ES2745525T3 - Compuestos de aminopiridina sustituida con heteroarilo - Google Patents
Compuestos de aminopiridina sustituida con heteroarilo Download PDFInfo
- Publication number
- ES2745525T3 ES2745525T3 ES16734538T ES16734538T ES2745525T3 ES 2745525 T3 ES2745525 T3 ES 2745525T3 ES 16734538 T ES16734538 T ES 16734538T ES 16734538 T ES16734538 T ES 16734538T ES 2745525 T3 ES2745525 T3 ES 2745525T3
- Authority
- ES
- Spain
- Prior art keywords
- pyridin
- pyrazolo
- carbonitrile
- triazol
- isopropylamino
- 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 CN(C1N=C2*)C=NC1C=C2[Rh] Chemical compound CN(C1N=C2*)C=NC1C=C2[Rh] 0.000 description 8
- SGTGXXLTWWAIDL-UHFFFAOYSA-N CC(C)Nc(cc(-[n]1ncc2c1ncc(C#N)c2)nc1)c1-c1c[n](CC(F)(F)F)nc1 Chemical compound CC(C)Nc(cc(-[n]1ncc2c1ncc(C#N)c2)nc1)c1-c1c[n](CC(F)(F)F)nc1 SGTGXXLTWWAIDL-UHFFFAOYSA-N 0.000 description 1
- WRWNPDTZJNLWHL-UHFFFAOYSA-N CC(C)Nc(cc(-[n]1ncc2c1ncc(C#N)c2)nc1)c1-c1cc(C2CNC2)n[o]1 Chemical compound CC(C)Nc(cc(-[n]1ncc2c1ncc(C#N)c2)nc1)c1-c1cc(C2CNC2)n[o]1 WRWNPDTZJNLWHL-UHFFFAOYSA-N 0.000 description 1
- SWRKUPLIPIEAOS-UHFFFAOYSA-N CC(C)Nc(cc(-[n]1ncc2cc(C#N)cnc12)nc1)c1-[n]1nnc(C2CCN(CC(F)F)CC2)c1 Chemical compound CC(C)Nc(cc(-[n]1ncc2cc(C#N)cnc12)nc1)c1-[n]1nnc(C2CCN(CC(F)F)CC2)c1 SWRKUPLIPIEAOS-UHFFFAOYSA-N 0.000 description 1
- CPLQNQBMMGLAAJ-UHFFFAOYSA-N CC(C)Nc(cc(-[n]1ncc2cc(C#N)cnc12)nc1)c1-[n]1nnc(C2CCNCC2)c1 Chemical compound CC(C)Nc(cc(-[n]1ncc2cc(C#N)cnc12)nc1)c1-[n]1nnc(C2CCNCC2)c1 CPLQNQBMMGLAAJ-UHFFFAOYSA-N 0.000 description 1
- GVPHIPBSKCVWBA-DLBZAZTESA-N CC(C)Nc(cc(nc1)Cl)c1-c1c[n]([C@@H](CCN(C2)C(OC(C)(C)C)=O)[C@@H]2O)nn1 Chemical compound CC(C)Nc(cc(nc1)Cl)c1-c1c[n]([C@@H](CCN(C2)C(OC(C)(C)C)=O)[C@@H]2O)nn1 GVPHIPBSKCVWBA-DLBZAZTESA-N 0.000 description 1
- CNAUUJIWAQALDJ-UHFFFAOYSA-N CC(C)Nc1cc(-[n]2ncc3c2ncc(C#N)c3)ncc1-c1c[n](C(C2)CN2C(C)C)nn1 Chemical compound CC(C)Nc1cc(-[n]2ncc3c2ncc(C#N)c3)ncc1-c1c[n](C(C2)CN2C(C)C)nn1 CNAUUJIWAQALDJ-UHFFFAOYSA-N 0.000 description 1
- HIUCJCFXTWGEIE-UHFFFAOYSA-N CC(C)Nc1cc(-[n]2ncc3c2ncc(C#N)c3)ncc1-c1c[n](C(C2)CN2C(CC2CC2)=O)nn1 Chemical compound CC(C)Nc1cc(-[n]2ncc3c2ncc(C#N)c3)ncc1-c1c[n](C(C2)CN2C(CC2CC2)=O)nn1 HIUCJCFXTWGEIE-UHFFFAOYSA-N 0.000 description 1
- JMLWLLVDDWTHOR-UHFFFAOYSA-N CC(C)Nc1cc(-[n]2ncc3c2ncc(C#N)c3)ncc1-c1cc(C(C2)CN2C(C)=O)n[o]1 Chemical compound CC(C)Nc1cc(-[n]2ncc3c2ncc(C#N)c3)ncc1-c1cc(C(C2)CN2C(C)=O)n[o]1 JMLWLLVDDWTHOR-UHFFFAOYSA-N 0.000 description 1
- BFKKIDHWWRDAPL-UHFFFAOYSA-N CC(C)Nc1cc(-[n]2ncc3cc(C#N)cnc23)ncc1-c1c[n](C(C2)CN2c2nnc(C)[o]2)nn1 Chemical compound CC(C)Nc1cc(-[n]2ncc3cc(C#N)cnc23)ncc1-c1c[n](C(C2)CN2c2nnc(C)[o]2)nn1 BFKKIDHWWRDAPL-UHFFFAOYSA-N 0.000 description 1
- ZRJCNMYMCUBLAI-UHFFFAOYSA-N CC(C)Nc1cc(Cl)ncc1-c1c[nH]nc1 Chemical compound CC(C)Nc1cc(Cl)ncc1-c1c[nH]nc1 ZRJCNMYMCUBLAI-UHFFFAOYSA-N 0.000 description 1
- QGSSQOPZQYGFHL-UHFFFAOYSA-N CC(C)Nc1cc(Cl)ncc1-c1c[n](CC(C)F)nn1 Chemical compound CC(C)Nc1cc(Cl)ncc1-c1c[n](CC(C)F)nn1 QGSSQOPZQYGFHL-UHFFFAOYSA-N 0.000 description 1
- UMBXYHRYEHEXSL-SFHVURJKSA-N CC(C)Nc1cc(Cl)ncc1-c1c[n](C[C@H](Cc2ccccc2)NC(OC(C)(C)C)=O)nn1 Chemical compound CC(C)Nc1cc(Cl)ncc1-c1c[n](C[C@H](Cc2ccccc2)NC(OC(C)(C)C)=O)nn1 UMBXYHRYEHEXSL-SFHVURJKSA-N 0.000 description 1
- JNDCZWRSJRYUDD-UHFFFAOYSA-N CC(C)Nc1cc(Cl)ncc1-c1nnc(C(N(CC2)CCN2C(OC(C)(C)C)=O)=O)[o]1 Chemical compound CC(C)Nc1cc(Cl)ncc1-c1nnc(C(N(CC2)CCN2C(OC(C)(C)C)=O)=O)[o]1 JNDCZWRSJRYUDD-UHFFFAOYSA-N 0.000 description 1
- IMFLIGANAFVVEX-UHFFFAOYSA-O CC(C)Nc1cc(Cl)ncc1C(N=N)=C[NH2+]CC(C)F Chemical compound CC(C)Nc1cc(Cl)ncc1C(N=N)=C[NH2+]CC(C)F IMFLIGANAFVVEX-UHFFFAOYSA-O 0.000 description 1
- GTVJTOUCOLLRGC-UHFFFAOYSA-N CC(C)[n]1ncc(O)c1 Chemical compound CC(C)[n]1ncc(O)c1 GTVJTOUCOLLRGC-UHFFFAOYSA-N 0.000 description 1
- JANHZYJACYIJQP-UHFFFAOYSA-N CCCN1C=NC2C=NC([Rh])=NC12 Chemical compound CCCN1C=NC2C=NC([Rh])=NC12 JANHZYJACYIJQP-UHFFFAOYSA-N 0.000 description 1
- NOEFIUWJGDCTGB-UHFFFAOYSA-N CCOC(c(c(NC(C)C)c1)cnc1-[n](cc1)c2c1cncn2)=O Chemical compound CCOC(c(c(NC(C)C)c1)cnc1-[n](cc1)c2c1cncn2)=O NOEFIUWJGDCTGB-UHFFFAOYSA-N 0.000 description 1
- BLHTXORQJNCSII-UHFFFAOYSA-N Cc1c[n](C)cn1 Chemical compound Cc1c[n](C)cn1 BLHTXORQJNCSII-UHFFFAOYSA-N 0.000 description 1
- SZQCPPRPWDXLMM-UHFFFAOYSA-N Cc1c[n](C)nc1 Chemical compound Cc1c[n](C)nc1 SZQCPPRPWDXLMM-UHFFFAOYSA-N 0.000 description 1
- FICAQKBMCKEFDI-UHFFFAOYSA-N Cc1n[o]c(C)c1 Chemical compound Cc1n[o]c(C)c1 FICAQKBMCKEFDI-UHFFFAOYSA-N 0.000 description 1
- ZOEPGDLOKCFSAJ-WOJBJXKFSA-N N#Cc1cc(cn[n]2-c(nc3)cc(NC4CC4)c3-c3c[n]([C@H](CNCC4)[C@@H]4O)nn3)c2nc1 Chemical compound N#Cc1cc(cn[n]2-c(nc3)cc(NC4CC4)c3-c3c[n]([C@H](CNCC4)[C@@H]4O)nn3)c2nc1 ZOEPGDLOKCFSAJ-WOJBJXKFSA-N 0.000 description 1
- DEJUUKULVAIMNF-UHFFFAOYSA-N Nc1cc(Cl)ncc1I Chemical compound Nc1cc(Cl)ncc1I DEJUUKULVAIMNF-UHFFFAOYSA-N 0.000 description 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
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/12—Antidiarrhoeals
-
- 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
-
- 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
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- 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
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- 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
- A61P19/06—Antigout agents, e.g. antihyperuricemic or uricosuric agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- 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
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (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)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Hospice & Palliative Care (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Transplantation (AREA)
- Psychiatry (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN1877DE2015 | 2015-06-24 | ||
| PCT/US2016/038858 WO2016210034A1 (en) | 2015-06-24 | 2016-06-23 | Heteroaryl substituted aminopyridine compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2745525T3 true ES2745525T3 (es) | 2020-03-02 |
Family
ID=56322320
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES16734538T Active ES2745525T3 (es) | 2015-06-24 | 2016-06-23 | Compuestos de aminopiridina sustituida con heteroarilo |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US10294229B2 (enExample) |
| EP (1) | EP3313840B1 (enExample) |
| JP (1) | JP6843775B2 (enExample) |
| CN (1) | CN107849039B (enExample) |
| AR (1) | AR105113A1 (enExample) |
| ES (1) | ES2745525T3 (enExample) |
| TW (1) | TW201718571A (enExample) |
| UY (1) | UY36748A (enExample) |
| WO (1) | WO2016210034A1 (enExample) |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3313844B1 (en) * | 2015-06-24 | 2020-08-26 | Bristol-Myers Squibb Company | Heteroaryl substituted aminopyridine compounds |
| CN115448916B (zh) * | 2016-10-14 | 2026-04-28 | 武田药品工业株式会社 | Tyk2抑制剂及其用途 |
| TWI733982B (zh) | 2017-02-16 | 2021-07-21 | 美商基利科學股份有限公司 | 吡咯并[1,2-b]嗒衍生物 |
| RS62430B1 (sr) | 2017-05-11 | 2021-11-30 | Bristol Myers Squibb Co | Tienopiridini i benzotiofeni korisni kao irak4 inhibitori |
| JP7366031B2 (ja) | 2017-09-22 | 2023-10-20 | カイメラ セラピューティクス, インコーポレイテッド | タンパク質分解剤およびそれらの使用 |
| WO2019060693A1 (en) | 2017-09-22 | 2019-03-28 | Kymera Therapeutics, Inc. | CRBN LIGANDS AND USES THEREOF |
| TWI812649B (zh) | 2017-10-10 | 2023-08-21 | 美商絡速藥業公司 | 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之調配物 |
| WO2019111218A1 (en) | 2017-12-08 | 2019-06-13 | Cadila Healthcare Limited | Novel heterocyclic compounds as irak4 inhibitors |
| IL315310A (en) | 2017-12-26 | 2024-10-01 | Kymera Therapeutics Inc | Irak degraders and uses thereof |
| EP3737666A4 (en) | 2018-01-12 | 2022-01-05 | Kymera Therapeutics, Inc. | PROTEIN DEGRADATION AGENTS AND ASSOCIATED USES |
| US11512080B2 (en) | 2018-01-12 | 2022-11-29 | Kymera Therapeutics, Inc. | CRBN ligands and uses thereof |
| EP3817822A4 (en) | 2018-07-06 | 2022-07-27 | Kymera Therapeutics, Inc. | PROTEIN DEGRADANTS AND USES THEREOF |
| WO2020010177A1 (en) | 2018-07-06 | 2020-01-09 | Kymera Therapeutics, Inc. | Tricyclic crbn ligands and uses thereof |
| TWI721483B (zh) | 2018-07-13 | 2021-03-11 | 美商基利科學股份有限公司 | 吡咯并[1,2-b]嗒𠯤衍生物 |
| US11572362B2 (en) | 2018-08-13 | 2023-02-07 | Gilead Sciences, Inc. | Pyrrolo[1,2-b]pyridazine derivatives |
| JP7164705B2 (ja) * | 2018-08-13 | 2022-11-01 | ギリアード サイエンシーズ, インコーポレイテッド | IRAK4阻害剤としてのピロロ[1,2-b]ピリダジン誘導体 |
| TWI727392B (zh) | 2018-08-13 | 2021-05-11 | 美商基利科學股份有限公司 | 噻二唑irak4抑制劑 |
| JP7623943B2 (ja) | 2018-11-30 | 2025-01-29 | カイメラ セラピューティクス, インコーポレイテッド | Irak分解剤およびそれらの使用 |
| CN109836376B (zh) * | 2019-04-10 | 2022-03-22 | 江苏汉阔生物有限公司 | 一种以2,3-吡啶二羧酸为原料制备2-氯代烟酸的方法 |
| BR112021026517A2 (pt) | 2019-06-28 | 2022-05-10 | Kymera Therapeutics Inc | Degradadores de irak e usos dos mesmos |
| WO2021011868A1 (en) | 2019-07-17 | 2021-01-21 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
| ES2961950T3 (es) | 2019-07-18 | 2024-03-14 | Bristol Myers Squibb Co | Compuestos heteroarílicos tricíclicos útiles como inhibidores de IRAK4 |
| EP3999512B1 (en) | 2019-07-18 | 2023-08-23 | Bristol-Myers Squibb Company | Pyrazolo[3,4-d]pyrrolo[1,2-b]pyridazinyl compounds useful as irak4 inhibitors |
| JP7573596B2 (ja) * | 2019-07-23 | 2024-10-25 | ブリストル-マイヤーズ スクイブ カンパニー | Irak4阻害剤として有用なチエノピリジニルおよびチアゾロピリジニル化合物 |
| JP7682154B2 (ja) | 2019-08-06 | 2025-05-23 | ブリストル-マイヤーズ スクイブ カンパニー | Irak4阻害剤として有用な二環ヘテロ環式化合物 |
| EP4013758B1 (en) | 2019-08-13 | 2025-12-24 | Bristol-Myers Squibb Company | Bicyclic heteroaryl compounds useful as irak4 inhibitors |
| US11578071B2 (en) | 2019-10-04 | 2023-02-14 | University Of Kentucky Research Foundation | Preparation of pyrazolo[3,4-B]pyridines as antimalarials |
| EP4072591A4 (en) | 2019-12-10 | 2024-06-05 | Kymera Therapeutics, Inc. | IRAQ DEGRADER AND USES THEREOF |
| JP2023509366A (ja) | 2019-12-17 | 2023-03-08 | カイメラ セラピューティクス, インコーポレイテッド | Irak分解剤およびそれらの使用 |
| WO2021127283A2 (en) | 2019-12-17 | 2021-06-24 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
| MX2022007455A (es) | 2019-12-18 | 2022-08-15 | Elanco Tiergesundheit Ag | Derivados de isoxazolina como plaguicidas. |
| US12391702B2 (en) | 2020-02-03 | 2025-08-19 | Bristol-Myers Squibb Company | Benzo[5,6][1,4]dioxino[2,3-b]pyridine compounds useful as IRAK4 inhibitors |
| US12528814B2 (en) | 2020-02-19 | 2026-01-20 | Nurix Therapeutics, Inc. | Bifunctional degraders of interleukin-1 receptor-associated kinases and therapeutic use thereof |
| TW202210483A (zh) | 2020-06-03 | 2022-03-16 | 美商凱麥拉醫療公司 | Irak降解劑之結晶型 |
| WO2022147465A1 (en) | 2020-12-30 | 2022-07-07 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
| TW202245788A (zh) | 2021-02-15 | 2022-12-01 | 美商凱麥拉醫療公司 | Irak4降解劑及其用途 |
| AU2022271290A1 (en) | 2021-05-07 | 2023-11-23 | Kymera Therapeutics, Inc. | Cdk2 degraders and uses thereof |
| EP4367118B1 (en) | 2021-08-18 | 2025-01-29 | Nurix Therapeutics, Inc. | Bifunctional degraders of interleukin-1 receptor-associated kinases and therapeutic use thereof |
| EP4422635A4 (en) | 2021-10-29 | 2025-11-26 | Kymera Therapeutics Inc | IRAQ4 DEGRADATION AGENTS AND THEIR SYNTHESIS |
| IL314437A (en) | 2022-01-31 | 2024-09-01 | Kymera Therapeutics Inc | IRAK joints and their uses |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60232510D1 (de) | 2001-06-15 | 2009-07-16 | Vertex Pharma | 5-(2-aminopyrimidin-4-yl)benzisoxazole als proteinkinasehemmer |
| AUPR688101A0 (en) | 2001-08-08 | 2001-08-30 | Luminis Pty Limited | Protein domains and their ligands |
| GB0211019D0 (en) | 2002-05-14 | 2002-06-26 | Syngenta Ltd | Novel compounds |
| EP1518855B1 (en) | 2002-06-28 | 2011-10-26 | Astellas Pharma Inc. | Diaminopyrimidinecarboxa mide derivative |
| MXPA05007503A (es) | 2003-01-17 | 2005-09-21 | Warner Lambert Co | Heterociclicos 2-aminopiridina sustituidos como inhibidores de proliferacion celular. |
| AU2004257260A1 (en) | 2003-07-10 | 2005-01-27 | Neurogen Corporation | Substituted heterocyclic diarylamine analogues |
| GB0402653D0 (en) | 2004-02-06 | 2004-03-10 | Cyclacel Ltd | Compounds |
| US7521457B2 (en) | 2004-08-20 | 2009-04-21 | Boehringer Ingelheim International Gmbh | Pyrimidines as PLK inhibitors |
| FR2896503B1 (fr) | 2006-01-23 | 2012-07-13 | Aventis Pharma Sa | Nouveaux derives soufres d'uree cyclique, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de kinases |
| EP2164841A1 (en) | 2007-06-08 | 2010-03-24 | Bayer CropScience SA | Fungicide heterocyclyl-pyrimidinyl-amino derivatives |
| WO2009046416A1 (en) | 2007-10-05 | 2009-04-09 | Targegen Inc. | Anilinopyrimidines as jak kinase inhibitors |
| JPWO2010058846A1 (ja) | 2008-11-21 | 2012-04-19 | アステラス製薬株式会社 | 4,6−ジアミノニコチンアミド化合物 |
| AU2009320683B2 (en) | 2008-11-28 | 2012-07-19 | Kowa Company, Ltd. | Pyridine-3-carboxyamide derivative |
| JP2012529535A (ja) | 2009-06-12 | 2012-11-22 | ブリストル−マイヤーズ スクイブ カンパニー | キナーゼモジュレーターとして有用なニコチンアミド化合物 |
| JP5770198B2 (ja) | 2009-10-30 | 2015-08-26 | ヤンセン ファーマシューティカ エヌ.ベー. | オピオイド受容体調節因子としてのフェノキシ置換ピリミジン |
| JPWO2011093501A1 (ja) | 2010-02-01 | 2013-06-06 | 日本ケミファ株式会社 | Gpr119作動薬 |
| BR112013027787A2 (pt) | 2011-04-29 | 2017-06-27 | Icahn School Med Mount Sinai | compostos, composição farmacêutica, método para tratar um distúrbio proliferativo celular, método para tratar um distúrbio neurológico, métodos para inibir uma ou mais quinases, método para inibir a proliferação celular de células cancerosas, método para induzir a morte celular de células cancerosas, método para induzir a apoptose de células cancerosas, método para induzir a apoptose em uma célula e métodos para produzir compostos |
| CN104169275B (zh) * | 2012-01-13 | 2017-06-09 | 百时美施贵宝公司 | 用作激酶抑制剂的三唑取代的吡啶化合物 |
| ES2575604T3 (es) | 2012-01-13 | 2016-06-29 | Bristol-Myers Squibb Company | Compuestos de piridilo sustituidos con tiazolilo o tiadiazolilo útiles como inhibidores cinasa |
| JP6109195B2 (ja) * | 2012-01-13 | 2017-04-05 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | キナーゼ阻害剤として有用な複素環置換されたピリジル化合物 |
| EP2903617B1 (en) * | 2012-10-08 | 2019-01-30 | Merck Sharp & Dohme Corp. | Inhibitors of irak4 activity |
| AR093403A1 (es) | 2012-11-08 | 2015-06-03 | Bristol Myers Squibb Co | COMPUESTOS DE PIRIDILO SUSTITUIDOS CON ALQUILAMIDA UTILES COMO MODULADORES DE LAS RESPUESTAS DE IL-12, IL23 Y/O INFa |
| US9546153B2 (en) | 2012-11-08 | 2017-01-17 | Bristol-Myers Squibb Company | Bicyclic heterocycle substituted pyridyl compounds useful as kinase modulators |
| SG11201503397YA (en) | 2012-11-08 | 2015-05-28 | Bristol Myers Squibb Co | Heteroaryl substituted pyridyl compounds useful as kinase modulators |
| AR094537A1 (es) | 2013-11-07 | 2015-08-12 | Bristol Myers Squibb Co | COMPUESTOS DE PIRIDILO SUSTITUIDOS CON ALQUILAMIDA ÚTILES COMO MODULADORES DE LAS RESPUESTAS DE IL-12, IL-23 Y/O IFNa |
| AR098991A1 (es) | 2014-01-03 | 2016-06-22 | Bristol Myers Squibb Co | Compuestos de nicotinamida sustituida con heteroarilo |
| EP3313844B1 (en) * | 2015-06-24 | 2020-08-26 | Bristol-Myers Squibb Company | Heteroaryl substituted aminopyridine compounds |
-
2016
- 2016-06-23 TW TW105119777A patent/TW201718571A/zh unknown
- 2016-06-23 UY UY0001036748A patent/UY36748A/es not_active Application Discontinuation
- 2016-06-23 AR ARP160101892A patent/AR105113A1/es unknown
- 2016-06-23 WO PCT/US2016/038858 patent/WO2016210034A1/en not_active Ceased
- 2016-06-23 ES ES16734538T patent/ES2745525T3/es active Active
- 2016-06-23 US US15/738,362 patent/US10294229B2/en active Active
- 2016-06-23 JP JP2017566643A patent/JP6843775B2/ja active Active
- 2016-06-23 EP EP16734538.8A patent/EP3313840B1/en active Active
- 2016-06-23 CN CN201680040987.7A patent/CN107849039B/zh active Active
Also Published As
| Publication number | Publication date |
|---|---|
| WO2016210034A1 (en) | 2016-12-29 |
| EP3313840A1 (en) | 2018-05-02 |
| TW201718571A (zh) | 2017-06-01 |
| AR105113A1 (es) | 2017-09-06 |
| JP2018522859A (ja) | 2018-08-16 |
| CN107849039B (zh) | 2020-07-03 |
| US10294229B2 (en) | 2019-05-21 |
| UY36748A (es) | 2016-12-30 |
| CN107849039A (zh) | 2018-03-27 |
| US20180186799A1 (en) | 2018-07-05 |
| EP3313840B1 (en) | 2019-07-24 |
| JP6843775B2 (ja) | 2021-03-17 |
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