PE20110424A1 - Isoindolonas que inhiben la cinasa mek - Google Patents
Isoindolonas que inhiben la cinasa mekInfo
- Publication number
- PE20110424A1 PE20110424A1 PE2010001200A PE2010001200A PE20110424A1 PE 20110424 A1 PE20110424 A1 PE 20110424A1 PE 2010001200 A PE2010001200 A PE 2010001200A PE 2010001200 A PE2010001200 A PE 2010001200A PE 20110424 A1 PE20110424 A1 PE 20110424A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- halo
- isoindolones
- mek kinase
- inhibit mek
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/46—Iso-indoles; Hydrogenated iso-indoles with an oxygen atom in position 1
-
- 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
- A61K31/4035—Isoindoles, e.g. phthalimide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
Abstract
REFERIDA A DERIVADOS DE ISOINDOLONAS DE FORMULA (I), DONDE Z1 ES CR1R1a O NRA; R1 Y R1a SON H, ALQUILO C1-C3, CF3, CHF2, CN O ORA; Z2 ES CR2 O N; R2 ES H, ALQUILO C1-C3, HALO, CF3, ENTRE OTROS; Z3 ES CR3 O N; R3 ES H, HALO, CN, CF3, ENTRE OTROS; R4 ES H, ALQUILO C1-C6, CARBOCICLILO C3-C4; Y ES W-C(O)- O W'; W ES X1-NR5- O R11-O-; R5 ES H O ALQUILO C1-C12; X1 ES R11 O OR11; R11' ES H, ALQUILO C1-C12, ALQUINILO C2-C8, ENTRE OTROS; R11 ES H, ALQUILO C1-C12, ALQUENILO C2-C8, ENTRE OTROS; W' ES Het-R7, -NH-SO2-R8, -NH-SO2-NR8R10; Het ES (a), (b), ENTRE OTROS; X2 ES O, S, ENTRE OTROS; R7 ES H, HALO, CN, CF3, ENTRE OTROS; R8 ES ALQUILO C1-C12, ARILO, ENTRE OTROS; R10 ES H, ALQUILO C1-C6 O CARBOCICLILO C3-C4; R6 ES H, HALO, ALQUILO C1-C6, ALQUENILO C2-C8, ENTRE OTROS; p ES 0, 1, 2 O 3. ES UN COMPUESTO PREFERIDO: (2-HIDROXI-ETOXI)-AMIDA DEL ACIDO 6-(2-FLUORO-4-YODO-FENILAMINO)-1-OXO-2,3-DIHIDRO-1H-ISOINDOL-5-CARBOXILICO. TAMBIEN ESTA REFERIDA A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS INHIBEN LA CINASA MEK Y SON UTILES EN EL TRATAMIENTO DEL CANCER
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US7743208P | 2008-07-01 | 2008-07-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20110424A1 true PE20110424A1 (es) | 2011-07-22 |
Family
ID=41128054
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2010001200A PE20110424A1 (es) | 2008-07-01 | 2009-07-01 | Isoindolonas que inhiben la cinasa mek |
Country Status (16)
Country | Link |
---|---|
US (1) | US8492427B2 (es) |
EP (1) | EP2307364B1 (es) |
JP (1) | JP5615274B2 (es) |
KR (1) | KR20110028376A (es) |
CN (1) | CN102137843A (es) |
AU (1) | AU2009266953A1 (es) |
BR (1) | BRPI0910200A2 (es) |
CA (1) | CA2727252A1 (es) |
CL (1) | CL2010001637A1 (es) |
ES (1) | ES2426096T3 (es) |
IL (1) | IL209892A0 (es) |
MX (1) | MX2010014565A (es) |
PE (1) | PE20110424A1 (es) |
RU (1) | RU2495028C2 (es) |
WO (1) | WO2010003022A1 (es) |
ZA (1) | ZA201008962B (es) |
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CN102020651B (zh) | 2010-11-02 | 2012-07-18 | 北京赛林泰医药技术有限公司 | 6-芳基氨基吡啶酮甲酰胺mek抑制剂 |
CA2890238A1 (en) | 2012-11-02 | 2014-05-08 | Merck Patent Gmbh | Method of reducing adverse effects in a cancer patient undergoing treatment with a mek inhibitor |
US9725703B2 (en) | 2012-12-20 | 2017-08-08 | Biomatrica, Inc. | Formulations and methods for stabilizing PCR reagents |
CN105491883B (zh) | 2013-06-13 | 2018-11-02 | 生物马特里卡公司 | 细胞稳定化 |
US9532987B2 (en) | 2013-09-05 | 2017-01-03 | Genentech, Inc. | Use of a combination of a MEK inhibitor and an ERK inhibitor for treatment of hyperproliferative diseases |
RU2667892C2 (ru) * | 2013-10-25 | 2018-09-25 | Шанхай Хэнжуй Фармасьютикал Ко., Лтд. | Производные пиридилкетона, способ их получения и их фармацевтическое применение |
SG11201606080SA (en) | 2014-02-03 | 2016-08-30 | Vitae Pharmaceuticals Inc | Dihydropyrrolopyridine inhibitors of ror-gamma |
CN103922992B (zh) * | 2014-04-25 | 2015-09-02 | 温州大学 | 一种抗癌活性吲哚酮衍生物、合成方法及其用途 |
JP6661554B2 (ja) | 2014-06-10 | 2020-03-11 | バイオマトリカ,インク. | 周囲温度における血小板の安定化 |
HUE042335T2 (hu) | 2014-10-14 | 2019-06-28 | Vitae Pharmaceuticals Inc | ROR-gamma dihidropirrolopiridin inhibitorai |
US9845308B2 (en) | 2014-11-05 | 2017-12-19 | Vitae Pharmaceuticals, Inc. | Isoindoline inhibitors of ROR-gamma |
US9663515B2 (en) | 2014-11-05 | 2017-05-30 | Vitae Pharmaceuticals, Inc. | Dihydropyrrolopyridine inhibitors of ROR-gamma |
CN104860869B (zh) * | 2015-04-03 | 2017-11-03 | 北京大学 | 具有mek激酶抑制功能的化合物及其制备方法与应用 |
PT3300500T (pt) | 2015-05-20 | 2020-05-19 | Amgen Inc | Agonistas triazóis do receptor apj |
EP3331876B1 (en) | 2015-08-05 | 2020-10-07 | Vitae Pharmaceuticals, LLC | Modulators of ror-gamma |
US20190008859A1 (en) | 2015-08-21 | 2019-01-10 | Acerta Pharma B.V. | Therapeutic Combinations of a MEK Inhibitor and a BTK Inhibitor |
EP3377482B1 (en) | 2015-11-20 | 2021-05-12 | Vitae Pharmaceuticals, LLC | Modulators of ror-gamma |
SG11201804776SA (en) | 2015-12-08 | 2018-07-30 | Biomatrica Inc | Reduction of erythrocyte sedimentation rate |
TWI757266B (zh) | 2016-01-29 | 2022-03-11 | 美商維它藥物有限責任公司 | ROR-γ調節劑 |
EP3443114A1 (en) | 2016-04-15 | 2019-02-20 | H. Hoffnabb-La Roche Ag | Diagnostic and therapeutic methods for cancer |
US9988369B2 (en) | 2016-05-03 | 2018-06-05 | Amgen Inc. | Heterocyclic triazole compounds as agonists of the APJ receptor |
US9481674B1 (en) | 2016-06-10 | 2016-11-01 | Vitae Pharmaceuticals, Inc. | Dihydropyrrolopyridine inhibitors of ROR-gamma |
WO2018093580A1 (en) | 2016-11-16 | 2018-05-24 | Amgen Inc. | Triazole pyridyl compounds as agonists of the apj receptor |
MA46827A (fr) | 2016-11-16 | 2019-09-25 | Amgen Inc | Composés de triazole à substitution cycloalkyle en tant qu'agonistes du récepteur apj |
WO2018097945A1 (en) | 2016-11-16 | 2018-05-31 | Amgen Inc. | Heteroaryl-substituted triazoles as apj receptor agonists |
US10736883B2 (en) | 2016-11-16 | 2020-08-11 | Amgen Inc. | Triazole furan compounds as agonists of the APJ receptor |
US11191762B2 (en) | 2016-11-16 | 2021-12-07 | Amgen Inc. | Alkyl substituted triazole compounds as agonists of the APJ Receptor |
EP3541810B1 (en) | 2016-11-16 | 2020-12-23 | Amgen Inc. | Triazole phenyl compounds as agonists of the apj receptor |
KR102580179B1 (ko) | 2017-06-23 | 2023-09-18 | 씨스톤 파마슈티컬즈 | Mek억제제로서의 쿠마린 고리계 화합물 및 이의 용도 |
MX2020000887A (es) | 2017-07-24 | 2020-07-22 | Vitae Pharmaceuticals Llc | Inhibidores de ror?. |
WO2019018975A1 (en) | 2017-07-24 | 2019-01-31 | Vitae Pharmaceuticals, Inc. | INHIBITORS OF ROR GAMMA |
EP3679159A1 (en) | 2017-09-08 | 2020-07-15 | H. Hoffnabb-La Roche Ag | Diagnostic and therapeutic methods for cancer |
MA50509A (fr) | 2017-11-03 | 2021-06-02 | Amgen Inc | Agonistes de triazole fusionnés du récepteur apj |
CN111801314B (zh) | 2018-01-02 | 2023-10-31 | 西尔洛克治疗公司 | Ask1抑制剂化合物及其用途 |
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WO2019213006A1 (en) | 2018-05-01 | 2019-11-07 | Amgen Inc. | Substituted pyrimidinones as agonists of the apj receptor |
WO2024033381A1 (en) | 2022-08-10 | 2024-02-15 | Vib Vzw | Inhibition of tcf4/itf2 in the treatment of cancer |
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US3736326A (en) * | 1971-03-29 | 1973-05-29 | Squibb & Sons Inc | Isoxazolopyridine carboxylic acids and esters |
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GB8404586D0 (en) * | 1984-02-22 | 1984-03-28 | Beecham Group Plc | Compounds |
GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
KR20020015376A (ko) | 1999-07-16 | 2002-02-27 | 로즈 암스트롱, 크리스틴 에이. 트러트웨인 | Mek 억제제를 사용한 만성 통증의 치료 방법 |
JP2002020386A (ja) | 2000-07-07 | 2002-01-23 | Ono Pharmaceut Co Ltd | ピラゾロピリジン誘導体 |
SI1301472T1 (sl) | 2000-07-19 | 2014-05-30 | Warner-Lambert Company Llc | Oksigenirani estri 4-jodo fenilamino benzihidroksamskih kislin |
PT2275102E (pt) | 2002-03-13 | 2015-10-27 | Array Biopharma Inc | Derivados de benzimidazole alquilado n3 como inibidores de mek |
TW200406203A (en) | 2002-03-13 | 2004-05-01 | Array Biopharma Inc | N3 alkylated banzimidazole derivatives as MEK inhibitors |
GB0220581D0 (en) | 2002-09-04 | 2002-10-09 | Novartis Ag | Organic Compound |
GB0316237D0 (en) | 2003-07-11 | 2003-08-13 | Astrazeneca Ab | Therapeutic agents |
GB0316232D0 (en) | 2003-07-11 | 2003-08-13 | Astrazeneca Ab | Therapeutic agents |
US20050049276A1 (en) * | 2003-07-23 | 2005-03-03 | Warner-Lambert Company, Llc | Imidazopyridines and triazolopyridines |
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US7144907B2 (en) * | 2003-09-03 | 2006-12-05 | Array Biopharma Inc. | Heterocyclic inhibitors of MEK and methods of use thereof |
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ES2299906T3 (es) | 2003-11-25 | 2008-06-01 | Eli Lilly And Company | Moduladores de receptores activados por proliferadores de peroxisomas. |
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RU2008112313A (ru) | 2005-09-01 | 2009-10-10 | Эррэй Биофарма Инк. (Us) | Соединения ингибиторы raf и способы их применения |
EA019983B1 (ru) | 2005-10-07 | 2014-07-30 | Экселиксис, Инк. | Ингибиторы mek и способы их применения |
CN101553492A (zh) | 2006-08-31 | 2009-10-07 | 阵列生物制药公司 | Raf抑制剂化合物及其使用方法 |
-
2009
- 2009-07-01 RU RU2011103434/04A patent/RU2495028C2/ru not_active IP Right Cessation
- 2009-07-01 EP EP09774472.6A patent/EP2307364B1/en active Active
- 2009-07-01 BR BRPI0910200A patent/BRPI0910200A2/pt not_active IP Right Cessation
- 2009-07-01 CA CA2727252A patent/CA2727252A1/en not_active Abandoned
- 2009-07-01 PE PE2010001200A patent/PE20110424A1/es not_active Application Discontinuation
- 2009-07-01 WO PCT/US2009/049449 patent/WO2010003022A1/en active Application Filing
- 2009-07-01 MX MX2010014565A patent/MX2010014565A/es active IP Right Grant
- 2009-07-01 KR KR1020117002455A patent/KR20110028376A/ko not_active Application Discontinuation
- 2009-07-01 ES ES09774472T patent/ES2426096T3/es active Active
- 2009-07-01 JP JP2011516857A patent/JP5615274B2/ja not_active Expired - Fee Related
- 2009-07-01 US US12/998,000 patent/US8492427B2/en not_active Expired - Fee Related
- 2009-07-01 AU AU2009266953A patent/AU2009266953A1/en not_active Abandoned
- 2009-07-01 CN CN2009801337804A patent/CN102137843A/zh active Pending
-
2010
- 2010-12-09 IL IL209892A patent/IL209892A0/en unknown
- 2010-12-13 ZA ZA2010/08962A patent/ZA201008962B/en unknown
- 2010-12-30 CL CL2010001637A patent/CL2010001637A1/es unknown
Also Published As
Publication number | Publication date |
---|---|
CL2010001637A1 (es) | 2011-07-15 |
CN102137843A (zh) | 2011-07-27 |
RU2011103434A (ru) | 2012-08-10 |
JP2011526924A (ja) | 2011-10-20 |
ZA201008962B (en) | 2012-03-28 |
CA2727252A1 (en) | 2010-01-07 |
JP5615274B2 (ja) | 2014-10-29 |
ES2426096T3 (es) | 2013-10-21 |
KR20110028376A (ko) | 2011-03-17 |
IL209892A0 (en) | 2011-02-28 |
BRPI0910200A2 (pt) | 2015-09-29 |
US20110124622A1 (en) | 2011-05-26 |
AU2009266953A1 (en) | 2010-01-07 |
RU2495028C2 (ru) | 2013-10-10 |
MX2010014565A (es) | 2011-03-04 |
EP2307364B1 (en) | 2013-06-19 |
EP2307364A1 (en) | 2011-04-13 |
WO2010003022A8 (en) | 2010-09-30 |
WO2010003022A1 (en) | 2010-01-07 |
US8492427B2 (en) | 2013-07-23 |
AU2009266953A2 (en) | 2011-01-27 |
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