EA034822B9 - Производные n-пиридинилацетамида в качестве ингибиторов сигнального пути wnt - Google Patents
Производные n-пиридинилацетамида в качестве ингибиторов сигнального пути wntInfo
- Publication number
- EA034822B9 EA034822B9 EA201790637A EA201790637A EA034822B9 EA 034822 B9 EA034822 B9 EA 034822B9 EA 201790637 A EA201790637 A EA 201790637A EA 201790637 A EA201790637 A EA 201790637A EA 034822 B9 EA034822 B9 EA 034822B9
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- compounds
- inhibitors
- relates
- signalling pathway
- wnt signalling
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 3
- 230000019491 signal transduction Effects 0.000 title abstract 3
- MIQSEHQDHNIQNF-UHFFFAOYSA-N N-(2H-pyridin-1-yl)acetamide Chemical class CC(=O)NN1CC=CC=C1 MIQSEHQDHNIQNF-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 6
- 206010028980 Neoplasm Diseases 0.000 abstract 2
- 201000009030 Carcinoma Diseases 0.000 abstract 1
- 241001481760 Erethizon dorsatum Species 0.000 abstract 1
- 206010025323 Lymphomas Diseases 0.000 abstract 1
- 101100408855 Mus musculus Porcn gene Proteins 0.000 abstract 1
- 206010039491 Sarcoma Diseases 0.000 abstract 1
- 208000000453 Skin Neoplasms Diseases 0.000 abstract 1
- 238000011394 anticancer treatment Methods 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 230000002708 enhancing effect Effects 0.000 abstract 1
- 230000002489 hematologic effect Effects 0.000 abstract 1
- 208000032839 leukemia Diseases 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 201000001441 melanoma Diseases 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 201000000849 skin cancer Diseases 0.000 abstract 1
Classifications
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- 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
-
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- 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
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- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- 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
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
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- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A61K31/535—Heterocyclic 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
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- 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
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- C07D413/14—Heterocyclic 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
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- C07D417/14—Heterocyclic 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
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- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Urology & Nephrology (AREA)
- Immunology (AREA)
- Biomedical Technology (AREA)
- Diabetes (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Psychology (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pulmonology (AREA)
- Gastroenterology & Hepatology (AREA)
- Pain & Pain Management (AREA)
- Oncology (AREA)
- Ophthalmology & Optometry (AREA)
- Cardiology (AREA)
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Abstract
Изобретение относится к соединениям. Конкретно, настоящее изобретение относится к соединениям формулы (III)Более конкретно, настоящее изобретение относится к соединениям, применимым в качестве ингибиторов сигнального пути Wnt. В частности, настоящее изобретение относится к ингибиторам поркупина (Porcn). Кроме того, изобретение относится к способам получения соединений и применениям соединений. Таким образом, соединения по настоящему изобретению могут применяться в лечении состояний, опосредуемых сигнальным путем Wnt, например, для лечения рака, саркомы, меланомы, рака кожи, гематологических опухолей, лимфомы, рака и лейкоза; или повышения эффективности противоракового лечения.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB1417829.7A GB201417829D0 (en) | 2014-10-08 | 2014-10-08 | Compounds |
GBGB1511387.1A GB201511387D0 (en) | 2015-06-29 | 2015-06-29 | Compounds |
PCT/GB2015/052939 WO2016055786A1 (en) | 2014-10-08 | 2015-10-08 | N-pyridinyl acetamide derivatives as inhibitors of the wnt signalling pathway |
Publications (3)
Publication Number | Publication Date |
---|---|
EA201790637A1 EA201790637A1 (ru) | 2017-10-31 |
EA034822B1 EA034822B1 (ru) | 2020-03-25 |
EA034822B9 true EA034822B9 (ru) | 2020-10-23 |
Family
ID=54337304
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201790637A EA034822B9 (ru) | 2014-10-08 | 2015-10-08 | Производные n-пиридинилацетамида в качестве ингибиторов сигнального пути wnt |
Country Status (23)
Country | Link |
---|---|
US (4) | US10047079B2 (ru) |
EP (1) | EP3204378B3 (ru) |
JP (2) | JP6722178B2 (ru) |
KR (1) | KR102525131B1 (ru) |
CN (1) | CN107108565B (ru) |
AU (1) | AU2015329784C1 (ru) |
CA (1) | CA2960446C (ru) |
CY (1) | CY1122243T1 (ru) |
DK (1) | DK3204378T6 (ru) |
EA (1) | EA034822B9 (ru) |
ES (1) | ES2754349T7 (ru) |
HR (1) | HRP20191826T4 (ru) |
HU (1) | HUE046914T2 (ru) |
IL (1) | IL251131B (ru) |
LT (1) | LT3204378T (ru) |
MX (1) | MX2017004637A (ru) |
PH (1) | PH12017500611A1 (ru) |
PL (1) | PL3204378T6 (ru) |
PT (1) | PT3204378T (ru) |
SG (1) | SG11201701837UA (ru) |
SI (1) | SI3204378T1 (ru) |
WO (1) | WO2016055786A1 (ru) |
ZA (1) | ZA201701842B (ru) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3204378B3 (en) | 2014-10-08 | 2022-05-25 | Redx Pharma PLC | N-pyridinyl acetamide derivatives as inhibitors of the wnt signalling pathway |
MX2017004639A (es) | 2014-10-08 | 2017-07-17 | Redx Pharma Plc | Derivados de n-piridinil acetamida como inhibidores de la via de señalizacion wnt. |
WO2017156350A1 (en) | 2016-03-09 | 2017-09-14 | K-Gen, Inc. | Methods of cancer treatment |
US10793544B2 (en) | 2016-09-01 | 2020-10-06 | The Board Of Regents Of The University Of Texas System | Disubstituted and trisubstituted 1,2,3-triazoles as Wnt inhibitors |
US10357493B2 (en) | 2017-03-10 | 2019-07-23 | Selenity Therapeutics (Bermuda), Ltd. | Metalloenzyme inhibitor compounds |
JP2019064975A (ja) * | 2017-10-03 | 2019-04-25 | 国立大学法人 熊本大学 | 抗がん剤 |
AU2019215799B2 (en) * | 2018-02-01 | 2022-04-14 | The University Of Sydney | Anti-cancer compounds |
PL3762368T3 (pl) | 2018-03-08 | 2022-06-06 | Incyte Corporation | ZWIĄZKI AMINOPIRAZYNODIOLOWE JAKO INHIBITORY PI3K-γ |
WO2020010003A1 (en) | 2018-07-02 | 2020-01-09 | Incyte Corporation | AMINOPYRAZINE DERIVATIVES AS PI3K-γ INHIBITORS |
US10961534B2 (en) | 2018-07-13 | 2021-03-30 | University of Pittsburgh—of the Commonwealth System of Higher Education | Methods of treating porphyria |
IL294052A (en) | 2019-12-20 | 2022-08-01 | Tenaya Therapeutics Inc | Fluoroalkyl-oxadiazoles and their uses |
WO2022094477A1 (en) * | 2020-11-02 | 2022-05-05 | Icahn School Of Medicine At Mount Sinai | Methods of treating tumors and cancers having dysregulated wnt signaling pathways |
GB202100526D0 (en) | 2021-01-15 | 2021-03-03 | Redx Pharma Plc | Pharmaceutical formulation |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
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SK86699A3 (en) | 1996-12-23 | 2000-11-07 | Du Pont Pharm Co | Nitrogen containing heteroaromatics as factor xa inhibitors |
ATE236890T1 (de) | 1996-12-23 | 2003-04-15 | Bristol Myers Squibb Pharma Co | Sauerstoff oder schwefel enthaltende 5-gliedrige heteroaromatishe derivative als factor xa hemmer |
GB0226583D0 (en) | 2002-11-14 | 2002-12-18 | Cyclacel Ltd | Compounds |
SE0203654D0 (sv) | 2002-12-09 | 2002-12-09 | Astrazeneca Ab | New compounds |
WO2004071447A2 (en) * | 2003-02-12 | 2004-08-26 | Transtech Pharma Inc. | Substituted azole derivatives as therapeutic agents |
JP2008515961A (ja) | 2004-10-12 | 2008-05-15 | アストラゼネカ アクチボラグ | 癌に対する使用のためのキナゾリン誘導体 |
EP2148865B1 (en) * | 2007-04-30 | 2017-05-17 | Genentech, Inc. | Pyrazole inhibitors of wnt signaling |
EP2231602A1 (en) | 2007-12-13 | 2010-09-29 | Amgen, Inc | Gamma secretase modulators |
UA103918C2 (en) * | 2009-03-02 | 2013-12-10 | Айерем Элелси | N-(hetero)aryl, 2-(hetero)aryl-substituted acetamides for use as wnt signaling modulators |
US8993612B2 (en) | 2009-10-08 | 2015-03-31 | Rhizen Pharmaceuticals Sa | Modulators of calcium release-activated calcium channel and methods for treatment of non-small cell lung cancer |
UY33469A (es) * | 2010-06-29 | 2012-01-31 | Irm Llc Y Novartis Ag | Composiciones y metodos para modular la via de señalizacion de wnt |
CN104302782A (zh) * | 2012-02-28 | 2015-01-21 | 诺华股份有限公司 | 利用rnf43突变状态选择wnt信号转导抑制剂给药的癌症患者 |
GB2513403A (en) | 2013-04-26 | 2014-10-29 | Agency Science Tech & Res | WNT pathway modulators |
MX2017004639A (es) | 2014-10-08 | 2017-07-17 | Redx Pharma Plc | Derivados de n-piridinil acetamida como inhibidores de la via de señalizacion wnt. |
EP3204378B3 (en) | 2014-10-08 | 2022-05-25 | Redx Pharma PLC | N-pyridinyl acetamide derivatives as inhibitors of the wnt signalling pathway |
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2015
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- 2015-10-08 LT LT15782041T patent/LT3204378T/lt unknown
- 2015-10-08 KR KR1020177011823A patent/KR102525131B1/ko active IP Right Grant
- 2015-10-08 MX MX2017004637A patent/MX2017004637A/es active IP Right Grant
- 2015-10-08 HU HUE15782041A patent/HUE046914T2/hu unknown
- 2015-10-08 ES ES15782041T patent/ES2754349T7/es active Active
- 2015-10-08 JP JP2017518951A patent/JP6722178B2/ja active Active
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