MA55593A - Cycles pyridine contenant des dérivés servant d'inhibiteurs de malt1 - Google Patents
Cycles pyridine contenant des dérivés servant d'inhibiteurs de malt1Info
- Publication number
- MA55593A MA55593A MA055593A MA55593A MA55593A MA 55593 A MA55593 A MA 55593A MA 055593 A MA055593 A MA 055593A MA 55593 A MA55593 A MA 55593A MA 55593 A MA55593 A MA 55593A
- Authority
- MA
- Morocco
- Prior art keywords
- containing derivatives
- cycles containing
- derivatives serving
- malt1 inhibitors
- pyridine
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/14—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201962832608P | 2019-04-11 | 2019-04-11 | |
| EP19178959 | 2019-06-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA55593A true MA55593A (fr) | 2022-02-16 |
Family
ID=70224393
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA055593A MA55593A (fr) | 2019-04-11 | 2020-04-10 | Cycles pyridine contenant des dérivés servant d'inhibiteurs de malt1 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US12404260B2 (fr) |
| EP (1) | EP3953345B1 (fr) |
| JP (1) | JP7554768B2 (fr) |
| KR (1) | KR20210151880A (fr) |
| CN (1) | CN113677674B (fr) |
| AU (1) | AU2020272156A1 (fr) |
| BR (1) | BR112021019799A2 (fr) |
| ES (1) | ES2949871T3 (fr) |
| MA (1) | MA55593A (fr) |
| MX (1) | MX2021012417A (fr) |
| WO (1) | WO2020208222A1 (fr) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI795381B (zh) | 2016-12-21 | 2023-03-11 | 比利時商健生藥品公司 | 作為ｍａｌｔ１抑制劑之吡唑衍生物 |
| MA55593A (fr) | 2019-04-11 | 2022-02-16 | Janssen Pharmaceutica Nv | Cycles pyridine contenant des dérivés servant d'inhibiteurs de malt1 |
| EP4243812A1 (fr) * | 2020-11-12 | 2023-09-20 | Monopteros Therapeutics, Inc. | Matériaux et procédés de traitement du cancer |
| IL313925A (en) | 2021-12-30 | 2024-08-01 | Jiangsu Hansoh Pharmaceutical Group Co Ltd | Inhibitor of tricyclic derivatives, method of preparation therefor and application |
Family Cites Families (67)
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|---|---|---|---|---|
| US6339099B1 (en) | 1997-06-20 | 2002-01-15 | Dupont Pharmaceuticals Company | Guanidine mimics as factor Xa inhibitors |
| DK173431B1 (da) | 1998-03-20 | 2000-10-23 | Gea Farmaceutisk Fabrik As | Farmaceutisk formulering omfattende en 2-[[(2-pyridinyl)methyl]sulfinyl]benzimidazol med anti-ulcusaktivitet samt fremgangs |
| FR2795726A1 (fr) | 1999-06-30 | 2001-01-05 | Aventis Cropscience Sa | Nouveaux pyrazoles fongicides |
| GB9925127D0 (en) | 1999-10-22 | 1999-12-22 | Pharmacia & Upjohn Spa | Oral formulations for anti-tumor compounds |
| DE60235114D1 (de) | 2001-11-01 | 2010-03-04 | Icagen Inc | Pyrazolamide zur anwendung in der behandlung von schmerz |
| JP2007525183A (ja) | 2003-04-30 | 2007-09-06 | アジェンシス， インコーポレイテッド | 癌の処置および検出において有用な１０９ｐ１ｄ４と称される、核酸および対応タンパク質 |
| ES2350837T3 (es) | 2003-05-01 | 2011-01-27 | Bristol-Myers Squibb Company | Compuestos de pirazol-amida sustituidos con arilo útiles como inhibidores de quinasas. |
| WO2006085685A1 (fr) | 2005-02-09 | 2006-08-17 | Takeda Pharmaceutical Company Limited | Dérivé de pyrazole |
| WO2007111904A2 (fr) | 2006-03-22 | 2007-10-04 | Vertex Pharmaceuticals Incorporated | Inhibiteurs de la c-met proteine kinase |
| AU2007273057A1 (en) | 2006-07-12 | 2008-01-17 | Merck Sharp & Dohme Corp. | Substituted pyrazoles as ghrelin receptor antagonists |
| US8389544B2 (en) | 2007-01-17 | 2013-03-05 | The Hong Kong University Of Science And Technology | Isoquinolone compounds as subtype-selective agonists for melatonin receptors MT1 and MT2 |
| CN101652359A (zh) | 2007-03-09 | 2010-02-17 | 高点制药有限责任公司 | 作为羟类固醇脱氢酶抑制剂的吲哚-和苯并咪唑酰胺类 |
| US8309523B2 (en) | 2007-11-21 | 2012-11-13 | Vib Vzw | Inhibitors of MALT1 proteolytic activity and uses thereof |
| CN102112447B (zh) * | 2008-06-04 | 2013-06-26 | 阿姆布里利亚生物制药公司 | 来自吡哆醇的hiv整合酶抑制剂 |
| WO2010034737A1 (fr) | 2008-09-24 | 2010-04-01 | Basf Se | Composés de pyrazole pour la lutte contre des parasites invertébrés |
| WO2010039039A1 (fr) | 2008-10-03 | 2010-04-08 | Clavis Pharma Asa | Formulations orales de dérivés de gemcitabine |
| KR101061599B1 (ko) | 2008-12-05 | 2011-09-02 | 한국과학기술연구원 | 비정상 세포 성장 질환의 치료를 위한 단백질 키나아제 저해제인 신규 인다졸 유도체, 이의 약학적으로 허용가능한염 및 이를 유효성분으로 함유하는 약학적 조성물 |
| DE102009003954A1 (de) | 2009-01-07 | 2010-07-08 | Merck Patent Gmbh | Pyridazinonderivate |
| US8252821B2 (en) | 2009-04-14 | 2012-08-28 | Bristol-Myers Squibb Company | Bioavailable capsule compositions of amorphous alpha-(N-sulfonamido)acetamide compound |
| WO2011036885A1 (fr) | 2009-09-25 | 2011-03-31 | 武田薬品工業株式会社 | Composé hétérocyclique |
| NZ772688A (en) | 2010-06-03 | 2022-09-30 | Pharmacyclics Llc | The use of inhibitors of bruton’s tyrosine kinase (btk) |
| US20120071497A1 (en) | 2010-06-03 | 2012-03-22 | Pharmacyclics, Inc. | Methods of treating abc-dlbcl using inhibitors of bruton's tyrosine kinase |
| ES2539379T3 (es) | 2010-06-22 | 2015-06-30 | Basf Se | Procedimiento de preparación de 4-hidroxipiridinas |
| JP2013530199A (ja) * | 2010-07-06 | 2013-07-25 | ノバルティス アーゲー | キナーゼ阻害剤として有用な環状エーテル化合物 |
| TW201236685A (en) | 2010-11-11 | 2012-09-16 | Daiichi Sankyo Co Ltd | New pyrazole amide derivatives |
| MX2014014531A (es) | 2012-05-31 | 2015-04-08 | Hoffmann La Roche | Derivados de aminoquinazolina y piridopirimidina. |
| US20150225373A1 (en) | 2012-08-29 | 2015-08-13 | Respivert Limited | Kinase inhibitors |
| AU2013342267B2 (en) | 2012-11-09 | 2017-01-12 | Cornell University | Small molecule inhibitors of MALT1 |
| WO2014086478A1 (fr) | 2012-12-03 | 2014-06-12 | Helmholtz Zentrum München - Deutsches Forschungszentrum für Gesundheit und Umwelt (GmbH) | Inhibiteurs de la protéase malt1 |
| EP2943196A1 (fr) | 2013-01-10 | 2015-11-18 | Grünenthal GmbH | Carboxamides i à base de pyrazolyl à utiliser en tant qu'inhibiteurs du canal crac |
| AP2016009487A0 (en) | 2014-05-28 | 2016-10-31 | Novartis Ag | Novel pyrazolo pyrimidine derivatives and their use as malt1 inhibitors |
| US20150361504A1 (en) | 2014-06-13 | 2015-12-17 | Pharmacyclics Llc | Biomarker for predicting response of cll to treatment with a btk inhibitor |
| WO2016005994A2 (fr) | 2014-07-06 | 2016-01-14 | Gattefosse India Pvt. Ltd. | Composition pharmaceutique comprenant une dispersion solide de médicaments de classe ii bcs avec gelucires |
| AU2015300966A1 (en) | 2014-08-08 | 2017-02-16 | Janssen Pharmaceutica Nv | Bruton's tyrosine kinase inhibitor combinations and uses thereof |
| CR20170094A (es) | 2014-09-10 | 2017-05-08 | Glaxosmithkline Ip Dev Ltd | Nuevos compuestos como inhibidores de reorganizado durante la transfección (ret) |
| AU2015357498B2 (en) | 2014-12-06 | 2019-09-12 | Intra-Cellular Therapies, Inc. | Organic compounds |
| US10835524B2 (en) | 2015-06-24 | 2020-11-17 | University Of Florida Research Foundation, Incorporated | Compositions for the treatment of pancreatic cancer and uses thereof |
| TWI744256B (zh) * | 2015-11-06 | 2021-11-01 | 美商英塞特公司 | 作為ＰＩ３Ｋ-γ抑制劑之雜環化合物 |
| JP2018533610A (ja) | 2015-11-13 | 2018-11-15 | ノバルティス アーゲー | 新規なピラゾロピリミジン誘導体 |
| JO3794B1 (ar) | 2015-12-10 | 2021-01-31 | Janssen Pharmaceutica Nv | المركبات متعددة الحلقات كمثبطات لتيروزين كيناز بروتون |
| CN107021963A (zh) * | 2016-01-29 | 2017-08-08 | 北京诺诚健华医药科技有限公司 | 吡唑稠环类衍生物、其制备方法及其在治疗癌症、炎症和免疫性疾病上的应用 |
| EP3423452B1 (fr) | 2016-03-01 | 2025-05-07 | University of Maryland, Baltimore | Inhibiteurs de la voie de signalisation wnt pour le traitement de maladies |
| MX2019001132A (es) * | 2016-07-29 | 2019-12-16 | Lupin Ltd | Compuestos de tiazolo-piridina sustituida como inhibidores de malt1. |
| WO2018103060A1 (fr) | 2016-12-09 | 2018-06-14 | Janssen Pharmaceutica Nv | Inhibiteurs de tyrosine kinase de bruton et leurs procédés d'utilisation |
| MY203083A (en) | 2016-12-21 | 2024-06-07 | Acerta Pharma Bv | Imidazopyrazine inhibitors of bruton's tyrosine kinase |
| TWI795381B (zh) | 2016-12-21 | 2023-03-11 | 比利時商健生藥品公司 | 作為ｍａｌｔ１抑制劑之吡唑衍生物 |
| JOP20190141A1 (ar) | 2016-12-21 | 2019-06-12 | Bayer Pharma AG | أشكال جرعات صيدلية تحتوي على مثبطات لقناة task-1 و task-3 واستخدامها في معالجة اضطراب تنفسي |
| MX2019007161A (es) | 2016-12-21 | 2020-02-12 | Mereo Biopharma 3 Ltd | Uso de anticuerpos anti-esclerostina en el tratamiento de osteogenesis imperfecta. |
| JOP20190148A1 (ar) | 2016-12-21 | 2019-06-18 | Bayer Pharma AG | أشكال جرعات صيدلية تحتوي على مثبطات قنوات task-1 و task-3 واستخدامها لمعالجة الاضطرابات التنفسية |
| JOP20190152A1 (ar) | 2016-12-21 | 2019-06-20 | Novartis Ag | مضادات الميوستاتين، الآكتيفين أو مستقبلات الآكتيفين للاستخدام في علاج السمنة والحالات ذات الصلة |
| US20200009135A1 (en) | 2017-02-01 | 2020-01-09 | Medivir Ab | Therapeutic applications of malt1 inhibitors |
| EP3592731A4 (fr) * | 2017-03-08 | 2020-10-07 | Cornell University | Inhibiteurs de malt1 et leurs utilisations |
| WO2018226150A1 (fr) * | 2017-06-05 | 2018-12-13 | Medivir Aktiebolag | Pyrazolopyrimidine utilisés en tant qu'inhibiteurs de malt-1 |
| SG11202006200RA (en) | 2017-12-28 | 2020-07-29 | Massachusetts Gen Hospital | Targeting the cbm signalosome complex induces regulatory t cells to inflame the tumor microenvironment |
| WO2019161921A1 (fr) | 2018-02-23 | 2019-08-29 | Industrieanlagen-Betriebsgesellschaft Mbh | Dispositif de génération d'un champ magnétique, notamment pour un système de charge inductif, et dispositif primaire d'un système de charge inductif pour la charge dynamique de véhicules |
| JP7296408B2 (ja) * | 2018-06-18 | 2023-06-22 | ヤンセン ファーマシューティカ エヌ．ベー． | Ｍａｌｔ１阻害剤としてのピラゾール誘導体 |
| EA202092962A1 (ru) | 2018-06-18 | 2021-09-06 | Янссен Фармацевтика Нв | Производные пиразола в качестве ингибиторов malt1 |
| SG11202109102PA (en) | 2019-02-22 | 2021-09-29 | Janssen Pharmaceutica Nv | Pharmaceutical formulations |
| WO2020169736A1 (fr) | 2019-02-22 | 2020-08-27 | Janssen Pharmaceutica Nv | Forme cristalline du monohydrate de 1-(1-oxo-1,2-dihydroisoquinoléin-5-yl)-5-(trifluorométhyl)-n-(2-(trifluorométhyl)pyridin-4-yl)-1h-pyrazole-4-carboxamide |
| MA55593A (fr) | 2019-04-11 | 2022-02-16 | Janssen Pharmaceutica Nv | Cycles pyridine contenant des dérivés servant d'inhibiteurs de malt1 |
| KR20220116460A (ko) | 2019-11-22 | 2022-08-23 | 얀센 파마슈티카 엔.브이. | NF-kB 전좌 분석을 사용하여 MALT1 억제제의 효능을 평가하기 위한 방법 |
| IL293143A (en) | 2019-11-22 | 2022-07-01 | Janssen Pharmaceutica Nv | Nf-kb regulated gene expression assay for assessing efficacy of malt1 inhibitors |
| WO2021138298A1 (fr) | 2019-12-30 | 2021-07-08 | Rheos Medicines, Inc. | Modulateurs de malt1 et leurs utilisations |
| EP4199911A1 (fr) | 2020-08-21 | 2023-06-28 | JANSSEN Pharmaceutica NV | Formulations pharmaceutiques comprenant un inhibiteur de malt1 et un mélange de polyéthylèneglycol et d'un acide gras |
| JP2023539729A (ja) | 2020-08-21 | 2023-09-19 | ヤンセン ファーマシューティカ エヌ．ベー． | Ｍａｌｔ１阻害剤の非晶質形態及びその製剤 |
| CA3212339A1 (fr) | 2021-03-03 | 2022-09-09 | Janssen Pharmaceutica Nv | Methode de traitement d'une affection a l'aide d'une dose therapeutiquement efficace de l'inhibiteur de malt1 jnj-67856633 (1-(1-oxo-1,2-dihydroisoquinolin-5-yl)-5-(trifluoromethy l)-n-(2-(trifluoromethyl)pyridin-4-yl)-1 h-pyrazole-4-carboxamide) |
| MX2023010314A (es) | 2021-03-03 | 2023-11-24 | Janssen Pharmaceutica Nv | Terapia de combinación usando un inhibidor de malt1 y un inhibidor de btk. |
-
2020
- 2020-04-10 MA MA055593A patent/MA55593A/fr unknown
- 2020-04-10 JP JP2021559711A patent/JP7554768B2/ja active Active
- 2020-04-10 EP EP20717667.8A patent/EP3953345B1/fr active Active
- 2020-04-10 ES ES20717667T patent/ES2949871T3/es active Active
- 2020-04-10 US US17/602,885 patent/US12404260B2/en active Active
- 2020-04-10 CN CN202080028070.1A patent/CN113677674B/zh active Active
- 2020-04-10 MX MX2021012417A patent/MX2021012417A/es unknown
- 2020-04-10 AU AU2020272156A patent/AU2020272156A1/en not_active Abandoned
- 2020-04-10 WO PCT/EP2020/060307 patent/WO2020208222A1/fr not_active Ceased
- 2020-04-10 KR KR1020217036345A patent/KR20210151880A/ko not_active Withdrawn
- 2020-04-10 BR BR112021019799A patent/BR112021019799A2/pt not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| KR20210151880A (ko) | 2021-12-14 |
| CN113677674A (zh) | 2021-11-19 |
| WO2020208222A1 (fr) | 2020-10-15 |
| US20220162187A1 (en) | 2022-05-26 |
| EP3953345A1 (fr) | 2022-02-16 |
| US12404260B2 (en) | 2025-09-02 |
| MX2021012417A (es) | 2021-11-12 |
| BR112021019799A2 (pt) | 2021-12-07 |
| CN113677674B (zh) | 2024-08-23 |
| ES2949871T3 (es) | 2023-10-03 |
| CA3131856A1 (fr) | 2020-10-15 |
| JP7554768B2 (ja) | 2024-09-20 |
| EP3953345B1 (fr) | 2023-04-05 |
| JP2022528919A (ja) | 2022-06-16 |
| AU2020272156A1 (en) | 2021-10-14 |
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