl derivatives and methods of use
US7115617B2 (en) 2001-08-22 2006-10-03 Amgen Inc. Amino-substituted pyrimidinyl derivatives and methods of use
JP4460292B2 (ja) 2001-10-17 2010-05-12 ベーリンガー インゲルハイム ファルマ ゲゼルシャフト ミット ベシュレンクテル ハフツング ウント コンパニー コマンディトゲゼルシャフト ピリミジン誘導体、これらの化合物を含む医薬組成物、その使用及びその調製方法
EP1453516A2 (fr) 2001-10-17 2004-09-08 Boehringer Ingelheim Pharma GmbH & Co.KG Nouvelles pyrimidines substituees, procede permettant de les produire et leur utilisation comme medicament
HUP0402330A3 (en) 2001-11-01 2010-03-29 Janssen Pharmaceutica Nv Amide derivatives as glycogen synthase kinase 3-beta inhibitors, process for producing them, pharmaceutical compositions containing them and use thereof
CA2463822A1 (fr) 2001-11-01 2003-05-08 Janssen Pharmaceutica N.V. Heteroaryl amines utiles comme inhibiteurs de glycogene synthase kinase 3beta (inhibiteurs de gsk3)
SE0104140D0 (sv) 2001-12-07 2001-12-07 Astrazeneca Ab Novel Compounds
TWI329105B (en) 2002-02-01 2010-08-21 Rigel Pharmaceuticals Inc 2,4-pyrimidinediamine compounds and their uses
WO2003075929A1 (fr) 2002-03-13 2003-09-18 Janssen Pharmaceutica N.V. Inhibiteurs de l'histone déacétylase
ATE396971T1 (de) 2002-03-13 2008-06-15 Janssen Pharmaceutica Nv Sulfonylaminoderivate als neue inhibitoren von histondeacetylase
GB0206215D0 (en) 2002-03-15 2002-05-01 Novartis Ag Organic compounds
CN1290893C (zh) * 2002-05-03 2006-12-20 詹森药业有限公司 聚合物微乳状液
AR039540A1 (es) * 2002-05-13 2005-02-23 Tibotec Pharm Ltd Compuestos microbicidas con contenido de pirimidina o triazina
TW200409629A (en) 2002-06-27 2004-06-16 Bristol Myers Squibb Co 2,4-disubstituted-pyridine N-oxides useful as HIV reverse transcriptase inhibitors
CN103169708B (zh) 2002-07-29 2018-02-02 里格尔药品股份有限公司 用2,4‑嘧啶二胺化合物治疗或者预防自体免疫性疾病的方法
WO2004016581A1 (fr) * 2002-08-09 2004-02-26 Janssen Pharmaceutica N.V. Procedes de preparation de 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]amino]benzonitrile
EP1551372B8 (fr) 2002-09-20 2018-08-01 Alpharma Pharmaceuticals LLC Sous-unite de sequestration et compositions et procedes associes
CA2502970A1 (fr) * 2002-11-28 2004-06-10 Schering Aktiengesellschaft Pyrimidines inhibitrices de chk-, pdk- et de akt, production et utilisation de ces composes comme agents pharmaceutiques
GEP20084540B (en) 2003-01-14 2008-11-25 Arena Pharm Inc 1,2,3-trisubstituted aryl and heteroaryl derivatives as modulators of metabolism and the prpphylaxis and treatment of disorders related thereto such as diabetes and hyperglycemia
AP2005003365A0 (en) * 2003-02-07 2005-09-30 Janssen Pharmaceutica Nv Hiv inhibiting 1, 2, 4-triazines.
KR20110132482A (ko) 2003-02-07 2011-12-07 얀센 파마슈티카 엔.브이. Hiv 감염 예방용 피리미딘 유도체
CL2004000303A1 (es) * 2003-02-20 2005-04-08 Tibotec Pharm Ltd Compuestos derivados de pirimidinas y triazinas; proceso de preparacion; composicion farmaceutica; y su uso para inhibir la replicacion del vih.
DE602004021472D1 (en) * 2003-02-20 2009-07-23 Smithkline Beecham Corp Pyrimiidinverbindungen
CN1822843B (zh) * 2003-07-17 2010-04-28 泰博特克药品有限公司 制备含有抗病毒药物颗粒的方法
RS53109B (en) 2003-07-30 2014-06-30 Rigel Pharmaceuticals Inc. 2,4 PIRIMIDINDIAMINE COMPOUNDS FOR USE IN TREATMENT OR PREVENTION OF AUTOIMMUNE DISEASES
DE602004031641D1 (de) * 2003-09-25 2011-04-14 Janssen Pharmaceutica Nv Die replikation von hiv hemmende purinderivate
JP5213228B2 (ja) 2004-03-02 2013-06-19 ビルコ・ビーブイビーエイ 臨床的カット−オフ値の推測
EP1598343A1 (fr) * 2004-05-19 2005-11-23 Boehringer Ingelheim International GmbH Dérivés de 2-arylaminopyrimidines comme des inhibiteurs de PLK
EA010652B1 (ru) 2004-07-28 2008-10-30 Янссен Фармацевтика Н.В. Замещенные индолильные алкиламинопроизводные в качестве новых ингибиторов гистондеацетилазы
EP1797050B1 (fr) 2004-08-10 2013-10-23 Janssen Pharmaceutica NV Dérivés de 1,2,4-triazin-6-one destinés à inhiber le hiv
MX2007003796A (es) 2004-09-30 2007-04-25 Tibotec Pharm Ltd Pirimidinas 5-sustituidas inhibidoras del virus de inmunodeficiencia humana.
US7531548B2 (en) * 2004-09-30 2009-05-12 Tibotec Pharmaceuticals Ltd HIV inhibiting 5-carbo- or heterocyclic substituted pyrimidines
TW200626574A (en) 2004-09-30 2006-08-01 Tibotec Pharm Ltd HIV inhibiting 5-heterocyclyl pyrimidines
CA2577588C (fr) 2004-10-29 2013-09-10 Tibotec Pharmaceuticals Ltd. Derives de pyrimidine bicycliques inhibant le vih
EP1812069A2 (fr) * 2004-11-08 2007-08-01 Boehringer Ingelheim International GmbH Methode de traitement d'infection vih par coadministration de tipranavir et etravirine
ATE540035T1 (de) 2004-11-24 2012-01-15 Rigel Pharmaceuticals Inc Spiro-2,4-pyrimidindiamin-verbindungen und ihre verwendungen
ES2337496T3 (es) 2005-01-19 2010-04-26 Rigel Pharmaceuticals, Inc. Profarmacos de compuestos de 2,4-pirimidindiamina y sus usos.
CN101107234B (zh) * 2005-01-27 2013-06-19 泰博特克药品有限公司 抑制hiv的2-(4-氰基苯氨基)嘧啶衍生物
PT1853588E (pt) 2005-02-16 2008-08-25 Astrazeneca Ab Compostos químicos
MX2007010051A (es) * 2005-02-18 2007-09-21 Tibotec Pharm Ltd Derivados de oxido de 2-(4-cianofenilamino)pirimidina que inhiben el virus de inmunodeficiencia humana.
BRPI0609291B1 (pt) * 2005-03-04 2022-02-08 Janssen Sciences Ireland Uc 2-(4-ciano-fenil)-o-hidroxilamina-pirimidinas que inibem hiv, composição farmacêutica que as compreende e processo para a preparação de ambas
US20080287437A1 (en) 2005-05-16 2008-11-20 Astrazeneca Ab Pyrazolylaminopyrimidine Derivatives Useful as Tyrosine Kinase Inhibitors
DK1888537T3 (da) 2005-05-26 2013-12-09 Janssen R & D Ireland Fremgangsmåde til fremstilling af 4[(1,6-dihydro-6-oxo-2-pyrimidinyl)amino]benzonitril
US20070203161A1 (en) 2006-02-24 2007-08-30 Rigel Pharmaceuticals, Inc. Compositions and methods for inhibition of the jak pathway
NZ563454A (en) 2005-06-08 2011-03-31 Rigel Pharmaceuticals Inc 2,4-diaminopyrimidine derivatives for inhibition of the JAK pathway
EP1945208A4 (fr) * 2005-10-06 2011-08-03 Univ Massachusetts Composition et synthese de nouveaux reactifs pour inhiber la replication du vih
PL1945631T3 (pl) 2005-10-28 2012-12-31 Astrazeneca Ab Pochodne 4-(3-aminopirazolo)pirymidyny do stosowania jako inhibitory kinazy tyrozynowej do leczenia raka
WO2007082874A1 (fr) 2006-01-19 2007-07-26 Janssen Pharmaceutica N.V. Dérivés de pyridine et de pyrimidine en tant qu'inhibiteurs d'histone désacétylase
SI1981874T1 (sl) 2006-01-19 2009-10-31 Janssen Pharmaceutica Nv Aminofenilni derivati kot novi inhibitorji histon deacetilaze
DK1981875T3 (da) 2006-01-19 2014-07-14 Janssen Pharmaceutica Nv Substituerede indolylalkylaminoderivater som inhibitorer af histondeacetylase
EP1991532B1 (fr) 2006-02-24 2017-01-11 Rigel Pharmaceuticals, Inc. Compositions et méthodes destinées à l'inhibition de la voie jak
EP2004632B1 (fr) 2006-03-30 2014-03-12 Janssen R&D Ireland Pyrimidines à substitution 5-amido inhibant le vih
DK2004641T3 (da) 2006-03-30 2011-01-24 Tibotec Pharm Ltd HIV-inhiberende 5-(hydroxymethylen og aminomethylen) substituerede pyrimidiner
US8623887B2 (en) 2006-05-15 2014-01-07 Boehringer Ingelheim International Gmbh Compounds
PT2029110E (pt) * 2006-06-06 2011-11-23 Tibotec Pharm Ltd Processo para preparar formulações secas por atomização de tmc125
EP2526932B1 (fr) 2006-06-19 2017-06-07 Alpharma Pharmaceuticals LLC Composition pharmaceutique
WO2008063301A2 (fr) * 2006-10-11 2008-05-29 Alpharma, Inc. Compositions pharmaceutiques
WO2008068299A2 (fr) 2006-12-06 2008-06-12 Tibotec Pharmaceuticals Ltd. Sel de bromhydrate d'un composé anti-vih
JP5185283B2 (ja) * 2006-12-29 2013-04-17 テイボテク・フアーマシユーチカルズ Hiv阻害6−置換ピリミジン
CN101573342A (zh) * 2006-12-29 2009-11-04 泰博特克药品有限公司 抑制hiv的5,6-取代的嘧啶类化合物
UA99459C2 (en) 2007-05-04 2012-08-27 Астразенека Аб 9-(pyrazol-3-yl)- 9h-purine-2-amine and 3-(pyraz0l-3-yl)-3h-imidazo[4,5-b]pyridin-5-amine derivatives and their use for the treatment of cancer
US8410124B2 (en) 2007-10-18 2013-04-02 Concert Pharmaceuticals Inc. Deuterated etravirine
US8623418B2 (en) 2007-12-17 2014-01-07 Alpharma Pharmaceuticals Llc Pharmaceutical composition
US20100151014A1 (en) * 2008-12-16 2010-06-17 Alpharma Pharmaceuticals, Llc Pharmaceutical composition
AU2008338442A1 (en) * 2007-12-17 2009-06-25 Alpharma Pharmaceuticals, Llc Pharmaceutical composition
SI2300013T1 (en) 2008-05-21 2018-03-30 Adriad Pharmacaceuticals, Inc. Phosphorus derivatives as kinase inhibitors
US9273077B2 (en) 2008-05-21 2016-03-01 Ariad Pharmaceuticals, Inc. Phosphorus derivatives as kinase inhibitors
US8338439B2 (en) 2008-06-27 2012-12-25 Celgene Avilomics Research, Inc. 2,4-disubstituted pyrimidines useful as kinase inhibitors
US11351168B1 (en) 2008-06-27 2022-06-07 Celgene Car Llc 2,4-disubstituted pyrimidines useful as kinase inhibitors
CA2986640C (fr) 2008-06-27 2019-03-26 Celgene Avilomics Research, Inc. Composes hetero-aryles et leurs utilisations
TW201016676A (en) * 2008-10-03 2010-05-01 Astrazeneca Ab Heterocyclic derivatives and methods of use thereof
US20110071158A1 (en) * 2009-03-18 2011-03-24 Boehringer Ingelheim International Gmbh New compounds
JP5748737B2 (ja) 2009-03-30 2015-07-15 ヤンセン・アールアンドデイ・アイルランド エトラビリンとニコチンアミドの共結晶
WO2010129053A2 (fr) 2009-05-05 2010-11-11 Dana Farber Cancer Institute Inhibiteurs d'egfr et procédés de traitement de troubles
WO2010131118A2 (fr) * 2009-05-12 2010-11-18 Pliva Hrvatska D.O.O. Formes polymorphes d'étravirine et leurs procédés de préparation
WO2010150279A2 (fr) 2009-06-22 2010-12-29 Emcure Pharmaceuticals Limited Procédé pour la synthèse d'inhibiteur non nucléosidique de la transcriptase inverse diarylpyrimidine
US8153790B2 (en) 2009-07-27 2012-04-10 Krizmanic Irena Process for the preparation and purification of etravirine and intermediates thereof
GR1007010B (el) 2009-10-08 2010-10-07 Χημικα Και Βιοφαρμακευτικα Εργαστηρια Πατρων Αε (Cbl-Patras), Ινσουλινοειδη πεπτιδια
CN103038230B (zh) 2010-06-04 2016-05-25 霍夫曼-拉罗奇有限公司 作为lrrk2调节剂的氨基嘧啶衍生物
WO2012001695A1 (fr) 2010-06-28 2012-01-05 Hetero Research Foundation Procédé de préparation d'intermédiaire de l'étravirine et de polymorphes de l'étravirine
BR112013003388A2 (pt) 2010-08-10 2016-07-12 Celgene Avilomics Res Inc sal de besilato de um inibidor de btk
CA2812061A1 (fr) 2010-09-22 2012-03-29 Arena Pharmaceuticals, Inc. Modulateurs du recepteur gpr119 et traitement des troubles qui lui sont lies
US9238629B2 (en) 2010-11-01 2016-01-19 Celgene Avilomics Research, Inc. Heteroaryl compounds and uses thereof
MX2013004894A (es) 2010-11-01 2013-10-17 Celgene Avilomics Res Inc Compuestos heterociclicos y usos de los mismos.
JP5986094B2 (ja) 2010-11-10 2016-09-06 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft Lrrk2調節薬としてのピラゾールアミノピリミジン誘導体
EP2637502B1 (fr) 2010-11-10 2018-01-10 Celgene CAR LLC Inhibiteurs d'egfr sélectifs d'un mutant et leurs utilisations
EP2702045B1 (fr) 2011-04-26 2017-10-18 Mylan Laboratories Ltd. Nouveau procédé de préparation d'étravirine
EP2704572B1 (fr) 2011-05-04 2015-12-30 Ariad Pharmaceuticals, Inc. Composés permettant d'inhiber la prolifération cellulaire dans les cancers induits par l'egfr
WO2012170647A1 (fr) * 2011-06-09 2012-12-13 Assia Chemical Industriew Ltd. Procédé pour la préparation d'étravirine et intermédiaires dans la synthèse de celle-ci
CN103974955B (zh) 2011-08-23 2018-06-19 阿萨纳生物科技有限责任公司 嘧啶并-哒嗪酮化合物及其用途
WO2013059572A1 (fr) 2011-10-19 2013-04-25 Assia Chemical Industries Ltd. Procédé de préparation d'etravarine et produits intermédiaires utiles dans la synthèse de ce composé
EP2770830A4 (fr) 2011-10-28 2015-05-27 Celgene Avilomics Res Inc Méthodes de traitement d'une maladie ou d'une affection associée à la tyrosine-kinase btk (bruton's tyrosine kinase)
US8703786B2 (en) * 2011-12-07 2014-04-22 Texas Southern University Etravirine formulations and uses thereof
US9108927B2 (en) 2012-03-15 2015-08-18 Celgene Avilomics Research, Inc. Salts of an epidermal growth factor receptor kinase inhibitor
CA2866852C (fr) 2012-03-15 2020-12-29 Celgene Avilomics Research, Inc. Formes solides d'un inhibiteur de kinases du recepteur du facteur de croissance epidermique
US20150166591A1 (en) 2012-05-05 2015-06-18 Ariad Pharmaceuticals, Inc. Methods and compositions for raf kinase mediated diseases
US20150336900A1 (en) * 2012-10-29 2015-11-26 Biophore India Pharmaceuticals Pvt. Ltd. Process for the Synthesis of Etravirine and Its Intermediates
WO2014072419A1 (fr) 2012-11-08 2014-05-15 Universiteit Antwerpen Nouveaux composés anti-vih
WO2014100748A1 (fr) 2012-12-21 2014-06-26 Celgene Avilomics Research, Inc. Composés hétéroarylés et leurs utilisations
KR20150126595A (ko) 2012-12-21 2015-11-12 벌릭스 파마 인코포레이티드 간 질환 또는 증상의 치료를 위한 용도 및 방법
MX2015009952A (es) 2013-02-08 2015-10-05 Celgene Avilomics Res Inc Inhibidores de cinasas reguladas por señales extracelulares (erk) y sus usos.
US9611283B1 (en) 2013-04-10 2017-04-04 Ariad Pharmaceuticals, Inc. Methods for inhibiting cell proliferation in ALK-driven cancers
US9492471B2 (en) 2013-08-27 2016-11-15 Celgene Avilomics Research, Inc. Methods of treating a disease or disorder associated with Bruton'S Tyrosine Kinase
US9415049B2 (en) 2013-12-20 2016-08-16 Celgene Avilomics Research, Inc. Heteroaryl compounds and uses thereof
US10005760B2 (en) 2014-08-13 2018-06-26 Celgene Car Llc Forms and compositions of an ERK inhibitor
AU2016205361C1 (en) 2015-01-06 2021-04-08 Arena Pharmaceuticals, Inc. Methods of treating conditions related to the S1P1 receptor
CN104926829A (zh) * 2015-06-08 2015-09-23 山东大学 一种噻吩并嘧啶类衍生物及其制备方法和应用
KR102603199B1 (ko) 2015-06-22 2023-11-16 아레나 파마슈티칼스, 인크. S1p1 수용체-관련 장애에서의 사용을 위한 (r)-2-(7-(4-시클로펜틸-3-(트리플루오로메틸)벤질옥시)-1,2,3,4-테트라히드로시클로-펜타[b]인돌-3-일)아세트산 (화합물 1)의 결정성 l-아르기닌 염
CN110066273A (zh) * 2019-06-05 2019-07-30 山东大学 一种含三氮唑环的单芳基嘧啶类hiv-1逆转录酶抑制剂及其制备方法与应用
EP3994132A1 (fr) 2019-07-03 2022-05-11 Sumitomo Dainippon Pharma Oncology, Inc. Inhibiteurs de tyrosine kinase non récepteur 1 (tnk1) et leurs utilisations
CN111217833B (zh) * 2020-02-21 2021-03-16 山东大学 噻吩并[2,3-d]嘧啶类HIV-1非核苷类逆转录酶抑制剂及其制备方法和应用
CN111875548A (zh) * 2020-07-16 2020-11-03 山东大学 一种5位芳环取代的二芳基嘧啶类衍生物及其制备方法与应用

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3459731A (en) 1966-12-16 1969-08-05 Corn Products Co Cyclodextrin polyethers and their production
US4659363A (en) * 1983-07-25 1987-04-21 Ciba-Geigy Corporation N-(2-nitrophenyl)-2-aminopyrimidine derivatives, the preparation and use thereof
DE3581570D1 (de) * 1984-06-25 1991-03-07 Ciba Geigy Ag Pyrimidinderivate wirksam als schaedlingsbekaempfungsmittel.
WO1989009213A1 (fr) 1988-03-31 1989-10-05 Mitsubishi Kasei Corporation Derives de nucleoside de pyrimidine acyclique substitue en 6 et agents antiviraux contenant ces composes en tant qu'ingredients actifs
JPH02308248A (ja) 1989-05-24 1990-12-21 Fuji Photo Film Co Ltd アミノピリミジン系色素形成カプラーおよび該カプラーを含有するハロゲン化銀カラー写真感光材料
JP2895680B2 (ja) * 1992-07-08 1999-05-24 シャープ株式会社 磁気ヘッドおよびその製造方法
US5516775A (en) 1992-08-31 1996-05-14 Ciba-Geigy Corporation Further use of pyrimidine derivatives
CN1142817A (zh) * 1993-10-12 1997-02-12 杜邦麦克制药有限公司 1n-烷基-n-芳基嘧啶胺及其衍生物
US5691364A (en) * 1995-03-10 1997-11-25 Berlex Laboratories, Inc. Benzamidine derivatives and their use as anti-coagulants
GB9523675D0 (en) * 1995-11-20 1996-01-24 Celltech Therapeutics Ltd Chemical compounds
CZ154398A3 (cs) 1995-11-23 1998-08-12 Janssen Pharmaceutica N.V. Pevné směsi cyklodextrinů připravené vytlačováním taveniny
KR100219922B1 (ko) * 1996-05-16 1999-09-01 이서봉 신규한 항바이러스성 6-아릴옥시 및 6-아릴카르보닐 2,4-피리미딘디온 유도체 및 그의 제조 방법
GB9619284D0 (en) * 1996-09-16 1996-10-30 Celltech Therapeutics Ltd Chemical compounds
NO311614B1 (no) * 1996-10-01 2001-12-17 Janssen Pharmaceutica Nv Substituerte diamino-1,3,5-triazinderivater
GB9705361D0 (en) * 1997-03-14 1997-04-30 Celltech Therapeutics Ltd Chemical compounds
DE29704863U1 (de) * 1997-03-17 1997-05-22 Gesellschaft für Innenhochdruckverfahren mbH & Co. KG, 73441 Bopfingen Achsschwinge
BR9908004A (pt) 1998-02-17 2001-12-18 Tularik Inc Composto, composição e método para prevençãoou supressão de uma infecção viral
EP0945442A1 (fr) 1998-03-27 1999-09-29 Janssen Pharmaceutica N.V. Dérivés de pyrimidine trisubstitués
AU751573C (en) * 1998-03-27 2003-10-09 Janssen Pharmaceutica N.V. HIV inhibiting pyrimidine derivatives
KR100643419B1 (ko) * 1998-03-27 2006-11-10 얀센 파마슈티카 엔.브이. Hiv를 억제하는 피리미딘 유도체
CZ301367B6 (cs) * 1998-11-10 2010-02-03 Janssen Pharmaceutica N. V. Derivát pyrimidinu, zpusob a meziprodukty pro jeho prípravu a lécivo pro lécení HIV na jeho bázi
EP1282607B1 (fr) * 2000-05-08 2015-11-11 Janssen Pharmaceutica NV Promedicaments a base de pyrimidines inhibant la replication du vih

Also Published As

Publication number Publication date
HRP20080359A2 (en) 2008-12-31
NZ511116A (en) 2003-08-29
ES2193664T3 (es) 2003-11-01
KR100658489B1 (ko) 2006-12-18
CY2008021I2 (el) 2010-07-28
NL300373I1 (nl) 2009-03-02
HRP20010161A2 (en) 2002-02-28
EP1002795A1 (fr) 2000-05-24
HK1025330A1 (en) 2000-11-10
US6878717B2 (en) 2005-04-12
JP3635238B2 (ja) 2005-04-06
HU227453B1 (en) 2011-06-28
HRP20010161B9 (hr) 2014-10-24
EP1270560A1 (fr) 2003-01-02
AU762523B2 (en) 2003-06-26
EP1270560B1 (fr) 2010-01-13
FR09C0004I2 (fr) 2010-06-11
FR09C0004I1 (fr) 2009-02-27
PL204427B1 (pl) 2010-01-29
PT1002795E (pt) 2003-07-31
HU230394B1 (hu) 2016-04-28
ATE233740T1 (de) 2003-03-15
CZ20011533A3 (cs) 2001-10-17
AU762523C (en) 2004-02-12
EA004049B1 (ru) 2003-12-25
CZ301367B6 (cs) 2010-02-03
DE69941934D1 (de) 2010-03-04
DE69905683T2 (de) 2004-03-18
KR20010075235A (ko) 2001-08-09
AR024227A1 (es) 2002-09-25
US20040039005A1 (en) 2004-02-26
WO2000027825A1 (fr) 2000-05-18
UA70966C2 (uk) 2004-11-15
HK1048817A1 (en) 2003-04-17
EP1002795B1 (fr) 2003-03-05
NO318801B1 (no) 2005-05-09
ATE455107T1 (de) 2010-01-15
BG65103B1 (bg) 2007-02-28
MY121108A (en) 2005-12-30
HRP20010161B1 (en) 2009-03-31
BRPI9915552B8 (pt) 2021-05-25
PL347586A1 (en) 2002-04-08
SK287269B6 (sk) 2010-05-07
AP1683A (en) 2006-11-29
TWI238161B (en) 2005-08-21
US20050288278A1 (en) 2005-12-29
EA200100536A1 (ru) 2002-02-28
CA2350801C (fr) 2008-05-20
AU6200899A (en) 2000-05-29
LTC1002795I2 (lt) 2021-06-10
HRP20080359B1 (hr) 2016-01-01
DE122009000003I1 (de) 2009-05-20
US20110263625A1 (en) 2011-10-27
LTPA2008016I1 (lt) 2021-04-26
JP2002529456A (ja) 2002-09-10
SK6032001A3 (en) 2002-01-07
CN1214013C (zh) 2005-08-10
HUP0104177A3 (en) 2003-01-28
OA11674A (en) 2005-01-12
US20080176880A1 (en) 2008-07-24
EE200100252A (et) 2002-10-15
BG105418A (en) 2001-11-30
NO2009003I1 (no) 2009-03-09
IL143023A0 (en) 2002-04-21
LU91528I2 (fr) 2009-04-20
SK287270B6 (sk) 2010-05-07
US20030114472A1 (en) 2003-06-19
ZA200103769B (en) 2002-08-12
SI1002795T1 (en) 2003-10-31
ES2338760T3 (es) 2010-05-12
CN1322198A (zh) 2001-11-14
BR9915552A (pt) 2001-08-14
US7037917B2 (en) 2006-05-02
US8003789B2 (en) 2011-08-23
CA2350801A1 (fr) 2000-05-18
AU2011200708A1 (en) 2011-03-10
CY2008021I1 (el) 2010-07-28
HK1048817B (zh) 2010-04-09
NO2009003I2 (no) 2010-06-07
NL300373I2 (nl) 2009-04-01
NO20011696L (no) 2001-04-04
NO2021015I1 (no) 2021-03-29
BR9915552B1 (pt) 2013-11-19
DE69905683D1 (de) 2003-04-10
DK1002795T3 (da) 2003-06-30
ID28376A (id) 2001-05-17
EE05086B1 (et) 2008-10-15
HUP0104177A2 (hu) 2002-03-28
NO20011696D0 (no) 2001-04-04
IL169949A (en) 2011-02-28
US8530655B2 (en) 2013-09-10
TR200101306T2 (tr) 2001-10-22

Similar Documents

Publication Publication Date Title
FR09C0004I1 (fr)
BRPI9917862A2 (fr)
BRPI9914151B8 (fr)
ECSDI980465S (fr)
ECSDI980486S (fr)
IN187753B (fr)
CN3078962S (fr)
CN3079181S (fr)
BY6371C1 (fr)
CL1998003164A1 (fr)
CN3072688S (fr)
CN3072756S (fr)
CN3073190S (fr)
CN3073771S (fr)
CN3074054S (fr)
CN3074474S (fr)
CN3074906S (fr)
CN3074964S (fr)
CN3075297S (fr)
CN3075591S (fr)
CN3077352S (fr)
CN3078087S (fr)
CN3078314S (fr)
CN3078569S (fr)
CN3073425S (fr)