MA47125A - Dérivés de pyrazole en tant qu'inhibiteurs de malt1 - Google Patents

Dérivés de pyrazole en tant qu'inhibiteurs de malt1

Info

Publication number
MA47125A
MA47125A MA047125A MA47125A MA47125A MA 47125 A MA47125 A MA 47125A MA 047125 A MA047125 A MA 047125A MA 47125 A MA47125 A MA 47125A MA 47125 A MA47125 A MA 47125A
Authority
MA
Morocco
Prior art keywords
pyrazole derivatives
malt1 inhibitors
malt1
inhibitors
pyrazole
Prior art date
Application number
MA047125A
Other languages
English (en)
Inventor
Brett Douglas Allison
Joseph Kent Barbay
Didier Jean-Claude Berthelot
Peter J Connolly
Maxwell David Cummings
Gaston Diels
James Patrick Edwards
Kevin D Kreutter
Tianbao Lu
Ulrike Philippar
Fang Shen
Johannes Wilhelmus John Fitzgerald Thuring
Tongfei Wu
Original Assignee
Janssen Pharmaceutica Nv
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of MA47125A publication Critical patent/MA47125A/fr

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/472Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/5381,4-Oxazines, e.g. morpholine ortho- or peri-condensed with carbocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic 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
    • C07D491/02Heterocyclic 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 two hetero rings
    • C07D491/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Pulmonology (AREA)
  • Epidemiology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Rheumatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
MA047125A 2016-12-21 2017-12-20 Dérivés de pyrazole en tant qu'inhibiteurs de malt1 MA47125A (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201662437384P 2016-12-21 2016-12-21

Publications (1)

Publication Number Publication Date
MA47125A true MA47125A (fr) 2021-04-28

Family

ID=61628454

Family Applications (1)

Application Number Title Priority Date Filing Date
MA047125A MA47125A (fr) 2016-12-21 2017-12-20 Dérivés de pyrazole en tant qu'inhibiteurs de malt1

Country Status (23)

Country Link
US (2) US10954214B2 (fr)
EP (1) EP3558969B1 (fr)
JP (1) JP7138641B2 (fr)
KR (1) KR102583317B1 (fr)
CN (1) CN110214136A (fr)
AR (1) AR110421A1 (fr)
AU (2) AU2017382185C1 (fr)
BR (1) BR112019012355A2 (fr)
CA (1) CA3048027A1 (fr)
CL (1) CL2019001709A1 (fr)
CO (1) CO2019006622A2 (fr)
EA (1) EA201991503A1 (fr)
ES (1) ES2992411T3 (fr)
IL (1) IL267343B2 (fr)
MA (1) MA47125A (fr)
MX (2) MX392673B (fr)
PE (1) PE20191755A1 (fr)
PH (1) PH12019501212A1 (fr)
TN (1) TN2019000192A1 (fr)
TW (1) TWI795381B (fr)
UA (1) UA127920C2 (fr)
UY (1) UY37537A (fr)
WO (1) WO2018119036A1 (fr)

Families Citing this family (68)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20170107216A1 (en) 2015-10-19 2017-04-20 Incyte Corporation Heterocyclic compounds as immunomodulators
AU2016358100B2 (en) 2015-11-19 2021-05-27 Incyte Corporation Heterocyclic compounds as immunomodulators
TW201726623A (zh) 2015-12-17 2017-08-01 英塞特公司 作為免疫調節劑之雜環化合物
TWI850624B (zh) 2015-12-22 2024-08-01 美商英塞特公司 作為免疫調節劑之雜環化合物
TW201808950A (zh) 2016-05-06 2018-03-16 英塞特公司 作為免疫調節劑之雜環化合物
US20170342060A1 (en) 2016-05-26 2017-11-30 Incyte Corporation Heterocyclic compounds as immunomodulators
DK3472167T3 (da) 2016-06-20 2022-09-05 Incyte Corp Heterocykliske forbindelser som immunomodulatorer
EP3484866B1 (fr) 2016-07-14 2022-09-07 Incyte Corporation Composés hétérocycliques utilisés comme immunomodulateurs
EP3504198B1 (fr) 2016-08-29 2023-01-25 Incyte Corporation Composés hétérocycliques utilisés comme immunomodulateurs
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
IL295660A (en) 2016-12-22 2022-10-01 Incyte Corp Benzooxazole derivatives as immunomodulators
EP3558973B1 (fr) 2016-12-22 2021-09-15 Incyte Corporation Dérivés pyridine utilisés en tant qu'immunomodulateurs
EP3558963B1 (fr) 2016-12-22 2022-03-23 Incyte Corporation Composés hétéroaromatiques bicycliques utilisés en tant qu'immunomodulateurs
ES2874756T3 (es) 2016-12-22 2021-11-05 Incyte Corp Derivados de triazolo[1,5-A]piridina como inmunomoduladores
BR112020005489A2 (pt) 2017-09-22 2020-09-24 Jubilant Epipad Llc, composto da fórmula (i), composto de fórmula (ii), composto de fórmula (iii), processo de preparação de compostos de fórmula (i), processo de preparação de compostos de fórmula (ii), processo de preparação de compostos de fórmula (iii), composição farmacêutica, método para inibir uma ou mais famílias pad em uma célula, método para tratar uma afeção mediada por um ou mais pads, utilização do composto, método para o tratamento e/ou prevenção de uma afeção mediada por um ou mais distúrbios da família pad, método para o tratamento de artrite reumatoide e método de tratamento de câncer
CN111225915B (zh) 2017-10-18 2023-03-07 朱比兰特埃皮帕德有限公司 作为pad抑制剂的咪唑并吡啶化合物
EP3707135A1 (fr) 2017-11-06 2020-09-16 Jubilant Prodel LLC Dérivés de pyrimidine utilisés en tant qu'inhibiteurs de l'activation de pd1/pd-l1
IL274762B2 (en) 2017-11-24 2023-10-01 Jubilant Episcribe Llc Novel heterocyclic compounds as prmt5 inhibitors
CN111770759A (zh) 2017-12-28 2020-10-13 通用医疗公司 靶向cbm信号体复合物诱导调节性t细胞使肿瘤微环境发炎
EP3765453A1 (fr) 2018-03-13 2021-01-20 Jubilant Prodel LLC Composés bicycliques utilisés en tant qu'inhibiteurs de l'interaction/activation de pd1/pd-l1
RS64055B1 (sr) 2018-03-30 2023-04-28 Incyte Corp Heterociklična jedinjenja kao imunomodulatori
EP4219492B1 (fr) 2018-05-11 2024-11-27 Incyte Corporation Composés hétérocycliques utilisés comme immunomodulateurs
CN112585128B (zh) * 2018-06-18 2023-02-21 詹森药业有限公司 作为malt1抑制剂的吡唑衍生物
MX2020013699A (es) * 2018-06-18 2021-05-12 Janssen Pharmaceutica Nv Derivados de pirazol como inhibidores de malt1.
TW202045008A (zh) * 2019-02-01 2020-12-16 印度商皮埃企業有限公司 4-取代的異噁唑/異噁唑啉(雜)芳基脒化合物、及其製備與用途
US12269813B2 (en) * 2019-02-22 2025-04-08 Janssen Pharmaceutica Nv Crystalline form of 1-(1-oxo-1,2-dihydroisoquinolin-5-yl)-5-(trifluoromethyl)-N-(2-(trifluoromethyl)pyridin-4-yl)-1H-pyrazole-4-carboxamide monohydrate
MX2021010144A (es) * 2019-02-22 2021-09-14 Janssen Pharmaceutica Nv Formulaciones farmaceuticas.
EP3953345B1 (fr) 2019-04-11 2023-04-05 Janssen Pharmaceutica NV Dérivés de pyridines comme inhibiteurs de malt1
JP7665593B2 (ja) 2019-08-09 2025-04-21 インサイト・コーポレイション Pd-1/pd-l1阻害剤の塩
EP4037773A1 (fr) 2019-09-30 2022-08-10 Incyte Corporation Composés pyrido[3,2-d]pyrimidine en tant qu'immunomodulateurs
JP2022553282A (ja) * 2019-10-24 2022-12-22 小野薬品工業株式会社 Trek(twik関連k+チャネル)チャネル機能のモジュレータ
ES3055177T3 (en) 2019-10-30 2026-02-10 Biogen Ma Inc Condensed pyridazine or pyrimidine as btk inhibitors
BR112022009031A2 (pt) 2019-11-11 2022-10-11 Incyte Corp Sais e formas cristalinas de um inibidor de pd-1/pd-l1
IL293146A (en) 2019-11-22 2022-07-01 Janssen Pharmaceutica Nv Methods for evaluating the efficacy of malt1 inhibitors using the nf-kb knockdown assay
US20210155990A1 (en) * 2019-11-22 2021-05-27 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
US20230235077A1 (en) 2020-06-24 2023-07-27 The General Hospital Corporation Materials and methods of treating cancer
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
KR20230054394A (ko) * 2020-08-21 2023-04-24 얀센 파마슈티카 엔.브이. 비정질 형태의 malt1 억제제 및 이의 제형
CA3198715A1 (fr) * 2020-10-16 2022-04-21 Rheos Medicines, Inc. Modulateurs de malt1 et leurs utilisations
US11760756B2 (en) 2020-11-06 2023-09-19 Incyte Corporation Crystalline form of a PD-1/PD-L1 inhibitor
EP4240739A1 (fr) 2020-11-06 2023-09-13 Incyte Corporation Processus de fabrication d'un inhibiteur pd-1/pd-l1 ainsi que de ses sels et formes cristallines
WO2022099018A1 (fr) 2020-11-06 2022-05-12 Incyte Corporation Procédé de préparation d'un inhibiteur de pd-1/pd-l1
US20230414629A1 (en) * 2020-11-12 2023-12-28 Monopteros Therapeutics, Inc. Materials and methods of treating cancer
GB202018412D0 (en) * 2020-11-23 2021-01-06 Exscientia Ltd Malt-1 modulators ii
US20240132475A1 (en) * 2021-02-04 2024-04-25 Aurigene Oncology Limited Substituted pyrazolyl compounds as malt-1 inhibitors
WO2022185097A1 (fr) 2021-03-03 2022-09-09 Janssen Pharmaceutica Nv Méthode de traitement d'une affection à l'aide d'une dose thérapeutiquement efficace de l'inhibiteur de malt1 jnj-67856633 (1-(1-oxo-1,2-dihydroisoquinolin-5-yl)-5-(trifluorométhyl)-n-(2-(trifluorométhyl)pyridin-4-yl)-1 h-pyrazole-4-carboxamide)
CA3212015A1 (fr) 2021-03-03 2022-09-09 Janssen Pharmaceutica Nv Polytherapie utilisant un inhibiteur de malt1 et un inhibiteur de btk
CN117120427A (zh) * 2021-06-18 2023-11-24 上海拓界生物医药科技有限公司 一种malt1抑制剂及其制备方法和用途
US20240336594A1 (en) * 2021-07-05 2024-10-10 Betta Pharmaceuticals Co., Ltd Six-membered aryl or heteroaryl amides, and composition and use thereof
CA3227033A1 (fr) 2021-08-09 2023-02-16 Eric Frederik ELDERING Compositions destinees a etre utilisees dans le traitement de malignites des lymphocytes b
CN113912511B (zh) * 2021-11-29 2024-02-13 广东广康生化科技股份有限公司 一种联苯肼酯中间体的合成方法
AU2022425324A1 (en) 2021-12-30 2024-05-30 Jiangsu Hansoh Pharmaceutical Group Co., Ltd. Tricyclic derivative inhibitor, preparation method therefor, and application thereof
JPWO2023149450A1 (fr) 2022-02-02 2023-08-10
EP4472734A1 (fr) * 2022-02-03 2024-12-11 C4X Discovery Limited Dérivés hétérocycliques en tant qu'inhibiteurs de malt1
TW202430031A (zh) 2022-09-30 2024-08-01 瑞士商先正達農作物保護股份公司 殺微生物之吡唑衍生物
TW202430514A (zh) 2022-09-30 2024-08-01 瑞士商先正達農作物保護股份公司 殺微生物之吡唑衍生物
JP2025539452A (ja) 2022-11-30 2025-12-05 シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト 殺微生物テトラヒドロイソキノリン誘導体
WO2024125628A1 (fr) * 2022-12-16 2024-06-20 江苏恒瑞医药股份有限公司 Promédicament ester de phosphate d'un inhibiteur de malt1
TW202515873A (zh) * 2023-06-29 2025-04-16 大陸商上海翰森生物醫藥科技有限公司 一種三并環類衍生物抑制劑的晶型及其製備方法
TW202515550A (zh) * 2023-06-29 2025-04-16 大陸商上海翰森生物醫藥科技有限公司 三并環類抑制劑與抗癌劑在製備抗腫瘤藥物中的聯合應用
WO2025069270A1 (fr) * 2023-09-27 2025-04-03 日本新薬株式会社 Composé d'azaindole et médicament
WO2025073968A1 (fr) 2023-10-06 2025-04-10 Ionctura Sa Combinaison de roginolisib avec un inhibiteur de malt1-gls
WO2025114167A1 (fr) 2023-11-28 2025-06-05 Syngenta Crop Protection Ag Dérivés de pyrazole microbiocides
WO2025174889A1 (fr) * 2024-02-13 2025-08-21 Board Of Regents, The University Of Texas System Inhibiteurs doubles de malt1 et de btk
WO2025191053A1 (fr) 2024-03-14 2025-09-18 Syngenta Crop Protection Ag Dérivés de pyrazole microbiocides
WO2025210095A1 (fr) 2024-04-03 2025-10-09 Syngenta Crop Protection Ag Composés de tétrahydroisoquinoléine microbiocides
WO2025210096A1 (fr) 2024-04-03 2025-10-09 Syngenta Crop Protection Ag Compositions fongicides

Family Cites Families (71)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6339099B1 (en) 1997-06-20 2002-01-15 Dupont Pharmaceuticals Company Guanidine mimics as factor Xa inhibitors
GB9721964D0 (en) * 1997-10-16 1997-12-17 Pfizer Ltd Isoquinolines
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
CA2522994C (fr) * 2003-04-30 2012-09-25 Agensys, Inc. Acides nucleiques et proteines correspondantes appelees 109p1d4 utiles dans le traitement et la detection du cancer
AU2004236240C1 (en) 2003-05-01 2010-11-04 Bristol-Myers Squibb Company Aryl-substituted pyrazole compounds useful as kinase inhibitors
US20090156582A1 (en) 2005-02-09 2009-06-18 Tetsuya Tsukamoto Pyrazole Compound
CN100526430C (zh) 2005-10-19 2009-08-12 中国石油化工股份有限公司 一种生产清洁汽油的方法
TW200738682A (en) * 2005-12-08 2007-10-16 Organon Nv Isoquinoline derivatives
RU2008141761A (ru) 2006-03-22 2010-04-27 Вертекс Фармасьютикалз Инкорпорейтед (Us) ИНГИБИТОРЫ с-МЕТ ПРОТЕИНКИНАЗЫ
CA2657660A1 (fr) 2006-07-12 2008-01-17 Merck & Co., Inc. Pyrazoles substitues servant d'antagonistes des recepteurs de la ghreline
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
BRPI0721430A2 (pt) 2007-03-09 2013-01-08 High Point Pharmaceuticals Llc amidas indol e benzimidazol como inibidoras de hidroxiesteràide deidrogenase
CN101366715A (zh) 2007-08-15 2009-02-18 上海医药工业研究院 一种雷帕霉素组合物及其制备方法
US8309523B2 (en) 2007-11-21 2012-11-13 Vib Vzw Inhibitors of MALT1 proteolytic activity and uses thereof
EA020661B1 (ru) 2008-09-24 2014-12-30 Басф Се Пиразольные соединения для борьбы с беспозвоночными вредителями
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
CA3007787C (fr) 2010-06-03 2020-03-10 Pharmacyclics Llc Utilisation d'inhibiteurs de la tyrosine kinase de bruton (btk)
US20120071497A1 (en) 2010-06-03 2012-03-22 Pharmacyclics, Inc. Methods of treating abc-dlbcl using inhibitors of bruton's tyrosine kinase
CN102947270B (zh) 2010-06-22 2015-04-08 巴斯夫欧洲公司 制备4-羟基吡啶的方法
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
KR20150020228A (ko) 2012-05-31 2015-02-25 에프. 호프만-라 로슈 아게 아미노퀴나졸린 및 피리도피리미딘 유도체
EP2890695A2 (fr) 2012-08-29 2015-07-08 Respivert Limited Inhibiteurs de kinase
EP2916656B1 (fr) 2012-11-09 2017-10-25 Cornell University Inhibiteurs de malt1 à petites molécules
WO2014086478A1 (fr) 2012-12-03 2014-06-12 Helmholtz Zentrum München - Deutsches Forschungszentrum für Gesundheit und Umwelt (GmbH) Inhibiteurs de la protéase malt1
HK1216300A1 (zh) 2013-01-10 2016-11-04 Grünenthal GmbH 作为crac通道抑制剂的基於吡唑基的甲醯胺i
JP2015096499A (ja) 2013-10-11 2015-05-21 田辺三菱製薬株式会社 医薬組成物
KR20170007311A (ko) * 2014-05-28 2017-01-18 노파르티스 아게 신규 피라졸로 피리미딘 유도체 및 malt1 억제제로서의 그의 용도
WO2015192081A1 (fr) 2014-06-13 2015-12-17 Byrd, John C. Biomarqueur permettant de prédire la réponse d'une llc à un traitement avec un inhibiteur de la btk
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
JP2017523207A (ja) 2014-08-08 2017-08-17 ファーマサイクリックス エルエルシー ブルトン型チロシンキナーゼ阻害薬の組み合わせ及びそれらの使用
MX381233B (es) 2014-09-10 2025-03-12 Glaxosmithkline Ip Dev Ltd Nuevos compuestos como inhibidores de reorganizado durante la transfección (ret).
US10105349B2 (en) 2014-12-06 2018-10-23 Intra-Cellular Therapies, Inc. Organic compounds
WO2016209688A1 (fr) 2015-06-24 2016-12-29 University Of Florida Research Foundation, Incorporated Compositions destinées au traitement du cancer, et leurs utilisations
EP4086259A1 (fr) 2015-11-06 2022-11-09 Incyte Corporation Composés hétérocycliques utilisés en tant qu'inhibiteurs de pi3k-gamma
MX2018005390A (es) 2015-11-13 2018-08-16 Novartis Ag Nuevos derivados de pirazolo pirimidina.
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
WO2017151786A1 (fr) 2016-03-01 2017-09-08 University Of Maryland, Baltimore Inhibiteurs de la voie de signalisation wnt pour le traitement de maladies
KR20190033607A (ko) 2016-07-29 2019-03-29 루핀 리미티드 Malt1 저해제로서의 치환 티아졸로-피리딘 화합물
WO2018103060A1 (fr) 2016-12-09 2018-06-14 Janssen Pharmaceutica Nv Inhibiteurs de tyrosine kinase de bruton et leurs procédés d'utilisation
ES2862922T7 (en) 2016-12-21 2025-02-26 Mereo Biopharma 3 Ltd Use of anti-sclerostin antibodies in the treatment of osteogenesis imperfecta
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
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
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
CA3046578A1 (fr) 2016-12-21 2018-06-28 Acerta Pharma B.V. Inhibiteurs de type imidazopyrazine de tyrosine kinase de bruton
EP3576744A1 (fr) 2017-02-01 2019-12-11 Medivir Aktiebolag Applications thérapeutiques d'inhibiteurs de malt1
WO2018165385A1 (fr) 2017-03-08 2018-09-13 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
CN111770759A (zh) 2017-12-28 2020-10-13 通用医疗公司 靶向cbm信号体复合物诱导调节性t细胞使肿瘤微环境发炎
CN111801245B (zh) 2018-02-23 2024-04-30 工业设备运营公司 产生磁场的设备以及对交通工具动态充电的感应式充电系统的初级装置
CN112585128B (zh) 2018-06-18 2023-02-21 詹森药业有限公司 作为malt1抑制剂的吡唑衍生物
MX2020013699A (es) 2018-06-18 2021-05-12 Janssen Pharmaceutica Nv Derivados de pirazol como inhibidores de malt1.
MX2021010144A (es) 2019-02-22 2021-09-14 Janssen Pharmaceutica Nv Formulaciones farmaceuticas.
US12269813B2 (en) 2019-02-22 2025-04-08 Janssen Pharmaceutica Nv Crystalline form of 1-(1-oxo-1,2-dihydroisoquinolin-5-yl)-5-(trifluoromethyl)-N-(2-(trifluoromethyl)pyridin-4-yl)-1H-pyrazole-4-carboxamide monohydrate
EP3953345B1 (fr) 2019-04-11 2023-04-05 Janssen Pharmaceutica NV Dérivés de pyridines comme inhibiteurs de malt1
IL293146A (en) 2019-11-22 2022-07-01 Janssen Pharmaceutica Nv Methods for evaluating the efficacy of malt1 inhibitors using the nf-kb knockdown assay
US20210155990A1 (en) 2019-11-22 2021-05-27 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
KR20230054394A (ko) 2020-08-21 2023-04-24 얀센 파마슈티카 엔.브이. 비정질 형태의 malt1 억제제 및 이의 제형
CA3212015A1 (fr) 2021-03-03 2022-09-09 Janssen Pharmaceutica Nv Polytherapie utilisant un inhibiteur de malt1 et un inhibiteur de btk
WO2022185097A1 (fr) 2021-03-03 2022-09-09 Janssen Pharmaceutica Nv Méthode de traitement d'une affection à l'aide d'une dose thérapeutiquement efficace de l'inhibiteur de malt1 jnj-67856633 (1-(1-oxo-1,2-dihydroisoquinolin-5-yl)-5-(trifluorométhyl)-n-(2-(trifluorométhyl)pyridin-4-yl)-1 h-pyrazole-4-carboxamide)

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