MA37650A1 - Forme amorphe d'un composé pyrimidinyl-cyclopentane inhibiteur de akt, compositions et procédés de celle-ci - Google Patents
Forme amorphe d'un composé pyrimidinyl-cyclopentane inhibiteur de akt, compositions et procédés de celle-ciInfo
- Publication number
- MA37650A1 MA37650A1 MA37650A MA37650A MA37650A1 MA 37650 A1 MA37650 A1 MA 37650A1 MA 37650 A MA37650 A MA 37650A MA 37650 A MA37650 A MA 37650A MA 37650 A1 MA37650 A1 MA 37650A1
- Authority
- MA
- Morocco
- Prior art keywords
- akt
- compositions
- methods
- amorphous form
- cyclopentane compound
- Prior art date
Links
- 230000002401 inhibitory effect Effects 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- -1 pyrimidinyl-cyclopentane compound Chemical class 0.000 title 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or 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
- A61K31/495—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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/505—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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Inorganic Chemistry (AREA)
Abstract
La présente invention concerne le monochlorhydrate de (
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261648536P | 2012-05-17 | 2012-05-17 | |
| PCT/US2013/041728 WO2013173811A1 (fr) | 2012-05-17 | 2013-05-17 | Forme amorphe d'un composé pyrimidinyl-cyclopentane inhibiteur de akt, compositions et procédés de celle-ci |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA37650A1 true MA37650A1 (fr) | 2016-11-30 |
Family
ID=48539412
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA37650A MA37650A1 (fr) | 2012-05-17 | 2014-12-12 | Forme amorphe d'un composé pyrimidinyl-cyclopentane inhibiteur de akt, compositions et procédés de celle-ci |
Country Status (30)
| Country | Link |
|---|---|
| US (2) | US9290458B2 (fr) |
| EP (2) | EP2858989B9 (fr) |
| JP (2) | JP6283663B2 (fr) |
| KR (5) | KR102678074B1 (fr) |
| CN (1) | CN104470912B (fr) |
| AU (2) | AU2013262548B2 (fr) |
| BR (1) | BR112014028593A2 (fr) |
| CA (1) | CA2873663C (fr) |
| CL (1) | CL2014003115A1 (fr) |
| CO (1) | CO7151489A2 (fr) |
| CR (1) | CR20140560A (fr) |
| DK (1) | DK2858989T3 (fr) |
| ES (1) | ES2799512T3 (fr) |
| HR (1) | HRP20200992T1 (fr) |
| HU (1) | HUE051254T2 (fr) |
| IL (2) | IL235712B (fr) |
| LT (1) | LT2858989T (fr) |
| MA (1) | MA37650A1 (fr) |
| MX (1) | MX353041B (fr) |
| MY (1) | MY170086A (fr) |
| NZ (1) | NZ702513A (fr) |
| PE (1) | PE20150725A1 (fr) |
| PH (1) | PH12014502538A1 (fr) |
| PL (1) | PL2858989T3 (fr) |
| PT (1) | PT2858989T (fr) |
| RS (1) | RS60417B9 (fr) |
| RU (1) | RU2650511C2 (fr) |
| SG (1) | SG11201407618VA (fr) |
| SI (1) | SI2858989T1 (fr) |
| WO (1) | WO2013173811A1 (fr) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9416110B2 (en) | 2012-05-17 | 2016-08-16 | Array Biopharma Inc. | Process for making hydroxylated cyclopentylpyrimidine compounds |
| KR102678074B1 (ko) | 2012-05-17 | 2024-06-26 | 제넨테크, 인크. | 무정형 형태의 akt 저해성 피리미디닐 - 사이클로펜탄 화합물, 조성물 및 이들의 방법 |
| SI3068770T1 (sl) | 2013-11-15 | 2020-02-28 | F. Hoffmann-La Roche Ag | Postopki za pripravo pirimidinilciklopentanskih spojin |
| SI2946774T1 (sl) | 2014-05-19 | 2020-07-31 | Tillotts Pharma Ag | Obložene kapsule s prirejenim sproščanjem |
| BR112019002007B1 (pt) | 2016-08-10 | 2024-01-16 | F. Hoffmann-La Roche Ag | Composição farmacêutica e uso de uma composição farmacêutica |
| US11576919B2 (en) * | 2019-08-12 | 2023-02-14 | Genentech, Inc. | Treatment of breast cancer using combination therapies comprising an ATP competitive AKT inhibitor, a CDK4/6 inhibitor, and fulvestrant |
| JP2024520798A (ja) * | 2021-06-09 | 2024-05-24 | ロンザ・ベンド・インコーポレーテッド | 非晶質固体分散体の調製のための噴霧乾燥のための混合溶媒 |
| WO2023043869A1 (fr) | 2021-09-15 | 2023-03-23 | Teva Pharmaceuticals International Gmbh | Formes à l'état solide de citrate d'ipatasertib |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1995015684A1 (fr) | 1993-12-12 | 1995-06-15 | Agrogene, Ltd. | Nouveau procede servant a proteger des vegetaux des infections fongiques |
| AU724216B2 (en) | 1997-04-07 | 2000-09-14 | Merck & Co., Inc. | A method of treating cancer |
| US6201023B1 (en) | 1997-06-10 | 2001-03-13 | Agrogene Ltd. | Methods and compositions to protect crops against plant parasitic nematodes |
| ES2137137B1 (es) | 1998-05-25 | 2000-08-16 | Medichem Sa | Nuevo polimorfo de gabapentina no hidratada, su procedimiento de obtencion y su utilizacion para la obtencion de gabapentina de calidad farmaceutica. |
| EP0982300A3 (fr) | 1998-07-29 | 2000-03-08 | Societe Civile Bioprojet | Non-imidazole alkylamines comme antagonistes du recepteur histamine H3 et leur application thérapeutique |
| AU3386600A (en) | 1999-03-03 | 2000-09-21 | Merck & Co., Inc. | Inhibitors of prenyl-protein transferase |
| AU7715300A (en) | 1999-09-27 | 2001-04-30 | Merck & Co., Inc. | Method of preventing osteoporosis |
| PL372247A1 (en) | 2002-02-01 | 2005-07-11 | Pfizer Products Inc. | Method for making homogeneous spray-dried solid amorphous drug dispersions utilizing modified spray-drying apparatus |
| CA2526506A1 (fr) | 2003-06-09 | 2004-12-16 | Boehringer Ingelheim International Gmbh | Inhibiteurs du papillomavirus |
| NZ590160A (en) | 2003-11-21 | 2012-07-27 | Array Biopharma Inc | AKT protein kinase inhibitors |
| MY139645A (en) * | 2004-02-11 | 2009-10-30 | Amgen Inc | Vanilloid receptor ligands and their use in treatments |
| US8927546B2 (en) | 2006-02-28 | 2015-01-06 | Dart Neuroscience (Cayman) Ltd. | Therapeutic piperazines |
| UA95641C2 (xx) | 2006-07-06 | 2011-08-25 | Эррей Биофарма Инк. | Гідроксильовані піримідильні циклопентани як інгібітори акт протеїнкінази$гидроксилированные пиримидильные циклопентаны как ингибиторы акт протеинкиназы |
| US8063050B2 (en) | 2006-07-06 | 2011-11-22 | Array Biopharma Inc. | Hydroxylated and methoxylated pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
| WO2009006567A2 (fr) | 2007-07-05 | 2009-01-08 | Array Biopharma Inc. | Cyclopentanes de pyrimidyle comme inhibiteurs de protéines kinases akt |
| US20100298289A1 (en) | 2007-10-09 | 2010-11-25 | Ucb Pharma, S.A. | Heterobicyclic compounds as histamine h4-receptor antagonists |
| ES2422733T3 (es) * | 2008-01-09 | 2013-09-13 | Array Biopharma Inc | Pirimidilciclopentanos hidroxilados como inhibidores de proteínas cinasas AKT |
| US9278922B2 (en) | 2009-04-15 | 2016-03-08 | Abbvie Inc. | Anti-viral compounds |
| EA020151B1 (ru) | 2009-10-23 | 2014-09-30 | Эли Лилли Энд Компани | Ингибиторы akt и фармацевтические составы, их содержащие |
| WO2011130654A1 (fr) * | 2010-04-16 | 2011-10-20 | Genentech, Inc. | Foxo3a utilisée comme biomarqueur prédictif pour l'efficacité d'un inhibiteur de la voie des kinases p13k/akt |
| US9050334B2 (en) | 2010-07-16 | 2015-06-09 | Innov88 Llc | MIF inhibitors and their uses |
| WO2012177925A1 (fr) | 2011-06-21 | 2012-12-27 | The Board Institute, Inc. | Inhibiteurs akt pour le traitement d'un cancer exprimant un gène de fusion magi3 - akt3 |
| EP2850200A1 (fr) | 2012-05-17 | 2015-03-25 | Genentech, Inc. | Procédé de fabrication de composés de cyclopentapyrimidine hydroxylée et sels de ceux-ci |
| KR102678074B1 (ko) | 2012-05-17 | 2024-06-26 | 제넨테크, 인크. | 무정형 형태의 akt 저해성 피리미디닐 - 사이클로펜탄 화합물, 조성물 및 이들의 방법 |
| HRP20180948T1 (hr) | 2012-05-17 | 2018-08-10 | Genentech, Inc. | Postupak za proizvodnju aminokiselinskih spojeva |
| ES2588878T3 (es) | 2012-05-17 | 2016-11-07 | Array Biopharma, Inc. | Proceso para preparar compuestos de ciclopentilpirimidina hidroxilada |
| US9416110B2 (en) | 2012-05-17 | 2016-08-16 | Array Biopharma Inc. | Process for making hydroxylated cyclopentylpyrimidine compounds |
| US20140121193A1 (en) | 2012-11-01 | 2014-05-01 | Robert S. Katz | Methods for treating fibromyalgia |
| CN105263910A (zh) | 2013-02-18 | 2016-01-20 | 斯克利普斯研究所 | 具有治疗潜力的血管加压素受体调节剂 |
| CN105473141A (zh) | 2013-03-15 | 2016-04-06 | 实发生物医学公司 | 治疗和/或预防心血管疾病的抗pcsk9化合物和方法 |
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2013
- 2013-05-17 KR KR1020227034985A patent/KR102678074B1/ko active Active
- 2013-05-17 JP JP2015512908A patent/JP6283663B2/ja active Active
- 2013-05-17 KR KR1020207017092A patent/KR20200074252A/ko not_active Withdrawn
- 2013-05-17 US US14/401,092 patent/US9290458B2/en active Active
- 2013-05-17 DK DK13726362.0T patent/DK2858989T3/da active
- 2013-05-17 KR KR1020147034925A patent/KR102125588B1/ko active Active
- 2013-05-17 MY MYPI2014703413A patent/MY170086A/en unknown
- 2013-05-17 EP EP13726362.0A patent/EP2858989B9/fr active Active
- 2013-05-17 SG SG11201407618VA patent/SG11201407618VA/en unknown
- 2013-05-17 PE PE2014002029A patent/PE20150725A1/es not_active Application Discontinuation
- 2013-05-17 CA CA2873663A patent/CA2873663C/fr active Active
- 2013-05-17 MX MX2014013856A patent/MX353041B/es active IP Right Grant
- 2013-05-17 KR KR1020217023442A patent/KR20210095238A/ko not_active Ceased
- 2013-05-17 PL PL13726362T patent/PL2858989T3/pl unknown
- 2013-05-17 RU RU2014151016A patent/RU2650511C2/ru active
- 2013-05-17 ES ES13726362T patent/ES2799512T3/es active Active
- 2013-05-17 WO PCT/US2013/041728 patent/WO2013173811A1/fr not_active Ceased
- 2013-05-17 RS RS20200729A patent/RS60417B9/sr unknown
- 2013-05-17 BR BR112014028593A patent/BR112014028593A2/pt not_active Application Discontinuation
- 2013-05-17 PT PT137263620T patent/PT2858989T/pt unknown
- 2013-05-17 LT LTEP13726362.0T patent/LT2858989T/lt unknown
- 2013-05-17 SI SI201331754T patent/SI2858989T1/sl unknown
- 2013-05-17 EP EP20162228.9A patent/EP3719014A1/fr active Pending
- 2013-05-17 AU AU2013262548A patent/AU2013262548B2/en active Active
- 2013-05-17 HR HRP20200992TT patent/HRP20200992T1/hr unknown
- 2013-05-17 CN CN201380037991.4A patent/CN104470912B/zh active Active
- 2013-05-17 KR KR1020247014285A patent/KR20240066293A/ko not_active Ceased
- 2013-05-17 NZ NZ702513A patent/NZ702513A/en not_active IP Right Cessation
- 2013-05-17 HU HUE13726362A patent/HUE051254T2/hu unknown
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2014
- 2014-11-13 IL IL235712A patent/IL235712B/en active IP Right Grant
- 2014-11-14 PH PH12014502538A patent/PH12014502538A1/en unknown
- 2014-11-17 CL CL2014003115A patent/CL2014003115A1/es unknown
- 2014-12-04 CR CR20140560A patent/CR20140560A/es unknown
- 2014-12-09 CO CO14270817A patent/CO7151489A2/es unknown
- 2014-12-12 MA MA37650A patent/MA37650A1/fr unknown
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2016
- 2016-02-08 US US15/018,636 patent/US9505725B2/en active Active
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2017
- 2017-12-19 AU AU2017279607A patent/AU2017279607C1/en active Active
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2018
- 2018-01-29 JP JP2018013099A patent/JP6518352B2/ja active Active
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2020
- 2020-01-14 IL IL272037A patent/IL272037B/en active IP Right Grant
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