AR075383A1 - Derivados de triazolo[4,3-b]piridazina - Google Patents
Derivados de triazolo[4,3-b]piridazinaInfo
- Publication number
- AR075383A1 AR075383A1 ARP100100350A ARP100100350A AR075383A1 AR 075383 A1 AR075383 A1 AR 075383A1 AR P100100350 A ARP100100350 A AR P100100350A AR P100100350 A ARP100100350 A AR P100100350A AR 075383 A1 AR075383 A1 AR 075383A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- cr3r4
- heteroatoms
- independently selected
- identically
- Prior art date
Links
- 229910052757 nitrogen Inorganic materials 0.000 abstract 9
- 125000005842 heteroatom Chemical group 0.000 abstract 6
- 229910052760 oxygen Inorganic materials 0.000 abstract 6
- 229910052717 sulfur Inorganic materials 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000002733 (C1-C6) fluoroalkyl group Chemical group 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- -1 indolyl pyrrolopyridinyl Chemical group 0.000 abstract 2
- 125000004043 oxo group Chemical group O=* 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000003341 7 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 1
- 206010060862 Prostate cancer Diseases 0.000 abstract 1
- 208000000236 Prostatic Neoplasms Diseases 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 102000001307 androgen receptors Human genes 0.000 abstract 1
- 108010080146 androgen receptors Proteins 0.000 abstract 1
- 125000001589 carboacyl group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 230000036651 mood Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/58—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids containing heterocyclic rings, e.g. danazol, stanozolol, pancuronium or digitogenin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic 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
- C07D403/04—Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Se refiere a procesos para la preparacion de dichos compuestos, composiciones farmacéuticas que los contienen y su uso en el tratamiento de afecciones asociadas con el receptor de androgenos, en particular el cáncer de prostata. Reivindicacion 1: Un compuesto caracterizado porque es de Formula 1, o una sal farmacéuticamente aceptable del mismo: en donde R1 representa haloalquilo C1-4; k representa 0, 1 o 2: n y p independientemente representan 1 o 2: Y representa N, C, CH o COH; la línea punteada representa un enlace simple cuando Y es N, CH o COH; la línea punteada representa un enlace doble cuando Y es C, L1 es un enlace directo y J es indolilo pirrolopiridinilo: L1 representa un enlace directo,-(CR3R4)t-, -(CR3R4)v-O-(CR3R4)v-, -N(R5)-(CH2)q-, -S-, -S(O)- o S(O)2-; R3 y R4, de forma idéntica o diferente en cada aparicion, representan hidrogeno o metilo; R5 representa hidrogeno o metilo: q, de forma idéntica o diferente en cada aparicion, representa 0, 1, 2, 3 o 4; t representa 1, 2 o 3; v, de forma idéntica o diferente en cada aparicion, representa 0, 1 o 2; j representa: arilo; cicloalquilo C3-6; un anillo heterocíclico de 4, 5, 6 o 7 miembros monocíclico que comprende 1, 2 o 3 heteroátomos que se seleccionan independientemente de O, N o S; Un anillo heteroarilo monocíclico de 5 o 6 miembros que comprende 1, 2, 3 o 4 heteroátomos que se seleccionan independientemente de O, N o S; o un sistema de anillos heteroarilo bicíclico de 9 o 10 miembros que comprende 1, 2, 3, 4 o 5 heteroátomos que se seleccionan independientemente de O, N o S; L2 representa un enlace directo. -(CR3R4)t-, -C(O)N(R5)-(CH2)q-, -C(O)N(R5)-(CH2)q- S(O)2-, -NR5C(O)-(CH2)q-, -C(O)-(CH2)q-, -O-(CR9R10)q-, -O-(CR3R4)q-NR5-(CH2)q-, -O-(CR3R4)q-C(O)NR5-(CH2)q-, -S-, -S(O)- o -S(O)2-; R9 y R10, de forma idéntica o diferente en cada aparicion, representan hidrogeno, metilo, etilo, isopropilo, ciclopropilo o metoximetilo: R2 representa: halo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, carboxi, alcoxi C1-6, ciano, oxo, fluoroalquilo C1-6, hidroxi, animo, N-alquil C1-4amino o N,N-di-alquil C1-4amino; arilo, en donde el anillo arilo está opcionalmente sustituido por 1, 2 o 3 sustituyentes que se seleccionan de R6; un anillo heterocíclico de 4, 5, 6 o 7 miembros monocíclico que comprende 1, 2 o 3 heteroátomos que se seleccionan independientemente de O, N o S y en donde el anillo heterocíclico está opcionalmente sustituido por 1, 2 o 3 sustituyentes que se seleccionan de R6; un anillo heteroarilo de 5 o 6 miembros monocíclico que comprende 1, 2, 3 o 4 heteroátomos que se seleccionan independientemente de O, N o S y en donde el anillo heteroarilo está opcionalmente sustituido por 1, 2 o 3 sustituyentes que se seleccionan de R6: o un sistema de anillos heteroarilo bicíclico de 9 o 10 miembros que comprenden 1, 2, 3, 4 o 5 heteroátomos que se seleccionan independientemente de O, N o S y en donde el anillo heterocíclico está opcionalmente sustituido por 1, 2 o 3 sustituyentes que se seleccionan de R6; R6 representa amino, halo, alquilo C1-6, cicloalquilo C3-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, alcanoilo C2-6, alcoxi C1-6 alquilo C1-6, carboxi, ciano, oxo, fluoroalquilo C1-6, hidroxi, hidroxialquilo C1-6, alquil C1-6 sulfanilo, alquil C1-6 sulfinilo, alquil C1-6 sulfonilo, oxetan-3-ilcarbonilo, N-alquil C1-4 amino N,N-di-alquil C1-4 amino o -C(O)NR7R8 en donde R7 y R8 independientemente representan hidrogeno o metilo; y r representa 0, 1, 2 o 3.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15122109P | 2009-02-10 | 2009-02-10 | |
| US18776609P | 2009-06-17 | 2009-06-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR075383A1 true AR075383A1 (es) | 2011-03-30 |
Family
ID=42115693
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100100350A AR075383A1 (es) | 2009-02-10 | 2010-02-09 | Derivados de triazolo[4,3-b]piridazina |
Country Status (26)
| Country | Link |
|---|---|
| US (2) | US8258140B2 (es) |
| EP (1) | EP2396333B1 (es) |
| JP (1) | JP5059977B2 (es) |
| KR (1) | KR20110113755A (es) |
| CN (1) | CN102388048B (es) |
| AR (1) | AR075383A1 (es) |
| AU (1) | AU2010212590B2 (es) |
| CA (1) | CA2749926A1 (es) |
| CL (1) | CL2011001920A1 (es) |
| CO (1) | CO6410299A2 (es) |
| CR (1) | CR20110427A (es) |
| CU (1) | CU20110158A7 (es) |
| DO (1) | DOP2011000258A (es) |
| EA (1) | EA019647B1 (es) |
| EC (1) | ECSP11011257A (es) |
| ES (1) | ES2427917T3 (es) |
| IL (1) | IL214112A0 (es) |
| MX (1) | MX2011008452A (es) |
| NI (1) | NI201100156A (es) |
| PE (1) | PE20120603A1 (es) |
| SG (1) | SG172986A1 (es) |
| SV (1) | SV2011003993A (es) |
| TW (1) | TW201033215A (es) |
| UY (1) | UY32426A (es) |
| WO (1) | WO2010092371A1 (es) |
| ZA (1) | ZA201106625B (es) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20120473A1 (es) * | 2009-05-11 | 2012-05-27 | Astrazeneca Ab | [1,2,4]triazolo[4,3-b]piridazinas como ligandos del receptor de androgenos |
| AU2012321110B2 (en) * | 2011-11-30 | 2014-10-23 | Astrazeneca Ab | Combination treatment |
| AU2013204533B2 (en) | 2012-04-17 | 2017-02-02 | Astrazeneca Ab | Crystalline forms |
| HRP20202050T1 (hr) | 2012-09-04 | 2021-02-19 | Shanghai Hengrui Pharmaceutical Co., Ltd. | Derivati imidazolina, postupci njihove pripreme i njihova medicinska primjena |
| WO2015042170A1 (en) | 2013-09-17 | 2015-03-26 | Wayne State University | Compositions and uses of combinations of dim-related indoles and selected anti-androgen compounds |
| NO2719005T3 (es) | 2014-07-28 | 2018-01-20 | ||
| BR112017019453A2 (pt) | 2015-03-13 | 2018-05-15 | Forma Therapeutics Inc | compostos e composições de alfa-cinamida como inibidores de hdac8 |
| EP3285764B1 (en) | 2015-03-31 | 2024-03-27 | University of Vermont and State Agricultural College | Triazolopyridazines for treating cryptosporidiosis |
| EP3824908A1 (en) | 2015-04-10 | 2021-05-26 | Capsugel Belgium NV | Abiraterone acetate lipid formulations |
| US11664093B2 (en) * | 2019-01-17 | 2023-05-30 | The Board Of Trustees Of The University Of Illinois | Extrapolative prediction of enantioselectivity enabled by computer-driven workflow, new molecular representations and machine learning |
| JP7183842B2 (ja) * | 2019-02-08 | 2022-12-06 | 富士通株式会社 | 結合自由エネルギー計算の前処理方法、前処理装置及び前処理プログラム、並びに、結合自由エネルギーの算出方法 |
| AU2020266604A1 (en) * | 2019-05-02 | 2021-11-18 | Constellation Pharmaceuticals, Inc. | Modulators of TREX1 |
| US20220218701A1 (en) * | 2019-05-31 | 2022-07-14 | United States Government As Represented By The Department Of Veterans Affairs | Compositions and methods comprising endothelin a receptor antagonists and androgen therapies |
| TWI813106B (zh) * | 2020-12-30 | 2023-08-21 | 財團法人工業技術研究院 | 雄性激素受體結合分子及其用途 |
| WO2022266162A1 (en) | 2021-06-16 | 2022-12-22 | Celgene Corporation | Azetidinyl compounds comprising a carboxylic acid group for the treatment of neurodegenerative diseases |
| WO2024137968A1 (en) * | 2022-12-21 | 2024-06-27 | Capulus Therapeutics, Llc | Androgen receptor modulators and methods for their use |
Family Cites Families (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USRE35956E (en) * | 1991-01-09 | 1998-11-10 | Roussel Uclaf | Phenylimidazolidines having antiandrogenic activity |
| FR2693461B1 (fr) | 1992-07-08 | 1994-09-02 | Roussel Uclaf | Nouvelles phénylimidazolidines substituées, leur procédé de préparation, leur application comme médicaments et les compositions pharmaceutiques les renfermant. |
| US5411981A (en) * | 1991-01-09 | 1995-05-02 | Roussel Uclaf | Phenylimidazolidines having antiandrogenic activity |
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| AU719434B2 (en) | 1996-02-13 | 2000-05-11 | Astrazeneca Ab | Quinazoline derivatives as VEGF inhibitors |
| ES2169355T3 (es) | 1996-03-05 | 2002-07-01 | Astrazeneca Ab | Derivados de 4-anilinoquinazolina. |
| GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
| GB9714249D0 (en) | 1997-07-08 | 1997-09-10 | Angiogene Pharm Ltd | Vascular damaging agents |
| GB9900334D0 (en) | 1999-01-07 | 1999-02-24 | Angiogene Pharm Ltd | Tricylic vascular damaging agents |
| GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
| MXPA01008182A (es) | 1999-02-10 | 2003-08-20 | Astrazeneca Ab | Derivados de quinazolina como inhibidores de angiotensina. |
| US6566372B1 (en) | 1999-08-27 | 2003-05-20 | Ligand Pharmaceuticals Incorporated | Bicyclic androgen and progesterone receptor modulator compounds and methods |
| EP1289952A1 (en) | 2000-05-31 | 2003-03-12 | AstraZeneca AB | Indole derivatives with vascular damaging activity |
| UA73993C2 (uk) | 2000-06-06 | 2005-10-17 | Астразенека Аб | Хіназолінові похідні для лікування пухлин та фармацевтична композиція |
| CA2411160A1 (en) | 2000-07-07 | 2002-01-17 | Angiogene Pharmaceuticals Limited | Colchinol derivatives as vascular damaging agents |
| MXPA02012903A (es) | 2000-07-07 | 2004-07-30 | Angiogene Pharm Ltd | Derivados de colquinol como inhibidores de angiogenesis. |
| US7268230B2 (en) | 2002-02-01 | 2007-09-11 | Astrazeneca Ab | Quinazoline compounds |
| US20040102360A1 (en) * | 2002-10-30 | 2004-05-27 | Barnett Stanley F. | Combination therapy |
| US20050124625A1 (en) | 2003-10-21 | 2005-06-09 | Salvati Mark E. | Piperazine derivatives and their use as modulators of nuclear hormone receptor function |
| US7388027B2 (en) | 2004-03-04 | 2008-06-17 | Bristol-Myers Squibb Company | Bicyclic compounds as modulators of androgen receptor function and method |
| CN1597671A (zh) * | 2004-07-20 | 2005-03-23 | 贵州大学 | 喹唑啉衍生物及制备方法和生物活性 |
| AU2005292134B2 (en) * | 2004-10-01 | 2010-12-23 | Merck Sharp & Dohme Corp. | Aminopiperidines as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes |
| US7572807B2 (en) * | 2005-06-09 | 2009-08-11 | Bristol-Myers Squibb Company | Heteroaryl 11-beta-hydroxysteroid dehydrogenase type I inhibitors |
| EP1963329B1 (en) * | 2005-11-30 | 2013-01-23 | Vertex Pharmaceuticals Incorporated | Inhibitors of c-met and uses thereof |
| JP5230448B2 (ja) | 2006-02-10 | 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 | 選択的アンドローゲン受容体モジュレーターとして有用な新イミダゾロピラゾール誘導体 |
| CA2642205C (en) | 2006-02-10 | 2015-01-27 | Janssen Pharmaceutica N.V. | Bicyclic imidazole or thiadiazole heterocycles useful as selective androgen receptor modulators |
| CA2651979A1 (en) * | 2006-05-30 | 2007-12-06 | Pfizer Products Inc. | Triazolopyridazine derivatives |
| AU2007279595A1 (en) | 2006-08-04 | 2008-02-07 | Takeda Pharmaceutical Company Limited | Fused heterocyclic derivative and use thereof |
| CN101563339A (zh) * | 2006-09-14 | 2009-10-21 | 阿斯利康(瑞典)有限公司 | 作为 p i 3 k和 m t o r抑制剂用于治疗增殖性疾病的 2 -苯并咪唑基 - 6 -吗啉代 - 4 - (氮杂环丁烷、吡咯烷、哌啶或氮杂)嘧啶衍生物 |
| WO2008044033A1 (en) | 2006-10-11 | 2008-04-17 | Astrazeneca Ab | Amide derivatives |
| BRPI0717317A2 (pt) * | 2006-10-23 | 2013-10-22 | Sgx Pharmaceuticals Inc | Modularoes da proteína cinase triazalopiridazina |
| WO2008109104A1 (en) * | 2007-03-07 | 2008-09-12 | The Regents Of The University Of California | Bivalent inhibitors of akt protein kinase |
| WO2009005675A1 (en) | 2007-06-28 | 2009-01-08 | Abbott Laboratories | Novel triazolopyridazines |
| PA8792501A1 (es) * | 2007-08-09 | 2009-04-23 | Sanofi Aventis | Nuevos derivados de 6-triazolopiridacina-sulfanil benzotiazol y bencimidazol,su procedimiento de preparación,su aplicación como medicamentos,composiciones farmacéuticas y nueva utilización principalmente como inhibidores de met. |
| FR2919870B1 (fr) | 2007-08-09 | 2014-05-16 | Sanofi Aventis | Nouveaux derives de 6-triazolopyridazine-sulfanyl benzothiazole et benzothiazole et benzimidazole, procede, compositions pharmaceutiques et nouvelle utilisation comme inhibiteurs de cmet |
| EA017144B1 (ru) | 2007-12-21 | 2012-10-30 | Астразенека Аб | N-содержащие бициклические производные для применения при лечении состояний, связанных с андрогенным рецептором |
| PE20120473A1 (es) | 2009-05-11 | 2012-05-27 | Astrazeneca Ab | [1,2,4]triazolo[4,3-b]piridazinas como ligandos del receptor de androgenos |
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2010
- 2010-02-08 CN CN201080016898.1A patent/CN102388048B/zh active Active
- 2010-02-08 WO PCT/GB2010/050191 patent/WO2010092371A1/en not_active Ceased
- 2010-02-08 MX MX2011008452A patent/MX2011008452A/es active IP Right Grant
- 2010-02-08 PE PE2011001469A patent/PE20120603A1/es not_active Application Discontinuation
- 2010-02-08 ES ES10703945T patent/ES2427917T3/es active Active
- 2010-02-08 EA EA201101180A patent/EA019647B1/ru not_active IP Right Cessation
- 2010-02-08 CA CA2749926A patent/CA2749926A1/en not_active Abandoned
- 2010-02-08 AU AU2010212590A patent/AU2010212590B2/en not_active Ceased
- 2010-02-08 JP JP2011549665A patent/JP5059977B2/ja active Active
- 2010-02-08 EP EP10703945.5A patent/EP2396333B1/en active Active
- 2010-02-08 KR KR1020117019968A patent/KR20110113755A/ko not_active Withdrawn
- 2010-02-08 SG SG2011051034A patent/SG172986A1/en unknown
- 2010-02-09 UY UY0001032426A patent/UY32426A/es not_active Application Discontinuation
- 2010-02-09 TW TW099104022A patent/TW201033215A/zh unknown
- 2010-02-09 US US12/702,603 patent/US8258140B2/en active Active
- 2010-02-09 AR ARP100100350A patent/AR075383A1/es unknown
-
2011
- 2011-07-14 IL IL214112A patent/IL214112A0/en unknown
- 2011-08-09 CL CL2011001920A patent/CL2011001920A1/es unknown
- 2011-08-09 NI NI201100156A patent/NI201100156A/es unknown
- 2011-08-10 CR CR20110427A patent/CR20110427A/es unknown
- 2011-08-10 CU CU20110158A patent/CU20110158A7/es unknown
- 2011-08-10 DO DO2011000258A patent/DOP2011000258A/es unknown
- 2011-08-10 EC EC2011011257A patent/ECSP11011257A/es unknown
- 2011-08-10 SV SV2011003993A patent/SV2011003993A/es unknown
- 2011-08-16 CO CO11103913A patent/CO6410299A2/es not_active Application Discontinuation
- 2011-09-09 ZA ZA2011/06625A patent/ZA201106625B/en unknown
-
2012
- 2012-08-01 US US13/564,029 patent/US20130203714A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| UY32426A (es) | 2010-09-30 |
| ECSP11011257A (es) | 2011-09-30 |
| CR20110427A (es) | 2011-09-21 |
| JP2012517462A (ja) | 2012-08-02 |
| EA019647B1 (ru) | 2014-05-30 |
| IL214112A0 (en) | 2011-08-31 |
| CN102388048A (zh) | 2012-03-21 |
| WO2010092371A1 (en) | 2010-08-19 |
| CU20110158A7 (es) | 2012-02-15 |
| US20130203714A1 (en) | 2013-08-08 |
| SV2011003993A (es) | 2012-01-06 |
| AU2010212590A1 (en) | 2011-08-04 |
| PE20120603A1 (es) | 2012-06-14 |
| CA2749926A1 (en) | 2010-08-19 |
| US20100267699A1 (en) | 2010-10-21 |
| EP2396333A1 (en) | 2011-12-21 |
| EP2396333B1 (en) | 2013-07-03 |
| AU2010212590B2 (en) | 2013-01-10 |
| EA201101180A1 (ru) | 2012-03-30 |
| KR20110113755A (ko) | 2011-10-18 |
| ES2427917T3 (es) | 2013-11-04 |
| HK1164870A1 (en) | 2012-09-28 |
| TW201033215A (en) | 2010-09-16 |
| CL2011001920A1 (es) | 2011-10-21 |
| CN102388048B (zh) | 2014-07-30 |
| MX2011008452A (es) | 2011-12-16 |
| SG172986A1 (en) | 2011-08-29 |
| US8258140B2 (en) | 2012-09-04 |
| CO6410299A2 (es) | 2012-03-30 |
| DOP2011000258A (es) | 2011-09-30 |
| JP5059977B2 (ja) | 2012-10-31 |
| ZA201106625B (en) | 2013-02-27 |
| NI201100156A (es) | 2012-03-19 |
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