WO2009156837A3 - Forme amorphe d'un sel de malate de 2-indolinone à substitution 3-pyrrole - Google Patents
Forme amorphe d'un sel de malate de 2-indolinone à substitution 3-pyrrole Download PDFInfo
- Publication number
- WO2009156837A3 WO2009156837A3 PCT/IB2009/006056 IB2009006056W WO2009156837A3 WO 2009156837 A3 WO2009156837 A3 WO 2009156837A3 IB 2009006056 W IB2009006056 W IB 2009006056W WO 2009156837 A3 WO2009156837 A3 WO 2009156837A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- amorphous form
- indolinone
- malate salt
- pyrrole substituted
- sunitinib
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- 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
- C07D403/06—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 linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- A61K31/40—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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
L'invention concerne de nouvelles formes de l'agent anticancéreux sunitinib de formule (I) ainsi que des sels pharmaceutiquement acceptables correspondants, et notamment du malate de sunitinib sous forme amorphe et du malate de sunitinib de forme III. L'invention concerne également un procédé de préparation correspondant et des compositions pharmaceutiques comprenant du malate de sunitinib sous forme amorphe.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US7603108P | 2008-06-26 | 2008-06-26 | |
| US61/076,031 | 2008-06-26 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2009156837A2 WO2009156837A2 (fr) | 2009-12-30 |
| WO2009156837A3 true WO2009156837A3 (fr) | 2010-08-05 |
Family
ID=41445029
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/IB2009/006056 Ceased WO2009156837A2 (fr) | 2008-06-26 | 2009-06-26 | Forme amorphe d'un sel de malate de 2-indolinone à substitution 3-pyrrole |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2009156837A2 (fr) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GEP20063777B (en) | 2001-08-15 | 2006-03-27 | Upjohn Co | Crystals Including Malic Acid Salt of N-[2-(Diethylamino) Ethyl]-5-[(5-Fluoro-2-Oxo-3h-Indole-3-Ylidene) Methyl]-2, 4-Dimethyl-1h-Pyrrole-3-Carboxamide, Processes for Its Preparation and Compositions Thereof |
| WO2011092664A1 (fr) | 2010-01-29 | 2011-08-04 | Ranbaxy Laboratories Limited | Formes cristallines du sel d'acide l-malique du sunitinib |
| WO2011100325A2 (fr) | 2010-02-09 | 2011-08-18 | Sicor Inc. | Polymorphes de sels de sunitinib |
| EP2802314B1 (fr) | 2012-01-13 | 2020-11-25 | XSpray Microparticles AB | Procédé de production de nanoparticules hybrides amorphes stables comprenant au moins un inhibiteur de la protéine kinase et au moins un constituant polymère stabilisant et matriciel |
| WO2013160916A1 (fr) * | 2012-04-25 | 2013-10-31 | Hetero Research Foundation | Dispersion solide de malate de sunitinib |
| CA2838587A1 (fr) * | 2013-10-18 | 2015-04-18 | Hari Babu Matta | Forme cristalline pure ii de sel d'acide l-malique de sunitinib et procede pour sa preparation |
| CN104693187A (zh) * | 2013-12-10 | 2015-06-10 | 安杰世纪生物科技(北京)有限公司 | 一种舒尼替尼L-苹果酸盐晶型λ及其制备方法 |
| CN105085490A (zh) * | 2014-05-09 | 2015-11-25 | 上海科胜药物研发有限公司 | 新的舒尼替尼苹果酸盐晶型及其制备方法 |
| WO2020216450A1 (fr) | 2019-04-25 | 2020-10-29 | Synthon B.V. | Composition pharmaceutique comprenant du sunitinib amorphe |
| KR20240025990A (ko) * | 2022-08-19 | 2024-02-27 | 주식회사 스카이테라퓨틱스 | 무정형 수니티닙, 그 제조방법 및 이를 포함한 의약 조성물 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20020156292A1 (en) * | 2000-02-15 | 2002-10-24 | Tang Peng Cho | Pyrrole substituted 2-indolinone protein kinase inhibitors |
| US20030069298A1 (en) * | 2001-08-15 | 2003-04-10 | Pharmacia & Upjohn Company | Crystals including a malic acid salt of a 3-pyrrole substituted 2-indolinone, and compositions thereof |
| US20030229229A1 (en) * | 2002-02-15 | 2003-12-11 | Qingwu Jin | Process for preparing indolinone derivatives |
| US20060009510A1 (en) * | 2004-07-09 | 2006-01-12 | Pharmacia & Upjohn Company Llc | Method of synthesizing indolinone compounds |
| WO2009067674A2 (fr) * | 2007-11-21 | 2009-05-28 | Teva Pharmaceutical Industries Ltd. | Polymorphes de base de sunitinib et procédés pour les préparer |
-
2009
- 2009-06-26 WO PCT/IB2009/006056 patent/WO2009156837A2/fr not_active Ceased
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20020156292A1 (en) * | 2000-02-15 | 2002-10-24 | Tang Peng Cho | Pyrrole substituted 2-indolinone protein kinase inhibitors |
| US20030069298A1 (en) * | 2001-08-15 | 2003-04-10 | Pharmacia & Upjohn Company | Crystals including a malic acid salt of a 3-pyrrole substituted 2-indolinone, and compositions thereof |
| US20030229229A1 (en) * | 2002-02-15 | 2003-12-11 | Qingwu Jin | Process for preparing indolinone derivatives |
| US20060009510A1 (en) * | 2004-07-09 | 2006-01-12 | Pharmacia & Upjohn Company Llc | Method of synthesizing indolinone compounds |
| WO2009067674A2 (fr) * | 2007-11-21 | 2009-05-28 | Teva Pharmaceutical Industries Ltd. | Polymorphes de base de sunitinib et procédés pour les préparer |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2009156837A2 (fr) | 2009-12-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| WO2009156837A3 (fr) | Forme amorphe d'un sel de malate de 2-indolinone à substitution 3-pyrrole | |
| WO2007135527A3 (fr) | Composés de benzimidazolyle | |
| WO2008133896A3 (fr) | Agents antihypertensifs à double action | |
| WO2008012622A3 (fr) | Composés d'azabenzimidazolyle | |
| WO2008097459A3 (fr) | Agents anti hypertension à double action | |
| WO2007141283A3 (fr) | Nouveaux sels et formes de sels cristallins d'un dérivé de l'indolinone | |
| WO2009155121A3 (fr) | Inhibiteurs de la pi3 kinase | |
| TN2012000125A1 (en) | Substituted carbamoylmethylamino acetic acid derivatives as novel nep inhibitors | |
| MY156552A (en) | Isoxazole derivatives and their use as metabotropic glutamate receptor potentiators | |
| IN2012DN03182A (fr) | ||
| WO2007150026A3 (fr) | Dérivés de purinone en tant qu'agonistes de hm74a | |
| WO2008006795A3 (fr) | Composés d'indole | |
| WO2011045232A3 (fr) | Agonistes du récepteur du neuropeptide-2 (y-2r) | |
| WO2010001257A3 (fr) | Nouvelles formes à l’état solide de laquinimod et son sel de sodium | |
| WO2010052144A3 (fr) | Agonistes du récepteur 2 de neuropeptide (y-2r) et leurs utilisations | |
| WO2012015681A3 (fr) | Conjugués médicaments-ligands, leur synthèse et intermédiaires correspondants | |
| WO2013042135A8 (fr) | Composés hétéroaryles convenant comme ligands du récepteur 5-ht4 | |
| WO2010049449A3 (fr) | Nouveaux sels de sunitinib | |
| WO2012135615A3 (fr) | Enopeptines, utilisations de celles-ci, et procédés de synthèse de celles-ci | |
| WO2010011811A3 (fr) | Composés de 3-(phénoxyphénylméthyl)pyrrolidine | |
| IN2012DN04868A (fr) | ||
| WO2010070677A3 (fr) | Procédé de préparation de prasugrel et de ses sels pharmaceutiquement acceptables | |
| WO2007112913A3 (fr) | Derives de benzimidazole | |
| WO2011084434A3 (fr) | Dérivés d'indole et d'indoline à cycles condensés et pontage aza | |
| WO2010012459A3 (fr) | Procédé de préparation de sels de solifénacine et inclusion de ces derniers dans des formes pharmaceutiques |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 09769649 Country of ref document: EP Kind code of ref document: A2 |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 09769649 Country of ref document: EP Kind code of ref document: A2 |