AR071856A1 - Derivados de indazoles sustituidos con fenilo o piridinilo, un proceso para su preparacion, una composicion farmaceutica que los comprende y su uso en la fabricacion de un medicamento para el tratamiento de enfermedades mediadas por el receptor de glucocorticoides. - Google Patents
Derivados de indazoles sustituidos con fenilo o piridinilo, un proceso para su preparacion, una composicion farmaceutica que los comprende y su uso en la fabricacion de un medicamento para el tratamiento de enfermedades mediadas por el receptor de glucocorticoides.Info
- Publication number
- AR071856A1 AR071856A1 ARP090101814A ARP090101814A AR071856A1 AR 071856 A1 AR071856 A1 AR 071856A1 AR P090101814 A ARP090101814 A AR P090101814A AR P090101814 A ARP090101814 A AR P090101814A AR 071856 A1 AR071856 A1 AR 071856A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- heteroaryl
- aryl
- optionally substituted
- Prior art date
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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
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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
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Abstract
La presente se refiere a derivados de indazolilo, a composiciones farmaceuticas que comprenden tales derivados, a procesos para preparar dichos nuevos derivados y al uso de tales derivados como medicamentos. Reivindicacion 1: Un compuesto caracterizado porque es de la formula (1) donde: A es alquilo C1-6, alcoxi C1-6, cicloalquilo C3-7, haloalquilo C1-6, alquiltio C1-6, alquil C1-6C(O), alquiloxi C1-6C(O), NR5R6, NR5R6C(O) o heteroarilo C5-10, todos opcionalmente sustituidos con uno o m s sustituyentes seleccionados independientemente entre halo, ciano, hidroxilo, alquilo C1-4, alcoxi C1-4 y haloalquilo C1-4; R5 y R6 se seleccionan independientemente de hidrogeno, alquilo C1-6, cicloalquilo C3-7, alquiI C1-6C(O) y cicloalquil C3-7C(O), o R5 y R6 pueden formar un anillo con el nitrogeno al cual est n unidos; R1 es hidrogeno, alquilo C1-4, hidroxialquilo C1-4, alquil C1-4O-alquilo C1-4, alquiltio C1-4-alquilo C1-4 o haloalquilo C1-4; R3 es arilo C5-10, aril C5-10-alquilo C1-4, aril C5-10-O, aril C5-10-alcoxi C1-4, ariloxi C5-10-alquilo C1-4, heteroarilo C5-10, heteroaril C5-10-alquilo C1-4, heteroaril C5-10-alcoxi C1-4 o heteroariloxi C5-10-alquilo C1-4, todos los cuales est n sin sustituir o opcionalmente sustituidos con uno o m s sustituyentes seleccionados independientemente de B; B es hidroxilo, halo, ciano, alquilo C1-4, alcoxi C1-4, hidroxialquilo C1-3, alcoxi C1-4-alquilo C1-4, cicloalquiloxi C3-6-alquilo C1-4, cicloalquil C3-6O, cicloalquiltio C3-6-alquilo C1-4, cicloalquiltio C3-6, aIquil C1-3S(O)k-alquilo C1-4, alquil C1-3S(O)k, haloalquilo C1-4 o haloalcoxi C1-4, o B es uno de los grupos siguientes que est n unidos a carbonos adyacentes en un anillo arilo o heteroarilo (CH2)tOalqueniI C1-4O(CH2)v o (CH2)tO(CH2)v; k es 0, 1; t y v son, independientemente, 0, 1, 2 o 3, y t y v no son ambos 0; X es O o NH; W es fenilo sustituido con uno o m s sustituyentes seleccionados independientemente entre (CH2)nC(O)NR7R8, (CH2)nNR9C(O)R8 o (CH2)nC(O)NR9(CR14R15)C(O)NR7R8; y W est adem s opcionalmente sustituido con halogeno o alquilo c1-4; R7 es hidrogeno o alquilo C1-4; R8 y R9 son, independientemente, hidrogeno, alquilo C1-4 (opcionalmente sustituido con uno o dos grupos seleccionados entre hidroxilo, alcoxi C1-4, NH2, oxo, C(O)NR10R11, NR10alquilo C1-4, C(O)NR10alquilo c1-4, NR10C(O)alquilo C1-4, alquiltio C1-4, heterociclilo C5-10, arilo C5-10 o heteroarilo C5-10), cicloalquilo C3-7 (opcionalmente sustituido con C(O)NH2), heterociclilo C5-10, arilo C5-10, heteroarilo C5-10 o C(O)NR10R11; donde arilo C5-10 o heteroarilo C5-10 est n opcionalmente sustituidos con halogeno, alquilo C1-4, alcoxi C1-4, CF3, OCF3, hidroxi o ciano; y donde cualquier heterociclilo est opcionalmente sustituido con alquilo C1-4, alcoxi C1-4-alquilo C1-4, oxo o hidroxilo; o R7 y R8, junto con el nitrogeno al cual est n unidos, forman un anillo de 5 o 6 miembros que comprende opcionalmente un segundo tomo de nitrogeno en el anillo, donde el anillo est opcionalmente sustituido con uno o dos grupos seleccionados entre oxo, hidroxilo, hidroxialquilo C1-4, alquilo C1-4, alcoxi C1-4-alquilo C1-4 o (CH2)pC(O)NR12R13, R10, R11, R12 y R13 son, independientemente, hidrogeno o alquilo C1-4; n y p son, independientemente, 0, 1, 2, 3 o 4; e Y es hidrogeno, halo, alquilo C1-4 o haloalquilo C1-4; o una de sus sales farmaceuticamente aceptables.
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US5461608P | 2008-05-20 | 2008-05-20 | |
US8031208P | 2008-07-14 | 2008-07-14 | |
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ARP090101814A AR071856A1 (es) | 2008-05-20 | 2009-05-20 | Derivados de indazoles sustituidos con fenilo o piridinilo, un proceso para su preparacion, una composicion farmaceutica que los comprende y su uso en la fabricacion de un medicamento para el tratamiento de enfermedades mediadas por el receptor de glucocorticoides. |
ARP090101815A AR071857A1 (es) | 2008-05-20 | 2009-05-20 | Derivados de indazol sustituidos con fenilo y benzodioxinilo, una composicion farmaceutica que los comprende y su uso en la fabricacion de un medicamento para el tratamiento de enfermedades mediadas por el receptor de glucocorticoides. |
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ARP090101815A AR071857A1 (es) | 2008-05-20 | 2009-05-20 | Derivados de indazol sustituidos con fenilo y benzodioxinilo, una composicion farmaceutica que los comprende y su uso en la fabricacion de un medicamento para el tratamiento de enfermedades mediadas por el receptor de glucocorticoides. |
Country Status (42)
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JO2754B1 (en) | 2006-12-21 | 2014-03-15 | استرازينكا ايه بي | Amylendazoleil derivatives for the treatment of glucocorticoid-mediated disorders |
TWI443098B (zh) | 2008-03-24 | 2014-07-01 | Medivation Technologies Inc | 吡啶并〔3,4-b〕吲哚及使用方法 |
UY31832A (es) * | 2008-05-20 | 2010-01-05 | Astrazeneca Ab | Derivados de indazol sustituidos con fenilo y benzodioxinilo |
US8853410B2 (en) | 2009-04-30 | 2014-10-07 | Basf Se | Process for preparing substituted isoxazoline compounds and their precursors |
WO2011061527A1 (en) * | 2009-11-17 | 2011-05-26 | Astrazeneca Ab | Combinations comprising a glucocorticoid receptor modulator for the treatment of respiratory diseases |
FR2955105B1 (fr) | 2010-01-11 | 2012-04-20 | Arkema France | Procede de preparation d'aminoethyl imidazolidone ou de son thiocarbonyle |
WO2011161130A1 (en) | 2010-06-23 | 2011-12-29 | Basf Se | Process for producing imine compounds for combating invertebrate pests |
US9006447B2 (en) | 2010-11-03 | 2015-04-14 | Basf Se | Method for preparing substituted isoxazoline compounds and their precursors 4-chloro, 4-bromo- or 4-iodobenzaldehyde oximes |
GB201021992D0 (en) | 2010-12-23 | 2011-02-02 | Astrazeneca Ab | Compound |
GB201021979D0 (en) | 2010-12-23 | 2011-02-02 | Astrazeneca Ab | New compound |
IN2013MN01699A (es) | 2011-02-18 | 2015-06-12 | Medivation Technologies Inc | |
US9974759B2 (en) | 2013-05-31 | 2018-05-22 | Indiana University Research And Technology Corporation | Beta 2 adrenoceptor antagonists for treating orthostatic hypotension |
AP2017009819A0 (en) * | 2014-09-26 | 2017-03-31 | Astrazeneca Ab | 1-alkyl-6-oxo-1,6-dihydropyridin-3-yl compounds and use as sgrm modulators |
WO2016124722A1 (en) * | 2015-02-06 | 2016-08-11 | Astrazeneca Ab | A process for the preparation of 3-5-{[(1r,2s)-2-[(2,2-difluoropropanyl)amino]-1 -(2,3-dihydro-1,4-benzodioxin-6-yl]propyl]oxy}-1h-indazol-1-yl)-n-[(3r)-tetrahydrofuran-3-yl] benzamide |
GB201511382D0 (en) | 2015-06-29 | 2015-08-12 | Imp Innovations Ltd | Novel compounds and their use in therapy |
JP6749399B2 (ja) * | 2015-09-15 | 2020-09-02 | レオ ファーマ アクティーゼルスカブ | 局所薬物送達のための非ステロイド性グルココルチコイド受容体モジュレーター |
WO2017161518A1 (en) * | 2016-03-23 | 2017-09-28 | Astrazeneca Ab | New physical form |
RU2018135607A (ru) | 2016-03-24 | 2020-04-24 | Астразенека Аб | Кристаллическая форма |
CN106083837B (zh) * | 2016-05-27 | 2018-08-31 | 浙江普洛得邦制药有限公司 | 一种噁唑烷酮类抗菌药物及其中间体的制备方法 |
JP2021506964A (ja) | 2017-12-18 | 2021-02-22 | グリュネンタール・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング | 置換ピロリジンアミドi |
TW201927769A (zh) * | 2017-12-18 | 2019-07-16 | 德商歌林達有限公司 | 經取代之吡咯啶醯胺ii |
CA3125929A1 (en) * | 2019-01-11 | 2020-07-16 | Grunenthal Gmbh | Substituted pyrrolidine amides iii |
EP3986885B1 (en) | 2019-06-19 | 2023-05-03 | Grünenthal GmbH | Substituted pyrrolidine amides iv |
WO2020254552A2 (en) | 2019-06-19 | 2020-12-24 | Grünenthal GmbH | Substituted pyrrolidine amides v |
EP4086247A4 (en) * | 2019-12-31 | 2023-12-06 | Medshine Discovery Inc. | BENZOPYRAZOLE COMPOUND |
EP4178954A1 (en) | 2020-07-09 | 2023-05-17 | Grünenthal GmbH | Substituted pyrrolidine amines and amides as mediator of the glucocortoid receptor |
CN117616020A (zh) * | 2021-06-28 | 2024-02-27 | 南京明德新药研发有限公司 | 一种三唑并吡啶取代的吲唑类化合物的晶型及其制备方法 |
KR102571432B1 (ko) * | 2023-02-08 | 2023-08-29 | 주식회사 에스씨엘테라퓨틱스 | 인다졸릴에스테르 및 아미드 유도체를 포함하는 암 치료용 조성물 |
Family Cites Families (81)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB607840A (en) | 1946-02-12 | 1948-09-06 | Bristol Aeroplane Co Ltd | Improvements in or relating to means for feeding ammunition to automatic fire arms |
US3992441A (en) * | 1972-12-26 | 1976-11-16 | Pfizer Inc. | Sulfamylbenzoic acids |
DE3000377A1 (de) | 1980-01-07 | 1981-07-09 | Boehringer Mannheim Gmbh, 6800 Mannheim | Neue sulfonamide, verfahren zu deren herstellung sowie diese verbindungen enthaltende arzneimittel |
DE3514696A1 (de) | 1985-04-24 | 1986-11-06 | Bayer Ag, 5090 Leverkusen | N-indolylethyl-sulfonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung |
DE3535167A1 (de) * | 1985-10-02 | 1987-04-09 | Boehringer Mannheim Gmbh | Neue sulfonyl-phenyl(alkyl)amine, verfahren zu ihrer herstellung sowie arzneimittel |
DE3632329A1 (de) | 1986-09-24 | 1988-03-31 | Bayer Ag | Substituierte phenylsulfonamide |
TW224462B (es) | 1992-02-24 | 1994-06-01 | Squibb & Sons Inc | |
NZ247440A (en) | 1992-05-06 | 1995-04-27 | Squibb & Sons Inc | Phenyl sulphonamide derivatives, preparation and pharmaceutical compositions thereof |
CA2114981A1 (en) | 1993-02-09 | 1994-08-10 | Kazumi Ogata | Quinolonecarboxylic acid derivatives |
DE4323916A1 (de) | 1993-07-16 | 1995-01-19 | Basf Ag | Substituierte 2-Phenylpyridine |
US5834462A (en) | 1993-07-26 | 1998-11-10 | Eisai Co., Ltd. | Tricyclic heterocyclic sulfonamide and sulfonic ester derivatives |
ATE216757T1 (de) | 1993-08-30 | 2002-05-15 | Bosch Robert Corp | Gehäuse mit rezirkulationsregelung zur anwendung in axiallüfter mit zarge |
GB9504854D0 (en) * | 1994-03-31 | 1995-04-26 | Zeneca Ltd | Nitrogen derivatives |
US5545669A (en) | 1994-06-02 | 1996-08-13 | Adams; Jerry L. | Anti-inflammatory compounds |
GB9417532D0 (en) | 1994-08-31 | 1994-10-19 | Zeneca Ltd | Aromatic compounds |
AU5772296A (en) | 1995-05-19 | 1996-11-29 | Chiroscience Limited | 3,4-disubstituted-phenylsulphonamides and their therapeutic use |
TW523506B (en) | 1996-12-18 | 2003-03-11 | Ono Pharmaceutical Co | Sulfonamide or carbamide derivatives and drugs containing the same as active ingredients |
TW542822B (en) | 1997-01-17 | 2003-07-21 | Ajinomoto Kk | Benzamidine derivatives |
ZA9811898B (en) | 1997-12-29 | 2000-06-28 | Ortho Mcneil Pharm Inc | Anti-Inflammatory Compounds. |
AU759255B2 (en) | 1998-01-29 | 2003-04-10 | Amgen, Inc. | PPAR-gamma modulators |
DE19856475A1 (de) * | 1998-11-27 | 2000-05-31 | Schering Ag | Nichtsteroidale Entzündungshemmer |
KR20020002501A (ko) | 1999-05-13 | 2002-01-09 | 시오노 요시히코 | 당뇨병의 예방 또는 치료약 |
US6569885B1 (en) | 1999-12-23 | 2003-05-27 | Icos Corporation | Cyclic AMP-specific phosphodiesterase inhibitors |
ATE281431T1 (de) | 2000-09-11 | 2004-11-15 | Pfizer Prod Inc | Resorcin-derivate |
FR2815030A1 (fr) | 2000-10-05 | 2002-04-12 | Lipha | Derives nitroso de la diphenylamine, compositions pharmaceutiques les contenant et leur utilisation pour la preparation de medicaments |
US6838074B2 (en) * | 2001-08-08 | 2005-01-04 | Bristol-Myers Squibb Company | Simultaneous imaging of cardiac perfusion and a vitronectin receptor targeted imaging agent |
WO2003028641A2 (en) | 2001-10-01 | 2003-04-10 | Taisho Pharmaceutical Co., Ltd. | Mch receptor antagonists |
HUP0500027A2 (hu) | 2001-11-22 | 2005-04-28 | Ono Pharmaceutical Co., Ltd. | Piperidin-2-on-származékok és hatóanyagként ezeket tartalmazó gyógyászati készítmények |
KR20040094672A (ko) | 2002-03-13 | 2004-11-10 | 얀센 파마슈티카 엔.브이. | 히스톤 디아세틸라제의 신규한 저해제로서의설포닐아미노-유도체 |
ATE496620T1 (de) | 2002-04-11 | 2011-02-15 | Merck Sharp & Dohme | 1h-benzo(f)indazol-5-yl-derivate als selektive glucocorticoid-rezeptor-modulatoren |
WO2003099773A1 (en) | 2002-05-24 | 2003-12-04 | Millennium Pharmaceuticals, Inc. | Ccr9 inhibitors and methods of use thereof |
JP2004059116A (ja) | 2002-07-31 | 2004-02-26 | Sharp Corp | ディスプレイ用基板収納用トレイ及びディスプレイ用基板の取り出し機構並びにディスプレイ用基板の取り出し方法 |
US20050113450A1 (en) | 2002-08-23 | 2005-05-26 | Atli Thorarensen | Antibacterial agents |
CN1678306A (zh) | 2002-08-29 | 2005-10-05 | 贝林格尔·英格海姆药物公司 | 在炎性、变应性和增生性疾病中用作糖皮质激素模拟物的3-(磺酰氨基乙基)-吲哚衍生物 |
US6894061B2 (en) | 2002-12-04 | 2005-05-17 | Wyeth | Substituted dihydrophenanthridinesulfonamides |
CA2767153A1 (en) | 2003-02-20 | 2004-09-02 | Encysive Pharmaceuticals Inc. | Phenylenediamine urotensin-ii receptor antagonists and ccr-9 antagonists |
GB0308466D0 (en) | 2003-04-11 | 2003-05-21 | Novartis Ag | Organic compounds |
US20040235892A1 (en) * | 2003-05-22 | 2004-11-25 | Yujia Dai | Indazole and benzisoxazole kinase inhibitors |
US7297709B2 (en) * | 2003-05-22 | 2007-11-20 | Abbott Laboratories | Indazole, benzisoxazole, and benzisothiazole kinase inhibitors |
EP1635800A2 (en) | 2003-06-10 | 2006-03-22 | Kalypsys, Inc. | Carbonyl compounds as inhibitors of histone deacetylase for the treatment of disease |
US7393873B2 (en) | 2003-07-02 | 2008-07-01 | Merck & Co., Inc. | Arylsulfonamide derivatives |
WO2005060963A1 (en) | 2003-12-19 | 2005-07-07 | Pfizer Inc. | Benzenesulfonylamino-pyridin-2-yl derivatives and related compounds as inhibitors of 11-beta-hydroxysteroid dehydrogenase type 1 (11-beta-hsd-1) for the treatment of diabetes and obesity |
JP4829506B2 (ja) | 2004-02-17 | 2011-12-07 | 石原産業株式会社 | チオアミド系化合物又はその塩、並びにそれらを含有するサイトカイン産生抑制剤 |
JP2007527918A (ja) | 2004-03-08 | 2007-10-04 | アムジェン インコーポレイテッド | Pparガンマ活性の治療的調節 |
DE102004028862A1 (de) | 2004-06-15 | 2005-12-29 | Merck Patent Gmbh | 3-Aminoindazole |
RS20070076A (en) * | 2004-10-29 | 2008-09-29 | Astrazeneca Ab., | Novel sulphonamide derivatives as glucocorticoid receptor modulators for the treatment of inflammatory diseases |
SE0402636D0 (sv) * | 2004-10-29 | 2004-10-29 | Astrazeneca Ab | Chemical compounds |
SE0402635D0 (sv) * | 2004-10-29 | 2004-10-29 | Astrazeneca Ab | Chemical compounds |
WO2006108699A1 (en) | 2005-04-14 | 2006-10-19 | Glaxo Group Limited | Indazoles as glucocorticoid receptor ligands |
AU2006257861A1 (en) | 2005-06-10 | 2006-12-21 | Boehringer Ingelheim International Gmbh | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
US7888381B2 (en) | 2005-06-14 | 2011-02-15 | Bristol-Myers Squibb Company | Modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity, and use thereof |
TW200815361A (en) * | 2005-10-20 | 2008-04-01 | Astrazeneca Ab | Chemical compounds |
GB0522880D0 (en) | 2005-11-09 | 2005-12-21 | Glaxo Group Ltd | Novel compounds |
US20090170898A1 (en) * | 2006-03-31 | 2009-07-02 | Malena Bengtsson | Sulphonamide Derivatives as Modulators of the Glucocorticoid Receptor |
GB0607840D0 (en) | 2006-04-20 | 2006-05-31 | Glaxo Group Ltd | Novel compounds |
AU2007242851A1 (en) * | 2006-04-20 | 2007-11-01 | Glaxo Group Limited | Novel compounds |
CA2655202A1 (en) | 2006-07-14 | 2008-01-17 | Eli Lilly And Company | Glucocorticoid receptor modulator and methods of use |
GB0620406D0 (en) | 2006-10-13 | 2006-11-22 | Glaxo Group Ltd | Novel compounds |
GB0620385D0 (en) | 2006-10-13 | 2006-11-22 | Glaxo Group Ltd | Novel compounds |
MX2009004385A (es) | 2006-10-23 | 2009-05-22 | Merck & Co Inc | Derivados de 2-[1-fenil-5-hidroxi-4alfa-metil-hexahidrociclopenta [f]indazol-5-il]etil fenilo como ligandos del receptor glucocorticoide. |
JP2010508358A (ja) | 2006-11-01 | 2010-03-18 | ブリストル−マイヤーズ スクイブ カンパニー | グルココルチコイド受容体、AP−1、および/またはNF−κB活性の調節剤、並びにその使用 |
US8067447B2 (en) | 2006-11-01 | 2011-11-29 | Bristol-Myers Squibb Company | Modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof |
US20120065173A1 (en) | 2006-11-23 | 2012-03-15 | Markus Berger | Chemical compounds |
TW200829578A (en) | 2006-11-23 | 2008-07-16 | Astrazeneca Ab | Chemical compounds 537 |
KR20090097908A (ko) | 2006-12-06 | 2009-09-16 | 베링거 인겔하임 인터내셔날 게엠베하 | 글루코코르티코이드 모사물, 이의 제조 방법, 이의 약제학적 조성물 및 용도 |
JO2754B1 (en) * | 2006-12-21 | 2014-03-15 | استرازينكا ايه بي | Amylendazoleil derivatives for the treatment of glucocorticoid-mediated disorders |
WO2008079073A1 (en) | 2006-12-22 | 2008-07-03 | Astrazeneca Ab | Indazolyl sulphonamide derivatives for the treatment of glucocorticoid receptor mediated disorders |
US20100048950A1 (en) | 2007-04-10 | 2010-02-25 | Boehringer Ingelheim International Gmbh | Glucocorticoid Mimetics, Methods of Making Them, Pharmaceutical Compositions and Uses Thereof |
WO2008124665A1 (en) | 2007-04-10 | 2008-10-16 | Boehringer Ingelheim International Gmbh | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
GB0708858D0 (en) | 2007-05-08 | 2007-06-13 | Glaxo Group Ltd | Novel compounds |
DE102007029419A1 (de) | 2007-06-26 | 2009-01-02 | Emsland-Stärke GmbH | Filamentfaserschlichtemittel und Verwendung desselben |
GB0720546D0 (en) | 2007-10-19 | 2007-11-28 | Glaxo Group Ltd | Novel compounds |
GB0720557D0 (en) | 2007-10-19 | 2007-11-28 | Glaxo Group Ltd | Novel compounds |
GB0720544D0 (en) | 2007-10-19 | 2007-11-28 | Glaxo Group Ltd | Novel compounds |
GB0720549D0 (en) | 2007-10-19 | 2007-11-28 | Glaxo Group Ltd | Novel compounds |
GB0720556D0 (en) | 2007-10-19 | 2007-11-28 | Glaxo Group Ltd | Novel compounds |
GB0722211D0 (en) | 2007-11-12 | 2007-12-27 | Glaxo Group Ltd | Novel compounds |
GB0724254D0 (en) | 2007-12-12 | 2008-01-23 | Glaxo Group Ltd | Novel compounds |
CA2714607A1 (en) | 2008-02-26 | 2009-09-03 | Merck Sharp & Dohme Corp. | Hexahydrocyclopentyl[f]indazole carboxamides and derivatives thereof as selective glucocorticoid receptor modulators |
AU2009220458A1 (en) | 2008-03-06 | 2009-09-11 | Merck Sharp & Dohme Corp. | Hexahydrocyclopentyl[f]findazole sulfonamides and derivates thereof as selective glucocorticoid receptor modulators |
UY31832A (es) * | 2008-05-20 | 2010-01-05 | Astrazeneca Ab | Derivados de indazol sustituidos con fenilo y benzodioxinilo |
-
2009
- 2009-05-19 UY UY0001031832A patent/UY31832A/es not_active Application Discontinuation
- 2009-05-19 US US12/468,561 patent/US8211930B2/en active Active
- 2009-05-19 TW TW098116534A patent/TW200951114A/zh unknown
- 2009-05-19 UY UY0001031831A patent/UY31831A/es not_active Application Discontinuation
- 2009-05-19 US US12/468,494 patent/US20100080786A1/en not_active Abandoned
- 2009-05-19 SA SA109300309A patent/SA109300309B1/ar unknown
- 2009-05-19 TW TW098116533A patent/TWI445705B/zh active
- 2009-05-20 MX MX2010012529A patent/MX2010012529A/es active IP Right Grant
- 2009-05-20 PA PA20098827001A patent/PA8827001A1/es unknown
- 2009-05-20 MX MX2010012390A patent/MX2010012390A/es not_active Application Discontinuation
- 2009-05-20 PA PA20098827101A patent/PA8827101A1/es unknown
- 2009-05-20 EP EP13165585.4A patent/EP2620435A1/en not_active Withdrawn
- 2009-05-20 AU AU2009249872A patent/AU2009249872A1/en not_active Abandoned
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