ES2522290T3 - Tratamiento de distrofia muscular de Duchenne - Google Patents
Tratamiento de distrofia muscular de Duchenne Download PDFInfo
- Publication number
- ES2522290T3 ES2522290T3 ES07705368.4T ES07705368T ES2522290T3 ES 2522290 T3 ES2522290 T3 ES 2522290T3 ES 07705368 T ES07705368 T ES 07705368T ES 2522290 T3 ES2522290 T3 ES 2522290T3
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- optionally substituted
- alkyl
- aryl
- substituted aryl
- hydrogen
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- 206010013801 Duchenne Muscular Dystrophy Diseases 0.000 title abstract 3
- 238000011282 treatment Methods 0.000 title abstract 2
- 125000003107 substituted aryl group Chemical group 0.000 abstract 13
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 150000002431 hydrogen Chemical group 0.000 abstract 7
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000002367 halogens Chemical class 0.000 abstract 4
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000005000 thioaryl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 101001043818 Mus musculus Interleukin-31 receptor subunit alpha Proteins 0.000 abstract 1
- 125000004450 alkenylene group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000004419 alkynylene group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000005647 linker group Chemical group 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000005415 substituted alkoxy group Chemical group 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000004001 thioalkyl group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
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- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
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- A61K31/41—Heterocyclic 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
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic 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
- A61K31/4192—1,2,3-Triazoles
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- A61K31/42—Oxazoles
- A61K31/423—Oxazoles condensed with carbocyclic rings
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- A61K31/4245—Oxadiazoles
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- A61K31/425—Thiazoles
- A61K31/426—1,3-Thiazoles
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- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4355—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having oxygen as a ring hetero atom
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4365—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
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- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A61P21/02—Muscle relaxants, e.g. for tetanus or cramps
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- Pharmacology & Pharmacy (AREA)
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Abstract
Compuesto de fórmula (1), o una sal farmacéuticamente aceptable del mismo, para su uso en el tratamiento o la profilaxis de distrofia muscular de Duchenne o distrofia muscular de Becker, en la que X es O; Y es N; R9 es -L-R3; L es (i) un enlace sencillo; o (ii) un grupo ligador seleccionado de: (a) -O-, -S- y -(CO)nNR18-; (b) alquileno, alquenileno y alquinileno, cada uno de los cuales está interrumpido opcionalmente por uno o más de -O-, -S- o -NR18-, o uno o más de enlace C-C sencillo, doble o triple; y (c) un enlace -N-N- sencillo o doble; en el que n es un número entero de desde 0 hasta 2; y R18 es hidrógeno, alquilo o C(O)R16; R3 es alquilo, alcoxilo o arilo, cada uno de los cuales está opcionalmente sustituido con de uno a tres R2, que pueden ser iguales o diferentes; cada aparición de R2 es independientemente alquilo opcionalmente sustituido con uno o más de halógeno, alcoxilo, arilo opcionalmente sustituido, tioarilo opcionalmente sustituido o ariloxilo opcionalmente sustituido; alcoxilo opcionalmente sustituido con alquilo o arilo opcionalmente sustituido; hidroxilo; arilo opcionalmente sustituido; tioalquilo opcionalmente sustituido con alquilo o arilo opcionalmente sustituido; tioarilo en el que el arilo está opcionalmente sustituido; halógeno; NO2; CN; OC(>=W)NR10R11; NR10R11; SO2R12; NR13SO2R14; C(>=W)R16; NR15C(>=W)R17; o P(>=O)OR40R41; W es O, S o NR20; A1, A2, A3 y A4, que pueden ser iguales o diferentes, son N o CR1, en los que todos de A1-A4 son CR1, o uno de A1-A4 es nitrógeno; cada aparición de R1 es independientemente (i) hidrógeno; o (ii) R2; en la que al menos una aparición de R1 es NR15C(>=W)R17; NHCONHR15', en los que R15' es fenilo, alquilo C1-C6 o CO-fenilo opcionalmente sustituido con uno o más de halógeno; NHSO2-(alquilo C1-C6); NHSO2-fenilo; SO2-(alquilo C1-C6); o P(>=O)OR40R41; cuando en una pareja adyacente de A1-A4 cada uno representa CR1, los átomos de carbono adyacentes junto con sus sustituyentes R1 forman opcionalmente un anillo B; R10 y R11 son cada uno independientemente hidrógeno, alquilo opcionalmente sustituido con arilo opcionalmente sustituido o arilo opcionalmente sustituido; o R10 y R11 junto con el nitrógeno al que están unidos forman un anillo; R12 es (a) hidrógeno, alquilo opcionalmente sustituido con arilo opcionalmente sustituido o arilo opcionalmente sustituido; o (b) NR10R11; R13, R14 y R15 son cada uno independientemente hidrógeno, alquilo opcionalmente sustituido con arilo opcionalmente sustituido o arilo opcionalmente sustituido; R16 es (a) hidrógeno, alquilo opcionalmente sustituido con arilo opcionalmente sustituido o arilo opcionalmente sustituido; o (b) hidroxilo, alcoxilo o NR10R11; R17 es (a) hidrógeno, alquilo opcionalmente sustituido con arilo opcionalmente sustituido o arilo opcionalmente sustituido; (b) NR10R11; (c) NR10'R11', en los que R10' y R11' son cada uno independientemente hidrógeno, CO-alquilo o CO-arilo opcionalmente sustituido; o (d) alquilo sustituido con uno o más de halógeno, alcoxilo, arilo opcionalmente sustituido o NR10R11;
Applications Claiming Priority (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0602768A GB0602768D0 (en) | 2006-02-10 | 2006-02-10 | Treatment of muscular dystrophy |
GB0602768 | 2006-02-10 | ||
GB0614690 | 2006-07-24 | ||
GB0614690A GB0614690D0 (en) | 2006-07-24 | 2006-07-24 | Method of treatment of duchenne muscular dystrophy |
GB0619281 | 2006-09-29 | ||
GB0619281A GB0619281D0 (en) | 2006-09-29 | 2006-09-29 | Treatment of duchenne muscular dystrophy |
GB0623983A GB0623983D0 (en) | 2006-11-30 | 2006-11-30 | Treatment of duchenne muscular dystrophy |
GB0623983 | 2006-11-30 | ||
PCT/GB2007/050055 WO2007091106A2 (en) | 2006-02-10 | 2007-02-09 | Treatment of duchenne muscular dystrophy |
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ES07705368.4T Active ES2522290T3 (es) | 2006-02-10 | 2007-02-09 | Tratamiento de distrofia muscular de Duchenne |
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EP (1) | EP1986633B1 (es) |
JP (1) | JP5376956B2 (es) |
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Families Citing this family (67)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2522290T3 (es) | 2006-02-10 | 2014-11-14 | Summit Corporation Plc | Tratamiento de distrofia muscular de Duchenne |
TW200813035A (en) * | 2006-06-19 | 2008-03-16 | Astrazeneca Ab | Novel heteroaryl substituted benzoxazoles |
US9108948B2 (en) | 2006-06-23 | 2015-08-18 | Abbvie Inc. | Cyclopropyl amine derivatives |
RU2449989C2 (ru) * | 2006-06-23 | 2012-05-10 | Эбботт Лэборетриз | Производные циклопропиламина в качестве модуляторов h3-гистаминового рецептора |
PE20080888A1 (es) * | 2006-10-18 | 2008-08-26 | Novartis Ag | COMPUESTOS HETEROCICLICOS COMO INHIBIDORES DE LA ACIL-TRANSFERASA DE ACIL-CoA-DIACIL-GLICEROL 1 (DGAT1) |
CL2008002279A1 (es) | 2007-08-03 | 2009-11-27 | Summit Corp Plc | Combinacion farmaceutica que comprende un compuesto heteroarilbiciclico o arilbiciclico y un agente auxiliar; proceso de preparacion; y envase farmaceutico, util en el tratamiento y/o profilaxis de la distrofia muscular de duchenne, distrofia muscular de becker y caquexia. |
GB0715937D0 (en) * | 2007-08-15 | 2007-09-26 | Vastox Plc | Method of treatment og duchenne muscular dystrophy |
GB0715938D0 (en) * | 2007-08-15 | 2007-09-26 | Vastox Plc | Method of treatment of duchenne muscular dystrophy |
GB0715939D0 (en) * | 2007-08-15 | 2007-09-26 | Vastox Plc | Method of treatment of duchenne muscular dystrophy |
WO2009080788A2 (en) * | 2007-12-21 | 2009-07-02 | Universite Catholique De Louvain | Antibacterial agents |
US20130023498A1 (en) * | 2008-02-20 | 2013-01-24 | The Wistar Institute and North Carolina State University | MicroRNA Modulators and Method for Identifying and Using the Same |
US20110020477A1 (en) * | 2008-03-31 | 2011-01-27 | Shiseido Company, Ltd. | Oral preparation, injection preparation, external skin preparation and cosmetic method for preventing or improving wrinkles |
JP5369854B2 (ja) | 2008-04-21 | 2013-12-18 | 住友化学株式会社 | 有害節足動物防除組成物および縮合複素環化合物 |
US20110065728A1 (en) * | 2008-05-14 | 2011-03-17 | Otsuka Pharmaceutical Factory, Inc. | Lipoprotein lipase-activating compositions comprising benzene derivatives |
WO2009155017A2 (en) * | 2008-05-30 | 2009-12-23 | Merck & Co., Inc. | Novel substituted azabenzoxazoles |
GB0815369D0 (en) * | 2008-08-22 | 2008-10-01 | Summit Corp Plc | Compounds for treatment of duchenne muscular dystrophy |
AU2009296820B2 (en) | 2008-09-26 | 2014-03-20 | Merck Sharp & Dohme Llc | Novel cyclic benzimidazole derivatives useful anti-diabetic agents |
EP2348857B1 (en) | 2008-10-22 | 2016-02-24 | Merck Sharp & Dohme Corp. | Novel cyclic benzimidazole derivatives useful anti-diabetic agents |
CA2741300A1 (en) | 2008-10-29 | 2010-05-06 | Merck Sharp & Dohme Corp. | Novel cyclic benzimidazole derivatives useful anti-diabetic agents |
US8329914B2 (en) | 2008-10-31 | 2012-12-11 | Merck Sharp & Dohme Corp | Cyclic benzimidazole derivatives useful as anti-diabetic agents |
GB0821307D0 (en) * | 2008-11-21 | 2008-12-31 | Summit Corp Plc | Compounds for treatment of duchenne muscular dystrophy |
CA2755251A1 (en) * | 2009-03-18 | 2010-09-23 | Schering Corporation | Bicyclic compounds as inhibitors of diacylglycerol acyltransferase |
EP2408753A4 (en) * | 2009-03-20 | 2012-11-07 | Univ Brandeis | COMPOUNDS AND METHOD FOR THE TREATMENT OF MICROBIAL STOMACH DARM INFECTIONS IN MAMMALS |
GB0905667D0 (en) * | 2009-04-02 | 2009-05-20 | Summit Corp Plc | Compounds for treatment of duchenne muscular dystrophy |
GB0905664D0 (en) * | 2009-04-02 | 2009-05-13 | Summit Corp Plc | Compounds for treatment of duchenne muscular dystrophy |
US9186353B2 (en) | 2009-04-27 | 2015-11-17 | Abbvie Inc. | Treatment of osteoarthritis pain |
CN102574788A (zh) * | 2009-09-24 | 2012-07-11 | 弗·哈夫曼-拉罗切有限公司 | 作为crac调节剂的吲哚衍生物 |
JP5540640B2 (ja) | 2009-10-07 | 2014-07-02 | 住友化学株式会社 | 複素環化合物及びその有害節足動物防除用途 |
WO2011106273A1 (en) | 2010-02-25 | 2011-09-01 | Merck Sharp & Dohme Corp. | Novel cyclic benzimidazole derivatives useful anti-diabetic agents |
US8686048B2 (en) * | 2010-05-06 | 2014-04-01 | Rhizen Pharmaceuticals Sa | Immunomodulator and anti-inflammatory compounds |
CN103037694B (zh) | 2010-06-23 | 2014-08-13 | 住友化学株式会社 | 防治有害节肢动物的组合物和杂环化合物 |
US8853390B2 (en) | 2010-09-16 | 2014-10-07 | Abbvie Inc. | Processes for preparing 1,2-substituted cyclopropyl derivatives |
CN103748085A (zh) | 2011-06-09 | 2014-04-23 | 诺华股份有限公司 | 杂环磺酰胺衍生物 |
JO3192B1 (ar) | 2011-09-06 | 2018-03-08 | Novartis Ag | مركب بنزوثيازولون |
ES2652136T3 (es) * | 2012-02-16 | 2018-01-31 | Atyr Pharma, Inc. | Histidil-tRNA sintetasas para tratar enfermedades autoinmunitarias e inflamatorias |
BR112014021809A2 (pt) | 2012-03-06 | 2017-07-11 | Compound Handling B V | aminometileno pirazolonas com atividade terapêutica |
EP2636673A1 (en) * | 2012-03-06 | 2013-09-11 | Compound Handling B.V. | Aminomethylene pyrazolones with therapeutic activity |
GB201208178D0 (en) | 2012-05-10 | 2012-06-20 | Summit Corp Plc | Pharmaceutical composition for the treatment of duchenne muscular dystrophy |
EA028626B1 (ru) * | 2012-06-11 | 2017-12-29 | Юсб Байофарма Спрл | БЕНЗИМИДАЗОЛЫ, МОДУЛИРУЮЩИЕ TNF-α |
BR112015008564A2 (pt) | 2012-10-17 | 2017-07-04 | Hoffmann La Roche | derivados de 6-aminoindol como antagonistas de canal trp |
ITMI20122065A1 (it) * | 2012-12-03 | 2014-06-04 | Univ Padova | Uso dei correttori del cftr nel trattamento delle patologie del muscolo striato |
WO2014116859A1 (en) * | 2013-01-23 | 2014-07-31 | The University Of Chicago | Methods and compositions for inhibiting human copper trafficking proteins atox1 and ccs |
US9587235B2 (en) | 2013-03-15 | 2017-03-07 | Atyr Pharma, Inc. | Histidyl-tRNA synthetase-Fc conjugates |
TWI652014B (zh) * | 2013-09-13 | 2019-03-01 | 美商艾佛艾姆希公司 | 雜環取代之雙環唑殺蟲劑 |
DK3133068T3 (da) * | 2014-04-14 | 2021-01-11 | Shanghai hengrui pharmaceutical co ltd | Amidderivater og farmaceutisk acceptable salte deraf, fremgangsmåde til fremstilling deraf og medicinske anvendelser deraf |
GB201412010D0 (en) | 2014-07-04 | 2014-08-20 | Summit Corp Plc | Treatment of hypertransaminasemia |
US20170298081A1 (en) * | 2014-08-08 | 2017-10-19 | Kasuma Partners Inc. | Condensed heterocyclic compound |
US9353093B2 (en) | 2014-10-07 | 2016-05-31 | Allergan, Inc. | Indole-1-carboxamides as kinase inhibitors |
US9371314B2 (en) | 2014-10-09 | 2016-06-21 | Allergan, Inc. | Pyridyl benzothiophenes as kinase inhibitors |
JP6603043B2 (ja) * | 2015-05-26 | 2019-11-06 | セイカ株式会社 | 芳香族ジアミン及びその中間体、並びにこれらの製造方法 |
CN107531652A (zh) * | 2015-03-31 | 2018-01-02 | 精化株式会社 | 芳香族二胺及其中间体和它们的制造方法 |
JP6603035B2 (ja) * | 2015-03-31 | 2019-11-06 | セイカ株式会社 | アミノ基及び/又はニトロ基を有するベンゾオキサゾール−2−イル−ジフェニルエーテル及びその誘導体、並びにこれらの製造方法 |
CA2989098A1 (en) | 2015-06-22 | 2016-12-29 | Actelion Pharmaceuticals Ltd | Nadph oxidase 4 inhibitors |
US20180296532A1 (en) * | 2015-09-18 | 2018-10-18 | The Scripps Research Institute | RNA-Focused Small Molecules for Inhibiting RNA Toxicity in Myotonic Dystrophy |
AU2017243198A1 (en) | 2016-03-30 | 2018-11-22 | Summit (Oxford) Limited | Composition for the treatment of duchenne muscular dystrophy |
ES2643856B1 (es) | 2016-05-24 | 2018-08-03 | Universidad Del Pais Vasco / Euskal Herriko Unibertsitatea | Triazoles para la regulación de la homeostasis de calcio intracelular |
WO2018195338A1 (en) | 2017-04-20 | 2018-10-25 | Atyr Pharma, Inc. | Compositions and methods for treating lung inflammation |
IL282021B1 (en) | 2018-10-05 | 2024-12-01 | Annapurna Bio Inc | Compounds and compositions for treating conditions associated with apj receptor activity |
CN113195084B (zh) * | 2018-10-10 | 2024-04-09 | 阿尔伯爱因斯坦医学院 | 可用作分子伴侣介导的自噬调节剂的苯并噁唑及相关化合物 |
CN114040760A (zh) | 2018-12-31 | 2022-02-11 | 拜欧米富士恩公司 | Menin-mll相互作用的不可逆抑制剂 |
CA3125353A1 (en) | 2018-12-31 | 2020-07-09 | Biomea Fusion, Llc | Inhibitors of menin-mll interaction |
KR102132459B1 (ko) | 2019-10-02 | 2020-07-09 | 손영재 | 알루미늄 커튼월 구조 |
EP4259607A1 (en) * | 2020-12-11 | 2023-10-18 | Tmem16A Limited | Benzimidazole derivatives for treating respiratory disease |
WO2023018825A1 (en) | 2021-08-11 | 2023-02-16 | Biomea Fusion, Inc. | Covalent inhibitors of menin-mll interaction for diabetes mellitus |
KR20240087693A (ko) | 2021-08-20 | 2024-06-19 | 바이오메아 퓨전, 인크. | 암 치료를 위한 비가역적 메닌-mll 억제제인 n-[4-[4-(4-모르폴리닐)-7h-피롤로[2,3-d]피리미딘-6-일]페닐]-4-[[3(r)-[(1-옥소-2-프로펜-1-일)아미노]-1-피페리디닐]메틸]-2-피리딘카르복스아미드의 결정질 형태 |
CN114057662A (zh) * | 2021-12-10 | 2022-02-18 | 湖南第一师范学院 | 一种Tafamidis的合成方法 |
WO2024155710A1 (en) | 2023-01-18 | 2024-07-25 | Biomea Fusion, Inc. | Crystalline forms of n-[4-[4-(4-morpholinyl)-7h-pyrrolo[2,3-d]pyrimidin-6- yl]phenyl]-4-[[3(r)-[(l-oxo-2-propen-l-yl)amino]-l-piperidinyl]methyl]-2-pyridinecarboxamide as a covalent inhibitor of menin-mll interaction |
Family Cites Families (97)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE628696A (es) | 1962-02-21 | |||
CH561242A5 (es) | 1971-08-10 | 1975-04-30 | Ciba Geigy Ag | |
US3993659A (en) | 1971-08-10 | 1976-11-23 | Ciba-Geigy Corporation | Bis-benzoxazolyl-naphthalenes as optical brighteners |
GB1488003A (en) * | 1973-10-23 | 1977-10-05 | Lilly Industries Ltd | 1,2-benzisoxazole derivatives processes for their preparation and their use as pharmaceuticals |
CH617809GA3 (es) | 1975-10-10 | 1980-06-30 | ||
DE2619547A1 (de) * | 1976-05-04 | 1977-11-24 | Dynamit Nobel Ag | Verfahren zur herstellung von 2-aryl- benzoxazolen und 2-aryl-benzthiazolen |
US4110246A (en) | 1976-05-13 | 1978-08-29 | Hoechst Aktiengesellschaft | Mixture of benzoxazole derivatives |
DE3027479A1 (de) | 1980-07-19 | 1982-03-04 | Hoechst Ag, 6000 Frankfurt | Mischungen von optischen aufhellern und deren verwendung |
JPS615071A (ja) | 1984-06-15 | 1986-01-10 | Fuji Photo Film Co Ltd | ベンゾオキサゾ−ル誘導体 |
DE3617451A1 (de) | 1986-05-23 | 1987-11-26 | Hoechst Ag | Sulfonat- oder sulfonamidgruppen-haltige bis-benzoxazolylnaphthaline, verfahren zu deren herstellung und deren verwendung |
JP2615805B2 (ja) | 1988-04-15 | 1997-06-04 | ミノルタ株式会社 | 感光体 |
DE3819051A1 (de) | 1988-06-04 | 1989-12-07 | Agfa Gevaert Ag | Farbfotografisches aufzeichnungsmaterial |
JPH0369292A (ja) | 1989-08-08 | 1991-03-25 | Sharp Corp | スロー再生における縦揺れ補正装置 |
ES2092080T3 (es) | 1991-08-08 | 1996-11-16 | Ciba Geigy Ag | Colorantes, procedimiento para su obtencion y su utilizacion. |
ES2157268T5 (es) | 1994-02-24 | 2004-12-01 | SYMRISE GMBH & CO KG | Preparados cosmeticos y dermatologicos que contienen acidos fenilen-1,4-bisbencimidazolsulfonicos. |
US6004719A (en) | 1994-04-25 | 1999-12-21 | Polaroid Corporation | Imaging medium and process for producing an image |
JP3928070B2 (ja) | 1994-06-30 | 2007-06-13 | スリーエム カンパニー | 硬化指示性成形及びコーティング組成物 |
JP3928071B2 (ja) | 1994-06-30 | 2007-06-13 | スリーエム カンパニー | 硬化指示性染料を含む歯科印象材料 |
JPH0815917A (ja) | 1994-07-01 | 1996-01-19 | Mitsubishi Chem Corp | 静電荷像現像用帯電制御剤 |
JPH08175992A (ja) | 1994-12-21 | 1996-07-09 | Sagami Chem Res Center | 神経成長因子産生促進剤および縮環型オキサゾール化合物 |
JP3216458B2 (ja) * | 1994-12-28 | 2001-10-09 | 富士レビオ株式会社 | アミド誘導体 |
US6222044B1 (en) | 1995-03-20 | 2001-04-24 | The Dow Chemical Company | Process for making 2-aryl benz (ox, thi, imid) azoles and 2-aminoaryl aminobenz (ox, thi, imid) azoles |
US5567843A (en) | 1995-03-20 | 1996-10-22 | The Dow Chemical Company | Process for making 2-aryl benz (ox, thi, imid)azoles and 2-aminoaryl aminobenz(ox, thi, imid)azoles |
US5977101A (en) | 1995-06-29 | 1999-11-02 | Smithkline Beecham Corporation | Benzimidazoles/Imidazoles Linked to a Fibrinogen Receptor Antagonist Template Having Vitronectin Receptor Antagonist Activity |
JP3069292B2 (ja) | 1996-06-13 | 2000-07-24 | 株式会社分子バイオホトニクス研究所 | カテコール化合物及びバニリル化合物の蛍光検出用固相化試薬および検出方法 |
US5645948A (en) | 1996-08-20 | 1997-07-08 | Eastman Kodak Company | Blue organic electroluminescent devices |
US5914213A (en) | 1996-11-27 | 1999-06-22 | Polaroid Corporation | Process and composition for generation of acid |
US6110638A (en) | 1996-11-27 | 2000-08-29 | Polaroid Corporation | Process and composition for generation of acid |
FR2757389B1 (fr) | 1996-12-24 | 1999-02-05 | Oreal | Composition cosmetique filtrante |
US6177572B1 (en) | 1997-08-20 | 2001-01-23 | Sepracor, Inc. | Solid and liquid-phase synthesis of benzoxazoles and benzothiazoles and their use |
WO1999016761A1 (en) | 1997-09-30 | 1999-04-08 | Mitsubishi Chemical Corporation | Oxygenic heterocyclic derivatives |
JPH11171881A (ja) | 1997-09-30 | 1999-06-29 | Mitsubishi Chemical Corp | 含酸素複素環誘導体 |
US6312822B1 (en) | 1998-05-28 | 2001-11-06 | Eastman Chem Co | Dispersion aids for optical brighteners in polyolefins |
GB9815880D0 (en) * | 1998-07-21 | 1998-09-16 | Pfizer Ltd | Heterocycles |
US6436558B1 (en) | 1998-08-07 | 2002-08-20 | Fuji Photo Film Co., Ltd. | Organic electroluminescence element |
SE9804465D0 (sv) | 1998-12-22 | 1998-12-22 | Amersham Pharm Biotech Ab | A method for the removal/purification of serum albumins and means for use in the method |
FR2789582B1 (fr) | 1999-02-12 | 2001-05-04 | Oreal | Compositions photoprotectrices contenant un derive de bis-resorcinyl triazine et un compose a groupements benzoazolyle ou benzodiazolyle |
FR2789581B1 (fr) | 1999-02-12 | 2001-05-04 | Oreal | Compositions photoprotectrices contenant un derive de benzotriazole, un derive de bis-resorcinyl triazine et un compose a groupements benzoazolyle ou benzodiazolyle |
JP2002544132A (ja) | 1999-05-07 | 2002-12-24 | ビーエーエスエフ アクチェンゲゼルシャフト | 除草剤としての4−(3’,4’−ヘテロシクリルベンゾイル)ピラゾール |
AU4755600A (en) | 1999-05-07 | 2000-11-21 | Basf Aktiengesellschaft | Benzohetero cyclylcyclo hexenones and their use as herbicides |
FR2794645B1 (fr) | 1999-06-08 | 2001-08-10 | Oreal | Compositions photoprotectrices contenant un compose hydrocarbone bis-hydroxyphenylbenzotriazole et un compose a groupements benzoazolyle ou benzodiazolyle |
JP2001039034A (ja) | 1999-08-03 | 2001-02-13 | Mitsui Chemicals Inc | 光記録媒体 |
GB2353038A (en) | 1999-08-12 | 2001-02-14 | Eastman Chem Co | Polyolefin composition comprising non-migrating optical brightener |
KR20020032618A (ko) | 1999-09-24 | 2002-05-03 | 우에노 도시오 | 히드록삼산 유도체 화합물, 그 제조 방법 및 그 화합물을유효 성분으로 하는 의약 |
US6565987B2 (en) | 1999-11-12 | 2003-05-20 | Eastman Chemical Company | Non-exuding optically brightened polyolefin blends |
GB0003256D0 (en) | 2000-02-11 | 2000-04-05 | Darwin Discovery Ltd | Heterocyclic compounds and their therapeutic use |
JP2001261664A (ja) | 2000-03-15 | 2001-09-26 | Konica Corp | ハロゲン化銀写真感光材料、画像形成方法並びに化合物及びその合成方法 |
JP2002047278A (ja) | 2000-08-02 | 2002-02-12 | Fuji Photo Film Co Ltd | チオエーテル化合物の製造方法 |
AU8670201A (en) | 2000-08-24 | 2002-03-04 | Univ Pittsburgh | Thioflavin derivatives for use in antemortem diagnosis of alzheimer's disease and in vivo imaging and prevention of amyloid deposition |
US6716413B1 (en) | 2000-10-16 | 2004-04-06 | Mallinckrodt, Inc. | Indole compounds as tissue-specific exogenous optical agents |
KR100865096B1 (ko) | 2000-11-30 | 2008-10-24 | 캐논 가부시끼가이샤 | 발광 소자 및 표시 장치 |
FR2818142B1 (fr) | 2000-12-18 | 2003-12-26 | Oreal | Compositions antisolaires a base d'un base melange synergetique de filtres et utilisations |
JP2003005356A (ja) | 2001-06-20 | 2003-01-08 | Fuji Photo Film Co Ltd | 電子線又はx線用ネガ型レジスト組成物 |
EP1513522A2 (en) | 2002-01-18 | 2005-03-16 | Sri International | Methods of treating conditions associated with an edg receptor |
US20050261298A1 (en) | 2002-01-18 | 2005-11-24 | David Solow-Cordero | Methods of treating conditions associated with an Edg-7 receptor |
US20050113283A1 (en) | 2002-01-18 | 2005-05-26 | David Solow-Cordero | Methods of treating conditions associated with an EDG-4 receptor |
CN101597262A (zh) | 2002-03-05 | 2009-12-09 | 特兰斯泰克制药公司 | 抑制配体与高级糖化终产物受体相互作用的单和双环吡咯衍生物 |
JP4294917B2 (ja) | 2002-07-02 | 2009-07-15 | 三井化学株式会社 | 光記録媒体およびオキサゾール化合物 |
EP1547996A4 (en) | 2002-08-30 | 2006-08-02 | Bf Res Inst Inc | DIAGNOSTIC PROBES AND REMEDIES FOR DISEASES IN WHICH PRION PROTEIN IS ACCUMULATED, AND ANIMAL FEVERING FOR PRION PROTEIN |
WO2004041277A1 (en) * | 2002-11-01 | 2004-05-21 | Merck & Co., Inc. | Carbonylamino-benzimidazole derivatives as androgen receptor modulators |
WO2004069394A2 (en) | 2003-02-03 | 2004-08-19 | The Trustees Of Columbia University In The City Of New York | Synthetic method for direct arylation of heterocyclic arenes |
JP2004250411A (ja) | 2003-02-21 | 2004-09-09 | Bf Kenkyusho:Kk | アミロイドβ蓄積性疾患の診断プローブおよび治療用化合物 |
WO2004098494A2 (en) | 2003-04-30 | 2004-11-18 | Cytokinetics, Inc. | Compounds, compositions, and methods |
AU2004247627A1 (en) | 2003-05-16 | 2004-12-23 | Ambit Biosciences Corporation | Pyrrole compounds and uses thereof |
CN1805743A (zh) | 2003-05-20 | 2006-07-19 | 特兰斯泰克制药公司 | 用作逆转淀粉样变性及其他与之相关疾病的rage拮抗剂 |
AU2004270733B2 (en) | 2003-09-11 | 2011-05-19 | Itherx Pharma, Inc. | Cytokine inhibitors |
WO2005029187A1 (en) | 2003-09-22 | 2005-03-31 | Agfa-Gevaert | Photopolymerizable composition. |
US7097888B2 (en) | 2003-12-15 | 2006-08-29 | Eastman Kodak Company | Aligned liquid crystal layer containing azolium salts and process for increasing the tilt |
US7592373B2 (en) | 2003-12-23 | 2009-09-22 | Boehringer Ingelheim International Gmbh | Amide compounds with MCH antagonistic activity and medicaments comprising these compounds |
CA2555313A1 (en) | 2004-02-06 | 2005-08-18 | Insight Biopharmaceuticals Ltd | Heparanase inhibitors and uses thereof |
MY144903A (en) | 2004-06-17 | 2011-11-30 | Novartis Ag | Pyrrolopyridine derivatives and their use as crth2 antagonists |
CN101035508A (zh) | 2004-08-09 | 2007-09-12 | 西巴特殊化学制品控股公司 | 荧光增白剂作为抗微生物剂的应用 |
EP1794255B1 (en) | 2004-08-19 | 2016-11-16 | LG Chem, Ltd. | Organic light-emitting device comprising buffer layer and method for fabricating the same |
CA2583159A1 (en) * | 2004-10-13 | 2006-04-27 | Ptc Therapeutics, Inc. | Compounds for nonsense suppression, and methods for their use |
BRPI0406040B1 (pt) | 2004-10-21 | 2018-09-11 | Universidade Federal Do Rio De Janeiro - Ufrj | compostos capazes de absorver radiação ultravioleta, composições contendo os mesmos e processos para sua preparação |
WO2006051410A1 (en) | 2004-11-15 | 2006-05-18 | Pfizer Inc. | Azabenzoxazoles for the treatment of cns disorders |
US20070060589A1 (en) * | 2004-12-21 | 2007-03-15 | Purandare Ashok V | Inhibitors of protein arginine methyl transferases |
US7723340B2 (en) | 2005-01-13 | 2010-05-25 | Signal Pharmaceuticals, Llc | Haloaryl substituted aminopurines, compositions thereof, and methods of treatment therewith |
WO2006091862A2 (en) | 2005-02-24 | 2006-08-31 | Kemia, Inc. | Cytokine inhibitors and their use in therapy |
EP1853610A1 (en) * | 2005-03-03 | 2007-11-14 | Sirtris Pharmaceuticals, Inc. | N-phenyl benzamide derivatives as sirtuin modulators |
EP1853590A1 (en) | 2005-03-03 | 2007-11-14 | Sirtris Pharmaceuticals, Inc. | Fused heterocyclic compounds and their use as sirtuin modulators |
WO2006099379A2 (en) | 2005-03-14 | 2006-09-21 | Transtech Pharma, Inc. | Benzazole derivatives, compositions, and methods of use as b-secretase inhibitors |
WO2006124780A2 (en) | 2005-05-12 | 2006-11-23 | Kalypsys, Inc. | Ih-benzo [d] imidazole compounds as inhibitors of b-raf kinase |
EP2388263A1 (en) | 2005-08-04 | 2011-11-23 | Sirtris Pharmaceuticals, Inc. | Imidazo[2,1-b]thiazole derivatives as sirtuin modulators |
FR2889700B1 (fr) | 2005-08-11 | 2012-11-23 | Synthinnove Lab | Marqueurs, leur procede de fabrication et leurs applications |
JP2007086165A (ja) | 2005-09-20 | 2007-04-05 | Fujifilm Corp | 感光性組成物、これを用いた平版印刷版原版及び画像記録方法 |
KR100890862B1 (ko) | 2005-11-07 | 2009-03-27 | 주식회사 엘지화학 | 유기 발광 소자 및 이의 제조 방법 |
WO2007058990A2 (en) | 2005-11-14 | 2007-05-24 | Kemia, Inc. | Therapy using cytokine inhibitors |
EP1960078B1 (en) | 2005-12-02 | 2014-03-12 | Sachem, Inc. | Anion-exchange displacement chromatography process |
KR101213485B1 (ko) | 2006-01-27 | 2012-12-18 | 삼성디스플레이 주식회사 | 유기 금속 착물 및 이를 이용한 유기 전계 발광 소자 |
KR101213486B1 (ko) | 2006-02-02 | 2012-12-20 | 삼성디스플레이 주식회사 | 유기 금속 착물 및 이를 이용한 유기 전계 발광 소자 |
ES2522290T3 (es) | 2006-02-10 | 2014-11-14 | Summit Corporation Plc | Tratamiento de distrofia muscular de Duchenne |
CA2643012A1 (en) | 2006-02-21 | 2007-08-30 | Trigen Limited | Heterocyclic compounds and their use in the treatment of cardiovascular disease |
JP4649645B2 (ja) | 2006-03-10 | 2011-03-16 | 独立行政法人科学技術振興機構 | 光学活性アルコール化合物の製法 |
KR101325062B1 (ko) | 2006-05-19 | 2013-11-05 | 삼성디스플레이 주식회사 | 발광 이종 핵 구리-이리듐 착체 및 이를 이용한 유기 전계발광 소자 |
AU2007257959A1 (en) | 2006-06-09 | 2007-12-21 | Kemia, Inc. | Therapy using cytokine inhibitors |
GB0715937D0 (en) * | 2007-08-15 | 2007-09-26 | Vastox Plc | Method of treatment og duchenne muscular dystrophy |
-
2007
- 2007-02-09 ES ES07705368.4T patent/ES2522290T3/es active Active
- 2007-02-09 PT PT77053684T patent/PT1986633E/pt unknown
- 2007-02-09 KR KR1020137027768A patent/KR101472248B1/ko active IP Right Grant
- 2007-02-09 PL PL07705368T patent/PL1986633T3/pl unknown
- 2007-02-09 MX MX2008010187A patent/MX2008010187A/es active IP Right Grant
- 2007-02-09 NZ NZ570625A patent/NZ570625A/en not_active IP Right Cessation
- 2007-02-09 DK DK07705368.4T patent/DK1986633T3/da active
- 2007-02-09 JP JP2008553834A patent/JP5376956B2/ja not_active Expired - Fee Related
- 2007-02-09 BR BRPI0707719-0A patent/BRPI0707719A2/pt not_active Application Discontinuation
- 2007-02-09 KR KR1020087022077A patent/KR101426093B1/ko active IP Right Grant
- 2007-02-09 SI SI200731544T patent/SI1986633T1/sl unknown
- 2007-02-09 AU AU2007213451A patent/AU2007213451B2/en not_active Ceased
- 2007-02-09 EP EP07705368.4A patent/EP1986633B1/en active Active
- 2007-02-09 CA CA2641880A patent/CA2641880C/en not_active Expired - Fee Related
- 2007-02-09 US US12/278,769 patent/US8518980B2/en not_active Expired - Fee Related
- 2007-02-09 WO PCT/GB2007/050055 patent/WO2007091106A2/en active Application Filing
-
2008
- 2008-08-07 IL IL193315A patent/IL193315A/en not_active IP Right Cessation
-
2009
- 2009-05-14 HK HK09104431.0A patent/HK1125577A1/xx not_active IP Right Cessation
-
2013
- 2013-07-11 US US13/939,771 patent/US20140018320A1/en not_active Abandoned
- 2013-09-29 IL IL228598A patent/IL228598A0/en unknown
-
2014
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Also Published As
Publication number | Publication date |
---|---|
CY1115657T1 (el) | 2017-01-25 |
CA2641880A1 (en) | 2007-08-16 |
EP1986633A2 (en) | 2008-11-05 |
KR101426093B1 (ko) | 2014-08-01 |
KR20130129476A (ko) | 2013-11-28 |
IL193315A (en) | 2016-02-29 |
AU2007213451A1 (en) | 2007-08-16 |
KR20090010025A (ko) | 2009-01-28 |
WO2007091106A3 (en) | 2008-03-06 |
CA2641880C (en) | 2014-09-09 |
US20090075938A1 (en) | 2009-03-19 |
EP1986633B1 (en) | 2014-07-30 |
HK1125577A1 (en) | 2009-08-14 |
NZ570625A (en) | 2011-10-28 |
BRPI0707719A2 (pt) | 2011-05-10 |
PT1986633E (pt) | 2014-11-05 |
MX2008010187A (es) | 2008-10-31 |
JP5376956B2 (ja) | 2013-12-25 |
KR101472248B1 (ko) | 2014-12-16 |
DK1986633T3 (da) | 2014-11-03 |
JP2009526034A (ja) | 2009-07-16 |
WO2007091106A2 (en) | 2007-08-16 |
SI1986633T1 (sl) | 2015-03-31 |
US20140018320A1 (en) | 2014-01-16 |
US8518980B2 (en) | 2013-08-27 |
IL193315A0 (en) | 2009-09-22 |
IL228598A0 (en) | 2013-12-31 |
AU2007213451B2 (en) | 2013-02-07 |
PL1986633T3 (pl) | 2015-01-30 |
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