IL283368B2 - Imidazo[2,1-b]pyridazin-7-yl urea compound and medicament containing the compound - Google Patents
Imidazo[2,1-b]pyridazin-7-yl urea compound and medicament containing the compoundInfo
- Publication number
- IL283368B2 IL283368B2 IL283368A IL28336821A IL283368B2 IL 283368 B2 IL283368 B2 IL 283368B2 IL 283368 A IL283368 A IL 283368A IL 28336821 A IL28336821 A IL 28336821A IL 283368 B2 IL283368 B2 IL 283368B2
- Authority
- IL
- Israel
- Prior art keywords
- pyridazin
- urea
- substituted
- pyridin
- chloro
- Prior art date
Links
Classifications
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- 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
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4841—Filling excipients; Inactive ingredients
- A61K9/4858—Organic compounds
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2018222530 | 2018-11-28 | ||
| PCT/JP2019/046261 WO2020111087A1 (ja) | 2018-11-28 | 2019-11-27 | 複素環化合物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| IL283368A IL283368A (en) | 2021-07-29 |
| IL283368B1 IL283368B1 (en) | 2024-09-01 |
| IL283368B2 true IL283368B2 (en) | 2025-01-01 |
Family
ID=70853784
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL303962A IL303962A (en) | 2018-11-28 | 2019-11-27 | The tricyclic compound |
| IL283368A IL283368B2 (en) | 2018-11-28 | 2019-11-27 | Imidazo[2,1-b]pyridazin-7-yl urea compound and medicament containing the compound |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL303962A IL303962A (en) | 2018-11-28 | 2019-11-27 | The tricyclic compound |
Country Status (16)
| Country | Link |
|---|---|
| US (4) | US12152027B2 (enExample) |
| EP (1) | EP3888652A4 (enExample) |
| JP (2) | JP6972384B2 (enExample) |
| KR (2) | KR102646470B1 (enExample) |
| CN (2) | CN113038948B (enExample) |
| AU (1) | AU2019390863B2 (enExample) |
| BR (1) | BR112021009994A2 (enExample) |
| CA (1) | CA3120774A1 (enExample) |
| IL (2) | IL303962A (enExample) |
| MX (2) | MX2021005877A (enExample) |
| MY (1) | MY209902A (enExample) |
| PH (1) | PH12021551251A1 (enExample) |
| SG (1) | SG11202105652XA (enExample) |
| TW (3) | TWI784213B (enExample) |
| WO (1) | WO2020111087A1 (enExample) |
| ZA (1) | ZA202104402B (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102646470B1 (ko) * | 2018-11-28 | 2024-03-11 | 다케다 야쿠힌 고교 가부시키가이샤 | 헤테로시클릭 화합물 |
| US20230192685A1 (en) * | 2020-05-27 | 2023-06-22 | Takeda Pharmaceutical Company Limited | Method for producing heterocyclic compound |
| CN116916924A (zh) * | 2020-10-16 | 2023-10-20 | 稀有生物科学股份有限公司 | Malt1调节剂及其用途 |
| GB202018412D0 (en) | 2020-11-23 | 2021-01-06 | Exscientia Ltd | Malt-1 modulators ii |
| JP2025501056A (ja) | 2021-12-30 | 2025-01-17 | シャンハイ ハンソー バイオメディカル カンパニー リミテッド | 三環系誘導体阻害剤、その製造方法と応用 |
| KR20240144146A (ko) | 2022-02-02 | 2024-10-02 | 오노 야꾸힝 고교 가부시키가이샤 | Malt1 저해약을 유효 성분으로서 포함하는 암 치료제 |
| US20250188081A1 (en) * | 2023-12-08 | 2025-06-12 | Shaman Pharma, LLC | Method for Production of Spiro-Oxindole and Indoxyl Derivatives of Mitragynine |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2015181747A1 (en) * | 2014-05-28 | 2015-12-03 | Novartis Ag | Novel pyrazolo pyrimidine derivatives and their use as malt1 inhibitors |
| WO2017081641A1 (en) * | 2015-11-13 | 2017-05-18 | Novartis Ag | Novel pyrazolo pyrimidine derivatives |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2288521A1 (fr) | 1974-10-25 | 1976-05-21 | Merck Patent Gmbh | Nouvelles penicillines et procede pour leur preparation |
| NZ308228A (en) * | 1995-05-31 | 1999-11-29 | Sumitomo Pharma | Substituted 1,8-naphthyridine derivatives |
| GB9720052D0 (en) | 1997-09-19 | 1997-11-19 | Smithkline Beecham Plc | Novel compounds |
| GB201321734D0 (en) | 2013-12-09 | 2014-01-22 | Ucb Pharma Sa | Therapeutic Agents |
| JP2019522035A (ja) | 2016-07-29 | 2019-08-08 | ルピン・リミテッド | Ｍａｌｔ１阻害剤としての置換チアゾロ−ピリジン化合物 |
| WO2018085247A1 (en) * | 2016-11-01 | 2018-05-11 | Cornell University | Compounds for malt1 degradation |
| WO2018165385A1 (en) * | 2017-03-08 | 2018-09-13 | Cornell University | Inhibitors of malt1 and uses thereof |
| US20200111087A1 (en) * | 2018-10-08 | 2020-04-09 | Jinlei Zhou | Method for encrypting digital contract document between contractors |
| KR102646470B1 (ko) * | 2018-11-28 | 2024-03-11 | 다케다 야쿠힌 고교 가부시키가이샤 | 헤테로시클릭 화합물 |
-
2019
- 2019-11-27 KR KR1020227003334A patent/KR102646470B1/ko active Active
- 2019-11-27 MY MYPI2021002948A patent/MY209902A/en unknown
- 2019-11-27 TW TW108143201A patent/TWI784213B/zh active
- 2019-11-27 EP EP19890558.0A patent/EP3888652A4/en active Pending
- 2019-11-27 US US17/296,434 patent/US12152027B2/en active Active
- 2019-11-27 CN CN201980078144.XA patent/CN113038948B/zh active Active
- 2019-11-27 AU AU2019390863A patent/AU2019390863B2/en active Active
- 2019-11-27 MX MX2021005877A patent/MX2021005877A/es unknown
- 2019-11-27 TW TW113120662A patent/TW202438498A/zh unknown
- 2019-11-27 KR KR1020217019537A patent/KR102359143B1/ko active Active
- 2019-11-27 CN CN202410510968.2A patent/CN118420620A/zh active Pending
- 2019-11-27 IL IL303962A patent/IL303962A/en unknown
- 2019-11-27 JP JP2020557754A patent/JP6972384B2/ja active Active
- 2019-11-27 BR BR112021009994-8A patent/BR112021009994A2/pt unknown
- 2019-11-27 CA CA3120774A patent/CA3120774A1/en active Pending
- 2019-11-27 IL IL283368A patent/IL283368B2/en unknown
- 2019-11-27 TW TW111139300A patent/TWI848400B/zh active
- 2019-11-27 SG SG11202105652XA patent/SG11202105652XA/en unknown
- 2019-11-27 WO PCT/JP2019/046261 patent/WO2020111087A1/ja not_active Ceased
-
2021
- 2021-05-19 MX MX2024003064A patent/MX2024003064A/es unknown
- 2021-05-28 PH PH12021551251A patent/PH12021551251A1/en unknown
- 2021-06-25 ZA ZA2021/04402A patent/ZA202104402B/en unknown
- 2021-07-02 US US17/367,171 patent/US11230545B2/en active Active
- 2021-11-02 JP JP2021179627A patent/JP7434249B2/ja active Active
- 2021-11-17 US US17/528,677 patent/US11897879B2/en active Active
-
2024
- 2024-10-07 US US18/908,457 patent/US20250034141A1/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2015181747A1 (en) * | 2014-05-28 | 2015-12-03 | Novartis Ag | Novel pyrazolo pyrimidine derivatives and their use as malt1 inhibitors |
| WO2017081641A1 (en) * | 2015-11-13 | 2017-05-18 | Novartis Ag | Novel pyrazolo pyrimidine derivatives |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| IL283368B2 (en) | Imidazo[2,1-b]pyridazin-7-yl urea compound and medicament containing the compound | |
| JP2022017461A5 (enExample) | ||
| JP7531595B2 (ja) | ピリド［３，４－ｄ］ピリミジン誘導体およびこれを含む治療用薬学組成物 | |
| ME02203B (me) | Hinolin i hinoksalin derivati kao inhibitori kinaza | |
| CN109983007A (zh) | 酰胺类衍生物抑制剂及其制备方法和应用 | |
| FI3932919T3 (fi) | Jak-inhibiittoriyhdiste ja sen käyttö | |
| MY206521A (en) | Heterocyclic compounds as kinase inhibitors, compositions comprising the heterocyclic compound, and methods of use thereof | |
| CA2403514A1 (en) | 8-quinolinxanthine and 8-isoquinolinxanthine derivatives as pde 5 inhibitors | |
| CA2687265A1 (en) | P70 s6 kinase inhibitors | |
| NZ591712A (en) | Imidazopyridazinecarbonitriles useful as kinase inhibitors | |
| JP2011507854A5 (enExample) | ||
| NZ592809A (en) | SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINE COMPOUNDS AS TRK KINASE INHIBITORS | |
| NZ592238A (en) | Pharmaceutical compositions comprising 4-isopropyl-1,4,6,7-tetrahydro-5H-imidazo[4,5-c]pyridine derivatives | |
| ZA202205900B (en) | 5-(2-(2,5-difluorophenyl)pyrrolidin-1 -yl)-3-(1h-pyrazol-1-yl)pyrazolo[1,5-a]pyrimidine derivatives and related compounds as trk kinase inhibitors for treating cancer | |
| JP2016520118A5 (enExample) | ||
| JP2019503337A5 (enExample) | ||
| RU2010143455A (ru) | Имидазохинолины и производные пиримидина в качестве потенциальных модуляторов vegf-стимулируемых ангиогенных процессов | |
| WO2014106800A8 (en) | Substituted 2-amino pyrimidine derivatives as kinase inhibitors | |
| RU2016120610A (ru) | Производное сульфонамида и его применение в медицине | |
| MY206359A (en) | Heteroaryl-substituted pyrazole compound and medicinal use thereof | |
| PH12021551386A1 (en) | Salt of syk inhibitor and crystalline form thereof | |
| MX2020013847A (es) | Forma cristalina del compuesto para inhibir la actividad de cdk4/6 y uso del mismo. | |
| TW200602344A (en) | Novel pyrrolo(2, 3-b)pyridine derivatives, preparation thereof and pharmaceutical use thereof as kinase inhibitors | |
| MX2017011423A (es) | Derivados de 7-(morfolin-4-il)pirazolo[1,5-a]pirimidina que son utiles para el tratamiento de enfermedades inmunes o inflamatorias o cancer. | |
| RU2021117869A (ru) | Гетероциклическое соединение |