MX2014010494A - Derivados de pirazolo-triazina como inhibidores selectivos de cinasas dependientes de ciclina. - Google Patents
Derivados de pirazolo-triazina como inhibidores selectivos de cinasas dependientes de ciclina.Info
- Publication number
- MX2014010494A MX2014010494A MX2014010494A MX2014010494A MX2014010494A MX 2014010494 A MX2014010494 A MX 2014010494A MX 2014010494 A MX2014010494 A MX 2014010494A MX 2014010494 A MX2014010494 A MX 2014010494A MX 2014010494 A MX2014010494 A MX 2014010494A
- Authority
- MX
- Mexico
- Prior art keywords
- pyrazolo
- triazine derivatives
- diseases
- inhinitors
- dependent kinase
- Prior art date
Links
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- 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
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
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- 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
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- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P11/02—Nasal agents, e.g. decongestants
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- A—HUMAN NECESSITIES
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- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- 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
- C07D471/10—Spiro-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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
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- Communicable Diseases (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Physical Education & Sports Medicine (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Virology (AREA)
- Heart & Thoracic Surgery (AREA)
- Dermatology (AREA)
- Neurology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Gastroenterology & Hepatology (AREA)
- Urology & Nephrology (AREA)
- Molecular Biology (AREA)
- Vascular Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Transplantation (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Pain & Pain Management (AREA)
Abstract
La presente invención se refiere a derivados de pirazolo[1,5-a] [1,3,5] triazina y/o sales farmacéuticamente aceptables de los mismos; el uso de estos derivados como agentes farmacéuticamente activos, especialmente para la profilaxis y/o tratamiento de enfermedades infecciosas, incluidas las enfermedades oportunistas, enfermedades inmunológicas, enfermedades autoinmunes, enfermedades cardiovasculares, enfermedades proliferativas celulares, inflamación, disfunción eréctil y accidente cerebrovascular; y composiciones farmacéuticas que contienen al menos uno de dichos derivados de pirazolo[1,5-a] [1,3,5] triazina y/o sales farmacéuticamente aceptables de los mismos. Además, la presente invención se refiere al uso de dichos derivados de pirazolo [1,5-a] [1,3,5] triazina como inhibidores de una proteína cinasa.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP12157751.4A EP2634190A1 (en) | 2012-03-01 | 2012-03-01 | Pyrazolo-triazine derivatives as selective cyclin-dependent kinase inhinitors |
PCT/EP2013/054224 WO2013128028A1 (en) | 2012-03-01 | 2013-03-01 | Pyrazolo - triazine derivatives as selective cyclin- dependent kinase inhinitors |
Publications (2)
Publication Number | Publication Date |
---|---|
MX2014010494A true MX2014010494A (es) | 2015-04-08 |
MX347359B MX347359B (es) | 2017-04-06 |
Family
ID=47757629
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2014010494A MX347359B (es) | 2012-03-01 | 2013-03-01 | Derivados de pirazolo-triazina como inhibidores selectivos de cinasas dependientes de ciclina. |
Country Status (18)
Country | Link |
---|---|
US (1) | US9567345B2 (es) |
EP (2) | EP2634190A1 (es) |
JP (1) | JP6182549B2 (es) |
KR (1) | KR101821452B1 (es) |
CN (1) | CN104350054B (es) |
AU (1) | AU2013224848B2 (es) |
BR (1) | BR112014021189B1 (es) |
CA (1) | CA2865946C (es) |
DK (1) | DK2820020T3 (es) |
ES (1) | ES2583231T3 (es) |
HK (1) | HK1206014A1 (es) |
HU (1) | HUE029264T2 (es) |
IL (1) | IL234183A (es) |
MX (1) | MX347359B (es) |
RU (1) | RU2645347C2 (es) |
SG (1) | SG11201405129RA (es) |
WO (1) | WO2013128028A1 (es) |
ZA (1) | ZA201406078B (es) |
Families Citing this family (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
UA119247C2 (uk) | 2013-09-06 | 2019-05-27 | РОЙВЕНТ САЙЕНСИЗ ҐмбГ | Спіроциклічні сполуки як інгібітори триптофангідроксилази |
GB201403093D0 (en) | 2014-02-21 | 2014-04-09 | Cancer Rec Tech Ltd | Therapeutic compounds and their use |
PL3126352T3 (pl) | 2014-04-04 | 2019-04-30 | Syros Pharmaceuticals Inc | Inhibitory kinazy cyklinozależnej 7 (cdk7) |
US10336760B2 (en) | 2014-04-05 | 2019-07-02 | Syros Pharmaceuticals, Inc. | Inhibitors of cyclin-dependent kinase 7 (CDK7) |
CN107074887B (zh) | 2014-10-31 | 2020-12-22 | 宇部兴产株式会社 | 取代二氢吡咯并吡唑化合物 |
CN107530329B (zh) * | 2015-03-09 | 2021-10-08 | 奥瑞基尼探索技术有限公司 | 用作CDK抑制剂的吡唑并[1,5-a][1,3,5]三嗪和吡唑并[1,5-a]嘧啶衍生物 |
JP6787314B2 (ja) | 2015-06-15 | 2020-11-18 | 宇部興産株式会社 | 置換ジヒドロピロロピラゾール誘導体 |
EP3313842B1 (en) * | 2015-06-24 | 2020-04-15 | Curovir Ab | Pyrazolo[1,5-a]triazin-4-amine derivatives useful in therapy |
EP3436054B2 (en) | 2016-09-13 | 2022-07-27 | Allergan, Inc. | Stabilized non-protein clostridial toxin compositions |
CN106432249B (zh) * | 2016-09-30 | 2018-12-04 | 陕西科技大学 | 一类吡咯并[2,1-f][1,2,4]三嗪母核化合物的合成及其医药用途 |
WO2019032720A1 (en) | 2017-08-09 | 2019-02-14 | Sanford Burnham Prebys Medical Discovery Institute | APELIN RECEPTOR AGONISTS AND METHODS OF USE |
GB201715194D0 (en) | 2017-09-20 | 2017-11-01 | Carrick Therapeutics Ltd | Compounds and their therapeutic use |
EP3740489A1 (en) | 2018-01-17 | 2020-11-25 | GlaxoSmithKline Intellectual Property Development Limited | Pi4kiiibeta inhibitors |
SG11202009466UA (en) * | 2018-04-11 | 2020-10-29 | Qurient Co Ltd | Pharmaceutically active pyrazolo-triazine and/or pyrazolo-pyrimidine derivatives |
IL277770B2 (en) | 2018-04-11 | 2024-01-01 | Qurient Co Ltd | History of pyrazolo-triazine and/or pyrazolo-pyrimidine as selective inhibitors of cyclin-dependent kinase |
US11364234B2 (en) | 2018-09-12 | 2022-06-21 | The Governing Council Of The University Of Toronto | Compounds and methods for treating nematode infections |
US11517568B2 (en) | 2018-09-12 | 2022-12-06 | The Governing Council Of The University Of Toronto | Compounds and methods for treating nematode infections |
JP7530297B2 (ja) | 2018-11-14 | 2024-08-07 | Ube株式会社 | ジヒドロピロロピラゾール誘導体 |
CN110101703B (zh) * | 2019-05-06 | 2021-06-11 | 暨南大学 | Cdk7抑制剂在制备溃疡性结肠炎或结肠癌药物的应用 |
RU2713152C1 (ru) * | 2019-08-30 | 2020-02-04 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Алтайский государственный медицинский университет" Министерства здравоохранения Российской Федерации | Способ лечения хронической аллергической крапивницы на фоне описторхоза |
TW202146416A (zh) * | 2019-12-11 | 2021-12-16 | 德商拜耳廠股份有限公司 | 吡唑并三𠯤 |
GB201918541D0 (en) * | 2019-12-16 | 2020-01-29 | Carrick Therapeutics Ltd | Therapeutic compounds and their use |
CN110950871B (zh) * | 2019-12-25 | 2022-05-17 | 陕西师范大学 | 2-取代-4-芳氨基吡唑并三嗪衍生物及制备抗肿瘤药物的应用 |
WO2022136174A1 (en) * | 2020-12-21 | 2022-06-30 | Janssen Pharmaceutica Nv | Tricyclic pyrimidines as cyclin-dependent kinase 7 (cdk7) inhibitors |
EP4305040A1 (en) * | 2021-03-09 | 2024-01-17 | JANSSEN Pharmaceutica NV | Tricyclic pyridines as cyclin-dependent kinase 7 (cdk7) inhibitors |
WO2022266418A1 (en) * | 2021-06-17 | 2022-12-22 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Triazine inhibitors of cyclin-dependent kinases |
WO2023001061A1 (en) * | 2021-07-17 | 2023-01-26 | Jingrui Biopharma Co., Ltd. | Cdk7 selective inhibitors as anticancer agents |
WO2023006789A1 (en) | 2021-07-29 | 2023-02-02 | Syngenta Crop Protection Ag | Pesticidally active fused bicyclic heteroaromatic compounds |
CN118284610A (zh) * | 2021-11-23 | 2024-07-02 | 原真股份有限公司 | 用作cdk9抑制剂的吡唑并三嗪衍生物 |
CN114181217B (zh) * | 2022-01-10 | 2022-12-27 | 陕西师范大学 | 吡唑并[1,5-a][1,3,5]三嗪衍生物及其盐和在制备抗癌药物中的应用 |
AU2023235439A1 (en) * | 2022-03-18 | 2024-09-19 | Lead Discovery Center Gmbh | Cdk7 inhibitors for antiviral treatment |
WO2024175024A1 (zh) * | 2023-02-21 | 2024-08-29 | 杭州德睿智药科技有限公司 | 作为CDKs抑制剂的新型并杂环类新化合物及其应用 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US615968A (en) | 1898-12-13 | Apparatus for treating ores | ||
CZ20012765A3 (cs) * | 1999-02-01 | 2002-08-14 | Cv Therapeutics, Inc. | Purinové inhibitory kinasy 2 a Ikappa - Aalfa dependentní na cyklinu |
US7119200B2 (en) * | 2002-09-04 | 2006-10-10 | Schering Corporation | Pyrazolopyrimidines as cyclin dependent kinase inhibitors |
TW200536536A (en) | 2004-02-25 | 2005-11-16 | Schering Corp | Pyrazolotriazines as kinase inhibitors |
CZ302122B6 (cs) * | 2009-01-28 | 2010-10-20 | Univerzita Palackého v Olomouci | Substituované deriváty 6-(2-aminobenzylamino)purinu, jejich použití jako léciva a prípravky tyto slouceniny obsahující |
FR2943058B1 (fr) * | 2009-03-11 | 2011-06-03 | Centre Nat Rech Scient | Derives de pyrazolo°1,5-a!-1,3,5-triazines, leur preparation et leur application en therapeutique. |
CZ302711B6 (cs) * | 2009-06-03 | 2011-09-14 | Univerzita Palackého v Olomouci | Substituované deriváty 6-(2-hydroxybenzylamino)purinu, jejich použití jako léciva a farmaceutické prípravky tyto slouceniny obsahující |
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2012
- 2012-03-01 EP EP12157751.4A patent/EP2634190A1/en not_active Withdrawn
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2013
- 2013-03-01 US US14/381,146 patent/US9567345B2/en active Active
- 2013-03-01 JP JP2014559259A patent/JP6182549B2/ja active Active
- 2013-03-01 DK DK13707008.2T patent/DK2820020T3/en active
- 2013-03-01 CN CN201380011917.5A patent/CN104350054B/zh active Active
- 2013-03-01 SG SG11201405129RA patent/SG11201405129RA/en unknown
- 2013-03-01 HU HUE13707008A patent/HUE029264T2/en unknown
- 2013-03-01 BR BR112014021189-2A patent/BR112014021189B1/pt active IP Right Grant
- 2013-03-01 CA CA2865946A patent/CA2865946C/en active Active
- 2013-03-01 WO PCT/EP2013/054224 patent/WO2013128028A1/en active Application Filing
- 2013-03-01 EP EP13707008.2A patent/EP2820020B1/en active Active
- 2013-03-01 KR KR1020147027812A patent/KR101821452B1/ko active IP Right Grant
- 2013-03-01 MX MX2014010494A patent/MX347359B/es active IP Right Grant
- 2013-03-01 ES ES13707008.2T patent/ES2583231T3/es active Active
- 2013-03-01 RU RU2014139705A patent/RU2645347C2/ru active
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US20150018329A1 (en) | 2015-01-15 |
CN104350054B (zh) | 2017-06-13 |
CA2865946C (en) | 2020-01-21 |
HK1206014A1 (en) | 2015-12-31 |
ES2583231T3 (es) | 2016-09-19 |
IL234183A (en) | 2016-11-30 |
MX347359B (es) | 2017-04-06 |
WO2013128028A8 (en) | 2014-10-02 |
JP6182549B2 (ja) | 2017-08-16 |
KR20140131994A (ko) | 2014-11-14 |
WO2013128028A1 (en) | 2013-09-06 |
SG11201405129RA (en) | 2014-09-26 |
CA2865946A1 (en) | 2013-09-06 |
US9567345B2 (en) | 2017-02-14 |
DK2820020T3 (en) | 2016-07-04 |
HUE029264T2 (en) | 2017-02-28 |
JP2015511952A (ja) | 2015-04-23 |
AU2013224848B2 (en) | 2017-06-29 |
BR112014021189B1 (pt) | 2022-08-16 |
RU2014139705A (ru) | 2016-04-20 |
ZA201406078B (en) | 2016-08-31 |
AU2013224848A1 (en) | 2014-08-28 |
CN104350054A (zh) | 2015-02-11 |
EP2820020B1 (en) | 2016-04-06 |
BR112014021189A2 (es) | 2017-06-20 |
RU2645347C2 (ru) | 2018-02-21 |
EP2820020A1 (en) | 2015-01-07 |
EP2634190A1 (en) | 2013-09-04 |
KR101821452B1 (ko) | 2018-01-23 |
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