PL3472165T3 - Pochodne n-(podstawione-fenylo)-sulfonamidowe jako inhibitory kinaz - Google Patents
Pochodne n-(podstawione-fenylo)-sulfonamidowe jako inhibitory kinazInfo
- Publication number
- PL3472165T3 PL3472165T3 PL17732075.1T PL17732075T PL3472165T3 PL 3472165 T3 PL3472165 T3 PL 3472165T3 PL 17732075 T PL17732075 T PL 17732075T PL 3472165 T3 PL3472165 T3 PL 3472165T3
- Authority
- PL
- Poland
- Prior art keywords
- phenyl
- substituted
- kinase inhibitors
- sulfonamide derivatives
- sulfonamide
- Prior art date
Links
- -1 N-(substituted-phenyl)-sulfonamide Chemical class 0.000 title 1
- 229940043355 kinase inhibitor Drugs 0.000 title 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 title 1
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
- A61K31/4355—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 five-membered ring having oxygen as a ring hetero atom
-
- 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
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic 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
- A61K31/4353—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
- A61K31/4365—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 having sulfur as a ring hetero atom, e.g. ticlopidine
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
-
- 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
- C07D491/02—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 two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic 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
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Immunology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP16175386 | 2016-06-21 | ||
| PCT/EP2017/064904 WO2017220477A1 (en) | 2016-06-21 | 2017-06-19 | N-(substituted-phenyl)-sulfonamide derivatives as kinase inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL3472165T3 true PL3472165T3 (pl) | 2024-05-27 |
Family
ID=56148248
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL17732075.1T PL3472165T3 (pl) | 2016-06-21 | 2017-06-19 | Pochodne n-(podstawione-fenylo)-sulfonamidowe jako inhibitory kinaz |
Country Status (18)
| Country | Link |
|---|---|
| US (4) | US10561660B2 (pl) |
| EP (1) | EP3472165B1 (pl) |
| JP (1) | JP6867417B2 (pl) |
| KR (1) | KR102500416B1 (pl) |
| CN (1) | CN109311894B (pl) |
| AU (1) | AU2017279878B9 (pl) |
| CA (1) | CA3029097A1 (pl) |
| DK (1) | DK3472165T3 (pl) |
| ES (1) | ES2964781T3 (pl) |
| FI (1) | FI3472165T3 (pl) |
| HU (1) | HUE064919T2 (pl) |
| IL (1) | IL263739B (pl) |
| MX (1) | MX388660B (pl) |
| PL (1) | PL3472165T3 (pl) |
| PT (1) | PT3472165T (pl) |
| RU (1) | RU2753520C2 (pl) |
| SI (1) | SI3472165T1 (pl) |
| WO (1) | WO2017220477A1 (pl) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2017279878B9 (en) | 2016-06-21 | 2021-04-29 | Nerviano Medical Sciences S.R.L. | N-(substituted-phenyl)-sulfonamide derivatives as kinase inhibitors |
| WO2021030238A2 (en) * | 2019-08-09 | 2021-02-18 | Ohm Oncology | Method of synthesis of compound for dual inhibition of jak2 and bet |
| KR20210056827A (ko) * | 2019-11-11 | 2021-05-20 | 일동제약(주) | 신규한 벤젠설폰아미드 유도체 및 그의 용도 |
| AU2021222818A1 (en) * | 2020-02-17 | 2022-09-01 | Alesta Therapeutics BV | GCN2 modulator compounds |
| PT4146348T (pt) | 2020-05-08 | 2024-10-04 | Halia Therapeutics Inc | Inibidores da quinase nek7 |
| CN111454261A (zh) * | 2020-05-27 | 2020-07-28 | 南京普锐达医药科技有限公司 | 一种4-氯吡咯并嘧啶化合物的合成方法 |
| AU2021381949A1 (en) | 2020-11-18 | 2023-06-15 | Deciphera Pharmaceuticals, Llc | Gcn2 and perk kinase inhibitors and methods of use thereof |
| US20240382488A1 (en) | 2021-03-29 | 2024-11-21 | Halia Therapeutics, Inc. | Nek7 inhibitors |
| IL307258A (en) | 2021-04-05 | 2023-11-01 | Halia Therapeutics Inc | NEK7 inhibitors |
| WO2023025912A1 (en) | 2021-08-25 | 2023-03-02 | Alesta Therapeutics BV | Use of gcn2 inhibitors in treating cancer |
| US20230382915A1 (en) * | 2021-12-03 | 2023-11-30 | Deciphera Pharmaceuticals, Llc | Gcn2 and perk kinase inhibitors and methods of use thereof |
| CN119677727A (zh) * | 2022-04-08 | 2025-03-21 | 阿莱斯塔治疗公司 | Gcn2调节剂化合物 |
| WO2023239165A1 (ko) * | 2022-06-08 | 2023-12-14 | 한국화학연구원 | 페닐설폰아마이드 유도체, 이의 제조방법 및 이를 유효성분으로 함유하는 암의 예방 또는 치료용 약학적 조성물 |
| WO2024249493A2 (en) * | 2023-05-30 | 2024-12-05 | Deciphera Pharmaceuticals, Llc | Gcn2 and perk kinase modulators and methods of use thereof |
| WO2025076441A1 (en) * | 2023-10-06 | 2025-04-10 | Alesta Therapeutics BV | Compounds of gcn2 modulators |
| GB202407386D0 (en) | 2024-05-24 | 2024-07-10 | Apollo Ap45 Ltd | 1H-pyrazolo(4,3-D)pyrimidine derivatives |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001516353A (ja) * | 1997-03-19 | 2001-09-25 | ビーエーエスエフ アクチェンゲゼルシャフト | ピロロ[2,3d]ピリミジンおよびチロシンキナーゼ阻害剤としてのこれらの使用 |
| HK1039325B (en) * | 1998-09-18 | 2006-02-24 | Abbott Gmbh & Co. Kg | 4-aminopyrrolopyrimidines as kinase inhibitors |
| GB0625827D0 (en) * | 2006-12-22 | 2007-02-07 | Astex Therapeutics Ltd | New compounds |
| CA2740885C (en) | 2008-10-16 | 2018-04-03 | The Regents Of The University Of California | Fused ring heteroaryl kinase inhibitors |
| UY33288A (es) | 2010-03-25 | 2011-10-31 | Glaxosmithkline Llc | Derivados de indolina inhibidores de la proteina quinasa r del reticulo endoplasmatico |
| GEP201706623B (en) * | 2012-10-16 | 2017-02-10 | Almirall Sa | Pyrrolotriazinone derivatives as pi3k inhibitors |
| BR112015024971B1 (pt) | 2013-04-04 | 2022-09-20 | Janssen Pharmaceutica Nv | Derivados de n-(2,3-di-hidro-1h-pirrolo[2,3-b]piridin-5-il)-4-quinazolinamina e n-(2,3-di-hidro-1hindol-5-il)-4-quinazolinamina como inibidores de perk e composição farmacêutica que os compreende |
| BR112015028845A2 (pt) * | 2013-05-30 | 2017-07-25 | Plexxikon Inc | compostos para a modulação da quinase e indicações da mesma |
| JP2017507967A (ja) * | 2014-03-11 | 2017-03-23 | グラクソスミスクライン、インテレクチュアル、プロパティー、(ナンバー2)、リミテッドGlaxosmithkline Intellectual Property (No.2) Limited | Perk阻害剤として作用する化合物 |
| AU2017279878B9 (en) * | 2016-06-21 | 2021-04-29 | Nerviano Medical Sciences S.R.L. | N-(substituted-phenyl)-sulfonamide derivatives as kinase inhibitors |
-
2017
- 2017-06-19 AU AU2017279878A patent/AU2017279878B9/en active Active
- 2017-06-19 JP JP2018566910A patent/JP6867417B2/ja active Active
- 2017-06-19 CA CA3029097A patent/CA3029097A1/en active Pending
- 2017-06-19 DK DK17732075.1T patent/DK3472165T3/da active
- 2017-06-19 KR KR1020197001839A patent/KR102500416B1/ko active Active
- 2017-06-19 HU HUE17732075A patent/HUE064919T2/hu unknown
- 2017-06-19 CN CN201780038709.2A patent/CN109311894B/zh active Active
- 2017-06-19 US US16/312,061 patent/US10561660B2/en active Active
- 2017-06-19 EP EP17732075.1A patent/EP3472165B1/en active Active
- 2017-06-19 SI SI201731456T patent/SI3472165T1/sl unknown
- 2017-06-19 ES ES17732075T patent/ES2964781T3/es active Active
- 2017-06-19 RU RU2019101002A patent/RU2753520C2/ru active
- 2017-06-19 PL PL17732075.1T patent/PL3472165T3/pl unknown
- 2017-06-19 PT PT177320751T patent/PT3472165T/pt unknown
- 2017-06-19 WO PCT/EP2017/064904 patent/WO2017220477A1/en not_active Ceased
- 2017-06-19 MX MX2018016419A patent/MX388660B/es unknown
- 2017-06-19 FI FIEP17732075.1T patent/FI3472165T3/fi active
-
2018
- 2018-12-16 IL IL263739A patent/IL263739B/en unknown
-
2019
- 2019-12-19 US US16/721,267 patent/US10918642B2/en active Active
-
2021
- 2021-01-04 US US17/140,471 patent/US11491158B2/en active Active
-
2022
- 2022-09-29 US US17/936,576 patent/US11833153B2/en active Active
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| IL263739B (en) | History of n-(converted-phenyl)-sulfonamide as kinase inhibitors | |
| IL268614B (en) | Aminotriazolopyridines as kinase inhibitors | |
| DK3298002T3 (da) | Heterocykliske amider som kinasehæmmere | |
| IL275207A (en) | An oxyfluoropiperidine derivative as a kinase inhibitor | |
| IL276269A (en) | Aminopyrrolotriazines as kinase inhibitors | |
| IL274207A (en) | Aminoimidazopyridazines as kinase inhibitors | |
| SG11202004918XA (en) | Amino-fluoropiperidine derivative as kinase inhibitor | |
| IL266789A (en) | Heterocyclic compounds as kinase inhibitors | |
| IL304547A (en) | 3-substituted benzamide derivatives as kinase inhibitors | |
| ZA201808238B (en) | Certain protein kinase inhibitors | |
| MA44607A (fr) | Inhibiteurs de kinase | |
| ZA201908372B (en) | Pyridoquinazoline derivatives useful as protein kinase inhibitors | |
| GB201613945D0 (en) | Compounds useful as kinase inhibitors | |
| TH1501004620A (th) | เฮทเทอโรไซคลิก เอไมด์ ในรูปสารยับยั้งไคเนส |