PA8603801A1 - Derivados de la quinazolina - Google Patents

Derivados de la quinazolina

Info

Publication number
PA8603801A1
PA8603801A1 PA20048603801A PA8603801A PA8603801A1 PA 8603801 A1 PA8603801 A1 PA 8603801A1 PA 20048603801 A PA20048603801 A PA 20048603801A PA 8603801 A PA8603801 A PA 8603801A PA 8603801 A1 PA8603801 A1 PA 8603801A1
Authority
PA
Panama
Prior art keywords
rent
alquil
represents hydrogen
amino
replaced
Prior art date
Application number
PA20048603801A
Other languages
English (en)
Inventor
Eddy Jean Edgard Freyne
Timothy Pietro Suren Perera
Peter Jacobus Johannes Antonius Buijnsters
Marc Willems
Gaston Stanislas Marcella Diels
Werner Constant Johan Embrechts
Holte Peter Ten
Carsten Schultz-Fademrecht
Frederik Jan Rita Rombouts
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=33493782&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PA8603801(A1) "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 PA8603801A1 publication Critical patent/PA8603801A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/06Peri-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/04Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C229/06Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton
    • C07C229/10Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
    • C07C229/16Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings to carbon atoms of hydrocarbon radicals substituted by amino or carboxyl groups, e.g. ethylenediamine-tetra-acetic acid, iminodiacetic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/40Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino groups bound to carbon atoms of at least one six-membered aromatic ring and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • 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
    • C07D239/86Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/88Oxygen atoms
    • 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
    • C07D239/86Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/93Sulfur atoms
    • 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
    • C07D239/86Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/94Nitrogen atoms

Abstract

LA PRESENTE INVENCION SE REFIERE A LOS COMPUESTOS DE FORMULA (I) LAS FORMAS N-OXIDOS, LAS SALES DE ADICION ACEPTABLES PARA USO FARMACEUTICO Y LAS FORMAS ESTEREOQUIMICAMENTE ISOMERAS DE LOS MISMOS, DONDE: Z REPRESENTA NH; Y REPRESENTA -ALQUILO C3-C9-, -ALQUENILO C2-C9, -ALQUIL-C3-C7-CO-NH- SUSTITUIDO EN FORMA OPTATIVA CON AMINO, MONO- O DI(ALQUIL-C1-4)AMINO O ALQUILOXICARBONILAMINO C1-4-, -ALQUENIL-C3-7-CO-NH-OPCIONALMENTE SUSTITUIDO CON AMINO, MONO- O DI(ALQUIL-C1-4)AMINO O ALQUILOXICARBONILAMINO C1-4-, -ALQUIL-C1-5-NR13-ALQUILO C1-5, -ALQUIL-C1-5-NR14-CO-ALQUILO C1-5, -ALQUIL-C1-6-CO-NH-, -ALQUIL-C1-5-CO-NR15-ALQUILO C1-5-, -ALQUIL-C1-6-CO-NH-, -ALQUIL-C1-6-NH-CO-, -ALQUIL-C1-3-NH-CS-HET20-, -ALQUIL-C1-3-NH-CO-HET20-, -ALQUIL-C1-2-CO-HET21-CO-, -ALQUIL-C1-2-NH-CO-CR16R17-NH-, ALQUIL-C1-2-CO-NH-CR18R19-CO-, -ALQUIL-C1-2-CO-NR20-ALQUIL-C1-3-CO- O NR22-CO-ALQUIL-C1-3-NH-; X1 REPRESENTA UNA UNION DIRECTA, O, -O-ALQUILO C1-2-; X2 REPRESENTA UNA UNION DIRECTA, -CO-ALQUILO C1-2-,NR12,-NR12- ALQUILO C1-2-, -O-N=CH- O -ALQUILO C1-2-; R1 Y R2 CADA UNO DE FORMA IDEPENDIENTE REPRESENTA HIDROGENO O HALO; R3 REPRESENTA HIDROGENO;R4 REPRESENTA HIDROGENO O ALQUILOXI C1-4; R12 Y R13 CADA UNO DE MANERA INDEPENDIENTE REPRESENTA HIDROGENO O ALQUILO C1-4; R14 Y R15 REPRESENTAN HIDROGENO; R16 Y R17 CADA UNO DE MANERA INDEPENDIENTE REPRESENTAN HIDROGENO O ALQUILO C1-4; R18 Y R19 CADA UNO DE MANERA INDEPENDIENTE REPRESENTA HIDROGENO O ALQUILO C1-4 SUSTITUIDO DE MANERA OPCIONAL CON FENILO O HIDROXI; R20 Y R21 CADA UNO DE MANERA INDEPENDIENTE REPRESENTA HIDROGENO O ALQUILO C1-4 SUSTITUIDO DE MANERA OPCIONAL CON ALQUILOXI C1-4. HET20, HET21 Y HET22 CADA UNO EN FORMA INDEPENDIENTE REPRESENTA UN HETEROCICLO SELECCIONADO DEL GRUPO INTEGRADO POR PIRROLIDINILO, 2-PIRROLIDINONILO O PIPERIDINILO SUSTITUIDO DE MANERA OPCIONAL CON HIDROXI.
PA20048603801A 2003-05-27 2004-05-24 Derivados de la quinazolina PA8603801A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP0305723 2003-05-27
EP0310266 2003-09-15
EP0351061 2003-12-18

Publications (1)

Publication Number Publication Date
PA8603801A1 true PA8603801A1 (es) 2004-12-16

Family

ID=33493782

Family Applications (1)

Application Number Title Priority Date Filing Date
PA20048603801A PA8603801A1 (es) 2003-05-27 2004-05-24 Derivados de la quinazolina

Country Status (32)

Country Link
US (4) US7648975B2 (es)
EP (2) EP2305687A1 (es)
JP (1) JP4887151B2 (es)
KR (1) KR101143878B1 (es)
CN (1) CN102718775B (es)
AR (2) AR045687A1 (es)
AT (1) ATE544454T1 (es)
AU (1) AU2004243487B2 (es)
BR (1) BRPI0410714B8 (es)
CA (1) CA2525214C (es)
CL (1) CL2004001267A1 (es)
CO (1) CO5640038A2 (es)
CY (1) CY1113002T1 (es)
DK (1) DK1633365T3 (es)
EA (1) EA009064B1 (es)
ES (1) ES2381976T3 (es)
HK (1) HK1176350A1 (es)
HR (1) HRP20120351T1 (es)
IL (3) IL172154A0 (es)
IS (1) IS3030B (es)
JO (1) JO2785B1 (es)
MX (1) MXPA05012762A (es)
MY (1) MY148633A (es)
NO (1) NO334209B1 (es)
NZ (1) NZ544154A (es)
PA (1) PA8603801A1 (es)
PL (1) PL1633365T3 (es)
PT (1) PT1633365E (es)
SI (1) SI1633365T1 (es)
TW (3) TWI468397B (es)
UA (1) UA84010C2 (es)
WO (1) WO2004105765A1 (es)

Families Citing this family (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JO2785B1 (en) * 2003-05-27 2014-03-15 شركة جانسين فارماسوتيكا ان. في Quinazoline derivatives
EP1684762A4 (en) * 2003-11-13 2009-06-17 Ambit Biosciences Corp UREA DERIVATIVES AS MODULATORS OF KINASE
NZ547795A (en) 2003-12-18 2009-07-31 Janssen Pharmaceutica Nv 3-Cyano-quinoline derivatives with antiproliferative activity
MXPA06007017A (es) 2003-12-18 2006-08-31 Janssen Pharmaceutica Nv Derivados de pirido y pirimidopirimidina como agentes antiproliferativos.
MY169441A (en) 2004-12-08 2019-04-11 Janssen Pharmaceutica Nv 2,4, (4,6) pyrimidine derivatives
JO3088B1 (ar) * 2004-12-08 2017-03-15 Janssen Pharmaceutica Nv مشتقات كوينازولين كبيرة الحلقات و استعمالها بصفتها موانع كينيز متعددة الاهداف
NI200700147A (es) 2004-12-08 2019-05-10 Janssen Pharmaceutica Nv Derivados de quinazolina inhibidores de cinasas dirigidos a multip
KR100910333B1 (ko) 2005-02-23 2009-07-31 시오노기세이야쿠가부시키가이샤 타이로신 키나아제 억제 활성을 갖는 퀴나졸린 유도체
GB0509227D0 (en) * 2005-05-05 2005-06-15 Chroma Therapeutics Ltd Intracellular enzyme inhibitors
CA2611438C (en) * 2005-06-30 2014-01-07 Janssen Pharmaceutica N.V. Cyclic anilino-pyridinotriazines
MX2009000456A (es) * 2006-07-13 2009-01-27 Janssen Pharmaceutica Nv Derivados de quinazolina mtki.
JP2009242240A (ja) * 2006-08-04 2009-10-22 Mebiopharm Co Ltd 含ホウ素キナゾリン誘導体
US7547781B2 (en) 2006-09-11 2009-06-16 Curis, Inc. Quinazoline based EGFR inhibitors containing a zinc binding moiety
MX2009002585A (es) 2006-09-11 2009-08-24 Curis Inc Inhibidores e egfr a base de quinolina que contienen porcion de enlace de zinc.
WO2008033748A2 (en) * 2006-09-11 2008-03-20 Curis, Inc. Quinazoline based egfr inhibitors containing a zinc binding moiety
EA200970420A1 (ru) * 2006-10-27 2009-12-30 Янссен Фармацевтика Нв Применение mtki 1 для лечения или предупреждения рака кости
EP2402752A3 (en) * 2006-10-27 2012-06-06 Janssen Pharmaceutica, N.V. A method for pharmacologically profiling compounds
KR20090091119A (ko) * 2006-10-27 2009-08-26 얀센 파마슈티카 엔.브이. 뇌암을 치료하거나 예방하기 위한 mt 키나아제 저해제의 용도
KR20090089849A (ko) * 2006-10-27 2009-08-24 얀센 파마슈티카 엔.브이. Vegfr3 저해제로서의 마크로사이클릭 퀴나졸린 유도체
EP2123627B1 (en) * 2007-01-19 2013-11-20 Ube Industries, Ltd. Process for producing aromatic amine having aralkyloxy or heteroaralkyloxy group
US8642067B2 (en) 2007-04-02 2014-02-04 Allergen, Inc. Methods and compositions for intraocular administration to treat ocular conditions
ES2562218T3 (es) 2007-07-27 2016-03-03 Janssen Pharmaceutica, N.V. Pirrolopirimidinas útiles para el tratamiento de enfermedades proliferativas
US8119616B2 (en) 2007-09-10 2012-02-21 Curis, Inc. Formulation of quinazoline based EGFR inhibitors containing a zinc binding moiety
CL2008003384A1 (es) * 2007-11-14 2009-12-11 Enanta Pharm Inc Compuestos derivados de quinoxalina macrocíclica, inhibidores de serina proteasa; composicion farmaceutica que los comprende; y su uso en el tratamiento de la hepatitis c.
US8426430B2 (en) 2008-06-30 2013-04-23 Hutchison Medipharma Enterprises Limited Quinazoline derivatives
US8450322B2 (en) 2008-09-22 2013-05-28 Array Biopharma Inc. Substituted imidazo[1,2b]pyridazine compounds as Trk kinase inhibitors
EP3372605B1 (en) 2008-10-22 2021-11-03 Array Biopharma, Inc. Substituted pyrazolo[1,5-a]pyrimidine compounds as trk kinase inhibitors
WO2010085597A1 (en) * 2009-01-23 2010-07-29 Incyte Corporation Macrocyclic compounds and their use as kinase inhibitors
AR077468A1 (es) 2009-07-09 2011-08-31 Array Biopharma Inc Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa
TWI406853B (zh) * 2010-04-07 2013-09-01 Dev Center Biotechnology Egfr與vegfr-2雙重抑制劑及其用途與製法
RU2594742C2 (ru) 2010-05-20 2016-08-20 Эррэй Биофарма Инк. Макроциклические соединения в качестве ингибиторов киназы trk
WO2013126015A1 (en) 2012-02-23 2013-08-29 N. V. Nutricia Composition comprising non- digestible oligosaccharides
PL2822953T3 (pl) * 2012-03-06 2017-07-31 Pfizer Inc. Makrocykliczne pochodne do leczenia chorób proliferacyjnych
CN104513253A (zh) * 2013-10-01 2015-04-15 南京波尔泰药业科技有限公司 用于治疗增殖性疾病的大环化合物
EP4309653A1 (en) * 2014-02-07 2024-01-24 Exithera Pharmaceuticals Inc. Therapeutic compounds and compositions
MA39822A (fr) 2014-04-03 2018-02-06 Janssen Pharmaceutica Nv Dérivés de pyrimidine bicycle
MA39823A (fr) 2014-04-03 2018-01-09 Janssen Pharmaceutica Nv Dérivés de pyridine macrocyclique
LT3699181T (lt) 2014-11-16 2023-05-10 Array Biopharma, Inc. Kristalinė (s)-n-(5-((r)-2-(2,5-difluorfenil)-pirolidin-1-il)-pirazolo[1,5-a] pirimidin-3-il)-3 -hidroksipirolidino-1-karboksamido vandenilio sulfato forma
BR112018006873A2 (pt) 2015-10-05 2018-11-06 The Trustees Of Columbia University In The City Of New York ativadores do fluxo autofágico e fosfolipase d e depuração de agregados de proteína incluindo tau e tratamento de proteinopatias
TN2019000271A1 (en) 2015-10-26 2021-01-07 Univ Colorado Regents Point mutations in trk inhibitor-resistant cancer and methods relating to the same
EP3423113B1 (en) * 2016-02-29 2020-09-02 Oncodesign S.A. Radiolabeled macrocyclic egfr inhibitor
US10045991B2 (en) 2016-04-04 2018-08-14 Loxo Oncology, Inc. Methods of treating pediatric cancers
MA44610A (fr) 2016-04-04 2019-02-13 Loxo Oncology Inc Formulations liquides de (s)-n-(5-((r)-2-(2,5-difluorophényl)-pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide
HUE053643T2 (hu) 2016-05-18 2021-07-28 Loxo Oncology Inc (S)-N-(5 -((R)-2-(2,5-difluor-fenil)-pirrolidin-1-il)-pirazolo[1,5-A] pirimidin-3-il)-3-hidroxi-pirrolidin-1-karboxamid elõkészítése
JOP20190092A1 (ar) 2016-10-26 2019-04-25 Array Biopharma Inc عملية لتحضير مركبات بيرازولو[1، 5-a]بيريميدين وأملاح منها
JOP20190213A1 (ar) 2017-03-16 2019-09-16 Array Biopharma Inc مركبات حلقية ضخمة كمثبطات لكيناز ros1
MA51052A (fr) * 2017-12-07 2021-04-21 Amplyx Pharmaceuticals Inc Agents antifongiques dérivés de pyridine substitués par un hétérocycle
CA3104653A1 (en) 2018-06-25 2020-01-02 Amplyx Pharmaceuticals, Inc. Pyridine derivatives substituted by heterocyclic ring and amino group
US20230159556A1 (en) * 2020-04-20 2023-05-25 Tenova Pharmaceuticals Inc. Novel protein kinase inhibitors
TW202333709A (zh) 2021-12-16 2023-09-01 美商奇奈特生物製藥公司 Met激酶抑制劑
WO2024017258A1 (zh) * 2022-07-19 2024-01-25 百极弘烨(南通)医药科技有限公司 Egfr小分子抑制剂、含其的药物组合物及其用途

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE558251A (es) * 1956-06-11
DE2423536A1 (de) * 1974-05-15 1975-11-27 Bayer Ag 3-amino-phenylessigsaeure-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als herbizide
US4066772A (en) * 1975-07-21 1978-01-03 Janssen Pharmaceutica N.V. 1,3-Dihydro-1-[3-(1-piperidinyl)propyl]-2H-benzimidazol-2-ones and related compounds
NZ181256A (en) * 1975-07-21 1978-04-28 Janssen Pharmaceutica Nv 1-(w-benzazol-11-ylalkyl)-piperidine derivatives and pharmaceutical compositions containing certain of these derivatives
US4126687A (en) 1976-05-17 1978-11-21 Janssen Pharmaceutica N.V. Antiemetic, 1-(benzimidazolyl-alkyl)-piperidine derivatives
US5721237A (en) 1991-05-10 1998-02-24 Rhone-Poulenc Rorer Pharmaceuticals Inc. Protein tyrosine kinase aryl and heteroaryl quinazoline compounds having selective inhibition of HER-2 autophosphorylation properties
GB9510757D0 (en) * 1994-09-19 1995-07-19 Wellcome Found Therapeuticaly active compounds
GB9508538D0 (en) * 1995-04-27 1995-06-14 Zeneca Ltd Quinazoline derivatives
CN100503580C (zh) * 1996-04-12 2009-06-24 沃尼尔·朗伯公司 酪氨酸激酶的不可逆抑制剂
GB9718972D0 (en) * 1996-09-25 1997-11-12 Zeneca Ltd Chemical compounds
PT1117653E (pt) 1998-10-01 2003-06-30 Astrazeneca Ab Derivados de quinolina e quinazolina e sua utilizacao como inibidores de doencas mediadas pela citosina
FR2809400B1 (fr) * 2000-05-25 2004-04-09 Inst Francais Du Petrole Materiaux comportant des groupements organiques contenant du soufre et du phosphore lie par l'intermediaire d'atomes d'oxygenes a un oxyde mineral
JO2785B1 (en) * 2003-05-27 2014-03-15 شركة جانسين فارماسوتيكا ان. في Quinazoline derivatives
JO3088B1 (ar) * 2004-12-08 2017-03-15 Janssen Pharmaceutica Nv مشتقات كوينازولين كبيرة الحلقات و استعمالها بصفتها موانع كينيز متعددة الاهداف
GB2446974B (en) * 2006-04-13 2009-01-14 Siemens Magnet Technology Ltd A solenoidal magnet structure

Also Published As

Publication number Publication date
TWI468397B (zh) 2015-01-11
TW200510431A (en) 2005-03-16
CA2525214C (en) 2012-11-27
TWI468372B (zh) 2015-01-11
US20160207938A1 (en) 2016-07-21
AU2004243487B2 (en) 2009-12-03
TW201245111A (en) 2012-11-16
IS3030B (is) 2021-06-15
CO5640038A2 (es) 2006-05-31
US7648975B2 (en) 2010-01-19
BRPI0410714B1 (pt) 2019-09-24
IS8077A (is) 2005-10-14
IL172154A0 (en) 2006-04-10
US20060247237A1 (en) 2006-11-02
AR045687A1 (es) 2005-11-09
NO20056196L (no) 2005-12-28
UA84010C2 (en) 2008-09-10
NO334209B1 (no) 2014-01-13
BRPI0410714B8 (pt) 2021-05-25
TW201245160A (en) 2012-11-16
ES2381976T3 (es) 2012-06-04
US20100105668A1 (en) 2010-04-29
EP1633365A1 (en) 2006-03-15
KR101143878B1 (ko) 2012-05-24
EA200501866A1 (ru) 2006-06-30
JP4887151B2 (ja) 2012-02-29
US8394786B2 (en) 2013-03-12
HK1176350A1 (zh) 2013-07-26
IL233045A0 (en) 2014-07-31
CN102718775B (zh) 2016-02-17
HRP20120351T1 (hr) 2012-05-31
CY1113002T1 (el) 2016-04-13
NZ544154A (en) 2009-01-31
CL2004001267A1 (es) 2005-04-22
MXPA05012762A (es) 2006-02-13
KR20060014415A (ko) 2006-02-15
WO2004105765A1 (en) 2004-12-09
IL233046A0 (en) 2014-07-31
CN102718775A (zh) 2012-10-10
BRPI0410714A (pt) 2006-06-13
IL233045B (en) 2018-07-31
SI1633365T1 (sl) 2012-06-29
MY148633A (en) 2013-05-15
PL1633365T3 (pl) 2012-07-31
AU2004243487A1 (en) 2004-12-09
PT1633365E (pt) 2012-05-07
EP1633365B1 (en) 2012-02-08
AR092137A2 (es) 2015-03-25
DK1633365T3 (da) 2012-05-14
ATE544454T1 (de) 2012-02-15
EA009064B1 (ru) 2007-10-26
US20130178624A1 (en) 2013-07-11
CA2525214A1 (en) 2004-12-09
JO2785B1 (en) 2014-03-15
EP2305687A1 (en) 2011-04-06
JP2007504276A (ja) 2007-03-01
TWI379835B (en) 2012-12-21
US9273013B2 (en) 2016-03-01

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