MA32232B1 - Nouveaux compoés hétérocycliques et leurs utilisations - Google Patents
Nouveaux compoés hétérocycliques et leurs utilisationsInfo
- Publication number
- MA32232B1 MA32232B1 MA33252A MA33252A MA32232B1 MA 32232 B1 MA32232 B1 MA 32232B1 MA 33252 A MA33252 A MA 33252A MA 33252 A MA33252 A MA 33252A MA 32232 B1 MA32232 B1 MA 32232B1
- Authority
- MA
- Morocco
- Prior art keywords
- heterocyclic compounds
- novel heterocyclic
- novel
- raf kinase
- compositions
- Prior art date
Links
- 150000002391 heterocyclic compounds Chemical class 0.000 title 1
- 239000000203 mixture Substances 0.000 abstract 2
- 102000009929 raf Kinases Human genes 0.000 abstract 2
- 108010077182 raf Kinases Proteins 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 150000001420 substituted heterocyclic compounds Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—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
- A61K31/435—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
- A61K31/4439—Non 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
-
- 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
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D405/14—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 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—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
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
La présente invention concerne de nouveaux composés hétérocycliques substitués, des compositions les contenant et leurs procédés d'utilisation dans le cadre de l'inhibition de l'activité de la raf kinase. Les nouveaux composés et compositions peuvent être utilisés soit seuls, soit en combinaison avec au moins un agent supplémentaire afin de traiter un trouble induit par la raf kinase, tel que le cancer.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3872308P | 2008-03-21 | 2008-03-21 | |
| US20845809P | 2009-02-24 | 2009-02-24 | |
| PCT/EP2009/053245 WO2009115572A2 (fr) | 2008-03-21 | 2009-03-19 | Nouveaux composés hétérocycliques et leurs utilisations |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA32232B1 true MA32232B1 (fr) | 2011-04-01 |
Family
ID=40734805
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA33252A MA32232B1 (fr) | 2008-03-21 | 2010-10-15 | Nouveaux compoés hétérocycliques et leurs utilisations |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US8129394B2 (fr) |
| EP (1) | EP2274300A2 (fr) |
| JP (2) | JP5384611B2 (fr) |
| KR (2) | KR101408517B1 (fr) |
| CN (1) | CN102015686B (fr) |
| AR (1) | AR071283A1 (fr) |
| AU (1) | AU2009227013B2 (fr) |
| BR (1) | BRPI0908906A2 (fr) |
| CA (1) | CA2718936A1 (fr) |
| CL (1) | CL2009000687A1 (fr) |
| CO (1) | CO6311078A2 (fr) |
| CR (1) | CR11681A (fr) |
| DO (1) | DOP2010000280A (fr) |
| EA (1) | EA201001456A1 (fr) |
| EC (1) | ECSP10010559A (fr) |
| IL (1) | IL208063A0 (fr) |
| MA (1) | MA32232B1 (fr) |
| MX (1) | MX2010010317A (fr) |
| NI (1) | NI201000156A (fr) |
| PE (1) | PE20091656A1 (fr) |
| SM (1) | SMAP201000115A (fr) |
| SV (1) | SV2010003673A (fr) |
| TW (1) | TW201000457A (fr) |
| UY (1) | UY31724A (fr) |
| WO (1) | WO2009115572A2 (fr) |
| ZA (1) | ZA201006505B (fr) |
Families Citing this family (81)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT2348023E (pt) | 2005-12-13 | 2015-09-15 | Incyte Corp | Pirrolo[2,3-b] pirimidinas e pirrolo[2,3-b]piridinas substituídas com heteroarilo como inibidores de janus quinase |
| EP2535330A3 (fr) * | 2006-10-23 | 2012-12-26 | Takeda Pharmaceutical Company Limited | Dérivé d'iminopyridine et son utilisation |
| ES2714092T3 (es) | 2007-06-13 | 2019-05-27 | Incyte Holdings Corp | Uso de sales del inhibidor de quinasas Janus (R)-3-(4-(7H-pirrolo[2,3-d]pirimidin-4-il)-1H-pirazol-1-il)-3-ciclopentilpropanonitrilo |
| US8268834B2 (en) | 2008-03-19 | 2012-09-18 | Novartis Ag | Pyrazine derivatives that inhibit phosphatidylinositol 3-kinase enzyme |
| US8865732B2 (en) * | 2008-03-21 | 2014-10-21 | Novartis Ag | Heterocyclic compounds and uses thereof |
| US8481569B2 (en) * | 2008-04-23 | 2013-07-09 | Takeda Pharmaceutical Company Limited | Iminopyridine derivatives and use thereof |
| US20110039892A1 (en) * | 2008-04-23 | 2011-02-17 | Takeda Pharmaceutical Company Limited | Iminopyridine derivative and use thereof |
| AU2009238938A1 (en) * | 2008-04-23 | 2009-10-29 | Takeda Pharmaceutical Company Limited | Iminopyridine derivatives and use thereof |
| ME03556B (fr) | 2009-05-22 | 2020-07-20 | Incyte Holdings Corp | 3-[4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl]octane- ou heptane-nitrile en tant qu'inhibiteurs de jak |
| SG176130A1 (en) | 2009-05-22 | 2011-12-29 | Incyte Corp | N-(HETERO)ARYL-PYRROLIDINE DERIVATIVES OF PYRAZOL-4-YL-PYRROLO[2,3-d]PYRIMIDINES AND PYRROL-3-YL-PYRROLO[2,3-d]PYRIMIDINES AS JANUS KINASE INHIBITORS |
| US8242260B2 (en) | 2009-08-28 | 2012-08-14 | Novartis Ag | Compounds and compositions as protein kinase inhibitors |
| JO3002B1 (ar) | 2009-08-28 | 2016-09-05 | Irm Llc | مركبات و تركيبات كمثبطات كيناز بروتين |
| AR078012A1 (es) | 2009-09-01 | 2011-10-05 | Incyte Corp | Derivados heterociclicos de las pirazol-4-il- pirrolo (2,3-d) pirimidinas como inhibidores de la quinasa janus |
| EP2519517B1 (fr) | 2009-12-29 | 2015-03-25 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de kinase raf de type ii |
| RU2571930C2 (ru) | 2010-02-25 | 2015-12-27 | Дана-Фарбер Кэнсер Инститьют, Инк. | Мутации braf, обеспечивающие резистентность к ингибиторам braf |
| TWI694826B (zh) | 2010-03-10 | 2020-06-01 | 美商英塞特公司 | 作為jak1抑制劑之哌啶-4-基三亞甲亞胺衍生物 |
| MY178634A (en) | 2010-05-21 | 2020-10-19 | Incyte Corp | Topical formulation for a jak inhibitor |
| EP2592130B1 (fr) * | 2010-07-09 | 2015-01-21 | Mitsubishi Gas Chemical Company, Inc. | Matériau photochromique |
| CN103097384B (zh) | 2010-07-12 | 2017-02-15 | 拜耳知识产权有限责任公司 | 取代的咪唑并[1,2‑a]嘧啶和吡啶 |
| EP2640723A1 (fr) | 2010-11-19 | 2013-09-25 | Incyte Corporation | Dérivés pyrrolopyridine et pyrrolopyrimidine à substitution cyclobutyle utilisés comme inhibiteurs des jak |
| CA2818545C (fr) | 2010-11-19 | 2019-04-16 | Incyte Corporation | Pyrrolopyridines et pyrrolopyrimidines a substitution heterocyclique utilisees en tant qu'inhibiteurs des jak |
| WO2012135631A1 (fr) * | 2011-03-30 | 2012-10-04 | Arrien Pharmaeuticals Llc | 5-(pyrazin-2-yl)-1h-pyrazolo[3,4-b]pyridine substituée et dérivés de pyrazolo[3,4-b]pyridine en tant qu'inhibiteurs de protéine kinase |
| KR20140040819A (ko) | 2011-06-20 | 2014-04-03 | 인사이트 코포레이션 | Jak 저해제로서의 아제티디닐 페닐, 피리딜 또는 피라지닐 카르복스아미드 유도체 |
| TW201313721A (zh) | 2011-08-18 | 2013-04-01 | Incyte Corp | 作為jak抑制劑之環己基氮雜環丁烷衍生物 |
| UA111854C2 (uk) | 2011-09-07 | 2016-06-24 | Інсайт Холдінгс Корпорейшн | Способи і проміжні сполуки для отримання інгібіторів jak |
| WO2013059634A1 (fr) | 2011-10-20 | 2013-04-25 | The Regents Of The University Of California | Utilisation d'inhibiteurs de cdk9 pour réduire la dégradation cartilagineuse |
| CN108542906A (zh) | 2011-11-11 | 2018-09-18 | 诺华股份有限公司 | 治疗增生性疾病的方法 |
| SI2782557T1 (sl) | 2011-11-23 | 2019-02-28 | Array Biopharma, Inc., | Farmacevtske formulacije |
| US9408885B2 (en) | 2011-12-01 | 2016-08-09 | Vib Vzw | Combinations of therapeutic agents for treating melanoma |
| CN103159735B (zh) * | 2011-12-10 | 2015-12-09 | 通化济达医药有限公司 | 取代的咪唑激酶抑制剂 |
| JP2015503505A (ja) * | 2011-12-23 | 2015-02-02 | ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. | ヘテロアリールおよびその使用 |
| EP2844251B1 (fr) * | 2012-05-03 | 2018-08-01 | Saint Louis College of Pharmacy | Compositions et procédés pour augmenter des peptides neurotrophiques |
| US9193733B2 (en) | 2012-05-18 | 2015-11-24 | Incyte Holdings Corporation | Piperidinylcyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as JAK inhibitors |
| WO2014047330A1 (fr) * | 2012-09-19 | 2014-03-27 | Jean-Michel Vernier | Nouveaux inhibiteurs de raf kinase |
| KR20210037012A (ko) | 2012-11-15 | 2021-04-05 | 인사이트 홀딩스 코포레이션 | 룩솔리티니브의 서방성 제형 |
| SI2964650T1 (sl) | 2013-03-06 | 2019-05-31 | Incyte Holdings Corporation | Postopki in vmesne spojine za izdelavo inhibitorja JAK |
| US9242969B2 (en) | 2013-03-14 | 2016-01-26 | Novartis Ag | Biaryl amide compounds as kinase inhibitors |
| EA201690357A1 (ru) | 2013-08-07 | 2016-07-29 | Инсайт Корпорейшн | Лекарственные формы с замедленным высвобождением для ингибитора jak1 |
| US9498467B2 (en) | 2014-05-30 | 2016-11-22 | Incyte Corporation | Treatment of chronic neutrophilic leukemia (CNL) and atypical chronic myeloid leukemia (aCML) by inhibitors of JAK1 |
| UY36294A (es) | 2014-09-12 | 2016-04-29 | Novartis Ag | Compuestos y composiciones como inhibidores de quinasa |
| HK1243021A1 (zh) | 2014-10-14 | 2018-07-06 | The Regents Of The University Of California | 使用cdk9和brd4抑制剂来抑制炎症 |
| AU2015371251B2 (en) | 2014-12-23 | 2020-06-11 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 (CDK7) |
| KR101665231B1 (ko) * | 2015-01-30 | 2016-10-13 | 순천향대학교 산학협력단 | 티오페닐 그룹을 갖는 티아졸계 화합물 및 이를 유효성분으로 포함하는 항진균제 |
| EP3253386B1 (fr) * | 2015-02-04 | 2023-03-01 | Medpacto Inc. | Composition pharmaceutique pour prévenir ou traiter la leucémie myéloïde chronique et son procédé d'utilisation |
| EP3273966B1 (fr) | 2015-03-27 | 2023-05-03 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de kinases cycline-dépendantes |
| GB201614940D0 (en) * | 2016-09-02 | 2016-10-19 | Glaxosmithkline Intellectual Property (No 2) Ltd | Chemical compounds |
| GB201614934D0 (en) * | 2016-09-02 | 2016-10-19 | Glaxosmithkline Intellectual Property (No 2) Ltd | Chemical compounds |
| US10973829B2 (en) | 2016-09-19 | 2021-04-13 | Novartis Ag | Therapeutic uses of a C-RAF inhibitor |
| AU2017363307B2 (en) | 2016-11-22 | 2021-07-29 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 12 (CDK12) and uses thereof |
| KR20230020566A (ko) | 2017-01-10 | 2023-02-10 | 바이엘 악티엔게젤샤프트 | 해충 방제제로서의 헤테로사이클 유도체 |
| KR102515694B1 (ko) | 2017-01-10 | 2023-03-29 | 바이엘 악티엔게젤샤프트 | 해충 방제제로서의 헤테로사이클 유도체 |
| JP7341060B2 (ja) | 2017-02-10 | 2023-09-08 | アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル | Mapk経路の活性化に関連付けられる癌の処置のための方法及び医薬組成物 |
| JP2020512400A (ja) * | 2017-03-23 | 2020-04-23 | クラヴィウス ファーマシューティカルズ,エルエルシー | TGFβの阻害のための三置換イミダゾールおよび治療方法 |
| IL311471A (en) | 2017-05-02 | 2024-05-01 | Novartis Ag | Combination therapy |
| JP7038994B2 (ja) * | 2017-10-16 | 2022-03-22 | 国立大学法人金沢大学 | 炭素繊維強化プラスチックの製造方法、炭素繊維強化プラスチック及びセルロース系樹脂 |
| AR113922A1 (es) | 2017-12-08 | 2020-07-01 | Incyte Corp | Terapia de combinación de dosis baja para el tratamiento de neoplasias mieloproliferativas |
| WO2019133810A1 (fr) | 2017-12-28 | 2019-07-04 | Tract Pharmaceuticals, Inc. | Systèmes de culture de cellules souches pour cellules souches épithéliales colonnaires, et leurs utilisations |
| UA127488C2 (uk) | 2018-01-30 | 2023-09-06 | Інсайт Корпорейшн | Способи одержання (1-(3-фтор-2-(трифторметил)ізонікотиноїл)піперидин-4-ону) |
| US11304949B2 (en) | 2018-03-30 | 2022-04-19 | Incyte Corporation | Treatment of hidradenitis suppurativa using JAK inhibitors |
| WO2020005807A1 (fr) | 2018-06-25 | 2020-01-02 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de kinase de la famille taire et utilisations correspondantes |
| JP7262843B2 (ja) * | 2018-07-12 | 2023-04-24 | 深▲チェン▼市塔吉瑞生物医薬有限公司 | ジアリールピラゾール化合物、該化合物を含む組成物およびその使用 |
| WO2020041562A1 (fr) | 2018-08-22 | 2020-02-27 | Clavius Pharmaceuticals, Llc | Imidazoles substitués pour l'inhibition de tgf-bêta et méthodes de traitement |
| US11066404B2 (en) | 2018-10-11 | 2021-07-20 | Incyte Corporation | Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors |
| JP7660063B2 (ja) | 2018-12-28 | 2025-04-10 | ダナ-ファーバー キャンサー インスティテュート, インコーポレイテッド | サイクリン依存性キナーゼ7のインヒビターおよびそれらの使用 |
| WO2020150091A1 (fr) | 2019-01-15 | 2020-07-23 | Merck Sharp & Dohme Corp. | Inhibiteurs d'histone désacétylase utiles pour le traitement ou la prévention d'une infection par le vih |
| US11384083B2 (en) | 2019-02-15 | 2022-07-12 | Incyte Corporation | Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors |
| WO2020180959A1 (fr) | 2019-03-05 | 2020-09-10 | Incyte Corporation | Composés de pyrazolyl pyrimidinylamine en tant qu'inhibiteurs de cdk2 |
| WO2020192302A1 (fr) * | 2019-03-27 | 2020-10-01 | 广州必贝特医药技术有限公司 | Composé d'imidazole tri-substitué contenant de la pyrimidine et utilisation associée |
| US11919904B2 (en) | 2019-03-29 | 2024-03-05 | Incyte Corporation | Sulfonylamide compounds as CDK2 inhibitors |
| US11447494B2 (en) | 2019-05-01 | 2022-09-20 | Incyte Corporation | Tricyclic amine compounds as CDK2 inhibitors |
| US11440914B2 (en) | 2019-05-01 | 2022-09-13 | Incyte Corporation | Tricyclic amine compounds as CDK2 inhibitors |
| EP4563150A3 (fr) | 2019-05-13 | 2025-07-23 | Novartis AG | Nouvelles formes cristallines de n-(3-(2-(2-hydroxyéthoxy)-6-morpholinopyridin-4-yl)-4-méthylphényl-2(trifluorométhyl)isonicotinamide en tant qu'inhibiteurs de raf pour le traitement du cancer |
| MX2022001940A (es) | 2019-08-14 | 2022-05-10 | Incyte Corp | Compuestos de imidazolil pirimidinilamina como inhibidores de cdk2. |
| CN115298177B (zh) | 2019-10-11 | 2025-01-17 | 因赛特公司 | 作为cdk2抑制剂的双环胺 |
| US11833155B2 (en) | 2020-06-03 | 2023-12-05 | Incyte Corporation | Combination therapy for treatment of myeloproliferative neoplasms |
| EP4175961A1 (fr) | 2020-07-02 | 2023-05-10 | Bayer Aktiengesellschaft | Dérivés d'hétérocyclène utiles en tant qu'agents de lutte contre les nuisibles |
| US11981671B2 (en) | 2021-06-21 | 2024-05-14 | Incyte Corporation | Bicyclic pyrazolyl amines as CDK2 inhibitors |
| US11976073B2 (en) | 2021-12-10 | 2024-05-07 | Incyte Corporation | Bicyclic amines as CDK2 inhibitors |
| US11905272B1 (en) | 2023-09-12 | 2024-02-20 | King Faisal University | 3-(2-(4-methoxypyridin-3-yl)-4,5-diphenyl-1H-imidazol-1-yl)-N,N-dimethylpropan-1-amine as an anti-cancer compound |
| US11932619B1 (en) | 2023-09-13 | 2024-03-19 | King Faisal University | 3-(2-(6-Methoxypyridin-3-yl)-4,5-diphenyl-1H-imidazol-1-yl)-N,N-dimethylpropan-1-amine as an anticancer compound |
| US11993579B1 (en) | 2023-09-13 | 2024-05-28 | King Faisal University | 3-(1-(3-(dimethylamino)propyl)-4,5-diphenyl-1h-imidazol-2-yl)pyridin-4-ol as an anti-microbial compound |
Family Cites Families (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3707475A (en) * | 1970-11-16 | 1972-12-26 | Pfizer | Antiinflammatory imidazoles |
| JPS5613715A (en) * | 1979-07-13 | 1981-02-10 | Nec Corp | Manufacture of coil |
| DE3029376A1 (de) * | 1980-07-31 | 1982-03-18 | Nepera Chemical Co. Inc., Harriman, N.Y. | Verfahren zur herstellung von 2,4,5-tris-pyridylimidazolen |
| US5243517A (en) * | 1988-08-03 | 1993-09-07 | Westinghouse Electric Corp. | Method and apparatus for physiological evaluation of short films and entertainment materials |
| JP2722586B2 (ja) | 1989-01-13 | 1998-03-04 | 大正製薬株式会社 | インドリルイミダゾール誘導体 |
| JP2808460B2 (ja) * | 1989-11-16 | 1998-10-08 | 大正製薬株式会社 | イミダゾール誘導体 |
| US6850252B1 (en) * | 1999-10-05 | 2005-02-01 | Steven M. Hoffberg | Intelligent electronic appliance system and method |
| US5436830A (en) * | 1993-02-01 | 1995-07-25 | Zaltman; Gerald | Metaphor elicitation method and apparatus |
| US5676148A (en) * | 1995-03-31 | 1997-10-14 | Siemens Medical Systems Inc. | Method and system for doppler ultrasound audio dealiasing |
| US5717100A (en) * | 1995-10-06 | 1998-02-10 | Merck & Co., Inc. | Substituted imidazoles having anti-cancer and cytokine inhibitory activity |
| AU702146B2 (en) * | 1995-10-06 | 1999-02-11 | Merck & Co., Inc. | Substituted imidazoles having anti-cancer and cytokine inhibitory activity |
| US5676138A (en) * | 1996-03-15 | 1997-10-14 | Zawilinski; Kenneth Michael | Emotional response analyzer system with multimedia display |
| EP0923579A1 (fr) * | 1996-08-27 | 1999-06-23 | Novartis AG | 1,2,4,6-thiatriazines s-substituees desherbantes |
| US6099319A (en) * | 1998-02-24 | 2000-08-08 | Zaltman; Gerald | Neuroimaging as a marketing tool |
| US6315569B1 (en) * | 1998-02-24 | 2001-11-13 | Gerald Zaltman | Metaphor elicitation technique with physiological function monitoring |
| US6358201B1 (en) * | 1999-03-02 | 2002-03-19 | Doc L. Childre | Method and apparatus for facilitating physiological coherence and autonomic balance |
| JP2000302680A (ja) * | 1999-04-23 | 2000-10-31 | Takeda Chem Ind Ltd | 脳保護剤 |
| DE60015594T2 (de) * | 1999-11-22 | 2005-10-27 | Smithkline Beecham P.L.C., Brentford | Imidazolderivate und deren verwendung als raf kinase inhibitoren |
| MXPA02007134A (es) * | 2000-01-18 | 2003-03-27 | Vertex Pharma | Inhibidores de girasa y usos de los mismos. |
| AR029803A1 (es) * | 2000-02-21 | 2003-07-16 | Smithkline Beecham Plc | Imidazoles sustituidos con piridilo y composiciones farmaceuticas que las comprenden |
| GB0005357D0 (en) * | 2000-03-06 | 2000-04-26 | Smithkline Beecham Plc | Compounds |
| GB0007405D0 (en) * | 2000-03-27 | 2000-05-17 | Smithkline Beecham Corp | Compounds |
| ES2233647T3 (es) * | 2000-05-19 | 2005-06-16 | The Nutrasweet Company | Sintesis de n- n-(3,3-dimetilbutil)-l-alfa- aspartil-l- fenilalanina 1-metil ester utilizando "nuevos derivados de laoxazolidinona". |
| US20040053943A1 (en) * | 2000-11-20 | 2004-03-18 | Adams Jerry L. | Novel compounds |
| ATE341539T1 (de) * | 2001-01-26 | 2006-10-15 | Chugai Pharmaceutical Co Ltd | Malonyl coa-decarboxylase inhibitoren als stoffwechselmodulatoren |
| AR039241A1 (es) * | 2002-04-04 | 2005-02-16 | Biogen Inc | Heteroarilos trisustituidos y metodos para su produccion y uso de los mismos |
| DE60328028D1 (de) * | 2002-09-18 | 2009-07-30 | Pfizer Prod Inc | Imidazolverbindungen als inhibitoren des transformierenden wachstumsfaktors (twf) |
| CA2545942C (fr) * | 2003-11-14 | 2012-07-10 | Lorus Therapeutics Inc. | Imidazoles d'aryle et leur utilisation comme agents anticancereux |
| CA2556944C (fr) * | 2004-03-05 | 2012-10-09 | Taisho Pharmaceutical Co., Ltd. | Derive de thiazole |
| KR100749566B1 (ko) * | 2004-04-21 | 2007-08-16 | 이화여자대학교 산학협력단 | Alk5 및/또는 alk4 억제제로 유효한 2-피리딜이치환된 이미다졸 유도체 |
| US20060106020A1 (en) * | 2004-04-28 | 2006-05-18 | Rodgers James D | Tetracyclic inhibitors of Janus kinases |
| PE20060315A1 (es) * | 2004-05-24 | 2006-05-15 | Irm Llc | Compuestos de tiazol como moduladores de ppar |
| US7453002B2 (en) * | 2004-06-15 | 2008-11-18 | Bristol-Myers Squibb Company | Five-membered heterocycles useful as serine protease inhibitors |
| JP2007246520A (ja) * | 2006-02-15 | 2007-09-27 | Takeda Yuichiro | Rage阻害剤 |
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2009
- 2009-03-19 KR KR1020107023491A patent/KR101408517B1/ko not_active Expired - Fee Related
- 2009-03-19 CN CN200980114791.8A patent/CN102015686B/zh not_active Expired - Fee Related
- 2009-03-19 KR KR1020137005251A patent/KR20130040258A/ko not_active Abandoned
- 2009-03-19 CA CA2718936A patent/CA2718936A1/fr not_active Abandoned
- 2009-03-19 BR BRPI0908906A patent/BRPI0908906A2/pt not_active IP Right Cessation
- 2009-03-19 WO PCT/EP2009/053245 patent/WO2009115572A2/fr not_active Ceased
- 2009-03-19 EP EP09722890A patent/EP2274300A2/fr not_active Withdrawn
- 2009-03-19 JP JP2011500226A patent/JP5384611B2/ja not_active Expired - Fee Related
- 2009-03-19 US US12/383,035 patent/US8129394B2/en not_active Expired - Fee Related
- 2009-03-19 EA EA201001456A patent/EA201001456A1/ru unknown
- 2009-03-19 AU AU2009227013A patent/AU2009227013B2/en not_active Ceased
- 2009-03-19 MX MX2010010317A patent/MX2010010317A/es active IP Right Grant
- 2009-03-20 AR ARP090101010A patent/AR071283A1/es unknown
- 2009-03-20 CL CL2009000687A patent/CL2009000687A1/es unknown
- 2009-03-20 PE PE2009000430A patent/PE20091656A1/es not_active Application Discontinuation
- 2009-03-20 TW TW098109220A patent/TW201000457A/zh unknown
- 2009-03-20 UY UY0001031724A patent/UY31724A/es not_active Application Discontinuation
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2010
- 2010-09-07 IL IL208063A patent/IL208063A0/en unknown
- 2010-09-10 ZA ZA2010/06505A patent/ZA201006505B/en unknown
- 2010-09-20 DO DO2010000280A patent/DOP2010000280A/es unknown
- 2010-09-20 NI NI201000156A patent/NI201000156A/es unknown
- 2010-09-21 CR CR11681A patent/CR11681A/es not_active Application Discontinuation
- 2010-09-21 SV SV2010003673A patent/SV2010003673A/es not_active Application Discontinuation
- 2010-10-15 MA MA33252A patent/MA32232B1/fr unknown
- 2010-10-20 SM SM201000115T patent/SMAP201000115A/it unknown
- 2010-10-21 CO CO10130723A patent/CO6311078A2/es not_active Application Discontinuation
- 2010-10-21 EC EC2010010559A patent/ECSP10010559A/es unknown
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2013
- 2013-10-02 JP JP2013207483A patent/JP2014040452A/ja not_active Withdrawn
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