ECSP14002014A - N-(3-{[(3-{[2-cloro-5-(metoxi) fenil] amino} quinoxalin-2-il) amino] sulfonil} fenil)-2-metilalaninamida como inhibidor de fosfatidilinositol 3-quinasa para el tratamiento de neoplasias linfoproliferativas - Google Patents
N-(3-{[(3-{[2-cloro-5-(metoxi) fenil] amino} quinoxalin-2-il) amino] sulfonil} fenil)-2-metilalaninamida como inhibidor de fosfatidilinositol 3-quinasa para el tratamiento de neoplasias linfoproliferativasInfo
- Publication number
- ECSP14002014A ECSP14002014A ECIEPI20142014A ECPI201402014A ECSP14002014A EC SP14002014 A ECSP14002014 A EC SP14002014A EC IEPI20142014 A ECIEPI20142014 A EC IEPI20142014A EC PI201402014 A ECPI201402014 A EC PI201402014A EC SP14002014 A ECSP14002014 A EC SP14002014A
- Authority
- EC
- Ecuador
- Prior art keywords
- phenyl
- amino
- treatment
- methylalaninamide
- sulfonil
- Prior art date
Links
Classifications
-
- 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
- A61K31/435—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
- A61K31/47—Quinolines; Isoquinolines
-
- 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
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/20—Oxygen atoms
- C07D215/22—Oxygen atoms attached in position 2 or 4
- C07D215/233—Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
- C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
- C07D241/40—Benzopyrazines
- C07D241/44—Benzopyrazines with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Se proporcionan métodos para el tratamiento de una neoplasia linfoproliferativa a un paciente en necesidad de dicho tratamiento, comprendiendo la administración al paciente de una cantidad efectiva del compuesto A como se describe aquí.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161553990P | 2011-11-01 | 2011-11-01 | |
| US201161568189P | 2011-12-08 | 2011-12-08 | |
| PCT/US2012/062999 WO2013067141A1 (en) | 2011-11-01 | 2012-11-01 | N- (3- { [ (3- { [2-chloro-5- (methoxy) phenyl] amino} quinoxalin- 2 -yl) amino] sulfonyl} phe nyl) - 2 -methylalaninamide as phosphatidylinositol 3 - kinase inhibitor for the treatment of lymphoproliferative malignancies |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP14002014A true ECSP14002014A (es) | 2015-11-30 |
Family
ID=47295148
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ECIEPI20142014A ECSP14002014A (es) | 2011-11-01 | 2014-05-26 | N-(3-{[(3-{[2-cloro-5-(metoxi) fenil] amino} quinoxalin-2-il) amino] sulfonil} fenil)-2-metilalaninamida como inhibidor de fosfatidilinositol 3-quinasa para el tratamiento de neoplasias linfoproliferativas |
Country Status (22)
| Country | Link |
|---|---|
| US (2) | US20140303172A1 (es) |
| EP (1) | EP2773353B1 (es) |
| JP (1) | JP6013498B2 (es) |
| KR (1) | KR20140096083A (es) |
| CN (2) | CN104302294A (es) |
| AU (2) | AU2012332486A1 (es) |
| BR (1) | BR112014010492A2 (es) |
| CA (1) | CA2854159A1 (es) |
| CL (1) | CL2014001138A1 (es) |
| CR (1) | CR20140253A (es) |
| DO (1) | DOP2014000092A (es) |
| EA (1) | EA201490905A1 (es) |
| EC (1) | ECSP14002014A (es) |
| HK (1) | HK1201480A1 (es) |
| IL (1) | IL232398A0 (es) |
| MX (1) | MX2014005249A (es) |
| NI (1) | NI201400037A (es) |
| PE (1) | PE20141794A1 (es) |
| PH (1) | PH12014500973A1 (es) |
| SG (1) | SG11201401961UA (es) |
| WO (1) | WO2013067141A1 (es) |
| ZA (1) | ZA201403258B (es) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG11201401961UA (en) | 2011-11-01 | 2014-05-29 | Exelixis Inc | N- (3- { [ (3- { [2-chloro-5- (methoxy) phenyl] amino} quinoxalin- 2 -yl) amino] sulfonyl} phe nyl) - 2 -methylalaninamide as phosphatidylinositol 3 - kinase inhibitor for the treatment of lymphoproliferative malignancies |
| AR092501A1 (es) * | 2012-09-13 | 2015-04-22 | Sanofi Sa | Compuestos cristalinos |
| HK1214159A1 (zh) | 2012-11-08 | 2016-07-22 | Rhizen Pharmaceuticals S.A. | 含有PDE4抑制剂和PI3δ或双重PI3δ-γ激酶抑制剂的药物组合物 |
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| HRP20130902T1 (hr) | 2005-10-07 | 2013-11-08 | Exelixis Inc. | PIRIDOPIRIMIDINONSKI INHIBITORI PI3Kalfa |
| HRP20140975T1 (hr) | 2005-10-07 | 2014-11-21 | Exelixis, Inc. | Derivati n-(3-amino-hinoksalin-2-il)-sulfonamida i njihova uporaba kao inhibitora fosfatidilinozitol 3-kinaze |
| PT1940839E (pt) | 2005-10-07 | 2013-10-10 | Exelixis Inc | Inibidores de piridopirimidinona pi3k alfa |
| CA2658725A1 (en) | 2006-08-16 | 2008-02-21 | Exelixis, Inc. | Using pi3k and mek modulators in treatments of cancer |
| PT2139484E (pt) | 2007-04-10 | 2013-10-31 | Exelixis Inc | Métodos de tratamento de cancro usando inibidores piridopirimidinona de pi3k-alfa |
| UA98141C2 (ru) * | 2007-04-11 | 2012-04-25 | Экселиксис, Инк. | Способы лечения с применением хинаксолиновых ингибиторов pi3k-альфа |
| AU2008239655B2 (en) | 2007-04-11 | 2013-06-20 | Exelixis, Inc. | Pyrido (2, 3-d) pyrimidin-7-one compounds as inhibitors of PI3k-alpha for the treatment of cancer |
| CA2683820A1 (en) | 2007-04-11 | 2008-10-23 | Exelixis, Inc. | Pyrido [2, 3-d] pyrimidin-7-one compounds as inhibitors of p13k-alpha for the treatment of cancer |
| WO2009017838A2 (en) * | 2007-08-01 | 2009-02-05 | Exelixis, Inc. | Combinations of jak-2 inhibitors and other agents |
| MX2010007746A (es) * | 2008-01-15 | 2010-08-18 | Wyeth Llc | Compuestos de 3h-[1,2,3]triazolo[4,5-d]pirimidina, su uso como inhibidores de diana de rapamicina de mamifero quinasa y fosfatidilinositol quinasa y su sintesis. |
| TW201018685A (en) | 2008-09-30 | 2010-05-16 | Exelixis Inc | Pyridopyrimidinone inhibitors of PI3Kα and mTOR |
| ES2439793T3 (es) * | 2009-04-17 | 2014-01-24 | Wyeth Llc | Compuestos de pirimidina, su uso como inhibidores de la mTOR quinasa y de la PI3 quinasa, y su síntesis |
| WO2010135524A1 (en) | 2009-05-22 | 2010-11-25 | Exelixis, Inc. | Benzoxazepines based p13k/mt0r inhibitors against proliferative diseases |
| MX2011012584A (es) | 2009-05-26 | 2012-02-21 | Exelixis Inc | Benzoxazepinas como inhibidores de pi3k/m tor, metodos para su uso y fabricación. |
| UY33221A (es) | 2010-02-09 | 2011-09-30 | Univ California | MÉTODOS PARA TRATAR CÁNCER USANDO INHIBIDORES DE PI3K Y mTOR EN COMBINACIÓN CON INHIBIDORES DE AUTOFAGIA |
| JP2013539453A (ja) * | 2010-07-09 | 2013-10-24 | エクセリクシス, インク. | 癌の治療のためのキナーゼ阻害物質の組み合わせ |
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| TWI642670B (zh) | 2010-09-14 | 2018-12-01 | 伊塞利克斯公司 | Pi3k-德爾塔抑制劑以及其應用和生產方法 |
| EP2444084A1 (en) * | 2010-10-21 | 2012-04-25 | Centro Nacional de Investigaciones Oncológicas (CNIO) | Use of PI3K inibitors for the treatment of obesity |
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| WO2012068106A2 (en) | 2010-11-15 | 2012-05-24 | Exelixis, Inc. | Benzoxazepines as inhibitors of pi3k/mtor and methods of their use and manufacture |
| EP2643316A2 (en) | 2010-11-24 | 2013-10-02 | Exelixis, Inc. | Benzoxazepines as inhibitors of p13k/mtor and methods of their use and manufacture |
| JP2013544827A (ja) | 2010-11-24 | 2013-12-19 | エクセリクシス, インク. | PI3K/mTORの阻害剤としてのベンゾオキサゼピン類ならびにそれらの使用法および製造法 |
| BR112013012950A2 (pt) | 2010-11-24 | 2017-08-29 | Exelixis Inc 210 | Benzoxazepinas asn inhibidoras de p13k/m tor e métodos de seu uso e fabricação |
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| SG11201401961UA (en) | 2011-11-01 | 2014-05-29 | Exelixis Inc | N- (3- { [ (3- { [2-chloro-5- (methoxy) phenyl] amino} quinoxalin- 2 -yl) amino] sulfonyl} phe nyl) - 2 -methylalaninamide as phosphatidylinositol 3 - kinase inhibitor for the treatment of lymphoproliferative malignancies |
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-
2012
- 2012-11-01 SG SG11201401961UA patent/SG11201401961UA/en unknown
- 2012-11-01 HK HK15102158.7A patent/HK1201480A1/xx unknown
- 2012-11-01 US US14/355,775 patent/US20140303172A1/en not_active Abandoned
- 2012-11-01 EA EA201490905A patent/EA201490905A1/ru unknown
- 2012-11-01 BR BR112014010492A patent/BR112014010492A2/pt not_active Application Discontinuation
- 2012-11-01 JP JP2014540068A patent/JP6013498B2/ja not_active Expired - Fee Related
- 2012-11-01 MX MX2014005249A patent/MX2014005249A/es unknown
- 2012-11-01 CA CA2854159A patent/CA2854159A1/en not_active Abandoned
- 2012-11-01 PE PE2014000632A patent/PE20141794A1/es not_active Application Discontinuation
- 2012-11-01 EP EP12795915.3A patent/EP2773353B1/en active Active
- 2012-11-01 PH PH1/2014/500973A patent/PH12014500973A1/en unknown
- 2012-11-01 CN CN201280065743.6A patent/CN104302294A/zh active Pending
- 2012-11-01 CN CN201710532924.XA patent/CN107375289A/zh active Pending
- 2012-11-01 WO PCT/US2012/062999 patent/WO2013067141A1/en not_active Ceased
- 2012-11-01 KR KR1020147014381A patent/KR20140096083A/ko not_active Ceased
- 2012-11-01 AU AU2012332486A patent/AU2012332486A1/en not_active Abandoned
-
2014
- 2014-04-30 IL IL232398A patent/IL232398A0/en unknown
- 2014-04-30 NI NI201400037A patent/NI201400037A/es unknown
- 2014-04-30 CL CL2014001138A patent/CL2014001138A1/es unknown
- 2014-04-30 DO DO2014000092A patent/DOP2014000092A/es unknown
- 2014-05-06 ZA ZA2014/03258A patent/ZA201403258B/en unknown
- 2014-05-26 EC ECIEPI20142014A patent/ECSP14002014A/es unknown
- 2014-05-28 CR CR20140253A patent/CR20140253A/es unknown
-
2017
- 2017-05-19 US US15/600,147 patent/US10328069B2/en active Active
- 2017-08-28 AU AU2017219131A patent/AU2017219131A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| MX2014005249A (es) | 2015-03-05 |
| BR112014010492A2 (pt) | 2017-04-25 |
| CL2014001138A1 (es) | 2014-08-01 |
| AU2017219131A1 (en) | 2017-09-28 |
| EP2773353B1 (en) | 2018-09-05 |
| ZA201403258B (en) | 2015-11-25 |
| CN104302294A (zh) | 2015-01-21 |
| EP2773353A1 (en) | 2014-09-10 |
| AU2012332486A1 (en) | 2014-06-19 |
| US20170296529A1 (en) | 2017-10-19 |
| PH12014500973A1 (en) | 2014-06-16 |
| JP2014532709A (ja) | 2014-12-08 |
| HK1201480A1 (en) | 2015-09-04 |
| IL232398A0 (en) | 2014-06-30 |
| WO2013067141A1 (en) | 2013-05-10 |
| NI201400037A (es) | 2014-12-22 |
| US20140303172A1 (en) | 2014-10-09 |
| DOP2014000092A (es) | 2015-02-15 |
| PE20141794A1 (es) | 2014-12-17 |
| KR20140096083A (ko) | 2014-08-04 |
| US10328069B2 (en) | 2019-06-25 |
| CN107375289A (zh) | 2017-11-24 |
| CA2854159A1 (en) | 2013-05-10 |
| SG11201401961UA (en) | 2014-05-29 |
| JP6013498B2 (ja) | 2016-10-25 |
| EA201490905A1 (ru) | 2014-11-28 |
| CR20140253A (es) | 2014-10-28 |
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