CN101861307B - 取代的酰胺、其制备方法及其用于治疗疾病例如癌症的用途 - Google Patents
取代的酰胺、其制备方法及其用于治疗疾病例如癌症的用途 Download PDFInfo
- Publication number
- CN101861307B CN101861307B CN2008801161200A CN200880116120A CN101861307B CN 101861307 B CN101861307 B CN 101861307B CN 2008801161200 A CN2008801161200 A CN 2008801161200A CN 200880116120 A CN200880116120 A CN 200880116120A CN 101861307 B CN101861307 B CN 101861307B
- Authority
- CN
- China
- Prior art keywords
- methyl
- oxo
- phenyl
- amino
- dihydro pyrazine
- 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.)
- Active
Links
- 0 CC(CCC1)c2c1[s]c(*)c2 Chemical compound CC(CCC1)c2c1[s]c(*)c2 0.000 description 23
- LCQKJBJNWJIAHT-UHFFFAOYSA-N Cc([s]c1c2CCCC1)c2F Chemical compound Cc([s]c1c2CCCC1)c2F LCQKJBJNWJIAHT-UHFFFAOYSA-N 0.000 description 2
- DUFOMETVDHTDAB-UHFFFAOYSA-N OC(c1cc(CCCC2=O)c2[s]1)=O Chemical compound OC(c1cc(CCCC2=O)c2[s]1)=O DUFOMETVDHTDAB-UHFFFAOYSA-N 0.000 description 2
- ZBLXLMAUMNIMCR-UHFFFAOYSA-N C=S(CC=S)c1cc(CCCCC2)c2[s]1 Chemical compound C=S(CC=S)c1cc(CCCCC2)c2[s]1 ZBLXLMAUMNIMCR-UHFFFAOYSA-N 0.000 description 1
- XDXQNXKXLOQDLQ-UHFFFAOYSA-N CC(C)(C)c1cc(/C=[O]/C)c(C)cc1 Chemical compound CC(C)(C)c1cc(/C=[O]/C)c(C)cc1 XDXQNXKXLOQDLQ-UHFFFAOYSA-N 0.000 description 1
- CBJYRLFTDYXONN-UHFFFAOYSA-N CC(CC1)Cc2c1[s]c(C)c2 Chemical compound CC(CC1)Cc2c1[s]c(C)c2 CBJYRLFTDYXONN-UHFFFAOYSA-N 0.000 description 1
- ZFFFSHWQGNCAIF-UHFFFAOYSA-N CCN(C)c1ccc(C)cc1 Chemical compound CCN(C)c1ccc(C)cc1 ZFFFSHWQGNCAIF-UHFFFAOYSA-N 0.000 description 1
- UVGSACQZVAUFKL-UHFFFAOYSA-N CCN(CC1)CCN1C(C(N(C)CCO)=O)c(cc1)ccc1NC1=NC(c2cccc(NC(c3cc(CCCCC4)c4[s]3)=O)c2C)=CN(C)C1=O Chemical compound CCN(CC1)CCN1C(C(N(C)CCO)=O)c(cc1)ccc1NC1=NC(c2cccc(NC(c3cc(CCCCC4)c4[s]3)=O)c2C)=CN(C)C1=O UVGSACQZVAUFKL-UHFFFAOYSA-N 0.000 description 1
- VUAQALGOUZDRPT-UHFFFAOYSA-N FC(CCC1)(c2c1[s]c(SS)c2)F Chemical compound FC(CCC1)(c2c1[s]c(SS)c2)F VUAQALGOUZDRPT-UHFFFAOYSA-N 0.000 description 1
- NTNCDTQDPQYJMU-UHFFFAOYSA-N FC(CCCC1)(c2c1[s]c(S)c2)F Chemical compound FC(CCCC1)(c2c1[s]c(S)c2)F NTNCDTQDPQYJMU-UHFFFAOYSA-N 0.000 description 1
- ROLXOQXKNDKXTA-UHFFFAOYSA-N OC(c1cc(CCCC2)c2[s]1)=O Chemical compound OC(c1cc(CCCC2)c2[s]1)=O ROLXOQXKNDKXTA-UHFFFAOYSA-N 0.000 description 1
- HSBPBXMYJKWSEK-UHFFFAOYSA-N Sc1cc(CCCC2)c2[s]1 Chemical compound Sc1cc(CCCC2)c2[s]1 HSBPBXMYJKWSEK-UHFFFAOYSA-N 0.000 description 1
- DODWVZSLOOEOKB-UHFFFAOYSA-N Sc1cc2ccccc2[s]1 Chemical compound Sc1cc2ccccc2[s]1 DODWVZSLOOEOKB-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/04—Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
-
- 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
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic 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
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/06—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having one or two double bonds between ring members or between ring members and non-ring members
- C07D241/08—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having one or two double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pulmonology (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Neurology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Hydrogenated Pyridines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US97399507P | 2007-09-20 | 2007-09-20 | |
| US60/973,995 | 2007-09-20 | ||
| US5077708P | 2008-05-06 | 2008-05-06 | |
| US61/050,777 | 2008-05-06 | ||
| PCT/US2008/077054 WO2009039397A2 (en) | 2007-09-20 | 2008-09-19 | Substituted amides, methods of making, use thereof for the treatment of diseases such as cancer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101861307A CN101861307A (zh) | 2010-10-13 |
| CN101861307B true CN101861307B (zh) | 2013-05-01 |
Family
ID=40377565
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2008801161200A Active CN101861307B (zh) | 2007-09-20 | 2008-09-19 | 取代的酰胺、其制备方法及其用于治疗疾病例如癌症的用途 |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US7884108B2 (enExample) |
| EP (1) | EP2188267B1 (enExample) |
| JP (1) | JP5485894B2 (enExample) |
| KR (1) | KR20100072032A (enExample) |
| CN (1) | CN101861307B (enExample) |
| AR (1) | AR068503A1 (enExample) |
| AU (1) | AU2008302099B2 (enExample) |
| BR (1) | BRPI0817130A2 (enExample) |
| CA (1) | CA2700443A1 (enExample) |
| CL (1) | CL2008002793A1 (enExample) |
| PE (1) | PE20091201A1 (enExample) |
| RU (1) | RU2470923C2 (enExample) |
| TW (1) | TWI423966B (enExample) |
| WO (1) | WO2009039397A2 (enExample) |
Families Citing this family (80)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR063706A1 (es) * | 2006-09-11 | 2009-02-11 | Cgi Pharmaceuticals Inc | Determinadas amidas sustituidas, el uso de las mismas para el tratamiento de enfermedades mediadas por la inhibicion de la actividad de btk y composiciones farmaceuticas que las comprenden. |
| US7838523B2 (en) * | 2006-09-11 | 2010-11-23 | Cgi Pharmaceuticals, Inc. | Certain substituted amides, method of making, and method of use thereof |
| US7683064B2 (en) | 2008-02-05 | 2010-03-23 | Roche Palo Alto Llc | Inhibitors of Bruton's tyrosine kinase |
| UA103319C2 (en) | 2008-05-06 | 2013-10-10 | Глаксосмитклайн Ллк | Thiazole- and oxazole-benzene sulfonamide compounds |
| CA2723237A1 (en) * | 2008-05-06 | 2009-11-12 | Peter A. Blomgren | Substituted amides, method of making, and use as btk inhibitors |
| PE20100851A1 (es) | 2008-06-24 | 2011-01-31 | Hoffmann La Roche | PIRIDIN-2-ONAS Y PIRIDAZIN-3-ONAS SUSTITUIDAS COMO INHIBIDORES DE Btk |
| PL2300459T3 (pl) | 2008-07-02 | 2013-10-31 | Hoffmann La Roche | Nowe fenylopirazynony jako inhibitory kinazy |
| CA3034600C (en) * | 2010-05-07 | 2020-11-10 | Genentech, Inc. | Pyridone and aza-pyridone compounds and methods of use |
| CA2809836C (en) | 2010-09-01 | 2019-01-15 | Gilead Connecticut, Inc. | Pyridinones/pyrazinones, method of making, and method of use thereof for the treatment of disorders mediated by bruton's tyrosine kinase |
| UA111756C2 (uk) | 2011-11-03 | 2016-06-10 | Ф. Хоффманн-Ля Рош Аг | Сполуки гетероарилпіридону та азапіридону як інгібітори тирозинкінази брутона |
| TW201326171A (zh) | 2011-11-03 | 2013-07-01 | Genentech Inc | 烷基化哌□化合物 |
| US8669251B2 (en) * | 2011-11-03 | 2014-03-11 | Genentech, Inc. | 8-fluorophthalazin-1(2H)-one compounds |
| CA2852964A1 (en) | 2011-11-03 | 2013-05-10 | F. Hoffmann-La Roche Ag | Bicyclic piperazine compounds |
| WO2013097052A1 (en) | 2011-12-30 | 2013-07-04 | Abbott Laboratories | Bromodomain inhibitors |
| WO2013106414A1 (en) | 2012-01-09 | 2013-07-18 | X-Rx, Inc. | Tryptoline derivatives having kinase inhibitory activity and uses thereof |
| WO2013157021A1 (en) | 2012-04-20 | 2013-10-24 | Advinus Therapeutics Limited | Bicyclic compounds, compositions and medicinal applications thereof |
| WO2014108820A1 (en) * | 2013-01-08 | 2014-07-17 | Aurigene Discovery Technologies Limited | Substituted 2-pyrazinone derivatives as kinase inhibitors |
| WO2014125410A1 (en) * | 2013-02-12 | 2014-08-21 | Aurigene Discovery Technologies Limited | N-substituted heterocyclic derivatives as kinase inhibitors |
| BR112015022263B1 (pt) * | 2013-03-15 | 2023-01-03 | Deciphera Pharmaceuticals Llc | N-acil-n-(piridin-2-il) uréias e análogos apresentando atividades anticâncer e antiproliferativas, seus usos, e composição farmacêutica |
| PL2989106T3 (pl) | 2013-04-25 | 2017-08-31 | Beigene, Ltd. | Połączone związki heterocykliczne jako inhibitory kinazy białkowej |
| JP6476174B2 (ja) * | 2013-06-19 | 2019-02-27 | ソム イノヴェーション バイオテック、ソシエダッド リミターダ | 運動過剰障害の予防および/または治療における使用のための治療剤 |
| HK1214820A1 (zh) | 2013-07-03 | 2016-08-05 | 豪夫迈.罗氏有限公司 | 杂芳基吡啶酮和氮杂-吡啶酮酰胺化合物 |
| EA029281B1 (ru) | 2013-07-30 | 2018-03-30 | Джилид Коннектикут, Инк. | Полиморф ингибиторов syk |
| PL3027171T3 (pl) | 2013-07-30 | 2020-08-24 | Gilead Connecticut, Inc. | Formulacja inhibitorów syk |
| SMT202300039T1 (it) | 2013-09-13 | 2023-03-17 | Beigene Switzerland Gmbh | Anticorpi anti-pd1 e loro uso come terapia e per diagnostica |
| EP3290407B1 (en) * | 2013-10-18 | 2020-01-01 | Celgene Quanticel Research, Inc | Bromodomain inhibitors |
| ES2716299T3 (es) | 2013-11-20 | 2019-06-11 | Uhde Inventa Fischer Gmbh | Procedimiento así como dispositivo para la preparación de una mezcla de ácido poliláctico cristalizable así como mezcla de ácido poliláctico |
| CN105793251B (zh) | 2013-12-05 | 2018-10-12 | 豪夫迈·罗氏有限公司 | 具有亲电子官能性的杂芳基吡啶酮和氮杂-吡啶酮化合物 |
| AU2014360446A1 (en) | 2013-12-05 | 2016-06-09 | Pharmacyclics, Llc | Inhibitors of Bruton's tyrosine kinase |
| TWI662037B (zh) | 2013-12-23 | 2019-06-11 | 美商基利科學股份有限公司 | 脾酪胺酸激酶抑制劑 |
| WO2015151006A1 (en) | 2014-03-29 | 2015-10-08 | Lupin Limited | Substituted purine compounds as btk inhibitors |
| WO2015170266A1 (en) | 2014-05-07 | 2015-11-12 | Lupin Limited | Substituted pyrimidine compounds as btk inhibitors |
| PL3160956T3 (pl) | 2014-06-27 | 2020-11-30 | Celgene Quanticel Research, Inc. | Inhibitory demetylazy-1 specyficznej dla lizyny |
| TWI726608B (zh) | 2014-07-03 | 2021-05-01 | 英屬開曼群島商百濟神州有限公司 | 抗pd-l1抗體及其作為治療及診斷之用途 |
| WO2016003917A1 (en) * | 2014-07-03 | 2016-01-07 | Quanticel Pharmaceuticals, Inc. | Inhibitors of lysine specific demethylase-1 |
| EP3265453B1 (en) * | 2015-03-05 | 2022-06-29 | Boehringer Ingelheim International GmbH | New pyridinones and isoquinolinones as inhibitors of the bromodomain brd9 |
| US20170107216A1 (en) | 2015-10-19 | 2017-04-20 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| MD3377488T2 (ro) | 2015-11-19 | 2023-02-28 | Incyte Corp | Compuși heterociclici ca imunomodulatori |
| ES2916874T3 (es) | 2015-12-17 | 2022-07-06 | Incyte Corp | Derivados de N-fenil-piridina-2-carboxamida y su uso como moduladores de la interacción proteína/proteína PD-1/PD-L1 |
| CA3009474A1 (en) | 2015-12-22 | 2017-06-29 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| CN107033069B (zh) | 2016-02-04 | 2022-03-04 | 中国科学院合肥物质科学研究院 | 一种新型布鲁顿酪氨酸激酶不可逆抑制剂 |
| PL4049660T3 (pl) | 2016-02-29 | 2025-06-09 | F. Hoffmann-La Roche Ag | Kompozycje postaci dawkowania zawierające inhibitor kinazy tyrozynowej Brutona |
| AU2017251537B2 (en) | 2016-04-15 | 2020-10-08 | Abbvie Inc. | Bromodomain inhibitors |
| ES2906460T3 (es) | 2016-05-06 | 2022-04-18 | Incyte Corp | Compuestos heterocíclicos como inmunomoduladores |
| EP3464279B1 (en) | 2016-05-26 | 2021-11-24 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| SG11201811414TA (en) | 2016-06-20 | 2019-01-30 | Incyte Corp | Heterocyclic compounds as immunomodulators |
| WO2018007885A1 (en) | 2016-07-05 | 2018-01-11 | Beigene, Ltd. | COMBINATION OF A PD-l ANTAGONIST AND A RAF INHIBITOR FOR TREATING CANCER |
| MA45669A (fr) | 2016-07-14 | 2019-05-22 | Incyte Corp | Composés hétérocycliques utilisés comme immunomodulateurs |
| IL293319B1 (en) | 2016-08-16 | 2026-01-01 | Beone Medicines Ltd | Crystal structure of s)–7–(1–acryloylpiperidin–4–yl)–2–(4–)phenoxyphenyl)–4,5,6,7–tetra–hydropyrazolo(1,5–a)pyrimidine–3–carboxamide, methods of preparation and uses thereof |
| CN110087680B (zh) | 2016-08-19 | 2024-03-19 | 百济神州有限公司 | 使用包含btk抑制剂的组合产品治疗癌症 |
| US20180057486A1 (en) | 2016-08-29 | 2018-03-01 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| CN109982687A (zh) | 2016-09-19 | 2019-07-05 | 梅制药公司 | 联合疗法 |
| US10842878B2 (en) | 2016-11-22 | 2020-11-24 | Dana-Farber Cancer Institute, Inc. | Degradation of Bruton's tyrosine kinase (BTK) by conjugation of BTK inhibitors with E3 ligase ligand and methods of use |
| WO2018119286A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Bicyclic heteroaromatic compounds as immunomodulators |
| WO2018119221A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Pyridine derivatives as immunomodulators |
| US10308644B2 (en) | 2016-12-22 | 2019-06-04 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| WO2018119236A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Triazolo[1,5-a]pyridine derivatives as immunomodulators |
| EP4223369A1 (en) | 2016-12-22 | 2023-08-09 | Incyte Corporation | Immunomodulator compounds and methods of use |
| WO2018124281A1 (ja) * | 2016-12-28 | 2018-07-05 | 富山化学工業株式会社 | 外用組成物 |
| EP3573989A4 (en) | 2017-01-25 | 2020-11-18 | Beigene, Ltd. | CRYSTALLINE FORMS OF (S) -7- (1- (BUT-2-YNOYL) PIPERIDIN-4-YL) -2- (4-PHENOXYPHENYL) -4, 5, 6, 7-TETRAHY DROPYRAZOLO [1, 5-A ] PYRIMIDINE-3-CARBOXAMIDE, PREPARATION AND ASSOCIATED USES |
| WO2018175863A1 (en) | 2017-03-24 | 2018-09-27 | Genentech, Inc. | Methods of treating autoimmune and inflammatory diseases |
| EP3645569A4 (en) | 2017-06-26 | 2021-03-24 | BeiGene, Ltd. | IMMUNOTHERAPY FOR LIVER CELL CARCINOMA |
| WO2019034009A1 (en) | 2017-08-12 | 2019-02-21 | Beigene, Ltd. | BTK INHIBITOR WITH ENHANCED DOUBLE SELECTIVITY |
| KR20220070056A (ko) | 2017-08-25 | 2022-05-27 | 길리애드 사이언시즈, 인코포레이티드 | Syk 억제제의 다형체 |
| KR102613433B1 (ko) * | 2017-10-11 | 2023-12-13 | 주식회사 대웅제약 | 신규한 페닐피리딘 유도체 및 이를 포함하는 약학 조성물 |
| US11786529B2 (en) | 2017-11-29 | 2023-10-17 | Beigene Switzerland Gmbh | Treatment of indolent or aggressive B-cell lymphomas using a combination comprising BTK inhibitors |
| JP2021512059A (ja) * | 2018-01-29 | 2021-05-13 | ダナ−ファーバー キャンサー インスティテュート,インコーポレイテッド | ブルトン型チロシンキナーゼ(btk)阻害剤のe3リガーゼリガンドとのコンジュゲーションによるbtkの分解および使用方法 |
| SMT202300065T1 (it) | 2018-03-30 | 2023-05-12 | Incyte Corp | Composti eterociclici come immunomodulatori |
| CN112752756B (zh) | 2018-05-11 | 2024-06-25 | 因赛特公司 | 作为PD-L1免疫调节剂的四氢-咪唑并[4,5-c]吡啶衍生物 |
| AU2020225455A1 (en) | 2019-02-22 | 2021-09-09 | Kronos Bio, Inc. | Solid forms of condensed pyrazines as Syk inhibitors |
| EP3981399A4 (en) | 2019-06-10 | 2023-05-31 | BeiGene Switzerland GmbH | ORAL SOLID TABLET WITH A TYROSINE KINAS INHIBITOR AND METHOD OF MANUFACTURE THEREOF |
| TW202115059A (zh) | 2019-08-09 | 2021-04-16 | 美商英塞特公司 | Pd—1/pd—l1抑制劑之鹽 |
| JP7559059B2 (ja) | 2019-09-30 | 2024-10-01 | インサイト・コーポレイション | 免疫調節剤としてのピリド[3,2-d]ピリミジン化合物 |
| EP4058461A1 (en) | 2019-11-11 | 2022-09-21 | Incyte Corporation | Salts and crystalline forms of a pd-1/pd-l1 inhibitor |
| CN112812113B (zh) * | 2019-11-15 | 2022-09-20 | 杭州和正医药有限公司 | 免疫调节化合物、组合物及其应用 |
| CN114380841B (zh) * | 2020-10-19 | 2025-12-30 | 南京正大天晴制药有限公司 | 作为akt抑制剂的三环喹唑啉或二氢喹唑啉化合物 |
| US11780836B2 (en) | 2020-11-06 | 2023-10-10 | Incyte Corporation | Process of preparing a PD-1/PD-L1 inhibitor |
| US11760756B2 (en) | 2020-11-06 | 2023-09-19 | Incyte Corporation | Crystalline form of a PD-1/PD-L1 inhibitor |
| IL302590A (en) | 2020-11-06 | 2023-07-01 | Incyte Corp | Process for preparing PD-1/PD-L1 inhibitor and salts and crystalline forms thereof |
| US11786531B1 (en) | 2022-06-08 | 2023-10-17 | Beigene Switzerland Gmbh | Methods of treating B-cell proliferative disorder |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006099075A2 (en) * | 2005-03-10 | 2006-09-21 | Cgi Pharmaceuticals, Inc. | Certain substituted amides, method of making, and method of use thereof |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR042586A1 (es) * | 2001-02-15 | 2005-06-29 | Sugen Inc | 3-(4-amidopirrol-2-ilmetiliden)-2-indolinona como inhibidores de la protein quinasa; sus composiciones farmaceuticas; un metodo para la modulacion de la actividad catalitica de la proteinquinasa; un metodo para tratar o prevenir una afeccion relacionada con la proteinquinasa |
| US7405295B2 (en) * | 2003-06-04 | 2008-07-29 | Cgi Pharmaceuticals, Inc. | Certain imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of Bruton's tyrosine kinase by such compounds |
| AR063706A1 (es) * | 2006-09-11 | 2009-02-11 | Cgi Pharmaceuticals Inc | Determinadas amidas sustituidas, el uso de las mismas para el tratamiento de enfermedades mediadas por la inhibicion de la actividad de btk y composiciones farmaceuticas que las comprenden. |
| JP2010502751A (ja) * | 2006-09-11 | 2010-01-28 | シージーアイ ファーマシューティカルズ,インコーポレイティド | キナーゼ阻害物質、およびキナーゼ阻害物質の使用および同定方法 |
-
2008
- 2008-09-17 CL CL2008002793A patent/CL2008002793A1/es unknown
- 2008-09-19 JP JP2010526003A patent/JP5485894B2/ja active Active
- 2008-09-19 EP EP08832237.5A patent/EP2188267B1/en active Active
- 2008-09-19 PE PE2008001640A patent/PE20091201A1/es not_active Application Discontinuation
- 2008-09-19 WO PCT/US2008/077054 patent/WO2009039397A2/en not_active Ceased
- 2008-09-19 BR BRPI0817130 patent/BRPI0817130A2/pt not_active Application Discontinuation
- 2008-09-19 US US12/234,281 patent/US7884108B2/en active Active
- 2008-09-19 RU RU2010115574/04A patent/RU2470923C2/ru active
- 2008-09-19 AR ARP080104094A patent/AR068503A1/es unknown
- 2008-09-19 CN CN2008801161200A patent/CN101861307B/zh active Active
- 2008-09-19 AU AU2008302099A patent/AU2008302099B2/en not_active Ceased
- 2008-09-19 TW TW097136216A patent/TWI423966B/zh not_active IP Right Cessation
- 2008-09-19 CA CA2700443A patent/CA2700443A1/en not_active Abandoned
- 2008-09-19 KR KR1020107008468A patent/KR20100072032A/ko not_active Withdrawn
-
2010
- 2010-11-04 US US12/939,518 patent/US8247550B2/en active Active
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006099075A2 (en) * | 2005-03-10 | 2006-09-21 | Cgi Pharmaceuticals, Inc. | Certain substituted amides, method of making, and method of use thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| RU2010115574A (ru) | 2011-10-27 |
| US8247550B2 (en) | 2012-08-21 |
| TW200914446A (en) | 2009-04-01 |
| RU2470923C2 (ru) | 2012-12-27 |
| CA2700443A1 (en) | 2009-03-26 |
| EP2188267B1 (en) | 2016-08-03 |
| US20090082330A1 (en) | 2009-03-26 |
| AR068503A1 (es) | 2009-11-18 |
| WO2009039397A3 (en) | 2009-05-22 |
| AU2008302099B2 (en) | 2013-03-28 |
| US20110059944A1 (en) | 2011-03-10 |
| KR20100072032A (ko) | 2010-06-29 |
| TWI423966B (zh) | 2014-01-21 |
| PE20091201A1 (es) | 2009-09-13 |
| CN101861307A (zh) | 2010-10-13 |
| JP2010540452A (ja) | 2010-12-24 |
| AU2008302099A1 (en) | 2009-03-26 |
| JP5485894B2 (ja) | 2014-05-07 |
| CL2008002793A1 (es) | 2009-09-04 |
| WO2009039397A2 (en) | 2009-03-26 |
| EP2188267A2 (en) | 2010-05-26 |
| BRPI0817130A2 (pt) | 2015-03-31 |
| US7884108B2 (en) | 2011-02-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101861307A (zh) | 取代的酰胺、其制备方法及其用于治疗疾病例如癌症的用途 | |
| JP7076432B2 (ja) | Hpk1調節薬としてのピラゾロピリジン誘導体及びがんの治療のためのその用法 | |
| CN104341388B (zh) | 芳香族酰胺类衍生物、其制备方法及其在医药上的应用 | |
| TW202115065A (zh) | Kras突變蛋白抑制劑 | |
| WO2021258010A1 (en) | Oxime compounds useful as t cell activators | |
| CN101605778A (zh) | 某些取代的酰胺、其制备方法及使用方法 | |
| US20080125417A1 (en) | Certain pyrimidines, method of making, and method of use thereof | |
| TW201910306A (zh) | Nlrp3發炎體之選擇性抑制劑 | |
| CN101223141A (zh) | 特定取代的酰胺,其制备方法和使用方法 | |
| CN108290863A (zh) | 可用作人壳多糖酶抑制剂的经取代的氨基三唑 | |
| CN110746424A (zh) | Mk2抑制剂和其用途 | |
| WO2015165279A1 (zh) | 多氟化合物作为布鲁顿酪氨酸激酶抑制剂 | |
| CN108478579A (zh) | 吡啶酮-吡啶基化合物及其用途 | |
| CA2661654A1 (en) | Certain substituted amides, method of making, and method of use thereof | |
| WO2016169504A1 (zh) | 稠环嘧啶氨基衍生物﹑其制备方法、中间体、药物组合物及应用 | |
| CN111566102A (zh) | 作为激活素受体样激酶抑制剂的取代的吡咯并吡啶 | |
| JP2021536436A (ja) | キノリン誘導体から調製される新規な阻害剤 | |
| WO2019154177A1 (zh) | 嘧啶类化合物、其制备方法及其医药用途 | |
| KR20170054421A (ko) | 브로모도메인 억제제로서의 테트라하이드로퀴놀린 유도체 | |
| CN105884695B (zh) | 杂环衍生物类酪氨酸激酶抑制剂 | |
| CN103261193A (zh) | 抑制白三烯生成的*二唑抑制剂 | |
| CN117980309A (zh) | 用作her2抑制剂的三环稠合嘧啶化合物 | |
| HK40065647A (en) | Fused thiazolopyrimidine derivatives as mnks inhibitors | |
| HK40065647B (en) | Fused thiazolopyrimidine derivatives as mnks inhibitors | |
| HK40043591B (en) | Heteroaryl compounds as type ii irak inhibitors and uses thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| ASS | Succession or assignment of patent right |
Owner name: GILEAD CONNECTICUT, INC. Free format text: FORMER OWNER: CGI PHARMACEUTICALS INC. Effective date: 20121109 |
|
| C41 | Transfer of patent application or patent right or utility model | ||
| TA01 | Transfer of patent application right |
Effective date of registration: 20121109 Address after: American Connecticut Applicant after: Gilead Connecticut, Inc. Address before: American Connecticut Applicant before: CGI Pharmaceuticals Inc. |
|
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant |