CR11568A - Compuestos de 3h-[1,2,3]triazolo[4,5-d]pirimidina, su uso como inhibidores de mtor quinasa y pi3 quinasa y su sintesis - Google Patents
Compuestos de 3h-[1,2,3]triazolo[4,5-d]pirimidina, su uso como inhibidores de mtor quinasa y pi3 quinasa y su sintesisInfo
- Publication number
- CR11568A CR11568A CR11568A CR11568A CR11568A CR 11568 A CR11568 A CR 11568A CR 11568 A CR11568 A CR 11568A CR 11568 A CR11568 A CR 11568A CR 11568 A CR11568 A CR 11568A
- Authority
- CR
- Costa Rica
- Prior art keywords
- quinasa
- triazolo
- compounds
- mtor
- inhibitors
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 101150097381 Mtor gene Proteins 0.000 title 1
- 102100023085 Serine/threonine-protein kinase mTOR Human genes 0.000 title 1
- 230000015572 biosynthetic process Effects 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 238000003786 synthesis reaction Methods 0.000 title 1
- GIIGHSIIKVOWKZ-UHFFFAOYSA-N 2h-triazolo[4,5-d]pyrimidine Chemical compound N1=CN=CC2=NNN=C21 GIIGHSIIKVOWKZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000000470 constituent Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- 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
-
- 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
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
La invencion se refiere a compuestos de 3H-[1,2,3]triazolo[4,5-d]pirimidina de Formula 1, o una sal farmaceuticamente aceptable de los mismos, en la que las variables constituyentes son como se definen en el presente documento, a composiciones que comprenden los compuestos y a procedimientos para fabricar y usar los compuestos.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2108408P | 2008-01-15 | 2008-01-15 | |
| US3468008P | 2008-03-07 | 2008-03-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CR11568A true CR11568A (es) | 2010-08-11 |
Family
ID=40377318
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CR11568A CR11568A (es) | 2008-01-15 | 2010-07-14 | Compuestos de 3h-[1,2,3]triazolo[4,5-d]pirimidina, su uso como inhibidores de mtor quinasa y pi3 quinasa y su sintesis |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US20090181963A1 (es) |
| EP (1) | EP2252296A1 (es) |
| JP (1) | JP2011510010A (es) |
| KR (1) | KR20100113567A (es) |
| CN (1) | CN102014914A (es) |
| AP (1) | AP2010005346A0 (es) |
| AU (1) | AU2009205501A1 (es) |
| BR (1) | BRPI0906519A2 (es) |
| CA (1) | CA2712267A1 (es) |
| CO (1) | CO6321259A2 (es) |
| CR (1) | CR11568A (es) |
| DO (1) | DOP2010000217A (es) |
| EA (1) | EA201001017A1 (es) |
| EC (1) | ECSP10010346A (es) |
| IL (1) | IL206820A0 (es) |
| MA (1) | MA32341B1 (es) |
| MX (1) | MX2010007746A (es) |
| NI (1) | NI201000119A (es) |
| SV (1) | SV2010003621A (es) |
| WO (1) | WO2009091788A1 (es) |
| ZA (2) | ZA201004603B (es) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20091268A1 (es) | 2007-12-19 | 2009-09-19 | Amgen Inc | Derivados heterociclicos como inhibidores de pi3 quinasa |
| JP2011515462A (ja) * | 2008-03-27 | 2011-05-19 | アウククランド ウニセルビセス リミテッド | 置換されたピリミジン、及びトリアジン、並びに癌療法におけるこれらの使用 |
| TWI378933B (en) | 2008-10-14 | 2012-12-11 | Daiichi Sankyo Co Ltd | Morpholinopurine derivatives |
| AU2010229468A1 (en) * | 2009-03-27 | 2011-10-13 | Vetdc, Inc. | Pyrimidinyl and 1,3,5-triazinyl benzimidazole sulfonamides and their use in cancer therapy |
| US20100331305A1 (en) * | 2009-06-24 | 2010-12-30 | Genentech, Inc. | Oxo-heterocycle fused pyrimidine compounds, compositions and methods of use |
| US8486939B2 (en) * | 2009-07-07 | 2013-07-16 | Pathway Therapeutics Inc. | Pyrimidinyl and 1,3,5-triazinyl benzimidazoles and their use in cancer therapy |
| SG183155A1 (en) | 2010-02-03 | 2012-09-27 | Signal Pharm Llc | Identification of lkb1 mutation as a predictive biomarker for sensitivity to tor kinase inhibitors |
| ES2616238T3 (es) | 2010-10-06 | 2017-06-12 | Glaxosmithkline Llc, Corporation Service Company | Derivados de bencimidazol como inhibidores de PI3 quinasa |
| EP2691384B1 (en) | 2011-03-28 | 2016-10-26 | MEI Pharma, Inc. | (alpha-substituted aralkylamino and heteroarylalkylamino) pyrimidinyl and 1,3,5-triazinyl benzimidazoles, pharmaceutical compositions containing them, and these compounds for use in treating proliferative diseases |
| PH12014500973A1 (en) * | 2011-11-01 | 2014-06-16 | Exelixis Inc | Phosphatidylinositol 3-kinase inhibitors for the treatment of lymphoproliferative malignancies |
| WO2013152717A1 (zh) * | 2012-04-10 | 2013-10-17 | 上海昀怡健康管理咨询有限公司 | 稠合嘧啶类化合物,其制备方法,中间体,组合物和应用 |
| EP2852661A1 (en) | 2012-05-23 | 2015-04-01 | F. Hoffmann-La Roche AG | Compositions and methods of obtaining and using endoderm and hepatocyte cells |
| AU2013203714B2 (en) | 2012-10-18 | 2015-12-03 | Signal Pharmaceuticals, Llc | Inhibition of phosphorylation of PRAS40, GSK3-beta or P70S6K1 as a marker for TOR kinase inhibitory activity |
| HK1221168A1 (zh) | 2013-04-17 | 2017-05-26 | 西格诺药品有限公司 | 用於治疗癌症的包括tor激酶抑制剂和n-(3-(5-氟-2-(4-(2-甲氧基乙氧基)苯基氨基)嘧啶-4-基氨基)苯基)丙烯醯胺的组合疗法 |
| MX368286B (es) | 2013-04-17 | 2019-09-27 | Signal Pharm Llc | Terapia de combinacion que comprende un inhibidor de tor cinasa y un compuesto de quinazolinona 5-sustituida para tratar cancer. |
| AU2014254059B2 (en) | 2013-04-17 | 2019-06-06 | Signal Pharmaceuticals, Llc | Combination therapy comprising a TOR kinase inhibitor and a cytidine analog for treating cancer |
| CA2908353C (en) | 2013-04-17 | 2021-11-02 | Signal Pharmaceuticals, Llc | Treatment of cancer with dihydropyrazino-pyrazines |
| CA2908957C (en) | 2013-04-17 | 2021-05-18 | Signal Pharmaceuticals, Llc | Combination therapy comprising a dihydropyrazino-pyrazine compound and an androgen receptor antagonist for treating prostate cancer |
| US9505764B2 (en) | 2013-04-17 | 2016-11-29 | Signal Pharmaceuticals, Llc | Treatment of cancer with dihydropyrazino-pyrazines |
| EA030726B1 (ru) | 2013-04-17 | 2018-09-28 | СИГНАЛ ФАРМАСЬЮТИКАЛЗ, ЭлЭлСи | ФАРМАЦЕВТИЧЕСКИЕ СОСТАВЫ, СПОСОБЫ, ТВЕРДЫЕ ФОРМЫ И СПОСОБЫ ПРИМЕНЕНИЯ, ОТНОСЯЩИЕСЯ К 1-ЭТИЛ-7-(2-МЕТИЛ-6-(1H-1,2,4-ТРИАЗОЛ-3-ИЛ)ПИРИДИН-3-ИЛ)-3,4-ДИГИДРОПИРАЗИНО[2,3-b]ПИРАЗИН-2(1H)-ОНУ |
| HK1223286A1 (zh) | 2013-05-29 | 2017-07-28 | 西格诺药品有限公司 | 7-(6-(2-羟基丙-2-基)吡啶-3-基)-1-((反式)-4-甲氧基环己基)-3,4-二氢吡嗪并[2,3-b]吡嗪-2(1h)-酮的药物组合物、其固体形式及它们的使用方法 |
| JP6441910B2 (ja) * | 2013-09-30 | 2018-12-19 | シャンハイ インリ ファーマシューティカル カンパニー リミティド | 縮合ピリミジン化合物、中間体、その調製方法、組成物及び使用 |
| JP2017511367A (ja) | 2014-04-16 | 2017-04-20 | シグナル ファーマシューティカルズ,エルエルシー | 1−エチル−7−(2−メチル−6−(1H−1,2,4−トリアゾール−3−イル)ピリジン−3−イル)−3,4−ジヒドロピラジノ[2,3−b]ピラジン−2(1H)−オン及び共形成物を含む固体形態、その組成物及び使用方法 |
| NZ714742A (en) | 2014-04-16 | 2017-04-28 | Signal Pharm Llc | Solid forms of 1-ethyl-7-(2-methyl-6-(1h-1,2,4-triazol-3-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1h)-one, compositions thereof and methods of their use |
| CN106459048A (zh) | 2014-05-14 | 2017-02-22 | 辉瑞公司 | 吡唑并吡啶类和吡唑并嘧啶类 |
| WO2017087818A1 (en) * | 2015-11-19 | 2017-05-26 | The Regents Of The University Of Michigan | Dual src/p38 kinase inhibitor compounds and their use as therapeutic agents |
| CA3063976A1 (en) | 2017-05-23 | 2018-11-29 | Mei Pharma, Inc. | Combination therapy |
| ES2959860T3 (es) | 2017-06-22 | 2024-02-28 | Celgene Corp | Tratamiento del carcinoma hepatocelular caracterizado por la infección por el virus de la hepatitis B |
| WO2020063636A1 (zh) * | 2018-09-27 | 2020-04-02 | 苏州锐明新药研发有限公司 | 吡唑并嘧啶化合物及制备方法与制备抗癌症药物的应用 |
| CN113549080B (zh) * | 2021-08-27 | 2023-05-16 | 中国医学科学院放射医学研究所 | 一类1,2,3-三氮唑并嘧啶类化合物、其制备方法和用途 |
| KR20240015978A (ko) | 2022-07-28 | 2024-02-06 | 박수산 | 다층 수력 발전시스템 |
| GB202415232D0 (en) | 2024-10-16 | 2024-11-27 | Nacamed As | Composition |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU5261001A (en) * | 2000-04-27 | 2001-11-12 | Imperial Cancer Research Technology Ltd | Condensed heteroaryl derivatives |
-
2009
- 2009-01-14 MX MX2010007746A patent/MX2010007746A/es not_active Application Discontinuation
- 2009-01-14 CA CA2712267A patent/CA2712267A1/en not_active Abandoned
- 2009-01-14 JP JP2010543208A patent/JP2011510010A/ja not_active Withdrawn
- 2009-01-14 BR BRPI0906519-9A patent/BRPI0906519A2/pt not_active IP Right Cessation
- 2009-01-14 KR KR1020107018006A patent/KR20100113567A/ko not_active Ceased
- 2009-01-14 EP EP09701825A patent/EP2252296A1/en not_active Withdrawn
- 2009-01-14 AP AP2010005346A patent/AP2010005346A0/en unknown
- 2009-01-14 WO PCT/US2009/030939 patent/WO2009091788A1/en not_active Ceased
- 2009-01-14 AU AU2009205501A patent/AU2009205501A1/en not_active Abandoned
- 2009-01-14 CN CN2009801084548A patent/CN102014914A/zh active Pending
- 2009-01-14 EA EA201001017A patent/EA201001017A1/ru unknown
- 2009-01-15 US US12/354,027 patent/US20090181963A1/en not_active Abandoned
-
2010
- 2010-06-30 ZA ZA2010/04603A patent/ZA201004603B/en unknown
- 2010-07-05 IL IL206820A patent/IL206820A0/en unknown
- 2010-07-14 CR CR11568A patent/CR11568A/es not_active Application Discontinuation
- 2010-07-14 DO DO2010000217A patent/DOP2010000217A/es unknown
- 2010-07-14 NI NI201000119A patent/NI201000119A/es unknown
- 2010-07-15 SV SV2010003621A patent/SV2010003621A/es not_active Application Discontinuation
- 2010-07-15 EC EC2010010346A patent/ECSP10010346A/es unknown
- 2010-07-15 MA MA33020A patent/MA32341B1/fr unknown
- 2010-08-12 CO CO10099284A patent/CO6321259A2/es not_active Application Discontinuation
- 2010-08-13 ZA ZA2010/05793A patent/ZA201005793B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU2009205501A1 (en) | 2009-07-23 |
| NI201000119A (es) | 2011-05-04 |
| ZA201004603B (en) | 2011-03-30 |
| CN102014914A (zh) | 2011-04-13 |
| SV2010003621A (es) | 2011-07-05 |
| EP2252296A1 (en) | 2010-11-24 |
| MA32341B1 (fr) | 2011-06-01 |
| CA2712267A1 (en) | 2009-07-23 |
| DOP2010000217A (es) | 2010-07-31 |
| BRPI0906519A2 (pt) | 2015-07-14 |
| EA201001017A1 (ru) | 2011-02-28 |
| WO2009091788A1 (en) | 2009-07-23 |
| ZA201005793B (en) | 2011-04-28 |
| AP2010005346A0 (en) | 2010-08-31 |
| JP2011510010A (ja) | 2011-03-31 |
| ECSP10010346A (es) | 2010-08-31 |
| KR20100113567A (ko) | 2010-10-21 |
| IL206820A0 (en) | 2010-12-30 |
| CO6321259A2 (es) | 2011-09-20 |
| MX2010007746A (es) | 2010-08-18 |
| US20090181963A1 (en) | 2009-07-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal (granting procedure) |